Kyle Thompson

1.6k citations

23 papers · 563 indexed · h-index 14

Impact in

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Molecular Biology
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA and protein synthesis mechanisms

Papers in ⓘ

Clinical Biochemistry 15
- Metabolism and Genetic Disorders 15
Molecular Biology 20
- Mitochondrial Function and Pathology 16
- RNA modifications and cancer 10
- RNA and protein synthesis mechanisms 3
- ATP Synthase and ATPases Research 3

Co-authors: Robert W. Taylor (19 shared papers)Monika Oláhová (5 shared papers)Robert McFarland (6 shared papers)Charlotte L. Alston (3 shared papers)Angela Pyle (2 shared papers)Emma L. Blakely (2 shared papers)Fiona Robertson (1 shared paper)Langping He (10 shared papers)
Journals: Journal of Inherited Metabolic Disease (2 papers)Human Molecular Genetics (2 papers)Frontiers in Genetics (2 papers)Clinical Genetics (2 papers)Neurology Genetics (2 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Kyle Thompson

22 papers receiving 561 citations

Peers

Countries citing papers authored by Kyle Thompson

Since Specialization

Citations

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

Fields of papers citing papers by Kyle Thompson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kyle Thompson. 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 Kyle Thompson. The network helps show where Kyle Thompson may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways International Journal of Molecular Sciences ·Jia Xin Tang, Kyle Thompson, Robert W. Taylor, Monika Oláhová	2020	121
2	Recent advances in understanding the molecular genetic basis of mitochondrial disease Journal of Inherited Metabolic Disease ·Kyle Thompson, Jack J. Collier, Ruth I.C. Glasgow, Fiona Robertson, Angela Pyle, Emma L. Blakely, Charlotte L. Alston, Monika Oláhová, Robert McFarland, Robert W. Taylor	2019	112
3	A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways Cell Reports ·Thomas Agnew, Michelle Goldsworthy, Carlos Aguilar, Anna Morgan, Michelle Simon, Helen Hilton, Chris Esapa, Yixing Wu, Heather Cater, Liz Bentley, Cheryl L. Scudamore, Joanna Poulton, Karl Morten, Kyle Thompson, Langping He, Steve D. M. Brown, Robert W. Taylor, Michael R. Bowl, Roger Cox	2018	32
4	Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23) Neurology Genetics ·Guido Zagnoli-Vieira, Francesco Bruni, Kyle Thompson, Langping He, Sarah Walker, Arjan P.M. de Brouwer, Robert W. Taylor, Dmitriy Niyazov, Keith W. Caldecott	2018	30
5	Biallelic mutations in mitochondrial tryptophanyl‐tRNA synthetase cause Levodopa‐responsive infantile‐onset Parkinsonism Clinical Genetics ·Elizabeth A. Burke, Steven J. Frucht, Kyle Thompson, Lynne A. Wolfe, Tadafumi Yokoyama, M. Bertoni, Yan Huang, Murat Sincan, David R. Adams, Robert W. Taylor, William A. Gahl, Camilo Toro, May Christine V. Malicdan	2017	30
6	Withaferin A Effectively Targets Soluble Vimentin in the Glaucoma Filtration Surgical Model of Fibrosis PLoS ONE ·Paola Bargagna‐Mohan, Sunil Deokule, Kyle Thompson, John Wizeman, Cidambi Srinivasan, Sunil K. Vooturi, Uday B. Kompella, Royce Mohan	2013	29
7	Species- and agonist-dependent differences in the deactivation-kinetics of P2X 7 receptors Naunyn-Schmiedeberg s Archives of Pharmacology ·A D Hibell, Kyle Thompson, Joseph Simon, Mengxue Xing, P.P.A. Humphrey, A.D. Michel	2001	28
8	Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy Human Molecular Genetics ·David Pacheu‐Grau, Sylvie Callegari, Sonia Emperador, Kyle Thompson, Abhishek Aich, Sarah E. Topol, Emily Spencer, Robert McFarland, Eduardo Ruiz‐Pesini, Ali Torkamani, Robert W. Taylor, Julio Montoya, Peter Rehling	2018	27
9	Pathogenic variants in HTRA2 cause an early‐onset mitochondrial syndrome associated with 3‐methylglutaconic aciduria Journal of Inherited Metabolic Disease ·Monika Oláhová, Kyle Thompson, Steven Hardy, Inês A. Barbosa, Arnaud Besse, Maria‐Eleni Anagnostou, Kathryn White, Tracey Davey, Michael A. Simpson, Michael Champion, Greg Enns, Susan Schelley, Robert N. Lightowlers, Zofia M. Chrzanowska‐Lightowlers, Robert McFarland, Charu Deshpande, Penelope E. Bonnen, Robert W. Taylor	2016	23
