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Industrial & Engineering Chemistry Research|January 31, 2014
Adapting Data Processing To Compare Model and Experiment Accurately: A Discrete Element Model and Magnetic Resonance Measurements of a 3D Cylindrical Fluidized BedChristopher M Boyce, Daniel J Holland, Stuart A Scott, et al.The Journal of Molecular Diagnostics : JMD|March 20, 2017
Chromosomal Microarray Detection of Constitutional Copy Number Variation Using Saliva DNAJennifer Reiner, Lisa Karger, Ninette Cohen, et al.Human Mutation|July 31, 2010
Experience with carrier screening and prenatal diagnosis for 16 Ashkenazi Jewish genetic diseasesStuart A Scott, Lisa Edelmann, Liu Liu, et al.Journal of Genetic Counseling|April 21, 2021
Pharmacogenomic education among genetic counseling training programs in North AmericaElizabeth Loudon, Stuart A Scott, Robert Rigobello, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2010
Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridizationStuart A Scott, Ninette Cohen, Tracy Brandt, et al.Clinical Pharmacology and Therapeutics|June 23, 2023
Response to the FDA Decision Regarding DPYD Testing Prior to Fluoropyrimidine ChemotherapyDaniel L Hertz, D Max Smith, Stuart A Scott, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 30, 2026
Hemophagocytic Lymphohistiocytosis and Fibroblast Growth Factor 23 (FGF23)-Induced HypophosphatemiaMartina Cacciapuoti, Jehan Z Bahrainwala, Wen-Kai Weng, et al.Pharmacogenomics|May 24, 2018
Multi-ethnic SULT1A1 copy number profiling with multiplex ligation-dependent probe amplificationRaymon Vijzelaar, Mariana R Botton, Lisette Stolk, et al.Pharmacogenomics and Personalized Medicine|September 11, 2014
Implementation and utilization of genetic testing in personalized medicineNoura S Abul-Husn, Aniwaa Owusu Obeng, Saskia C Sanderson, et al.Pageof 146