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Clinical Case Reports|April 22, 2016
A patient with constitutional ring 1 chromosome characterized by SNP array CGHSheila Saliganan, Joanna Lee, Sainan WeiGenetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2025
Impact of laboratory-driven proactive reanalysis: Reclassification to positive in 5% of initially negative or uncertain exome sequencing casesMeghan C Towne, Jennifer Huang, Sheila Saliganan, et al.Neurogenetics|August 5, 2015
Mutations in ARID2 are associated with intellectual disabilitiesLinshan Shang, Megan T Cho, Kyle Retterer, et al.Journal of Genetic Counseling|August 4, 2023
Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic CounselorsKristin A Maloney, Elizabeth Mizerik, Robin H King, et al.HGG Advances|July 21, 2022
Erratum: Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3Divya Nair, Dong Li, Hannah Erdogan, et al.HGG Advances|January 20, 2022
Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3Divya Nair, Dong Li, Hannah Erdogan, et al.Science Advances|May 1, 2023
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafishVictoria Patterson, Farid Ullah, Laura Bryant, et al.Pageof 1