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Amina Barhdadi

Showing results (21-30 of 37) with videos related to

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Pharmacogenetics and Genomics|February 11, 2012
PRKCB is associated with calcineurin inhibitor-induced renal dysfunction in heart transplant recipientsKim Lachance, Amina Barhdadi, Ian Mongrain, et al.
Journal of the American Heart Association|October 30, 2018
Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein CholesterolCécile Low-Kam, David Rhainds, Ken Sin Lo, et al.
Plos One|September 7, 2012
Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterolIan Tietjen, G Kees Hovingh, Roshni R Singaraja, et al.
Elife|October 5, 2021
A sex-specific evolutionary interaction between <i>ADCY9</i> and <i>CETP</i>Isabel Gamache, Marc-André Legault, Jean-Christophe Grenier, et al.
Plos One|October 11, 2016
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy IndividualsSimon L Girard, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, et al.
BMC Medical Genomics|March 26, 2026
Pharmacogenomic study of the effects of saxagliptin on glucose control and hypoglycemic eventsMarc-Olivier Pilon, Simon de Denus, Géraldine Asselin, et al.
Nature Genetics|November 10, 2009
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapyColin J D Ross, Hagit Katzov-Eckert, Marie-Pierre Dubé, et al.
Epigenetics & Chromatin|July 1, 2016
DNA methylation signature of human fetal alcohol spectrum disorderElodie Portales-Casamar, Alexandre A Lussier, Meaghan J Jones, et al.
Genetic Epidemiology|November 30, 2007
Multistage designs in the genomic era: providing balance in complex disease studiesMarie-Pierre Dubé, Silke Schmidt, Elizabeth Hauser, et al.
Circulation. Cardiovascular Genetics|September 13, 2014
CKM and LILRB5 are associated with serum levels of creatine kinaseMarie-Pierre Dubé, Rosa Zetler, Amina Barhdadi, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Pharmacogenetics and Genomics|February 11, 2012
PRKCB is associated with calcineurin inhibitor-induced renal dysfunction in heart transplant recipientsKim Lachance, Amina Barhdadi, Ian Mongrain, et al.
Journal of the American Heart Association|October 30, 2018
Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein CholesterolCécile Low-Kam, David Rhainds, Ken Sin Lo, et al.
Plos One|September 7, 2012
Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterolIan Tietjen, G Kees Hovingh, Roshni R Singaraja, et al.
Elife|October 5, 2021
A sex-specific evolutionary interaction between <i>ADCY9</i> and <i>CETP</i>Isabel Gamache, Marc-André Legault, Jean-Christophe Grenier, et al.
Plos One|October 11, 2016
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy IndividualsSimon L Girard, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, et al.
BMC Medical Genomics|March 26, 2026
Pharmacogenomic study of the effects of saxagliptin on glucose control and hypoglycemic eventsMarc-Olivier Pilon, Simon de Denus, Géraldine Asselin, et al.
Nature Genetics|November 10, 2009
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapyColin J D Ross, Hagit Katzov-Eckert, Marie-Pierre Dubé, et al.
Epigenetics & Chromatin|July 1, 2016
DNA methylation signature of human fetal alcohol spectrum disorderElodie Portales-Casamar, Alexandre A Lussier, Meaghan J Jones, et al.
Genetic Epidemiology|November 30, 2007
Multistage designs in the genomic era: providing balance in complex disease studiesMarie-Pierre Dubé, Silke Schmidt, Elizabeth Hauser, et al.
Circulation. Cardiovascular Genetics|September 13, 2014
CKM and LILRB5 are associated with serum levels of creatine kinaseMarie-Pierre Dubé, Rosa Zetler, Amina Barhdadi, et al.
Pageof 4