Neda Zadeh

Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children’s hospitals demonstrates improved clinical outcomes and reduced costs of care

David Dimmock, Sara Caylor, Bryce Waldman et al. · The American Journal of Human Genetics · 2021 · 238 citations · Full text

Project Baby Bear, Neonatology, Preventive Pediatrics +8

De Novo Nonsense Mutations in KAT6A, a Lysine Acetyl-Transferase Gene, Cause a Syndrome Including Microcephaly and Global Developmental Delay

Valerie A. Arboleda, Hane Lee, Naghmeh Dorrani et al. · The American Journal of Human Genetics · 2015 · 136 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +9

Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome

Sarah E. Sheppard, Ian M. Campbell, Margaret Harr et al. · American Journal of Medical Genetics Part A · 2021 · 66 citations · Full text

Phenotypic expansion of <i>POGZ</i>‐related intellectual disability syndrome (White‐Sutton syndrome)

Nurit Assia Batzir, Jennifer E. Posey, Xiaofei Song et al. · American Journal of Medical Genetics Part A · 2019 · 60 citations · Full text

REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis

Yavuz Bayram, Janson J. White, Nursel Elçioğlu et al. · The American Journal of Human Genetics · 2017 · 58 citations · Full text

Fibrosis, Mendelian Disorder, Genetics +3