Bernard Le Marec

1.4k citations
62 papers · 1.1k · h-index 20

Impact in

  • Genetics top 5%
    • Connective tissue disorders research
    • Genetic and rare skin diseases.
    • Cleft Lip and Palate Research
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genomic variations and chromosomal abnormalities 5
    • Genomics and Rare Diseases 5
    • Connective tissue disorders research 5
    • Ocular Disorders and Treatments 5
    • Fetal and Pediatric Neurological Disorders 4
    • Prenatal Screening and Diagnostics 4

Bernard Le Marec

61 papers receiving 1.0k citations

Peers

Bernard Le Marec
Comparison fields: 5 of 84
  • Genetics 506
  • Developmental Biology 37
  • Clinical Biochemistry 58
  • Genetics 87
  • Molecular Biology 520
Replace Kouji Narahara with:
Kouji Narahara Japan
Ann Haskins Olney United States
R. Sid Wilroy United States
Georg Klaus Hinkel Germany
Irfan Saadi United States
M Shohat Israel
Alexa Kidd New Zealand
Valerio Ventruto Italy
Pamela S. Karnes United States
Yasutsugu Chinen Japan
Bernard Le Marec relative to Kouji Narahara Japan Kouji Narahara's profile →
Citations per field
00.5×2×2.9×
Kouji Narahara · 1×
Citations per year

Countries citing papers authored by Bernard Le Marec

Since Specialization
Citations

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

Fields of papers citing papers by Bernard Le Marec

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernard Le Marec. 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 Bernard Le Marec. The network helps show where Bernard Le Marec may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 62 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1999132
2 197781
3 199853
4 200053
5 198252
6 199450
7 198643
8 199843
9 198440
10 199540
11 198640
12 199537
13 198732
14 198829
15 199126
16 198926
17 198726
18 199125
19 198625
20 199820

About Bernard Le Marec

Bernard Le Marec is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Genetics, Developmental Biology and Clinical Biochemistry, having authored 62 papers that have together received 1.1k indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (5 papers), Connective tissue disorders research (5 papers), Ocular Disorders and Treatments (5 papers), Metabolism and Genetic Disorders (4 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (506 citations), Developmental Biology (37 citations), Clinical Biochemistry (58 citations), Genetics (87 citations) and Molecular Biology (520 citations). Bernard Le Marec has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Sylvie Odent, Hubert Journel, M. Roussey, Martine Blayau, Véronique David, PIERRE MAROTEAUX, Michel Bourel, M. K. Simon, M Mathieu and Tania Attié‐Bitach. Their work appears in journals such as Human Genetics, Clinical Genetics, Human Molecular Genetics, Prenatal Diagnosis and Acta Paediatrica.

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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