Gerli Rosengren Pielberg

A novel canine reference genome resolves genomic architecture and uncovers transcript complexity

Wang, Chao; Wallerman, Ola; Arendt, Maja-Louise; Sundström, Elisabeth et al.

Part of Communications Biology, 2021

• DOI for A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
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Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs

Bianchi, Matteo; Rafati, Nima; Karlsson, Åsa; Murén, Eva et al.

Part of BMC Genomics, 2020

• DOI for Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs
• Download full text (pdf) of Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs

Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1

Eriksson, Daniel; Dalin, Frida; Eriksson, Gabriel Nordling; Landegren, Nils et al.

Part of Journal of Clinical Endocrinology and Metabolism, p. 179-186, 2018

• DOI for Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1
• Download full text (pdf) of Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1

Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden

Eriksson, Daniel; Bianchi, Matteo; Landegren, Nils; Dalin, Frida et al.

Part of Scientific Reports, 2018

• DOI for Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden
• Download full text (pdf) of Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden

Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease

Eriksson, D.; Bianchi, Matteo; Landegren, Nils; Nordin, Jessika et al.

Part of Journal of Internal Medicine, p. 595-608, 2016

• DOI for Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease
• Download full text (pdf) of Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease

A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12

Bianchi, Matteo; Dahlgren, Stina; Massey, Jonathan; Dietschi, Elisabeth et al.

Part of PLOS ONE, 2015

• DOI for A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12
• Download full text (pdf) of A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12

Rabbit genome analysis reveals a polygenic basis for phenotypic change during domestication

Carneiro, Miguel; Rubin, Carl-Johan; Di Palma, Federica; Albert, Frank W. et al.

Part of Science, p. 1074-1079, 2014

• DOI for Rabbit genome analysis reveals a polygenic basis for phenotypic change during domestication

Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping

Vaysse, Amaury; Ratnakumar, Abhirami; Derrien, Thomas; Axelsson, Erik et al.

Part of PLOS Genetics, 2011

• DOI for Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping
• Download full text (pdf) of Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping

A Novel Unstable Duplication Upstream of HAS2 Predisposes to a Breed-Defining Skin Phenotype and a Periodic Fever Syndrome in Chinese Shar-Pei Dogs

Olsson, Mia; Meadows, Jennifer R. S.; Truve, Katarina; Pielberg, Gerli Rosengren et al.

Part of PLoS Genetics, 2011

• DOI for A Novel Unstable Duplication Upstream of HAS2 Predisposes to a Breed-Defining Skin Phenotype and a Periodic Fever Syndrome in Chinese Shar-Pei Dogs

A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse

Pielberg, Gerli Rosengren; Golovko, Anna; Sundström, Elisabeth; Curik, Ino et al.

Part of Nature Genetics, p. 1004-1009, 2008

• DOI for A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse

Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs

Salmon Hillbertz, Nicolette H. C.; Isaksson, Magnus; Karlsson, Elinor K.; Hellmén, Eva et al.

Part of Nature Genetics, p. 1318-1320, 2007

• DOI for Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs

Efficient mapping of mendelian traits in dogs through genome-wide association

Karlsson, Elinor K.; Baranowska, Izabella; Wade, Claire M.; Salmon Hillbertz, Nicolette H. C. et al.

Part of Nature Genetics, p. 1321-1328, 2007

• DOI for Efficient mapping of mendelian traits in dogs through genome-wide association

Gene copy number detection in animal studies

Pielberg, Gerli; Andersson, Leif

Part of Methods in Molecular Biology, p. 147-156, 2007

• DOI for Gene copy number detection in animal studies

A sensitive method for detecting variation in copy numbers of duplicatedgenes

Pielberg, Gerli; Day, A E; Plastow, G S; Andersson, Leif

Part of Genome Research, p. 2171-2177, 2003

• DOI for A sensitive method for detecting variation in copy numbers of duplicatedgenes

Comparative sequence analysis of the PRKAG3 region between human and pig: evolution of repetitive sequences and potential new exons

Amarger, V; Erlandsson, R; Pielberg, G; Jeon, J T et al.

