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David B Goldstein

Showing results (101-110 of 338) with videos related to

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Genome Research|February 8, 2008
WGAViewer: software for genomic annotation of whole genome association studiesDongliang Ge, Kunlin Zhang, Anna C Need, et al.
American Journal of Human Genetics|April 17, 2007
Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug-responsive splice variants of SCN1AErin L Heinzen, Woohyun Yoon, Sarah K Tate, et al.
Genetic Epidemiology|February 12, 2020
Incorporating external information to improve sparse signal detection in rare-variant gene-set-based analysesMengqi Zhang, Sahar Gelfman, Janice McCarthy, et al.
American Journal of Human Genetics|May 20, 2014
Utilizing population controls in rare-variant case-parent association testsYu Jiang, Glen A Satten, Yujun Han, et al.
European Journal of Human Genetics : EJHG|January 22, 2009
Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysisAnna C Need, Richard S E Keefe, Dongliang Ge, et al.
Briefings in Bioinformatics|December 1, 2021
Focused goodness of fit tests for gene set analysesMengqi Zhang, Sahar Gelfman, Cristiane Araujo Martins Moreno, et al.
American Journal of Epidemiology|April 15, 2011
Impact of phenotype definition on genome-wide association signals: empirical evaluation in human immunodeficiency virus type 1 infectionEvangelos Evangelou, Jacques Fellay, Sara Colombo, et al.
The New England Journal of Medicine|April 11, 2003
Association of multidrug resistance in epilepsy with a polymorphism in the drug-transporter gene ABCB1Asra Siddiqui, Reinhold Kerb, Michael E Weale, et al.
Current Biology : CB|July 30, 2005
Positive selection on a high-sensitivity allele of the human bitter-taste receptor TAS2R16Nicole Soranzo, Bernd Bufe, Pardis C Sabeti, et al.
The Journal of Pediatrics|November 28, 2017
A Novel Mutation in Junctional Plakoglobin Causing Lethal Congenital Epidermolysis BullosaVeronica Rotemberg, Maria Garzon, Christine Lauren, et al.
Pageof 34

Showing results (101-110 of 338) with videos related to

Sort By:
Pageof 34
Genome Research|February 8, 2008
WGAViewer: software for genomic annotation of whole genome association studiesDongliang Ge, Kunlin Zhang, Anna C Need, et al.
American Journal of Human Genetics|April 17, 2007
Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug-responsive splice variants of SCN1AErin L Heinzen, Woohyun Yoon, Sarah K Tate, et al.
Genetic Epidemiology|February 12, 2020
Incorporating external information to improve sparse signal detection in rare-variant gene-set-based analysesMengqi Zhang, Sahar Gelfman, Janice McCarthy, et al.
American Journal of Human Genetics|May 20, 2014
Utilizing population controls in rare-variant case-parent association testsYu Jiang, Glen A Satten, Yujun Han, et al.
European Journal of Human Genetics : EJHG|January 22, 2009
Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysisAnna C Need, Richard S E Keefe, Dongliang Ge, et al.
Briefings in Bioinformatics|December 1, 2021
Focused goodness of fit tests for gene set analysesMengqi Zhang, Sahar Gelfman, Cristiane Araujo Martins Moreno, et al.
American Journal of Epidemiology|April 15, 2011
Impact of phenotype definition on genome-wide association signals: empirical evaluation in human immunodeficiency virus type 1 infectionEvangelos Evangelou, Jacques Fellay, Sara Colombo, et al.
The New England Journal of Medicine|April 11, 2003
Association of multidrug resistance in epilepsy with a polymorphism in the drug-transporter gene ABCB1Asra Siddiqui, Reinhold Kerb, Michael E Weale, et al.
Current Biology : CB|July 30, 2005
Positive selection on a high-sensitivity allele of the human bitter-taste receptor TAS2R16Nicole Soranzo, Bernd Bufe, Pardis C Sabeti, et al.
The Journal of Pediatrics|November 28, 2017
A Novel Mutation in Junctional Plakoglobin Causing Lethal Congenital Epidermolysis BullosaVeronica Rotemberg, Maria Garzon, Christine Lauren, et al.
Pageof 34