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A Ashley-Koch

Showing results (1-10 of 13) with videos related to

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American Journal of Epidemiology|May 3, 2000
Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE reviewA Ashley-Koch, Q Yang, R S Olney
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
Contribution of sickle cell disease to the occurrence of developmental disabilities: a population-based studyA Ashley-Koch, C C Murphy, M J Khoury, et al.
Acta Neurologica Scandinavica|December 17, 2011
Design, methodological issues and participation in a multiple sclerosis case-control studyD M Williamson, R A Marrie, A Ashley-Koch, et al.
Genes, Brain, and Behavior|January 10, 2012
Impact of BDNF Val66Met and 5-HTTLPR polymorphism variants on neural substrates related to sadness and executive functionL Wang, A Ashley-Koch, D C Steffens, et al.
Journal of Medical Genetics|September 10, 2003
Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational classA G Yip, A Dürr, D A Marchuk, et al.
The Pharmacogenomics Journal|March 3, 2010
BDNF Val66Met genotype and 6-month remission rates in late-life depressionW D Taylor, D R McQuoid, A Ashley-Koch, et al.
Molecular Psychiatry|March 11, 2009
Angiotensin receptor gene polymorphisms and 2-year change in hyperintense lesion volume in menW D Taylor, D C Steffens, A Ashley-Koch, et al.
Molecular Psychiatry|September 28, 2006
SLITRK1 mutations in trichotillomaniaS Zuchner, M L Cuccaro, K N Tran-Viet, et al.
Genetic Epidemiology|December 22, 1999
Complete genomic screen for disease susceptibility loci in nuclear familiesJ L Anderson, E R Hauser, E R Martin, et al.
Scientific Reports|February 12, 2021
Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migrationK S Au, L Hebert, P Hillman, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
American Journal of Epidemiology|May 3, 2000
Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE reviewA Ashley-Koch, Q Yang, R S Olney
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
Contribution of sickle cell disease to the occurrence of developmental disabilities: a population-based studyA Ashley-Koch, C C Murphy, M J Khoury, et al.
Acta Neurologica Scandinavica|December 17, 2011
Design, methodological issues and participation in a multiple sclerosis case-control studyD M Williamson, R A Marrie, A Ashley-Koch, et al.
Genes, Brain, and Behavior|January 10, 2012
Impact of BDNF Val66Met and 5-HTTLPR polymorphism variants on neural substrates related to sadness and executive functionL Wang, A Ashley-Koch, D C Steffens, et al.
Journal of Medical Genetics|September 10, 2003
Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational classA G Yip, A Dürr, D A Marchuk, et al.
The Pharmacogenomics Journal|March 3, 2010
BDNF Val66Met genotype and 6-month remission rates in late-life depressionW D Taylor, D R McQuoid, A Ashley-Koch, et al.
Molecular Psychiatry|March 11, 2009
Angiotensin receptor gene polymorphisms and 2-year change in hyperintense lesion volume in menW D Taylor, D C Steffens, A Ashley-Koch, et al.
Molecular Psychiatry|September 28, 2006
SLITRK1 mutations in trichotillomaniaS Zuchner, M L Cuccaro, K N Tran-Viet, et al.
Genetic Epidemiology|December 22, 1999
Complete genomic screen for disease susceptibility loci in nuclear familiesJ L Anderson, E R Hauser, E R Martin, et al.
Scientific Reports|February 12, 2021
Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migrationK S Au, L Hebert, P Hillman, et al.
Pageof 2