S. Fauré

771 citations
14 papers · 523 · h-index 10

Impact in

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

Papers in

    • Glycosylation and Glycoproteins Research 2
    • Muscle Physiology and Disorders 2
    • Genomics and Phylogenetic Studies 2
    • Genomic variations and chromosomal abnormalities 3

S. Fauré

14 papers receiving 480 citations

Peers

S. Fauré
Comparison fields: 5 of 67
  • Genetics 101
  • Horticulture 8
  • Plant Science 172
  • Genetics 93
  • Molecular Biology 177
Replace Christophe Battail with:
Christophe Battail France
Gopal Pandi India
Aleksandr V. Makeyev United States
Kutay Taysi United States
Mélissa Beaudoin Canada
Peter G. Hendrickson United States
V. D. Marković Canada
Concetta G.A. Marfella United States
Mildred L. Kistenmacher United States
Xingguo Zhu United States
S. Fauré relative to Christophe Battail France Christophe Battail's profile →
Citations per field
00.5×3.1×
Christophe Battail · 1×
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

14 of 14 papers shown
#Work
1 1993129
2 1995103
3 199760
4 199454
5 199541
6 199737
7
[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].
199630
8
A locus for Fanconi anemia on 16q determined by homozygosity mapping.
199625
9
Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis.
199722
10 200816
11 19963
12 19991
13
Insertion Site-Based Polymorphism: A Swiss army knife for wheat genomics
20081
14
Recombination analysis on bread wheat chromosome 3B
20081

About S. Fauré

S. Fauré is a scholar working on Molecular Biology, Genetics, Plant Science, Surgery and Genetics, having authored 14 papers that have together received 523 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (3 papers), Glycosylation and Glycoproteins Research (2 papers), Plant Disease Resistance and Genetics (2 papers), Banana Cultivation and Research (2 papers), Muscle Physiology and Disorders (2 papers), Genomics and Phylogenetic Studies (2 papers) and Wheat and Barley Genetics and Pathology (2 papers). The work is most often cited by research in Genetics (101 citations), Horticulture (8 citations), Plant Science (172 citations), Genetics (93 citations) and Molecular Biology (177 citations). S. Fauré has collaborated with scholars based in France, United States and Hungary. Frequent co-authors include Frédéric Bakry, D. González de León, Claire Lanaud, J. Weissenbach, Jean-Pierre Horry, Jean‐Louis Noyer, Jacqueline Godet, Jamïlé Hazan, Henri Plauchu and Mogens Thomsen. Their work appears in journals such as Human Molecular Genetics, Theoretical and Applied Genetics, Psychiatric Genetics, Genomics and Genetics Selection Evolution.

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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