Ghislaine Plessis

4.6k total citations
31 papers, 810 citations indexed

About

Ghislaine Plessis is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Ghislaine Plessis has authored 31 papers receiving a total of 810 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 17 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Ghislaine Plessis's work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Connective tissue disorders research (4 papers). Ghislaine Plessis is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Connective tissue disorders research (4 papers). Ghislaine Plessis collaborates with scholars based in France, United Kingdom and Germany. Ghislaine Plessis's co-authors include Joris Andrieux, Cédric Le Maréchal, Jian‐Min Chen, Nadia Chuzhanova, Claude Férec, Odile Raguénès, J Chipponi, Moira Blyth, C. Gall and Anne Moncla and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and Hypertension.

In The Last Decade

Ghislaine Plessis

31 papers receiving 780 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ghislaine Plessis France 18 431 341 129 116 103 31 810
Zeynep Coban‐Akdemir United States 18 544 1.3× 396 1.2× 51 0.4× 69 0.6× 66 0.6× 50 965
Serena Redaelli Italy 16 372 0.9× 185 0.5× 288 2.2× 60 0.5× 104 1.0× 48 814
Rodger Palmer United Kingdom 13 397 0.9× 494 1.4× 78 0.6× 105 0.9× 76 0.7× 20 915
Anas M. Alazami Saudi Arabia 22 857 2.0× 584 1.7× 127 1.0× 52 0.4× 95 0.9× 55 1.5k
Shlomit Rienstein Israel 14 277 0.6× 161 0.5× 69 0.5× 49 0.4× 46 0.4× 28 559
Bénédicte Duriez France 17 698 1.6× 724 2.1× 56 0.4× 291 2.5× 125 1.2× 25 1.5k
Marie‐France Portnoï France 19 446 1.0× 574 1.7× 100 0.8× 57 0.5× 71 0.7× 29 908
Silvia Majore Italy 16 427 1.0× 319 0.9× 133 1.0× 32 0.3× 42 0.4× 48 808
Martine Blayau France 18 649 1.5× 404 1.2× 116 0.9× 234 2.0× 118 1.1× 44 1.1k
A M van den Ouweland Netherlands 13 312 0.7× 286 0.8× 32 0.2× 62 0.5× 69 0.7× 19 737

Countries citing papers authored by Ghislaine Plessis

Since Specialization
Citations

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

Fields of papers citing papers by Ghislaine Plessis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ghislaine Plessis

