Concepedia

Rachel Hart

RH

Statistics

Publications

4

Citations

112

H-Index

4

Active since

2014

Affiliations

National Human Genome Research Institute(Current)

National Institutes of Health

Virginia Commonwealth University

Rachel Hart is an author at National Human Genome Research Institute specializing in genetics, molecular genetics, and life sciences.

Publications per year

2014–2021

4

Publications

4

Mutations in <i>SPECC1L</i>, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome

Paul Kruszka, Dong Li, Margaret Harr et al. · Journal of Medical Genetics · 2014 · 49 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling

Erich Roessler, Ping Hu, Juliana Marino et al. · Human Mutation · 2018 · 29 citations

Life Sciences, Genetics, Molecular Genetics +16

Severe Vitamin B12 Deficiency Mimicking Microangiopathic Hemolytic Anemia

Ramzi Hassouneh, Olivia Lee, Rachel Hart et al. · Journal of Hematology · 2021 · 24 citations · Full text

Medicine, Hematology, Internal Medicine +13

Executive Function and Adaptive Behavior in Muenke Syndrome

Colin M. P. Yarnell, Yonit A. Addissie, Donald W. Hadley et al. · The Journal of Pediatrics · 2015 · 10 citations

Social Sciences, Neuroscience, Psychology +15

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