Kyle Thompson

1.7k citations

42 papers · 1.3k · h-index 21

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Molecular Biology top 10%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- RNA Research and Splicing

Papers in

Clinical Biochemistry 20
- Metabolism and Genetic Disorders 20
Molecular Biology 36
- Mitochondrial Function and Pathology 30
- RNA modifications and cancer 11
- ATP Synthase and ATPases Research 9
- RNA and protein synthesis mechanisms 5

Co-authors: Robert William Taylor (20 shared papers)Monika Oláhová (5 shared papers)Robert McFarland (7 shared papers)Charlotte L. Alston (4 shared papers)Angela Pyle (3 shared papers)Langping He (11 shared papers)Jack J. Collier (1 shared paper)Emma L. Blakely (2 shared papers)
Journals: The American Journal of Human Genetics (8 papers)Journal of Inherited Metabolic Disease (3 papers)EMBO Molecular Medicine (3 papers)Frontiers in Genetics (2 papers)Clinical Genetics (2 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Kyle Thompson

42 papers receiving 1.3k 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 42 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 William Taylor, Monika Oláhová	2020	143
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 M. Robertson, Angela Pyle, Emma L. Blakely, Charlotte L. Alston, Monika Oláhová	2019	126
3	Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number The American Journal of Human Genetics ·Kyle Thompson, Homa Majd, Cristina Dallabona, Karit Reinson, Martin S. King, Charlotte L. Alston, Langping He, Tiziana Lodi	2016	108
4	Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies The American Journal of Human Genetics ·Metodi Dimitrov Metodiev, Kyle Thompson, Charlotte L. Alston, Andrew A. M. Morris, Langping He, Zarah Assouline, Marlene Rio, Nadia Bahi‐Buisson	2016	105
5	Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder The American Journal of Human Genetics ·Monika Oláhová, Wan Hee Yoon, Kyle Thompson, Sharayu V. Jangam, Liliana Fernández, Jean M. Davidson, Jennifer E Kyle, Megan E. Grove	2018	80
6	OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect EMBO Molecular Medicine ·Kyle Thompson, Nicole Mai, Monika Oláhová, Filippo Scialò, Luke E. Formosa, David Arthur Stroud, Madeleine Garrett, Nichola Zoe Lax	2018	65
7	Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies The American Journal of Human Genetics ·René Günther Feichtinger, Monika Oláhová, Yoshihito Kishita, Caterina Garone, Laura Sophie Kremer, Mikako Yagi, Takeshi Uchiumi, Alexis A. Jourdain	2017	55
8	Clinical presentation and proteomic signature of patients with TANGO2 mutations Journal of Inherited Metabolic Disease ·Nadja Mingirulli, Angela Pyle, Denisa Hathazi, Charlotte L. Alston, Nicolai Kohlschmidt, Gina L. O’Grady, Leigh B. Waddell, Frances J. Evesson	2019	50
9	Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations The American Journal of Human Genetics ·Irit Hochberg, Leigh A. M. Demain, Julie Richer, Kyle Thompson, Jill E. Urquhart, Alessandro Rea, Waheeda Pagarkar, Agustí Rodríguez‐Palmero	2021	40
10	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	2017	37
11	A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways Cell Reports ·Thomas Agnew, Michelle E. Goldsworthy, Carlos Aguilar, Anna Morgan, Michelle Simon, Helen Hilton, Chris T. Esapa, Yixing Wu	2018	34
12	Withaferin A Effectively Targets Soluble Vimentin in the Glaucoma Filtration Surgical Model of Fibrosis PLoS ONE ·Paola Bargagna‐Mohan, Sunil P. Deokule, Kyle Thompson, John W. Wizeman, Cidambi Srinivasan, Sunil K. Vooturi, Uday B. Kompella, Royce Mohan	2013	33
13	Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23) Neurology Genetics ·Guido Zagnoli-Vieira, Francesco Bruni, Kyle Thompson, Langping He, Sarah K. Walker, Arjan P.M. de Brouwer, Robert William Taylor, Dmitriy M. Niyazov	2018	32
14	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 G. Spencer, Robert McFarland	2018	30
15	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, Patrick P.A. Humphrey, A.D. Michel	2001	28
16	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 A. Hardy, Inês A. Barbosa, Arnaud Besse, Maria‐Eleni Anagnostou, Kathryn White, Tracey Davey	2016	28
17	Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults JAMA Neurology ·Majida Charif, Alessia Nasca, Kyle Thompson, Sylvie Gerber, Christine C. Makowski, Neda Mazaheri, Céline Bris, David Goudenège	2017	27
18	Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number The American Journal of Human Genetics ·Kyle Thompson, Homa Majd, Cristina Dallabona, Karit Reinson, Martin S. King, Charlotte L. Alston, Langping He, Tiziana Lodi	2016	26
19	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 Menezes Nunes, Angela Pyle, Manuela M. Grazina, Patrick Francis Chinnery, Luísa M. Diogo	2016	24
20	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	2020	24

About Kyle Thompson

Kyle Thompson is a scholar working on Clinical Biochemistry, Molecular Biology, Neurology, Genetics and Physiology, having authored 42 papers that have together received 1.3k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (30 papers), Metabolism and Genetic Disorders (20 papers), RNA modifications and cancer (11 papers), ATP Synthase and ATPases Research (9 papers), RNA and protein synthesis mechanisms (5 papers), Salivary Gland Disorders and Functions (3 papers), Neurological diseases and metabolism (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Clinical Biochemistry (396 citations), Molecular Biology (1.0k citations), Physiology (30 citations), Neurology (47 citations) and Aging (10 citations). Kyle Thompson has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Robert William Taylor, Monika Oláhová, Robert McFarland, Charlotte L. Alston, Angela Pyle, Langping He, Jack J. Collier, Emma L. Blakely, Fiona M. Robertson and Patrick Francis Chinnery. Their work appears in journals such as The American Journal of Human Genetics, Journal of Inherited Metabolic Disease, EMBO Molecular Medicine, Frontiers in Genetics and Clinical Genetics.

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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