Part of Cytogenetic and Genome Research, p. 163-172, 2003

• DOI for Comparative sequence analysis of the PRKAG3 region between human and pig: evolution of repetitive sequences and potential new exons

Unexpectedly High Allelic Diversity at the KIT Locus Causing DominantWhite Color in the Domestic Pig

Pielberg, Gerli; Olsson, Christian; Syvänen, Ann-Christine; Andersson, L

Part of Genetics, p. 305-311, 2002

A novel canine reference genome resolves genomic architecture and uncovers transcript complexity

Wang, Chao; Wallerman, Ola; Arendt, Maja-Louise; Sundström, Elisabeth et al.

Part of Communications Biology, 2021

• DOI for A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
• Download full text (pdf) of A novel canine reference genome resolves genomic architecture and uncovers transcript complexity

Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA

Dahlqvist, Johanna; Ekman, Diana; Sennblad, Bengt; Kozyrev, Sergey V. et al.

Part of Rheumatology, p. 3461-3470, 2021

• DOI for Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
• Download full text (pdf) of Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA

Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs

Bianchi, Matteo; Rafati, Nima; Karlsson, Åsa; Murén, Eva et al.

Part of BMC Genomics, 2020

• DOI for Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs
• Download full text (pdf) of Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs

A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts

Farias, Fabiana H. G.; Dahlqvist, Johanna; Kozyrev, Sergey V.; Leonard, Dag et al.

Part of European Journal of Human Genetics, p. 432-441, 2019

• DOI for A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts
• Download full text (pdf) of A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts

Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1

Eriksson, Daniel; Dalin, Frida; Eriksson, Gabriel Nordling; Landegren, Nils et al.

Part of Journal of Clinical Endocrinology and Metabolism, p. 179-186, 2018

• DOI for Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1
• Download full text (pdf) of Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1

A novel canine reference genome resolves genomic architecture and uncovers transcript complexity

Wang, Chao; Wallerman, Ola; Arendt, Maja-Louise; Sundström, Elisabeth et al.

Part of Communications Biology, 2021

• DOI for A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
• Download full text (pdf) of A novel canine reference genome resolves genomic architecture and uncovers transcript complexity

Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA

Dahlqvist, Johanna; Ekman, Diana; Sennblad, Bengt; Kozyrev, Sergey V. et al.

Part of Rheumatology, p. 3461-3470, 2021

• DOI for Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
• Download full text (pdf) of Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA

Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs

Bianchi, Matteo; Rafati, Nima; Karlsson, Åsa; Murén, Eva et al.

Part of BMC Genomics, 2020

• DOI for Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs
• Download full text (pdf) of Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs

A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts

Farias, Fabiana H. G.; Dahlqvist, Johanna; Kozyrev, Sergey V.; Leonard, Dag et al.

Part of European Journal of Human Genetics, p. 432-441, 2019

• DOI for A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts
• Download full text (pdf) of A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts

Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1

Eriksson, Daniel; Dalin, Frida; Eriksson, Gabriel Nordling; Landegren, Nils et al.

Part of Journal of Clinical Endocrinology and Metabolism, p. 179-186, 2018

• DOI for Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1
• Download full text (pdf) of Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1

The risk allele A of rs200395694 associated with SLE in Swedish patients affects on MEF2D gene regulation and alternative splicing

Abramov, Sergei; Kozyrev, Sergey V.; Farias, Fabiana H. G.; Dahlqvist, Johanna et al.

Part of Human Gene Therapy, 2018

Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden

Eriksson, Daniel; Bianchi, Matteo; Landegren, Nils; Dalin, Frida et al.

Part of Scientific Reports, 2018

• DOI for Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden
• Download full text (pdf) of Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden

Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd dogs

Tengvall, Katarina; Kozyrev, Sergey; Kierczak, Marcin; Bergvall, Kerstin et al.

Part of BMC Genetics, 2016

• DOI for Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd dogs
• Download full text (pdf) of Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd dogs

Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus

Truve, Katarina; Dickinson, Peter; Xiong, Anqi; York, Daniel et al.

Part of PLOS Genetics, 2016

• DOI for Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus
• Download full text (pdf) of Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus

Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease

Eriksson, D.; Bianchi, Matteo; Landegren, Nils; Nordin, Jessika et al.

Part of Journal of Internal Medicine, p. 595-608, 2016

• DOI for Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease
• Download full text (pdf) of Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease

A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12

Bianchi, Matteo; Dahlgren, Stina; Massey, Jonathan; Dietschi, Elisabeth et al.

