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Nature Genetics
|
March 26, 2013
Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity
Austin M Dulak, Petar Stojanov, Shouyong Peng, et al.
Circulation. Genomic and Precision Medicine
|
March 24, 2023
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program
Amanda A Seyerle, Cecelia A Laurie, Brandon J Coombes, et al.
Science (New York, N.Y.)
|
July 30, 2011
The mutational landscape of head and neck squamous cell carcinoma
Nicolas Stransky, Ann Marie Egloff, Aaron D Tward, et al.
Circulation. Cardiovascular Genetics
|
April 20, 2010
Candidate gene association resource (CARe): design, methods, and proof of concept
Kiran Musunuru, Guillaume Lettre, Taylor Young, et al.
Human Genetics
|
March 20, 2014
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans
Jaclyn Ellis, Ethan M Lange, Jin Li, et al.
Cell
|
July 24, 2012
A landscape of driver mutations in melanoma
Eran Hodis, Ian R Watson, Gregory V Kryukov, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 27, 2024
Dysanapsis Genetic Risk Predicts Lung Function Across the Lifespan
Catherine L Debban, Amirthagowri Ambalavanan, Auyon Ghosh, et al.
Nature
|
February 11, 2011
The genomic complexity of primary human prostate cancer
Michael F Berger, Michael S Lawrence, Francesca Demichelis, et al.
Neuron
|
January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders
Elaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Nature Genetics
|
November 6, 2007
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
Robert M Plenge, Chris Cotsapas, Leela Davies, et al.
Page
of 14
Search research articles
Search
Showing results (71-80 of 133) with videos related to
Sort By:
Page
of 14
Nature Genetics
|
March 26, 2013
Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity
Austin M Dulak, Petar Stojanov, Shouyong Peng, et al.
Circulation. Genomic and Precision Medicine
|
March 24, 2023
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program
Amanda A Seyerle, Cecelia A Laurie, Brandon J Coombes, et al.
Science (New York, N.Y.)
|
July 30, 2011
The mutational landscape of head and neck squamous cell carcinoma
Nicolas Stransky, Ann Marie Egloff, Aaron D Tward, et al.
Circulation. Cardiovascular Genetics
|
April 20, 2010
Candidate gene association resource (CARe): design, methods, and proof of concept
Kiran Musunuru, Guillaume Lettre, Taylor Young, et al.
Human Genetics
|
March 20, 2014
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans
Jaclyn Ellis, Ethan M Lange, Jin Li, et al.
Cell
|
July 24, 2012
A landscape of driver mutations in melanoma
Eran Hodis, Ian R Watson, Gregory V Kryukov, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 27, 2024
Dysanapsis Genetic Risk Predicts Lung Function Across the Lifespan
Catherine L Debban, Amirthagowri Ambalavanan, Auyon Ghosh, et al.
Nature
|
February 11, 2011
The genomic complexity of primary human prostate cancer
Michael F Berger, Michael S Lawrence, Francesca Demichelis, et al.
Neuron
|
January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders
Elaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Nature Genetics
|
November 6, 2007
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
Robert M Plenge, Chris Cotsapas, Leela Davies, et al.
Page
of 14