The Research Institute at Nationwide Children's Hospital Genetics of Congenital Heart Disease (CHD)

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease

S. LaHaye, Don Corsmeier, Madhumita Basu, et al.. (2016). Circulation: Cardiovascular Genetics. Cited 80 times. https://doi.org/10.1161/CIRCGENETICS.115.001324

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.

N. Hanchard, S. Swaminathan, K. Bucasas, et al.. (2016). Human molecular genetics. Cited 34 times. https://doi.org/10.1093/HMG/DDW071

Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy

S. Manivannan, S. Darouich, A. Masmoudi, et al.. (2019). PLoS Genetics. Cited 21 times. https://doi.org/10.1371/journal.pgen.1008639

Assessment of large copy number variants in patients with apparently isolated congenital left‐sided cardiac lesions reveals clinically relevant genomic events

N. Hanchard, Luis A Umana, Lisa C. A. D’Alessandro, et al.. (2017). American Journal of Medical Genetics Part A. Cited 19 times. https://doi.org/10.1002/ajmg.a.38309

Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery

David M. Gordon, D. Cunningham, Gloria A Zender, et al.. (2022). PLoS Genetics. Cited 17 times. https://doi.org/10.1371/journal.pgen.1010236