Gérald Bussy

905 total citations
17 papers, 176 citations indexed

About

Gérald Bussy is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Gérald Bussy has authored 17 papers receiving a total of 176 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Cognitive Neuroscience and 6 papers in Molecular Biology. Recurrent topics in Gérald Bussy's work include Genetics and Neurodevelopmental Disorders (11 papers), Congenital heart defects research (4 papers) and Autism Spectrum Disorder Research (4 papers). Gérald Bussy is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Congenital heart defects research (4 papers) and Autism Spectrum Disorder Research (4 papers). Gérald Bussy collaborates with scholars based in France, United States and Japan. Gérald Bussy's co-authors include Vincent des Portes, Aurore Curie, V. des Portes, Gaëtan Lesca, Damien Sanlaville, Renaud Touraine, Brun Amandine, Daniel Gérard, Massimiliano Rossi and Laurence Lion‐François and has published in prestigious journals such as Behavioral Neuroscience, Journal of Intellectual Disability Research and Clinical Genetics.

In The Last Decade

Gérald Bussy

16 papers receiving 156 citations

Peers

Gérald Bussy

GENET

DEP

PHEOH

Watfa Al‐Mamari Oman

Amber Boys Australia

William Arias Colombia

Simone Schröder Germany

Lucy Wilde United Kingdom

Lien Le Germany

Alinoë Lavillaureix France

Alejandro Q. Nato United States

Tianyun Wang China

She Min Zeng United States

Watfa Al‐Mamari Oman

Gérald Bussy

112 ×1.4

GENET

48 ×0.7

87 ×2.8

16 ×0.6

DEP

14 ×0.6

PHEOH

Citations per year, relative to Gérald Bussy Gérald Bussy (= 1×) peers Watfa Al‐Mamari

Countries citing papers authored by Gérald Bussy

Since Specialization

Citations

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

Fields of papers citing papers by Gérald Bussy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gérald Bussy

This figure shows the co-authorship network connecting the top 25 collaborators of Gérald Bussy. A scholar is included among the top collaborators of Gérald Bussy 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 Gérald Bussy. Gérald Bussy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

Labalme, Audrey, Marianne Till, Gérald Bussy, et al.. (2018). Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations. Clinical Case Reports. 6(5). 827–834. 3 indexed citations

Curie, Aurore, Gaëlle Friocourt, Vincent des Portes, et al.. (2018). Basal ganglia involvement in ARX patients: The reason for ARX patients very specific grasping?. NeuroImage Clinical. 19. 454–465. 6 indexed citations

Curie, Aurore, Gaëtan Lesca, Gérald Bussy, et al.. (2017). Asperger syndrome and early-onset schizophrenia associated with a novel MECP2 deleterious missense variant. Psychiatric Genetics. 27(3). 105–109. 14 indexed citations

Portes, Vincent des, et al.. (2015). Évaluation neuropsychologique du trouble de l’inhibition dans le TDAH : de la théorie à la clinique. Revue de neuropsychologie. 7(4). 291–291. 1 indexed citations

Fréminville, Bénédicte de, et al.. (2014). Variability of the Aging Process in Dementia-Free Adults With Down Syndrome. American Journal on Intellectual and Developmental Disabilities. 120(1). 3–15. 12 indexed citations

Bussy, Gérald, et al.. (2014). Impact d’un entraînement de la mémoire à court terme verbale sur le langage d’enfants ayant une déficience intellectuelle. Érudit (Université de Montréal). 24. 141–151. 2 indexed citations

Lesca, Gaëtan, Marie‐Pierre Moizard, Gérald Bussy, et al.. (2013). Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation. American Journal of Medical Genetics Part A. 161(12). 3063–3071. 30 indexed citations

Lesca, Gaëtan, et al.. (2012). Childhood apraxia of speech without intellectual deficit in a patient with cri du chat syndrome. European Journal of Medical Genetics. 55(6-7). 433–436. 19 indexed citations

Bussy, Gérald, et al.. (2011). Implicit procedural learning in fragile X and Down syndrome. Journal of Intellectual Disability Research. 55(5). 521–528. 24 indexed citations

10.

Bussy, Gérald, et al.. (2011). Apprentissage procédural implicite dans la dyslexie de surface et la dyslexie phonologique. Revue de neuropsychologie. Volume 3(3). 141–146. 3 indexed citations

11.

Bussy, Gérald, et al.. (2011). Apprentissage procédural implicite dans la dyslexie de surface et la dyslexie phonologique. Revue de neuropsychologie. 3(3). 141–141. 2 indexed citations

12.

Germanaud, David, Massimiliano Rossi, Gérald Bussy, et al.. (2010). The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males. Clinical Genetics. 79(3). 225–235. 36 indexed citations

13.

Michael, George A., et al.. (2009). Reactivity to visual signals and the cerebellar vermis: Evidence from a rare case with rhombencephalosynapsis.. Behavioral Neuroscience. 123(1). 86–96. 12 indexed citations

14.

Bussy, Gérald & Vincent des Portes. (2008). Définition du retard mental, épidémiologie, évaluation clinique. MTP. Médecine thérapeutique pédiatrie. 11(4). 196–201. 3 indexed citations

15.

Bussy, Gérald, et al.. (2008). Déficiences intellectuelles liées au chromosome X. MTP. Médecine thérapeutique pédiatrie. 11(4). 218–223. 1 indexed citations

16.

Curie, Aurore, Silvia Sacco, Gérald Bussy, et al.. (2008). Impairment of cerebello-thalamo-frontal pathway in Rab-GDI mutated patients with pure mental deficiency. European Journal of Medical Genetics. 52(1). 6–13. 8 indexed citations

17.

Bussy, Gérald, et al.. (2007). R - 1 Trouble hyperactif avec déficit attentionnel chez un enfant de dix ans ayant une malformation cérébelleuse. Revue Neurologique. 163(4). 135–135.

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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