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Showing results (1191-1200 of 1,225) with videos related to

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Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Nature Genetics|August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputationShane McCarthy, Sayantan Das, Warren Kretzschmar, et al.
Nature Genetics|December 9, 2008
Variants in MTNR1B influence fasting glucose levelsInga Prokopenko, Claudia Langenberg, Jose C Florez, et al.
Human Genetics|May 21, 2011
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriersKate M Im, Tomas Kirchhoff, Xianshu Wang, et al.
Plos Genetics|November 10, 2010
Common genetic variants and modification of penetrance of BRCA2-associated breast cancerMia M Gaudet, Tomas Kirchhoff, Todd Green, et al.
Journal of the American College of Cardiology|October 12, 2010
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studiesThemistocles L Assimes, Hilma Hólm, Sekar Kathiresan, et al.
Plos Genetics|April 2, 2013
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer riskMia M Gaudet, Karoline B Kuchenbaecker, Joseph Vijai, et al.
Lancet (London, England)|May 22, 2012
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyBenjamin F Voight, Gina M Peloso, Marju Orho-Melander, et al.
Nature Genetics|December 17, 2008
Six new loci associated with body mass index highlight a neuronal influence on body weight regulationCristen J Willer, Elizabeth K Speliotes, Ruth J F Loos, et al.
Pageof 123

Showing results (1191-1200 of 1,225) with videos related to

Sort By:
Pageof 123
Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Nature Genetics|August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputationShane McCarthy, Sayantan Das, Warren Kretzschmar, et al.
Nature Genetics|December 9, 2008
Variants in MTNR1B influence fasting glucose levelsInga Prokopenko, Claudia Langenberg, Jose C Florez, et al.
Human Genetics|May 21, 2011
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriersKate M Im, Tomas Kirchhoff, Xianshu Wang, et al.
Plos Genetics|November 10, 2010
Common genetic variants and modification of penetrance of BRCA2-associated breast cancerMia M Gaudet, Tomas Kirchhoff, Todd Green, et al.
Journal of the American College of Cardiology|October 12, 2010
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studiesThemistocles L Assimes, Hilma Hólm, Sekar Kathiresan, et al.
Plos Genetics|April 2, 2013
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer riskMia M Gaudet, Karoline B Kuchenbaecker, Joseph Vijai, et al.
Lancet (London, England)|May 22, 2012
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyBenjamin F Voight, Gina M Peloso, Marju Orho-Melander, et al.
Nature Genetics|December 17, 2008
Six new loci associated with body mass index highlight a neuronal influence on body weight regulationCristen J Willer, Elizabeth K Speliotes, Ruth J F Loos, et al.
Pageof 123