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Medrxiv : the Preprint Server for Health Sciences|April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disordersYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Cell|September 5, 2020
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global PopulationsMing-Huei Chen, Laura M Raffield, Abdou Mousas, et al.
Cell|September 5, 2020
The Polygenic and Monogenic Basis of Blood Traits and DiseasesDragana Vuckovic, Erik L Bao, Parsa Akbari, et al.
Nature|July 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndromeYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
The New England Journal of Medicine|March 3, 2016
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease, Nathan O Stitziel, Kathleen E Stirrups, et al.
Journal of the American College of Cardiology|February 18, 2017
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery DiseaseThomas R Webb, Jeanette Erdmann, Kathleen E Stirrups, et al.
The Journal of Infectious Diseases|March 28, 2024
Epidemiological and Clinical Insights into the Enterovirus D68 Upsurge in Europe 2021-2022 and Emergence of Novel B3-Derived Lineages, ENPEN Multicentre StudyMargarida Pires Simoes, Emma B Hodcroft, Peter Simmonds, et al.
Science Translational Medicine|June 3, 2016
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart diseaseRobert A Scott, Daniel F Freitag, Li Li, et al.
Circulation. Cardiovascular Genetics|October 15, 2017
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 IndividualsAldi T Kraja, James P Cook, Helen R Warren, et al.
Nature Genetics|April 30, 2024
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traitsJacob M Keaton, Zoha Kamali, Tian Xie, et al.
Pageof 55

Showing results (511-520 of 542) with videos related to

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Pageof 55
Medrxiv : the Preprint Server for Health Sciences|April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disordersYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Cell|September 5, 2020
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global PopulationsMing-Huei Chen, Laura M Raffield, Abdou Mousas, et al.
Cell|September 5, 2020
The Polygenic and Monogenic Basis of Blood Traits and DiseasesDragana Vuckovic, Erik L Bao, Parsa Akbari, et al.
Nature|July 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndromeYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
The New England Journal of Medicine|March 3, 2016
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease, Nathan O Stitziel, Kathleen E Stirrups, et al.
Journal of the American College of Cardiology|February 18, 2017
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery DiseaseThomas R Webb, Jeanette Erdmann, Kathleen E Stirrups, et al.
The Journal of Infectious Diseases|March 28, 2024
Epidemiological and Clinical Insights into the Enterovirus D68 Upsurge in Europe 2021-2022 and Emergence of Novel B3-Derived Lineages, ENPEN Multicentre StudyMargarida Pires Simoes, Emma B Hodcroft, Peter Simmonds, et al.
Science Translational Medicine|June 3, 2016
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart diseaseRobert A Scott, Daniel F Freitag, Li Li, et al.
Circulation. Cardiovascular Genetics|October 15, 2017
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 IndividualsAldi T Kraja, James P Cook, Helen R Warren, et al.
Nature Genetics|April 30, 2024
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traitsJacob M Keaton, Zoha Kamali, Tian Xie, et al.
Pageof 55