Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Elizabeth J. Leslie, Jacqueline T. Hecht et al.|Human Genetics and Genomics Advances|2023Cited by 14
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Elizabeth J. Leslie, Randy L. Parrish et al.|Human Genetics|2024Cited by 4
A mutational hotspot in <scp><i>AMOTL1</i></scp> defines a new syndrome of orofacial clefting, cardiac anomalies, and tall statureAlanna Strong, Timothy C. Cox, David A. Koolen et al.|American Journal of Medical Genetics Part A|2023Cited by 3
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Elizabeth J. Leslie-Clarkson, Sunil Kumar Singh et al.|The American Journal of Human Genetics|2025Cited by 3
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey Robinson, Elizabeth J. Leslie-Clarkson, Sarah W. Curtis et al.|The American Journal of Human Genetics|2025Cited by 3