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American Journal of Respiratory and Critical Care Medicine
|
March 7, 2018
Whole-Genome Sequencing of Pharmacogenetic Drug Response in Racially Diverse Children with Asthma
Angel C Y Mak, Marquitta J White, Walter L Eckalbar, et al.
Plos One
|
March 5, 2013
Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene
Blanca E Himes, Keith Sheppard, Annerose Berndt, et al.
Nature Communications
|
October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height
Gareth Hawkes, Robin N Beaumont, Zilin Li, et al.
Human Molecular Genetics
|
March 19, 2015
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals
Kevin T Nead, Aihua Li, Mackenzie R Wehner, et al.
Cell Genomics
|
November 1, 2024
Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas
Victor Borda, Douglas P Loesch, Bing Guo, et al.
American Journal of Epidemiology
|
April 16, 2021
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program
Adrienne M Stilp, Leslie S Emery, Jai G Broome, et al.
Nature Genetics
|
August 2, 2011
Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations
Dara G Torgerson, Elizabeth J Ampleford, Grace Y Chiu, et al.
Plos Genetics
|
December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Madeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
Genome Medicine
|
March 3, 2020
Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age
Simon Kebede Merid, Alexei Novoloaca, Gemma C Sharp, et al.
Biorxiv : the Preprint Server for Biology
|
February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortium
Goo Jun, Adam C English, Ginger A Metcalf, et al.
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Search research articles
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Showing results (631-640 of 655) with videos related to
Sort By:
Page
of 66
American Journal of Respiratory and Critical Care Medicine
|
March 7, 2018
Whole-Genome Sequencing of Pharmacogenetic Drug Response in Racially Diverse Children with Asthma
Angel C Y Mak, Marquitta J White, Walter L Eckalbar, et al.
Plos One
|
March 5, 2013
Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene
Blanca E Himes, Keith Sheppard, Annerose Berndt, et al.
Nature Communications
|
October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height
Gareth Hawkes, Robin N Beaumont, Zilin Li, et al.
Human Molecular Genetics
|
March 19, 2015
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals
Kevin T Nead, Aihua Li, Mackenzie R Wehner, et al.
Cell Genomics
|
November 1, 2024
Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas
Victor Borda, Douglas P Loesch, Bing Guo, et al.
American Journal of Epidemiology
|
April 16, 2021
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program
Adrienne M Stilp, Leslie S Emery, Jai G Broome, et al.
Nature Genetics
|
August 2, 2011
Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations
Dara G Torgerson, Elizabeth J Ampleford, Grace Y Chiu, et al.
Plos Genetics
|
December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Madeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
Genome Medicine
|
March 3, 2020
Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age
Simon Kebede Merid, Alexei Novoloaca, Gemma C Sharp, et al.
Biorxiv : the Preprint Server for Biology
|
February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortium
Goo Jun, Adam C English, Ginger A Metcalf, et al.
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of 66