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

align trajectories

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.

Defective myosin VIIA gene responsible for Usher syndrome type IB

1995 819 citations Stéphane Blanchard, Parry Guilford et al. profile →
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 →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness 2014 ·PLoS ONE ·(unknown), Crystel Bonnet, (unknown), Malek Louha, Yosra Bouyacoub, (unknown), (unknown), Rym Kéfi, Laurence Jonard, Imen Dorboz, Jean‐Pierre Hardelin, (unknown), Jacqueline Levilliers, Dominique Weil, Kenneth McElreavey, Odile Boespflug‐Tanguy, G. Besbes, Sonia Abdelhak, Christine Petit	21
2	Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2 2006 ·PLoS Genetics ·Catherine Dodé, Luís Teixeira, Jacqueline Levilliers, Corinne Fouveaut, Philippe Bouchard, Marie-Laure Kottler, James Lespinasse, Anne Lienhardt-Roussie, Michèle Mathieu, Alexandre Moerman, Graeme Morgan, Arnaud Murat, (unknown), Sławomir Wołczyński, Marc Delpech, Christine Petit, Jacques Young, Jean-Pierre Hardelin	315
3	Sequence Characterization of a Newly Identified Human α-Tubulin Gene (TUBA2) 1998 ·Genomics ·Catherine Dodé, Dominique Weil, Jacqueline Levilliers, Fabien Crozet, Hassan Chaı̈b, Fabienne Lévi-Acobas, Parry Guilford, Christine Petit	5
4	A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy 1995 ·Cell ·Brunella Franco, Germana Meroni, Giancarlo Parenti, Jacqueline Levilliers, Loris Bernard, Marinella Gebbia, Liza L. Cox, P Maroteaux, Leslie J. Sheffield, Gudrun Rappold, Generoso Andria, Christine Petit, Andrea Ballabio	233
5	Prevalence and Molecular Analysis of Two Hot Spots for Ectopic Recombination Leading to XX Maleness 1995 ·Genomics ·(unknown), (unknown), Jacqueline Levilliers, Nabeel A. Affara, Albert de la Chapelle, Christine Petit	16
6	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) 1995 ·Genomics ·(unknown), Brunella Franco, Giovanni Battista Ferrero, A. Craig Chinault, Jean Weissenbach, Ilya Chumakov, Denis Le Paslier, Jacqueline Levilliers, Albrecht Klink, Gudrun Rappold, Andrea Ballabio, Christine Petit	4
7	A YAC Contig and an EST Map in the Pericentromeric Region of Chromosome 13 Surrounding the Loci for Neurosensory Nonsyndromic Deafness (DFNB1 and DFNA3) and Limb-Girdle Muscular Dystrophy Type 2C (LGMD2C) 1995 ·Genomics ·Parry Guilford, Catherine Dodé, Fabien Crozet, Stéphane Blanchard, Hassan Chaı̈b, Jacqueline Levilliers, Fabienne Lévi-Acobas, Dominique Weil, Jean Weissenbach, Daniel Cohen, Denis Le Paslier, Jean‐Claude Kaplan, Christine Petit	24
8	A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval 1994 ·Human Molecular Genetics ·Hassan Chaı̈b, Geneviève Lina‐Granade, Parry Guilford, Henri Plauchu, Jacqueline Levilliers, A Morgon, Christine Petit	66
9	A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q 1994 ·Nature Genetics ·Parry Guilford, Saïda Ben Arab, Stéphane Blanchard, Jacqueline Levilliers, Jean Weissenbach, (unknown), Christine Petit	208
10	Construction of a Yeast Artificial Chromosome Contig Spanning the Pseudoautosomal Region and Isolation of 25 New Sequence-Tagged Sites 1993 ·Genomics ·Rima Slim, Denis Le Paslier, Sylvie Compain, Jacqueline Levilliers, Pierre Ougen, Alain Billault, Susan J. Donohue, David C. Klein, (unknown), Alain Bernheim, Daniel Cohen, Jean Weissenbach, Christine Petit	16
11	No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome families 1993 ·American Journal of Medical Genetics ·(unknown), Michel Bahuau, Stanislas Lyonnet, (unknown), Didier Lacombe, François Marçon, Jacqueline Levilliers, J Kachaner, Arnold Münnich, Martine Le Merrer	17
12	Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome 1993 ·Human Molecular Genetics ·Jean‐Pierre Hardelin, Jacqueline Levilliers, Stéphane Blanchard, Jean‐Claude Carel, M Leuténegger, (unknown), Pierre Bouloux, Christine Petit	155
13	A Human Pseudoautosomal Gene Encodes the ANT3 ADP/ATP Translocase and Escapes X-Inactivation 1993 ·Genomics ·Rima Slim, Jacqueline Levilliers, Hermann‐Josef Lüdecke, Uwe Claussen, Công Văn Nguyến, Nicholas M. Gough, Bernhard Horsthemke, Christine Petit	41
14	Characterization of the Chicken and Quail Homologues of the Human Gene Responsible for the X-Linked Kallmann Syndrome 1993 ·Genomics ·Renaud Legouis, Martine Cohen‐Salmon, Ignacio del Castillo, Jacqueline Levilliers, (unknown), Jean‐Paul Mornon, Christine Petit	35
15	A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3) 1991 ·Nucleic Acids Research ·(unknown), Jean‐Pierre Hardelin, Patricia B. Munroe, Jeremy Kirk, Renaud Legouis, Jacqueline Levilliers, Jamïlé Hazan, J. Weissenbach, Christine Petit	25
16	An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature 1990 ·Human Genetics ·Christine Petit, Judith Melki, Jacqueline Levilliers, (unknown), Jean Weissenbach, P Maroteaux	33
17	Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals 1990 ·Genomics ·Christine Petit, Jacqueline Levilliers, François Rouyer, (unknown), Eric Herouin, Jean Weissenbach	20
18	Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232. 1990 ·PubMed ·Thomas Meitinger, Babett Heye, Christine Petit, Jacqueline Levilliers, Astrid Golla, Claude Moraine, (unknown), Wolfgang G. Sippell, Jan Murken, Andrea Ballabio	53
19	Modulation by substrate and cations of guanylate cyclase activity in detergent-dispersed plasma membranes from rat adipocytes 1978 ·Biochemical and Biophysical Research Communications ·Jacqueline Levilliers, (unknown), Jacques Pairault	9
20	Hormone‐stimulated cAMP production in human placenta perfused in vitro 1974 ·FEBS Letters ·Jacqueline Levilliers, E. Alsat, P Laudat, L. Cédard	15

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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