Guy D’Anjou
Impact in
- Genetics top 1%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Psychiatry and Mental health top 5%
- Epilepsy research and treatment
Papers in
- Genetics 9
- Neurogenetic and Muscular Disorders Research 9
- Genetics and Neurodevelopmental Disorders 4
-
- Epilepsy research and treatment 4
- Co-authors
- Kathryn J. Swoboda (6 shared papers)Charles Scott (6 shared papers)Sandra P. Reyna (6 shared papers)Gyula Acsádi (6 shared papers)Kristin J. Krosschell (6 shared papers)Mary K. Schroth (6 shared papers)Thomas O. Crawford (6 shared papers)John T. Kissel (6 shared papers)
- Journals
- Journal of Child Neurology (4 papers)PLoS ONE (3 papers)Muscle & Nerve (3 papers)The American Journal of Human Genetics (3 papers)Pediatric Neurology (2 papers)
- Partner nations
- CanadaUnited StatesGermany
In The Last Decade
Guy D’Anjou
22 papers receiving 1.9k citations
Guy D’Anjou's Hit Papers
Peers
Comparison fields: 5 of 79
- Genetics 624
- Genetics 548
- Psychiatry and Mental health 334
- Cellular and Molecular Neuroscience 198
- Neurology 92
Countries citing papers authored by Guy D’Anjou
This map shows the geographic impact of Guy D’Anjou'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 Guy D’Anjou with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Guy D’Anjou more than expected).
Fields of papers citing papers by Guy D’Anjou
This network shows the impact of papers produced by Guy D’Anjou. 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 Guy D’Anjou. The network helps show where Guy D’Anjou may publish in the future.
Co-authors
The 25 scholars most cited alongside Guy D’Anjou, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies Hit paper breakdown → | 2017 | 364 |
| 2 | 2011 | 294 | |
| 3 | 2009 | 270 | |
| 4 | 2009 | 152 | |
| 5 | 2010 | 147 | |
| 6 | 2017 | 107 | |
| 7 | 2011 | 106 | |
| 8 | 2010 | 98 | |
| 9 | 2011 | 84 | |
| 10 | 2013 | 64 | |
| 11 | 2007 | 51 | |
| 12 | 2012 | 45 | |
| 13 | 2007 | 36 | |
| 14 | 2019 | 31 | |
| 15 | 2015 | 25 | |
| 16 | 2017 | 24 | |
| 17 | 2007 | 22 | |
| 18 | 2010 | 14 | |
| 19 | 2008 | 8 | |
| 20 | 2009 | 4 |
About Guy D’Anjou
Guy D’Anjou is a scholar working on Genetics, Psychiatry and Mental health, Neurology, Genetics and Critical Care and Intensive Care Medicine, having authored 22 papers that have together received 2k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (9 papers), Genetics and Neurodevelopmental Disorders (4 papers), Epilepsy research and treatment (4 papers), Peripheral Neuropathies and Disorders (3 papers), Muscle Physiology and Disorders (2 papers), Down syndrome and intellectual disability research (1 paper), Child Abuse and Related Trauma (1 paper) and Hereditary Neurological Disorders (1 paper). The work is most often cited by research in Genetics (624 citations), Genetics (548 citations), Psychiatry and Mental health (334 citations), Cellular and Molecular Neuroscience (198 citations) and Neurology (92 citations). Guy D’Anjou has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Kathryn J. Swoboda, Charles Scott, Sandra P. Reyna, Gyula Acsádi, Kristin J. Krosschell, Mary K. Schroth, Thomas O. Crawford, John T. Kissel, Louise R. Simard and Mark B. Bromberg. Their work appears in journals such as Journal of Child Neurology, PLoS ONE, Muscle & Nerve, The American Journal of Human Genetics and Pediatric Neurology.
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.