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Genome Research
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February 8, 2008
WGAViewer: software for genomic annotation of whole genome association studies
Dongliang 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 SCN1A
Erin 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 analyses
Mengqi Zhang, Sahar Gelfman, Janice McCarthy, et al.
American Journal of Human Genetics
|
May 20, 2014
Utilizing population controls in rare-variant case-parent association tests
Yu 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 analysis
Anna C Need, Richard S E Keefe, Dongliang Ge, et al.
Briefings in Bioinformatics
|
December 1, 2021
Focused goodness of fit tests for gene set analyses
Mengqi 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 infection
Evangelos 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 ABCB1
Asra 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 TAS2R16
Nicole 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 Bullosa
Veronica Rotemberg, Maria Garzon, Christine Lauren, et al.
Page
of 34
Search research articles
Search
Showing results (101-110 of 338) with videos related to
Sort By:
Page
of 34
Genome Research
|
February 8, 2008
WGAViewer: software for genomic annotation of whole genome association studies
Dongliang 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 SCN1A
Erin 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 analyses
Mengqi Zhang, Sahar Gelfman, Janice McCarthy, et al.
American Journal of Human Genetics
|
May 20, 2014
Utilizing population controls in rare-variant case-parent association tests
Yu 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 analysis
Anna C Need, Richard S E Keefe, Dongliang Ge, et al.
Briefings in Bioinformatics
|
December 1, 2021
Focused goodness of fit tests for gene set analyses
Mengqi 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 infection
Evangelos 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 ABCB1
Asra 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 TAS2R16
Nicole 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 Bullosa
Veronica Rotemberg, Maria Garzon, Christine Lauren, et al.
Page
of 34