Angela Pyle

8.9k citations

90 papers · 3.4k indexed · h-index 36

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism

Papers in

Clinical Biochemistry 36
- Metabolism and Genetic Disorders 36
Cellular and Molecular Neuroscience 26
- Genetic Neurodegenerative Diseases 19
- Hereditary Neurological Disorders 9

Co-authors: Patrick F. Chinnery Gavin Hudson Rita Horváth Helen Griffin David J. Burn Robert W. Taylor Marzena Kurzawa‐Akanbi Mauro Santibanez‐Koref
Journals: Neuromuscular Disorders (6 papers)Neurology Genetics (6 papers)Human Molecular Genetics (5 papers)Neurology (5 papers)Scientific Reports (4 papers)
Partner nations: United Kingdom Germany United States

In The Last Decade

Angela Pyle

88 papers receiving 3.3k citations

Peers

Countries citing papers authored by Angela Pyle

Since Specialization

Citations

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

Fields of papers citing papers by Angela Pyle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Early-stage idiopathic Parkinson’s disease is associated with reduced circular RNA expression npj Parkinson s Disease ·이세진, Osagie Izuogu, H. ERTON, E. Pajot, Angela Pyle, Ivan Pineda Velasco, Rachael A. Lawson, Alison J. Yarnall, Michael S. Jackson, Mauro Santibanez‐Koref, Gavin Hudson	2024	11
2	Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues Scientific Reports ·Сергій МАЦЮК, Angela Pyle, Amy E. Vincent, Paolo Actis, Gavin Hudson	2024	1
3	Genomic Strategies in Mitochondrial Diagnostics Methods in molecular biology ·E. Pajot, Charlotte L. Alston, Gavin Hudson, Robert W. Taylor, Angela Pyle	2023	0
4	Feasibility and impact of haplogroup matching for mitochondrial replacement treatment EMBO Reports ·Yuko Takeda, Louise Hyslop, Meenakshi Choudhary, Fiona Robertson, Angela Pyle, Ian Wilson, Mauro Santibanez‐Koref, Douglass M. Turnbull, Mary Herbert, Gavin Hudson	2023	3
5	Two type I topoisomerases maintain DNA topology in human mitochondria Nucleic Acids Research ·Katja E. Menger, James Chapman, Paula Berkel, Sanyog Pathak, E. Pajot, 肖丽婷, John Casement, I. D. van Felius, Angela Pyle, В. А. Блохин, Ian G. Cowell, Maria Falkenberg, Caroline A. Austin, Thomas J. Nicholls	2022	10
6	A subcellular cookie cutter for spatial genomics in human tissue Analytical and Bioanalytical Chemistry ·Сергій МАЦЮК, Angela Pyle, L. H. Luttrull, Douglass M. Turnbull, Amy E. Vincent, Gavin Hudson, Paolo Actis	2022	9
7	Homozygous TAF1C variants are associated with a novel childhood‐onset neurological phenotype Clinical Genetics ·胡雄, Angela Pyle, Maria Suo‐Palosaari, Jennifer Duff, Tawfiq Froukh, Anna‐Elina Lehesjoki, Salla M. Kangas, Julien Cazala, A Liang, Riikka Keski‐Filppula, Hannaleena Kokkonen, Johanna Uusimaa, Rita Horváth, Päivi Vieira	2020	3
8	Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion Journal of Neurology ·Grace McMacken, Hanns Lochmüller, Boglárka Bánsági, Angela Pyle, W. F. Danesi, Patrick F. Chinnery, Steven Laurie, Sergi Beltrán, Leslie Matalonga, Rita Horváth	2020	5
9	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
10	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
11	Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells Scientific Reports ·Jami King, Angela Pyle, Maria Lucia Valentino, Rocco Liguori, Patrick Yu‐Wai‐Man, Florence Burté, Jennifer Duff, Stephanie Kleinle, Isabel Diebold, Michela Rugolo, Rita Horváth, Valério Carelli	2018	17
12	Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans PLoS Genetics ·Angela Pyle, Gavin Hudson, Ian Wilson, Jonathan Coxhead, Michelle M. Hood, Mary Herbert, Mauro Santibanez‐Koref, Patrick F. Chinnery	2015	55
