Search research articles
Contact Us
Filters
Showing results (161-170 of 194) with videos related to
Page
of 20
Sort By:
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 3, 2025
Postoperative Lymph Is a Proximal Source of ctDNA for Detection of Recurrence in HPV-Independent Head and Neck Cancer
Seka Lazare, Zhuosheng Gu, Noah Earland, et al.
Birth Defects Research
|
July 23, 2019
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data
Mary M Jenkins, Lynn M Almli, Faith Pangilinan, et al.
Human Mutation
|
June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans
Timothy C Cox, Andrew C Lidral, Jason C McCoy, et al.
Nature Methods
|
August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variants
Zev Kronenberg, Cillian Nolan, David Porubsky, et al.
European Journal of Human Genetics : EJHG
|
January 14, 2016
Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project
Mengyuan Kan, Paul L Auer, Gao T Wang, et al.
Nature Genetics
|
June 30, 2015
Rare A2ML1 variants confer susceptibility to otitis media
Regie Lyn P Santos-Cortez, Charlotte M Chiong, Ma Rina T Reyes-Quintos, et al.
American Journal of Human Genetics
|
May 29, 2018
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate
Liza L Cox, Timothy C Cox, Lina M Moreno Uribe, et al.
American Journal of Human Genetics
|
February 17, 2015
De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay
Jessica X Chong, Margaret J McMillin, Kathryn M Shively, et al.
Plos One
|
November 22, 2017
Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data
Stephanie A Bien, Paul L Auer, Tabitha A Harrison, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
A telomere-to-telomere map of somatic mutation burden and functional impact in cancer
Min-Hwan Sohn, Danilo Dubocanin, Mitchell R Vollger, et al.
Page
of 20
Search research articles
Search
Showing results (161-170 of 194) with videos related to
Sort By:
Page
of 20
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 3, 2025
Postoperative Lymph Is a Proximal Source of ctDNA for Detection of Recurrence in HPV-Independent Head and Neck Cancer
Seka Lazare, Zhuosheng Gu, Noah Earland, et al.
Birth Defects Research
|
July 23, 2019
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data
Mary M Jenkins, Lynn M Almli, Faith Pangilinan, et al.
Human Mutation
|
June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans
Timothy C Cox, Andrew C Lidral, Jason C McCoy, et al.
Nature Methods
|
August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variants
Zev Kronenberg, Cillian Nolan, David Porubsky, et al.
European Journal of Human Genetics : EJHG
|
January 14, 2016
Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project
Mengyuan Kan, Paul L Auer, Gao T Wang, et al.
Nature Genetics
|
June 30, 2015
Rare A2ML1 variants confer susceptibility to otitis media
Regie Lyn P Santos-Cortez, Charlotte M Chiong, Ma Rina T Reyes-Quintos, et al.
American Journal of Human Genetics
|
May 29, 2018
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate
Liza L Cox, Timothy C Cox, Lina M Moreno Uribe, et al.
American Journal of Human Genetics
|
February 17, 2015
De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay
Jessica X Chong, Margaret J McMillin, Kathryn M Shively, et al.
Plos One
|
November 22, 2017
Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data
Stephanie A Bien, Paul L Auer, Tabitha A Harrison, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
A telomere-to-telomere map of somatic mutation burden and functional impact in cancer
Min-Hwan Sohn, Danilo Dubocanin, Mitchell R Vollger, et al.
Page
of 20