Ulf Gyllensten

Detecting TP53 mutations in paired liquid and tissue biopsies from patients with high-grade serous ovarian carcinoma

Widjaja, Amanda Olsson; Micallef, Peter; Lycke, Maria; Österlund, Tobias et al.

Part of International Journal of Cancer, p. 2043-2050, 2026

• DOI for Detecting TP53 mutations in paired liquid and tissue biopsies from patients with high-grade serous ovarian carcinoma
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Composite proteomic and metabolomic plasma biomarkers for detection of colorectal, lung and ovarian cancers

Åkerrén Ögren, Jim; Ekström, Joakim; Rameika, Natallia; Torell, Emma et al.

Part of Molecular Cancer, 2026

• DOI for Composite proteomic and metabolomic plasma biomarkers for detection of colorectal, lung and ovarian cancers
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Deep plasma proteomics identifies and validates an eight-protein biomarker panel that separate benign from malignant tumors in ovarian cancer

Moskov, Mikaela; Hedlund Lindberg, Julia; Lycke, Maria; Ivansson, Emma et al.

Part of Communications Medicine, 2025

• DOI for Deep plasma proteomics identifies and validates an eight-protein biomarker panel that separate benign from malignant tumors in ovarian cancer
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Novel diagnostics for improved treatment of gynecological cancer

Gyllensten, Ulf B.

Part of Upsala Journal of Medical Sciences, 2025

• DOI for Novel diagnostics for improved treatment of gynecological cancer
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The genetic landscape of neuro-related proteins in human plasma

Repetto, Linda; Chen, Jiantao; Yang, Zhijian; Zhai, Ranran et al.

Part of Nature Human Behaviour, p. 2222-2234, 2024

• DOI for The genetic landscape of neuro-related proteins in human plasma

Detecting TP53 mutations in paired liquid and tissue biopsies from patients with high-grade serous ovarian carcinoma

Widjaja, Amanda Olsson; Micallef, Peter; Lycke, Maria; Österlund, Tobias et al.

Part of International Journal of Cancer, p. 2043-2050, 2026

• DOI for Detecting TP53 mutations in paired liquid and tissue biopsies from patients with high-grade serous ovarian carcinoma
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Composite proteomic and metabolomic plasma biomarkers for detection of colorectal, lung and ovarian cancers

Åkerrén Ögren, Jim; Ekström, Joakim; Rameika, Natallia; Torell, Emma et al.

Part of Molecular Cancer, 2026

• DOI for Composite proteomic and metabolomic plasma biomarkers for detection of colorectal, lung and ovarian cancers
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Deep plasma proteomics identifies and validates an eight-protein biomarker panel that separate benign from malignant tumors in ovarian cancer

Moskov, Mikaela; Hedlund Lindberg, Julia; Lycke, Maria; Ivansson, Emma et al.

Part of Communications Medicine, 2025

• DOI for Deep plasma proteomics identifies and validates an eight-protein biomarker panel that separate benign from malignant tumors in ovarian cancer
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Novel diagnostics for improved treatment of gynecological cancer

Gyllensten, Ulf B.

Part of Upsala Journal of Medical Sciences, 2025

• DOI for Novel diagnostics for improved treatment of gynecological cancer
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The genetic landscape of neuro-related proteins in human plasma

Repetto, Linda; Chen, Jiantao; Yang, Zhijian; Zhai, Ranran et al.

Part of Nature Human Behaviour, p. 2222-2234, 2024

• DOI for The genetic landscape of neuro-related proteins in human plasma

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

Keaton, Jacob M; Kamali, Zoha; Xie, Tian; Vaez, Ahmad et al.

Part of Nature Genetics, p. 778-791, 2024

• DOI for Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
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Large-scale proteomics reveals precise biomarkers for detection of ovarian cancer in symptomatic women

Ivansson, Emma; Hedlund Lindberg, Julia; Stålberg, Karin; Sundfeldt, Karin et al.

Part of Scientific Reports, 2024

• DOI for Large-scale proteomics reveals precise biomarkers for detection of ovarian cancer in symptomatic women
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Whole-genome resequencing facilitates the development of a 50K single nucleotide polymorphism genotyping array for Scots pine (Pinus sylvestris L.) and its transferability to other pine species

Barcala, Maximiliano Estravis; van der Valk, Tom; Chen, Zhiqiang; Funda, Tomas et al.

Part of The Plant Journal, p. 944-955, 2024

• DOI for Whole-genome resequencing facilitates the development of a 50K single nucleotide polymorphism genotyping array for Scots pine (Pinus sylvestris L.) and its transferability to other pine species
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Toward ovarian cancer screening with protein biomarkers using dried, self-sampled cervico-vaginal fluid

Hedlund Lindberg, Julia; Widgren, Anna; Ivansson, Emma; Gustavsson, Inger M. et al.

Part of iScience, 2024

• DOI for Toward ovarian cancer screening with protein biomarkers using dried, self-sampled cervico-vaginal fluid
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Next generation pan-cancer blood proteome profiling using proximity extension assay

Alvez, Maria Bueno; Edfors, Fredrik; von Feilitzen, Kalle; Zwahlen, Martin et al.

Part of Nature Communications, 2023

• DOI for Next generation pan-cancer blood proteome profiling using proximity extension assay
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Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

Zhao, Jing Hua; Stacey, David; Eriksson, Niclas; Macdonald-Dunlop, Erin et al.

Part of Nature Immunology, p. 1540-1551, 2023

• DOI for Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
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Genetic insights into resting heart rate and its role in cardiovascular disease

van de Vegte, Yordi; Eppinga, Ruben P.; van der Ende, M. Yldau; Hagemeijer, Yanick et al.

Part of Nature Communications, 2023

• DOI for Genetic insights into resting heart rate and its role in cardiovascular disease
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Forensic prediction of sex, age, height, body mass index, hip-to-waist ratio, smoking status and lipid lowering drugs using epigenetic markers and plasma proteins

Llobet, Mònica Ortega; Johansson, Åsa; Gyllensten, Ulf B.; Allen, Marie et al.

Part of Forensic Science International, 2023

• DOI for Forensic prediction of sex, age, height, body mass index, hip-to-waist ratio, smoking status and lipid lowering drugs using epigenetic markers and plasma proteins
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Complete Mitochondrial DNA Genome Variation in the Swedish Population

Andreaggi, Kimberly; Bodner, Martin; Ring, Joseph D.; Ameur, Adam et al.

Part of Genes, p. 1989-1989, 2023

• DOI for Complete Mitochondrial DNA Genome Variation in the Swedish Population
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Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia

Wen, Jia; Trost, Brett; Engchuan, Worrawat; Halvorsen, Matthew et al.

Part of Molecular Psychiatry, p. 475-482, 2023

• DOI for Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
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Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas

Weishaupt, Holger; Čančer, Matko; Rosén, Gabriela; Holmberg, Karl O. et al.

Part of Neuro-Oncology, p. 97-107, 2023

• DOI for Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas
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Incidence of oncogenic HPV and HPV-related dysplasia five years after a negative HPV test by self-sampling in elderly women

Hermansson, Ruth S.; Olovsson, Matts; Gustavsson, Inger M.; Gyllensten, Ulf B. et al.

Part of Infectious Agents and Cancer, 2022

• DOI for Incidence of oncogenic HPV and HPV-related dysplasia five years after a negative HPV test by self-sampling in elderly women
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Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability

Kierczak, Marcin; Rafati, Nima; Höglund, Julia; Gourlé, Hadrien et al.

Part of Nature Communications, 2022

• DOI for Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability
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Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

Wang, Zhe; Emmerich, Andrew; Pillon, Nicolas J; Moore, Tim et al.

Part of Nature Genetics, p. 1332-1344, 2022

• DOI for Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
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CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations

Höijer, Ida; Emmanouilidou, Anastasia; Östlund, Rebecka; van Schendel, Robin et al.

Part of Nature Communications, 2022

• DOI for CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations
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Genetic Landscape of the ACE2 Coronavirus Receptor

Yang, Zhijian; Macdonald-Dunlop, Erin; Chen, Jiantao; Zhai, Ranran et al.

Part of Circulation, p. 1398-1411, 2022

• DOI for Genetic Landscape of the ACE2 Coronavirus Receptor
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The Value of Whole-Genome Sequencing for Mitochondrial DNA Population Studies: Strategies and Criteria for Extracting High-Quality Mitogenome Haplotypes

Sturk-Andreaggi, Kimberly; Ring, Joseph D.; Ameur, Adam; Gyllensten, Ulf et al.

Part of International Journal of Molecular Sciences, 2022

• DOI for The Value of Whole-Genome Sequencing for Mitochondrial DNA Population Studies: Strategies and Criteria for Extracting High-Quality Mitogenome Haplotypes
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Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.

Gyllensten, Ulf B.; Hedlund-Lindberg, Julia; Svensson, Johanna; Manninen, Johanna et al.

Part of Cancers, 2022

• DOI for Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.
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Data-driven analysis of a validated risk score for ovarian cancer identifies clinically distinct patterns during follow-up and treatment

Enroth, Stefan; Ivansson, Emma; Hedlund Lindberg, Julia; Lycke, Maria et al.

Part of Communications Medicine, 2022

• DOI for Data-driven analysis of a validated risk score for ovarian cancer identifies clinically distinct patterns during follow-up and treatment
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Implementing precision medicine in a regionally organized healthcare system in Sweden.

Fioretos, Thoas; Wirta, Valtteri; Cavelier, Lucia; Berglund, Eva et al.

Part of Nature Medicine, p. 1980-1982, 2022

• DOI for Implementing precision medicine in a regionally organized healthcare system in Sweden.

Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19

Klaric, Lucija; Gisby, Jack S; Papadaki, Artemis; Muckian, Marisa D et al.

Part of medRxiv : the preprint server for health sciences, p. 1-28, 2021

• DOI for Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19

Identification of Candidate Protein Biomarkers for CIN2+ Lesions from Self-Sampled, Dried Cervico-Vaginal Fluid Using LC-MS/MS

Lara Gutiérrez, Ariadna; Hedlund Lindberg, Julia; Shevchenko, Ganna; Gustavsson, Inger et al.

