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Mary V Relling

Showing results (151-160 of 257) with videos related to

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Clinical Pharmacology and Therapeutics|December 17, 2024
Clinical Actionability of the NUDT15 *4 (p.R139H) Allele and Its Association With Hispanic EthnicityMaud Maillard, Jenny Q Nguyen, Wenjian Yang, et al.
Nature|March 9, 2007
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemiaCharles G Mullighan, Salil Goorha, Ina Radtke, et al.
Annals of Internal Medicine|November 23, 2006
Pharmacogenomics: challenges and opportunitiesDan M Roden, Russ B Altman, Neal L Benowitz, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 30, 2011
Anthracycline-related cardiomyopathy after childhood cancer: role of polymorphisms in carbonyl reductase genes--a report from the Children's Oncology GroupJavier G Blanco, Can-Lan Sun, Wendy Landier, et al.
Journal of the American Medical Informatics Association : JAMIA|August 28, 2013
Development and use of active clinical decision support for preemptive pharmacogenomicsGillian C Bell, Kristine R Crews, Mark R Wilkinson, et al.
The Lancet. Haematology|May 13, 2019
The changing burden of long-term health outcomes in survivors of childhood acute lymphoblastic leukaemia: a retrospective analysis of the St Jude Lifetime Cohort StudyDaniel A Mulrooney, Geehong Hyun, Kirsten K Ness, et al.
Annals of Human Genetics|May 12, 2015
SVSI: fast and powerful set-valued system identification approach to identifying rare variants in sequencing studies for ordered categorical traitsWenjian Bi, Guolian Kang, Yanlong Zhao, et al.
Cancer|May 16, 2020
Association of GSTM1 null variant with anthracycline-related cardiomyopathy after childhood cancer-A Children's Oncology Group ALTE03N1 reportPurnima Singh, Xuexia Wang, Lindsey Hageman, et al.
Nature Genetics|May 23, 2018
Multiplex assessment of protein variant abundance by massively parallel sequencingKenneth A Matreyek, Lea M Starita, Jason J Stephany, et al.
Genome Research|December 8, 2011
Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate dispositionLaura B Ramsey, Gitte H Bruun, Wenjian Yang, et al.
Pageof 26

Showing results (151-160 of 257) with videos related to

Sort By:
Pageof 26
Clinical Pharmacology and Therapeutics|December 17, 2024
Clinical Actionability of the NUDT15 *4 (p.R139H) Allele and Its Association With Hispanic EthnicityMaud Maillard, Jenny Q Nguyen, Wenjian Yang, et al.
Nature|March 9, 2007
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemiaCharles G Mullighan, Salil Goorha, Ina Radtke, et al.
Annals of Internal Medicine|November 23, 2006
Pharmacogenomics: challenges and opportunitiesDan M Roden, Russ B Altman, Neal L Benowitz, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 30, 2011
Anthracycline-related cardiomyopathy after childhood cancer: role of polymorphisms in carbonyl reductase genes--a report from the Children's Oncology GroupJavier G Blanco, Can-Lan Sun, Wendy Landier, et al.
Journal of the American Medical Informatics Association : JAMIA|August 28, 2013
Development and use of active clinical decision support for preemptive pharmacogenomicsGillian C Bell, Kristine R Crews, Mark R Wilkinson, et al.
The Lancet. Haematology|May 13, 2019
The changing burden of long-term health outcomes in survivors of childhood acute lymphoblastic leukaemia: a retrospective analysis of the St Jude Lifetime Cohort StudyDaniel A Mulrooney, Geehong Hyun, Kirsten K Ness, et al.
Annals of Human Genetics|May 12, 2015
SVSI: fast and powerful set-valued system identification approach to identifying rare variants in sequencing studies for ordered categorical traitsWenjian Bi, Guolian Kang, Yanlong Zhao, et al.
Cancer|May 16, 2020
Association of GSTM1 null variant with anthracycline-related cardiomyopathy after childhood cancer-A Children's Oncology Group ALTE03N1 reportPurnima Singh, Xuexia Wang, Lindsey Hageman, et al.
Nature Genetics|May 23, 2018
Multiplex assessment of protein variant abundance by massively parallel sequencingKenneth A Matreyek, Lea M Starita, Jason J Stephany, et al.
Genome Research|December 8, 2011
Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate dispositionLaura B Ramsey, Gitte H Bruun, Wenjian Yang, et al.
Pageof 26