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Plos One
|
November 14, 2013
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes
Elijah R Behr, Marylyn D Ritchie, Toshihiro Tanaka, et al.
Clinical Pharmacology and Therapeutics
|
April 12, 2017
Pharmacogenomics-Based Point-of-Care Clinical Decision Support Significantly Alters Drug Prescribing
P H O'Donnell, N Wadhwa, K Danahey, et al.
Lancet (London, England)
|
May 4, 2010
Clinical assessment incorporating a personal genome
Euan A Ashley, Atul J Butte, Matthew T Wheeler, et al.
Frontiers in Psychiatry
|
March 22, 2018
Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder
Azmeraw T Amare, Klaus Oliver Schubert, Fasil Tekola-Ayele, et al.
Plos Genetics
|
September 22, 2011
Phased whole-genome genetic risk in a family quartet using a major allele reference sequence
Frederick E Dewey, Rong Chen, Sergio P Cordero, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
January 6, 2019
The association of obesity and coronary artery disease genes with response to SSRIs treatment in major depression
Azmeraw T Amare, Klaus Oliver Schubert, Fasil Tekola-Ayele, et al.
Cell
|
March 20, 2012
Personal omics profiling reveals dynamic molecular and medical phenotypes
Rui Chen, George I Mias, Jennifer Li-Pook-Than, et al.
Clinical Pharmacology and Therapeutics
|
November 8, 2012
Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis
E Danese, M Montagnana, J A Johnson, et al.
Lancet (London, England)
|
June 13, 2013
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study
Minoli A Perera, Larisa H Cavallari, Nita A Limdi, et al.
Human Mutation
|
June 22, 2017
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges
Roxana Daneshjou, Yanran Wang, Yana Bromberg, et al.
Page
of 52
Search research articles
Search
Showing results (501-510 of 514) with videos related to
Sort By:
Page
of 52
Plos One
|
November 14, 2013
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes
Elijah R Behr, Marylyn D Ritchie, Toshihiro Tanaka, et al.
Clinical Pharmacology and Therapeutics
|
April 12, 2017
Pharmacogenomics-Based Point-of-Care Clinical Decision Support Significantly Alters Drug Prescribing
P H O'Donnell, N Wadhwa, K Danahey, et al.
Lancet (London, England)
|
May 4, 2010
Clinical assessment incorporating a personal genome
Euan A Ashley, Atul J Butte, Matthew T Wheeler, et al.
Frontiers in Psychiatry
|
March 22, 2018
Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder
Azmeraw T Amare, Klaus Oliver Schubert, Fasil Tekola-Ayele, et al.
Plos Genetics
|
September 22, 2011
Phased whole-genome genetic risk in a family quartet using a major allele reference sequence
Frederick E Dewey, Rong Chen, Sergio P Cordero, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
January 6, 2019
The association of obesity and coronary artery disease genes with response to SSRIs treatment in major depression
Azmeraw T Amare, Klaus Oliver Schubert, Fasil Tekola-Ayele, et al.
Cell
|
March 20, 2012
Personal omics profiling reveals dynamic molecular and medical phenotypes
Rui Chen, George I Mias, Jennifer Li-Pook-Than, et al.
Clinical Pharmacology and Therapeutics
|
November 8, 2012
Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis
E Danese, M Montagnana, J A Johnson, et al.
Lancet (London, England)
|
June 13, 2013
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study
Minoli A Perera, Larisa H Cavallari, Nita A Limdi, et al.
Human Mutation
|
June 22, 2017
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges
Roxana Daneshjou, Yanran Wang, Yana Bromberg, et al.
Page
of 52