Paul Thiry
Impact in
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment
- Genetics top 10%
- 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
- Blood disorders and treatments 1
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- Genomics and Chromatin Dynamics 1
- Co-authors
- Thomy de Ravel (3 shared papers)Berten Ceulemans (3 shared papers)Lieve Claes (2 shared papers)Jean‐Pierre Frijns (2 shared papers)Lina Basel‐Vanagaite (1 shared paper)Katrien Smets (1 shared paper)Peter De Jonghe (1 shared paper)Ann Löfgren (1 shared paper)
- Journals
- European Journal of Medical Genetics (2 papers)Human Mutation (1 paper)Journal of Child Neurology (1 paper)Molecular Syndromology (1 paper)American Journal of Medical Genetics (1 paper)
- Partner nations
- BelgiumUnited StatesIndia
In The Last Decade
Paul Thiry
8 papers receiving 324 citations
Peers
Comparison fields: 5 of 52
- Psychiatry and Mental health 165
- Genetics 186
- Cellular and Molecular Neuroscience 84
- Pediatrics, Perinatology and Child Health 72
- Clinical Biochemistry 21
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 | 152 | |
| 2 | 2012 | 75 | |
| 3 | 2004 | 45 | |
| 4 | 2009 | 21 | |
| 5 | 2005 | 19 | |
| 6 | 1990 | 11 | |
| 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 333 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), Pharmacological Effects and Toxicity Studies (1 paper), Blood groups and transfusion (1 paper), Blood disorders and treatments (1 paper), Autism Spectrum Disorder Research (1 paper) and Genomics and Chromatin Dynamics (1 paper). The work is most often cited by research in Psychiatry and Mental health (165 citations), Genetics (186 citations), Cellular and Molecular Neuroscience (84 citations), Pediatrics, Perinatology and Child Health (72 citations) and Clinical Biochemistry (21 citations). Paul Thiry has collaborated with scholars based in Belgium, United States and India. Frequent co-authors include Thomy de Ravel, Berten Ceulemans, Lieve Claes, Jean‐Pierre Frijns, Lina Basel‐Vanagaite, Katrien Smets, Peter De Jonghe, Ann Löfgren, Salmo Raskin and Jurgen Del‐Favero. Their work appears in journals such as European Journal of Medical Genetics, Human Mutation, Journal of Child Neurology, Molecular Syndromology and American Journal of Medical 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.