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Genome Biology
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September 20, 2005
The biology of genomes: sequence gives way to function
David A Hinds
Bioinformatics (Oxford, England)
|
October 24, 2014
minimac2: faster genotype imputation
Christian Fuchsberger, Gonçalo R Abecasis, David A Hinds
Genetic Epidemiology
|
August 19, 2010
Pooled versus individual genotyping in a breast cancer genome-wide association study
Ying Huang, David A Hinds, Lihong Qi, et al.
Plos Genetics
|
October 17, 2012
Comparison of family history and SNPs for predicting risk of complex disease
Chuong B Do, David A Hinds, Uta Francke, et al.
Nature Genetics
|
December 1, 2009
Variant in PNPLA3 is associated with alcoholic liver disease
Chao Tian, Renee P Stokowski, David Kershenobich, et al.
Nature Genetics
|
December 6, 2005
Common deletions and SNPs are in linkage disequilibrium in the human genome
David A Hinds, Andrew P Kloek, Michael Jen, et al.
Applied Health Economics and Health Policy
|
March 6, 2014
Economic evaluation of using a genetic test to direct breast cancer chemoprevention in white women with a previous breast biopsy
Linda E Green, Tuan A Dinh, David A Hinds, et al.
Nature Communications
|
February 3, 2016
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person
Youna Hu, Alena Shmygelska, David Tran, et al.
American Journal of Human Genetics
|
September 9, 2006
A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping
Chao Tian, David A Hinds, Russell Shigeta, et al.
Nature Genetics
|
September 30, 2016
Erratum: Detection and interpretation of shared genetic influences on 42 human traits
Joseph K Pickrell, Tomaz Berisa, Jimmy Z Liu, et al.
Page
of 12
Search research articles
Search
Showing results (1-10 of 120) with videos related to
Sort By:
Page
of 12
Genome Biology
|
September 20, 2005
The biology of genomes: sequence gives way to function
David A Hinds
Bioinformatics (Oxford, England)
|
October 24, 2014
minimac2: faster genotype imputation
Christian Fuchsberger, Gonçalo R Abecasis, David A Hinds
Genetic Epidemiology
|
August 19, 2010
Pooled versus individual genotyping in a breast cancer genome-wide association study
Ying Huang, David A Hinds, Lihong Qi, et al.
Plos Genetics
|
October 17, 2012
Comparison of family history and SNPs for predicting risk of complex disease
Chuong B Do, David A Hinds, Uta Francke, et al.
Nature Genetics
|
December 1, 2009
Variant in PNPLA3 is associated with alcoholic liver disease
Chao Tian, Renee P Stokowski, David Kershenobich, et al.
Nature Genetics
|
December 6, 2005
Common deletions and SNPs are in linkage disequilibrium in the human genome
David A Hinds, Andrew P Kloek, Michael Jen, et al.
Applied Health Economics and Health Policy
|
March 6, 2014
Economic evaluation of using a genetic test to direct breast cancer chemoprevention in white women with a previous breast biopsy
Linda E Green, Tuan A Dinh, David A Hinds, et al.
Nature Communications
|
February 3, 2016
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person
Youna Hu, Alena Shmygelska, David Tran, et al.
American Journal of Human Genetics
|
September 9, 2006
A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping
Chao Tian, David A Hinds, Russell Shigeta, et al.
Nature Genetics
|
September 30, 2016
Erratum: Detection and interpretation of shared genetic influences on 42 human traits
Joseph K Pickrell, Tomaz Berisa, Jimmy Z Liu, et al.
Page
of 12