V. des Portes

1.6k citations
47 papers · 1.1k indexed · h-index 16
Topics
Genetics and Neurodevelopmental Disorders (18 papers)Fetal and Pediatric Neurological Disorders (13 papers)Autism Spectrum Disorder Research (7 papers)
Partner nations
FranceUnited StatesItaly

In The Last Decade

V. des Portes

44 papers receiving 1.0k citations

Peers

V. des Portes
Comparison fields: 5 of 92
  • Molecular Biology 389
  • Genetics 325
  • Pediatrics, Perinatology and Child Health 249
  • Cellular and Molecular Neuroscience 188
  • Cell Biology 159
Replace Richard P. Morse with:
Richard P. Morse United States
Tomohide Goto Japan
Férechté Encha‐Razavi France
Sandrine Passemard France
J. Motte France
Kenzo Takeshita Japan
Alex R. Paciorkowski United States
Julie S. Cohen United States
Susan Walker Canada
Susan Moore United Kingdom
V. des Portes relative to Richard P. Morse United States Richard P. Morse's profile →
Citations per field
00.5×1.5×
Richard P. Morse · 1×
Citations per year

Countries citing papers authored by V. des Portes

Since Specialization
Citations

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

Fields of papers citing papers by V. des Portes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. des Portes. 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 V. des Portes. The network helps show where V. des Portes may publish in the future.

Co-authorship network of co-authors of V. des Portes

This figure shows the co-authorship network connecting the top 25 collaborators of V. des Portes. A scholar is included among the top collaborators of V. des Portes 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 V. des Portes. V. des Portes 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 3
2 5
3 7
4 6
5 20
6 2
7 24
8 3
9 6
10 24
11 36
12
La dyspraxie verbale: trouble spécifique complexe du neurodéveloppement
0
13 32
14 0
15 1
16 3
17 10
18 1
19
Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation.
33
20 7

About V. des Portes

V. des Portes is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Psychiatry and Mental health, having authored 47 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (18 papers), Fetal and Pediatric Neurological Disorders (13 papers) and Autism Spectrum Disorder Research (7 papers). The work is most often cited by research in Developmental Neuroscience (116 citations), Pediatrics, Perinatology and Child Health (249 citations) and Genetics (325 citations). V. des Portes has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Laurent Guibaud, G Ponsot, C. Beldjord, Isabelle Desguerre, Olivier Dulac, J.-M. Pinard, J. Motte, Pierre Lebon, Bénédicte Héron and Fiona Francis. Their work appears in journals such as NeuroImage, Neurology and Human Molecular 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