Part of Cancers, 2021

• DOI for Identification of Candidate Protein Biomarkers for CIN2+ Lesions from Self-Sampled, Dried Cervico-Vaginal Fluid Using LC-MS/MS
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Comparison of vaginal self-sampling and cervical sampling by medical professionals for the detection of HPV and CIN2+: a randomized study

Aarnio, Riina; Isacson, Isabella; Sanner, Karin; Gustavsson, Inger M. et al.

Part of International Journal of Cancer, p. 3051-3059, 2021

• DOI for Comparison of vaginal self-sampling and cervical sampling by medical professionals for the detection of HPV and CIN2+: a randomized study
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Immune cells lacking Y chromosome show dysregulation of autosomal gene expression

Dumanski, Jan P.; Halvardson, Jonatan; Davies, Hanna; Rychlicka-Buniowska, Edyta et al.

Part of Cellular and Molecular Life Sciences (CMLS), p. 4019-4033, 2021

• DOI for Immune cells lacking Y chromosome show dysregulation of autosomal gene expression
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Patterns of Human Leukocyte Antigen Class I and Class II Associations and Cancer

Liu, Zhiwei; Derkach, Andriy; Yu, Kelly J.; Yeager, Meredith et al.

Part of Cancer Research, p. 1148-1152, 2021

• DOI for Patterns of Human Leukocyte Antigen Class I and Class II Associations and Cancer

Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomes

Ilumae, Anne-Mai; Post, Helen; Flores, Rodrigo; Karmin, Monika et al.

Part of European Journal of Human Genetics, p. 1510-1519, 2021

• DOI for Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomes

Brush Samples of Oral Lesions to FTA Elute Card for High-risk Human Papilloma Virus Diagnosis

Runow Stark, Christina; Gustavsson, Inger; Horal, Peter; Kotopouli, Maria et al.

Part of Anticancer Research, p. 269-277, 2021

• DOI for Brush Samples of Oral Lesions to FTA Elute Card for High-risk Human Papilloma Virus Diagnosis

Acceptability of self- collection for human papillomavirus detection in the Eastern Cape, South Africa

Taku, Ongeziwe; Meiring, Tracy L.; Gustavsson, Inger M.; Phohlo, Keletso et al.

Part of PLOS ONE, 2020

• DOI for Acceptability of self- collection for human papillomavirus detection in the Eastern Cape, South Africa
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Temporal changes in the vaginal microbiota in self-samples and its association with persistent HPV16 infection and CIN2+

Berggrund, Malin; Gustavsson, Inger M.; Aarnio, Riina; Lindberg, Julia Hedlund et al.

Part of Virology Journal, 2020

• DOI for Temporal changes in the vaginal microbiota in self-samples and its association with persistent HPV16 infection and CIN2+
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Cost-effectiveness analysis of repeated self-sampling for HPV testing in primary cervical screening: a randomized study

Aarnio, Riina; Östensson, Ellinor; Olovsson, Matts; Gustavsson, Inger M. et al.

Part of BMC Cancer, 2020

• DOI for Cost-effectiveness analysis of repeated self-sampling for HPV testing in primary cervical screening: a randomized study

SweHLA: the high confidence HLA typing bio-resource drawn from 1000 Swedish genomes

Nordin, Jessika; Ameur, Adam; Lindblad-Toh, Kerstin; Gyllensten, Ulf et al.

Part of European Journal of Human Genetics, p. 627-635, 2020

• DOI for SweHLA: the high confidence HLA typing bio-resource drawn from 1000 Swedish genomes
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Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

Halvorsen, Matthew; Huh, Ruth; Oskolkov, Nikolay; Wen, Jia et al.

Part of Nature Communications, 2020

• DOI for Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia
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The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderly

Pinese, Mark; Lacaze, Paul; Rath, Emma M.; Stone, Andrew et al.

Part of Nature Communications, 2020

• DOI for The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderly
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Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

Höijer, Ida; Johansson, Josefin; Gudmundsson, Sanna; Chin, Chen-Shan et al.

Part of Genome Biology, 2020

• DOI for Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity
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Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

Folkersen, Lasse; Gustafsson, Stefan; Wang, Qin; Hvidberg Hansen, Daniel et al.

Part of Nature Metabolism, p. 1135-1148, 2020

• DOI for Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human Genomes

Fatima, Nazeefa; Petri, Anna; Gyllensten, Ulf; Feuk, Lars et al.

Part of Genes, 2020

• DOI for Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human Genomes
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Preoperative Fasting and General Anaesthesia Alter the Plasma Proteome

Gyllensten, Ulf B.; Bosdotter Enroth, Sofia; Stålberg, Karin; Sundfeldt, Karin et al.

Part of Cancers, 2020

• DOI for Preoperative Fasting and General Anaesthesia Alter the Plasma Proteome
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Human papillomavirus prevalence and risk factors among HIV-negative and HIV-positive women residing in rural Eastern Cape, South Africa

Taku, Ongeziwe; Businge, Charles B.; Mdaka, Mana L.; Phohlo, Keletso et al.

Part of International Journal of Infectious Diseases, p. 176-182, 2020

• DOI for Human papillomavirus prevalence and risk factors among HIV-negative and HIV-positive women residing in rural Eastern Cape, South Africa
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Identification of Candidate Plasma Protein Biomarkers for Cervical Cancer Using the Multiplex Proximity Extension Assay

Berggrund, Malin; Enroth, Stefan; Lundberg, Martin; Assarsson, Erika et al.

Part of Molecular & Cellular Proteomics, p. 735-743, 2019

• DOI for Identification of Candidate Plasma Protein Biomarkers for Cervical Cancer Using the Multiplex Proximity Extension Assay

HPV viral load in self-collected vaginal fluid samples as predictor for presence of cervical intraepithelial neoplasia.

Berggrund, Malin; Gustavsson, Inger M.; Aarnio, Riina; Lindberg, Julia Hedlund et al.

Part of Virology Journal, 2019

• DOI for HPV viral load in self-collected vaginal fluid samples as predictor for presence of cervical intraepithelial neoplasia.
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Diagnostic excision of the cervix in women over 40 years with human papilloma virus persistency and normal cytology

Aarnio, Riina; Wikström, Ingrid; Gustavsson, Inger M.; Gyllensten, Ulf B. et al.

Part of European journal of obstetrics & gynecology and reproductive biology: X, 2019

• DOI for Diagnostic excision of the cervix in women over 40 years with human papilloma virus persistency and normal cytology
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Associations of autozygosity with a broad range of human phenotypes

Clark, David W.; Karlsson, Torgny; Sennblad, Bengt; Gyllensten, Ulf B. et al.

Part of Nature Communications, 2019

• DOI for Associations of autozygosity with a broad range of human phenotypes
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New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

Shrine, Nick; Guyatt, Anna L.; Erzurumluoglu, A. Mesut; Jackson, Victoria E. et al.

Part of Nature Genetics, p. 481-493, 2019

• DOI for New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

Sakornsakolpat, Phuwanat; Prokopenko, Dmitry; Lamontagne, Maxime; Reeve, Nicola F. et al.

Part of Nature Genetics, p. 494-505, 2019

• DOI for Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

Clinical validation of the HPVIR high-risk HPV test on cervical samples according to the international guidelines for human papillomavirus DNA test requirements for cervical cancer screening

Gustavsson, Inger M.; Aarnio, Riina; Myrnäs, Mattias; Lindberg, Julia Hedlund et al.

Part of Virology Journal, 2019

• DOI for Clinical validation of the HPVIR high-risk HPV test on cervical samples according to the international guidelines for human papillomavirus DNA test requirements for cervical cancer screening
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High throughput proteomics identifies a high-accuracy 11 plasma protein biomarker signature for ovarian cancer

Enroth, Stefan; Berggrund, Malin; Lycke, Maria; Broberg, John et al.

Part of Communications Biology, 2019

• DOI for High throughput proteomics identifies a high-accuracy 11 plasma protein biomarker signature for ovarian cancer
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Randomised study of HPV prevalence and detection of CIN2+ in vaginal self-sampling compared to cervical specimens collected by medical personnel.

Gustavsson, Inger M.; Aarnio, Riina; Berggrund, Malin; Lindberg, Julia Hedlund et al.

Part of International Journal of Cancer, p. 89-97, 2019

• DOI for Randomised study of HPV prevalence and detection of CIN2+ in vaginal self-sampling compared to cervical specimens collected by medical personnel.

Epigenome-wide association study of lung function level and its change

Imboden, Medea; Wielscher, Matthias; Rezwan, Faisal I; Amaral, André F S et al.

Part of European Respiratory Journal, 2019

• DOI for Epigenome-wide association study of lung function level and its change
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Invasive cervical tumors with high and low HPV titer represent molecular subgroups with different disease etiology

Cui, Tao; Enroth, Stefan; Ameur, Adam; Gustavsson, Inger et al.

Part of Carcinogenesis, p. 269-278, 2019

• DOI for Invasive cervical tumors with high and low HPV titer represent molecular subgroups with different disease etiology

Cervical dysplasia in elderly women performing repeated self-sampling for HPV testing

Lindström, Annika; Sanchez Hermansson, Ruth; Gustavsson, Inger M.; Lindberg, Julia Hedlund et al.

Part of PLOS ONE, 2018

• DOI for Cervical dysplasia in elderly women performing repeated self-sampling for HPV testing
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A two-step strategy for identification of plasma protein biomarkers for endometrial and ovarian cancer

Enroth, Stefan; Berggrund, Malin; Lycke, Maria; Lundberg, Martin et al.

Part of Clinical Proteomics, 2018

• DOI for A two-step strategy for identification of plasma protein biomarkers for endometrial and ovarian cancer
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A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood

Jiang, Jiyang; Thalamuthu, Anbupalam; Ho, Jennifer E.; Mahajan, Anubha et al.

Part of Frontiers in Genetics, 2018

• DOI for A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

Evangelou, Evangelos; Warren, Helen R; Mosen-Ansorena, David; Mifsud, Borbala et al.

Part of Nature Genetics, p. 1412-1425, 2018

• DOI for Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

Meta-analysis of exome array data identifies six novel genetic loci for lung function.

