Brigitte Gilbert‐Dussardier

8.6k total citations
48 papers, 1.4k citations indexed

About

Brigitte Gilbert‐Dussardier is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Brigitte Gilbert‐Dussardier has authored 48 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 15 papers in Genetics and 15 papers in Genetics. Recurrent topics in Brigitte Gilbert‐Dussardier's work include Tracheal and airway disorders (11 papers), Genomic variations and chromosomal abnormalities (9 papers) and Vascular Anomalies and Treatments (7 papers). Brigitte Gilbert‐Dussardier is often cited by papers focused on Tracheal and airway disorders (11 papers), Genomic variations and chromosomal abnormalities (9 papers) and Vascular Anomalies and Treatments (7 papers). Brigitte Gilbert‐Dussardier collaborates with scholars based in France, United States and Switzerland. Brigitte Gilbert‐Dussardier's co-authors include Patrick Edery, Dominique Bonneau, Albert David, Valérie Layet, Françoise Bonnet, Michel Longy, F. Caux, Catherine Dugast, Nicolas Sévenet and Gaëtan Lesca and has published in prestigious journals such as JAMA, PLoS ONE and Annals of Neurology.

In The Last Decade

Brigitte Gilbert‐Dussardier

47 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brigitte Gilbert‐Dussardier France	19	636	444	369	325	225	48	1.4k
J.G. Seidman United States	20	634 1.0×	215 0.5×	244 0.7×	169 0.5×	90 0.4×	35	1.3k
Jon Warner United Kingdom	21	770 1.2×	204 0.5×	276 0.7×	146 0.4×	387 1.7×	37	1.8k
Johanna M. van Hagen Netherlands	17	446 0.7×	263 0.6×	322 0.9×	275 0.8×	195 0.9×	41	1.0k
Lilian Bomme Ousager Denmark	17	428 0.7×	114 0.3×	420 1.1×	157 0.5×	186 0.8×	57	1.1k
Ghislaine Plessis France	18	431 0.7×	129 0.3×	341 0.9×	116 0.4×	103 0.5×	31	810
Stryder M. Meadows United States	21	926 1.5×	110 0.2×	104 0.3×	126 0.4×	148 0.7×	38	1.3k
James M. Dunn Canada	14	749 1.2×	95 0.2×	145 0.4×	94 0.3×	106 0.5×	29	1.3k
Geneviève Piétu France	26	839 1.3×	219 0.5×	323 0.9×	174 0.5×	266 1.2×	69	2.0k
Marc Valentine United States	19	932 1.5×	321 0.7×	156 0.4×	226 0.7×	122 0.5×	31	1.7k
Hana M. Odeh United States	15	751 1.2×	132 0.3×	194 0.5×	256 0.8×	108 0.5×	20	1.8k

Countries citing papers authored by Brigitte Gilbert‐Dussardier

Since Specialization

Citations

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

Fields of papers citing papers by Brigitte Gilbert‐Dussardier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brigitte Gilbert‐Dussardier. 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 Brigitte Gilbert‐Dussardier. The network helps show where Brigitte Gilbert‐Dussardier may publish in the future.

Co-authorship network of co-authors of Brigitte Gilbert‐Dussardier

This figure shows the co-authorship network connecting the top 25 collaborators of Brigitte Gilbert‐Dussardier. A scholar is included among the top collaborators of Brigitte Gilbert‐Dussardier 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 Brigitte Gilbert‐Dussardier. Brigitte Gilbert‐Dussardier 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

Quartier, Angélique, Nathalie Drouot, Damien Plassard, et al.. (2023). Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome. Molecular Psychiatry. 29(2). 287–296. 4 indexed citations

Giraud, Sophie, Claire Bardel, Sophie Dupuis‐Girod, et al.. (2020). Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia. Orphanet Journal of Rare Diseases. 15(1). 254–254. 5 indexed citations

Guyader, Gwenaël Le, Claire Bénéteau, Madeleine Joubert, et al.. (2020). 12q21 deletion syndrome: Narrowing the critical region down to 1.6 Mb including SYT1 and PPP1R12A. American Journal of Medical Genetics Part A. 182(9). 2133–2138. 5 indexed citations

Bilan, Frédéric, et al.. (2019). A functional assay to study the pathogenicity of CHD7 protein variants encountered in CHARGE syndrome patients. European Journal of Human Genetics. 27(11). 1683–1691. 6 indexed citations

