Alain Verloès

24.6k total citations
314 papers, 8.7k citations indexed

About

Alain Verloès is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Alain Verloès has authored 314 papers receiving a total of 8.7k indexed citations (citations by other indexed papers that have themselves been cited), including 185 papers in Genetics, 158 papers in Molecular Biology and 41 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Alain Verloès's work include Genomic variations and chromosomal abnormalities (55 papers), Genetics and Neurodevelopmental Disorders (39 papers) and Hedgehog Signaling Pathway Studies (30 papers). Alain Verloès is often cited by papers focused on Genomic variations and chromosomal abnormalities (55 papers), Genetics and Neurodevelopmental Disorders (39 papers) and Hedgehog Signaling Pathway Studies (30 papers). Alain Verloès collaborates with scholars based in France, Belgium and United States. Alain Verloès's co-authors include Damien Sanlaville, L Koulischer, Sandrine Passemard, Clarisse Baumann, Natzi Sakalihasan, Isabelle Bailleul‐Forestier, Raymond Limet, Ariane Berdal, Didier Lacombe and Pierre Gressèns and has published in prestigious journals such as Circulation, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Alain Verloès

307 papers receiving 8.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Alain Verloès France 46 4.4k 3.8k 1.1k 1.1k 1.0k 314 8.7k
Ben C.J. Hamel Netherlands 54 6.6k 1.5× 6.0k 1.6× 1.2k 1.2× 880 0.8× 687 0.7× 201 11.3k
Didier Lacombe France 48 4.0k 0.9× 2.7k 0.7× 1.1k 1.1× 647 0.6× 791 0.8× 322 7.8k
Eric Legius Belgium 57 4.6k 1.1× 3.1k 0.8× 1.4k 1.3× 820 0.8× 2.2k 2.1× 296 12.1k
William Reardon United Kingdom 53 6.5k 1.5× 5.2k 1.4× 1.2k 1.2× 515 0.5× 668 0.6× 195 11.9k
Martijn H. Breuning Netherlands 50 6.2k 1.4× 5.9k 1.6× 735 0.7× 611 0.6× 727 0.7× 160 11.0k
Valérie Cormier‐Daire France 62 8.4k 1.9× 7.2k 1.9× 1.3k 1.3× 927 0.9× 1.2k 1.2× 393 14.3k
Koenraad Devriendt Belgium 56 6.8k 1.6× 6.0k 1.6× 1.5k 1.4× 798 0.8× 1.5k 1.5× 444 12.6k
Egbert Bakker Netherlands 62 7.2k 1.7× 4.1k 1.1× 638 0.6× 1.4k 1.4× 554 0.5× 246 12.3k
James F. Reynolds United States 48 4.7k 1.1× 3.3k 0.9× 1.5k 1.4× 622 0.6× 400 0.4× 294 9.1k
Michel Vekemans France 44 4.1k 0.9× 3.3k 0.9× 1.2k 1.2× 439 0.4× 901 0.9× 248 8.7k

