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Patrick F. Chinnery

Showing results (121-130 of 370) with videos related to

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Journal of Neurology|May 11, 2015
Whole exome sequencing and the clinician: we need clinical skills and functional validation in variant filteringDaniyal Daud, Helen Griffin, Konstantinos Douroudis, et al.
Interface Focus|December 27, 2021
How COVID-19 has changed medical research fundingPatrick F Chinnery, Jonathan J Pearce, Anna M Kinsey, et al.
Neurotrauma Reports|October 7, 2022
Cell-Free Mitochondrial DNA in Acute Brain InjurySaeed Kayhanian, Angelos Glynos, Richard Mair, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 11, 2011
Genetic variations within the OPA1 gene are not associated with neuromyelitis opticaKamil S Sitarz, Patrick Yu-Wai-Man, Gavin Hudson, et al.
Mitochondrion|March 15, 2011
Variation in MAPT is not a contributing factor to the incomplete penetrance in LHONGavin Hudson, Patrick Yu-Wai-Man, Philip G Griffiths, et al.
Neurology. Genetics|January 23, 2023
High-Depth PRNP Sequencing in Brains With Sporadic Creutzfeldt-Jakob DiseaseAlexander G Murley, Yu Nie, Zoe Golder, et al.
Investigative Ophthalmology & Visual Science|May 16, 2009
Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophyPatrick Yu-Wai-Man, Vanessa J Davies, Malgorzata J Piechota, et al.
Science Advances|November 12, 2025
The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagyLaura S Kremer, Zoe Golder, Tom Barton-Owen, et al.
Journal of Medical Genetics|September 5, 2006
Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutationAngela Pyle, Robert W Taylor, Steve E Durham, et al.
Neurobiology of Aging|August 5, 2015
Inherited mtDNA variations are not strong risk factors in human prion diseaseGavin Hudson, James Uphill, Holger Hummerich, et al.
Pageof 37

Showing results (121-130 of 370) with videos related to

Sort By:
Pageof 37
Journal of Neurology|May 11, 2015
Whole exome sequencing and the clinician: we need clinical skills and functional validation in variant filteringDaniyal Daud, Helen Griffin, Konstantinos Douroudis, et al.
Interface Focus|December 27, 2021
How COVID-19 has changed medical research fundingPatrick F Chinnery, Jonathan J Pearce, Anna M Kinsey, et al.
Neurotrauma Reports|October 7, 2022
Cell-Free Mitochondrial DNA in Acute Brain InjurySaeed Kayhanian, Angelos Glynos, Richard Mair, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 11, 2011
Genetic variations within the OPA1 gene are not associated with neuromyelitis opticaKamil S Sitarz, Patrick Yu-Wai-Man, Gavin Hudson, et al.
Mitochondrion|March 15, 2011
Variation in MAPT is not a contributing factor to the incomplete penetrance in LHONGavin Hudson, Patrick Yu-Wai-Man, Philip G Griffiths, et al.
Neurology. Genetics|January 23, 2023
High-Depth PRNP Sequencing in Brains With Sporadic Creutzfeldt-Jakob DiseaseAlexander G Murley, Yu Nie, Zoe Golder, et al.
Investigative Ophthalmology & Visual Science|May 16, 2009
Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophyPatrick Yu-Wai-Man, Vanessa J Davies, Malgorzata J Piechota, et al.
Science Advances|November 12, 2025
The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagyLaura S Kremer, Zoe Golder, Tom Barton-Owen, et al.
Journal of Medical Genetics|September 5, 2006
Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutationAngela Pyle, Robert W Taylor, Steve E Durham, et al.
Neurobiology of Aging|August 5, 2015
Inherited mtDNA variations are not strong risk factors in human prion diseaseGavin Hudson, James Uphill, Holger Hummerich, et al.
Pageof 37