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Therapeutic Advances in Cardiovascular Disease
|
July 6, 2017
Clinical determinants of clopidogrel responsiveness in a heterogeneous cohort of Puerto Rican Hispanics
Dagmar F Hernandez-Suarez, Stuart A Scott, Matthew I Tomey, et al.
Clinical Chemistry
|
January 3, 2025
Integrating Pharmacogenomics into the Broader Construct of Genomic Medicine: Efforts by the ClinGen Pharmacogenomics Working Group (PGxWG)
Li Gong, Clarissa J Klein, Kelly E Caudle, et al.
The Journal of Molecular Diagnostics : JMD
|
February 24, 2018
Recommendations for Clinical CYP2C19 Genotyping Allele Selection: A Report of the Association for Molecular Pathology
Victoria M Pratt, Andria L Del Tredici, Houda Hachad, et al.
Genome Research
|
January 19, 2023
An efficient genotyper and star-allele caller for pharmacogenomics
Ananth Hari, Qinghui Zhou, Nina Gonzaludo, et al.
Genome Research
|
April 11, 2025
Analytical validation of germline small variant detection using long-read HiFi genome sequencing
Nathan Hammond, Linda Liao, Pun Wai Tong, et al.
Pharmacogenetics and Genomics
|
October 27, 2011
PharmGKB summary: very important pharmacogene information for cytochrome P450, family 2, subfamily C, polypeptide 19
Stuart A Scott, Katrin Sangkuhl, Alan R Shuldiner, et al.
Circulation. Cardiovascular Interventions
|
October 6, 2011
CYP2C19 but not PON1 genetic variants influence clopidogrel pharmacokinetics, pharmacodynamics, and clinical efficacy in post-myocardial infarction patients
Jean-Sébastien Hulot, Jean-Philippe Collet, Guillaume Cayla, et al.
Current Opinion in Biotechnology
|
April 20, 2010
Biodiesel from algae: challenges and prospects
Stuart A Scott, Matthew P Davey, John S Dennis, et al.
Clinical Pharmacology and Therapeutics
|
June 28, 2020
Clinical Pharmacogenetic Testing and the Posttest Counseling Conundrum
Robert Rigobello, Shahad Rahawi, Richard Wallsten, et al.
American Journal of Medical Genetics. Part A
|
March 21, 2017
Maternal uniparental disomy of chromosome 15 and concomitant STRC and CATSPER2 deletion-mediated deafness-infertility syndrome
Lisa Karger, Wahab A Khan, Rafaela Calabio, et al.
Page
of 15
Search research articles
Search
Showing results (51-60 of 147) with videos related to
Sort By:
Page
of 15
Therapeutic Advances in Cardiovascular Disease
|
July 6, 2017
Clinical determinants of clopidogrel responsiveness in a heterogeneous cohort of Puerto Rican Hispanics
Dagmar F Hernandez-Suarez, Stuart A Scott, Matthew I Tomey, et al.
Clinical Chemistry
|
January 3, 2025
Integrating Pharmacogenomics into the Broader Construct of Genomic Medicine: Efforts by the ClinGen Pharmacogenomics Working Group (PGxWG)
Li Gong, Clarissa J Klein, Kelly E Caudle, et al.
The Journal of Molecular Diagnostics : JMD
|
February 24, 2018
Recommendations for Clinical CYP2C19 Genotyping Allele Selection: A Report of the Association for Molecular Pathology
Victoria M Pratt, Andria L Del Tredici, Houda Hachad, et al.
Genome Research
|
January 19, 2023
An efficient genotyper and star-allele caller for pharmacogenomics
Ananth Hari, Qinghui Zhou, Nina Gonzaludo, et al.
Genome Research
|
April 11, 2025
Analytical validation of germline small variant detection using long-read HiFi genome sequencing
Nathan Hammond, Linda Liao, Pun Wai Tong, et al.
Pharmacogenetics and Genomics
|
October 27, 2011
PharmGKB summary: very important pharmacogene information for cytochrome P450, family 2, subfamily C, polypeptide 19
Stuart A Scott, Katrin Sangkuhl, Alan R Shuldiner, et al.
Circulation. Cardiovascular Interventions
|
October 6, 2011
CYP2C19 but not PON1 genetic variants influence clopidogrel pharmacokinetics, pharmacodynamics, and clinical efficacy in post-myocardial infarction patients
Jean-Sébastien Hulot, Jean-Philippe Collet, Guillaume Cayla, et al.
Current Opinion in Biotechnology
|
April 20, 2010
Biodiesel from algae: challenges and prospects
Stuart A Scott, Matthew P Davey, John S Dennis, et al.
Clinical Pharmacology and Therapeutics
|
June 28, 2020
Clinical Pharmacogenetic Testing and the Posttest Counseling Conundrum
Robert Rigobello, Shahad Rahawi, Richard Wallsten, et al.
American Journal of Medical Genetics. Part A
|
March 21, 2017
Maternal uniparental disomy of chromosome 15 and concomitant STRC and CATSPER2 deletion-mediated deafness-infertility syndrome
Lisa Karger, Wahab A Khan, Rafaela Calabio, et al.
Page
of 15