Robert W. Taylor

39.0k citations

453 papers · 23.1k indexed · 3 hit papers · h-index 77

Impact in

Clinical Biochemistry top 0.01%
- Metabolism and Genetic Disorders
Molecular Biology top 0.1%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- Metabolomics and Mass Spectrometry Studies

Papers in

Clinical Biochemistry 245
- Metabolism and Genetic Disorders 245
Molecular Biology 362
- Mitochondrial Function and Pathology 329
- ATP Synthase and ATPases Research 141
- RNA modifications and cancer 65
- RNA and protein synthesis mechanisms 29

Co-authors: Douglass M. Turnbull Robert McFarland Patrick F. Chinnery Emma L. Blakely Andrew M. Schaefer Charlotte L. Alston Robert N. Lightowlers Amy K. Reeve
Journals: Neuromuscular Disorders (31 papers)Annals of Neurology (16 papers)European Journal of Human Genetics (15 papers)Neurology (13 papers)Critical Care Medicine (12 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Robert W. Taylor

436 papers receiving 22.7k citations

Hit Papers

align trajectories log scale

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease 2015 · 643 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.

2015 Annals of Neurology
2006 Nature Genetics
2005 Nature Reviews Genetics

Peers

Countries citing papers authored by Robert W. Taylor

Since Specialization

Citations

This map shows the geographic impact of Robert W. Taylor'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 Robert W. Taylor with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert W. Taylor more than expected).

