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Katherine Inskeep - Publications

Affiliations: 
Cincinnati Children's Hospital Medical Center, University of Cincinnati 
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4 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Inskeep KA, Crase B, Stottmann RW. mediated sphingolipid metabolism regulates brain and primary cilia development. Biorxiv : the Preprint Server For Biology. PMID 38168190 DOI: 10.1101/2023.12.15.571873  0.558
2023 Smallwood K, Watt KEN, Ide S, Baltrunaite K, Brunswick C, Inskeep K, Capannari C, Adam MP, Begtrup A, Bertola DR, Demmer L, Demo E, Devinsky O, Gallagher ER, Guillen Sacoto MJ, et al. POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies. American Journal of Human Genetics. PMID 37075751 DOI: 10.1016/j.ajhg.2023.03.014  0.551
2022 Khalaf-Nazzal R, Fasham J, Inskeep KA, Blizzard LE, Leslie JS, Wakeling MN, Ubeyratna N, Mitani T, Griffith JL, Baker W, Al-Hijawi F, Keough KC, Gezdirici A, Pena L, Spaeth CG, et al. Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder. American Journal of Human Genetics. PMID 36283405 DOI: 10.1016/j.ajhg.2022.09.012  0.549
2021 Inskeep KA, Zarate YA, Monteil D, Spranger J, Doherty D, Stottmann RW, Weaver KN. Genetic and phenotypic heterogeneity in KIAA0753-related ciliopathies. American Journal of Medical Genetics. Part A. PMID 34523780 DOI: 10.1002/ajmg.a.62497  0.569
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