De novo <i>POGZ</i> mutations are associated with neurodevelopmental disorders and microcephaly
Yizhou Ye(GenVec), Wendy K. Chung(Oregon Health & Science University), Mariam Al‐Mureikhi(Hamad Medical Corporation), Rebecca McClellan(School of the Art Institute of Chicago), Patricia G. Wheeler(Nemours Children's Clinic), Ingrid Cristian(Arnold Palmer Hospital for Children), Francisca Millan, Kyle Retterer(Geisinger Health System), Tawfeg Ben‐Omran(Qatar Airways (Qatar)), Dina J. Zand(Children's National), Veronique Weinstein(Children's National), Hilary J. Vernon(Johns Hopkins University), Megan T. Cho, Nora Alexander(GenVec), Carrie Crain(Nemours Children's Clinic), Vidya Krishnamurthy(Pediatrics and Genetics), Patrik Vitazka(Inserm)
Cited by 70
Related Papers
Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer
|New England Journal of Medicine|2022|2.5k
Pediatric Pulmonary Hypertension
|Circulation|2015|1.1k
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
|Science|2015|980
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
|Nature Genetics|2017|945