Patrick F. Chinnery

62.9k citations

488 papers · 29.3k indexed · 8 hit papers · h-index 87

Impact in

Clinical Biochemistry top 0.01%
- Metabolism and Genetic Disorders
Molecular Biology top 0.05%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- Metabolomics and Mass Spectrometry Studies

Papers in

Clinical Biochemistry 224
- Metabolism and Genetic Disorders 224
Neurology 49
- Neurological diseases and metabolism 41

Co-authors: Douglass M. Turnbull David C. Samuels Patrick Yu‐Wai‐Man Robert W. Taylor Gavin Hudson James B. Stewart Philip G. Griffiths Rita Horváth
Journals: Neurology (40 papers)Brain (23 papers)Annals of Neurology (21 papers)The American Journal of Human Genetics (19 papers)Neuromuscular Disorders (19 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Patrick F. Chinnery

478 papers receiving 28.7k citations

Hit Papers

8 papers align trajectories log scale

Pro-inflammatory macrophages produce mitochondria-derived superoxide by reverse electron transport at complex I that regulates IL-1β release during NLRP3 inflammasome activation 2025 · 22 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2025 Nature Metabolism
2024 Cell
2016 Nature Reviews Disease Primers
2015 Cell
2015 Annals of Neurology
2015 Nature Reviews Genetics
2014 Nature Reviews Neurology
2013 Neurology

Peers

Countries citing papers authored by Patrick F. Chinnery

Since Specialization

Citations

This map shows the geographic impact of Patrick F. Chinnery's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Patrick F. Chinnery with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick F. Chinnery more than expected).

Fields of papers citing papers by Patrick F. Chinnery

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick F. Chinnery. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Patrick F. Chinnery. The network helps show where Patrick F. Chinnery may publish in the future.

