Laurence Faivre
Impact in
- Genetics top 0.2%
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Developmental Biology top 2%
Papers in
- Genetics 137
- Genomic variations and chromosomal abnormalities 38
- Genomics and Rare Diseases 35
- Connective tissue disorders research 30
- Genetics and Neurodevelopmental Disorders 29
- Genetic Syndromes and Imprinting 20
- Genetic and Kidney Cyst Diseases 10
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- RNA modifications and cancer 14
- Co-authors
- Guillaume Jondeau (13 shared papers)Valérie Cormier‐Daire (26 shared papers)Bart Loeys (3 shared papers)Dianna M. Milewicz (2 shared papers)Arnold Münnich (25 shared papers)Julie De Backer (1 shared paper)Richard B. Devereux (1 shared paper)Bert Callewaert (1 shared paper)
- Journals
- European Journal of Medical Genetics (18 papers)European Journal of Human Genetics (16 papers)Clinical Genetics (13 papers)Human Mutation (13 papers)Prenatal Diagnosis (12 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Laurence Faivre
208 papers receiving 6.2k citations
Laurence Faivre's Hit Papers
Peers
Comparison fields: 5 of 131
- Genetics 3.3k
- Developmental Biology 106
- Pulmonary and Respiratory Medicine 1.4k
- Cancer Research 618
- Cardiology and Cardiovascular Medicine 881
Countries citing papers authored by Laurence Faivre
This map shows the geographic impact of Laurence Faivre'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 Laurence Faivre with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laurence Faivre more than expected).
Fields of papers citing papers by Laurence Faivre
This network shows the impact of papers produced by Laurence Faivre. 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 Laurence Faivre. The network helps show where Laurence Faivre may publish in the future.
Co-authors
The 25 scholars most cited alongside Laurence Faivre, 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 215 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The revised Ghent nosology for the Marfan syndrome: Table 1 Hit paper breakdown → | 2010 | 1350 |
| 2 | 2001 | 295 | |
| 3 | 2004 | 207 | |
| 4 | 2003 | 205 | |
| 5 | 2010 | 171 | |
| 6 | 2011 | 148 | |
| 7 | 2013 | 115 | |
| 8 | 2003 | 107 | |
| 9 | 2002 | 97 | |
| 10 | 2016 | 95 | |
| 11 | 2007 | 94 | |
| 12 | 2008 | 81 | |
| 13 | 2012 | 80 | |
| 14 | 2005 | 75 | |
| 15 | 2006 | 74 | |
| 16 | 2009 | 72 | |
| 17 | 2005 | 67 | |
| 18 | 2005 | 60 | |
| 19 | 2019 | 60 | |
| 20 | 2007 | 58 |
About Laurence Faivre
Laurence Faivre is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Cardiology and Cardiovascular Medicine, having authored 215 papers that have together received 6.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (38 papers), Genomics and Rare Diseases (35 papers), Connective tissue disorders research (30 papers), Genetics and Neurodevelopmental Disorders (29 papers), Prenatal Screening and Diagnostics (21 papers), Genetic Syndromes and Imprinting (20 papers), RNA modifications and cancer (14 papers) and Genetic and Kidney Cyst Diseases (10 papers). The work is most often cited by research in Genetics (3.3k citations), Developmental Biology (106 citations), Pulmonary and Respiratory Medicine (1.4k citations), Cancer Research (618 citations) and Cardiology and Cardiovascular Medicine (881 citations). Laurence Faivre has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Guillaume Jondeau, Valérie Cormier‐Daire, Bart Loeys, Dianna M. Milewicz, Arnold Münnich, Julie De Backer, Richard B. Devereux, Bert Callewaert, Harry C. Dietz and Anne M. De Paepe. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Clinical Genetics, Human Mutation 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.