Ghislaine Plessis

4.6k citations

31 papers · 810 indexed · h-index 18

Co-authors: Joris Andrieux Jian‐Min Chen C. Gall Claude Férec J Chipponi Cédric Le Maréchal Moira Blyth Nadia Chuzhanova
Topics: Genomic variations and chromosomal abnormalities (10 papers)Genetics and Neurodevelopmental Disorders (8 papers)Connective tissue disorders research (4 papers)
Cited by: Genetics Reproductive Medicine
Journals: Blood The Journal of Clinical Endocrinology & Metabolism Hypertension
Partner nations: France United Kingdom Germany

In The Last Decade

Ghislaine Plessis

31 papers receiving 780 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome 2015 ·Journal of Medical Genetics ·(unknown),Alistair T. Pagnamenta,Moira Blyth,Sahar Mansour,Vivienne McConnell,Ikuyo Kou,Shiro Ikegawa,Yoshinori Tsurusaki,Naomichi Matsumoto,Adriana Lo‐Castro,Ghislaine Plessis,Beate Albrecht,Agatino Battaglia,Jenny C. Taylor,Malcolm F. Howard,David A. Keays,(unknown),Susanne J. Kühl,Usha Kini,Alisdair McNeill	53
2	21q21 deletion involving NCAM2: Report of 3 cases with neurodevelopmental disorders 2014 ·European Journal of Medical Genetics ·Florence Petit,Ghislaine Plessis,Matthieu Décamp,Jean‐Marie Cuisset,Moira Blyth,(unknown),Joris Andrieux	27
3	Clinical Comparison of Overlapping Deletions of 19p13.3 2013 ·American Journal of Medical Genetics Part A ·Hiba Risheg,Romela Pasion,(unknown),Virginia K. Proud,LaDonna Immken,Stuart Schwartz,(unknown),Peter Papenhausen,Tiong Yang Tan,Joris Andrieux,Ghislaine Plessis,David J. Amor,Elisabeth A. Keitges	9
4	A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features 2012 ·European Journal of Medical Genetics ·(unknown),Bénédicte Demeer,Cédric Le Caignec,Bertrand Isidor,Michèle Mathieu‐Dramard,Ghislaine Plessis,Alice M. George,Juliet Taylor,Salim Aftimos,Adelheid Wiemer‐Kruel,Jürgen Kohlhase,Göran Annerén,Helen V. Firth,Ingrid Simonic,Joris Vermeesch,Ann‐Charlotte Thuresson,Henri Copin,Donald R. Love,Joris Andrieux	41
5	Wilms’ tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas 2012 ·European Journal of Human Genetics ·Bertrand Isidor,Franck Bourdeaut,(unknown),Ghislaine Plessis,(unknown),Caroline Kannengiesser,Sylvie Rossignol,Olivier Pichon,(unknown),Dominique Martin‐Coignard,Maria Piccione,Albert David,Olivier Delattre,Marc Jeanpierre,Nicolas Sévenet,Cédric Le Caignec	19
6	Duplication 16p13.3 and the CREBBP gene: Confirmation of the phenotype 2012 ·European Journal of Medical Genetics ·Bénédicte Demeer,Joris Andrieux,Aline Receveur,G Morin,Florence Petit,Sophie Julia,Ghislaine Plessis,Dominique Martin‐Coignard,Bruno Delobel,Helen V. Firth,Ann‐Charlotte Thuresson,(unknown),(unknown),Cédric Le Caignec,Koenraad Devriendt,Michèle Mathieu‐Dramard	41
7	Evidence that FGFR1 loss-of-function mutations may cause variable skeletal malformations in patients with Kallmann syndrome 2012 ·Advances in Medical Sciences ·Katarzyna Jarząbek,Sławomir Wołczyński,R Leśniewicz,Ghislaine Plessis,(unknown)	29
8	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 2012 ·European Journal of Medical Genetics ·Kerstin Becker,Nataliya Di Donato,Muriel Holder‐Espinasse,Joris Andrieux,Jean‐Marie Cuisset,Louis Vallée,Ghislaine Plessis,(unknown),Bruno Delobel,Ann‐Charlotte Thuresson,Göran Annerén,Kirstine Ravn,Zeynep Tümer,Sigrid Tinschert,Evelin Schröck,Aia Elise Jønch,Karl Hackmann	19
9	5q12.1 deletion: Delineation of a phenotype including mental retardation and ocular defects 2011 ·American Journal of Medical Genetics Part A ·(unknown),Joris Andrieux,Ghislaine Plessis,Ana Cristina Victorino Krepischi,Josette Lucas,Véronique David,(unknown),Débora Romeo Bertola,Albert David,(unknown),Jean Mosser,Leïla Lazaro,Catherine Tréguier,Carla Rosenberg,Sylvie Odent,Christèle Dubourg	19