Co-authors

The 25 scholars most cited alongside Patrick F. Chinnery, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Patrick F. Chinnery Line = papers co-authored together Patrick F. Chinnery links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Ubiquitin-mediated mitophagy regulates the inheritance of mitochondrial DNA mutations Science ·Michele Frison, Brandon S. Lockey, Yu Nie, Zoe Golder, Eleni Theiaspra, Cameron Ryall, C J Lyons, Stephen P. Burr, Malwina Prater, Lyuba V. Bozhilova, Angelos Glynos, James B. Stewart, Nick S. Jones, Marcos Roberto Chiaratti, Patrick F. Chinnery	2025	0
2	The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagy Science Advances ·Laura S. Kremer, Zoe Golder, Tom Barton-Owen, Polyxeni Papadea, Camilla Koolmeister, Patrick F. Chinnery, Nils‐Göran Larsson	2025	0
3	LRPPRC and SLIRP synergize to maintain sufficient and orderly mammalian mitochondrial translation Nucleic Acids Research ·Diana Rubalcava-Gracia, Kristina Bubb, Fredrik Levander, Stephen P. Burr, Amelie V August, Patrick F. Chinnery, Camilla Koolmeister, Nils‐Göran Larsson	2024	5
4	Dynamics of cognitive variability with age and its genetic underpinning in NIHR BioResource Genes and Cognition cohort participants Nature Medicine ·Md Shafiqur Rahman, Emma Harrison, Heather Biggs, Chloe Seikus, Paul Elliott, Gerome Breen, Nathalie Kingston, John R. Bradley, Steven M. Hill, Brian D. M. Tom, Patrick F. Chinnery	2024	5
5	Evidence for sodium valproate toxicity in mitochondrial diseases: a systematic analysis BMJ Neurology Open ·Thiloka Ratnaike, Nour Elkhateeb, Angela Lochmüller, Christopher Gilmartin, Katherine Schon, Rita Horváth, Patrick F. Chinnery	2024	5
6	Mitochondrial DNA heteroplasmy is modulated during oocyte development propagating mutation transmission Science Advances ·Haixin Zhang, Marco Esposito, Mikael G. Pezet, Juvid Aryaman, Wei Wei, Florian Klimm, Claudia Calabrese, Stephen P. Burr, Carolina H. Macabelli, Carlo Viscomi, Mitinori Saitou, Marcos Roberto Chiaratti, James B. Stewart, Nick S. Jones, Patrick F. Chinnery	2021	25
7	Biparental inheritance of mitochondrial DNA revisited Nature Reviews Genetics ·Alistair T. Pagnamenta, Wei Wei, Shamima Rahman, Patrick F. Chinnery	2021	18
8	MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases Nucleic Acids Research ·Thiloka Ratnaike, Daniel Greene, Wei Wei, Alba Sanchis‐Juan, Katherine Schon, Jelle van den Ameele, Lucy Raymond, Rita Horváth, Ernest Turro, Patrick F. Chinnery	2021	22
9	Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project European Journal of Human Genetics ·Thomas Bourinaris, Damian Smedley, Valentina Cipriani, Isabella Sheikh, Alkyoni Athanasiou‐Fragkouli, Patrick F. Chinnery, Huw R. Morris, Raquel Real, Victoria Harrison, Evan Reid, Nicholas Wood, Jana Vandrovcová, Henry Houlden, Arianna Tucci	2020	11
10	Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion Journal of Neurology ·Grace McMacken, Hanns Lochmüller, Boglárka Bánsági, Angela Pyle, Angela Lochmüller, Patrick F. Chinnery, Steven Laurie, Sergi Beltrán, Leslie Matalonga, Rita Horváth	2020	5
11	Metabolic effects of bezafibrate in mitochondrial disease. Apollo (University of Cambridge) ·Hannah E. Steele, Aurora Gómez-Durán, Angela Pyle, Sila Hopton, Jane Newman, Renae J. Stefanetti, Sarah J. Charman, Jehill Parikh, Langping He, Carlo Viscomi, Djordje G. Jakovljević, Kieren G. Hollingsworth, Alan J. Robinson, Robert W. Taylor, Leonardo Bottolo, Rita Horváth, Patrick F. Chinnery	2020	0
12	Identification of a novel heterozygous guanosine monophosphate reductase ( GMPR ) variant in a patient with a late‐onset disorder of mitochondrial DNA maintenance Clinical Genetics ·Ewen W. Sommerville, Ilaria Dalla Rosa, Masha M. Rosenberg, Francesco Bruni, Kyle Thompson, Mariana C. Rocha, Emma L. Blakely, Langping He, Gavin Falkous, Andrew M. Schaefer, Patrick Yu‐Wai‐Man, Patrick F. Chinnery, Lizbeth Hedstrom, Antonella Spinazzola, Robert W. Taylor, Gráinne S. Gorman	2019	7
13	Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo PTEN mutation Neurology ·Boglárka Bánsági, Vietxuan Phan, Mark R. Baker, Julia O’Sullivan, Matthew J. Jennings, Roger G. Whittaker, Juliane Müller, Jennifer Duff, Helen Griffin, James Miller, Gráinne S. Gorman, Hanns Lochmüller, Patrick F. Chinnery, Andreas Roos, Laura E. Swan, Rita Horváth	2018	5
14	Mutations in mitochondrial DNA causing tubulointerstitial kidney disease PLoS Genetics ·Thomas M. Connor, Simon Hoer, Andrew J. Mallett, Daniel P. Gale, Aurora Gómez-Durán, Viktor Posse, Robin Antrobus, Pablo Moreno, Marco Sciacovelli, Christian Frezza, Jennifer Duff, Neil Sheerin, John A. Sayer, Margaret Ashcroft, Michael S. Wiesener, Gavin Hudson, Claes M. Gustafsson, Patrick F. Chinnery, Patrick H. Maxwell	2017	40
15	Hereditary Myopathy with Early Respiratory Failure Gerald Pfeffer, Patrick F. Chinnery	2014	3
16	Dissociation of duration-based and beat-based auditory timing in cerebellar degeneration Proceedings of the National Academy of Sciences ·Manon Grube, Freya E. Cooper, Patrick F. Chinnery, Timothy D. Griffiths	2010	147
17	In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes Human Molecular Genetics ·Stefanie Bulst, Angela Abicht, Elke Holinski‐Feder, Solvig Müller-Ziermann, Udo Koehler, Christian Thirion, Maggie C. Walter, Joanna D. Stewart, Patrick F. Chinnery, Hanns Lochmüller, Rita Horváth	2009	44
18	Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis Neurology ·Emma Matthews, Robyn Labrum, Mary G. Sweeney, Richa Sud, A. Haworth, Patrick F. Chinnery, G. Meola, Stéphanie Schorge, Dimitri M. Kullmann, Mary B. Davis, Michael G. Hanna	2008	144
19	Andersen's syndrome: A skeletal muscle potassium channel disorder UCL Discovery (University College London) ·Nigel P. Davies, Alyssa J. Weber, Robert A. Mueller, David Hilton‐Jones, Patrick F. Chinnery, Michael G. Hanna	2002	1
20	Proceedings of the Association of British Neurologists, University of Oxford, 3 April - 5 April 2002 Journal of Neurology Neurosurgery & Psychiatry ·Patrick F. Chinnery, Curtis Ar, Jackson Mj, Christopher M. Morris, Laurence A. Bindoff, Ince Pg, Khan Valente, David J. Brooks, Bhatia Kp, Quinn Np, Pauline Monro, Dale Rc, A. H. Church, Surtees Rah, Alexander Charles Lees, Neville Bgr, Chard Dt, P A Brex, Griffin Cmb, Alan J. Thompson	2002	4

About Patrick F. Chinnery

Patrick F. Chinnery is a scholar working on Clinical Biochemistry, Neurology, Molecular Biology, Cellular and Molecular Neuroscience and Neurology, having authored 488 papers that have together received 29.3k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (329 papers), Metabolism and Genetic Disorders (224 papers), ATP Synthase and ATPases Research (97 papers), Genetic Neurodegenerative Diseases (72 papers), Neurological diseases and metabolism (41 papers), RNA modifications and cancer (30 papers), Genomics and Rare Diseases (28 papers) and Hereditary Neurological Disorders (25 papers). The work is most often cited by research in Clinical Biochemistry (10.3k citations), Molecular Biology (23.2k citations), Aging (529 citations), Neurology (2.1k citations) and Cellular and Molecular Neuroscience (3.9k citations). Patrick F. Chinnery has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Douglass M. Turnbull, David C. Samuels, Patrick Yu‐Wai‐Man, Robert W. Taylor, Gavin Hudson, James B. Stewart, Philip G. Griffiths, Rita Horváth, Neil Howell and Robert McFarland. Their work appears in journals such as Neurology, Brain, Annals of Neurology, The American Journal of Human Genetics and Neuromuscular Disorders.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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