Patrick Callier
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Connective tissue disorders research
- Developmental Biology top 5%
Papers in
- Genetics 112
- Genomic variations and chromosomal abnormalities 53
- Genomics and Rare Diseases 40
- Genetics and Neurodevelopmental Disorders 22
- Connective tissue disorders research 6
- Genetic and rare skin diseases. 5
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- Prenatal Screening and Diagnostics 6
- Fetal and Pediatric Neurological Disorders 4
- Co-authors
- Laurence Olivier Faivre (45 shared papers)Christel Thauvin‐Robinet (41 shared papers)Frédéric Huet (29 shared papers)Alice Masurel (18 shared papers)Francine Mugneret (29 shared papers)Nathalie Marle (20 shared papers)Julien Thévenon (12 shared papers)Anne‐Laure Mosca‐Boidron (20 shared papers)
- Journals
- Clinical Genetics (13 papers)European Journal of Human Genetics (13 papers)Journal of Medical Genetics (12 papers)European Journal of Medical Genetics (10 papers)Genetics in Medicine (5 papers)
- Partner nations
- FranceUnited StatesNetherlands
In The Last Decade
Patrick Callier
129 papers receiving 3.8k citations
Peers
Comparison fields: 5 of 116
- Genetics 2.5k
- Developmental Biology 53
- Pediatrics, Perinatology and Child Health 224
- Developmental Neuroscience 38
- Cancer Research 155
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 137 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 371 | |
| 2 | 2011 | 246 | |
| 3 | 2016 | 199 | |
| 4 | 2013 | 162 | |
| 5 | 2011 | 160 | |
| 6 | 2017 | 141 | |
| 7 | 2018 | 135 | |
| 8 | 2011 | 115 | |
| 9 | 2010 | 112 | |
| 10 | 2012 | 95 | |
| 11 | 2012 | 84 | |
| 12 | 2012 | 78 | |
| 13 | 2010 | 74 | |
| 14 | 2018 | 60 | |
| 15 | 2014 | 59 | |
| 16 | 2018 | 57 | |
| 17 | 2003 | 54 | |
| 18 | 2011 | 53 | |
| 19 | 2019 | 51 | |
| 20 | 2018 | 49 |
About Patrick Callier
Patrick Callier is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Developmental Biology, Public Health, Environmental and Occupational Health and Health Informatics, having authored 137 papers that have together received 4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (53 papers), Genomics and Rare Diseases (40 papers), Genetics and Neurodevelopmental Disorders (22 papers), Congenital limb and hand anomalies (6 papers), Prenatal Screening and Diagnostics (6 papers), Connective tissue disorders research (6 papers), Genetic and rare skin diseases. (5 papers) and Fetal and Pediatric Neurological Disorders (4 papers). The work is most often cited by research in Genetics (2.5k citations), Developmental Biology (53 citations), Pediatrics, Perinatology and Child Health (224 citations), Developmental Neuroscience (38 citations) and Cancer Research (155 citations). Patrick Callier has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Laurence Olivier Faivre, Christel Thauvin‐Robinet, Frédéric Huet, Alice Masurel, Francine Mugneret, Nathalie Marle, Julien Thévenon, Anne‐Laure Mosca‐Boidron, Salima El Chehadeh and Mondher Chouchane. Their work appears in journals such as Clinical Genetics, European Journal of Human Genetics, Journal of Medical Genetics, European Journal of Medical Genetics and Genetics in Medicine.
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.