Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence DataJoseph Glessner, Wendy K. Chung, Alexander G. Bick et al.|Circulation Research|2014Cited by 277
Na<sub>V</sub>channel variants in patients with painful and nonpainful peripheral neuropathySamir Wadhawan, J. Robinson Singleton, John Thompson et al.|Neurology Genetics|2017Cited by 38