Jackson, Victoria E; Latourelle, Jeanne C; Wain, Louise V; Smith, Albert V et al.

Part of Wellcome open research, 2018

• DOI for Meta-analysis of exome array data identifies six novel genetic loci for lung function.

Genetic variants influencing phenotypic variance heterogeneity

Ek, Weronica E; Rask-Andersen, Mathias; Karlsson, Torgny; Enroth, Stefan et al.

Part of Human Molecular Genetics, p. 799-810, 2018

• DOI for Genetic variants influencing phenotypic variance heterogeneity

Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing

Höijer, Ida; Tsai, Yu-Chih; Clark, Tyson A.; Kotturi, Paul et al.

Part of Human Mutation, p. 1262-1272, 2018

• DOI for Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing
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De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data

Ameur, Adam; Che, Huiwen; Martin, Marcel; Bunikis, Ignas et al.

Part of Genes, 2018

• DOI for De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data
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Systemic and specific effects of antihypertensive and lipid-lowering medication on plasma protein biomarkers for cardiovascular diseases

Enroth, Stefan; Maturi, Varun; Berggrund, Malin; Bosdotter Enroth, Sofia et al.

Part of Scientific Reports, 2018

• DOI for Systemic and specific effects of antihypertensive and lipid-lowering medication on plasma protein biomarkers for cardiovascular diseases
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Targeted plasma proteomics identifies a novel, robust association between cornulin and Swedish moist snuff

Sundkvist, Anneli; Myte, Robin; Bodén, Stina; Enroth, Stefan et al.

Part of Scientific Reports, 2018

• DOI for Targeted plasma proteomics identifies a novel, robust association between cornulin and Swedish moist snuff
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Randomised study shows that repeated self-sampling and HPV test has more than two-fold higher detection rate of women with CIN2+ histology than Pap smear cytology

Gustavsson, Inger M.; Aarnio, Riina; Berggrund, Malin; Lindberg, Julia Hedlund et al.

Part of British Journal of Cancer, p. 896-904, 2018

• DOI for Randomised study shows that repeated self-sampling and HPV test has more than two-fold higher detection rate of women with CIN2+ histology than Pap smear cytology
• Download full text (pdf) of Randomised study shows that repeated self-sampling and HPV test has more than two-fold higher detection rate of women with CIN2+ histology than Pap smear cytology

Epigenome-wide DNA methylation study of IgE concentration in relation to self-reported allergies

Ek, Weronica E.; Ahsan, Muhammad; Rask-Andersen, Mathias; Liang, Liming et al.

Part of Epigenomics, p. 407-418, 2017

• DOI for Epigenome-wide DNA methylation study of IgE concentration in relation to self-reported allergies

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

Wain, Louise V.; Vaez, Ahmad; Jansen, Rick; Joehanes, Roby et al.

Part of Hypertension, 2017

• DOI for Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

Genome-wide physical activity interactions in adiposity: A meta-analysis of 200,452 adults.

Graff, Mariaelisa; Scott, Robert A; Justice, Anne E; Young, Kristin L et al.

Part of PLOS Genetics, 2017

• DOI for Genome-wide physical activity interactions in adiposity: A meta-analysis of 200,452 adults.
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Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease

Folkersen, Lasse; Fauman, Eric; Sabater-Lleal, Maria; Strawbridge, Rona J et al.

Part of PLOS Genetics, 2017

• DOI for Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease
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The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases.

Ahsan, Muhammad; Ek, Weronica E; Rask-Andersen, Mathias; Karlsson, Torgny et al.

Part of PLOS Genetics, 2017

• DOI for The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases.
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SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population

Ameur, Adam; Dahlberg, Johan; Olason, Pall; Vezzi, Francesco et al.

Part of European Journal of Human Genetics, p. 1253-1260, 2017

• DOI for SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Warren, Helen R.; Evangelou, Evangelos; Cabrera, Claudia P.; Gao, He et al.

Part of Nature Genetics, p. 403-415, 2017

• DOI for Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.

Wain, Louise V; Shrine, Nick; Artigas, María Soler; Erzurumluoglu, A Mesut et al.

Part of Nature Genetics, p. 416-425, 2017

• DOI for Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.

Evidence for large-scale gene-by-smoking interaction effects on pulmonary function

Aschard, Hugues; Tobin, Martin D; Hancock, Dana B; Skurnik, David et al.

Part of International Journal of Epidemiology, p. 894-904, 2017

• DOI for Evidence for large-scale gene-by-smoking interaction effects on pulmonary function
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PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c

Pan, Gang; Ameur, Adam; Enroth, Stefan; Bysani, Madhusudhan et al.

Part of Nucleic Acids Research, p. 2408-2422, 2017

• DOI for PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c

Genome-wide DNA methylation study identifies genes associated with the cardiovascular biomarker GDF-15

Ek, Weronica E; Hedman, Åsa K; Enroth, Stefan; Morris, Andrew P et al.

Part of Human Molecular Genetics, p. 817-827, 2016

• DOI for Genome-wide DNA methylation study identifies genes associated with the cardiovascular biomarker GDF-15

Identification of novel genetic causes of Rett syndrome-like phenotypes

Lopes, Fatima; Barbosa, Mafalda; Ameur, Adam; Soares, Gabriela et al.

Part of Journal of Medical Genetics, p. 190-199, 2016

• DOI for Identification of novel genetic causes of Rett syndrome-like phenotypes

A multiple-phenotype imputation method for genetic studies

Dahl, Andrew; Iotchkova, Valentina; Baud, Amelie; Johansson, Åsa et al.

Part of Nature Genetics, p. 466-472, 2016

• DOI for A multiple-phenotype imputation method for genetic studies

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

Ehret, Georg B.; Ferreira, Teresa; Chasman, Daniel I.; Jackson, Anne U. et al.

Part of Nature Genetics, p. 1171-1184, 2016

• DOI for The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

Epigenome-wide association study reveals differential DNA methylation in individuals with a history of myocardial infarction

Rask-Andersen, Mathias; Martinsson, David; Ahsan, Muhammad; Enroth, Stefan et al.

Part of Human Molecular Genetics, p. 4739-4748, 2016

• DOI for Epigenome-wide association study reveals differential DNA methylation in individuals with a history of myocardial infarction

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Pattaro, Cristian; Teumer, Alexander; Gorski, Mathias; Chu, Audrey Y et al.

Part of Nature Communications, 2016

• DOI for Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
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Pooled analysis of genome-wide association studies of cervical intraepithelial neoplasia 3 (CIN3) identifies a new susceptibility locus

Chen, Dan; Enroth, Stefan; Liu, Han; Sun, Yang et al.

Part of Oncotarget, p. 42216-42224, 2016

• DOI for Pooled analysis of genome-wide association studies of cervical intraepithelial neoplasia 3 (CIN3) identifies a new susceptibility locus

Effects of Long-Term Storage Time and Original Sampling Month on Biobank Plasma Protein Concentrations

Enroth, Stefan; Hallmans, Göran; Grankvist, Kjell; Gyllensten, Ulf

Part of EBioMedicine, p. 309-314, 2016

• DOI for Effects of Long-Term Storage Time and Original Sampling Month on Biobank Plasma Protein Concentrations
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KLB is associated with alcohol drinking, and its gene product beta-Klotho is necessary for FGF21 regulation of alcohol preference

Schumann, Gunter; Liu, Chunyu; O'Reilly, Paul; Gao, He et al.

Part of Proceedings of the National Academy of Sciences of the United States of America, p. 14372-14377, 2016

• DOI for KLB is associated with alcohol drinking, and its gene product beta-Klotho is necessary for FGF21 regulation of alcohol preference

Protein profiling reveals consequences of lifestyle choices on predicted biological aging

Enroth, Stefan; Bosdotter Enroth, Sofia; Johansson, Åsa; Gyllensten, Ulf

Part of Scientific Reports, 2015

• DOI for Protein profiling reveals consequences of lifestyle choices on predicted biological aging
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Protein profiling reveals consequences of lifestyle choices on predicted biological aging

Enroth, Stefan; Enroth, Sofia Bosdotter; Johansson, Åsa; Gyllensten, Ulf

Part of Scientific Reports, 2015

• DOI for Protein profiling reveals consequences of lifestyle choices on predicted biological aging

Daily self-sampling for high-risk human papillomavirus (HR-HPV) testing.

Sanner, Karin; Wikström, Ingrid; Gustavsson, Inger; Wilander, Erik et al.

Part of Journal of Clinical Virology, p. 1-7, 2015

• DOI for Daily self-sampling for high-risk human papillomavirus (HR-HPV) testing.

MEG3 long noncoding RNA regulates the TGF-β pathway genes through formation of RNA-DNA triplex structures

Mondal, Tanmoy; Subhash, Santhilal; Vaid, Roshan; Enroth, Stefan et al.

Part of Nature Communications, 2015

• DOI for MEG3 long noncoding RNA regulates the TGF-β pathway genes through formation of RNA-DNA triplex structures
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Determination of obesity associated gene variants related to TMEM18 through ultra-deep targeted re-sequencing in a case-control cohort for pediatric obesity.

Rask-Andersen, Mathias; Sällman Almén, Markus; Jacobsson, Josefin A; Ameur, Adam et al.

Part of Genetical Research, 2015

• DOI for Determination of obesity associated gene variants related to TMEM18 through ultra-deep targeted re-sequencing in a case-control cohort for pediatric obesity.

A systematic investigation of the contribution of genetic variation within the MHC region to HPV seropositivity

Chen, Dan; Gaborieau, Valerie; Zhao, Yao; Chabrier, Amelie et al.

Part of Human Molecular Genetics, p. 2681-2688, 2015

• DOI for A systematic investigation of the contribution of genetic variation within the MHC region to HPV seropositivity

Homozygous loss-of-function variants in European cosmopolitan and isolate populations

Kaiser, Vera B; Svinti, Victoria; Prendergast, James G; Chau, You-Ying et al.

