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Psychiatric co‐morbidity is associated with increased risk of surgery in Crohn's disease

Alimentary pharmacology & therapeutics, 2013-02, Vol.37 (4), p.445-454

2013

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Predictors of severe outcomes associated with Clostridium difficile infection in patients with inflammatory bowel disease

Alimentary pharmacology & therapeutics, 2012-04, Vol.35 (7), p.789-795

2012

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Polygenic inheritance of paclitaxel-induced sensory peripheral neuropathy driven by axon outgrowth gene sets in CALGB 40101 (Alliance)

The pharmacogenomics journal, 2014-08, Vol.14 (4), p.336-342

2014

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Fine mapping the TAGAP risk locus in rheumatoid arthritis

Genes and immunity, 2011-06, Vol.12 (4), p.314-318

2011

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Associations between Human leukocyte antigen, PTPN22, CTLA4 genotypes and rheumatoid arthritis phenotypes of autoantibody status, age at diagnosis and erosions in a large cohort study

Annals of the rheumatic diseases, 2008-03, Vol.67 (3), p.358-363

2008

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The influence of polygenic risk scores on heritability of anti-CCP level in RA

Genes and immunity, 2014-03, Vol.15 (2), p.107-114

2014

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Gene-Gene and Gene-Environment Interactions Involving HLA-DRB1, PTPN22, and Smoking in Two Subsets of Rheumatoid Arthritis

American journal of human genetics, 2007-05, Vol.80 (5), p.867-875

2007

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A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation

Nature genetics, 1997-11, Vol.17 (3), p.353-356

1997

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Heritability of X chromosome-inactivation phenotype in a large family

American journal of human genetics, 1996-06, Vol.58 (6), p.1111-1119

1996

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Skewed X-Chromosome Inactivation Is a Common Feature of X-Linked Mental Retardation Disorders

American journal of human genetics, 2002-07, Vol.71 (1), p.168-173

2002

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GWAS in IMIDs

Journal of translational medicine, 2010-11, Vol.8 (S1), p.I5-I5, Article I5

Plenge, R M

2010

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The BLIMP-1 risk allele is associated with increased synovial inflammation in rheumatoid arthritis

Annals of the rheumatic diseases, 2011-03, Vol.70 (Suppl 2), p.A23-A23

2011

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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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Evidence That Mutations in the X-linked DDP Gene Cause Incompletely Penetrant and Variable Skewed X Inactivation

American journal of human genetics, 1999-03, Vol.64 (3), p.759-767

1999

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Disruption of dominant B cell/plasma cell clones in rheumatoid arthritis synovium by rituximab correlates with treatment response

Annals of the rheumatic diseases, 2012-02, Vol.71 (Suppl 1), p.A37-A38

2012

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Autosomal Dominant Mutations Affecting X Inactivation Choice in the Mouse

Science (American Association for the Advancement of Science), 2002-05, Vol.296 (5570), p.1136-1139

2002

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High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

Nature genetics, 2012-12, Vol.44 (12), p.1336-1340

2012

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Predictors of severe outcomes associated with C lostridium difficile infection in patients with inflammatory bowel disease

Alimentary pharmacology & therapeutics, 2012-04, Vol.35 (7), p.789-795

2012

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Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis

Nature genetics, 2012-05, Vol.44 (5), p.483-489

2012

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Using genetic and clinical data to understand response to disease-modifying anti-rheumatic drug therapy: data from the Brigham and Women's Hospital Rheumatoid Arthritis Sequential Study

Rheumatology (Oxford, England), 2011-01, Vol.50 (1), p.40-46

2011

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Quantifying missing heritability at known GWAS loci

PLoS genetics, 2013-12, Vol.9 (12), p.e1003993-e1003993

2013

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STAT4 and the Risk of Rheumatoid Arthritis and Systemic Lupus Erythematosus

The New England journal of medicine, 2007-09, Vol.357 (10), p.977-986

2007

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Analysis and application of European genetic substructure using 300 K SNP information

PLoS genetics, 2008, Vol.4 (1), p.e4-e4

2008

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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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Psychiatric co‐morbidity is associated with increased risk of surgery in Crohn's disease

Predictors of severe outcomes associated with Clostridium difficile infection in patients with inflammatory bowel disease

Polygenic inheritance of paclitaxel-induced sensory peripheral neuropathy driven by axon outgrowth gene sets in CALGB 40101 (Alliance)

Fine mapping the TAGAP risk locus in rheumatoid arthritis

Associations between Human leukocyte antigen, PTPN22, CTLA4 genotypes and rheumatoid arthritis phenotypes of autoantibody status, age at diagnosis and erosions in a large cohort study

The influence of polygenic risk scores on heritability of anti-CCP level in RA

Gene-Gene and Gene-Environment Interactions Involving HLA-DRB1, PTPN22, and Smoking in Two Subsets of Rheumatoid Arthritis

A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation

Heritability of X chromosome-inactivation phenotype in a large family

Skewed X-Chromosome Inactivation Is a Common Feature of X-Linked Mental Retardation Disorders

GWAS in IMIDs

The BLIMP-1 risk allele is associated with increased synovial inflammation in rheumatoid arthritis

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

Evidence That Mutations in the X-linked DDP Gene Cause Incompletely Penetrant and Variable Skewed X Inactivation

Disruption of dominant B cell/plasma cell clones in rheumatoid arthritis synovium by rituximab correlates with treatment response

Autosomal Dominant Mutations Affecting X Inactivation Choice in the Mouse

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

Predictors of severe outcomes associated with C lostridium difficile infection in patients with inflammatory bowel disease

Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis

Using genetic and clinical data to understand response to disease-modifying anti-rheumatic drug therapy: data from the Brigham and Women's Hospital Rheumatoid Arthritis Sequential Study

Quantifying missing heritability at known GWAS loci

STAT4 and the Risk of Rheumatoid Arthritis and Systemic Lupus Erythematosus

Analysis and application of European genetic substructure using 300 K SNP information

A common haplotype of interferon regulatory factor 5 ( IRF5 ) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus

A Role for Noncoding Variation in Schizophrenia

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