Béatrice Laudier

2.4k total citations · 2 hit papers
16 papers, 1.7k citations indexed

About

Béatrice Laudier is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Béatrice Laudier has authored 16 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Béatrice Laudier's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (3 papers). Béatrice Laudier is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (3 papers). Béatrice Laudier collaborates with scholars based in France, Germany and Singapore. Béatrice Laudier's co-authors include Jeanne Amiel, Stanislas Lyonnet, Arnold Münnich, Delphine Trochet, Ha Trang, Claude Gaultier, Michel Vekemans, Pierre F. Ray, Heather Etchevers and Blanca Gener and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Reproduction.

In The Last Decade

Béatrice Laudier

16 papers receiving 1.6k 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.

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

2003 619 citations Jeanne Amiel, Béatrice Laudier et al. Nature Genetics profile →
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

2004 553 citations Frédéric Laumonnier, Frédérique Bonnet‐Brilhault et al. The American Journal of Human Genetics profile →

Peers

Béatrice Laudier

GENET

EAS

PRM

Silvia Pagliardini Canada

Kimberly H. Cox United States

Julia R. Wilkerson United States

Dawna D. Armstrong United States

Peter Huppke Germany

Michaël Ogier France

Georg M. Stettner Germany

Kunihiro Kawashima Japan

Kazunari Yuri Japan

Yusuke Tanahashi Japan

Silvia Pagliardini Canada

Béatrice Laudier

302 ×0.4

GENET

1.0k ×1.7

EAS

466 ×0.8

707 ×1.5

313 ×0.7

PRM

Citations per year, relative to Béatrice Laudier Béatrice Laudier (= 1×) peers Silvia Pagliardini

Countries citing papers authored by Béatrice Laudier

Since Specialization

Citations

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

Fields of papers citing papers by Béatrice Laudier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Béatrice Laudier

This figure shows the co-authorship network connecting the top 25 collaborators of Béatrice Laudier. A scholar is included among the top collaborators of Béatrice Laudier 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 Béatrice Laudier. Béatrice Laudier is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Laudier, Béatrice, et al.. (2016). Molecular and clinical analyses with neuropsychological assessment of a case of del(10)(q26.2qter) without intellectual disability: Genomic and transcriptomic combined approach and review of the literature. American Journal of Medical Genetics Part A. 170(7). 1806–1812. 3 indexed citations

Nadal, Marga, et al.. (2015). Kératodermie aquagénique palmaire chez une patiente hétérozygote pour la mutation c.3197G>C du gène CFTR. Annales de Dermatologie et de Vénéréologie. 142(3). 201–205. 3 indexed citations

Clot, Fabienne, Anne Rovelet‐Lecrux, Foudil Lamari, et al.. (2014). Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration. Neurogenetics. 15(2). 95–100. 7 indexed citations

Pietropaolo, Susanna, Sandra Même, Béatrice Laudier, et al.. (2014). Rescue of fragile X syndrome phenotypes in Fmr1KO mice by a BKCa channel opener molecule. Orphanet Journal of Rare Diseases. 9(1). 124–124. 75 indexed citations

Perche, Olivier, Arnaud Menuet, Kagistia Hana Utami, et al.. (2013). Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency. European Journal of Medical Genetics. 56(11). 635–641. 21 indexed citations

Nadal, Marga, Béatrice Laudier, & É. Estève. (2013). Pseudo-kératodermie aquagénique chez une patiente hétérozygote pour une nouvelle mutation de la mucoviscidose. Annales de Dermatologie et de Vénéréologie. 140(12). S568–S568. 1 indexed citations

Perche, Olivier, Georges Haddad, Arnaud Menuet, et al.. (2013). Dysregulation of FOXG1 pathway in a 14q12 microdeletion case. American Journal of Medical Genetics Part A. 161(12). 3072–3077. 19 indexed citations

Perche, Olivier, Béatrice Laudier, Arnaud Menuet, et al.. (2012). FG syndrome: The FGS2 locus revisited. American Journal of Medical Genetics Part A. 158A(6). 1489–1492. 3 indexed citations

Keren, Boris, Annick Toutain, Delphine Héron, et al.. (2007). Pure proximal deletion of chromosome 21 and kyphosis. European Journal of Medical Genetics. 50(6). 469–474. 4 indexed citations

10.

Perrin, Aurore, Nathalie Douet‐Guilbert, Béatrice Laudier, et al.. (2006). Meiotic segregation in spermatozoa of a 45,XY,-14,der(18)t(14;18)(q11;p11.3) translocation carrier: A Case Report. Human Reproduction. 22(3). 729–732. 10 indexed citations

11.

Morel, Fréderic, Béatrice Laudier, Fabrice Guérif, et al.. (2006). Meiotic segregation analysis in spermatozoa of pericentric inversion carriers using fluorescence in-situ hybridization. Human Reproduction. 22(1). 136–141. 79 indexed citations

12.

Trochet, Delphine, Louise M. O’Brien, David Gozal, et al.. (2005). PHOX2B Genotype Allows for Prediction of Tumor Risk in Congenital Central Hypoventilation Syndrome. The American Journal of Human Genetics. 76(3). 421–426. 183 indexed citations

13.

Laumonnier, Frédéric, Frédérique Bonnet‐Brilhault, Marie Gomot, et al.. (2004). X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family. The American Journal of Human Genetics. 74(3). 552–557. 553 indexed citations breakdown →

14.

Trang, Ha, Béatrice Laudier, Delphine Trochet, et al.. (2004). PHOX2B gene mutation in a patient with late‐onset central hypoventilation. Pediatric Pulmonology. 38(4). 349–351. 39 indexed citations

15.

Laudier, Béatrice, et al.. (2003). PMX2B, a new candidate gene for Hirschsprung's disease. Clinical Genetics. 64(3). 204–209. 45 indexed citations

16.

Amiel, Jeanne, Béatrice Laudier, Tania Attié‐Bitach, et al.. (2003). Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nature Genetics. 33(4). 459–461. 619 indexed citations breakdown →

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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