Fields of papers citing papers by Robert W. Taylor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert W. Taylor. 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 Robert W. Taylor. The network helps show where Robert W. Taylor may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Robert W. Taylor, 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 Robert W. Taylor Line = papers co-authored together Robert W. Taylor links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A novel missense mutation in ISCA2 causes aberrant splicing and leads to multiple mitochondrial dysfunctions syndrome 4 Frontiers in Psychiatry ·Zuhair N. Al‐Hassnan, Mazhor Aldosary, Yang Yao-nin, Olivia Jorisch-Mühlebach, Rawan Almass, Fisk Mb, Saif Alshahrani, Albandary AlBakheet, Mohammad A. Al–Muhaizea, Robert W. Taylor, Dilek Çolak, Namik Kaya	2024	0
2	Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study Orphanet Journal of Rare Diseases ·王士娜, Izelle Smuts, Anderson Francklin Soares, Mutia Shaza Fita, Barend Christiaan Vorster, Gail-Ann P. Wilson, Careni Spencer, 孟祥豪, Maiyeti Fitri, Hongqi Wang, Robert McFarland, Robert W. Taylor, Graeme Levy, Mahmoud R. Fassad, Jana Vandrovcová, Ronald J. A. Wanders, Francois H. van der Westhuizen	2024	2
3	Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54 European Journal of Human Genetics ·Thomas B. Smith, Jim Bologna, Huw B. Thomas, Kyle Thompson, Monika Oláhová, Reza Maroofian, Mina Zamani, Langping He, Saeid Sadeghian, Vicki Cohen, Gota TAKAHASHI, Tal Gilboa, Kristin Herman, Thomas J. McCorvie, Wyatt W. Yue, Henry Houlden, Robert W. Taylor, William G. Newman, Raymond T. O’Keefe	2023	3
4	Delineating selective vulnerability of inhibitory interneurons in Alpers' syndrome Neuropathology and Applied Neurobiology ·Kakembo Aisha Annet, Daniel Erskine, Alasdair Blain, Robert W. Taylor, Robert McFarland, Nichola Z. Lax	2022	11
5	Nonstop mRNAs generate a ground state of mitochondrial gene expression noise Science Advances ·Joseph Replat, Ching Lan Esther Lin, Uwe Richter, Omid Safronov, Lars Paulín, Cory D. Dunn, Ville O. Paavilainen, Julie Richer, William G. Newman, Robert W. Taylor, Brendan J. Battersby	2022	10
6	A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families Cells ·Mazhor Aldosary, Maysoon Alsagob, Olivia Jorisch-Mühlebach, H. Libikova, Stefan T. Arold, C.Y. Li, Javier A. Madrigal, Rawan Almass, Albandary AlBakheet, Anne rer. nat. Morgenstern, Alya Qari, Mysoon M. Al‐Ansari, Monika Oláhová, Saif Alshahrani, Moeenaldeen AlSayed, Dilek Çolak, Robert W. Taylor, Mohammed Al‐Owain, Namik Kaya	2022	0
7	The Effect of tRNA[Ser]Sec Isopentenylation on Selenoprotein Expression International Journal of Molecular Sciences ·Noelia Fradejas‐Villar, Bahori Bahori, Wenchao Zhao, Uwe Reuter, Annika Kötter, Mark Helm, Rainer Knoll, Robert McFarland, Robert W. Taylor, Tianguo Hong, Kenjyo Miyauchi, Yuriko Sakaguchi, Tsutomu Suzuki, Ulrich Schweizer	2021	11
8	Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease Human Molecular Genetics ·Gerald Cullen, А Сейтбаев, Kyle Thompson, Emanuele Bellacchio, Courtney E. French, Sathya .P, Toni S. Pearson, Julie Vogt, Daria Diodato, R. Fleischer, Anja Ernst, Rita Horváth, Manali Chitre, Jakob Ek, Flemming Wibrand, Dorothy K. Grange, Lucy Raymond, Xiao-Long Zhou, Robert W. Taylor, Elsebet Østergaard	2021	13
9	The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi‐omic pipelines The Journal of Pathology ·Charlotte L. Alston, Sarah L. Stenton, Gavin Hudson, Holger Prokisch, Robert W. Taylor	2021	36
10	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
11	Metabolic effects of bezafibrate in mitochondrial disease EMBO Molecular Medicine ·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	56
12	FBXL 4 deficiency increases mitochondrial removal by autophagy EMBO Molecular Medicine ·David Alsina, Oleksandr Lytovchenko, С. Т. Болдарев, Ilian Atanassov, F. Schober, Min Jiang, Camilla Koolmeister, Anna Wedell, Robert W. Taylor, Anna Wredenberg, Nils‐Göran Larsson	2020	43
13	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
14	Mitochondrial stress response triggered by defects in protein synthesis quality control Life Science Alliance ·Uwe Richter, Joseph Replat, Fumi Suomi, Paula Marttinen, Axmann in Erfurt, Christopher B. Jackson, Anu Suomalainen, Helena Vihinen, Eija Jokitalo, Tuula A. Nyman, Martha Alicia Jarquin Cerda, James B. Stewart, Cecilia Mancini, Alfredo Brusco, Sara Seneca, Anne Lombès, Robert W. Taylor, Brendan J. Battersby	2019	33
15	Designing General Anesthetics That Have a Better Safety Profile Pharmacology &amp Pharmacy ·Robert B. Raffa, Joseph V. Pergolizzi, Robert W. Taylor	2019	1
16	SURF1 deficiency: a multi-centre natural history study Orphanet Journal of Rare Diseases ·Yehani Wedatilake, Ruth M. Brown, Robert McFarland, Joy Yaplito‐Lee, Andrew A. M. Morris, Mike Champion, C H Fang, Antonia Clarke, David R. Thorburn, Robert W. Taylor, John M. Land, Katharine Forrest, Angus Dobbie, Louise Simmons, Erlend T. Aasheim, David Ketteridge, Donncha Hanrahan, Anupam Chakrapani, Garry K. Brown, Shamima Rahman	2013	91
17	P02 Impaired subendocardial myofibre function in primary biliary cirrhosis: Abstract P02 Table 1 Gut ·Imran Patanwala, Wei Mingguo, Julia L. Newton, Robert W. Taylor, Andrew M. Blamire, D. I. Jones	2010	1
18	M.P.3.08 Resistance exercise training in mitochondrial myopathy due to single, large-scale deletions: Implications for therapy Neuromuscular Disorders ·Tanja Taivassalo, 唐风, Robert W. Taylor, Chong Chung Foong, Ronald G. Haller, Doris A. Taylor	2007	1
19	False-Positive Diagnosis of a Single, Large-Scale Mitochondrial DNA Deletion by Southern Blot Analysis: The Role of Neutral Polymorphisms Genetic Testing ·Marcus Deschauer, Anna Krasnianski, Stephan Zierz, Robert W. Taylor	2004	6
20	Techniques and procedures in critical care Lippincott eBooks ·Robert W. Taylor, Joseph M. Civetta, Robert R. Kirby	1990	1

About Robert W. Taylor

Robert W. Taylor is a scholar working on Clinical Biochemistry, Molecular Biology, Cellular and Molecular Neuroscience, Genetics and Critical Care and Intensive Care Medicine, having authored 453 papers that have together received 23.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (329 papers), Metabolism and Genetic Disorders (245 papers), ATP Synthase and ATPases Research (141 papers), RNA modifications and cancer (65 papers), Genetic Neurodegenerative Diseases (41 papers), RNA and protein synthesis mechanisms (29 papers), Genomics and Rare Diseases (15 papers) and Cardiomyopathy and Myosin Studies (11 papers). The work is most often cited by research in Clinical Biochemistry (9.0k citations), Molecular Biology (18.4k citations), Aging (420 citations), Cellular and Molecular Neuroscience (2.5k citations) and Neurology (1.3k citations). Robert W. Taylor has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Douglass M. Turnbull, Robert McFarland, Patrick F. Chinnery, Emma L. Blakely, Andrew M. Schaefer, Charlotte L. Alston, Robert N. Lightowlers, Amy K. Reeve, Laura C. Greaves and Helen Tuppen. Their work appears in journals such as Neuromuscular Disorders, Annals of Neurology, European Journal of Human Genetics, Neurology and Critical Care Medicine.

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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