Part of Human Molecular Genetics, p. 5464-5475, 2015

• DOI for Homozygous loss-of-function variants in European cosmopolitan and isolate populations
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Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans

Huffman, Jennifer E.; Albrecht, Eva; Teumer, Alexander; Mangino, Massimo et al.

Part of PLOS ONE, 2015

• DOI for Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans
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Identification of novel genetic causes of Rett syndrome-like phenotypes by whole exome sequencing

Lopes, Fatima; Barbosa, Mafalda; Temudo, Teresa; de Sa, Joaquim et al.

Part of International Journal of Developmental Neuroscience, p. 99-99, 2015

• DOI for Identification of novel genetic causes of Rett syndrome-like phenotypes by whole exome sequencing

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Winkler, Thomas W.; Justice, Anne E.; Graff, Mariaelisa; Barata, Llilda et al.

Part of PLOS Genetics, 2015

• DOI for The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
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Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

Soler Artigas, María; Wain, Louise V; Miller, Suzanne; Kheirallah, Abdul Kader et al.

Part of Nature Communications, 2015

• DOI for Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
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Analysis of the genetic architecture of susceptibility to cervical cancer indicates that common SNPs explain a large proportion of the heritability

Chen, Dan; Cui, Tao; Ek, Weronica E.; Liu, Han et al.

Part of Carcinogenesis, p. 992-998, 2015

• DOI for Analysis of the genetic architecture of susceptibility to cervical cancer indicates that common SNPs explain a large proportion of the heritability

Genetic studies of body mass index yield new insights for obesity biology

Locke, Adam E; Kahali, Bratati; Berndt, Sonja I; Justice, Anne E et al.

Part of Nature, p. 197-206, 2015

• DOI for Genetic studies of body mass index yield new insights for obesity biology

Effect of genetic and environmental factors on protein biomarkers for common non-communicable disease and use of personally normalized plasma protein profiles (PNPPP)

Enroth, Stefan; Enroth, Sofia Bosdotter; Johansson, Åsa; Gyllensten, Ulf

Part of Biomarkers, p. 355-364, 2015

• DOI for Effect of genetic and environmental factors on protein biomarkers for common non-communicable disease and use of personally normalized plasma protein profiles (PNPPP)

Directional dominance on stature and cognition in diverse human populations

Joshi, Peter K; Esko, Tonu; Mattsson, Hannele; Eklund, Niina et al.

Part of Nature, p. 459-462, 2015

• DOI for Directional dominance on stature and cognition in diverse human populations

Pathway analysis of cervical cancer genome-wide association study highlights the MHC region and pathways involved in response to infection

Chen, Dan; Enroth, Stefan; Ivansson, Emma; Gyllensten, Ulf

Part of Human Molecular Genetics, p. 6047-6060, 2014

• DOI for Pathway analysis of cervical cancer genome-wide association study highlights the MHC region and pathways involved in response to infection

Systematic validation of hypothesis-driven candidate genes for cervical cancer in a genome-wide association study

Johanneson, Bo; Chen, Dan; Enroth, Stefan; Cui, Tao et al.

Part of Carcinogenesis, p. 2084-2088, 2014

• DOI for Systematic validation of hypothesis-driven candidate genes for cervical cancer in a genome-wide association study

Genome-wide association analysis identifies six new loci associated with forced vital capacity

Loth, Daan W; Artigas, María Soler; Gharib, Sina A; Wain, Louise V et al.

Part of Nature Genetics, p. 669-677, 2014

• DOI for Genome-wide association analysis identifies six new loci associated with forced vital capacity

HLA Typing By SMRT Sequencing: Advantages Of Full Length HLA Genotyping In Clinical Routine

Cahill, Nicola; Ameur, Adam; Knutson, Carina; Orebrand, Ulrika et al.

Part of Tissue Antigens, p. 113-113, 2014

Defining the role of common variation in the genomic and biological architecture of adult human height

Wood, Andrew R; Esko, Tonu; Yang, Jian; Vedantam, Sailaja et al.

Part of Nature Genetics, p. 1173-1186, 2014

• DOI for Defining the role of common variation in the genomic and biological architecture of adult human height

CanvasDB: a local database infrastructure for analysis of targeted- and whole genome re-sequencing projects

Ameur, Adam; Bunikis, Ignas; Enroth, Stefan; Gyllensten, Ulf

Part of Database, 2014

• DOI for CanvasDB: a local database infrastructure for analysis of targeted- and whole genome re-sequencing projects

Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs

Enroth, Stefan; Johansson, Åsa; Bosdotter Enroth, Sofia; Gyllensten, Ulf

Part of Nature Communications, p. 4684, 2014

• DOI for Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs

A cis-eQTL of HLA-DRB1 and a frameshift mutation of MICA contribute to the pattern of association of HLA alleles with cervical cancer

Chen, Dan; Gyllensten, Ulf

Part of Cancer Medicine, p. 445-452, 2014

• DOI for A cis-eQTL of HLA-DRB1 and a frameshift mutation of MICA contribute to the pattern of association of HLA alleles with cervical cancer
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A variant upstream of HLA-DRB1 and multiple variants in MICA influence susceptibility to cervical cancer in a Swedish population

Chen, Dan; Hammer, Joanna; Lindquist, David; Idahl, Annika et al.

Part of Cancer Medicine, p. 190-198, 2014

• DOI for A variant upstream of HLA-DRB1 and multiple variants in MICA influence susceptibility to cervical cancer in a Swedish population
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Increased alpha-9 human papillomavirus species viral load in human immunodeficiency virus positive women

Mbulawa, Zizipho Z. A.; Johnson, Leigh F.; Marais, Dianne J.; Gustavsson, Inger et al.

Part of BMC Infectious Diseases, p. 51, 2014

• DOI for Increased alpha-9 human papillomavirus species viral load in human immunodeficiency virus positive women
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Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencing

Ameur, Adam; Meiring, Tracy L.; Bunikis, Ignas; Häggqvist, Susana et al.

Part of Scientific Reports, p. 4398, 2014

• DOI for Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencing
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TGFβ Receptor 1: An Immune Susceptibility Gene in HPV-Associated Cancer

Levovitz, Chaya; Chen, Dan; Ivansson, Emma; Gyllensten, Ulf et al.

Part of Cancer Research, p. 6833-6844, 2014

• DOI for TGFβ Receptor 1: An Immune Susceptibility Gene in HPV-Associated Cancer

Systematic investigation of contribution of genetic variation in the HLA-DP region to cervical cancer susceptibility

Chen, Dan; Gyllensten, Ulf

Part of Carcinogenesis, p. 1765-1769, 2014

• DOI for Systematic investigation of contribution of genetic variation in the HLA-DP region to cervical cancer susceptibility

Uneven distribution of human papillomavirus 16111 cervical carcinoma in situ and squamous cell carcinoma in older females: A retrospective database study

Andersson, Sonia; Mints, Miriam; Gyllensten, Ulf; Lindell, Monica et al.

Part of Oncology Letters, p. 1528-1532, 2014

• DOI for Uneven distribution of human papillomavirus 16111 cervical carcinoma in situ and squamous cell carcinoma in older females: A retrospective database study

TGFBR1 and other immune-related genes modify susceptibility to HPV-associated head and neck cancer

Levovitz, Chaya; Chen, Dan; Ivansson, Emma; Gyllensten, Ulf et al.

Part of Cancer Research, 2014

• DOI for TGFBR1 and other immune-related genes modify susceptibility to HPV-associated head and neck cancer

Human enterovirus species B in ileocecal Crohn's disease

Nyström, Niklas; Berg, Tove; Lundin, Elin; Skog, Oskar et al.

Part of Clinical and Translational Gastroenterology, 2013

• DOI for Human enterovirus species B in ileocecal Crohn's disease
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Berndt, Sonja I.; Gustafsson, Stefan; Maegi, Reedik; Ganna, Andrea et al.

Part of Nature Genetics, p. 501-U69, 2013

• DOI for Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
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Prevalence and sensitization of atopic allergy and coeliac disease in the Northern Sweden Population Health Study

Enroth, Stefan; Dahlbom, Ingrid; Hansson, Tony; Johansson, Åsa et al.

Part of International Journal of Circumpolar Health, p. 21403, 2013

• DOI for Prevalence and sensitization of atopic allergy and coeliac disease in the Northern Sweden Population Health Study
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Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Koettgen, Anna; Albrecht, Eva; Teumer, Alexander; Vitart, Veronique et al.

Part of Nature Genetics, p. 145-154, 2013

• DOI for Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Genome-wide Association Study of Susceptibility Loci for Cervical Cancer

Chen, Dan; Juko-Pecirep, Ivana; Hammer, Joanna; Ivansson, Emma et al.

Part of Journal of the National Cancer Institute, p. 624-633, 2013

• DOI for Genome-wide Association Study of Susceptibility Loci for Cervical Cancer

Discovery and refinement of loci associated with lipid levels

Willer, Cristen J.; Schmidt, Ellen M.; Sengupta, Sebanti; Peloso, Gina M. et al.

Part of Nature Genetics, p. 1274-1283, 2013

• DOI for Discovery and refinement of loci associated with lipid levels

Common variants associated with plasma triglycerides and risk for coronary artery disease

Do, Ron; Willer, Cristen J.; Schmidt, Ellen M.; Sengupta, Sebanti et al.

Part of Nature Genetics, p. 1345-+, 2013

• DOI for Common variants associated with plasma triglycerides and risk for coronary artery disease

Continuous Aging of the Human DNA Methylome Throughout the Human Lifespan

Johansson, Åsa; Enroth, Stefan; Gyllensten, Ulf

Part of PLOS ONE, 2013

• DOI for Continuous Aging of the Human DNA Methylome Throughout the Human Lifespan
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Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

den Hoed, Marcel; Eijgelsheim, Mark; Esko, Tonu; Brundel, Bianca J. J. M. et al.

Part of Nature Genetics, p. 621-+, 2013

• DOI for Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Animal source food intake and association with blood cholesterol, glycerophospholipids and sphingolipids in a northern Swedish population

Igl, Wilmar; Kamal-Eldin, Afaf; Johansson, Asa; Liebisch, Gerhard et al.

