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Nature Genetics
|
November 23, 2006
Automating resequencing-based detection of insertion-deletion polymorphisms
Tushar R Bhangale, Matthew Stephens, Deborah A Nickerson
Nature Genetics
|
June 24, 2008
Estimating coverage and power for genetic association studies using near-complete variation data
Tushar R Bhangale, Mark J Rieder, Deborah A Nickerson
Bioinformatics (Oxford, England)
|
December 31, 2016
geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation
Arthur Wuster, Diana Chang, Timothy W Behrens, et al.
Human Molecular Genetics
|
November 5, 2004
Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes
Tushar R Bhangale, Mark J Rieder, Robert J Livingston, et al.
Human Heredity
|
August 7, 2014
Using gene expression to improve the power of genome-wide association analysis
Yen-Yi Ho, Emily C Baechler, Ward Ortmann, et al.
BMC Bioinformatics
|
July 26, 2017
Identifying and mitigating batch effects in whole genome sequencing data
Jennifer A Tom, Jens Reeder, William F Forrest, et al.
Plos Genetics
|
November 3, 2011
Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus
Deborah S Cunninghame Graham, David L Morris, Tushar R Bhangale, et al.
Nature Genetics
|
September 12, 2017
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Diana Chang, Mike A Nalls, Ingileif B Hallgrímsdóttir, et al.
The Journal of Infectious Diseases
|
May 23, 2017
Evaluation of IFITM3 rs12252 Association With Severe Pediatric Influenza Infection
Adrienne G Randolph, Wai-Ki Yip, Emma Kaitlynn Allen, et al.
Genes and Immunity
|
March 19, 2018
Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms
Asher Haug-Baltzell, Tushar R Bhangale, Diana Chang, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Nature Genetics
|
November 23, 2006
Automating resequencing-based detection of insertion-deletion polymorphisms
Tushar R Bhangale, Matthew Stephens, Deborah A Nickerson
Nature Genetics
|
June 24, 2008
Estimating coverage and power for genetic association studies using near-complete variation data
Tushar R Bhangale, Mark J Rieder, Deborah A Nickerson
Bioinformatics (Oxford, England)
|
December 31, 2016
geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation
Arthur Wuster, Diana Chang, Timothy W Behrens, et al.
Human Molecular Genetics
|
November 5, 2004
Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes
Tushar R Bhangale, Mark J Rieder, Robert J Livingston, et al.
Human Heredity
|
August 7, 2014
Using gene expression to improve the power of genome-wide association analysis
Yen-Yi Ho, Emily C Baechler, Ward Ortmann, et al.
BMC Bioinformatics
|
July 26, 2017
Identifying and mitigating batch effects in whole genome sequencing data
Jennifer A Tom, Jens Reeder, William F Forrest, et al.
Plos Genetics
|
November 3, 2011
Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus
Deborah S Cunninghame Graham, David L Morris, Tushar R Bhangale, et al.
Nature Genetics
|
September 12, 2017
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Diana Chang, Mike A Nalls, Ingileif B Hallgrímsdóttir, et al.
The Journal of Infectious Diseases
|
May 23, 2017
Evaluation of IFITM3 rs12252 Association With Severe Pediatric Influenza Infection
Adrienne G Randolph, Wai-Ki Yip, Emma Kaitlynn Allen, et al.
Genes and Immunity
|
March 19, 2018
Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms
Asher Haug-Baltzell, Tushar R Bhangale, Diana Chang, et al.
Page
of 2