Jacqueline Levilliers

7.1k total citations · 2 hit papers
45 papers, 4.1k citations indexed

About

Jacqueline Levilliers is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Jacqueline Levilliers has authored 45 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 15 papers in Genetics and 11 papers in Reproductive Medicine. Recurrent topics in Jacqueline Levilliers's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), Hypothalamic control of reproductive hormones (11 papers) and Hearing, Cochlea, Tinnitus, Genetics (7 papers). Jacqueline Levilliers is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), Hypothalamic control of reproductive hormones (11 papers) and Hearing, Cochlea, Tinnitus, Genetics (7 papers). Jacqueline Levilliers collaborates with scholars based in France, United States and United Kingdom. Jacqueline Levilliers's co-authors include Christine Petit, Jean‐Pierre Hardelin, Renaud Legouis, Stéphane Blanchard, Parry Guilford, J. Weissenbach, Jean‐Michel Claverie, Denis Le Paslier, Daniel Cohen and Philippe Millasseau and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Jacqueline Levilliers

45 papers receiving 4.0k citations

Hit Papers

Defective myosin VIIA gen... 1991 2026 2002 2014 1995 1991 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Defective myosin VIIA gene responsible for Usher syndrome type IB
    1995 819 citations Stéphane Blanchard, Parry Guilford et al. profile →
  2. The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
    1991 513 citations Renaud Legouis, Jean‐Pierre Hardelin et al. Cell profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Jacqueline Levilliers 2.5k 1.5k 1.2k 997 357 45 4.1k
Jean‐Pierre Hardelin 2.8k 1.1× 1.3k 0.9× 1.6k 1.4× 2.0k 2.0× 331 0.9× 79 5.2k
Hannie Kremer 5.1k 2.0× 1.2k 0.8× 287 0.2× 2.3k 2.3× 728 2.0× 188 8.0k
Kimia Kahrizi 1.8k 0.7× 835 0.6× 271 0.2× 826 0.8× 252 0.7× 141 3.0k
Stéphane Blanchard 1.9k 0.7× 370 0.3× 183 0.2× 1.4k 1.4× 449 1.3× 32 2.9k
Karen Brøndum‐Nielsen 2.3k 0.9× 2.0k 1.4× 113 0.1× 407 0.4× 454 1.3× 137 4.1k
Aimee K. Ryan 4.0k 1.6× 1.9k 1.3× 140 0.1× 362 0.4× 351 1.0× 48 5.7k
Jiangang Gao 1.7k 0.7× 617 0.4× 131 0.1× 1.5k 1.5× 275 0.8× 122 4.0k
Brunella Franco 4.5k 1.8× 3.4k 2.3× 614 0.5× 85 0.1× 688 1.9× 138 7.0k
Stéphane Schurmans 2.3k 0.9× 912 0.6× 94 0.1× 541 0.5× 632 1.8× 94 4.1k
Qiuxia Guo 2.3k 0.9× 535 0.4× 231 0.2× 119 0.1× 376 1.1× 33 3.5k

Countries citing papers authored by Jacqueline Levilliers

Since Specialization
Citations

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

Fields of papers citing papers by Jacqueline Levilliers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacqueline Levilliers

This figure shows the co-authorship network connecting the top 25 collaborators of Jacqueline Levilliers. A scholar is included among the top collaborators of Jacqueline Levilliers based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jacqueline Levilliers. Jacqueline Levilliers is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bonnet, Crystel, Malek Louha, Yosra Bouyacoub, et al.. (2014). Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness. PLoS ONE. 9(6). e99797–e99797. 21 indexed citations
2.
Dodé, Catherine, Luís Teixeira, Jacqueline Levilliers, et al.. (2006). Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2. PLoS Genetics. 2(10). e175–e175. 315 indexed citations
3.
Hardelin, Jean‐Pierre, Françoise Denoyelle, Jacqueline Levilliers, Marie‐Christine Simmler, & Christine Petit. (2004). Les surdités héréditaires : génétique moléculaire. médecine/sciences. 20(3). 311–316. 8 indexed citations
4.
Dodé, Catherine, Dominique Weil, Jacqueline Levilliers, et al.. (1998). Sequence Characterization of a Newly Identified Human α-Tubulin Gene (TUBA2). Genomics. 47(1). 125–130. 5 indexed citations
5.
Levilliers, Jacqueline, et al.. (1995). Prevalence and Molecular Analysis of Two Hot Spots for Ectopic Recombination Leading to XX Maleness. Genomics. 28(1). 52–58. 16 indexed citations
6.
Franco, Brunella, Giovanni Battista Ferrero, A. Craig Chinault, et al.. (1995). High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1). Genomics. 26(2). 229–238. 4 indexed citations
7.
Franco, Brunella, Germana Meroni, Giancarlo Parenti, et al.. (1995). A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy. Cell. 81(1). 15–25. 233 indexed citations
8.
9.
Chaı̈b, Hassan, Geneviève Lina‐Granade, Parry Guilford, et al.. (1994). A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval. Human Molecular Genetics. 3(12). 2219–2222. 66 indexed citations
10.
Guilford, Parry, Saïda Ben Arab, Stéphane Blanchard, et al.. (1994). A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nature Genetics. 6(1). 24–28. 208 indexed citations
11.
Slim, Rima, Denis Le Paslier, Sylvie Compain, et al.. (1993). Construction of a Yeast Artificial Chromosome Contig Spanning the Pseudoautosomal Region and Isolation of 25 New Sequence-Tagged Sites. Genomics. 16(3). 691–697. 16 indexed citations
12.
Slim, Rima, Jacqueline Levilliers, Hermann‐Josef Lüdecke, et al.. (1993). A Human Pseudoautosomal Gene Encodes the ANT3 ADP/ATP Translocase and Escapes X-Inactivation. Genomics. 16(1). 26–33. 41 indexed citations
13.
Claverie, Jean‐Michel, Jean-Pierre Hardelin, Renaud Legouis, et al.. (1993). Characterization and Chromosomal Assignment of a Human cDNA Encoding a Protein Related to the Murine 102-kDa Cadherin-Associated Protein (α-Catenin). Genomics. 15(1). 13–20. 27 indexed citations
14.
Bahuau, Michel, Stanislas Lyonnet, Didier Lacombe, et al.. (1993). No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome families. American Journal of Medical Genetics. 46(6). 700–705. 17 indexed citations
15.
Hardelin, Jean‐Pierre, Jacqueline Levilliers, Stéphane Blanchard, et al.. (1993). Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome. Human Molecular Genetics. 2(4). 373–377. 155 indexed citations
16.
Legouis, Renaud, Martine Cohen‐Salmon, Ignacio del Castillo, et al.. (1993). Characterization of the Chicken and Quail Homologues of the Human Gene Responsible for the X-Linked Kallmann Syndrome. Genomics. 17(2). 516–518. 35 indexed citations
17.
Hawkins, J. Ross, Annabel L. Taylor, Philippe Berta, et al.. (1992). Mutational analysis of SRY: nonsense and missense mutations in XY sex reversal. Human Genetics. 88(4). 471–474. 187 indexed citations
18.
Hardelin, Jean‐Pierre, Patricia B. Munroe, Jeremy Kirk, et al.. (1991). A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3). Nucleic Acids Research. 19(19). 5453–5453. 25 indexed citations
19.
20.
Petit, Christine, et al.. (1990). An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature. Human Genetics. 85(2). 247–50. 33 indexed citations

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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