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David Curtis

Showing results (41-50 of 203) with videos related to

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Advances and Applications in Bioinformatics and Chemistry : AABC|June 29, 2013
Approaches to the detection of recessive effects using next generation sequencing data from outbred populationsDavid Curtis
Human Heredity|January 7, 2021
Multiple Linear Regression Allows Weighted Burden Analysis of Rare Coding Variants in an Ethnically Heterogeneous PopulationDavid Curtis
BMC Genetics|June 15, 2007
Allelic association studies of genome wide association data can reveal errors in marker position assignmentsDavid Curtis
BMC Genetics|October 5, 2007
Extended homozygosity is not usually due to cytogenetic abnormalityDavid Curtis
The British Journal of Psychiatry : the Journal of Mental Science|October 26, 2020
Author's replyDavid Curtis
Psychiatric Genetics|March 17, 2016
Pathway analysis of whole exome sequence data provides further support for the involvement of histone modification in the aetiology of schizophreniaDavid Curtis
Annals of Human Genetics|March 31, 2015
Investigation of Recessive Effects in Schizophrenia Using Next-Generation Exome Sequence DataDavid Curtis
Psychiatric Genetics|January 8, 2024
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disordersDavid Curtis
Human Heredity|December 9, 2025
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMIDavid Curtis
Psychiatric Genetics|June 24, 2022
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesisDavid Curtis
Pageof 21

Showing results (41-50 of 203) with videos related to

Sort By:
Pageof 21
Advances and Applications in Bioinformatics and Chemistry : AABC|June 29, 2013
Approaches to the detection of recessive effects using next generation sequencing data from outbred populationsDavid Curtis
Human Heredity|January 7, 2021
Multiple Linear Regression Allows Weighted Burden Analysis of Rare Coding Variants in an Ethnically Heterogeneous PopulationDavid Curtis
BMC Genetics|June 15, 2007
Allelic association studies of genome wide association data can reveal errors in marker position assignmentsDavid Curtis
BMC Genetics|October 5, 2007
Extended homozygosity is not usually due to cytogenetic abnormalityDavid Curtis
The British Journal of Psychiatry : the Journal of Mental Science|October 26, 2020
Author's replyDavid Curtis
Psychiatric Genetics|March 17, 2016
Pathway analysis of whole exome sequence data provides further support for the involvement of histone modification in the aetiology of schizophreniaDavid Curtis
Annals of Human Genetics|March 31, 2015
Investigation of Recessive Effects in Schizophrenia Using Next-Generation Exome Sequence DataDavid Curtis
Psychiatric Genetics|January 8, 2024
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disordersDavid Curtis
Human Heredity|December 9, 2025
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMIDavid Curtis
Psychiatric Genetics|June 24, 2022
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesisDavid Curtis
Pageof 21