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Host genetic risk factors for West Nile virus infection and disease progression

PloS one, 2011-09, Vol.6 (9), p.e24745-e24745

2011

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Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis

PLoS genetics, 2015-06, Vol.11 (6), p.e1005273-e1005273

2015

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Survey of innate immune responses to Burkholderia pseudomallei in human blood identifies a central role for lipopolysaccharide

PloS one, 2013-11, Vol.8 (11), p.e81617-e81617

2013

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Disruption of protein kinase A in mice enhances healthy aging

PloS one, 2009-06, Vol.4 (6), p.e5963-e5963

2009

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Chromosomal instability in ulcerative colitis is related to telomere shortening

Nature genetics, 2002-10, Vol.32 (2), p.280-284

2002

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CpG Island Methylator Phenotype Is Associated With Response to Adjuvant Irinotecan-Based Therapy for Stage III Colon Cancer

Gastroenterology (New York, N.Y. 1943), 2014-09, Vol.147 (3), p.637-645

2014

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Mitochondrial DNA Mutations are Associated with Ulcerative Colitis Preneoplasia but Tend to be Negatively Selected in Cancer

Molecular cancer research, 2019-02, Vol.17 (2), p.488-498

2019

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Inflammasome Genetic Variants, Macrophage Function, and Clinical Outcomes in Cystic Fibrosis

American journal of respiratory cell and molecular biology, 2021-08, Vol.65 (2), p.157-166

2021

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Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload

Hepatology (Baltimore, Md.), 2015-08, Vol.62 (2), p.429-439

2015

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Mitochondria and Tumor Progression in Ulcerative Colitis

JNCI : Journal of the National Cancer Institute, 2013-08, Vol.105 (16), p.1239-1248

2013

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The Epithelial Sodium Channel Is a Modifier of the Long-Term Nonprogressive Phenotype Associated with F508del CFTR Mutations

American journal of respiratory cell and molecular biology, 2017-12, Vol.57 (6), p.711-720

2017

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Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole‐Exome Sequencing

Arthritis & rheumatology (Hoboken, N.J.), 2016-01, Vol.68 (1), p.191-200

2016

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Ursodiol use is associated with lower prevalence of colonic neoplasia in patients with ulcerative colitis and primary sclerosing cholangitis

Annals of internal medicine, 2001-01, Vol.134 (2), p.89

2001

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Impaired TLR5 functionality is associated with survival in melioidosis

The Journal of immunology (1950), 2013-04, Vol.190 (7), p.3373-3379

2013

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Apurinic Endonuclease Activity in Adult Gliomas and Time to Tumor Progression after Alkylating Agent-Based Chemotherapy and after Radiotherapy

Clinical cancer research, 2004-12, Vol.10 (23), p.7875-7883

2004

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Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype

Scientific reports, 2017-03, Vol.7 (1), p.44081, Article 44081

2017

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Increased prevalence of gastroesophageal reflux in patients with idiopathic pulmonary fibrosis

American journal of respiratory and critical care medicine, 1998-12, Vol.158 (6), p.1804-1808

1998

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Hepatitis C, iron status, and disease severity: Relationship with HFE mutations

Gastroenterology (New York, N.Y. 1943), 2003-02, Vol.124 (2), p.318-326

2003

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GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes

Blood cells, molecules, & diseases, 2017-03, Vol.63, p.15-20

2017

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Pancolonic chromosomal instability precedes dysplasia and cancer in ulcerative colitis

Cancer research (Chicago, Ill.), 1999-10, Vol.59 (20), p.5148-5153

1999

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Genomic Biomarkers to Improve Ulcerative Colitis Neoplasia Surveillance

The American journal of pathology, 2008-12, Vol.173 (6), p.1853-1860

2008

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Clinical response to azithromycin in cystic fibrosis correlates with in vitro effects on Pseudomonas aeruginosa phenotypes

Pediatric pulmonology, 2007-06, Vol.42 (6), p.533-541

2007

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Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

American journal of human genetics, 2014-02, Vol.94 (2), p.233-245

2014

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Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes

Cancer research (Chicago, Ill.), 2000-05, Vol.60 (9), p.2492-2496

2000

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TLR4 genetic variation is associated with inflammatory responses in Gram-positive sepsis

Clinical microbiology and infection, 2017-01, Vol.23 (1), p.47.e1-47.e10

2017

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Host genetic risk factors for West Nile virus infection and disease progression

Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis

Survey of innate immune responses to Burkholderia pseudomallei in human blood identifies a central role for lipopolysaccharide

Disruption of protein kinase A in mice enhances healthy aging

Chromosomal instability in ulcerative colitis is related to telomere shortening

CpG Island Methylator Phenotype Is Associated With Response to Adjuvant Irinotecan-Based Therapy for Stage III Colon Cancer

Mitochondrial DNA Mutations are Associated with Ulcerative Colitis Preneoplasia but Tend to be Negatively Selected in Cancer

Inflammasome Genetic Variants, Macrophage Function, and Clinical Outcomes in Cystic Fibrosis

Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload

Mitochondria and Tumor Progression in Ulcerative Colitis

The Epithelial Sodium Channel Is a Modifier of the Long-Term Nonprogressive Phenotype Associated with F508del CFTR Mutations

Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole‐Exome Sequencing

Ursodiol use is associated with lower prevalence of colonic neoplasia in patients with ulcerative colitis and primary sclerosing cholangitis

Impaired TLR5 functionality is associated with survival in melioidosis

Apurinic Endonuclease Activity in Adult Gliomas and Time to Tumor Progression after Alkylating Agent-Based Chemotherapy and after Radiotherapy

Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype

Increased prevalence of gastroesophageal reflux in patients with idiopathic pulmonary fibrosis

Hepatitis C, iron status, and disease severity: Relationship with HFE mutations

GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes

Pancolonic chromosomal instability precedes dysplasia and cancer in ulcerative colitis

Genomic Biomarkers to Improve Ulcerative Colitis Neoplasia Surveillance

Clinical response to azithromycin in cystic fibrosis correlates with in vitro effects on Pseudomonas aeruginosa phenotypes

Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes

TLR4 genetic variation is associated with inflammatory responses in Gram-positive sepsis

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