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David Curtis

Showing results (61-70 of 203) with videos related to

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Molecular Genetics and Metabolism|August 5, 2020
Analysis of exome-sequenced UK Biobank subjects implicates genes affecting risk of hyperlipidaemiaDavid Curtis
European Journal of Human Genetics : EJHG|August 3, 2024
Assessment of ability of AlphaMissense to identify variants affecting susceptibility to common diseaseDavid Curtis
Journal of Human Genetics|March 7, 2024
Weighted burden analysis of rare coding variants in 470,000 exome-sequenced UK Biobank participants characterises effects on hyperlipidaemia riskDavid Curtis
Human Heredity|February 11, 2024
Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank ParticipantsDavid Curtis
Pulse (Basel, Switzerland)|February 26, 2024
Genetic Variants Associated with Hypertension Risk: Progress and ImplicationsDavid Curtis
Psychiatric Bulletin (2014)|September 20, 2014
OCTET does not demonstrate a lack of effectiveness for community treatment ordersDavid Curtis
BMC Psychiatry|October 21, 2006
Case report: rapidly fatal bowel ischaemia on clozapine treatmentGiles Townsend, David Curtis
Journal of Neurogenetics|September 24, 2025
Analysis of whole genome sequence data shows association of Alzheimer's disease with rare coding variants in <i>ABCA7</i>, <i>PSEN1</i>, <i>SORL1</i> and <i>TREM2</i>David Curtis, Shujaani Joseph,
Lancet (London, England)|January 22, 2013
Report fails to acknowledge problems with at-home HIV testSam Curtis, David Curtis
Schizophrenia Research|November 22, 2017
Association study of schizophrenia with variants in miR-137 binding sitesDavid Curtis, Warren Emmett
Pageof 21

Showing results (61-70 of 203) with videos related to

Sort By:
Pageof 21
Molecular Genetics and Metabolism|August 5, 2020
Analysis of exome-sequenced UK Biobank subjects implicates genes affecting risk of hyperlipidaemiaDavid Curtis
European Journal of Human Genetics : EJHG|August 3, 2024
Assessment of ability of AlphaMissense to identify variants affecting susceptibility to common diseaseDavid Curtis
Journal of Human Genetics|March 7, 2024
Weighted burden analysis of rare coding variants in 470,000 exome-sequenced UK Biobank participants characterises effects on hyperlipidaemia riskDavid Curtis
Human Heredity|February 11, 2024
Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank ParticipantsDavid Curtis
Pulse (Basel, Switzerland)|February 26, 2024
Genetic Variants Associated with Hypertension Risk: Progress and ImplicationsDavid Curtis
Psychiatric Bulletin (2014)|September 20, 2014
OCTET does not demonstrate a lack of effectiveness for community treatment ordersDavid Curtis
BMC Psychiatry|October 21, 2006
Case report: rapidly fatal bowel ischaemia on clozapine treatmentGiles Townsend, David Curtis
Journal of Neurogenetics|September 24, 2025
Analysis of whole genome sequence data shows association of Alzheimer's disease with rare coding variants in <i>ABCA7</i>, <i>PSEN1</i>, <i>SORL1</i> and <i>TREM2</i>David Curtis, Shujaani Joseph,
Lancet (London, England)|January 22, 2013
Report fails to acknowledge problems with at-home HIV testSam Curtis, David Curtis
Schizophrenia Research|November 22, 2017
Association study of schizophrenia with variants in miR-137 binding sitesDavid Curtis, Warren Emmett
Pageof 21