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David Curtis

Showing results (71-80 of 203) with videos related to

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Annals of Human Genetics|February 25, 2020
Editorial: Topical ethical issues in the publication of human genetics researchDavid Curtis, François Balloux
Psychiatric Genetics|January 22, 2019
In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophreniaAntonia Tsavou, David Curtis
Schizophrenia Bulletin|May 22, 2019
Assessment of Potential Clinical Role for Exome Sequencing in SchizophreniaThivia Balakrishna, David Curtis
Blood|January 22, 2005
SCL/Tal1 and lymphoid versus myeloid lineage assignmentMark Hall, David Curtis
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Analysis of whole genome sequence data shows association of Alzheimer's disease with rare coding variants in <i>ABCA7, PSEN1, SORL1</i> and <i>TREM2</i>David Curtis, Shujaani Joseph,
Journal of Neurogenetics|June 27, 2025
Analysis of 470,000 exome-sequenced UK biobank participants identifies genes containing rare variants which confer dementia riskLily Gibbons, David Curtis
Archives of General Psychiatry|August 9, 2006
Estimation of haplotypes at DRD2 may have produced misleading resultsDavid Curtis, Hugh Gurling
Annals of Human Genetics|January 12, 2020
LD scores are associated with differences in allele frequencies between populations but LD score regression can still distinguish confounding from polygenicityMason Alexander, David Curtis
Annals of Human Genetics|June 21, 2018
Mini-review: Update on the genetics of schizophreniaLeda Coelewij, David Curtis
European Journal of Human Genetics : EJHG|June 12, 2023
The human genome harbours widespread exclusive yin yang haplotypesDavid Curtis, William Amos
Pageof 21

Showing results (71-80 of 203) with videos related to

Sort By:
Pageof 21
Annals of Human Genetics|February 25, 2020
Editorial: Topical ethical issues in the publication of human genetics researchDavid Curtis, François Balloux
Psychiatric Genetics|January 22, 2019
In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophreniaAntonia Tsavou, David Curtis
Schizophrenia Bulletin|May 22, 2019
Assessment of Potential Clinical Role for Exome Sequencing in SchizophreniaThivia Balakrishna, David Curtis
Blood|January 22, 2005
SCL/Tal1 and lymphoid versus myeloid lineage assignmentMark Hall, David Curtis
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Analysis of whole genome sequence data shows association of Alzheimer's disease with rare coding variants in <i>ABCA7, PSEN1, SORL1</i> and <i>TREM2</i>David Curtis, Shujaani Joseph,
Journal of Neurogenetics|June 27, 2025
Analysis of 470,000 exome-sequenced UK biobank participants identifies genes containing rare variants which confer dementia riskLily Gibbons, David Curtis
Archives of General Psychiatry|August 9, 2006
Estimation of haplotypes at DRD2 may have produced misleading resultsDavid Curtis, Hugh Gurling
Annals of Human Genetics|January 12, 2020
LD scores are associated with differences in allele frequencies between populations but LD score regression can still distinguish confounding from polygenicityMason Alexander, David Curtis
Annals of Human Genetics|June 21, 2018
Mini-review: Update on the genetics of schizophreniaLeda Coelewij, David Curtis
European Journal of Human Genetics : EJHG|June 12, 2023
The human genome harbours widespread exclusive yin yang haplotypesDavid Curtis, William Amos
Pageof 21