Exome‐wide assessment of isolated biliary atresia: A report from the <scp>National Birth Defects Prevention Study</scp> using child–parent trios and a case–control design to identify novel rare variantsPagna Sok, Philip J. Lupo, Aniko Sabo et al.|American Journal of Medical Genetics Part A|2023Cited by 7
Germline genetic variants and pediatric rhabdomyosarcoma outcomes: a report from the Children’s Oncology GroupBailey A. Martin‐Giacalone, Philip J. Lupo, Melissa A. Richard et al.|JNCI Journal of the National Cancer Institute|2023Cited by 4
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variantsShannon Dugan‐Perez, Pagna Sok, Jessica X. Chong et al.|UNC Libraries|2024Cited by 2
Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split‐Hand/Ft Malformation: A Report From the National Birth Defects Prevention StudyTonia C. Carter, Meredith M. Howley, Lawrence C. Brody et al.|Birth Defects Research|2025Cited by 1
Abstract 683: Identification of common germline variants associated with pediatric rhabdomyosarcoma survival: A report from the Children's Oncology Group (COG)Bailey A. Martin‐Giacalone, Philip J. Lupo, Michael E. Scheurer et al.|Cancer Research|2022Cited by 0