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Effects of immunomodulatory drugs on depressive symptoms: A mega-analysis of randomized, placebo-controlled clinical trials in inflammatory disorders

Molecular psychiatry, 2020-06, Vol.25 (6), p.1275-1285

2020

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Modular Analysis of Peripheral Blood Gene Expression in Rheumatoid Arthritis Captures Reproducible Gene Expression Changes in Tumor Necrosis Factor Responders

Arthritis & rheumatology (Hoboken, N.J.), 2015-02, Vol.67 (2), p.344-351

2015

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Comprehensive analysis of treatment response phenotypes in rheumatoid arthritis for pharmacogenetic studies

Arthritis research & therapy, 2017-05, Vol.19 (1), p.90-90, Article 90

2017

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Ethnic Differences in Cardiac Potassium Channel Variants: Implications for Genetic Susceptibility to Sudden Cardiac Death and Genetic Testing for Congenital Long QT Syndrome

Mayo Clinic proceedings, 2003-12, Vol.78 (12), p.1479-1487

2003

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Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing

Heart rhythm, 2004-11, Vol.1 (5), p.600-607

2004

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Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

American journal of medical genetics. Part A, 2003-12, Vol.123A (3), p.267-278

2003

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A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel

Cell, 1995-04, Vol.81 (2), p.299-307

1995

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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

Cell, 1995-03, Vol.80 (5), p.795-803

1995

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Conference Scene: Diagnostics and personalized medicine: observations from the World Companion Diagnostics Summit

Pharmacogenomics, 2011-04, Vol.12 (4), p.465-470

2011

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Integrative genomic deconvolution of rheumatoid arthritis GWAS loci into gene and cell type associations

Genome Biology, 2016-04, Vol.17 (1), p.79-79, Article 79

2016

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Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies

BMC bioinformatics, 2015-09, Vol.16 (1), p.304-304, Article 304

2015

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Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6

European journal of human genetics : EJHG, 2002-04, Vol.10 (4), p.259-265

2002

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Sudden infant death syndrome: Case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development

Pediatric research, 2004-09, Vol.56 (3), p.391-395

2004

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Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel : open-channel block by methanesulfonanilides

Circulation research, 1996-03, Vol.78 (3), p.499-503

1996

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Fast inactivation causes rectification of the IKr channel

The Journal of general physiology, 1996-05, Vol.107 (5), p.611-619

1996

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A Genomewide Analysis Provides Evidence for Novel Linkages in Inflammatory Bowel Disease in a Large European Cohort

American journal of human genetics, 1999-03, Vol.64 (3), p.808-816

1999

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Linkage of Inflammatory Bowel Disease to Human Chromosome 6p

American journal of human genetics, 1999-12, Vol.65 (6), p.1647-1655

1999

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Sudden infant death syndrome: Association with a promoter polymorphism of the serotonin transporter gene

American journal of medical genetics. Part A, 2003-03, Vol.117A (3), p.268-274

2003

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Potassium ion channels and human disease: phenotypes to drug targets?

Current opinion in biotechnology, 1998-12, Vol.9 (6), p.565-572

Curran, Mark E

1998

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Direct Activation of an Inwardly Rectifying Potassium Channel by Arachidonic Acid

Molecular pharmacology, 2001-05, Vol.59 (5), p.1061-1068

2001

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Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility loci

Human genetics, 2003-11, Vol.113 (6), p.514-521

2003

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Spectrum of HERG K+-Channel Dysfunction in an Inherited Cardiac Arrhythmia

Proceedings of the National Academy of Sciences - PNAS, 1996-03, Vol.93 (5), p.2208-2212

1996

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Diagnostics and personalized medicine: observations from the World Companion Diagnostics Summit

Pharmacogenomics, 2011, Vol.12 (4), p.465-470

2011

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Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16

Gastroenterology (New York, N.Y. 1943), 1998-11, Vol.115 (5), p.1066-1071

1998

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The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

Cell, 1993-04, Vol.73 (1), p.159-168

1993

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Effects of immunomodulatory drugs on depressive symptoms: A mega-analysis of randomized, placebo-controlled clinical trials in inflammatory disorders

Modular Analysis of Peripheral Blood Gene Expression in Rheumatoid Arthritis Captures Reproducible Gene Expression Changes in Tumor Necrosis Factor Responders

Comprehensive analysis of treatment response phenotypes in rheumatoid arthritis for pharmacogenetic studies

Ethnic Differences in Cardiac Potassium Channel Variants: Implications for Genetic Susceptibility to Sudden Cardiac Death and Genetic Testing for Congenital Long QT Syndrome

Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing

Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

Conference Scene: Diagnostics and personalized medicine: observations from the World Companion Diagnostics Summit

Integrative genomic deconvolution of rheumatoid arthritis GWAS loci into gene and cell type associations

Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies

Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6

Sudden infant death syndrome: Case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development

Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel : open-channel block by methanesulfonanilides

Fast inactivation causes rectification of the IKr channel

A Genomewide Analysis Provides Evidence for Novel Linkages in Inflammatory Bowel Disease in a Large European Cohort

Linkage of Inflammatory Bowel Disease to Human Chromosome 6p

Sudden infant death syndrome: Association with a promoter polymorphism of the serotonin transporter gene

Potassium ion channels and human disease: phenotypes to drug targets?

Direct Activation of an Inwardly Rectifying Potassium Channel by Arachidonic Acid

Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility loci

Spectrum of HERG K+-Channel Dysfunction in an Inherited Cardiac Arrhythmia

Diagnostics and personalized medicine: observations from the World Companion Diagnostics Summit

Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

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