Countries citing papers authored by Alain Verloès

Since Specialization
Citations

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

Fields of papers citing papers by Alain Verloès

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alain Verloès

This figure shows the co-authorship network connecting the top 25 collaborators of Alain Verloès. A scholar is included among the top collaborators of Alain Verloès 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 Alain Verloès. Alain Verloès 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
1.
Chevarin, Martin, Antonio Vitobello, Cyril Fournier, et al.. (2022). A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort. European Journal of Human Genetics. 31(7). 761–768. 6 indexed citations
2.
Lévy, Jonathan, Anna Maruani, Céline Dupont, et al.. (2021). Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder. Clinical Genetics. 101(3). 364–370. 8 indexed citations
3.
Ebstein, Frédéric, Geoffroy Delplancq, Stéphane Auvin, et al.. (2020). Report of the first patient with a homozygous OTUD7A variant responsible for epileptic encephalopathy and related proteasome dysfunction. Clinical Genetics. 97(4). 567–575. 18 indexed citations
4.
Gaston, Véronique, Isabelle Meunier, Sabine Sigaudy, et al.. (2020). Confirmation of FZD5 implication in a cohort of 50 patients with ocular coloboma. European Journal of Human Genetics. 29(1). 131–140. 10 indexed citations
5.
Capri, Yline, Catherine Pienkowski, Benoît Lepage, et al.. (2019). Gonadal Function of Female Patients with Noonan Syndrome. 92. 1 indexed citations
6.
Bruel, Ange‐Line, Jonathan Lévy, Narcisse Elenga, et al.. (2018). INTU‐related oral‐facial‐digital syndrome type VI: A confirmatory report. Clinical Genetics. 93(6). 1205–1209. 6 indexed citations
7.
Lévy, Jonathan, Damien Haye, Nicola Marziliano, et al.. (2018). EFNB2haploinsufficiency causes a syndromic neurodevelopmental disorder. Clinical Genetics. 93(6). 1141–1147. 19 indexed citations
8.
Lévy, Jonathan, Sarah Grotto, Cyril Mignot, et al.. (2018). NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder. Clinical Genetics. 94(2). 264–268. 25 indexed citations
9.
Piard, Juliette, George K. E. Umanah, Frederike L. Harms, et al.. (2017). A homozygous ATAD1 mutation impairs postsynaptic AMPA receptor trafficking and causes a lethal encephalopathy. Brain. 141(3). 651–661. 35 indexed citations
10.
Lévy, Jonathan, Aurélie Coussement, Céline Dupont, et al.. (2017). Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome. American Journal of Medical Genetics Part A. 173(8). 2081–2087. 15 indexed citations
11.
Tabet, Anne‐Claude, Marion Pilorge, Richard Delorme, et al.. (2012). Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother. European Journal of Human Genetics. 20(5). 540–546. 33 indexed citations
12.
Rambaud, Jérôme, Isabelle Marey, Céline Dupont, et al.. (2012). Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication. American Journal of Medical Genetics Part A. 158A(9). 2277–2282. 2 indexed citations
13.
Méchinaud, Françoise, Claire Galambrun, Neïla Ben Romdhane, et al.. (2010). Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia. Journal of Medical Genetics. 47(10). 686–691. 90 indexed citations
14.
Gérard‐Blanluet, Marion, Stéphane Serero, Clarisse Baumann, et al.. (2008). Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome. American Journal of Medical Genetics Part A. 146A(14). 1871–1874. 9 indexed citations
15.
Verloès, Alain, Dominique Brémond‐Gignac, Bertrand Isidor, et al.. (2006). Blepharophimosis‐mental retardation (BMR) syndromes: A proposed clinical classification of the so‐called Ohdo syndrome, and delineation of two new BMR syndromes, one X‐linked and one autosomal recessive. American Journal of Medical Genetics Part A. 140A(12). 1285–1296. 52 indexed citations
16.
Sznajer, Yves, Clarisse Baumann, Albert David, et al.. (2003). Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome). European Journal of Pediatrics. 162(12). 863–867. 51 indexed citations
17.
Campo, Miguel Del, Bryan D. Hall, Alec Aeby, et al.. (1999). Albinism and agenesis of the corpus callosum with profound developmental delay: Vici syndrome, evidence for autosomal recessive inheritance. American Journal of Medical Genetics. 85(5). 479–485. 3 indexed citations
18.
Verloès, Alain, et al.. (1994). Osteocraniostenosis.. Journal of Medical Genetics. 31(10). 772–778. 20 indexed citations
19.
Gibson, K. Michael, W. G. Sherwood, Georg F. Hoffmann, et al.. (1991). Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria. The Journal of Pediatrics. 118(6). 885–890. 48 indexed citations
20.
Verloès, Alain, Martine Le Merrer, J. P. Farriaux, & P Maroteaux. (1991). Metaphyseal acroscyphodysplasia. Clinical Genetics. 39(5). 362–369. 10 indexed citations

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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