Angus Clarke
Impact in
- Genetics top 0.2%
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 1%
- Autism Spectrum Disorder Research
Papers in
- Genetics 113
- BRCA gene mutations in cancer 55
- Genomics and Rare Diseases 38
- Genetics and Neurodevelopmental Disorders 33
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- Ethics and Legal Issues in Pediatric Healthcare 26
- Prenatal Screening and Diagnostics 19
- Co-authors
- Srikant SarangiJohn ChristodoulouHelen LeonardEvelyn ParsonsMark E.S. BaileyNadia Bahi‐BuissonMichele ZappellaDaniel G. Glaze
- Journals
- European Journal of Human Genetics (26 papers)Journal of Medical Genetics (18 papers)Archives of Disease in Childhood (8 papers)Social Science & Medicine (6 papers)Clinical Genetics (4 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Angus Clarke
209 papers receiving 8.1k citations
Hit Papers
Peers
Comparison fields: 5 of 169
- Genetics 4.5k
- Cognitive Neuroscience 1.3k
- Pediatrics, Perinatology and Child Health 1.3k
- Molecular Biology 3.3k
- Oral Surgery 351
Countries citing papers authored by Angus Clarke
This map shows the geographic impact of Angus Clarke'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 Angus Clarke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Angus Clarke more than expected).
Fields of papers citing papers by Angus Clarke
This network shows the impact of papers produced by Angus Clarke. 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 Angus Clarke. The network helps show where Angus Clarke may publish in the future.
Co-authors
The 25 scholars most cited alongside Angus Clarke, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2025 | 0 | |
| 3 | 2024 | 4 | |
| 4 | 2024 | 1 | |
| 5 | 2024 | 0 | |
| 6 | 2023 | 3 | |
| 7 | 2023 | 10 | |
| 8 | 2022 | 17 | |
| 9 | 2021 | 4 | |
| 10 | 2018 | 33 | |
| 11 | 2018 | 32 | |
| 12 | 2017 | 53 | |
| 13 | 2016 | 57 | |
| 14 | 2011 | 40 | |
| 15 | Non-directiveness in genetic counselling? | 2000 | 2 |
| 16 | 2000 | 12 | |
| 17 | Culture, kinship and genes: Towards cross-cultural genetics | 1997 | 21 |
| 18 | 1997 | 2 | |
| 19 | Genetic screening: a response to Nuffield. | 1994 | 4 |
| 20 | 1988 | 3 |
About Angus Clarke
Angus Clarke is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience, Clinical Psychology and Public Health, Environmental and Occupational Health, having authored 217 papers that have together received 8.5k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (55 papers), Genomics and Rare Diseases (38 papers), Genetics and Neurodevelopmental Disorders (33 papers), Ethics and Legal Issues in Pediatric Healthcare (26 papers), Autism Spectrum Disorder Research (23 papers), Prenatal Screening and Diagnostics (19 papers), Ethics in Clinical Research (17 papers) and dental development and anomalies (17 papers). The work is most often cited by research in Genetics (4.5k citations), Cognitive Neuroscience (1.3k citations), Pediatrics, Perinatology and Child Health (1.3k citations), Molecular Biology (3.3k citations) and Oral Surgery (351 citations). Angus Clarke has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Srikant Sarangi, John Christodoulou, Helen Leonard, Evelyn Parsons, Mark E.S. Bailey, Nadia Bahi‐Buisson, Michele Zappella, Daniel G. Glaze, Jeffrey L. Neul and Alan K. Percy. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Archives of Disease in Childhood, Social Science & Medicine 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.