This figure shows the co-authorship network connecting the top 25 collaborators of Ghislaine Plessis. A scholar is included among the top collaborators of Ghislaine Plessis 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 Ghislaine Plessis. Ghislaine Plessis 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.
Pagnamenta, Alistair T., Moira Blyth, Sahar Mansour, et al.. (2015). Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome. Journal of Medical Genetics. 53(3). 152–162. 53 indexed citations
2.
Petit, Florence, Ghislaine Plessis, Matthieu Décamp, et al.. (2014). 21q21 deletion involving NCAM2: Report of 3 cases with neurodevelopmental disorders. European Journal of Medical Genetics. 58(1). 44–46. 27 indexed citations
3.
Risheg, Hiba, Romela Pasion, Virginia K. Proud, et al.. (2013). Clinical Comparison of Overlapping Deletions of 19p13.3. American Journal of Medical Genetics Part A. 161(5). 1110–1116. 9 indexed citations
4.
Demeer, Bénédicte, Cédric Le Caignec, Bertrand Isidor, et al.. (2012). A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features. European Journal of Medical Genetics. 56(3). 163–170. 41 indexed citations
5.
Isidor, Bertrand, Franck Bourdeaut, Ghislaine Plessis, et al.. (2012). Wilms’ tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas. European Journal of Human Genetics. 21(7). 784–787. 19 indexed citations
6.
Jarząbek, Katarzyna, et al.. (2012). Evidence that FGFR1 loss-of-function mutations may cause variable skeletal malformations in patients with Kallmann syndrome. Advances in Medical Sciences. 57(2). 314–321. 29 indexed citations
7.
Demeer, Bénédicte, Joris Andrieux, Aline Receveur, et al.. (2012). Duplication 16p13.3 and the CREBBP gene: Confirmation of the phenotype. European Journal of Medical Genetics. 56(1). 26–31. 41 indexed citations
8.
Becker, Kerstin, Nataliya Di Donato, Muriel Holder‐Espinasse, et al.. (2012). De novo microdeletions of chromosome 6q14.1-q14.3 and 6q12.1-q14.1 in two patients with intellectual disability - further delineation of the 6q14 microdeletion syndrome and review of the literature. European Journal of Medical Genetics. 55(8-9). 490–497. 19 indexed citations
9.
Andrieux, Joris, Ghislaine Plessis, Ana Cristina Victorino Krepischi, et al.. (2011). 5q12.1 deletion: Delineation of a phenotype including mental retardation and ocular defects. American Journal of Medical Genetics Part A. 155(4). 725–731. 19 indexed citations
10.
Moncla, Anne, Chantal Missirian, Pierre Cacciagli, et al.. (2007). A cluster of translocation breakpoints in 2q37 is associated with overexpression of NPPC in patients with a similar overgrowth phenotype. Human Mutation. 28(12). 1183–1188. 66 indexed citations
11.
Lesca, Gaëtan, Henri Plauchu, Florence Coulet, et al.. (2004). Molecular screening ofALK1/ACVRL1andENGgenes in hereditary hemorrhagic telangiectasia in France. Human Mutation. 23(4). 289–299. 91 indexed citations
12.
Bourdon, Violaine, et al.. (2003). Chromosome imbalances in oligodendroglial tumors detected by comparative genomic hybridization. Annales de Génétique. 47(2). 105–111. 10 indexed citations
13.
Desmasures, Nathalie, et al.. (2002). Intra-species chromosome-length polymorphism in Geotrichum candidum revealed by pulsed field gel electrophoresis. International Journal of Food Microbiology. 76(1-2). 127–134. 11 indexed citations
14.
Krausz, Csilla, Lluís Quintana‐Murci, Sandrine Barbaux, et al.. (1999). A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic Infertility1. The Journal of Clinical Endocrinology & Metabolism. 84(10). 3606–3612. 73 indexed citations
15.
Ghazi, Imad, Jean‐Michel Rozet, Sophie Châtelin, et al.. (1997). Severe manifestations in carrier females in X linked retinitis pigmentosa.. Journal of Medical Genetics. 34(10). 793–797. 36 indexed citations
16.
Plessis, Ghislaine, et al.. (1997). Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay‐Marks syndrome. Clinical Genetics. 52(4). 231–234. 11 indexed citations
17.
Cossée, Mireille, Céline Moutou, Valérie Biancalana, et al.. (1997). Le syndrome X fragile est encore méconnu: efficacité du diagnostic moléculaire chez les proposants avec retard mental. Archives de Pédiatrie. 4(3). 227–236. 1 indexed citations
18.
Martin, Dominique, et al.. (1994). Molecular analysis of 53 fragile X families with the probe StB12.3. American Journal of Medical Genetics. 53(4). 370–373. 4 indexed citations
19.
Bonaventure, Jacky, C. Philippe, Ghislaine Plessis, et al.. (1992). Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene. Human Genetics. 90(1-2). 164–8. 25 indexed citations
20.
Turleau, C, et al.. (1989). X‐linked hypohidrotic ectodermal dysplasia and t(X;12) in a female. Clinical Genetics. 35(6). 462–466. 20 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Zeynep Coban‐Akdemir Breakdown of academic impact, for papers by Serena Redaelli Breakdown of academic impact, for papers by Rodger Palmer Breakdown of academic impact, for papers by Anas M. Alazami Breakdown of academic impact, for papers by Shlomit Rienstein Breakdown of academic impact, for papers by Bénédicte Duriez Breakdown of academic impact, for papers by Marie‐France Portnoï Breakdown of academic impact, for papers by Silvia Majore Breakdown of academic impact, for papers by Martine Blayau Breakdown of academic impact, for papers by A M van den Ouweland
Rankless by CCL
2026