Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Shamil Sunyaev

Showing results (61-70 of 75) with videos related to

Pageof 8
Sort By:
Science (New York, N.Y.)|May 19, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomesJacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, et al.
Blood|December 14, 2023
Low-frequency inherited complement receptor variants are associated with purpura fulminansPavan K Bendapudi, Sumaiya Nazeen, Justine Ryu, et al.
Nature Genetics|May 22, 2012
Extremely low-coverage sequencing and imputation increases power for genome-wide association studiesBogdan Pasaniuc, Nadin Rohland, Paul J McLaren, et al.
American Journal of Human Genetics|December 25, 2012
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritisDorothée Diogo, Fina Kurreeman, Eli A Stahl, et al.
Protein Science : a Publication of the Protein Society|April 25, 2012
The interface of protein structure, protein biophysics, and molecular evolutionDavid A Liberles, Sarah A Teichmann, Ivet Bahar, et al.
Cell|August 2, 2022
A cross-disorder dosage sensitivity map of the human genomeRyan L Collins, Joseph T Glessner, Eleonora Porcu, et al.
Cell|April 25, 2015
Widespread macromolecular interaction perturbations in human genetic disordersNidhi Sahni, Song Yi, Mikko Taipale, et al.
Science (New York, N.Y.)|August 13, 2021
Population sequencing data reveal a compendium of mutational processes in the human germ lineVladimir B Seplyarskiy, Ruslan A Soldatov, Evan Koch, et al.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Nature|June 18, 2013
Mutational heterogeneity in cancer and the search for new cancer-associated genesMichael S Lawrence, Petar Stojanov, Paz Polak, et al.
Pageof 8

Showing results (61-70 of 75) with videos related to

Sort By:
Pageof 8
Science (New York, N.Y.)|May 19, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomesJacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, et al.
Blood|December 14, 2023
Low-frequency inherited complement receptor variants are associated with purpura fulminansPavan K Bendapudi, Sumaiya Nazeen, Justine Ryu, et al.
Nature Genetics|May 22, 2012
Extremely low-coverage sequencing and imputation increases power for genome-wide association studiesBogdan Pasaniuc, Nadin Rohland, Paul J McLaren, et al.
American Journal of Human Genetics|December 25, 2012
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritisDorothée Diogo, Fina Kurreeman, Eli A Stahl, et al.
Protein Science : a Publication of the Protein Society|April 25, 2012
The interface of protein structure, protein biophysics, and molecular evolutionDavid A Liberles, Sarah A Teichmann, Ivet Bahar, et al.
Cell|August 2, 2022
A cross-disorder dosage sensitivity map of the human genomeRyan L Collins, Joseph T Glessner, Eleonora Porcu, et al.
Cell|April 25, 2015
Widespread macromolecular interaction perturbations in human genetic disordersNidhi Sahni, Song Yi, Mikko Taipale, et al.
Science (New York, N.Y.)|August 13, 2021
Population sequencing data reveal a compendium of mutational processes in the human germ lineVladimir B Seplyarskiy, Ruslan A Soldatov, Evan Koch, et al.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Nature|June 18, 2013
Mutational heterogeneity in cancer and the search for new cancer-associated genesMichael S Lawrence, Petar Stojanov, Paz Polak, et al.
Pageof 8