Multiple Research Fellow positions are available in the Stottmann lab in the Divisions of Human Genetics and Developmental Biology at Cincinnati Children’s Hospital Medical Center. Our interests are in the genetic basis of congenital malformations affecting the forebrain and craniofacial structures. The successful candidate will primarily be involved in characterizing novel genes and variants identified through genome sequencing analysis of affected patients with complex cortical and/or syndromic craniofacial malformations. Candidates will be expected to develop a vigorous research program in close consultation with the PI. Applicants with multiple first-author publications and experience in mouse genetics, molecular biology and/or embryology are preferred. Further preference will be given to applicants with demonstrable experience with iPSC culture and/or analysis of exome/genome sequencing datasets.