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Author Details
Full Name
Michael F Seldin
Affiliation
University of California davis
ORCID
Career Start Year
1978
Papers
379
H Index
90
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36639314
Corrigendum to: "An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs" [J Hepatol 75 (2021) 572-581].
J Hepatol
2023
36639314
Corrigendum to: "An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs" [J Hepatol 75 (2021) 572-581].
J Hepatol
2023
37348755
Differential regulation of JAK1 expression by ETS1 associated with predisposition to primary biliary cholangitis.
J Genet Genomics
2023
36977669
A regulatory variant at 19p13.3 is associated with primary biliary cholangitis risk and ARID3A expression.
Nat Commun
2023
37348755
Differential regulation of JAK1 expression by ETS1 associated with predisposition to primary biliary cholangitis.
J Genet Genomics
2023
36977669
A regulatory variant at 19p13.3 is associated with primary biliary cholangitis risk and ARID3A expression.
Nat Commun
2023
34971632
Increased sensitivity of gp210 autoantibody detection using a newly designed gp210 antigen.
J Immunol Methods
2022
35961613
Genetic admixture and cardiovascular disease risk in postmenopausal Hispanic women.
Int J Cardiol
2022
34971632
Increased sensitivity of gp210 autoantibody detection using a newly designed gp210 antigen.
J Immunol Methods
2022
35184318
Genome-wide meta-analysis identifies susceptibility loci for autoimmune hepatitis type 1.
Hepatology
2022
35961613
Genetic admixture and cardiovascular disease risk in postmenopausal Hispanic women.
Int J Cardiol
2022
35184318
Genome-wide meta-analysis identifies susceptibility loci for autoimmune hepatitis type 1.
Hepatology
2022
33284381
Replication study and meta-analysis indicate a suggestive association of RUNX3 locus with primary biliary cholangitis.
Immunogenetics
2020
31810856
Fine mapping of the MHC region identifies major independent variants associated with Han Chinese primary biliary cholangitis.
J Autoimmun
2020
33284381
Replication study and meta-analysis indicate a suggestive association of RUNX3 locus with primary biliary cholangitis.
Immunogenetics
2020
31810856
Fine mapping of the MHC region identifies major independent variants associated with Han Chinese primary biliary cholangitis.
J Autoimmun
2020
30854688
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis.
Hepatology
2019
30854688
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis.
Hepatology
2019
29953444
Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients.
PLoS One
2018
29953444
Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients.
PLoS One
2018
27697780
The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers.
Cancer Epidemiol Biomarkers Prev
2017
28425483
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis.
Nat Commun
2017
28714469
Transancestral mapping and genetic load in systemic lupus erythematosus.
Nat Commun
2017
28794437
Genetic variation at the CD28 locus and its impact on expansion of pro-inflammatory CD28 negative T cells in healthy individuals.
Sci Rep
2017
29037167
Ancestry inference using principal component analysis and spatial analysis: a distance-based analysis to account for population substructure.
BMC Genomics
2017
28086002
Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum.
Arthritis Rheumatol
2017
27697780
The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers.
Cancer Epidemiol Biomarkers Prev
2017
28086002
Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum.
Arthritis Rheumatol
2017
28425483
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis.
Nat Commun
2017
29037167
Ancestry inference using principal component analysis and spatial analysis: a distance-based analysis to account for population substructure.
BMC Genomics
2017
28794437
Genetic variation at the CD28 locus and its impact on expansion of pro-inflammatory CD28 negative T cells in healthy individuals.
Sci Rep
2017
28714469
Transancestral mapping and genetic load in systemic lupus erythematosus.
Nat Commun
2017
26842849
A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density.
Sci Rep
2016
26842849
A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density.
Sci Rep
2016
26961892
FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data.
BMC Bioinformatics
2016
27467283
Genetic risk and longitudinal disease activity in systemic lupus erythematosus using targeted maximum likelihood estimation.
Genes Immun
2016
26562150
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of <i>TNFRSF11A</i> and Identification of <i>ZBTB10</i> and Three Distinct HLA Associations.
Mol Med
2016
27723758
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.
Nat Genet
2016
26562150
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of <i>TNFRSF11A</i> and Identification of <i>ZBTB10</i> and Three Distinct HLA Associations.
Mol Med
2016
27723758
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.
Nat Genet
2016
27467283
Genetic risk and longitudinal disease activity in systemic lupus erythematosus using targeted maximum likelihood estimation.
Genes Immun
2016
26961892
FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data.
BMC Bioinformatics
2016
25373792
Independent origin of c.57 Câ¿¿>â¿¿T mutation in MIR184 associated with inherited corneal and lens abnormalities.
Ophthalmic Genet
2015
25752262
Relationship of pain and ancestry in African American women.
Eur J Pain
2015
25373792
Independent origin of c.57 Câ¿¿>â¿¿T mutation in MIR184 associated with inherited corneal and lens abnormalities.
Ophthalmic Genet
2015
25906362
The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk.
Genes Immun
2015
25690649
Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese population.
Clin Rev Allergy Immunol
2015
25569263
The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk.
Genes Immun
2015
25849893
TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits.
PLoS One
2015
26394269
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways.
Nat Commun
2015
1 - 50 of 758
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Robert R Graham
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Pietro Invernizzi
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11
Lars Klareskog
Co-authored papers
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John A Robbins
Department of Medicine University of California Davis Davis CA USA.
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10
Katherine A Siminovitch
University of Toronto, Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers
10
Leonid Padyukov
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10
Patrick M Gaffney
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9
John B Harley
US Department of Veterans Affairs Medical Center
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9
Rick A Kittles
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