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Stuart A Scott

Showing results (31-40 of 147) with videos related to

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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.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 11, 2015
Paroxysmal kinesigenic dyskinesia caused by 16p11.2 microdeletionPichet Termsarasab, Amy C Yang, Jennifer Reiner, et al.
Human Mutation|November 26, 2015
Long-Read Single Molecule Real-Time Full Gene Sequencing of Cytochrome P450-2D6Wanqiong Qiao, Yao Yang, Robert Sebra, et al.
Pharmacogenomics|August 12, 2009
CYP2C9*8 is prevalent among African-Americans: implications for pharmacogenetic dosingStuart A Scott, Malgorzata Jaremko, Steven A Lubitz, et al.
NPJ Genomic Medicine|December 22, 2017
Erratum: A <i>de novo</i> 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotypeJames D Weisfeld-Adams, Amanda K Tkachuk, Kenneth N Maclean, et al.
Pageof 15

Showing results (31-40 of 147) with videos related to

Sort By:
Pageof 15
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.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 11, 2015
Paroxysmal kinesigenic dyskinesia caused by 16p11.2 microdeletionPichet Termsarasab, Amy C Yang, Jennifer Reiner, et al.
Human Mutation|November 26, 2015
Long-Read Single Molecule Real-Time Full Gene Sequencing of Cytochrome P450-2D6Wanqiong Qiao, Yao Yang, Robert Sebra, et al.
Pharmacogenomics|August 12, 2009
CYP2C9*8 is prevalent among African-Americans: implications for pharmacogenetic dosingStuart A Scott, Malgorzata Jaremko, Steven A Lubitz, et al.
NPJ Genomic Medicine|December 22, 2017
Erratum: A <i>de novo</i> 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotypeJames D Weisfeld-Adams, Amanda K Tkachuk, Kenneth N Maclean, et al.
Pageof 15