Fanny Laffargue

1.5k citations
9 papers · 89 indexed · h-index 5
Topics
Genetics and Neurodevelopmental Disorders (2 papers)Congenital heart defects research (2 papers)Genomic variations and chromosomal abnormalities (2 papers)
Partner nations
France

In The Last Decade

Fanny Laffargue

8 papers receiving 83 citations

Peers

Fanny Laffargue
Comparison fields: 5 of 33
  • Molecular Biology 47
  • Surgery 43
  • Genetics 37
  • Pulmonary and Respiratory Medicine 12
  • Endocrinology, Diabetes and Metabolism 11
Replace Roisin Finn with:
Roisin Finn United Kingdom
Bob McClellan United States
Cécile Laroche France
Jani K. Haukka Finland
Priyanka Nandakumar United States
Jun Hosoe Japan
Alberto Casertano Italy
Christoph Naber Germany
Aurélien Lorthioir France
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Citations per field
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Citations per year

Countries citing papers authored by Fanny Laffargue

Since Specialization
Citations

This map shows the geographic impact of Fanny Laffargue'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 Fanny Laffargue with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fanny Laffargue more than expected).

Fields of papers citing papers by Fanny Laffargue

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fanny Laffargue. 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 Fanny Laffargue. The network helps show where Fanny Laffargue may publish in the future.

Co-authorship network of co-authors of Fanny Laffargue

This figure shows the co-authorship network connecting the top 25 collaborators of Fanny Laffargue. A scholar is included among the top collaborators of Fanny Laffargue 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 Fanny Laffargue. Fanny Laffargue is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

9 of 9 papers shown
#WorkIndexed citations
1 1
2 1
3 0
4 7
5 19
6 39
7 7
8 3
9 12

About Fanny Laffargue

Fanny Laffargue is a scholar working on Pharmacy, Genetics and Emergency Medicine, having authored 9 papers that have together received 89 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (37 citations), Nephrology (7 citations) and Surgery (43 citations). Fanny Laffargue has collaborated with scholars based in France. Frequent co-authors include Didier Lacombe, Marie‐Ange Delrue, Catherine Yardin, Vincent Guigonis, Sylvie Bourthoumieu, Cécile Laroche, Sylvie Cloarec, Christine Francannet, Lucie Bessenay and Éléonore Eymard-Pierre. Their work appears in journals such as Archives of Disease in Childhood, Journal of Inherited Metabolic Disease and American Journal of Medical Genetics Part A.

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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