Bruce D. Gelb

Bruce D. Gelb

Pediatric Cardiology
1 Gustave L Levy Pl
New York, NY 10029

Last Updated: 09/26/2026

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Found 241 publications

Rigosertib Reverses Hypertrophic Cardiomyopathy in Noonan Syndrome.

Rigosertib Reverses Hypertrophic Cardiomyopathy in Noonan Syndrome.

Journal: Circulation
Published: August 18, 2026

Uniparental Disomy Reveals Hidden Genetic Causes of Congenital Heart Disease.

Uniparental Disomy Reveals Hidden Genetic Causes of Congenital Heart Disease.

Journal: Research square
Published: August 01, 2026

Pediatric Genomic Medicine-rapid progress, but not too fast: American Pediatric Society's 2026 John Howland Award Lecture.

Pediatric Genomic Medicine-rapid progress, but not too fast: American Pediatric Society's 2026 John Howland Award Lecture.

Journal: Pediatric research
Published: May 18, 2026

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

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

Journal: Circulation. Genomic and precision medicine
Published: April 22, 2026

Feeder-Free Generation of Lymphatic Endothelial Cells from Human Induced Pluripotent Stem Cells.

Feeder-Free Generation of Lymphatic Endothelial Cells from Human Induced Pluripotent Stem Cells.

Journal: bioRxiv : the preprint server for biology
Published: April 03, 2026

Identifying Genes Associated with Obstructive Congenital Heart Defects Using a Family-Based Genetic Random Field Method: Results from the National Birth Defects Prevention Study.

Identifying Genes Associated with Obstructive Congenital Heart Defects Using a Family-Based Genetic Random Field Method: Results from the National Birth Defects Prevention Study.

Journal: HGG advances
Published: March 10, 2026

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

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

Journal: Journal of the American Heart Association
Published: March 04, 2026

The 9th International RASopathies Symposium.

The 9th International RASopathies Symposium.

Journal: American journal of medical genetics. Part A
Published: February 25, 2026

ROBO2 Variants Associated With Atrial Septal Defect Define a Novel Regulatory Element.

ROBO2 Variants Associated With Atrial Septal Defect Define a Novel Regulatory Element.

Journal: Circulation. Genomic and precision medicine
Published: February 16, 2026

Dysregulated TGFβ-ERK Signaling Drives Aberrant Extracellular Matrix Production in Noonan Syndrome-Associated Pulmonary Valve Stenosis.

Dysregulated TGFβ-ERK Signaling Drives Aberrant Extracellular Matrix Production in Noonan Syndrome-Associated Pulmonary Valve Stenosis.

Journal: bioRxiv : the preprint server for biology
Published: February 06, 2026

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

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

Journal: medRxiv : the preprint server for health sciences
Published: November 24, 2025

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

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

Journal: American journal of human genetics
Published: October 19, 2025
Showing 1-12 of 241

Last Updated: 09/26/2026