Claude Moraine

7.5k citations
83 papers · 4.4k indexed · 1 hit paper · h-index 31
Topics
Genetics and Neurodevelopmental Disorders (49 papers)Genomic variations and chromosomal abnormalities (17 papers)RNA modifications and cancer (15 papers)
Partner nations
FranceGermanyNetherlands

In The Last Decade

Claude Moraine

82 papers receiving 4.3k citations

Hit Papers

X-Linked Mental Retardation and Autism Are Associated wit...20042026201120182004100200300400500

Peers

Claude Moraine
Comparison fields: 5 of 105
  • Molecular Biology 2.9k
  • Genetics 2.6k
  • Cognitive Neuroscience 710
  • Cellular and Molecular Neuroscience 529
  • Cell Biology 512
Replace Elena Maestrini with:
Elena Maestrini Italy
Vera M. Kalscheuer Germany
Sylvain Briault France
André Hanauer France
Montserrat Milà Spain
Jamel Chelly France
Patrick Calvas France
Hilde Van Esch Belgium
Bert B.A. de Vries Netherlands
Chérif Beldjord France
Claude Moraine relative to Elena Maestrini Italy Elena Maestrini's profile →
Citations per field
00.5×1.7×
Elena Maestrini · 1×
Citations per year

Countries citing papers authored by Claude Moraine

Since Specialization
Citations

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

Fields of papers citing papers by Claude Moraine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claude Moraine

This figure shows the co-authorship network connecting the top 25 collaborators of Claude Moraine. A scholar is included among the top collaborators of Claude Moraine 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 Claude Moraine. Claude Moraine 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
#WorkIndexed citations
1 10
2 15
3 5
4 12
5 19
6
High prevalence of SLC6A8 deficiency, a novel X-linked mental retardation syndrome
1
7 32
8
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Familybreakdown →
553
9 148
10 65
11 2
12 9
13 9
14 10
15 10
16 41
17 21
18 382
19 19
20
[2 uncommon malformations of the nose. Attempt at an explanation].
1

About Claude Moraine

Claude Moraine is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 83 papers that have together received 4.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (49 papers), Genomic variations and chromosomal abnormalities (17 papers) and RNA modifications and cancer (15 papers). The work is most often cited by research in Genetics (2.6k citations), Molecular Biology (2.9k citations) and Cognitive Neuroscience (710 citations). Claude Moraine has collaborated with scholars based in France, Germany and Netherlands. Frequent co-authors include Jean‐Pierre Fryns, Martine Raynaud, Hans‐Hilger Ropers, Ben C.J. Hamel, Jamel Chelly, Sylvain Briault, Nathalie Ronce, Jozef Gécz, Hans van Bokhoven and Annick Toutain. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and Nature Genetics.

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026