Michel Leibovici

4.1k citations
25 papers · 2.9k · 2 hit papers · h-index 20

Impact in

Papers in

    • Hearing, Cochlea, Tinnitus, Genetics 12
    • Olfactory and Sensory Function Studies 3
    • Ion Channels and Receptors 3
    • RNA Research and Splicing 5
    • Connexins and lens biology 5

Michel Leibovici

25 papers receiving 2.8k citations

Michel Leibovici's Hit Papers

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome 1997 · 659 citations
6590+9+19Years since publication200400600

Peers

Michel Leibovici
Comparison fields: 5 of 107
  • Sensory Systems 1.3k
  • Neurology 400
  • Otorhinolaryngology 184
  • Molecular Biology 1.8k
  • Cardiology and Cardiovascular Medicine 429
Replace Stéphane Blanchard with:
Stéphane Blanchard France
Philomena Mburu United Kingdom
Michael D. Weston United States
Konrad Noben‐Trauth United States
Edward R. Wilcox United States
Karen P. Steel United Kingdom
Hanno J. Bolz Germany
Jean‐Pierre Hardelin France
Jacqueline Levilliers France
Markus Pfister Germany
Michel Leibovici relative to Stéphane Blanchard France Stéphane Blanchard's profile →
Citations per field
00.5×1.5×2.4×
Stéphane Blanchard · 1×
Citations per year

Countries citing papers authored by Michel Leibovici

Since Specialization
Citations

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

Fields of papers citing papers by Michel Leibovici

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
Hit paper breakdown →
1997659
2
A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family
Hit paper breakdown →
1997467
3 2000357
4 2006239
5 2001132
6 2002130
7 1997118
8 2008108
9 199997
10 201095
11 199271
12 199364
13 199657
14 200845
15 199039
16 201037
17 199633
18 200931
19 199228
20 200519

About Michel Leibovici

Michel Leibovici is a scholar working on Sensory Systems, Molecular Biology, Cognitive Neuroscience, Neurology and Genetics, having authored 25 papers that have together received 2.9k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), Hearing Loss and Rehabilitation (5 papers), RNA Research and Splicing (5 papers), Vestibular and auditory disorders (5 papers), Connexins and lens biology (5 papers), Olfactory and Sensory Function Studies (3 papers), Ion Channels and Receptors (3 papers) and Biochemical Analysis and Sensing Techniques (2 papers). The work is most often cited by research in Sensory Systems (1.3k citations), Neurology (400 citations), Otorhinolaryngology (184 citations), Molecular Biology (1.8k citations) and Cardiology and Cardiovascular Medicine (429 citations). Michel Leibovici has collaborated with scholars based in France, United Kingdom and Germany. Frequent co-authors include Christine Petit, Elisabeth Verpy, Dominique Weil, Sabine Fauré, Pascale Guicheney, Nathalie Neyroud, Françoise Gary, Jacques Barhanin, Isabelle Denjoy and Ketty Schwartz. Their work appears in journals such as Nature Genetics, Proceedings of the National Academy of Sciences, Developmental Biology, Biology of the Cell and Current topics in developmental biology.

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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