Béatrice Laudier

2.4k citations
16 papers · 1.7k indexed · 2 hit papers · h-index 10
Topics
Genetics and Neurodevelopmental Disorders (5 papers)Genomic variations and chromosomal abnormalities (5 papers)Chromosomal and Genetic Variations (3 papers)
Partner nations
FranceGermanySingapore

In The Last Decade

Béatrice Laudier

16 papers receiving 1.6k citations

Hit Papers

Polyalanine expansion and frameshift mutations of the pai...200320262010201820032004200400600

Peers

Béatrice Laudier
Comparison fields: 5 of 78
  • Genetics 675
  • Endocrine and Autonomic Systems 614
  • Molecular Biology 559
  • Cognitive Neuroscience 477
  • Pulmonary and Respiratory Medicine 425
Replace Silvia Pagliardini with:
Silvia Pagliardini Canada
Julia R. Wilkerson United States
Kimberly H. Cox United States
Dawna D. Armstrong United States
Peter Huppke Germany
Georg M. Stettner Germany
Michaël Ogier France
Christopher M. Bocchiaro United States
Shahriar SheikhBahaei United States
Daniel Richter Germany
Béatrice Laudier relative to Silvia Pagliardini Canada Silvia Pagliardini's profile →
Citations per field
00.5×1.5×2.2×
Silvia Pagliardini · 1×
Citations per year

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

16 of 16 papers shown
#WorkIndexed citations
1 3
2 3
3 7
4 75
5 21
6 1
7 19
8 3
9 4
10 10
11 79
12 183
13
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Familybreakdown →
553
14 39
15 45
16
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndromebreakdown →
619

About Béatrice Laudier

Béatrice Laudier is a scholar working on Endocrine and Autonomic Systems, Genetics and Developmental Neuroscience, having authored 16 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Endocrine and Autonomic Systems (614 citations), Cognitive Neuroscience (477 citations) and Genetics (675 citations). Béatrice Laudier has collaborated with scholars based in France, Germany and Singapore. Frequent 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. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics and Human Reproduction.

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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