Laurence Faivre

650 citations
7 papers · 108 indexed · h-index 5
Topics
Genetic Syndromes and Imprinting (4 papers)Connective tissue disorders research (2 papers)Prenatal Screening and Diagnostics (2 papers)
Partner nations
FranceUnited StatesItaly

In The Last Decade

Laurence Faivre

7 papers receiving 107 citations

Peers

Laurence Faivre
Comparison fields: 5 of 25
  • Genetics 93
  • Pulmonary and Respiratory Medicine 44
  • Cardiology and Cardiovascular Medicine 43
  • Molecular Biology 38
  • Surgery 20
Replace Steven Gazal with:
Steven Gazal United States
Alison H. Trainer United Kingdom
Rob Hastings United Kingdom
Elisabeth Gillis Netherlands
Mar Borregán Spain
Katharina Löhner Netherlands
Susanne Kaufmann Australia
Rósa B. Þórólfsdóttir Iceland
Michelle Steinraths Canada
Charlotte Pöe France
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Citations per field
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Countries citing papers authored by Laurence Faivre

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Laurence Faivre

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence Faivre. A scholar is included among the top collaborators of Laurence Faivre based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Laurence Faivre. Laurence Faivre is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

7 of 7 papers shown
#WorkIndexed citations
1 2
2 1
3 8
4 18
5 8
6 16
7 55

About Laurence Faivre

Laurence Faivre is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Oncology, having authored 7 papers that have together received 108 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (4 papers), Connective tissue disorders research (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (93 citations), Cardiology and Cardiovascular Medicine (43 citations) and Pulmonary and Respiratory Medicine (44 citations). Laurence Faivre has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Mireille Claustres, Cathérine Boileau, Guillaume Jondeau, Anne De Paepe, Élodie Gautier, Eloisa Arbustini, Karin Mayer, Bertrand Chevallier, Damien Bonnet and Christine Binquet. Their work appears in journals such as Human Molecular Genetics, Pediatric Research and Clinical Genetics.

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.

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