13	Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene Journal of Neuromuscular Diseases ·Angela Pyle, Venkateswaran Ramesh, Marina Bartsakoulia, Kimura Toshikazu, Aurora Gómez-Durán, Ágnes Herczegfalvi, Emma L. Blakely, Michelle M. Hood, Jennifer Duff, Gail Eglon, David Moore, Zidny Rahmawati, Konstantinos Douroudis, Mauro Santibanez‐Koref, Helen Griffin, Hanns Lochmüller, Veronika Karcagi, Robert W. Taylor, Patrick F. Chinnery, Rita Horváth	2014	14
14	Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy The American Journal of Human Genetics ·D. Herrmann, Rita Horváth, Janet E. Sowden, Michael Gonzalez, Avencia Sánchez-Mejías, Zhuo Guan, Roger G. Whittaker, 伸裕中村, Elodie Joyce Lucrece Malonga-Loukoula, Boglárka Bánsági, Angela Pyle, Veronika Boczonadi, Hanns Lochmüller, Helen Griffin, Patrick F. Chinnery, Thomas E. Lloyd, J. Troy Littleton, Natasha Timmer	2014	2
15	Late-Onset Sacsinopathy Diagnosed by Exome Sequencing and Comparative Genomic Hybridization Journal of Neurogenetics ·Angela Pyle, Helen Griffin, Jennifer Duff, Risaburo OBA, Simon Zwolinski, Michelle M. Hood, Haeranah Haeranah, Mauro Santibanez‐Koref, Rita Horváth, Patrick F. Chinnery	2013	6
16	Non-Random mtDNA Segregation Patterns Indicate a Metastable Heteroplasmic Segregation Unit in m.3243A>G Cybrid Cells PLoS ONE ·Anton K. Raap, В М Леонов, Frans M. van de Rijke, Angela Pyle, Carolina Wählby, Károly Szuhai, Raimond B. G. Ravelli, I.F.M. de Coo, Harsha Rajasimha, Mats Nilsson, Patrick F. Chinnery, David C. Samuels, George M. C. Janssen	2012	17
17	Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution Mitochondrion ·A.M. Voets, B.J.C. van den Bosch, Alphons P. M. Stassen, Alexandra T.M. Hendrickx, Debby M.E.I. Hellebrekers, L. Van Laer, Els Van Eyken, Guy Van Camp, Angela Pyle, Simon Baudouin, Patrick F. Chinnery, Hubert J.M. Smeets	2011	6
18	Clinical and neuropathological findings in patients with TACO1 mutations Neuromuscular Disorders ·Jürgen Seeger, Bertold Schrank, Angela Pyle, Rolf Stucka, H. Yoshimura, Soham S Patel, Angela Abicht, Birgit Czermin, Elke Holinski‐Feder, Hanns Lochmüller, Rita Horváth	2010	26
19	Mitochondrial DNA and survival after sepsis: a prospective study The Lancet ·Simon Baudouin, David Saunders, Watcharee Tiangyou, Joanna L. Elson, Yago Guidini, Angela Pyle, Sharon Keers, Douglass M. Turnbull, Neil Howell, Patrick F. Chinnery	2005	136
20	Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies Neuromuscular Disorders ·Robert Pogue, Louise V.B. Anderson, Angela Pyle, Caroline A. Sewry, C. Pollitt, Margaret A. Johnson, Keith Davison, Jennifer A. Moss, Eugenio Mercuri, Francesco Muntoni, K. Bushby	2001	32

About Angela Pyle

Angela Pyle is a scholar working on Clinical Biochemistry, Cellular and Molecular Neuroscience, Neurology, Molecular Biology and Neurology, having authored 90 papers that have together received 3.4k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (61 papers), Metabolism and Genetic Disorders (36 papers), Genetic Neurodegenerative Diseases (19 papers), ATP Synthase and ATPases Research (13 papers), Neurological diseases and metabolism (9 papers), Hereditary Neurological Disorders (9 papers), Metabolomics and Mass Spectrometry Studies (7 papers) and Parkinson's Disease Mechanisms and Treatments (7 papers). The work is most often cited by research in Clinical Biochemistry (881 citations), Neurology (329 citations), Cellular and Molecular Neuroscience (699 citations), Molecular Biology (2.6k citations) and Neurology (470 citations). Angela Pyle has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Patrick F. Chinnery, Gavin Hudson, Rita Horváth, Helen Griffin, David J. Burn, Robert W. Taylor, Marzena Kurzawa‐Akanbi, Mauro Santibanez‐Koref, Alison J. Yarnall and Jennifer Duff. Their work appears in journals such as Neuromuscular Disorders, Neurology Genetics, Human Molecular Genetics, Neurology and Scientific Reports.

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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