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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 22, 2013
An Ashkenazi Jewish SMN1 haplotype specific to duplication alleles improves pan-ethnic carrier screening for spinal muscular atrophyMinjie Luo, Liu Liu, Inga Peter, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 19, 2011
Personalizing medicine with clinical pharmacogeneticsStuart A ScottJournal of Parkinson'S Disease|April 17, 2023
Immunological Features of LRRK2 Function and Its Role in the Gut-Brain Axis Governing Parkinson's DiseaseInga Peter, Warren StroberGene|July 16, 2013
Evidence of expression variation and allelic imbalance in Crohn's disease susceptibility genes NOD2 and ATG16L1 in human dendritic cellsJianzhong Hu, Inga PeterGenome Research|April 11, 2025
Analytical validation of germline small variant detection using long-read HiFi genome sequencingNathan Hammond, Linda Liao, Pun Wai Tong, et al.The Journal of Molecular Diagnostics : JMD|September 10, 2013
An allele-specific PCR system for rapid detection and discrimination of the CYP2C19∗4A, ∗4B, and ∗17 alleles: implications for clopidogrel response testingStuart A Scott, Qian Tan, Usman Baber, et al.Genes|April 3, 2021
Pharmacogenomic Determinants of Interindividual Drug Response Variability: From Discovery to ImplementationStuart A Scott, Jesse J SwenVascular Medicine (London, England)|September 14, 2013
Warfarin pharmacogenetics: a controlled dose-response study in healthy subjectsDaniella L Kadian-Dodov, Sarina A van der Zee, Stuart A Scott, et al.Human Mutation|September 18, 2022
Human Mutation special issue on innovations in genomic diagnosticsStuart A Scott, Kai Wang, Nancy B SpinnerPageof 162