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.

Ingår i Communications Biology, 2021

• DOI för A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
• Ladda ner fulltext (pdf) av A novel canine reference genome resolves genomic architecture and uncovers transcript complexity

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.

Ingår i BMC Genomics, 2020

• DOI för Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs
• Ladda ner fulltext (pdf) av 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.

Ingår i Journal of Clinical Endocrinology and Metabolism, s. 179-186, 2018

• DOI för Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1
• Ladda ner fulltext (pdf) av 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.

Ingår i Scientific Reports, 2018

• DOI för Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden
• Ladda ner fulltext (pdf) av 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.

Ingår i Journal of Internal Medicine, s. 595-608, 2016

• DOI för Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease
• Ladda ner fulltext (pdf) av 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.

Ingår i PLOS ONE, 2015

• DOI för A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12
• Ladda ner fulltext (pdf) av 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.

Ingår i Science, s. 1074-1079, 2014

• DOI för 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.

Ingår i PLOS Genetics, 2011

• DOI för Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping
• Ladda ner fulltext (pdf) av 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.

Ingår i PLoS Genetics, 2011

• DOI för 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.

Ingår i Nature Genetics, s. 1004-1009, 2008

• DOI för 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.

Ingår i Nature Genetics, s. 1318-1320, 2007

• DOI för 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.

Ingår i Nature Genetics, s. 1321-1328, 2007

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

Gene copy number detection in animal studies

Pielberg, Gerli; Andersson, Leif

Ingår i Methods in Molecular Biology, s. 147-156, 2007

• DOI för 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

Ingår i Genome Research, s. 2171-2177, 2003

• DOI för 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.

Ingår i Cytogenetic and Genome Research, s. 163-172, 2003

• DOI för 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

Ingår i Genetics, s. 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.

Ingår i Communications Biology, 2021

• DOI för A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
• Ladda ner fulltext (pdf) av 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.

Ingår i Rheumatology, s. 3461-3470, 2021

• DOI för Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
• Ladda ner fulltext (pdf) av 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.

Ingår i BMC Genomics, 2020

• DOI för Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs
• Ladda ner fulltext (pdf) av 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.

Ingår i European Journal of Human Genetics, s. 432-441, 2019

• DOI för A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts
• Ladda ner fulltext (pdf) av 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.

Ingår i Journal of Clinical Endocrinology and Metabolism, s. 179-186, 2018

• DOI för Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1
• Ladda ner fulltext (pdf) av 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.

Ingår i Communications Biology, 2021

• DOI för A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
• Ladda ner fulltext (pdf) av 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.

Ingår i Rheumatology, s. 3461-3470, 2021

• DOI för Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
• Ladda ner fulltext (pdf) av 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.

Ingår i BMC Genomics, 2020

• DOI för Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs
• Ladda ner fulltext (pdf) av 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.

Ingår i European Journal of Human Genetics, s. 432-441, 2019

• DOI för A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts
• Ladda ner fulltext (pdf) av 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.

Ingår i Journal of Clinical Endocrinology and Metabolism, s. 179-186, 2018

• DOI för Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1
• Ladda ner fulltext (pdf) av 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.

Ingår i 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.

Ingår i Scientific Reports, 2018

• DOI för Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden
• Ladda ner fulltext (pdf) av 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.

Ingår i BMC Genetics, 2016

• DOI för 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
• Ladda ner fulltext (pdf) av 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.

Ingår i PLOS Genetics, 2016

• DOI för 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
• Ladda ner fulltext (pdf) av 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.

Ingår i Journal of Internal Medicine, s. 595-608, 2016

• DOI för Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease
• Ladda ner fulltext (pdf) av 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.

Ingår i PLOS ONE, 2015

• DOI för A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12
• Ladda ner fulltext (pdf) av 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.

Ingår i PLOS Genetics, 2015

• DOI för Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease
• Ladda ner fulltext (pdf) av 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.

Ingår i BMC Genomics, 2015

• DOI för Linked genetic variants on chromosome 10 control ear morphology and body mass among dog breeds
• Ladda ner fulltext (pdf) av 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.

Ingår i 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.

Ingår i Science, s. 1074-1079, 2014

• DOI för 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.

Ingår i BMC Cancer, s. 857, 2014

• DOI för Constitutive activation of the ERK pathway in melanoma and skin melanocytes in Grey horses
• Ladda ner fulltext (pdf) av 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.

Ingår i PLOS ONE, 2014

• DOI för A Simple Repeat Polymorphism in the MITF-M Promoter Is a Key Regulator of White Spotting in Dogs
• Ladda ner fulltext (pdf) av 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.

Ingår i PLOS Genetics, 2013

• DOI för Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis
• Ladda ner fulltext (pdf) av 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.

Ingår i PLOS ONE, 2013

• DOI för Thorough investigation of a canine autoinflammatory disease (AID) syndrome confirms one main risk factor and suggests a modifier locus for amyloidosis
• Ladda ner fulltext (pdf) av 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.

Ingår i PLOS Genetics, 2013

• DOI för Complex Inheritance of Melanoma and Pigmentation of Coat and Skin in Grey Horses
• Ladda ner fulltext (pdf) av 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.

Ingår i BMC Genomics, s. 365, 2012

• DOI för 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.

Ingår i BMC Genomics, s. 365, 2012

• DOI för Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses
• Ladda ner fulltext (pdf) av 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.

Ingår i PLOS Genetics, 2011

• DOI för Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping
• Ladda ner fulltext (pdf) av 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.

Ingår i PLoS Genetics, 2011

• DOI för 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.

Ingår i Nature Genetics, s. 1004-1009, 2008

• DOI för 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

Ingår i Journal of Dairy Science, s. 2127-2134, 2008

• DOI för 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.

Ingår i Nature Genetics, s. 1318-1320, 2007

• DOI för 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.

Ingår i Nature Genetics, s. 1321-1328, 2007

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

Gene copy number detection in animal studies

Pielberg, Gerli; Andersson, Leif

Ingår i Methods in Molecular Biology, s. 147-156, 2007

• DOI för 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

Ingår i Animal Genetics, s. 288-296, 2005

• DOI för 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.

Ingår i Anim Genet, s. 337-45, 2005

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

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

Ingår i Anim Genet, s. 390-5, 2005

A sensitive method for detecting variation in copy numbers of duplicatedgenes

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

Ingår i Genome Research, s. 2171-2177, 2003

• DOI för 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.

Ingår i Cytogenetic and Genome Research, s. 163-172, 2003

• DOI för 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

Ingår i Genetics, s. 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.