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Human Mutation|March 2, 2017
Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early developmentYiyun Chen, Justin Bartanus, Desheng Liang, et al.
American Journal of Medical Genetics. Part A|September 13, 2019
An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3Valerie J Castelluccio, Francesco Vetrini, Ty Lynnes, et al.
Human Genetics|May 19, 2009
Regional genomic instability predisposes to complex dystrophin gene rearrangementsJunko Oshima, Daniel B Magner, Jennifer A Lee, et al.
Stem Cells and Development|August 30, 2008
Interphase FISH demonstrates that human adipose stromal cells maintain a high level of genomic stability in long-term cultureBrenda R Grimes, Camie M Steiner, Stephanie Merfeld-Clauss, et al.
Prenatal Diagnosis|February 27, 2024
Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical studyMichelle Bellair, Elisabete Amaral, Mason Ouren, et al.
Prenatal Diagnosis|October 21, 2016
Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant womenSteen Kølvraa, Ripudaman Singh, Elizabeth A Normand, et al.
Nature|October 25, 2013
SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic propertiesKihoon Han, J Lloyd Holder, Christian P Schaaf, et al.
Human Mutation|September 9, 2020
Cytogenetically visible inversions are formed by multiple molecular mechanismsMaria Pettersson, Christopher M Grochowski, Josephine Wincent, et al.
Clinical Pharmacology and Therapeutics|August 22, 2024
Development of a Multifaceted Program for Pharmacogenetics Adoption at an Academic Medical Center: Practical Considerations and Lessons LearnedTyler Shugg, Emma M Tillman, Amy M Breman, et al.
Clinical Pharmacology and Therapeutics|May 12, 2025
Evaluation of CYP2C19 Clinical Decision Support Alerts to Guide P2Y<sub>12</sub> Inhibitor PrescribingAshley N Springer, Leah A Alicea, Yemi Gafari, et al.
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