Richard, Anne, Anne Rovelet‐Lecrux, Elsa Delaby, et al.. (2016). The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(3). 377–382. 1 indexed citations

Thoreau, Vincent, Montserrat Rodríguez-Ballesteros, Eva Hamade, et al.. (2015). Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia. PLoS ONE. 10(7). e0132111–e0132111. 18 indexed citations

Hyon, Capucine, Sandra Chantot‐Bastaraud, Radu Harbuz, et al.. (2015). Refining the regulatory region upstream of SOX9 associated with 46,XX testicular disorders of Sex Development (DSD). American Journal of Medical Genetics Part A. 167(8). 1851–1858. 44 indexed citations

Bubien, Virginie, Françoise Bonnet, Véronique Brouste, et al.. (2013). High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome. Journal of Medical Genetics. 50(4). 255–263. 225 indexed citations

Petit, Florence, Joris Andrieux, Geneviève Baujat, et al.. (2013). Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families. Clinical Genetics. 85(5). 464–469. 17 indexed citations

10.

Morice‐Picard, Fanny, Eulalie Lasseaux, Dorothée Cailley, et al.. (2013). High‐resolution array‐CGH in patients with oculocutaneous albinism identifies new deletions of the TYR, OCA2, and SLC45A2 genes and a complex rearrangement of the OCA2 gene. Pigment Cell & Melanoma Research. 27(1). 59–71. 21 indexed citations

11.

Harbuz, Radu, et al.. (2013). Osteogenesis imperfecta, tricho‐dento‐osseous syndrome and intellectual disability: A familial case with 17q21.33‐q22 (COL1A1 and DLX3) deletion and 7q32.3‐q33 duplication resulting from a reciprocal interchromosomal insertion. American Journal of Medical Genetics Part A. 161(10). 2504–2511. 12 indexed citations

12.

Ingrand, Isabelle, Pierre Ingrand, Brigitte Gilbert‐Dussardier, et al.. (2011). Altered quality of life in Rendu-Osler-Weber disease related to recurrent epistaxis. Rhinology Journal. 49(2). 155–162. 38 indexed citations

13.

Lacroix, Agnès, Mylène Pezet, Damien Bonnet, et al.. (2008). Le syndrome de Williams-Beuren : une approche pluridisciplinaire. Archives de Pédiatrie. 16(3). 273–282. 9 indexed citations

14.

Lesca, Gaëtan, Carla Olivieri, Nelly Burnichon, et al.. (2007). Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network. Genetics in Medicine. 9(1). 14–22. 157 indexed citations

15.

Chassaing, Nicolas, Brigitte Gilbert‐Dussardier, Florence Nicot, et al.. (2007). Germinal mosaicism and familial recurrence of a SOX2 mutation with highly variable phenotypic expression extending from AEG syndrome to absence of ocular involvement. American Journal of Medical Genetics Part A. 143A(3). 289–291. 38 indexed citations

16.

Boissonnot, M, et al.. (2007). Syndrome d’Oguchi ou cécité nocturne congénitale stationnaire : à propos d’un cas. Journal Français d Ophtalmologie. 30(1). 74.e1–74.e4. 2 indexed citations

17.

Saugier-Véber, Pascale, Alice Goldenberg, Valérie Drouin‐Garraud, et al.. (2006). Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation. European Journal of Human Genetics. 14(9). 1009–1017. 27 indexed citations

18.

Poirier, Karine, Didier Lacombe, Brigitte Gilbert‐Dussardier, et al.. (2005). Screening of ARX in mental retardation families: consequences for the strategy of molecular diagnosis. Neurogenetics. 7(1). 39–46. 32 indexed citations

19.

Chassaing, Nicolas, Dominique Carles, Anne Lise Delezoïde, et al.. (2005). X-linked dominant chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia. American Journal of Medical Genetics Part A. 136A(4). 307–312. 11 indexed citations

20.

Gilbert‐Dussardier, Brigitte, Jean‐Michel Rozet, Daniel Rabier, et al.. (1996). Partial duplication [dup. TCAC (178)] and novel point mutations (T125M, G188R, A209V, and H302L) of the ornithine transcarbamylase gene in congenital hyperammonemia. Human Mutation. 8(1). 74–76. 12 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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