Patrick F. Chinnery

Also affiliated with National Institute for Health and Care Research, MRC Mitochondrial Biology Unit, Medical Research Council

Biochemistry, Genetics and Molecular BiologyNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 12 papers. Top paper: “Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease”.

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease

Annals of Neurology(2015)10.1002/ana.24362

N/A

1.0DataRank · unranked

950 citations

Andrew M. Schaefer, Yi Ng, Nicholas Gomez, Emma L. Blakely, Charlotte L. Alston +8 more

Rare disease gene association discovery in the 100,000 GenomesProject

Nature(2025)10.1038/s41586-025-08623-w

N/A

0.515DataRank · unranked

18 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

RRM1 variants cause a mitochondrial DNA maintenance disorder via impaired de novo nucleotide synthesis

Journal of Clinical Investigation(2022)10.1172/jci145660

N/A

0DataRank · unranked

15 citations

Wolfgang M. Pernice, Wafaa Eyaid, B. Jeevan, Zuben P. Brown, Martí Juanola‐Falgarona +19 more

Nuclear genetic control of mtDNA copy number and heteroplasmy in humans

Nature(2023)10.1038/s41586-023-06426-5

N/A

0DataRank · unranked

182 citations

Masahiro Kanai, Timothy Durham, Kristin Tsuo, Jason G. McCoy, Anna V. Kotrys +7 more

CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signature

Human Molecular Genetics(2023)10.1093/hmg/ddad161

N/A

0DataRank · unranked

6 citations

Yu Nie, Alexandra J Gilsrud, Xiaoping Huang, Derek P. Narendra, Patrick F. Chinnery +1 more

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

medRxiv(2023)10.1101/2023.12.20.23300294

N/A

0DataRank · unranked

3 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion

Brain(2020)10.1093/brain/awz418

N/A

0DataRank · unranked

221 citations

Stefano Tozza, Wai Yan Yau, Salvatore Rossi, Sarah J. Beecroft, Zane Jaunmuktane +37 more

Preventing excessive autophagy protects from the pathology of mtDNA mutations in Drosophila melanogaster

Nature Communications(2024)10.1038/s41467-024-55559-2

N/A

0DataRank · unranked

5 citations

Florian A. Rosenberger, Kai Chang, Alissa Wilhalm, Tom Barton-Owen, Fynn M. Hansen +8 more

Mitochondrial DNA disorders in neuromuscular diseases in diverse populations

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52141

N/A

0DataRank · unranked

2 citations

Katherine Schon, Jana Vandrovcová, Özlem Yayıcı Köken, Sharika Raga, Kireshnee Naidu +30 more

An oligodendrocyte silencer element underlies the pathogenic impact of lamin B1 structural variants

Nature Communications(2025)10.1038/s41467-025-56378-9

N/A

0DataRank · unranked

7 citations

Guillermo Rodríguez Bey, Talia DeFrancesco Oranburg, Kseniia Dudnyk, Santana M. Lardo, Nathan Herdman +28 more

An oligodendrocyte silencer element underlies the pathogenic impact of lamin B1 structural variants

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.03.551473

N/A

0DataRank · unranked

2 citations

Guillermo Rodríguez Bey, Talia DeFrancesco Oranburg, Kseniia Dudnyk, Santana M. Lardo, Nathan Herdman +28 more

GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements

Nature Communications(2022)10.1038/s41467-022-29931-z

N/A

0DataRank · unranked

46 citations

Adam P. Levine, Inês Cebola, Melanie Chan, Aliya S. Amin, Anshul Aich +94 more