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David Curtis

Showing results (31-40 of 203) with videos related to

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Journal of Human Genetics|August 14, 2025
Assessment of ability of a DNA language model to predict pathogenicity of rare coding variantsDavid Curtis
Acta Neuropsychiatrica|June 30, 2025
Analysis of 470,000 exome-sequenced cases and controls fails to identify any genes impacting risk of developing affective disorderDavid Curtis
Pulse (Basel, Switzerland)|December 13, 2023
Analysis of Rare Variants in 470,000 Exome-Sequenced UK Biobank Participants Implicates Novel Genes Affecting Risk of HypertensionDavid Curtis
Annals of Human Genetics|March 26, 2019
Clinical relevance of genome-wide polygenic score may be less than claimedDavid Curtis
Human Heredity|March 22, 2021
Variants in ACE2 and TMPRSS2 Genes Are Not Major Determinants of COVID-19 Severity in UK Biobank SubjectsDavid Curtis
BMJ (Clinical Research Ed.)|September 18, 2008
Effect of antipsychotics on stroke risk remains unprovedDavid Curtis
European Journal of Human Genetics : EJHG|April 23, 2015
Rare missense variants within a single gene form yin yang haplotypesDavid Curtis
BMJ (Clinical Research Ed.)|October 15, 2010
Antipsychotics and venous thrombosis. Confounding factors may account for the associationDavid Curtis
Molecular Genetics and Metabolism|February 9, 2021
Corrigendum to "Analysis of exome-sequenced UK Biobank subjects implicates genes affecting risk of hyperlipidaemia " [131/1-2 (2020) 277-283]David Curtis
Plos One|December 12, 2024
Analysis of rare coding variants in 470,000 exome-sequenced subjects characterises contributions to risk of type 2 diabetesDavid Curtis
Pageof 21

Showing results (31-40 of 203) with videos related to

Sort By:
Pageof 21
Journal of Human Genetics|August 14, 2025
Assessment of ability of a DNA language model to predict pathogenicity of rare coding variantsDavid Curtis
Acta Neuropsychiatrica|June 30, 2025
Analysis of 470,000 exome-sequenced cases and controls fails to identify any genes impacting risk of developing affective disorderDavid Curtis
Pulse (Basel, Switzerland)|December 13, 2023
Analysis of Rare Variants in 470,000 Exome-Sequenced UK Biobank Participants Implicates Novel Genes Affecting Risk of HypertensionDavid Curtis
Annals of Human Genetics|March 26, 2019
Clinical relevance of genome-wide polygenic score may be less than claimedDavid Curtis
Human Heredity|March 22, 2021
Variants in ACE2 and TMPRSS2 Genes Are Not Major Determinants of COVID-19 Severity in UK Biobank SubjectsDavid Curtis
BMJ (Clinical Research Ed.)|September 18, 2008
Effect of antipsychotics on stroke risk remains unprovedDavid Curtis
European Journal of Human Genetics : EJHG|April 23, 2015
Rare missense variants within a single gene form yin yang haplotypesDavid Curtis
BMJ (Clinical Research Ed.)|October 15, 2010
Antipsychotics and venous thrombosis. Confounding factors may account for the associationDavid Curtis
Molecular Genetics and Metabolism|February 9, 2021
Corrigendum to "Analysis of exome-sequenced UK Biobank subjects implicates genes affecting risk of hyperlipidaemia " [131/1-2 (2020) 277-283]David Curtis
Plos One|December 12, 2024
Analysis of rare coding variants in 470,000 exome-sequenced subjects characterises contributions to risk of type 2 diabetesDavid Curtis
Pageof 21