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Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis

Nature genetics, 2012-03, Vol.44 (3), p.291-296

2012

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Self-labelled encoder-decoder (SLED) for multi-echo gradient echo-based myelin water imaging

NeuroImage (Orlando, Fla.), 2022-12, Vol.264, p.119717-119717, Article 119717

2022

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Pervasive sharing of genetic effects in autoimmune disease

PLoS genetics, 2011-08, Vol.7 (8), p.e1002254-e1002254

2011

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Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants

The New England journal of medicine, 2009-06, Vol.360 (24), p.2544-2555

2009

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A Role for Noncoding Variation in Schizophrenia

Cell reports (Cambridge), 2014-11, Vol.9 (4), p.1417-1429

2014

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Transcriptional regulators of the Golli/myelin basic protein locus integrate additive and stealth activities

PLoS genetics, 2020-08, Vol.16 (8), p.e1008752-e1008752

2020

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Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis

Nature communications, 2023-02, Vol.14 (1), p.1069-1069, Article 1069

2023

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Genetics and the environment converge to dysregulate N-glycosylation in multiple sclerosis

Nature communications, 2011-05, Vol.2 (1), p.334, Article 334

2011

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Nonreceptor protein-tyrosine phosphatases in immune cell signaling

Annual Review of Immunology, 2007-01, Vol.25 (1), p.473-523

2007

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RFC1 80G>A Is a Genetic Determinant of Methotrexate Efficacy in Rheumatoid Arthritis: A Human Genome Epidemiologic Review and Meta‐Analysis of Observational Studies

Arthritis & rheumatology (Hoboken, N.J.), 2014-05, Vol.66 (5), p.1111-1120

2014

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Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway

PLoS genetics, 2013-05, Vol.9 (5), p.e1003487-e1003487

2013

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Genetics in PBC: What Do the “Risk Genes” Teach Us?

Clinical reviews in allergy & immunology, 2015-06, Vol.48 (2-3), p.176-181

2015

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The human OCTN1 (SLC22A4) reconstituted in liposomes catalyzes acetylcholine transport which is defective in the mutant L503F associated to the Crohn's disease

Biochimica et biophysica acta, 2012-03, Vol.1818 (3), p.559-565

2012

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The mDial Formin Is Required for Neutrophil Polarization, Migration, and Activation of the LARG/RhoA/ROCK Signaling Axis during Chemotaxis

The Journal of immunology (1950), 2009-03, Vol.182 (6), p.3837-3845

2009

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Monoclonal Antibodies for the Treatment of Hypercholesterolemia: Targeting PCSK9

Canadian journal of cardiology, 2016-12, Vol.32 (12), p.1552-1560

2016

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T Cell Responses in Mammalian Diaphanous-related Formin mDia1 Knock-out Mice

The Journal of biological chemistry, 2007-08, Vol.282 (34), p.25152-25158

2007

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N-WASp is required for Schwann cell cytoskeletal dynamics, normal myelin gene expression and peripheral nerve myelination

Development (Cambridge), 2011-04, Vol.138 (7), p.1329-1337

2011

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Mammalian diaphanous-related formin 1 regulates GSK3β-dependent microtubule dynamics required for T cell migratory polarization

PloS one, 2013-11, Vol.8 (11), p.e80500-e80500

2013

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Pharmacogenetics of the G protein-coupled receptors

Methods in molecular biology (Clifton, N.J.), 2014-01, Vol.1175, p.189

2014

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Interaction of the Wiskott-Aldrich syndrome protein with sorting nexin 9 is required for CD28 endocytosis and cosignaling in T cells

Proceedings of the National Academy of Sciences - PNAS, 2007-01, Vol.104 (5), p.1593-1598

2007

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Genetic Variants in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A Bayesian Approach and Systematic Review

Journal of clinical medicine, 2019-02, Vol.8 (2), p.266

2019

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The SHP-1 protein tyrosine phosphatase negatively modulates glucose homeostasis

Nature medicine, 2006-05, Vol.12 (5), p.549-556

2006

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Utility of Incorporating Genetic Variants for the Early Detection of Prostate Cancer

Clinical cancer research, 2009-03, Vol.15 (5), p.1787-1793

2009

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Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis

Self-labelled encoder-decoder (SLED) for multi-echo gradient echo-based myelin water imaging

Pervasive sharing of genetic effects in autoimmune disease

Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants

A Role for Noncoding Variation in Schizophrenia

Transcriptional regulators of the Golli/myelin basic protein locus integrate additive and stealth activities

Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis

Genetics and the environment converge to dysregulate N-glycosylation in multiple sclerosis

Nonreceptor protein-tyrosine phosphatases in immune cell signaling

Rare, Low-Frequency, and Common Variants in the Protein-Coding Sequence of Biological Candidate Genes from GWASs Contribute to Risk of Rheumatoid Arthritis

RFC1 80G>A Is a Genetic Determinant of Methotrexate Efficacy in Rheumatoid Arthritis: A Human Genome Epidemiologic Review and Meta‐Analysis of Observational Studies

Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway

Genetics in PBC: What Do the “Risk Genes” Teach Us?

The human OCTN1 (SLC22A4) reconstituted in liposomes catalyzes acetylcholine transport which is defective in the mutant L503F associated to the Crohn's disease

The mDial Formin Is Required for Neutrophil Polarization, Migration, and Activation of the LARG/RhoA/ROCK Signaling Axis during Chemotaxis

Monoclonal Antibodies for the Treatment of Hypercholesterolemia: Targeting PCSK9

T Cell Responses in Mammalian Diaphanous-related Formin mDia1 Knock-out Mice

N-WASp is required for Schwann cell cytoskeletal dynamics, normal myelin gene expression and peripheral nerve myelination

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

Mammalian diaphanous-related formin 1 regulates GSK3β-dependent microtubule dynamics required for T cell migratory polarization

Pharmacogenetics of the G protein-coupled receptors

Interaction of the Wiskott-Aldrich syndrome protein with sorting nexin 9 is required for CD28 endocytosis and cosignaling in T cells

Genetic Variants in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A Bayesian Approach and Systematic Review

The SHP-1 protein tyrosine phosphatase negatively modulates glucose homeostasis

Utility of Incorporating Genetic Variants for the Early Detection of Prostate Cancer

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