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Alan F Wright

Showing results (41-50 of 239) with videos related to

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Human Genetics|January 16, 2008
Mortality risks in patients with constitutional autosomal chromosome deletions in Britain: a cohort studyAnthony J Swerdlow, Minouk J Schoemaker, Craig D Higgins, et al.
American Journal of Epidemiology|December 12, 2018
Mortality and Cancer Incidence in Carriers of Balanced Robertsonian Translocations: A National Cohort StudyMinouk J Schoemaker, Michael E Jones, Craig D Higgins, et al.
Human Molecular Genetics|December 4, 2009
Zebrafish Rpgr is required for normal retinal development and plays a role in dynein-based retrograde transport processesXinhua Shu, Zhiqiang Zeng, Philippe Gautier, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
A microdeletion in Xp11.3 accounts for co-segregation of retinitis pigmentosa and mental retardation in a large kindredLilei Zhang, Tao Wang, Alan F Wright, et al.
Neuroscience Letters|June 28, 2005
The functional COMT polymorphism, Val 158 Met, is associated with logical memory and the personality trait intellect/imagination in a cohort of healthy 79 year oldsSarah E Harris, Alan F Wright, Caroline Hayward, et al.
American Journal of Human Genetics|March 26, 2005
Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study designVeronique Vitart, Andrew D Carothers, Caroline Hayward, et al.
Advances in Experimental Medicine and Biology|January 26, 2007
Biochemical characterisation of the C1QTNF5 gene associated with late-onset retinal degeneration. A genetic model of age-related macular degenerationXinhua Shu, Brian Tulloch, Alan Lennon, et al.
International Journal of Epidemiology|March 30, 2010
Bayesian methods for instrumental variable analysis with genetic instruments ('Mendelian randomization'): example with urate transporter SLC2A9 as an instrumental variable for effect of urate levels on metabolic syndromePaul M McKeigue, Harry Campbell, Sarah Wild, et al.
BMC Genetics|July 3, 2007
A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognitionSarah E Harris, Helen Fox, Alan F Wright, et al.
Investigative Ophthalmology & Visual Science|February 2, 2011
Knockdown of the zebrafish ortholog of the retinitis pigmentosa 2 (RP2) gene results in retinal degenerationXinhua Shu, Zhiqiang Zeng, Philippe Gautier, et al.
Pageof 24

Showing results (41-50 of 239) with videos related to

Sort By:
Pageof 24
Human Genetics|January 16, 2008
Mortality risks in patients with constitutional autosomal chromosome deletions in Britain: a cohort studyAnthony J Swerdlow, Minouk J Schoemaker, Craig D Higgins, et al.
American Journal of Epidemiology|December 12, 2018
Mortality and Cancer Incidence in Carriers of Balanced Robertsonian Translocations: A National Cohort StudyMinouk J Schoemaker, Michael E Jones, Craig D Higgins, et al.
Human Molecular Genetics|December 4, 2009
Zebrafish Rpgr is required for normal retinal development and plays a role in dynein-based retrograde transport processesXinhua Shu, Zhiqiang Zeng, Philippe Gautier, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
A microdeletion in Xp11.3 accounts for co-segregation of retinitis pigmentosa and mental retardation in a large kindredLilei Zhang, Tao Wang, Alan F Wright, et al.
Neuroscience Letters|June 28, 2005
The functional COMT polymorphism, Val 158 Met, is associated with logical memory and the personality trait intellect/imagination in a cohort of healthy 79 year oldsSarah E Harris, Alan F Wright, Caroline Hayward, et al.
American Journal of Human Genetics|March 26, 2005
Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study designVeronique Vitart, Andrew D Carothers, Caroline Hayward, et al.
Advances in Experimental Medicine and Biology|January 26, 2007
Biochemical characterisation of the C1QTNF5 gene associated with late-onset retinal degeneration. A genetic model of age-related macular degenerationXinhua Shu, Brian Tulloch, Alan Lennon, et al.
International Journal of Epidemiology|March 30, 2010
Bayesian methods for instrumental variable analysis with genetic instruments ('Mendelian randomization'): example with urate transporter SLC2A9 as an instrumental variable for effect of urate levels on metabolic syndromePaul M McKeigue, Harry Campbell, Sarah Wild, et al.
BMC Genetics|July 3, 2007
A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognitionSarah E Harris, Helen Fox, Alan F Wright, et al.
Investigative Ophthalmology & Visual Science|February 2, 2011
Knockdown of the zebrafish ortholog of the retinitis pigmentosa 2 (RP2) gene results in retinal degenerationXinhua Shu, Zhiqiang Zeng, Philippe Gautier, et al.
Pageof 24