Claude Bendavid

3.4k citations
81 papers · 1.7k · h-index 23

Impact in

    • Congenital limb and hand anomalies
  • Genetics top 2%
    • Genomic variations and chromosomal abnormalities
    • Cleft Lip and Palate Research
    • Ocular Disorders and Treatments

Papers in

    • Hedgehog Signaling Pathway Studies 15
    • Genomic variations and chromosomal abnormalities 12
    • Cleft Lip and Palate Research 5

Claude Bendavid

75 papers receiving 1.7k citations

Peers

Claude Bendavid
Comparison fields: 5 of 112
  • Developmental Biology 112
  • Genetics 727
  • Pediatrics, Perinatology and Child Health 384
  • Molecular Biology 994
  • Reproductive Medicine 80
Replace U. Heinrich with:
U. Heinrich Germany
Andrew Dauber United States
Véronique David France
Leonard Pinsky Canada
Shuan‐Pei Lin Taiwan
Angelo M. DiGeorge United States
Xu Ma China
D. Hoefnagel United States
Narsingh D. Agnish United States
Carol E. Anderson United States
Claude Bendavid relative to U. Heinrich Germany U. Heinrich's profile →
Citations per field
00.5×3.6×
U. Heinrich · 1×
Citations per year

Countries citing papers authored by Claude Bendavid

Since Specialization
Citations

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

Fields of papers citing papers by Claude Bendavid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Claude Bendavid, 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 Claude Bendavid Line = papers co-authored together Claude Bendavid links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 81 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2007234
2 2019159
3 2004104
4 201173
5 200869
6 200968
7 201758
8 200854
9 200950
10 200949
11 200448
12 200544
13 201142
14 201037
15 200537
16 200936
17 200935
18 200535
19 201033
20 201031

About Claude Bendavid

Claude Bendavid is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 81 papers that have together received 1.7k indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (15 papers), Genomic variations and chromosomal abnormalities (12 papers), Breast Cancer Treatment Studies (5 papers), Cleft Lip and Palate Research (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Bacterial Identification and Susceptibility Testing (4 papers), Prenatal Screening and Diagnostics (4 papers) and Trace Elements in Health (4 papers). The work is most often cited by research in Developmental Biology (112 citations), Genetics (727 citations), Pediatrics, Perinatology and Child Health (384 citations), Molecular Biology (994 citations) and Reproductive Medicine (80 citations). Claude Bendavid has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Christèle Dubourg, Laurent Pasquier, Sylvie Odent, Véronique David, Cathérine Henry, Sylvie Odent, Véronique David, Isabelle Gicquel, Philippe Loget and Lucie Rochard. Their work appears in journals such as Human Mutation, Clinical Biochemistry, European Journal of Medical Genetics, European Journal of Obstetrics & Gynecology and Reproductive Biology and 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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