Robert W. Taylor

Newcastle upon Tyne Hospitals NHS Foundation Trust

Also affiliated with Charles Darwin University, Wellcome Centre for Mitochondrial Research, MRC Mitochondrial Biology Unit, Newcastle University

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 26 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

NovelDNM1Lvariants impair mitochondrial dynamics through divergent mechanisms

Life Science Alliance(2022)10.26508/lsa.202101284

N/A

0.871DataRank · unranked

25 citations

John M. Egner, Jack J. Collier, Oliver M. Russell, Charlotte L. Alston, Megan Cleland Harwig +19 more

LONP1 and mtHSP70 cooperate to promote mitochondrial protein folding

Nature Communications(2021)10.1038/s41467-020-20597-z

N/A

0DataRank · unranked

134 citations

Shuxia Meng, Spiros D. Garbis, Annie Moradian, Robert W. Taylor, Michael J. Sweredoski +3 more

POLRMT mutations impair mitochondrial transcription causing neurological disease

Nature Communications(2021)10.1038/s41467-021-21279-0

N/A

0DataRank · unranked

60 citations

Bradley Peter, Zsolt Szilágyi, Héctor Díaz-Maldonado, Meenakshi Singh, Ewen W. Sommerville +34 more

Clinical implementation of RNA sequencing for Mendelian disease diagnostics

medRxiv(2021)10.1101/2021.04.01.21254633

N/A

0DataRank · unranked

33 citations

Mirjana Gušić, Robert Kopajtich, Christian Mertes, Nicholas H. Smith, Charlotte L. Alston +48 more

Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants

Genetics in Medicine(2022)10.1016/j.gim.2022.09.015

N/A

0DataRank · unranked

17 citations

Yael Mozer‐Glassberg, Yuval E. Landau, Lea D. Schlieben, Holger Prokisch, René G. Feichtinger +56 more

Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100097

N/A

0DataRank · unranked

15 citations

L Bianchi, Francesca Rastelli, Florence Piron‐Prunier, Sophie Ayciriex, Claude Besmond +21 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

FBXL4 suppresses mitophagy by restricting the accumulation of NIX and BNIP3 mitophagy receptors

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.12.511867

N/A

0DataRank · unranked

9 citations

Keri‐Lyn Kozul, Yi Cui, Brendan Townsend, Prajakta Gosavi, Soo Siang Ooi +12 more

Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders

Brain(2023)10.1093/brain/awad380

N/A

0DataRank · unranked

19 citations

Abolfazl Rad, Sheng‐Jia Lin, Aida M. Bertoli‐Avella, Wouter W. Kallemeijn, Annie Godwin +84 more

Astrocytic pathology in Alpers’ syndrome

Acta Neuropathologica Communications(2023)10.1186/s40478-023-01579-w

N/A

0DataRank · unranked

14 citations

Chun Chen, Nichola Z. Lax, Robert W. Taylor, Daniel Erskine, Robert McFarland +1 more

Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental disease

Brain(2023)10.1093/brain/awad434

N/A

0DataRank · unranked

8 citations

Xinfu Jiao, J. Christopher Hennings, Jan Giesecke, Geeta Palsule, Stefanie Beck‐Wödl +35 more

Ultrasensitive deletion detection links mitochondrial DNA replication, disease, and aging

Genome biology(2020)10.1186/s13059-020-02138-5

N/A

0DataRank · unranked

103 citations

Matthew J. Longley, Margaret H. Humble, Christopher A. Lavender, Adam Burkholder, Emma L. Blakely +8 more

Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy

Nature Genetics(2024)10.1038/s41588-023-01651-0

N/A

0DataRank · unranked

33 citations

Dan Cox, Irina Zaharieva, Valeria Di Leo, J. Sarparanta, Per Harald Jonson +80 more

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial disease

Nature Metabolism(2024)10.1038/s42255-024-01039-2

N/A

0DataRank · unranked

22 citations

Rachel M. Guerra, Laura Steenberge, Charlotte L. Alston, Kei Murayama, Yasushi Okazaki +10 more

Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.007

N/A

0DataRank · unranked

7 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +34 more

Biallelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered intrinsic and extrinsic apoptosis and a Perrault syndrome-spectrum phenotype

medRxiv(2024)10.1101/2024.08.19.24312079

N/A

0DataRank · unranked

2 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +35 more

Biallelic variants in MRPL49 cause variable clinical presentations, including sensorineural hearing loss, leukodystrophy, and ovarian insufficiency

medRxiv(2024)10.1101/2024.10.10.24315152

N/A

0DataRank · unranked

2 citations

Leigh Demain, Alfredo Cabrera‐Orefice, Isabelle Schrauwen, Hanan E. Shamseldin, Alessandro Rea +26 more

RTN4IP1 is essential for the final stages of mitochondrial complex I assembly and coenzyme Q biosynthesis

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.04.610987

N/A

0DataRank · unranked

0 citations

Rachel M. Guerra, Jack J. Collier, Juliana Heidler, Kyle Thompson, Chelsea R. White +8 more

Bi-allelic variants in MRPL49 cause variable clinical presentations, including sensorineural hearing loss, leukodystrophy, and ovarian insufficiency

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.02.005

N/A

0DataRank · unranked

7 citations

Leigh Demain, Alfredo Cabrera‐Orefice, Isabelle Schrauwen, Hanan E. Shamseldin, Alessandro Rea +41 more

Delineating the mechanisms of cerebellar degeneration in paediatric and adult primary mitochondrial disease

Acta Neuropathologica(2025)10.1007/s00401-025-02891-6

N/A

0DataRank · unranked

1 citations

Elizaveta A. Olkhova, Nichola Z. Lax, Yi Shiau Ng, Robert W. Taylor, Gráinne S. Gorman +3 more

RTN4IP1 is required for the final stages of mitochondrial complex I assembly and CoQ biosynthesis

The EMBO Journal(2025)10.1038/s44318-025-00533-x

N/A

0DataRank · unranked

1 citations

Rachel M. Guerra, Jack J. Collier, Juliana Heidler, Kyle Thompson, Chelsea R. White +9 more

Biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency

Brain Communications(2025)10.1093/braincomms/fcaf369

N/A

0DataRank · unranked

1 citations

Lucie S Taylor, Sahar Sedighzadeh, Dalila Moualek, Mariasavina Severino, Daniel N. Grba +23 more

Genetic analysis and multimodal imaging confirm m.12148 T > C mitochondrial variant pathogenicity leading to multisystem dysfunction

Molecular Genetics and Metabolism(2025)10.1016/j.ymgme.2025.109049

N/A

0DataRank · unranked

1 citations

Alexander Kreymerman, Jill L Young, Nirmal Vadgama, Marco H. Ji, Sandeep Randhawa +14 more

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial disease

Research Square(2023)10.21203/rs.3.rs-3332602/v1

N/A

0DataRank · unranked

0 citations

Andrew Y. Sung, Rachel M. Guerra, Laura Steenberge, Charlotte L. Alston, Kei Murayama +10 more

Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.01.007

N/A

0DataRank · unranked

52 citations

Klaudia Strucinska, Mikel Muñoz Oreja, Andrew Parrish, Richard Caswell, Karen Stals +24 more