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Hydrocarbon production reduces natural methane seeps in the Santa Barbara channel

Marine and petroleum geology, 2023-05, Vol.151 (C), p.106187, Article 106187

2023

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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

Nature genetics, 2009-01, Vol.41 (1), p.35-46

2009

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Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

Genetics in medicine, 2021-08, Vol.23 (8), p.1506-1513

2021

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Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene

American journal of human genetics, 2010-02, Vol.86 (2), p.285-291

2010

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Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

Nature genetics, 2011-02, Vol.43 (2), p.117-120

2011

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Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

Human molecular genetics, 2011-01, Vol.20 (2), p.345-353

2011

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Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Nature genetics, 2011-08, Vol.43 (8), p.761-767

2011

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Common genetic determinants of vitamin D insufficiency: a genome-wide association study

The Lancet (British edition), 2010-07, Vol.376 (9736), p.180-188

2010

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Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis

Nature genetics, 2012-10, Vol.44 (10), p.1137-1141

2012

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National trends in total cholesterol obscure heterogeneous changes in HDL and non-HDL cholesterol and total-to-HDL cholesterol ratio: a pooled analysis of 458 population-based studies in Asian and Western countries

International journal of epidemiology, 2020-02, Vol.49 (1), p.173-192

2020

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Aire deficient mice develop multiple features of APECED phenotype and show altered immune response

Human molecular genetics, 2002-02, Vol.11 (4), p.397-409

2002

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Aire deficient mice develop multiple features of APECED phenotype and show altered immune response

Human molecular genetics, 2002-02, Vol.11 (4), p.397-409

2002

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Distinct Variants at LIN28B Influence Growth in Height from Birth to Adulthood

American journal of human genetics, 2010-05, Vol.86 (5), p.773-782

2010

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Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

Nature genetics, 2013-02, Vol.45 (2), p.208-213

2013

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Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

Circulation. Cardiovascular genetics, 2012-04, Vol.5 (2), p.242-249

2012

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The correlation between reading and mathematics ability at age twelve has a substantial genetic component

Nature communications, 2014-07, Vol.5 (1), p.4204, Article 4204

2014

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Systematic mutagenesis of the functional domains of AIRE reveals their role in intracellular targeting

Human molecular genetics, 2002-12, Vol.11 (26), p.3299-3308

2002

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Increased antigen presenting cell‐mediated T cell activation in mice and patients without the autoimmune regulator

European Journal of Immunology, 2006-02, Vol.36 (2), p.305-317

2006

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Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

Genome research, 2010-10, Vol.20 (10), p.1344-1351

2010

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The genetic association of variants in CD6, TNFRSF1A and IRF8 to multiple sclerosis: a multicenter case-control study

PloS one, 2011-04, Vol.6 (4), p.e18813-e18813

2011

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Aire-deficient mice develop hematopoetic irregularities and marginal zone B-cell lymphoma

Blood, 2006-09, Vol.108 (6), p.1941-1948

2006

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Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus

Human molecular genetics, 2013-11, Vol.22 (22), p.4653-4660

2013

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Common variants in the HLA-DRB1-HLA-DQA1 Class II region are associated with susceptibility to visceral leishmaniasis

Nature genetics, 2013-01, Vol.45 (2), p.208-213

2013

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Multiple common variants for celiac disease influencing immune gene expression

Nature genetics, 2010-05, Vol.42 (5), p.465

2010

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Erratum: Corrigendum: Multiple common variants for celiac disease influencing immune gene expression

Nature genetics, 2010-05, Vol.42 (5), p.465-465

2010

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Hydrocarbon production reduces natural methane seeps in the Santa Barbara channel

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Common genetic determinants of vitamin D insufficiency: a genome-wide association study

Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis

National trends in total cholesterol obscure heterogeneous changes in HDL and non-HDL cholesterol and total-to-HDL cholesterol ratio: a pooled analysis of 458 population-based studies in Asian and Western countries

Aire deficient mice develop multiple features of APECED phenotype and show altered immune response

Aire deficient mice develop multiple features of APECED phenotype and show altered immune response

Distinct Variants at LIN28B Influence Growth in Height from Birth to Adulthood

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

Systematic mutagenesis of the functional domains of AIRE reveals their role in intracellular targeting

Increased antigen presenting cell‐mediated T cell activation in mice and patients without the autoimmune regulator

Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

The genetic association of variants in CD6, TNFRSF1A and IRF8 to multiple sclerosis: a multicenter case-control study

Aire-deficient mice develop hematopoetic irregularities and marginal zone B-cell lymphoma

Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus

Common variants in the HLA-DRB1-HLA-DQA1 Class II region are associated with susceptibility to visceral leishmaniasis

Multiple common variants for celiac disease influencing immune gene expression

Erratum: Corrigendum: Multiple common variants for celiac disease influencing immune gene expression

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