Part of International Journal of Circumpolar Health, p. 421-427, 2013

• DOI for Animal source food intake and association with blood cholesterol, glycerophospholipids and sphingolipids in a northern Swedish population
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Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function

Parsa, Afshin; Fuchsberger, Christian; Koettgen, Anna; O'Seaghdha, Conall M. et al.

Part of Journal of the American Society of Nephrology, p. 2105-2117, 2013

• DOI for Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function

Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits

Randall, Joshua C.; Winkler, Thomas W.; Kutalik, Zoltan; Berndt, Sonja I. et al.

Part of PLOS Genetics, 2013

• DOI for Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits
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Identification of genetic variants influencing the human plasma proteome

Johansson, Åsa; Enroth, Stefan; Palmblad, Magnus; Deelder, Andre M. et al.

Part of Proceedings of the National Academy of Sciences of the United States of America, p. 4673-4678, 2013

• DOI for Identification of genetic variants influencing the human plasma proteome

Omega-3 and omega-6 fatty acids are more efficiently synthesized in populations having a high frequency of the derived FADS-haplotype

Enroth, Stefan; Ameur, Adam; Johansson, Åsa; Gyllensten, Ulf

Part of International Journal of Circumpolar Health, p. 511-512, 2013

Assessing The Effects Of Climate Change On Health And Lifestyle In Sub-Arctic Areas In Sweden - The Northern Sweden Population Health Study

Gyllensten, Ulf; Johansson, Åsa; Enroth, Stefan; Jonasson, Inger

Part of International Journal of Circumpolar Health, p. 516-517, 2013

Projected cost-effectiveness of repeat high-risk human papillomavirus testing using self-collected vaginal samples in the Swedish cervical cancer screening program

Ostensson, Ellinor; Hellstrom, Ann-Cathrin; Hellman, Kristina; Gustavsson, Inger et al.

Part of Acta Obstetricia et Gynecologica Scandinavica, p. 830-840, 2013

• DOI for Projected cost-effectiveness of repeat high-risk human papillomavirus testing using self-collected vaginal samples in the Swedish cervical cancer screening program

Mutations in HNF1A Result in Marked Alterations of Plasma Glycan Profile

Thanabalasingham, Gaya; Huffman, Jennifer E.; Kattla, Jayesh J.; Novokmet, Mislav et al.

Part of Diabetes, p. 1329-1337, 2013

• DOI for Mutations in HNF1A Result in Marked Alterations of Plasma Glycan Profile

Plasma phosphatidylcholine and sphingomyelin concentrations are associated with depression and anxiety symptoms in a Dutch family-based lipidomics study

Demirkan, Ayse; Isaacs, Aaron; Ugocsai, Peter; Liebisch, Gerhard et al.

Part of Journal of Psychiatric Research, p. 357-362, 2013

• DOI for Plasma phosphatidylcholine and sphingomyelin concentrations are associated with depression and anxiety symptoms in a Dutch family-based lipidomics study

Loci Associated with N-Glycosylation of Human Immunoglobulin G Show Pleiotropy with Autoimmune Diseases and Haematological Cancers

Lauc, Gordan; Huffman, Jennifer E.; Pucic, Maja; Zgaga, Lina et al.

Part of PLOS Genetics, 2013

• DOI for Loci Associated with N-Glycosylation of Human Immunoglobulin G Show Pleiotropy with Autoimmune Diseases and Haematological Cancers
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Fine-Mapping of Restless Legs Locus 4 (RLS4) Identifies a Haplotype over the SPATS2L and KCTD18 Genes

Pichler, Irene; Schwienbacher, Christine; Zanon, Alessandra; Fuchsberger, Christian et al.

Part of Journal of Molecular Neuroscience, p. 600-605, 2013

• DOI for Fine-Mapping of Restless Legs Locus 4 (RLS4) Identifies a Haplotype over the SPATS2L and KCTD18 Genes

Causal and Synthetic Associations of Variants in the SERPINA Gene Cluster with Alpha1-antitrypsin Serum Levels

Thun, Gian Andri; Imboden, Medea; Ferrarotti, Ilaria; Kumar, Ashish et al.

Part of PLOS Genetics, 2013

• DOI for Causal and Synthetic Associations of Variants in the SERPINA Gene Cluster with Alpha1-antitrypsin Serum Levels
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Determination of the obesity-associated gene variants within the entire FTO gene by ultra-deep targeted sequencing in obese and lean children.

Sällman Almén, Markus; Rask-Andersen, Mathias; Jacobsson, Josefin A; Ameur, Adam et al.

Part of International Journal of Obesity, p. 424-431, 2013

• DOI for Determination of the obesity-associated gene variants within the entire FTO gene by ultra-deep targeted sequencing in obese and lean children.

Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function

Pattaro, Cristian; Koettgen, Anna; Teumer, Alexander; Garnaas, Maija et al.

Part of PLoS Genetics, 2012

• DOI for Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function
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Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids

Ameur, Adam; Enroth, Stefan; Johansson, Åsa; Zaboli, Ghazal et al.

Part of American Journal of Human Genetics, p. 809-820, 2012

• DOI for Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids

Evidence of Inbreeding Depression on Human Height

McQuillan, Ruth; Eklund, Niina; Pirastu, Nicola; Kuningas, Maris et al.

Part of PLOS Genetics, 2012

• DOI for Evidence of Inbreeding Depression on Human Height
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Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

Chasman, Daniel I.; Fuchsberger, Christian; Pattaro, Cristian; Teumer, Alexander et al.

Part of Human Molecular Genetics, p. 5329-5343, 2012

• DOI for Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

Polymorphisms in sh2b1 and spns1 loci are associated with triglyceride levels in a healthy population in northern Sweden

Västermark, Åke; Jacobsson, Josefin; Johansson, Åsa; Fredriksson, Robert et al.

Part of Journal of Genetics, p. 237-240, 2012

• DOI for Polymorphisms in sh2b1 and spns1 loci are associated with triglyceride levels in a healthy population in northern Sweden

Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations

Demirkan, Ayse; van Duijn, Cornelia M.; Ugocsai, Peter; Isaacs, Aaron et al.

Part of PLoS Genetics, 2012

• DOI for Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations
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Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits

Zaboli, Ghazal; Ameur, Adam; Igl, Wilmar; Johansson, Åsa et al.

Part of European Journal of Human Genetics, p. 77-83, 2012

• DOI for Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits

Data-driven unbiased curation of the TP53 tumor suppressor gene mutation database and validation by ultradeep sequencing of human tumors

Edlund, Karolina; Larsson, Ola; Ameur, Adam; Bunikis, Ignas et al.

Part of Proceedings of the National Academy of Sciences of the United States of America, p. 9551-9556, 2012

• DOI for Data-driven unbiased curation of the TP53 tumor suppressor gene mutation database and validation by ultradeep sequencing of human tumors

Genetic variants near the MGAT1 gene are associated with body weight, BMI and fatty acid metabolism among adults and children

Jacobsson, Josefin; Rask-Andersen, Mathias; Risérus, Ulf; Moschonis, G et al.

Part of International Journal of Obesity, p. 119-129, 2012

• DOI for Genetic variants near the MGAT1 gene are associated with body weight, BMI and fatty acid metabolism among adults and children

Contribution of TMC6 and TMC8 (EVER1 and EVER2) variants to cervical cancer susceptibility

Castro, Felipe A; Ivansson, Emma L; Schmitt, Markus; Juko-Pecirep, Ivana et al.

Part of International Journal of Cancer, p. 349-355, 2012

• DOI for Contribution of TMC6 and TMC8 (EVER1 and EVER2) variants to cervical cancer susceptibility

Detection of Human Papillomavirus Among Women in Laos Feasibility of Using Filter Paper Card and Prevalence of High-Risk Types

Phongsavan, Keokedthong; Gustavsson, Inger; Marions, Lena; Phengsavanh, Alongkone et al.

Part of International Journal of Gynecological Cancer, p. 1398-1406, 2012

• DOI for Detection of Human Papillomavirus Among Women in Laos Feasibility of Using Filter Paper Card and Prevalence of High-Risk Types

Multiply-primed rolling circle amplification of human papillomavirus using sequence-specific primers

Marincevic-Zuniga, Yanara; Gustavsson, Inger; Gyllensten, Ulf

Part of Virology, p. 57-62, 2012

• DOI for Multiply-primed rolling circle amplification of human papillomavirus using sequence-specific primers

Long noncoding RNA-mediated maintenance of DNA methylation and transcriptional gene silencing

Mohammad, Faizaan; Pandey, Gaurav Kumar; Mondal, Tanmoy; Enroth, Stefan et al.

Part of Development, p. 2792-2803, 2012

• DOI for Long noncoding RNA-mediated maintenance of DNA methylation and transcriptional gene silencing

Next generation RNA-sequencing in prognostic subsets of chronic lymphocytic leukemia

Mansouri, Larry; Gunnarsson, Rebeqa; Sutton, Lesley-Ann; Ameur, Adam et al.

Part of American Journal of Hematology, p. 737-740, 2012

• DOI for Next generation RNA-sequencing in prognostic subsets of chronic lymphocytic leukemia

Primary high-risk HPV screening for cervical cancer in post-menopausal women

Gyllensten, Ulf; Gustavsson, Inger; Lindell, Monica; Wilander, Erik

Part of Gynecologic Oncology, p. 343-345, 2012

• DOI for Primary high-risk HPV screening for cervical cancer in post-menopausal women

Short-time repeat high-risk HPV testing by self-sampling for screening of cervical cancer

Gyllensten, Ulf; Sanner, Karin; Gustavsson, Inger; Lindell, Monica et al.

Part of British Journal of Cancer, p. 694-697, 2011

• DOI for Short-time repeat high-risk HPV testing by self-sampling for screening of cervical cancer

Evaluation of Fanconi anaemia genes FANCA, FANCC and FANCL in cervical cancer susceptibility

Juko-Pecirep, Ivana; Ivansson, Emma L.; Gyllensten, Ulf B.

Part of Gynecologic Oncology, p. 377-381, 2011

• DOI for Evaluation of Fanconi anaemia genes FANCA, FANCC and FANCL in cervical cancer susceptibility

Ultra-deep sequencing of mouse mitochondrial DNA: Mutational patterns and their origins

Ameur, Adam; Stewart, James B.; Freyer, Christoph; Hagström, Erik et al.

