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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 populations
David Curtis
Human Heredity
|
January 7, 2021
Multiple Linear Regression Allows Weighted Burden Analysis of Rare Coding Variants in an Ethnically Heterogeneous Population
David Curtis
BMC Genetics
|
June 15, 2007
Allelic association studies of genome wide association data can reveal errors in marker position assignments
David Curtis
BMC Genetics
|
October 5, 2007
Extended homozygosity is not usually due to cytogenetic abnormality
David Curtis
The British Journal of Psychiatry : the Journal of Mental Science
|
October 26, 2020
Author's reply
David 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 schizophrenia
David Curtis
Annals of Human Genetics
|
March 31, 2015
Investigation of Recessive Effects in Schizophrenia Using Next-Generation Exome Sequence Data
David Curtis
Psychiatric Genetics
|
January 8, 2024
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disorders
David Curtis
Human Heredity
|
December 9, 2025
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI
David Curtis
Psychiatric Genetics
|
June 24, 2022
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis
David Curtis
Page
of 21
Search research articles
Search
Showing results (41-50 of 203) with videos related to
Sort By:
Page
of 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 populations
David Curtis
Human Heredity
|
January 7, 2021
Multiple Linear Regression Allows Weighted Burden Analysis of Rare Coding Variants in an Ethnically Heterogeneous Population
David Curtis
BMC Genetics
|
June 15, 2007
Allelic association studies of genome wide association data can reveal errors in marker position assignments
David Curtis
BMC Genetics
|
October 5, 2007
Extended homozygosity is not usually due to cytogenetic abnormality
David Curtis
The British Journal of Psychiatry : the Journal of Mental Science
|
October 26, 2020
Author's reply
David 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 schizophrenia
David Curtis
Annals of Human Genetics
|
March 31, 2015
Investigation of Recessive Effects in Schizophrenia Using Next-Generation Exome Sequence Data
David Curtis
Psychiatric Genetics
|
January 8, 2024
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disorders
David Curtis
Human Heredity
|
December 9, 2025
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI
David Curtis
Psychiatric Genetics
|
June 24, 2022
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis
David Curtis
Page
of 21