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Caroline Hayward

Showing results (361-370 of 527) with videos related to

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Nature Genetics|December 23, 2018
Trans-ethnic association study of blood pressure determinants in over 750,000 individualsAyush Giri, Jacklyn N Hellwege, Jacob M Keaton, et al.
American Journal of Human Genetics|June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated DiseasesSalman M Tajuddin, Ursula M Schick, John D Eicher, et al.
Circulation. Genomic and Precision Medicine|May 12, 2018
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR IntervalHonghuang Lin, Jessica van Setten, Albert V Smith, et al.
Nature Communications|October 1, 2017
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traitsAurélien Macé, Marcus A Tuke, Patrick Deelen, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 1, 2014
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2Jie Huang, Jennifer E Huffman, Munekazu Yamakuchi, et al.
Nature Genetics|May 9, 2022
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effectsLaurence J Howe, Michel G Nivard, Tim T Morris, et al.
American Journal of Human Genetics|October 2, 2012
Discovery and fine mapping of serum protein loci through transethnic meta-analysisNora Franceschini, Frank J A van Rooij, Bram P Prins, et al.
Nature Genetics|February 27, 2019
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestriesNick Shrine, Anna L Guyatt, A Mesut Erzurumluoglu, et al.
Journal of Medical Genetics|April 3, 2016
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsElisabeth M van Leeuwen, Aniko Sabo, Joshua C Bis, et al.
Pageof 53

Showing results (361-370 of 527) with videos related to

Sort By:
Pageof 53
Nature Genetics|December 23, 2018
Trans-ethnic association study of blood pressure determinants in over 750,000 individualsAyush Giri, Jacklyn N Hellwege, Jacob M Keaton, et al.
American Journal of Human Genetics|June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated DiseasesSalman M Tajuddin, Ursula M Schick, John D Eicher, et al.
Circulation. Genomic and Precision Medicine|May 12, 2018
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR IntervalHonghuang Lin, Jessica van Setten, Albert V Smith, et al.
Nature Communications|October 1, 2017
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traitsAurélien Macé, Marcus A Tuke, Patrick Deelen, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 1, 2014
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2Jie Huang, Jennifer E Huffman, Munekazu Yamakuchi, et al.
Nature Genetics|May 9, 2022
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effectsLaurence J Howe, Michel G Nivard, Tim T Morris, et al.
American Journal of Human Genetics|October 2, 2012
Discovery and fine mapping of serum protein loci through transethnic meta-analysisNora Franceschini, Frank J A van Rooij, Bram P Prins, et al.
Nature Genetics|February 27, 2019
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestriesNick Shrine, Anna L Guyatt, A Mesut Erzurumluoglu, et al.
Journal of Medical Genetics|April 3, 2016
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsElisabeth M van Leeuwen, Aniko Sabo, Joshua C Bis, et al.
Pageof 53