Part of PLoS Genetics, 2011

• DOI for Ultra-deep sequencing of mouse mitochondrial DNA: Mutational patterns and their origins

Glycomics meets lipidomics-associations of N-glycans with classical lipids, glycerophospholipids, and sphingolipids in three European populations

Igl, Wilmar; Polasek, Ozren; Gornik, Olga; Knezevic, Ana et al.

Part of Molecular BioSystems, p. 1852-1862, 2011

• DOI for Glycomics meets lipidomics-associations of N-glycans with classical lipids, glycerophospholipids, and sphingolipids in three European populations

A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample

Obeidat, Ma'en; Wain, Louise V.; Shrine, Nick; Kalsheker, Noor et al.

Part of PLOS ONE, 2011

• DOI for A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample

Variants in STAT5B Associate with Serum TC and LDL-C Levels

Kornfeld, Jan-Wilhelm; Isaacs, Aaron; Vitart, Veronique; Pospisilik, J. Andrew et al.

Part of Journal of Clinical Endocrinology and Metabolism, 2011

• DOI for Variants in STAT5B Associate with Serum TC and LDL-C Levels

Type-specific detection of high-risk human papillomavirus (HPV) in self-sampled cervicovaginal cells applied to FTA elute cartridge

Gustavsson, Inger; Sanner, Karin; Lindell, Monica; Strand, Anders et al.

Part of Journal of Clinical Virology, p. 255-258, 2011

• DOI for Type-specific detection of high-risk human papillomavirus (HPV) in self-sampled cervicovaginal cells applied to FTA elute cartridge

Genetic architecture of circulating lipid levels

Demirkan, Ayse; Amin, Najaf; Isaacs, Aaron; Jarvelin, Marjo-Riitta et al.

Part of European Journal of Human Genetics, p. 813-819, 2011

• DOI for Genetic architecture of circulating lipid levels

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Wain, Louise V.; Verwoert, Germaine C.; O'Reilly, Paul F.; Shi, Gang et al.

Part of Nature Genetics, p. 1005-1122, 2011

• DOI for Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults

Huffman, Jennifer E.; Knezevic, Ana; Vitart, Veronique; Kattla, Jayesh et al.

Part of Human Molecular Genetics, p. 5000-5011, 2011

• DOI for Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults

A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol

Surakka, Ida; Isaacs, Aaron; Karssen, Lennart C.; Laurila, Pirkka-Pekka P. et al.

Part of PLoS Genetics, 2011

• DOI for A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol

Pathway-based analysis of genetic susceptibility to cervical cancer in situ: HLA-DPB1 affects risk in Swedish women

Ivansson, Emma L.; Juko-Pecirep, Ivana; Erlich, H. A.; Gyllensten, Ulf B.

Part of Genes and Immunity, p. 605-614, 2011

• DOI for Pathway-based analysis of genetic susceptibility to cervical cancer in situ: HLA-DPB1 affects risk in Swedish women

Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain

Ameur, Adam; Zaghlool, Ammar; Halvardson, Jonatan; Wetterbom, Anna et al.

Part of Nature Structural & Molecular Biology, p. 1435-1440, 2011

• DOI for Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

Ehret, Georg B.; Munroe, Patricia B.; Rice, Kenneth M.; Bochud, Murielle et al.

Part of Nature, p. 103-109, 2011

• DOI for Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

The Northern Swedish Population Health Study (NSPHS): a paradigmatic study in a rural population combining community health and basic research

Igl, Wilmar; Johansson, Åsa; Gyllensten, Ulf

Part of Rural and remote health, p. 1363, 2010

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

Pattaro, Cristian; De Grandi, Alessandro; Vitart, Veronique; Hayward, Caroline et al.

Part of BMC Medical Genetics, p. 41, 2010

• DOI for A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

Polasek, Ozren; Hayward, Caroline; Bellenguez, Celine; Vitart, Veronique et al.

Part of BMC Genomics, p. 139, 2010

• DOI for Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

HPV test shows low sensitivity of Pap screen in older women

Gyllensten, Ulf; Lindell, Monica; Gustafsson, Inger; Wilander, Erik

Part of The Lancet Oncology, p. 509-510, 2010

• DOI for HPV test shows low sensitivity of Pap screen in older women

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Voight, Benjamin F.; Scott, Laura J.; Steinthorsdottir, Valgerdur; Morris, Andrew P. et al.

Part of Nature Genetics, p. 579-589, 2010

• DOI for Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Allen, Hana Lango; Estrada, Karol; Lettre, Guillaume; Berndt, Sonja I. et al.

Part of Nature, p. 832-838, 2010

• DOI for Hundreds of variants clustered in genomic loci and biological pathways affect human height

Modeling of Environmental Effects in Genome-Wide Association Studies Identifies SLC2A2 and HP as Novel Loci Influencing Serum Cholesterol Levels

Igl, Wilmar; Johansson, Åsa; Wilson, James F.; Wild, Sarah H. et al.

Part of PLoS Genetics, 2010

• DOI for Modeling of Environmental Effects in Genome-Wide Association Studies Identifies SLC2A2 and HP as Novel Loci Influencing Serum Cholesterol Levels

Genes predict village of origin in rural Europe

O'Dushlaine, Colm; McQuillan, Ruth; Weale, Michael E.; Crouch, Daniel J. M. et al.

Part of European Journal of Human Genetics, p. 1269-1270, 2010

• DOI for Genes predict village of origin in rural Europe

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Heid, Iris M; Jackson, Anne U; Randall, Joshua C; Winkler, Thomas W et al.

Part of Nature Genetics, p. 949-960, 2010

• DOI for Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Biological, clinical and population relevance of 95 loci for blood lipids

Teslovich, Tanya M.; Musunuru, Kiran; Smith, Albert V.; Edmondson, Andrew C. et al.

Part of Nature, p. 707-713, 2010

• DOI for Biological, clinical and population relevance of 95 loci for blood lipids

Genomics Meets Glycomics-The First GWAS Study of Human N-Glycome Identifies HNF1 alpha as a Master Regulator of Plasma Protein Fucosylation

Lauc, Gordan; Essafi, Abdelkader; Huffman, Jennifer E.; Hayward, Caroline et al.

Part of PLoS Genetics, 2010

• DOI for Genomics Meets Glycomics-The First GWAS Study of Human N-Glycome Identifies HNF1 alpha as a Master Regulator of Plasma Protein Fucosylation

Ska HPV-test ersätta gynekologisk cellprovtagning hos kvinnor i menopaus?

Gustavsson, Inger; Gyllensten, Ulf; Lindell, Monica; Wilander, Erik

Part of Läkartidningen, p. 528-529, 2010

Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene

Johansson, Åsa; Marroni, Fabio; Hayward, Caroline; Franklin, Christopher S. et al.

Part of Obesity, p. 803-808, 2010

• DOI for Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene

New loci associated with kidney function and chronic kidney disease

Köttgen, Anna; Pattaro, Cristian; Böger, Carsten A.; Fuchsberger, Christian et al.

Part of Nature Genetics, p. 376-384, 2010

• DOI for New loci associated with kidney function and chronic kidney disease

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Dupuis, Josée; Langenberg, Claudia; Prokopenko, Inga; Saxena, Richa et al.

Part of Nature Genetics, p. 105-116, 2010

• DOI for New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Interaction of immunological genes on chromosome 2q33 and IFNG in susceptibility to cervical cancer

Ivansson, Emma L.; Juko-Pecirep, Ivana; Gyllensten, Ulf B.

Part of Gynecologic Oncology, p. 544-548, 2010

• DOI for Interaction of immunological genes on chromosome 2q33 and IFNG in susceptibility to cervical cancer

Genome-wide association study identifies five loci associated with lung function

Repapi, Emmanouela; Sayers, Ian; Wain, Louise V.; Burton, Paul R. et al.

Part of Nature Genetics, p. 36-44, 2010

• DOI for Genome-wide association study identifies five loci associated with lung function

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Speliotes, Elizabeth K.; Willer, Cristen J.; Berndt, Sonja I.; Monda, Keri L. et al.

Part of Nature Genetics, p. 937-948, 2010

• DOI for Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

A Fas Gene Polymorphism Influences Herpes Simplex Virus Type 2 Infection in South African Women

Chatterjee, Koushik; Dandara, Collet; Gyllensten, Ulf; van der Merwe, Lize et al.

Part of Journal of Medical Virology, p. 2082-2086, 2010

• DOI for A Fas Gene Polymorphism Influences Herpes Simplex Virus Type 2 Infection in South African Women

Comparison of participant information and informed consent forms of five European studies in genetic isolated populations

Mascalzoni, Deborah; Janssens, A. Cecile J. W.; Stewart, Alison; Pramstaller, Peter et al.

Part of European Journal of Human Genetics, p. 296-302, 2010

• DOI for Comparison of participant information and informed consent forms of five European studies in genetic isolated populations

Global and unbiased detection of splice junctions from RNA-seq data

Ameur, Adam; Wetterbom, Anna; Feuk, Lars; Gyllensten, Ulf

Part of Genome Biology, 2010

• DOI for Global and unbiased detection of splice junctions from RNA-seq data

Identification of novel exons and transcribed regions by chimpanzee transcriptome sequencing

Wetterbom, Anna; Ameur, Adam; Feuk, Lars; Gyllensten, Ulf et al.

Part of Genome Biology, 2010

• DOI for Identification of novel exons and transcribed regions by chimpanzee transcriptome sequencing

Genome-wide analysis of chimpanzee genes with premature termination codons

Wetterbom, Anna; Gyllensten, Ulf; Cavelier, Lucia; Bergström, Tomas F.

Part of BMC Genomics, p. 56, 2009

• DOI for Genome-wide analysis of chimpanzee genes with premature termination codons

Extended haplotypes in the growth hormone releasing hormone receptor gene (GHRHR) are associated with normal variation in height

Johansson, Åsa; Jonasson, Inger; Gyllensten, Ulf

Part of PLOS ONE, 2009

• DOI for Extended haplotypes in the growth hormone releasing hormone receptor gene (GHRHR) are associated with normal variation in height

Genetic determinants of circulating sphingolipid concentrations in European populations

Hicks, Andrew A.; Pramstaller, Peter P.; Johansson, Åsa; Vitart, Veronique et al.