10	A cluster of translocation breakpoints in 2q37 is associated with overexpression of NPPC in patients with a similar overgrowth phenotype 2007 ·Human Mutation ·Anne Moncla,Chantal Missirian,Pierre Cacciagli,(unknown),Laurence Legeai‐Mallet,Jean-Luc Jouve,B. Chabrol,Martine Le Merrer,Ghislaine Plessis,Laurent Villard,Nicole Philip	66
11	Molecular screening ofALK1/ACVRL1andENGgenes in hereditary hemorrhagic telangiectasia in France 2004 ·Human Mutation ·Gaëtan Lesca,Henri Plauchu,Florence Coulet,Sylvain Lefèbvre,Ghislaine Plessis,Sylvie Odent,Sophie Rivière,Bruno Leheup,Cyril Goizet,Marie‐France Carette,Jean-François Cordier,S. Pinson,Florent Soubrier,Alain Calender,Sophie Giraud	91
12	Chromosome imbalances in oligodendroglial tumors detected by comparative genomic hybridization 2003 ·Annales de Génétique ·Violaine Bourdon,Ghislaine Plessis,Françoise Chapon,(unknown),J M Derlon,Philippe Jonveaux	10
13	Intra-species chromosome-length polymorphism in Geotrichum candidum revealed by pulsed field gel electrophoresis 2002 ·International Journal of Food Microbiology ·(unknown),Nathalie Desmasures,(unknown),Ghislaine Plessis,(unknown),Jean-Michel Panoff,Micheline Guéguen	11
14	A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic Infertility¹ 1999 ·The Journal of Clinical Endocrinology & Metabolism ·Csilla Krausz,Lluís Quintana‐Murci,Sandrine Barbaux,Jean‐Pierre Siffroi,Hassan Rouba,D Delafontaine,(unknown),(unknown),J.-M. Antoine,(unknown),(unknown),Attila Tar,Éric Jeandidier,Ghislaine Plessis,Thomas Bourgeron,J. P. Dadoune,Marc Fellous,Ken McElreavey	73
15	Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay‐Marks syndrome 1997 ·Clinical Genetics ·Ghislaine Plessis,(unknown),M. Le Merrer	11
16	Le syndrome X fragile est encore méconnu: efficacité du diagnostic moléculaire chez les proposants avec retard mental 1997 ·Archives de Pédiatrie ·Mireille Cossée,Céline Moutou,Valérie Biancalana,(unknown),Ghislaine Plessis,B Delobel,M. F. Croquette,S Gilgenkrantz,Jean‐Philippe Lambert,G Malpuech,Claude Stoll,(unknown),(unknown),Jean‐Louis Mandel	1
17	Severe manifestations in carrier females in X linked retinitis pigmentosa. 1997 ·Journal of Medical Genetics ·(unknown),(unknown),Imad Ghazi,Jean‐Michel Rozet,Sophie Châtelin,S. Gerber,Isabelle Perrault,(unknown),Marie‐Louise Briard,Ghislaine Plessis,Jean‐Louis Dufier,A Munnich,Josseline Kaplan	36
18	Molecular analysis of 53 fragile X families with the probe StB12.3 1994 ·American Journal of Medical Genetics ·(unknown),(unknown),(unknown),Dominique Martin,(unknown),Sylvie Odent,Ghislaine Plessis,P. Parent,(unknown),(unknown)	4
19	Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene 1992 ·Human Genetics ·Jacky Bonaventure,C. Philippe,Ghislaine Plessis,Jacqueline Vigneron,C. Lasselin,P Maroteaux,S Gilgenkrantz	25
20	X‐linked hypohidrotic ectodermal dysplasia and t(X;12) in a female 1989 ·Clinical Genetics ·C Turleau,Patrick Niaudet,(unknown),Ghislaine Plessis,D. Cau,J. de Grouchy	20

About Ghislaine Plessis

Ghislaine Plessis is a scholar working on Genetics, Developmental Biology and Genetics, having authored 31 papers that have together received 810 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Genetics (341 citations), Genetics (129 citations) and Reproductive Medicine (79 citations). Ghislaine Plessis has collaborated with scholars based in France, United Kingdom and Germany. Frequent co-authors include Joris Andrieux, Jian‐Min Chen, C. Gall, Claude Férec, J Chipponi, Cédric Le Maréchal, Moira Blyth, Nadia Chuzhanova, Odile Raguénès and Florence Coulet. Their work appears in journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and Hypertension.

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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