Cheryl A. Hill

DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental Disorders

Diana L. Christian, Dennis Y. Wu, Jenna R. Martin et al. · Cell Reports · 2020 · 88 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice

Yingli Wang, Miao Sun, Victoria L Uhlhorn et al. · BMC Developmental Biology · 2010 · 82 citations · Full text

Dentistry, Genetics, Molecular Genetics +16

Beyond the closed suture in apert syndrome mouse models: Evidence of primary effects of FGFR2 signaling on facial shape at birth

Neus Martínez‐Abadías, Christopher J. Percival, Kristina Aldridge et al. · Developmental Dynamics · 2010 · 68 citations · Full text

Dentistry, Developmental Biology, Genetics +15

Brain phenotypes in two FGFR2 mouse models for Apert syndrome

Kristina Aldridge, Cheryl A. Hill, Jordan R. Austin et al. · Developmental Dynamics · 2010 · 51 citations

Life Sciences, Developmental Biology, Neuroscience +16

Functional and epigenetic phenotypes of humans and mice with DNMT3A Overgrowth Syndrome

Amanda M. Smith, Taylor A. LaValle, Marwan Shinawi et al. · Nature Communications · 2021 · 49 citations · Full text

Life Sciences, Genetics, Hematology +17