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Mark Daly

Showing results (41-50 of 149) with videos related to

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Human Heredity|July 19, 2014
(Epi)Genetic analyses of age-related macular degeneration: case-control and discordant twin studiesJohn N Hutchinson, Jes Fagerness, Andrew Kirby, et al.
Nature|April 4, 2006
A mutation in Orai1 causes immune deficiency by abrogating CRAC channel functionStefan Feske, Yousang Gwack, Murali Prakriya, et al.
Human Molecular Genetics|March 17, 2023
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancerMariann Koel, Urmo Võsa, Maarja Jõeloo, et al.
Genome Research|July 21, 2010
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing dataAaron McKenna, Matthew Hanna, Eric Banks, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United KingdomHimanshu Chheda, Priit Palta, Matti Pirinen, et al.
Cellular and Molecular Gastroenterology and Hepatology|March 5, 2019
Host Genetic Variant in CXCL16 May Be Associated With Hepatitis B Virus-Related Acute Liver FailureVeeral Ajmera, Hailiang Huang, Doan Dao, et al.
Inflammatory Bowel Diseases|June 4, 2018
Late-Onset Crohn's Disease Is A Subgroup Distinct in Genetic and Behavioral Risk Factors With UC-Like CharacteristicsDalin Li, Talin Haritunians, Carol Landers, et al.
Frontiers in Genetics|February 13, 2024
Risk and protection of different rare protein-coding variants of complement component C4A in age-related macular degenerationJohanna M Seddon, Dikha De, William Casazza, et al.
Nature Communications|September 16, 2022
Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanksRounak Dey, Wei Zhou, Tuomo Kiiskinen, et al.
Research Square|April 22, 2024
Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsiaA Lokki, Michael Triebwasser, Emma Daly, et al.
Pageof 15

Showing results (41-50 of 149) with videos related to

Sort By:
Pageof 15
Human Heredity|July 19, 2014
(Epi)Genetic analyses of age-related macular degeneration: case-control and discordant twin studiesJohn N Hutchinson, Jes Fagerness, Andrew Kirby, et al.
Nature|April 4, 2006
A mutation in Orai1 causes immune deficiency by abrogating CRAC channel functionStefan Feske, Yousang Gwack, Murali Prakriya, et al.
Human Molecular Genetics|March 17, 2023
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancerMariann Koel, Urmo Võsa, Maarja Jõeloo, et al.
Genome Research|July 21, 2010
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing dataAaron McKenna, Matthew Hanna, Eric Banks, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United KingdomHimanshu Chheda, Priit Palta, Matti Pirinen, et al.
Cellular and Molecular Gastroenterology and Hepatology|March 5, 2019
Host Genetic Variant in CXCL16 May Be Associated With Hepatitis B Virus-Related Acute Liver FailureVeeral Ajmera, Hailiang Huang, Doan Dao, et al.
Inflammatory Bowel Diseases|June 4, 2018
Late-Onset Crohn's Disease Is A Subgroup Distinct in Genetic and Behavioral Risk Factors With UC-Like CharacteristicsDalin Li, Talin Haritunians, Carol Landers, et al.
Frontiers in Genetics|February 13, 2024
Risk and protection of different rare protein-coding variants of complement component C4A in age-related macular degenerationJohanna M Seddon, Dikha De, William Casazza, et al.
Nature Communications|September 16, 2022
Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanksRounak Dey, Wei Zhou, Tuomo Kiiskinen, et al.
Research Square|April 22, 2024
Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsiaA Lokki, Michael Triebwasser, Emma Daly, et al.
Pageof 15