Philippe Loget
Impact in
-
- Fetal and Pediatric Neurological Disorders
- Prenatal Screening and Diagnostics
- Developmental Neuroscience top 2%
- Neurogenesis and neuroplasticity mechanisms
Papers in
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- Fetal and Pediatric Neurological Disorders 17
- Prenatal Screening and Diagnostics 5
- Genetics 30
- Genetic and Kidney Cyst Diseases 10
- Genomics and Rare Diseases 7
- Connective tissue disorders research 5
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- Laurent Pasquier (14 shared papers)Sylvie Odent (20 shared papers)Claude Bendavid (6 shared papers)Véronique David (6 shared papers)Christèle Dubourg (9 shared papers)Catherine Fallet‐Bianco (4 shared papers)Laurence Lœuillet (3 shared papers)Chloé Quēlin (10 shared papers)
- Journals
- Journal of Medical Genetics (9 papers)Prenatal Diagnosis (9 papers)European Journal of Medical Genetics (7 papers)Clinical Genetics (5 papers)Human Mutation (3 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Philippe Loget
65 papers receiving 2.7k citations
Peers
Comparison fields: 5 of 79
- Pediatrics, Perinatology and Child Health 835
- Developmental Neuroscience 162
- Genetics 989
- Developmental Biology 70
- Cell Biology 188
Countries citing papers authored by Philippe Loget
This map shows the geographic impact of Philippe Loget'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 Philippe Loget with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Philippe Loget more than expected).
Fields of papers citing papers by Philippe Loget
This network shows the impact of papers produced by Philippe Loget. 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 Philippe Loget. The network helps show where Philippe Loget may publish in the future.
Co-authors
The 25 scholars most cited alongside Philippe Loget, 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 70 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 306 | |
| 2 | 2012 | 139 | |
| 3 | 2012 | 121 | |
| 4 | 2014 | 114 | |
| 5 | 2014 | 102 | |
| 6 | 2005 | 101 | |
| 7 | 2017 | 101 | |
| 8 | 2013 | 96 | |
| 9 | 2008 | 95 | |
| 10 | 2008 | 93 | |
| 11 | 2003 | 91 | |
| 12 | 2013 | 87 | |
| 13 | 2011 | 86 | |
| 14 | 2008 | 79 | |
| 15 | 2009 | 79 | |
| 16 | 2017 | 78 | |
| 17 | 2012 | 75 | |
| 18 | 2010 | 71 | |
| 19 | 2007 | 59 | |
| 20 | 2011 | 53 |
About Philippe Loget
Philippe Loget is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Developmental Biology, Clinical Biochemistry and Molecular Biology, having authored 70 papers that have together received 2.8k indexed citations. Recurring topics across this work include Fetal and Pediatric Neurological Disorders (17 papers), Genetic and Kidney Cyst Diseases (10 papers), Congenital limb and hand anomalies (9 papers), Genomics and Rare Diseases (7 papers), Prenatal Screening and Diagnostics (5 papers), Connective tissue disorders research (5 papers), Renal and related cancers (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (835 citations), Developmental Neuroscience (162 citations), Genetics (989 citations), Developmental Biology (70 citations) and Cell Biology (188 citations). Philippe Loget has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Laurent Pasquier, Sylvie Odent, Claude Bendavid, Véronique David, Christèle Dubourg, Catherine Fallet‐Bianco, Laurence Lœuillet, Chloé Quēlin, Sylvie Jaillard and Josette Lucas. Their work appears in journals such as Journal of Medical Genetics, Prenatal Diagnosis, European Journal of Medical Genetics, Clinical Genetics and Human Mutation.
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.