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Charles Kooperberg

Showing results (351-360 of 530) with videos related to

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Nature Genetics|September 27, 2016
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation mapsValentina Iotchkova, Jie Huang, John A Morris, et al.
Circulation|April 7, 2022
Genetic Landscape of the ACE2 Coronavirus ReceptorZhijian Yang, Erin Macdonald-Dunlop, Jiantao Chen, et al.
Medrxiv : the Preprint Server for Health Sciences|April 14, 2021
Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19Lucija Klaric, Jack S Gisby, Artemis Papadaki, et al.
Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.
Plos One|September 24, 2013
An absolute risk model to identify individuals at elevated risk for pancreatic cancer in the general populationAlison P Klein, Sara Lindström, Julie B Mendelsohn, et al.
Carcinogenesis|March 26, 2014
Genome-wide interaction study of smoking and bladder cancer riskJonine D Figueroa, Summer S Han, Montserrat Garcia-Closas, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMedPeter Orchard, Thomas W Blackwell, Linda Kachuri, et al.
HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Blood|August 18, 2019
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolismSara Lindström, Lu Wang, Erin N Smith, et al.
Diabetologia|May 6, 2023
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Pageof 53

Showing results (351-360 of 530) with videos related to

Sort By:
Pageof 53
Nature Genetics|September 27, 2016
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation mapsValentina Iotchkova, Jie Huang, John A Morris, et al.
Circulation|April 7, 2022
Genetic Landscape of the ACE2 Coronavirus ReceptorZhijian Yang, Erin Macdonald-Dunlop, Jiantao Chen, et al.
Medrxiv : the Preprint Server for Health Sciences|April 14, 2021
Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19Lucija Klaric, Jack S Gisby, Artemis Papadaki, et al.
Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.
Plos One|September 24, 2013
An absolute risk model to identify individuals at elevated risk for pancreatic cancer in the general populationAlison P Klein, Sara Lindström, Julie B Mendelsohn, et al.
Carcinogenesis|March 26, 2014
Genome-wide interaction study of smoking and bladder cancer riskJonine D Figueroa, Summer S Han, Montserrat Garcia-Closas, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMedPeter Orchard, Thomas W Blackwell, Linda Kachuri, et al.
HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Blood|August 18, 2019
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolismSara Lindström, Lu Wang, Erin N Smith, et al.
Diabetologia|May 6, 2023
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Pageof 53