Part of PLOS ONE, 2015

• DOI for A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12
• Download full text (pdf) of A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12

Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease

Wilbe, Maria; Kozyrev, Sergey V.; Farias, Fabiana H. G.; Bremer, Hanna D. et al.

Part of PLOS Genetics, 2015

• DOI for Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease
• Download full text (pdf) of Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease

Linked genetic variants on chromosome 10 control ear morphology and body mass among dog breeds

Webster, Matthew T.; Kamgari, Nona; Perloski, Michele; Höppner, Marc P. et al.

Part of BMC Genomics, 2015

• DOI for Linked genetic variants on chromosome 10 control ear morphology and body mass among dog breeds
• Download full text (pdf) of Linked genetic variants on chromosome 10 control ear morphology and body mass among dog breeds

High-Throughput Sequencing of 219 Candidate Genes for Identification of SLE-Associated Risk Variants

Farias, Fabiana; Wilbe, Maria; Dahlqvist, Johanna; Leonard, Dag et al.

Part of Arthritis & Rheumatology, 2014

Rabbit genome analysis reveals a polygenic basis for phenotypic change during domestication

Carneiro, Miguel; Rubin, Carl-Johan; Di Palma, Federica; Albert, Frank W. et al.

Part of Science, p. 1074-1079, 2014

• DOI for Rabbit genome analysis reveals a polygenic basis for phenotypic change during domestication

Constitutive activation of the ERK pathway in melanoma and skin melanocytes in Grey horses

Jiang, Lin; Campagne, Cécile; Sundström, Elisabeth; Sousa, Pedro et al.

Part of BMC Cancer, p. 857, 2014

• DOI for Constitutive activation of the ERK pathway in melanoma and skin melanocytes in Grey horses
• Download full text (pdf) of Constitutive activation of the ERK pathway in melanoma and skin melanocytes in Grey horses

A Simple Repeat Polymorphism in the MITF-M Promoter Is a Key Regulator of White Spotting in Dogs

Baranowska Körberg, Izabella; Sundström, Elisabeth; Meadows, Jennifer R. S.; Pielberg, Gerli Rosengren et al.

Part of PLOS ONE, 2014

• DOI for A Simple Repeat Polymorphism in the MITF-M Promoter Is a Key Regulator of White Spotting in Dogs
• Download full text (pdf) of A Simple Repeat Polymorphism in the MITF-M Promoter Is a Key Regulator of White Spotting in Dogs

Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis

Tengvall, Katarina; Kierczak, Marcin; Bergvall, Kerstin; Olsson, Mia et al.

Part of PLOS Genetics, 2013

• DOI for Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis
• Download full text (pdf) of Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis

Thorough investigation of a canine autoinflammatory disease (AID) syndrome confirms one main risk factor and suggests a modifier locus for amyloidosis

Olsson, Mia; Tintle, Linda; Kierczak, Marcin; Perloski, Michele et al.

Part of PLOS ONE, 2013

• DOI for Thorough investigation of a canine autoinflammatory disease (AID) syndrome confirms one main risk factor and suggests a modifier locus for amyloidosis
• Download full text (pdf) of Thorough investigation of a canine autoinflammatory disease (AID) syndrome confirms one main risk factor and suggests a modifier locus for amyloidosis

Complex Inheritance of Melanoma and Pigmentation of Coat and Skin in Grey Horses

Curik, Ino; Druml, Thomas; Seltenhammer, Monika; Sundström, Elisabeth et al.

Part of PLOS Genetics, 2013

• DOI for Complex Inheritance of Melanoma and Pigmentation of Coat and Skin in Grey Horses
• Download full text (pdf) of Complex Inheritance of Melanoma and Pigmentation of Coat and Skin in Grey Horses

Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses

Sundström, Elisabeth; Imsland, Freyja; Mikko, Sofia; Wade, Claire et al.

Part of BMC Genomics, p. 365, 2012

• DOI for Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses

Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses

Sundström, Elisabeth; Imsland, Freyja; Mikko, Sofia; Wade, Claire et al.

Part of BMC Genomics, p. 365, 2012

• DOI for Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses
• Download full text (pdf) of Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses

Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping

Vaysse, Amaury; Ratnakumar, Abhirami; Derrien, Thomas; Axelsson, Erik et al.

