Patrick Callier
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Linguistics and Language top 5%
- Linguistic Variation and Morphology
Papers in
- Genetics 39
- Genomic variations and chromosomal abnormalities 21
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 7
- Genetic Syndromes and Imprinting 7
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- Congenital heart defects research 9
- Co-authors
- Robert J. Podesva (4 shared papers)Laurence Faivre (35 shared papers)Frédéric Huet (24 shared papers)Francine Mugneret (23 shared papers)Alice Masurel‐Paulet (14 shared papers)Nathalie Marle (19 shared papers)Julien Thévenon (11 shared papers)Stanislas Lyonnet (3 shared papers)
- Journals
- European Journal of Medical Genetics (6 papers)European Journal of Human Genetics (3 papers)Clinical Genetics (3 papers)American Journal of Medical Genetics Part A (19 papers)Diabetes & Metabolism (2 papers)
- Partner nations
- FranceUnited StatesBelgium
In The Last Decade
Patrick Callier
65 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 133
- Genetics 624
- Linguistics and Language 104
- Cancer Research 180
- Urology 45
- Molecular Biology 535
Countries citing papers authored by Patrick Callier
This map shows the geographic impact of Patrick Callier'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 Patrick Callier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick Callier more than expected).
Fields of papers citing papers by Patrick Callier
This network shows the impact of papers produced by Patrick Callier. 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 Patrick Callier. The network helps show where Patrick Callier may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick Callier, 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 68 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 243 | |
| 2 | 2016 | 144 | |
| 3 | 2012 | 81 | |
| 4 | 2015 | 59 | |
| 5 | 2015 | 56 | |
| 6 | 2018 | 54 | |
| 7 | 2003 | 51 | |
| 8 | 2011 | 49 | |
| 9 | 2011 | 41 | |
| 10 | 2019 | 39 | |
| 11 | 2000 | 33 | |
| 12 | 2005 | 31 | |
| 13 | 2016 | 29 | |
| 14 | 2013 | 27 | |
| 15 | 2013 | 27 | |
| 16 | 2012 | 24 | |
| 17 | 2011 | 23 | |
| 18 | 2008 | 22 | |
| 19 | 2009 | 21 | |
| 20 | 2013 | 21 |
About Patrick Callier
Patrick Callier is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Linguistics and Language, having authored 68 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Congenital heart defects research (9 papers), Prenatal Screening and Diagnostics (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (7 papers), Genetic Syndromes and Imprinting (7 papers), Linguistic Variation and Morphology (6 papers) and Phonetics and Phonology Research (5 papers). The work is most often cited by research in Genetics (624 citations), Linguistics and Language (104 citations), Cancer Research (180 citations), Urology (45 citations) and Molecular Biology (535 citations). Patrick Callier has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Robert J. Podesva, Laurence Faivre, Frédéric Huet, Francine Mugneret, Alice Masurel‐Paulet, Nathalie Marle, Julien Thévenon, Stanislas Lyonnet, Alice Goldenberg and Jeanne Amiel. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Clinical Genetics, American Journal of Medical Genetics Part A and Diabetes & Metabolism.
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.