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Whole-Genome Sequencing of a Healthy Aging Cohort

Cell, 2016-05, Vol.165 (4), p.1002-1011

2016

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The Asthma Mobile Health Study, a large-scale clinical observational study using ResearchKit

Nature biotechnology, 2017-04, Vol.35 (4), p.354-362

2017

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Sequencing the CYP2D6 gene: from variant allele discovery to clinical pharmacogenetic testing

Pharmacogenomics, 2017-05, Vol.18 (7), p.673-685

2017

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Estimating the causal effects of multiple intermittent treatments with application to COVID-19

Journal of the Royal Statistical Society Series C: Applied Statistics, 2023-12, Vol.72 (5), p.1162-1186

2023

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Microbial Cell-Free DNA Identifies Etiology of Bloodstream Infections, Persists Longer Than Conventional Blood Cultures, and Its Duration of Detection Is Associated With Metastatic Infection in Patients With Staphylococcus aureus and Gram-Negative Bacteremia

Clinical infectious diseases, 2022-06, Vol.74 (11), p.2020-2027

2022

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Microbial Cell-Free DNA Identifies the Causative Pathogen in Infective Endocarditis and Remains Detectable Longer Than Conventional Blood Culture in Patients with Prior Antibiotic Therapy

Clinical infectious diseases, 2023-02, Vol.76 (3), p.e1492-e1500

2023

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An Examination of the Relationship between Lipid Levels and Associated Genetic Markers across Racial/Ethnic Populations in the Multi-Ethnic Study of Atherosclerosis

PloS one, 2015-05, Vol.10 (5), p.e0126361-e0126361

2015

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Pharmacogenomic education among genetic counseling training programs in North America

Journal of genetic counseling, 2021-10, Vol.30 (5), p.1500-1508

2021

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VarCover: Allele Min-Set Cover Software

The Journal of molecular diagnostics : JMD, 2020-02, Vol.22 (2), p.123-131

2020

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Long‐read HiFi sequencing of NUDT15: Phased full‐gene haplotyping and pharmacogenomic allele discovery

Human mutation, 2022-11, Vol.43 (11), p.1557-1566

2022

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Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

European journal of human genetics : EJHG, 2020-04, Vol.28 (4), p.424-434

2020

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Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia

Annals of neurology, 2014-04, Vol.75 (4), p.542-549

2014

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Evidence for Alteration of Gene Regulatory Networks through MicroRNAs of the HIV-infected brain: novel analysis of retrospective cases

PloS one, 2010-04, Vol.5 (4), p.e10337-e10337

2010

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Whole Genome Sequencing Coverage & Quality at Prenatal Carrier Screening Loci: An Analysis of 15,496 gnomAD Genomes [23K]

Obstetrics and gynecology (New York. 1953), 2018-05, Vol.131 (1), p.125-125S

2018

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Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection

Clinical and translational science, 2021-01, Vol.14 (1), p.204-213

2021

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APPLaUD: access for patients and participants to individual level uninterpreted genomic data

Human genomics, 2018-02, Vol.12 (1), p.7-7, Article 7

2018

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Sensitive, multiplex and direct quantification of RNA sequences using a modified RASL assay

Nucleic acids research, 2014-08, Vol.42 (14), p.9146-9157

2014

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Institutional profile: translational pharmacogenomics at the Icahn School of Medicine at Mount Sinai

Pharmacogenomics, 2017-10, Vol.18 (15), p.1381-1386

2017

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Phased Haplotype Resolution of the SLC6A4 Promoter Using Long-Read Single Molecule Real-Time (SMRT) Sequencing

Genes, 2020-11, Vol.11 (11), p.1333

2020

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Estimating Local Costs Associated With Clostridium difficile Infection Using Machine Learning and Electronic Medical Records

Infection control and hospital epidemiology, 2017-12, Vol.38 (12), p.1478-1486

2017

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Multiplexed analysis of fixed tissue RNA using Ligation in situ Hybridization

Nucleic acids research, 2017-08, Vol.45 (14), p.e128-e128

2017

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Assessing calibration and bias of a deployed machine learning malnutrition prediction model within a large healthcare system

NPJ digital medicine, 2024-06, Vol.7 (1), p.149-7

2024

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A genome sequencing program for novel undiagnosed diseases

Genetics in medicine, 2015-12, Vol.17 (12), p.995-1001

2015

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METHODS FOR CLUSTERING TIME SERIES DATA ACQUIRED FROM MOBILE HEALTH APPS

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2017, Vol.22, p.300

2017

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'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods

Personalized medicine, 2018-07, Vol.15 (4), p.311-318

2018

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Whole-Genome Sequencing of a Healthy Aging Cohort

The Asthma Mobile Health Study, a large-scale clinical observational study using ResearchKit

Sequencing the CYP2D6 gene: from variant allele discovery to clinical pharmacogenetic testing

Estimating the causal effects of multiple intermittent treatments with application to COVID-19

Microbial Cell-Free DNA Identifies Etiology of Bloodstream Infections, Persists Longer Than Conventional Blood Cultures, and Its Duration of Detection Is Associated With Metastatic Infection in Patients With Staphylococcus aureus and Gram-Negative Bacteremia

Microbial Cell-Free DNA Identifies the Causative Pathogen in Infective Endocarditis and Remains Detectable Longer Than Conventional Blood Culture in Patients with Prior Antibiotic Therapy

An Examination of the Relationship between Lipid Levels and Associated Genetic Markers across Racial/Ethnic Populations in the Multi-Ethnic Study of Atherosclerosis

Pharmacogenomic education among genetic counseling training programs in North America

VarCover: Allele Min-Set Cover Software

Long‐read HiFi sequencing of NUDT15: Phased full‐gene haplotyping and pharmacogenomic allele discovery

Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia

Evidence for Alteration of Gene Regulatory Networks through MicroRNAs of the HIV-infected brain: novel analysis of retrospective cases

Whole Genome Sequencing Coverage & Quality at Prenatal Carrier Screening Loci: An Analysis of 15,496 gnomAD Genomes [23K]

Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection

APPLaUD: access for patients and participants to individual level uninterpreted genomic data

Sensitive, multiplex and direct quantification of RNA sequences using a modified RASL assay

Institutional profile: translational pharmacogenomics at the Icahn School of Medicine at Mount Sinai

Phased Haplotype Resolution of the SLC6A4 Promoter Using Long-Read Single Molecule Real-Time (SMRT) Sequencing

Estimating Local Costs Associated With Clostridium difficile Infection Using Machine Learning and Electronic Medical Records

Multiplexed analysis of fixed tissue RNA using Ligation in situ Hybridization

Assessing calibration and bias of a deployed machine learning malnutrition prediction model within a large healthcare system

A genome sequencing program for novel undiagnosed diseases

METHODS FOR CLUSTERING TIME SERIES DATA ACQUIRED FROM MOBILE HEALTH APPS

'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods

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