Part of PLOS Genetics, 2011

• DOI for Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping
• Download full text (pdf) of Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping

A Novel Unstable Duplication Upstream of HAS2 Predisposes to a Breed-Defining Skin Phenotype and a Periodic Fever Syndrome in Chinese Shar-Pei Dogs

Olsson, Mia; Meadows, Jennifer R. S.; Truve, Katarina; Pielberg, Gerli Rosengren et al.

Part of PLoS Genetics, 2011

• DOI for A Novel Unstable Duplication Upstream of HAS2 Predisposes to a Breed-Defining Skin Phenotype and a Periodic Fever Syndrome in Chinese Shar-Pei Dogs

A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse

Pielberg, Gerli Rosengren; Golovko, Anna; Sundström, Elisabeth; Curik, Ino et al.

Part of Nature Genetics, p. 1004-1009, 2008

• DOI for A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse

Frequency and effect of the bovine acyl-CoA: diacylglycerol acyltransferase 1 (DGAT1) K232A polymorphism in Swedish dairy cattle

Näslund, J; Fikse, W F; Pielberg, Gerli; Lundén, A

Part of Journal of Dairy Science, p. 2127-2134, 2008

• DOI for Frequency and effect of the bovine acyl-CoA: diacylglycerol acyltransferase 1 (DGAT1) K232A polymorphism in Swedish dairy cattle

Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs

Salmon Hillbertz, Nicolette H. C.; Isaksson, Magnus; Karlsson, Elinor K.; Hellmén, Eva et al.

Part of Nature Genetics, p. 1318-1320, 2007

• DOI for Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs

Efficient mapping of mendelian traits in dogs through genome-wide association

Karlsson, Elinor K.; Baranowska, Izabella; Wade, Claire M.; Salmon Hillbertz, Nicolette H. C. et al.

Part of Nature Genetics, p. 1321-1328, 2007

• DOI for Efficient mapping of mendelian traits in dogs through genome-wide association

Gene copy number detection in animal studies

Pielberg, Gerli; Andersson, Leif

Part of Methods in Molecular Biology, p. 147-156, 2007

• DOI for Gene copy number detection in animal studies

Polymorphism at the porcine Dominant white/KIT locus influence coat colour and peripheral blood cell measures

Johansson, A; Pielberg, Gerli; Andersson, Leif; Edfors-Lilja, I

Part of Animal Genetics, p. 288-296, 2005

• DOI for Polymorphism at the porcine Dominant white/KIT locus influence coat colour and peripheral blood cell measures

Confirmation of QTL on porcine chromosomes 1 and 8 influencing leukocyte numbers, haematological parameters and leukocyte function.

Wattrang, E; Almqvist, M; Johansson, A; Fossum, C et al.

Part of Anim Genet, p. 337-45, 2005

Comparative linkage mapping of the Grey coat colour gene in horses.

Pielberg, G; Mikko, S; Sandberg, K; Andersson, L

Part of Anim Genet, p. 390-5, 2005

A sensitive method for detecting variation in copy numbers of duplicatedgenes

Pielberg, Gerli; Day, A E; Plastow, G S; Andersson, Leif

Part of Genome Research, p. 2171-2177, 2003

• DOI for A sensitive method for detecting variation in copy numbers of duplicatedgenes

Comparative sequence analysis of the PRKAG3 region between human and pig: evolution of repetitive sequences and potential new exons

Amarger, V; Erlandsson, R; Pielberg, G; Jeon, J T et al.

Part of Cytogenetic and Genome Research, p. 163-172, 2003

• DOI for Comparative sequence analysis of the PRKAG3 region between human and pig: evolution of repetitive sequences and potential new exons

Unexpectedly High Allelic Diversity at the KIT Locus Causing DominantWhite Color in the Domestic Pig

Pielberg, Gerli; Olsson, Christian; Syvänen, Ann-Christine; Andersson, L

Part of Genetics, p. 305-311, 2002

Replication and fine mapping of ankylosing spondylitis replicated loci in the Swedish population reveal different CCHCR1 protective haplotypes

Mathioudaki, Argyri; Nordin, Jessika; Murén, Eva; Karlsson, Åsa et al.

The sex-stratified genetic architecture of ankylosing spondylitis

Mathioudaki, Argyri; Nordin, Jessika; Karlsson, Åsa; Murén, Eva et al.