Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis
2018 · Cell · 414 citations
https://doi.org/10.1016/j.cell.2018.02.036
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Karen W. Gripp
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Karen W. Gripp is an academic researcher from Alfred I. duPont Hospital for Children. The author has contributed to research in topics: Protein Tyrosine Phosphatases & Genomic variations and chromosomal abnormalities & Genomics and Rare Diseases. The author has an h-index of 67, co-authored 264 publications.
ORCID: 0000-0001-8200-1733Papers by this author
worksThe genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
2016 · Nature Genetics · 350 citations
https://doi.org/10.1038/ng.3720
Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848
2017 · The American Journal of Human Genetics · 203 citations
https://doi.org/10.1016/j.ajhg.2017.12.001
Diamond–Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes <i>TSR2</i> and <i>RPS28</i>
2014 · American Journal of Medical Genetics Part A · 144 citations
https://doi.org/10.1002/ajmg.a.36633
PEDIA: prioritization of exome data by image analysis
2019 · Genetics in Medicine · 86 citations
https://doi.org/10.1038/s41436-019-0566-2
Truncating mutations in the last exon of <i>NOTCH3</i> cause lateral meningocele syndrome
2014 · American Journal of Medical Genetics Part A · 81 citations
https://doi.org/10.1002/ajmg.a.36863
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