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Bruce Gelb

Has grant

Director

Icahn School of Medicine at Mount Sinai

United States

Research Interests

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Professors in United States

Recent Grants

Grant: Close

Human Induced Pluripotent Cell Models of Pediatric Cardiac Disorders

Open Date: 2013-08-01

Close Date: 2017-07-31

Grant: Close

Understanding intellectual disability in Noonan syndrome and related disorders

Open Date: 2011-08-25

Close Date: 2014-07-31

Grant: Close

International Meeting on Genetic Syndromes of the Ras/MAPK Pathway

Open Date: 2011-04-01

Close Date: 2011-12-31

Grant: Close

Impact of CNVs on outcomes for infants with single ventricle heart defects

Open Date: 2010-07-15

Close Date: 2013-06-30

Grant: Close

Genomic studies of secundum atrial septal defects

Open Date: 2009-09-30

Close Date: 2015-07-31

Articles (20)

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Collaborators (10)

S. Stephen Yi

Associate Professor and Research Member

Baylor College of Medicine

UNITED STATES

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Stephen Kingsmore

Chair

Cleveland Clinic

UNITED STATES

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Edgar Hernandez

Research Assistant Professor

University of Utah

UNITED STATES

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Nathan Blue

Assistant Professor

University of Utah

UNITED STATES

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Michael Wagner

Associate Professor

Cincinnati Children's Hospital Medical Center

UNITED STATES

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Sofia Douzgou

Honorary Senior Lecturer

UNITED KINGDOM

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Warren Tai

University of California, Los Angeles

UNITED STATES

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Qiongshi Lu

Assistant Professor

University of Wisconsin-Madison

UNITED STATES

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Tess Levy

Icahn School of Medicine at Mount Sinai

UNITED STATES

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Peter J. Gruber

Karolinska Institutet

SWEDEN

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Bruce Gelb

Research Interests

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Recent Grants

Articles (20)

ADNP‐Related Helsmoortel–Van der Aa Syndrome: A Review of the Literature and Clinical Recommendations for Assessment and Monitoring

Rare KDR Variants Define a Distinct Genetic Contribution to Congenital Heart Disease

Prothrombin G20210A and Factor V Leiden Variants Are Not Associated With Thrombotic Events in Congenital Heart Disease: An Observational Trial

Machine learning to infer neurocognitive testing scores among adolescents and young adults with congenital heart disease

Drivers of Diagnostic Delay in Mitochondrial Disease: Missed Recognition of Canonical Features.

Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genes

Recessive genetic contribution to congenital heart disease in 5,424 probands

Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery

Modeling SMAD2 Mutations in Induced Pluripotent Stem Cells Provides Insights Into Cardiovascular Disease Pathogenesis

Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach.

Rapid Genome Sequencing Compared with a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic Evaluation.

The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.

Toward governance of artificial intelligence in pediatric healthcare.

Patient and providers' perspectives on using the GUÍA digital tool to enhance genomic results disclosure.

Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencing.

Genome-Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DS.

Deficiency of the Fanconi anemia core complex protein FAAP100 results in severe Fanconi anemia.

Updated ACMG/AMP specifications for variant interpretation and gene curations from the ClinGen RASopathy expert panels.

2024 ASHG presidential address: Incomplete penetrance and variable expressivity: Old concepts, new urgency

Efficient identification of de novo mutations in family trios: a consensus-based informatic approach.

Collaborators (10)

S. Stephen Yi

Stephen Kingsmore

Edgar Hernandez

Nathan Blue

Michael Wagner

Sofia Douzgou

Warren Tai

Qiongshi Lu

Tess Levy

Peter J. Gruber

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