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Denise Harold

Showing results (21-30 of 56) with videos related to

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Human Molecular Genetics|November 14, 2012
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease riskJade Chapman, Elliott Rees, Denise Harold, et al.
Journal of Huntington'S Disease|October 8, 2015
The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's DiseaseKevin Correia, Denise Harold, Kyung-Hee Kim, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 3, 2014
Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesityAnke Hinney, Ozgür Albayrak, Jochen Antel, et al.
Human Molecular Genetics|September 22, 2017
A modifier of Huntington's disease onset at the MLH1 locusJong-Min Lee, Michael J Chao, Denise Harold, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 26, 2019
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophreniaDenise Harold, Siobhan Connolly, Brien P Riley, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 23, 2020
Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort studyClaire Foley, Elizabeth A Heron, Denise Harold, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2018
Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controlsDonna Cosgrove, David O Mothersill, Laura Whitton, et al.
Plos One|March 3, 2011
Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's diseaseMichelle K Lupton, Petroula Proitsi, Makrina Danillidou, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|June 14, 2017
Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working MemoryDonna Cosgrove, Omar Mothersill, Kimberley Kendall, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
Haplotype-based stratification of Huntington's diseaseMichael J Chao, Tammy Gillis, Ranjit S Atwal, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|November 14, 2012
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease riskJade Chapman, Elliott Rees, Denise Harold, et al.
Journal of Huntington'S Disease|October 8, 2015
The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's DiseaseKevin Correia, Denise Harold, Kyung-Hee Kim, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 3, 2014
Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesityAnke Hinney, Ozgür Albayrak, Jochen Antel, et al.
Human Molecular Genetics|September 22, 2017
A modifier of Huntington's disease onset at the MLH1 locusJong-Min Lee, Michael J Chao, Denise Harold, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 26, 2019
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophreniaDenise Harold, Siobhan Connolly, Brien P Riley, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 23, 2020
Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort studyClaire Foley, Elizabeth A Heron, Denise Harold, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2018
Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controlsDonna Cosgrove, David O Mothersill, Laura Whitton, et al.
Plos One|March 3, 2011
Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's diseaseMichelle K Lupton, Petroula Proitsi, Makrina Danillidou, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|June 14, 2017
Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working MemoryDonna Cosgrove, Omar Mothersill, Kimberley Kendall, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
Haplotype-based stratification of Huntington's diseaseMichael J Chao, Tammy Gillis, Ranjit S Atwal, et al.
Pageof 6