10	Bi‐allelic pathogenic variants in NDUFC2 cause early‐onset Leigh syndrome and stalled biogenesis of complex I EMBO Molecular Medicine ·Ahmad Alahmad, Alessia Nasca, Juliana Heidler, Kyle Thompson, Monika Oláhová, Andrea Legati, Eleonora Lamantea, Jana Meisterknecht, Manuela Spagnolo, Langping He, Seham Alameer, Fahad Hakami, Abeer Almehdar, Anna Ardissone, Charlotte L. Alston, Robert McFarland, Ilka Wittig, Daniele Ghezzi, Robert W. Taylor	2020	22
11	Lethal Neonatal LTBL Associated with Biallelic EARS2 Variants: Case Report and Review of the Reported Neuroradiological Features JIMD Reports ·Renata Maria Souza Oliveira, Ewen W. Sommerville, Kyle Thompson, Joana Nunes, Angela Pyle, Manuela Grazina, Patrick F. Chinnery, Luísa Diogo, Paula Garcia, Robert W. Taylor	2016	17
12	Novel MT-ND Gene Variants Causing Adult-Onset Mitochondrial Disease and Isolated Complex I Deficiency Frontiers in Genetics ·Yi Shiau Ng, Kyle Thompson, Daniela Loher, Sila Hopton, Gavin Falkous, Steven Hardy, Andrew M. Schaefer, Sandip Shaunak, Mark Roberts, James B Lilleker, Robert W. Taylor	2020	16
13	Expanding the phenotype of de novo SLC25A4 -linked mitochondrial disease to include mild myopathy Neurology Genetics ·Martin King, Kyle Thompson, Sila Hopton, Langping He, Edmund R.S. Kunji, Robert W. Taylor, Xilma R. Ortiz‐González	2018	16
14	Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations Frontiers in Genetics ·Sara Brito, Kyle Thompson, Jaume Campistol, J. Colomer, Steven Hardy, Langping He, Ana FernÃ¡ndez-Marmiesse, Lourdes Palacios, Cristina Jou, C. Jimenez‐Mallebrera, Judith Armstrong, Raquel Montero, Rafael Artuch, Christin Tischner, Tina Wenz, Robert McFarland, Robert W. Taylor	2015	14
15	Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease Human Molecular Genetics ·Wen-Qiang Zheng, Signe Vandal Pedersen, Kyle Thompson, Emanuele Bellacchio, Courtney E. French, Benjamin Munro, Toni S. Pearson, Julie Vogt, Daria Diodato, Tue Diemer, 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
16	Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits Neurogenetics ·Ruth I.C. Glasgow, Kyle Thompson, Inês A. Barbosa, Langping He, Charlotte L. Alston, Charu Deshpande, Michael A. Simpson, Andrew A. M. Morris, Axel Neu, Ulrike Löbel, Julie Hall, Holger Prokisch, Tobias B. Haack, Maja Hempel, Robert McFarland, Robert W. Taylor	2017	12
17	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
18	Periventricular Calcification, Abnormal Pterins and Dry Thickened Skin: Expanding the Clinical Spectrum of RMND1? JIMD Reports ·Jillian P. Casey, Ellen Crushell, Kyle Thompson, Eilish Twomey, Langping He, Sean Ennis, Roy K. Philip, Robert W. Taylor, Mary D. King, Sally Ann Lynch	2015	5
19	Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54 European Journal of Human Genetics ·Thomas B. Smith, Alessandro Rea, Huw B. Thomas, Kyle Thompson, Monika Oláhová, Reza Maroofian, Mina Zamani, Langping He, Saeid Sadeghian, Hamid Galehdari, Nava Shaul Lotan, Tal Gilboa, Kristin Herman, Thomas J. McCorvie, Wyatt W. Yue, Henry Houlden, Robert W. Taylor, William G. Newman, Raymond T. O’Keefe	2023	3
20	Investigation of oxidative phosphorylation activity and complex composition in mitochondrial disease Handbook of clinical neurology ·Kyle Thompson, David A. Stroud, David R. Thorburn, Robert W. Taylor	2023	3

About Kyle Thompson

Kyle Thompson is a scholar working on Clinical Biochemistry, Molecular Biology, Physiology, Endocrine and Autonomic Systems and Rehabilitation, having authored 23 papers that have together received 563 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (16 papers), Metabolism and Genetic Disorders (15 papers), RNA modifications and cancer (10 papers), RNA and protein synthesis mechanisms (3 papers), ATP Synthase and ATPases Research (3 papers), Neuroscience of respiration and sleep (1 paper), Genetic and Kidney Cyst Diseases (1 paper) and Trace Elements in Health (1 paper). The work is most often cited by research in Clinical Biochemistry (196 citations), Molecular Biology (448 citations), Physiology (28 citations), Neurology (26 citations) and Cellular and Molecular Neuroscience (44 citations). Kyle Thompson has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Robert W. Taylor, Monika Oláhová, Robert McFarland, Charlotte L. Alston, Angela Pyle, Emma L. Blakely, Fiona Robertson, Langping He, Jack J. Collier and P.P.A. Humphrey. Their work appears in journals such as Journal of Inherited Metabolic Disease, Human Molecular Genetics, Frontiers in Genetics, Clinical Genetics and Neurology Genetics.

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