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Overexpression of Catalase Targeted to Mitochondria Attenuates Murine Cardiac Aging

Circulation (New York, N.Y.), 2009-06, Vol.119 (21), p.2789-2797

2009

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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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Age‐dependent cardiomyopathy in mitochondrial mutator mice is attenuated by overexpression of catalase targeted to mitochondria

Aging cell, 2010-08, Vol.9 (4), p.536-544

2010

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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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Genome Capture Sequencing Selectively Enriches Bacterial DNA and Enables Genome-Wide Measurement of Intrastrain Genetic Diversity in Human Infections

mBio, 2022-10, Vol.13 (5), p.e0142422-e0142422

2022

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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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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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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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Homologous Recombination Resolution Defect in Werner Syndrome

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

2002

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

PLoS pathogens, 2019-02, Vol.15 (2), p.e1007588-e1007588

2019

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Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes

Annals of hepatology, 2018-09, Vol.17 (5), p.871-879

2018

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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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An exome-wide study of renal operational tolerance

Frontiers in medicine, 2023-05, Vol.9, p.976248-976248

2023

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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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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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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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Respiratory chain protein turnover rates in mice are highly heterogeneous but strikingly conserved across tissues, ages, and treatments

The FASEB journal, 2015-08, Vol.29 (8), p.3582-3592

2015

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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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Overexpression of Catalase Targeted to Mitochondria Attenuates Murine Cardiac Aging

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

Age‐dependent cardiomyopathy in mitochondrial mutator mice is attenuated by overexpression of catalase targeted to mitochondria

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

Genome Capture Sequencing Selectively Enriches Bacterial DNA and Enables Genome-Wide Measurement of Intrastrain Genetic Diversity in Human Infections

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

Exome sequencing as a tool for Mendelian disease gene discovery

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

Homologous Recombination Resolution Defect in Werner Syndrome

Disruption of protein kinase A in mice enhances healthy aging

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

Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes

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

An exome-wide study of renal operational tolerance

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

Sphingosine, a Modulator of Human Translesion DNA Polymerase Activity

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

Respiratory chain protein turnover rates in mice are highly heterogeneous but strikingly conserved across tissues, ages, and treatments

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

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