Search research articles
Contact Us
Filters
Showing results (91-100 of 133) with videos related to
Page
of 14
Sort By:
Nature Communications
|
May 3, 2019
Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation
Yanni Zeng, Carmen Amador, Charley Xia, et al.
Scientific Reports
|
February 4, 2017
IL1B-CGTC haplotype is associated with colorectal cancer in admixed individuals with increased African ancestry
María Carolina Sanabria-Salas, Gustavo Hernández-Suárez, Adriana Umaña-Pérez, et al.
Human Molecular Genetics
|
April 16, 2013
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment
Mirna Kirin, Aman Chandra, David G Charteris, et al.
Human Genomics
|
September 10, 2024
The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes
Mahmoud Amiri Roudbar, Seyed Milad Vahedi, Jin Jin, et al.
Nature Genetics
|
August 11, 2022
A multi-tissue atlas of regulatory variants in cattle
Shuli Liu, Yahui Gao, Oriol Canela-Xandri, et al.
Plos Genetics
|
August 31, 2011
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee
Taye H Hamza, Honglei Chen, Erin M Hill-Burns, et al.
Nature Genetics
|
December 18, 2007
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk
Emma Jaeger, Emily Webb, Kimberley Howarth, et al.
Human Molecular Genetics
|
April 17, 2014
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis
Nicola Whiffin, Fay J Hosking, Susan M Farrington, et al.
Plos Computational Biology
|
March 2, 2018
Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human disease
J Kenneth Baillie, Andrew Bretherick, Christopher S Haley, et al.
Human Molecular Genetics
|
October 28, 2008
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis
Asa Johansson, Fabio Marroni, Caroline Hayward, et al.
Page
of 14
Search research articles
Search
Showing results (91-100 of 133) with videos related to
Sort By:
Page
of 14
Nature Communications
|
May 3, 2019
Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation
Yanni Zeng, Carmen Amador, Charley Xia, et al.
Scientific Reports
|
February 4, 2017
IL1B-CGTC haplotype is associated with colorectal cancer in admixed individuals with increased African ancestry
María Carolina Sanabria-Salas, Gustavo Hernández-Suárez, Adriana Umaña-Pérez, et al.
Human Molecular Genetics
|
April 16, 2013
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment
Mirna Kirin, Aman Chandra, David G Charteris, et al.
Human Genomics
|
September 10, 2024
The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes
Mahmoud Amiri Roudbar, Seyed Milad Vahedi, Jin Jin, et al.
Nature Genetics
|
August 11, 2022
A multi-tissue atlas of regulatory variants in cattle
Shuli Liu, Yahui Gao, Oriol Canela-Xandri, et al.
Plos Genetics
|
August 31, 2011
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee
Taye H Hamza, Honglei Chen, Erin M Hill-Burns, et al.
Nature Genetics
|
December 18, 2007
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk
Emma Jaeger, Emily Webb, Kimberley Howarth, et al.
Human Molecular Genetics
|
April 17, 2014
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis
Nicola Whiffin, Fay J Hosking, Susan M Farrington, et al.
Plos Computational Biology
|
March 2, 2018
Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human disease
J Kenneth Baillie, Andrew Bretherick, Christopher S Haley, et al.
Human Molecular Genetics
|
October 28, 2008
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis
Asa Johansson, Fabio Marroni, Caroline Hayward, et al.
Page
of 14