Frédérique Tihy
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 2
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- Prenatal Screening and Diagnostics 7
- Fetal and Pediatric Neurological Disorders 2
- Nephrology top 10%
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- Glycogen Storage Diseases and Myoclonus 2
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- Lysosomal Storage Disorders Research 2
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- Sarcoma Diagnosis and Treatment 2
- Co-authors
- Nicole LemieuxEmmanuelle LemyreDimitri J. StavropoulosJo‐Ann BrockTanya N. NelsonClaudine H. KosGéraldine MathonnetHeini Murer
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Frédérique Tihy
16 papers receiving 348 citations
Peers
Comparison fields: 5 of 57
- Genetics 215
- Pediatrics, Perinatology and Child Health 146
- Nephrology 41
- Oral Surgery 13
- Molecular Biology 120
Countries citing papers authored by Frédérique Tihy
This map shows the geographic impact of Frédérique Tihy'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 Frédérique Tihy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Frédérique Tihy more than expected).
Fields of papers citing papers by Frédérique Tihy
This network shows the impact of papers produced by Frédérique Tihy. 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 Frédérique Tihy. The network helps show where Frédérique Tihy may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Frédérique Tihy, 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 | 2024 | 0 | |
| 2 | 2019 | 4 | |
| 3 | 2018 | 45 | |
| 4 | 2018 | 77 | |
| 5 | 2018 | 5 | |
| 6 | 2014 | 63 | |
| 7 | 2014 | 12 | |
| 8 | 2011 | 36 | |
| 9 | 2006 | 19 | |
| 10 | 2006 | 4 | |
| 11 | 2006 | 12 | |
| 12 | 2006 | 14 | |
| 13 | 2006 | 0 | |
| 14 | 2005 | 16 | |
| 15 | 1998 | 20 | |
| 16 | 1994 | 44 | |
| 17 | 1993 | 7 | |
| 18 | 1992 | 6 |
About Frédérique Tihy
Frédérique Tihy is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Rheumatology, having authored 18 papers that have together received 384 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (3 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Genomics and Rare Diseases (2 papers), Lysosomal Storage Disorders Research (2 papers), Sarcoma Diagnosis and Treatment (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). The work is most often cited by research in Genetics (215 citations), Pediatrics, Perinatology and Child Health (146 citations) and Nephrology (41 citations). Frédérique Tihy has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Nicole Lemieux, Emmanuelle Lemyre, Dimitri J. Stavropoulos, Jo‐Ann Brock, Tanya N. Nelson, Claudine H. Kos, Géraldine Mathonnet, Heini Murer, Harriet S. Tenenhouse and Michael J. Econs. Their work appears in journals such as Journal of Bone and Mineral Research, JAMA Psychiatry and Genomics.
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.