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MHC associations with clinical and autoantibody manifestations in European SLE

Genes and immunity, 2014-06, Vol.15 (4), p.210-217

2014

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Genotype–phenotype correlations in Peutz-Jeghers syndrome

Journal of medical genetics, 2004-05, Vol.41 (5), p.327-333

2004

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Relationship between adiposity and admixture in African-American and Hispanic-American women

International Journal of Obesity, 2012-02, Vol.36 (2), p.304-313

2012

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Accounting for ancestry: population substructure and genome-wide association studies

Human molecular genetics, 2008-10, Vol.17 (R2), p.R143-R150

2008

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Relationship between diabetes risk and admixture in postmenopausal African-American and Hispanic-American women

Diabetologia, 2012-05, Vol.55 (5), p.1329-1337

2012

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Uncoupling protein-2: a novel gene linked to obesity and hyperinsulinemia

Nature genetics, 1997-03, Vol.15 (3), p.269-272

1997

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Mouse Wnt receptor gene Fzd5 is essential for yolk sac and placental angiogenesis

Development (Cambridge), 2001-01, Vol.128 (1), p.25-33

2001

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Smoking interacts with genetic risk factors in the development of rheumatoid arthritis among older Caucasian women

Annals of the rheumatic diseases, 2006-09, Vol.65 (9), p.1163-1167

2006

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Relationship between hypertension and admixture in post-menopausal African American and Hispanic American women

Journal of human hypertension, 2012-06, Vol.26 (6), p.365-373

2012

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Association of PDCD1 genetic variation with risk and clinical manifestations of systemic lupus erythematosus in a multiethnic cohort

Genes and immunity, 2007-06, Vol.8 (4), p.279-287

2007

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Human/Mouse Homology Relationships

Genomics (San Diego, Calif.), 1996-05, Vol.33 (3), p.337-351

1996

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Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis

Genes and immunity, 2010-04, Vol.11 (3), p.199-208

2010

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Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency

Nature genetics, 2016-11, Vol.48 (11), p.1425-1429

2016

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Finnish case-control and family studies support PTPN22 R620W polymorphism as a risk factor in rheumatoid arthritis, but suggest only minimal or no effect in juvenile idiopathic arthritis

Genes and immunity, 2005-12, Vol.6 (8), p.720-722

2005

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Colonic hamartoma development by anomalous duplication in Cdx2 knockout mice

Cancer research (Chicago, Ill.), 1999-06, Vol.59 (12), p.2965-2970

1999

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Genetic analysis of MRL-lpr mice : relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci

The Journal of experimental medicine, 1992-12, Vol.176 (6), p.1645-1656

1992

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Role for Ceramide as an Endogenous Mediator of Fas-Induced Cytotoxicity

Proceedings of the National Academy of Sciences - PNAS, 1995-08, Vol.92 (18), p.8443-8447

1995

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Genetic risk and longitudinal disease activity in systemic lupus erythematosus using targeted maximum likelihood estimation

Genes and immunity, 2016-09, Vol.17 (6), p.358-362

2016

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Genes and (auto)immunity in primary biliary cirrhosis

Genes and immunity, 2005-10, Vol.6 (7), p.543-556

2005

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The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk

Genes and immunity, 2015-04, Vol.16 (3), p.193-198

2015

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Genomic organization, promoter region analysis, and chromosome localization of the mouse bcl-x gene

The Journal of immunology (1950), 1997-05, Vol.158 (10), p.4750

1997

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Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p

Cancer research (Chicago, Ill.), 1997-09, Vol.57 (17), p.3653-3656

1997

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Cloning of the human glycine transporter type 1: molecular and pharmacological characterization of novel isoform variants and chromosomal localization of the gene in the human and mouse genomes

Molecular pharmacology, 1994-04, Vol.45 (4), p.608-617

1994

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Glycine receptor β-subunit gene mutation in spastic mouse associated with LINE-1 element insertion

Nature genetics, 1994-06, Vol.7 (2), p.136-142

1994

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A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis

Genes and immunity, 2010-09, Vol.11 (6), p.504-508

2010

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MHC associations with clinical and autoantibody manifestations in European SLE

Genotype–phenotype correlations in Peutz-Jeghers syndrome

Relationship between adiposity and admixture in African-American and Hispanic-American women

Accounting for ancestry: population substructure and genome-wide association studies

Relationship between diabetes risk and admixture in postmenopausal African-American and Hispanic-American women

Uncoupling protein-2: a novel gene linked to obesity and hyperinsulinemia

Mouse Wnt receptor gene Fzd5 is essential for yolk sac and placental angiogenesis

Smoking interacts with genetic risk factors in the development of rheumatoid arthritis among older Caucasian women

Relationship between hypertension and admixture in post-menopausal African American and Hispanic American women

Association of PDCD1 genetic variation with risk and clinical manifestations of systemic lupus erythematosus in a multiethnic cohort

Human/Mouse Homology Relationships

Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis

Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency

Finnish case-control and family studies support PTPN22 R620W polymorphism as a risk factor in rheumatoid arthritis, but suggest only minimal or no effect in juvenile idiopathic arthritis

Colonic hamartoma development by anomalous duplication in Cdx2 knockout mice

Genetic analysis of MRL-lpr mice : relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci

Role for Ceramide as an Endogenous Mediator of Fas-Induced Cytotoxicity

Genetic risk and longitudinal disease activity in systemic lupus erythematosus using targeted maximum likelihood estimation

Genes and (auto)immunity in primary biliary cirrhosis

The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk

Genomic organization, promoter region analysis, and chromosome localization of the mouse bcl-x gene

Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p

Cloning of the human glycine transporter type 1: molecular and pharmacological characterization of novel isoform variants and chromosomal localization of the gene in the human and mouse genomes

Glycine receptor β-subunit gene mutation in spastic mouse associated with LINE-1 element insertion

A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis

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