Patrick Callier
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- 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 (3 shared papers)Laurence Faivre (35 shared papers)Frédéric Huet (24 shared papers)Alice Masurel‐Paulet (14 shared papers)Francine Mugneret (23 shared papers)Nathalie Marle (19 shared papers)Julien Thévenon (11 shared papers)Alice Goldenberg (3 shared papers)
- Journals
- European Journal of Medical Genetics (6 papers)Clinical Genetics (3 papers)European Journal of Human Genetics (3 papers)American Journal of Medical Genetics Part A (19 papers)Prenatal Diagnosis (2 papers)
- Partner nations
- FranceUnited StatesBelgium
In The Last Decade
Patrick Callier
64 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 131
- Genetics 585
- Linguistics and Language 93
- Cancer Research 170
- Molecular Biology 496
- Developmental Biology 15
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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 226 | |
| 2 | 2016 | 141 | |
| 3 | 2012 | 81 | |
| 4 | 2015 | 55 | |
| 5 | 2018 | 51 | |
| 6 | 2015 | 49 | |
| 7 | 2011 | 45 | |
| 8 | 2003 | 43 | |
| 9 | 2011 | 41 | |
| 10 | 2019 | 39 | |
| 11 | 2000 | 32 | |
| 12 | 2016 | 26 | |
| 13 | 2005 | 26 | |
| 14 | 2013 | 26 | |
| 15 | 2013 | 24 | |
| 16 | 2011 | 23 | |
| 17 | 2012 | 22 | |
| 18 | 2009 | 20 | |
| 19 | 2008 | 20 | |
| 20 | 2013 | 19 |
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 67 papers that have together received 1.3k 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 (585 citations), Linguistics and Language (93 citations), Cancer Research (170 citations), Molecular Biology (496 citations) and Developmental Biology (15 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, Alice Masurel‐Paulet, Francine Mugneret, Nathalie Marle, Julien Thévenon, Alice Goldenberg, Jeanne Amiel and Stanislas Lyonnet. Their work appears in journals such as European Journal of Medical Genetics, Clinical Genetics, European Journal of Human Genetics, American Journal of Medical Genetics Part A and Prenatal Diagnosis.
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.