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Unsupervised detection of cancer driver mutations with parsimony-guided learning

Nature genetics, 2016-10, Vol.48 (10), p.1288-1294

2016

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Analysis of somatic mutations across the kinome reveals loss-of-function mutations in multiple cancer types

Scientific reports, 2017-07, Vol.7 (1), p.6418-12, Article 6418

2017

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DGIdb: mining the druggable genome

Nature methods, 2013-12, Vol.10 (12), p.1209-1210

2013

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Statistically identifying tumor suppressors and oncogenes from pan-cancer genome-sequencing data

Bioinformatics (Oxford, England), 2015-11, Vol.31 (22), p.3561-3568

2015

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Prioritizing Potentially Druggable Mutations with dGene: An Annotation Tool for Cancer Genome Sequencing Data

PloS one, 2013-06, Vol.8 (6), p.e67980-e67980

2013

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Deciphering a global network of functionally associated post‐translational modifications

Molecular systems biology, 2012-07, Vol.8 (1), p.599-n/a

2012

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The prognostic effects of somatic mutations in ER-positive breast cancer

Nature communications, 2018-09, Vol.9 (1), p.3476-16, Article 3476

2018

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Clinical genome sequencing: Three years’ experience at a tertiary children’s hospital

Genetics in medicine, 2023-10, Vol.25 (10), p.100916-100916, Article 100916

2023

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P716: Real-world implications of new population genomic datasets for clinical variant interpretation

Genetics in Medicine Open, 2024, Vol.2, p.101620, Article 101620

2024

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Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis

American journal of medical genetics. Part A, 2022-11, Vol.188 (11), p.3184-3190

2022

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The germline p53 activation syndrome: A new patient further refines the clinical phenotype

American journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.2204-2208

2022

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Brain abscesses, neutropenia, and B-ALL: Multiple testing modalities required to confirm PDCD10 and ETV6 dual diagnoses

Cancer genetics, 2024-11, Vol.288-289, p.5-9

2024

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PoxA, YjeK, and Elongation Factor P Coordinately Modulate Virulence and Drug Resistance in Salmonella enterica

Molecular cell, 2010-07, Vol.39 (2), p.209-221

2010

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Cross‐talk between phosphorylation and lysine acetylation in a genome‐reduced bacterium

Molecular systems biology, 2012-02, Vol.8 (1), p.571-n/a

2012

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A TMPRSS2‐ERG gene signature predicts prognosis of patients with prostate adenocarcinoma

Clinical and translational medicine, 2020-12, Vol.10 (8), p.e216-n/a

2020

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P564: Genetic test stewardship for clinical exome sequencing: Review of critical care orders at Texas Children’s Hospital

Genetics in Medicine Open, 2023, Vol.1 (1), p.100611, Article 100611

2023

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A deep intronic variant is a common cause of OTC deficiency in individuals with previously negative genetic testing

Molecular genetics and metabolism reports, 2021-03, Vol.26, p.100706-100706, Article 100706

2021

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Facial Nerve Palsy in a Child With Fever of Unknown Origin

Clinical pediatrics, 2020-05, Vol.59 (4-5), p.516-518

2020

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Selection for or against escape from nonsense mediated decay is a novel signature for the detection of cancer genes

Cancer genetics, 2021-11, Vol.258-259, p.80-84

2021

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eP135 - A case of p53 related intellectual disability, seizures, microcephaly, anemia and small stature

Molecular genetics and metabolism, 2021-04, Vol.132, p.S89-S90

2021

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A case of p53 related intellectual disability, seizures, microcephaly, anemia and small stature

Molecular genetics and metabolism, 2021-04, Vol.132, p.S89-S90

2021

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Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer

Nature communications, 2018-11, Vol.9 (1), p.4850-2, Article 4850

2018

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Response of a Metastatic Breast Carcinoma With a Previously Uncharacterized ERBB2 G776V Mutation to Human Epidermal Growth Factor Receptor 2–Targeted Therapy

JCO precision oncology, 2017-11 (1), p.1-9

2017

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Initiation of Inappropriate Antimicrobial Therapy Results in a Fivefold Reduction of Survival in Human Septic Shock

Chest, 2009-11, Vol.136 (5), p.1237-1248

2009

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Association between Source of Infection and Hospital Mortality in Patients Who Have Septic Shock

American journal of respiratory and critical care medicine, 2014-05, Vol.189 (10), p.1204-1213

2014

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Unsupervised detection of cancer driver mutations with parsimony-guided learning

Analysis of somatic mutations across the kinome reveals loss-of-function mutations in multiple cancer types

DGIdb: mining the druggable genome

Statistically identifying tumor suppressors and oncogenes from pan-cancer genome-sequencing data

Prioritizing Potentially Druggable Mutations with dGene: An Annotation Tool for Cancer Genome Sequencing Data

Deciphering a global network of functionally associated post‐translational modifications

The prognostic effects of somatic mutations in ER-positive breast cancer

Clinical genome sequencing: Three years’ experience at a tertiary children’s hospital

P716: Real-world implications of new population genomic datasets for clinical variant interpretation

Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis

The germline p53 activation syndrome: A new patient further refines the clinical phenotype

Brain abscesses, neutropenia, and B-ALL: Multiple testing modalities required to confirm PDCD10 and ETV6 dual diagnoses

PoxA, YjeK, and Elongation Factor P Coordinately Modulate Virulence and Drug Resistance in Salmonella enterica

Cross‐talk between phosphorylation and lysine acetylation in a genome‐reduced bacterium

A TMPRSS2‐ERG gene signature predicts prognosis of patients with prostate adenocarcinoma

P564: Genetic test stewardship for clinical exome sequencing: Review of critical care orders at Texas Children’s Hospital

A deep intronic variant is a common cause of OTC deficiency in individuals with previously negative genetic testing

Facial Nerve Palsy in a Child With Fever of Unknown Origin

Selection for or against escape from nonsense mediated decay is a novel signature for the detection of cancer genes

eP135 - A case of p53 related intellectual disability, seizures, microcephaly, anemia and small stature

A case of p53 related intellectual disability, seizures, microcephaly, anemia and small stature

Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer

Response of a Metastatic Breast Carcinoma With a Previously Uncharacterized ERBB2 G776V Mutation to Human Epidermal Growth Factor Receptor 2–Targeted Therapy

Initiation of Inappropriate Antimicrobial Therapy Results in a Fivefold Reduction of Survival in Human Septic Shock

Association between Source of Infection and Hospital Mortality in Patients Who Have Septic Shock

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