Patrick F. Chinnery - Concepedia

Author

Patrick F. Chinnery

Also Known As

Adrienne M Flanagan, Afina W. Lemstra, Andy G Lynch, Chinnery Pf, Chinnery, P, Chinnery, PF, Chinnery, Patrick, Chinnery, Patrick F, Chinnery, Patrick F., Day, Christopher P.

929

Publications

62.3K

Citations

127

H-Index

285

Concepts

All Affiliations

Newcastle University Wellcome Centre for Mitochondrial Research University of Cambridge MRC Mitochondrial Biology Unit Royal Victoria Infirmary

About

Patrick F. Chinnery is an author at Newcastle University specializing in medicine, genetics, and mitochondrial function.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	74	179	18.6K
2	Natural Sciences	37	43	4.8K
3	Health Sciences	9	9	694
4	Engineering	3	3	181
5	Arts	1	1	152

Patrick F. Chinnery

390

Publications

39.2K

Citations

105

H-Index

Page 1

	Year	Citations
Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity Bo Meng, Adam Abdullahi, Isabella A.T.M. Ferreira, Nature	2022	1.1K
Prevalence of nuclear and mitochondrial <scp>DNA</scp> mutations related to adult mitochondrial disease Gráinne S. Gorman, Andrew M. Schaefer, Yi Shiau Ng, Annals of Neurology	2015	915
A Unique Gene Regulatory Network Resets the Human Germline Epigenome for Development Walfred W. C. Tang, Sabine Dietmann, Naoko Irie, Cell	2015	656
Pathogenic Mitochondrial DNA Mutations Are Common in the General Population Hannah R. Elliott, David C. Samuels, James A. Eden, The American Journal of Human Genetics	2008	599
Prevalence of mitochondrial DNA disease in adults Andrew M. Schaefer, Robert McFarland, Emma L. Blakely, Annals of Neurology	2007	578
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease Andrew R.J. Curtis, Constanze Fey, Christopher M. Morris, Nature Genetics Neurodegenerative DiseasesMolecular NeuroscienceGenetic DisorderMedicineGenetics	2001	539
A randomized placebo-controlled trial of idebenone in Leber’s hereditary optic neuropathy Thomas Klopstock, Patrick Yu‐Wai‐Man, Konstantinos Dimitriadis, Brain	2011	533
Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population Fiona Norwood, Chris Harling, Patrick F. Chinnery, Brain	2009	525
Mitochondrial DNA mutations in human colonic crypt stem cells Robert W. Taylor, Martin Barron, Gillian M. Borthwick, Journal of Clinical Investigation Essential SubunitsGenome InstabilityRespiratory ChainSomatic VariantMitochondrial Biogenesis	2003	518
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes Lynsey Cree, David C. Samuels, Susana M. Chuva de Sousa Lopes, Nature Genetics Developmental BiologyRapid SegregationCell DivisionMitochondrial FunctionMedicine	2008	505

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