Part of PLoS genetics, 2009

• DOI for Genetic determinants of circulating sphingolipid concentrations in European populations

Temporal trends over 3 decades and intrafamilial clustering of HPV types in Swedish patients with cervical cancer in situ

Ivansson, Emma L; Gustavsson, Inger M; Wilander, Erik; Magnusson, Patrik K E et al.

Part of International Journal of Cancer, p. 2930-2935, 2009

• DOI for Temporal trends over 3 decades and intrafamilial clustering of HPV types in Swedish patients with cervical cancer in situ

Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

Johansson, Åsa; Marroni, Fabio; Hayward, Caroline; Franklin, Christopher S. et al.

Part of Human Molecular Genetics, p. 373-380, 2009

• DOI for Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium

Heard-Costa, Nancy L; Zillikens, M Carola; Monda, Keri L; Johansson, Åsa et al.

Part of PLoS genetics, 2009

• DOI for NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Aulchenko, Yurii S; Ripatti, Samuli; Lindqvist, Ida; Boomsma, Dorret et al.

Part of Nature Genetics, p. 47-55, 2009

• DOI for Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Adherence to a traditional lifestyle affects food and nutrient intake among modern Swedish Sami

Ross, Alastair B; Johansson, Åsa; Vavruch-Nilsson, Veronika; Hassler, Sven et al.

Part of International Journal of Circumpolar Health, p. 372-385, 2009

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

Kolz, Melanie; Johnson, Toby; Sanna, Serena; Teumer, Alexander et al.

Part of PLoS genetics, 2009

• DOI for Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

Use of FTA card for dry collection, transportation and storage of cervical cell specimen to detect high-risk HPV

Gustavsson, Inger; Lindell, Monica; Wilander, Erik; Strand, Anders et al.

Part of Journal of Clinical Virology, p. 112-116, 2009

• DOI for Use of FTA card for dry collection, transportation and storage of cervical cell specimen to detect high-risk HPV

TP53 codon 72 polymorphism and cervical cancer: a pooled analysis of individual data from 49 studies

Klug, Stefanie J; Ressing, Meike; Koenig, Jochem; Abba, Martin C et al.

Part of The Lancet Oncology, p. 772-784, 2009

• DOI for TP53 codon 72 polymorphism and cervical cancer: a pooled analysis of individual data from 49 studies

Comparison between the Hybrid Capture 2 and the hpVIR real-time PCR for detection of human papillomavirus in women with ASCUS or low grade dysplasia

Gustavsson, Inger; Juko-Pecirep, Ivana; Backlund, Ingrid; Wilander, Erik et al.

Part of Journal of Clinical Virology, p. 85-89, 2009

• DOI for Comparison between the Hybrid Capture 2 and the hpVIR real-time PCR for detection of human papillomavirus in women with ASCUS or low grade dysplasia

Genome-wide linkage analysis of serum creatinine in three isolated European populations

Pattaro, Cristian; Aulchenko, Yurii S.; Isaacs, Aaron; Vitart, Veronique et al.

Part of Kidney International, p. 297-306, 2009

• DOI for Genome-wide linkage analysis of serum creatinine in three isolated European populations

A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project

Marroni, Fabio; Pfeufer, Arne; Aulchenko, Yurii S.; Franklin, Christopher S. et al.

Part of Circulation: Cardiovascular Genetics, p. 322-328, 2009

• DOI for A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project

Fas and FasL gene polymorphisms are not associated with cervical cancer but differ among Black and Mixed-ancestry South Africans

Chatterjee, Koushik; Engelmark, Malin; Gyllensten, Ulf; Dandara, Collet et al.

Part of BMC research notes, p. 238, 2009

• DOI for Fas and FasL gene polymorphisms are not associated with cervical cancer but differ among Black and Mixed-ancestry South Africans

Novel genetic variant in FTO influences insulin levels and insulin resistance in severely obese children and adolescents.

Jacobsson, J. A.; Klovins, Janis; Kapa, I.; Danielsson, P et al.

Part of International Journal of Obesity, p. 1730-1735, 2008

• DOI for Novel genetic variant in FTO influences insulin levels and insulin resistance in severely obese children and adolescents.

Identification of local selective sweeps in human populations since the exodus from Africa

Johansson, Åsa; Gyllensten, Ulf

Part of Hereditas, p. 126-137, 2008

• DOI for Identification of local selective sweeps in human populations since the exodus from Africa

Major gender difference in association of FTO gene variant among severely obese children with obesity and obesity related phenotypes.

Jacobsson, Josefin A.; Danielsson, Pernilla; Svensson, Victoria; Klovins, Janis et al.

Part of Biochemical and Biophysical Research Communications - BBRC, p. 476-482, 2008

• DOI for Major gender difference in association of FTO gene variant among severely obese children with obesity and obesity related phenotypes.

Genetic origin of the Swedish Sami inferred from HLA class I and class II allele frequencies

Johansson, Åsa; Ingman, Max; Mack, Steven J; Erlich, Henry et al.

Part of European Journal of Human Genetics, p. 1341-1349, 2008

• DOI for Genetic origin of the Swedish Sami inferred from HLA class I and class II allele frequencies

SNP frequency estimation using massively parallel sequencing of pooled DNA

Ingman, Max; Gyllensten, Ulf

Part of European Journal of Human Genetics, p. 383-386, 2008

• DOI for SNP frequency estimation using massively parallel sequencing of pooled DNA

MHC loci affecting cervical cancer risk: distinguishing the effects of HLA-DQB1 and non-HLA genes TNF, LTA, TAP1 and TAP2

Ivansson, Emma; Magnusson, Jessica; Magnusson, Patrik; Erlich, Henry et al.

Part of Genes and Immunity, p. 613-623, 2008

• DOI for MHC loci affecting cervical cancer risk: distinguishing the effects of HLA-DQB1 and non-HLA genes TNF, LTA, TAP1 and TAP2

Polymorphisms in 9q32 and TSCOT are linked to cervical cancer in affected sib-pairs with high mean age at diagnosis

Engelmark, Malin; Ivansson, Emma; Magnusson, Jessica; Gustavsson, Inger et al.

Part of Human Genetics, p. 437-443, 2008

• DOI for Polymorphisms in 9q32 and TSCOT are linked to cervical cancer in affected sib-pairs with high mean age at diagnosis

Rate variation between mitochondrial domains and adaptive evolution in humans

Ingman, Max; Gyllensten, Ulf

Part of Human Molecular Genetics, p. 2281-2287, 2007

• DOI for Rate variation between mitochondrial domains and adaptive evolution in humans

Variants of chemokine receptor 2 and interleukin 4 receptor, but not interleukin 10 or Fas ligand, increase risk of cervical cancer

Ivansson, Emma; Gustavsson, Inger M.; Magnusson, Jessica; Steiner, Lori et al.

Part of International Journal of Cancer, p. 2451-2457, 2007

• DOI for Variants of chemokine receptor 2 and interleukin 4 receptor, but not interleukin 10 or Fas ligand, increase risk of cervical cancer

Evaluation of the SNP tagging approach in an independent population sample: Array-based SNP discovery in Sami

Johansson, Åsa; Vavruch-Nilsson, Veronika; Cox, David; Frazer, Kelly et al.

Part of Human Genetics, p. 141-150, 2007

• DOI for Evaluation of the SNP tagging approach in an independent population sample: Array-based SNP discovery in Sami

A recent genetic link between Sami and the Volga-Ural region of Russia

Ingman, Max; Gyllensten, Ulf

Part of European Journal of Human Genetics, p. 115-120, 2007

• DOI for A recent genetic link between Sami and the Volga-Ural region of Russia

Full-length sequence analysis of the HLA-DRB1 locus suggests a recent origin of alleles

von Salomé, Jenny; Gyllensten, Ulf; Bergström, Tomas F.

Part of Immunogenetics, p. 261-271, 2007

• DOI for Full-length sequence analysis of the HLA-DRB1 locus suggests a recent origin of alleles

Type-specific persistence of high-risk human papillomavirus infections in the New Independent States of the former Soviet Union Cohort Study

Kulmala, Satu-Maria A.; Shabalova, Irena P.; Petrovitchev, Nikolay; Syrjänen, Kari J. et al.

Part of Cancer Epidemiology, Biomarkers and Prevention, p. 17-22, 2007

• DOI for Type-specific persistence of high-risk human papillomavirus infections in the New Independent States of the former Soviet Union Cohort Study

Prevalence of the most common high-risk HPV genotypes among women in three new independent states of the former Soviet Union

Kulmala, Satu-Maria A.; Shabalova, Irena P.; Petrovitchev, Nikolay; Syrjänen, Kari J. et al.

Part of Journal of Medical Virology, p. 771-781, 2007

• DOI for Prevalence of the most common high-risk HPV genotypes among women in three new independent states of the former Soviet Union

Identification of susceptibility loci for cervical carcinoma by genome scan of affected sib-pairs

Engelmark, Malin T.; Ivansson, Emma L.; Magnusson, Jessica J.; Gustavsson, Inger M. et al.

Part of Human Molecular Genetics, p. 3351-3360, 2006

• DOI for Identification of susceptibility loci for cervical carcinoma by genome scan of affected sib-pairs

Lifestyle, genetics, and disease in Sami.

Ross, Alastair B; Johansson, Asa; Ingman, Max; Gyllensten, Ulf

Part of Croat Med J, p. 553-65, 2006

Early integration of high copy HPV16 detectable in women with normal and low grade cervical cytology and histology.

Kulmala, S-M A; Syrjänen, S M; Gyllensten, Ulf B; Shabalova, I P et al.

Part of J Clin Pathol, p. 513-7, 2006

Height at age 18 years is a strong predictor of attained education later in life: cohort study of over 950,000 Swedish men.

