Paul Thiry
Impact in
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 7
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
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- Ion Transport and Channel Regulation 1
- Co-authors
- Thomy de Ravel (3 shared papers)Lieve Claes (2 shared papers)Berten Ceulemans (3 shared papers)Jean‐Pierre Frijns (2 shared papers)Dominique Audenaert (1 shared paper)Jurgen Del‐Favero (1 shared paper)Barbara Plecko (1 shared paper)Salmo Raskin (1 shared paper)
- Journals
- European Journal of Medical Genetics (2 papers)Human Mutation (1 paper)Journal of Child Neurology (1 paper)American Journal of Medical Genetics (1 paper)Molecular Syndromology (1 paper)
- Partner nations
- BelgiumUnited StatesAustria
In The Last Decade
Paul Thiry
8 papers receiving 339 citations
Peers
Comparison fields: 5 of 48
- Psychiatry and Mental health 153
- Genetics 165
- Cellular and Molecular Neuroscience 77
- Pediatrics, Perinatology and Child Health 58
- Clinical Biochemistry 19
Countries citing papers authored by Paul Thiry
This map shows the geographic impact of Paul Thiry'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 Paul Thiry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paul Thiry more than expected).
Fields of papers citing papers by Paul Thiry
This network shows the impact of papers produced by Paul Thiry. 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 Paul Thiry. The network helps show where Paul Thiry may publish in the future.
Co-authors
The 25 scholars most cited alongside Paul Thiry, 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 | 2003 | 158 | |
| 2 | 2012 | 84 | |
| 3 | 2004 | 47 | |
| 4 | 2009 | 21 | |
| 5 | 2005 | 20 | |
| 6 | 1990 | 12 | |
| 7 | Angelman syndrome in three adult patients with atypical presentation and severe neurological complications. | 2000 | 8 |
| 8 | Severe myoclonic epilepsy in infancy: towards an optimal treatment | 2004 | 2 |
About Paul Thiry
Paul Thiry is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Genetics and Cellular and Molecular Neuroscience, having authored 8 papers that have together received 352 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (3 papers), Epilepsy research and treatment (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Autism Spectrum Disorder Research (1 paper), Genomics and Rare Diseases (1 paper), Ion Transport and Channel Regulation (1 paper), Genetic Syndromes and Imprinting (1 paper) and Immunodeficiency and Autoimmune Disorders (1 paper). The work is most often cited by research in Psychiatry and Mental health (153 citations), Genetics (165 citations), Cellular and Molecular Neuroscience (77 citations), Pediatrics, Perinatology and Child Health (58 citations) and Clinical Biochemistry (19 citations). Paul Thiry has collaborated with scholars based in Belgium, United States and Austria. Frequent co-authors include Thomy de Ravel, Lieve Claes, Berten Ceulemans, Jean‐Pierre Frijns, Dominique Audenaert, Jurgen Del‐Favero, Barbara Plecko, Salmo Raskin, Lina Basel‐Vanagaite and Ann Löfgren. Their work appears in journals such as European Journal of Medical Genetics, Human Mutation, Journal of Child Neurology, American Journal of Medical Genetics and Molecular Syndromology.
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.