S. Fauré

776 citations
18 papers · 588 · h-index 12

Impact in

  • Genetics top 10%
    • Vascular Anomalies and Treatments
    • Genetic Mapping and Diversity in Plants and Animals

Papers in

    • Genomic variations and chromosomal abnormalities 4
    • Chromosomal and Genetic Variations 4
    • Plant Disease Resistance and Genetics 2
    • Wheat and Barley Genetics and Pathology 2
    • Banana Cultivation and Research 2

S. Fauré

18 papers receiving 538 citations

Peers

S. Fauré
Comparison fields: 5 of 68
  • Genetics 101
  • Horticulture 8
  • Plant Science 177
  • Genetics 101
  • Immunology 64
Replace Vera D. Markovic with:
Vera D. Markovic Canada
Aleksandr V. Makeyev United States
Kutay Taysi United States
Tao Qin China
Takaya Tohma Japan
Xingguo Zhu United States
Zi Yan China
Cornelia Daumer‐Haas Germany
Mildred L. Kistenmacher United States
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Citations per field
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Citations per year

Countries citing papers authored by S. Fauré

Since Specialization
Citations

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

Fields of papers citing papers by S. Fauré

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside S. Fauré, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with S. Fauré Line = papers co-authored together S. Fauré links everyone, so they are left out of the graph.

All Works

18 of 18 papers shown
#Work
1 1993131
2 1995104
3 199760
4 199454
5 199540
6 199737
7
[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].
199633
8
A locus for Fanconi anemia on 16q determined by homozygosity mapping.
199628
9
European genetic study on rheumatoid arthritis: is there a linkage of the interleukin-1 (IL-1), IL-10 or IL-4 genes to RA?
200225
10 199923
11
Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis.
199722
12 200816
13 19967
14 19963
15
Rheumatoid arthritis genome scan and putative autoimmunity locus
19972
16
Insertion Site-Based Polymorphism: A Swiss army knife for wheat genomics
20081
17 19991
18
Recombination analysis on bread wheat chromosome 3B
20081

About S. Fauré

S. Fauré is a scholar working on Genetics, Plant Science, Molecular Biology, Rheumatology and Cell Biology, having authored 18 papers that have together received 588 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers), Glycosylation and Glycoproteins Research (2 papers), Genomics and Phylogenetic Studies (2 papers), Muscle Physiology and Disorders (2 papers), Plant Disease Resistance and Genetics (2 papers), Wheat and Barley Genetics and Pathology (2 papers) and Banana Cultivation and Research (2 papers). The work is most often cited by research in Genetics (101 citations), Horticulture (8 citations), Plant Science (177 citations), Genetics (101 citations) and Immunology (64 citations). S. Fauré has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include D. González de León, Frédéric Bakry, Claire Lanaud, Jean Weissenbach, Jean-Pierre Horry, Jean‐Louis Noyer, Henri Plauchu, Jamïlé Hazan, Jacqueline Godet and Mogens Thomsen. Their work appears in journals such as Animal Genetics, Neuromuscular Disorders, Theoretical and Applied Genetics, Neurogenetics and Annals of Human 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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