Moltu Guy

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Tanya M. Teslovich, E. Cook, A. Chakravarti, 2008, American journal of human genetics.

Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability.

Jeffrey J. Gray, Albee Y. Ling, Seneca L. Bessling, 2015, American journal of human genetics.