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Ultra-Sensitive TP53 Sequencing for Cancer Detection Reveals Progressive Clonal Selection in Normal Tissue over a Century of Human Lifespan

Cell reports (Cambridge), 2019-07, Vol.28 (1), p.132-144.e3

2019

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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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Whole genome sequencing of extreme phenotypes identifies variants in CD101 and UBE2V1 associated with increased risk of sexually acquired HIV-1

PLoS pathogens, 2017-11, Vol.13 (11), p.e1006703-e1006703

2017

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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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The Human WRN and BLM RecQ Helicases Differentially Regulate Cell Proliferation and Survival after Chemotherapeutic DNA Damage

Cancer research (Chicago, Ill.), 2010-08, Vol.70 (16), p.6548-6555

2010

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Exome sequencing as a tool for Mendelian disease gene discovery

Nature reviews. Genetics, 2011-11, Vol.12 (11), p.745-755

2011

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Homologous Recombination Resolution Defect in Werner Syndrome

Molecular and Cellular Biology, 2002-10, Vol.22 (20), p.6971-6978

2002

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Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies

American journal of human genetics, 2012-08, Vol.91 (2), p.224-237

2012

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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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Sphingosine, a Modulator of Human Translesion DNA Polymerase Activity

The Journal of biological chemistry, 2014-08, Vol.289 (31), p.21663-21672

2014

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Ultra-deep sequencing detects ovarian cancer cells in peritoneal fluid and reveals somatic TP53 mutations in noncancerous tissues

Proceedings of the National Academy of Sciences - PNAS, 2016-05, Vol.113 (21), p.6005-6010

2016

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Exonic sequencing identifies TLR1 genetic variation associated with mortality in Thais with melioidosis

Emerging microbes & infections, 2019-01, Vol.8 (1), p.282-290

2019

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Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

Nature genetics, 2012-08, Vol.44 (8), p.886-889

2012

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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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Characterization of TP53 mutations in Pap test DNA of women with and without serous ovarian carcinoma

Gynecologic oncology, 2020-02, Vol.156 (2), p.407-414

2020

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Club cell secretory protein and lung function in children with cystic fibrosis

Journal of cystic fibrosis, 2022-09, Vol.21 (5), p.811-820

2022

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Overdiagnosis of high-grade dysplasia in Barrett's esophagus: a multicenter, international study

Modern pathology, 2015-06, Vol.28 (6), p.758-765

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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Ultra-Sensitive TP53 Sequencing for Cancer Detection Reveals Progressive Clonal Selection in Normal Tissue over a Century of Human Lifespan

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

Whole genome sequencing of extreme phenotypes identifies variants in CD101 and UBE2V1 associated with increased risk of sexually acquired HIV-1

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

The Human WRN and BLM RecQ Helicases Differentially Regulate Cell Proliferation and Survival after Chemotherapeutic DNA Damage

Exome sequencing as a tool for Mendelian disease gene discovery

Homologous Recombination Resolution Defect in Werner Syndrome

Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies

Chromosomal instability in ulcerative colitis is related to telomere shortening

Sphingosine, a Modulator of Human Translesion DNA Polymerase Activity

Ultra-deep sequencing detects ovarian cancer cells in peritoneal fluid and reveals somatic TP53 mutations in noncancerous tissues

Exonic sequencing identifies TLR1 genetic variation associated with mortality in Thais with melioidosis

Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

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

Characterization of TP53 mutations in Pap test DNA of women with and without serous ovarian carcinoma

Club cell secretory protein and lung function in children with cystic fibrosis

Overdiagnosis of high-grade dysplasia in Barrett's esophagus: a multicenter, international study

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

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