Magnusson, Patrik K E; Rasmussen, Finn; Gyllensten, Ulf B

Part of Int J Epidemiol, p. 658-63, 2006

Forensic analysis of the mitochondrial coding region and association to disease.

Budowle, B.; Gyllensten, Ulf; Chakraborty, R.; Allen, Marie

Part of International journal of legal medicine, p. 314-315, 2005

• DOI for Forensic analysis of the mitochondrial coding region and association to disease.

Linkage disequilibrium between microsatellite markers in the Swedish Sami relative to a worldwide selection of populations.

Johansson, Asa; Vavruch-Nilsson, Veronika; Edin-Liljegren, Anette; Sjölander, Per et al.

Part of Hum Genet, p. 105-13, 2005

Interaction of host and viral risk factors for development of cervical carcinoma in situ

Beskow, Anna H.; Engelmark, Malin T.; Magnusson, Jessica J.; Gyllensten, Ulf B.

Part of International Journal of Cancer, p. 690-692, 2005

• DOI for Interaction of host and viral risk factors for development of cervical carcinoma in situ

High viral loads of human papillomavirus predict risk of invasive cervical carcinoma.

Moberg, M; Gustavsson, I; Wilander, E; Gyllensten, U

Part of Br J Cancer, p. 891-4, 2005

Type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (CIN).

Andersson, S; Safari, H; Mints, M; Lewensohn-Fuchs, I et al.

Part of Br J Cancer, p. 2195-200, 2005

HLA class II allele control of HPV load in carcinoma in situ of the cervix uteri.

Beskow, Anna H; Moberg, Martin; Gyllensten, Ulf B

Part of Int J Cancer, p. 510-4, 2005

Type-specific associations of human papillomavirus load with risk of developing cervical carcinoma in situ.

Moberg, Martin; Gustavsson, Inger; Gyllensten, Ulf

Part of Int J Cancer, p. 854-9, 2004

No evidence of the involvement of the Fas -670 promoter polymorphism in cervical cancer in situ.

Engelmark, Malin T; Renkema, Kirsten Y; Gyllensten, Ulf B

Part of Int J Cancer, p. 1084-5, 2004

Affected sib-pair analysis of the contribution of HLA class I and class II loci to development of cervical cancer.

Engelmark, Malin; Beskow, Anna; Magnusson, Jessica; Erlich, Henry et al.

Part of Hum Mol Genet, p. 1951-8, 2004

A novel method for automatic genotyping of microsatellite markers based on parametric pattern recognition.

Johansson, Åsa; Karlsson, P; Gyllensten, Ulf

Part of Hum Genet, p. 316, 2003

Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines

Ingman, Max; Gyllensten, Ulf

Part of Genome Research, p. 1600-6, 2003

• DOI for Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines

Analysis of the mitochondrial genome in sudden infant death syndrome.

Divne, AM; Rasten-Almqvist, P; Rajs, J; Gyllensten, U et al.

Part of Acta Paediatr, p. 386, 2003

Real-time PCR-based system for simultaneous quantification of human papillomavirus types associated with high risk of cervical cancer

Moberg, Martin; Gustavsson, Inger; Gyllensten, Ulf

Part of J Clin Microbiol, p. 3221, 2003

Real-Time DNA Quantification of Nuclear and Mitochondrial DNA in Forensic Analysis

Andréasson, H.; Gyllensten, Ulf; Allen, Marie

Part of BioTechniques, p. 402-411, 2002

Mitochondrial sequence analysis for forensic identification using pyrosequencing technology.

Andreasson, H; Asp, A; Alderborn, A; Gyllensten, U et al.

Part of Biotechniques, p. 124, 2002

Analysis of the complete human mtDNA genome: methodology and inferences for human evolution

Ingman, Max; Gyllensten, Ulf

Part of Journal of Heredity, p. 454-61, 2001

Susceptibility locus for epidermodysplasia verruciformis not linked to cervical cancer in situ

Beskow, Anna; Rönnholm, Jessica; Magnusson, Patrik K; Gyllensten, Ulf B

Part of Hereditas, p. 61-63, 2001

• DOI for Susceptibility locus for epidermodysplasia verruciformis not linked to cervical cancer in situ

Phylogenetic history of hominoid DRB loci and alleles inferred from intron sequences.

Bergström, Tomas; Erlandsson, Rickard; Engkvist, Hans; Josefsson, Agneta et al.

Part of Immunol Rev, p. 351-65, 1999

Tracing the origin of HLA-DRB1 alleles by microsatellite polymorphism.

Bergström, Tomas; Engkvist, Hans; Erlandsson, Rickard; Josefsson, Agneta et al.

Part of Am J Hum Genet, p. 1709-18, 1999

High resolution genetic typing of the class II HLA-DRB1 locus using group-specific amplification and SSO-hybridisation in microplates

Allen, Marie; Eriksson, Inger; Liu, Limin; Gyllensten, Ulf

Part of Hereditas, p. 161-167, 1998

• DOI for High resolution genetic typing of the class II HLA-DRB1 locus using group-specific amplification and SSO-hybridisation in microplates

Mitochondrial DNA sequencing of shed hairs and saliva on robbery caps: sensitivity and matching probabilities

Allen, Marie; Engström, A-S.; Meyers, S.; Handt, O. et al.

Part of Journal of Forensic Sciences, p. 453-464, 1998

Recent origin of HLA-DRB1 alleles and implications for human evolution.

Bergström, Tomas; Josefsson, Agneta; Erlich, Henry; Gyllensten, Ulf

Part of Nat Genet, p. 237-42, 1998

HLA DQ-DR haplotype and susceptibility to cervical carcinoma: indications of increased risk for development of cervical carcinoma in individuals infected with HPV 18

Allen, Marie; Kalantari, M.; Ylitalo, Natalie; Pettersson, B. et al.

Part of Tissue Antigens, p. 32-37, 1996

HLA sequence polymorphism and the origin of humans.

Erlich, Henry; Bergström, Tomas; Stoneking, Mark; Gyllensten, Ulf

Part of Science, p. 1552-4, 1996

Analysis of HLA-Class II DQA1, DQB1, DRB1 and DPB1 in Italian Multiple Sclerosis Patients

Ciusani, E.; Allen, Marie; Sandberg-Wollheim, M.; Eoli, M. et al.

Part of European journal of immunogenetics, p. 171-178, 1995

Allele-specific HLA-DRB1 amplification of forensic evidence samples with mixed genotypes

Allen, Marie; Saldeen, Tom; Gyllensten, Ulf

Part of BioTechniques, p. 454-463, 1995

PCR-based DNA typing of saliva on stamps and envelopes

Allen, Marie; Saldeen, Tom; Gyllensten, Ulf

Part of BioTechniques, p. 546-552, 1994

Association of susceptibility to multiple sclerosis in Sweden with HLA class II DRB1 and DQB1 alleles

Allen, Marie; Sandberg-Wollheim, Magnhild; Sjögren, Karin; Erlich, Henry A. et al.

Part of Human Immunology, p. 41-8, 1994

• DOI for Association of susceptibility to multiple sclerosis in Sweden with HLA class II DRB1 and DQB1 alleles

A comprehensive polymerase chain reaction-oligonucleotide typing system for the HLA class I A locus

Allen, Marie; Liu, Limin; Gyllensten, Ulf

Part of Human Immunology, p. 25-32, 1994

• DOI for A comprehensive polymerase chain reaction-oligonucleotide typing system for the HLA class I A locus

Genetic typing of HLA class II genes in Swedish populations: application to forensic analysis

Allen, Marie; Saldeen, T.; Pettersson, Ulf; Gyllensten, Ulf

Part of Journal of Forensic Sciences, p. 554-70, 1993

Sequencing of in vitro amplified DNA

Gyllensten, Ulf; Allen, Marie

Part of Methods in Enzymology, p. 3-16, 1993

• DOI for Sequencing of in vitro amplified DNA

Frequency of four cystic fibrosis mutations in a Swedish population

Dahl, Niklas; Grandell, U.; Martinsson, T.; Allen, Marie et al.

Part of Acta Paediatrica, p. 609, 1993

Screening for the major cystic fibrosis mutation in non-Caucasian populations

Devoto, M.; Castagnola, S.; Saha, N.; Chetsanga, C. et al.

Part of American Journal of Human Genetics, p. 903-4, 1991

PCR-based HLA class II typing

Gyllensten, Ulf; Allen, Marie

Part of PCR methods and applications, p. 91-8, 1991

• DOI for PCR-based HLA class II typing

Lessons and implications from association studies and post-GWAS analyses of cervical cancer

Chen, Dan; Gyllensten, Ulf

Part of Trends in Genetics, p. 41-54, 2015

• DOI for Lessons and implications from association studies and post-GWAS analyses of cervical cancer

MICA polymorphism: biology and importance in cancer

Chen, Dan; Gyllensten, Ulf

Part of Carcinogenesis, p. 2633-2642, 2014

• DOI for MICA polymorphism: biology and importance in cancer

Brush Biopsy For HR-HPV Detection With FTA Card And AI For Cytology Analysis - A Viable Non-invasive Alternative

Runow Stark, Christina; Gustavsson, Inger M.; Gyllensten, Ulf B.; Darai Ramqvist, Eva et al.

Part of EAOM2018, 2018

SSO: genetic typing with sequence-specific oligonucleotides

Gyllensten, Ulf; Allen, Marie

Part of Laboratory protocols for mutation detection, p. 78, 1996

Ultra-deep targeted re-sequencing of TMEM18 in two cohorts of European children detects new genetic variants associated with obesity

Rask-Andersen, Mathias; Sällman Almén, Markus; Jacobsson, Josefin; Ameur, Adam et al.

2013

Mitochondrial DNA genome variation in the Swedish population

Sturk-Andreaggi, Kimberly; Bodner, Martin; Ring, Joseph; Ameur, Adam et al.

Part of SUPPLEMENTARY MATERIALS for Mitochondrial DNA genome variation in the Swedish population

A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

Prokunina, Ludmila; Castillejo-Lopez, Casimiro; Öberg, Fredrik; Gunnarsson, Iva et al.

Part of Nature Genetics, p. 666-669, 2002

• DOI for A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans