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David A Dyment

Showing results (21-30 of 120) with videos related to

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Neurology. Genetics|April 12, 2016
Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblingsPatrick Ferreira, Stephanie M Luco, Sarah L Sawyer, et al.
Human Mutation|December 2, 2017
Evaluation of exome filtering techniques for the analysis of clinically relevant genesKristin D Kernohan, Taila Hartley, Najmeh Alirezaie, et al.
American Journal of Epidemiology|June 24, 2009
Age of onset in concordant twins and other relative pairs with multiple sclerosisA Dessa Sadovnick, Irene M Yee, Colleen Guimond, et al.
Journal of Human Genetics|February 24, 2017
Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1Priya T Bhola, Taila Hartley, Eric Bareke, et al.
BMC Medical Genetics|February 6, 2009
An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 geneSreeram V Ramagopalan, Roisin McMahon, David A Dyment, et al.
Journal of the Neurological Sciences|May 24, 2011
Early life child exposure and the risk of multiple sclerosis: a population based studySreeram V Ramagopalan, Colleen Guimond, David A Dyment, et al.
American Journal of Medical Genetics. Part A|November 1, 2021
A disease-causing variant in HNRNPH2 inherited from an unaffected mother with skewed X-inactivationAlexandre M White-Brown, Gabrielle Lemire, Yoko A Ito, et al.
Neuroepidemiology|January 7, 2010
No effect of parental age on risk of multiple sclerosis: a population-based studySreeram V Ramagopalan, David A Dyment, Colleen Guimond, et al.
Clinical Genetics|August 9, 2019
p21 protein-activated kinase 1 is associated with severe regressive autism, and epilepsyKristin D Kernohan, Arran McBride, Taila Hartley, et al.
American Journal of Medical Genetics. Part A|August 18, 2021
Whole genome sequencing identifies pathogenic RNU4ATAC variants in a child with recurrent encephalitis, microcephaly, and normal statureHugh J McMillan, Jorge Davila, Matt Osmond, et al.
Pageof 12

Showing results (21-30 of 120) with videos related to

Sort By:
Pageof 12
Neurology. Genetics|April 12, 2016
Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblingsPatrick Ferreira, Stephanie M Luco, Sarah L Sawyer, et al.
Human Mutation|December 2, 2017
Evaluation of exome filtering techniques for the analysis of clinically relevant genesKristin D Kernohan, Taila Hartley, Najmeh Alirezaie, et al.
American Journal of Epidemiology|June 24, 2009
Age of onset in concordant twins and other relative pairs with multiple sclerosisA Dessa Sadovnick, Irene M Yee, Colleen Guimond, et al.
Journal of Human Genetics|February 24, 2017
Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1Priya T Bhola, Taila Hartley, Eric Bareke, et al.
BMC Medical Genetics|February 6, 2009
An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 geneSreeram V Ramagopalan, Roisin McMahon, David A Dyment, et al.
Journal of the Neurological Sciences|May 24, 2011
Early life child exposure and the risk of multiple sclerosis: a population based studySreeram V Ramagopalan, Colleen Guimond, David A Dyment, et al.
American Journal of Medical Genetics. Part A|November 1, 2021
A disease-causing variant in HNRNPH2 inherited from an unaffected mother with skewed X-inactivationAlexandre M White-Brown, Gabrielle Lemire, Yoko A Ito, et al.
Neuroepidemiology|January 7, 2010
No effect of parental age on risk of multiple sclerosis: a population-based studySreeram V Ramagopalan, David A Dyment, Colleen Guimond, et al.
Clinical Genetics|August 9, 2019
p21 protein-activated kinase 1 is associated with severe regressive autism, and epilepsyKristin D Kernohan, Arran McBride, Taila Hartley, et al.
American Journal of Medical Genetics. Part A|August 18, 2021
Whole genome sequencing identifies pathogenic RNU4ATAC variants in a child with recurrent encephalitis, microcephaly, and normal statureHugh J McMillan, Jorge Davila, Matt Osmond, et al.
Pageof 12