Angela Pyle
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Molecular Biology top 1%
- Mitochondrial Function and Pathology
- Muscle Physiology and Disorders
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
Papers in
-
- Mitochondrial Function and Pathology 70
-
- Hereditary Neurological Disorders 19
- Genetic Neurodegenerative Diseases 10
- Co-authors
- Patrick Francis Chinnery (75 shared papers)Gavin Hudson (30 shared papers)Rita Horváth (44 shared papers)Helen R Griffin (34 shared papers)Robert William Taylor (31 shared papers)David John Burn (8 shared papers)Mauro Santibanez‐Koref (19 shared papers)Marzena Kurzawa‐Akanbi (8 shared papers)
- Journals
- Brain (10 papers)The American Journal of Human Genetics (9 papers)Neurology Genetics (6 papers)Human Molecular Genetics (6 papers)Mitochondrion (6 papers)
- Partner nations
- United KingdomGermanyUnited States
In The Last Decade
Angela Pyle
135 papers receiving 7.3k citations
Angela Pyle's Hit Papers
Peers
Comparison fields: 5 of 125
- Clinical Biochemistry 533
- Molecular Biology 4.2k
- Cellular and Molecular Neuroscience 770
- Neurology 546
- Genetics 1.1k
Countries citing papers authored by Angela Pyle
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
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-authors
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.
All Works
Showing the 20 most-cited of 137 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Whole-genome sequencing of patients with rare diseases in a national health system Hit paper breakdown → | 2020 | 418 |
| 2 | 2014 | 316 | |
| 3 | 2007 | 305 | |
| 4 | 2013 | 240 | |
| 5 | 2015 | 219 | |
| 6 | 2018 | 179 | |
| 7 | 2020 | 179 | |
| 8 | 2019 | 178 | |
| 9 | 2005 | 153 | |
| 10 | 2005 | 148 | |
| 11 | 2014 | 140 | |
| 12 | 2014 | 134 | |
| 13 | 2021 | 134 | |
| 14 | 2000 | 129 | |
| 15 | 2019 | 127 | |
| 16 | 2016 | 124 | |
| 17 | 2014 | 118 | |
| 18 | 2014 | 117 | |
| 19 | 2014 | 113 | |
| 20 | 2015 | 111 |
About Angela Pyle
Angela Pyle is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Clinical Biochemistry, Neurology and Genetics, having authored 137 papers that have together received 7.4k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (70 papers), Hereditary Neurological Disorders (19 papers), Genomics and Rare Diseases (16 papers), Metabolism and Genetic Disorders (15 papers), Parkinson's Disease Mechanisms and Treatments (13 papers), Genetic Neurodegenerative Diseases (10 papers), Sepsis Diagnosis and Treatment (5 papers) and Neurological diseases and metabolism (4 papers). The work is most often cited by research in Clinical Biochemistry (533 citations), Molecular Biology (4.2k citations), Cellular and Molecular Neuroscience (770 citations), Neurology (546 citations) and Genetics (1.1k citations). Angela Pyle has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Patrick Francis Chinnery, Gavin Hudson, Rita Horváth, Helen R Griffin, Robert William Taylor, David John Burn, Mauro Santibanez‐Koref, Marzena Kurzawa‐Akanbi, Alison Jane Yarnall and Jennifer Duff. Their work appears in journals such as Brain, The American Journal of Human Genetics, Neurology Genetics, Human Molecular Genetics and Mitochondrion.
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.