National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Gabriella Miller Kids First Pediatric Research Program of the Pediatric Cardiac Genetics Consortium (PCGC)

Request Access

De novo mutations in histone modifying genes in congenital heart disease

Samir Zaidi, Murim Choi, H. Wakimoto, et al.. (2013). Nature. Cited 875 times. https://doi.org/10.1038/nature12141

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

S. Jin, Jason G. Homsy, Samir Zaidi, et al.. (2017). Nature genetics. Cited 742 times. https://doi.org/10.1038/ng.3970

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies

Jason G. Homsy, Samir Zaidi, Yufeng Shen, et al.. (2015). Science. Cited 725 times. https://doi.org/10.1126/science.aac9396

Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data

J. Glessner, A. Bick, K. Ito, et al.. (2014). Circulation Research. Cited 229 times. https://doi.org/10.1161/CIRCRESAHA.115.304458

The Congenital Heart Disease Genetic Network Study: Rationale, Design, and Early Results

B. Gelb, M. Brueckner, W. Chung, et al.. (2013). Circulation Research. Cited 158 times. https://doi.org/10.1161/CIRCRESAHA.111.300297

De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects

J. Priest, K. Osoegawa, Nebil Mohammed, et al.. (2016). PLoS Genetics. Cited 115 times. https://doi.org/10.1371/journal.pgen.1005963
NCPI Dataset Catalog
Feedback & Support
v0.10.0-b29ba7e