Brigitte Gilbert‐Dussardier

8.6k citations

48 papers · 1.4k indexed · h-index 19

Molecular Biology
Genetics top 2%
Genetics top 5%
Pulmonary and Respiratory Medicine top 10%
Surgery

Co-authors: Dominique Bonneau Patrick Edery Albert David Valérie Layet Nicolas Sévenet Françoise Bonnet Michel Longy F. Caux
Topics: Tracheal and airway disorders (11 papers)Genomic variations and chromosomal abnormalities (9 papers)Vascular Anomalies and Treatments (7 papers)
Cited by: Genetics Sensory Systems
Journals: JAMA PLoS ONE Annals of Neurology
Partner nations: France United States Switzerland

In The Last Decade

Brigitte Gilbert‐Dussardier

47 papers receiving 1.4k citations

Peers

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

#	Work	Indexed citations
1	Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome 2023 ·Molecular Psychiatry ·(unknown),(unknown),Angélique Quartier,Nathalie Drouot,(unknown),Damien Plassard,Arthur Sorlin,Elise Brischoux‐Boucher,(unknown),Lionel Van Maldergem,Massimiliano Rossi,Gaëtan Lesca,Patrick Edery,Audrey Putoux,Frédéric Bilan,Brigitte Gilbert‐Dussardier,Isis Atallah,Vera M. Kalscheuer,Jean‐Louis Mandel,Amélie Piton	4
2	Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions 2022 ·Cytogenetic and Genome Research ·(unknown),Gwenaël Le Guyader,(unknown),Brigitte Gilbert‐Dussardier,Matthieu Egloff	0
3	Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia 2020 ·Orphanet Journal of Rare Diseases ·Sophie Giraud,Claire Bardel,Sophie Dupuis‐Girod,Marie‐France Carette,Brigitte Gilbert‐Dussardier,Sophie Rivière,Jean‐Christophe Saurin,Mélanie Eyries,(unknown),Évelyne Decullier,Alain Calender,Gaëtan Lesca	5
4	A functional assay to study the pathogenicity of CHD7 protein variants encountered in CHARGE syndrome patients 2019 ·European Journal of Human Genetics ·(unknown),Frédéric Bilan,Brigitte Gilbert‐Dussardier,Alain Kitzis,Vincent Thoreau	6
5	Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability 2016 ·European Journal of Medical Genetics ·(unknown),Marine Legendre,(unknown),Brigitte Gilbert‐Dussardier,Alain Kitzis,Frédéric Bilan,Radu Harbuz	2
6	Dose – response relationship of bevacizumab in hereditary hemorrhagic telangiectasia 2015 ·mAbs ·Nicolas Azzopardi,Sophie Dupuis‐Girod,David Ternant,(unknown),Isabelle Ginon,Fréderic Faure,Évelyne Decullier,Adeline Roux,Marie‐France Carette,Brigitte Gilbert‐Dussardier,Pierre‐Yves Hatron,Pascal Lacombe,V. Leguy‐Seguin,Sophie Rivière,R. Corre,Sabine Bailly,Gilles Paintaud	16
7	Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia 2015 ·PLoS ONE ·(unknown),(unknown),Vincent Thoreau,Montserrat Rodríguez-Ballesteros,Eva Hamade,Sabine Bailly,Brigitte Gilbert‐Dussardier,Raghida Abou Merhi,Alain Kitzis	18
8	Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families 2013 ·Clinical Genetics ·Florence Petit,(unknown),Joris Andrieux,Geneviève Baujat,Clarisse Baumann,Claire Bénéteau,A. David,Laurence Faivre,Dominique Gaillard,Brigitte Gilbert‐Dussardier,Pierre‐Simon Jouk,Cédric Le Caignec,Philippe Loget,Laurent Pasquier,Nicole Porchet,Muriel Holder‐Espinasse,Sylvie Manouvrier‐Hanu,Fabienne Escande	17
9	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 2013 ·American Journal of Medical Genetics Part A ·Radu Harbuz,Frédéric Bilan,(unknown),(unknown),Alain Kitzis,Brigitte Gilbert‐Dussardier	12
10	Altered quality of life in Rendu-Osler-Weber disease related to recurrent epistaxis 2011 ·Rhinology Journal ·Isabelle Ingrand,Pierre Ingrand,Brigitte Gilbert‐Dussardier,Gautier Défossez,Vianney Jouhet,(unknown),Xavier Dufour,J.‐M. Klossek	38
11	Isolated Congenital Asplenia: A French Nationwide Retrospective Survey of 20 Cases 2010 ·The Journal of Pediatrics ·Nizar Mahlaoui,Véronique Minard‐Colin,Capucine Pïcard,Alexandre Bolze,Cheng‐Lung Ku,Olivier Tournilhac,Brigitte Gilbert‐Dussardier,Brigitte Pautard,Philippe Durand,Denis Devictor,Eric Lachassinne,B. Guillois,Michel Morin,François Gouraud,Françoise Valensi,Alain Fischer,Anne Puel,Laurent Abel,Damien Bonnet,Jean‐Laurent Casanova	36
12	Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Type 2 Caused by Mitofusin 2 Mutations 2009 ·Archives of Neurology ·(unknown),Benoît Funalot,Robert Ouvrier,Leïla Lazaro,Annick Toutain,P. De Mas,P. Bouché,Brigitte Gilbert‐Dussardier,Marie‐Christine Arné‐Bes,(unknown),Hubert Journel,Marie-Christine Minot-Myhié,Claire Le Guillou,Karima Ghorab,Laurent Magy,Franck Sturtz,Jean‐Michel Vallat,Corinne Magdelaine	92
13	Le syndrome de Williams-Beuren : une approche pluridisciplinaire 2008 ·Archives de Pédiatrie ·Agnès Lacroix,Mylène Pezet,(unknown),Damien Bonnet,Martine Hennèquin,M.P. Jacob,(unknown),(unknown),Gilles Faury,Josie Bernicot,Brigitte Gilbert‐Dussardier	9
14	Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network 2007 ·Genetics in Medicine ·Gaëtan Lesca,Carla Olivieri,Nelly Burnichon,Fabio Pagella,Marie‐France Carette,Brigitte Gilbert‐Dussardier,Cyril Goizet,J. Roume,Muriel Rabilloud,Jean‐Christophe Saurin,Vincent Cottin,Jérôme Honnorat,Florence Coulet,Sophie Giraud,Alain Calender,Cesare Danesino,Elisabetta Buscarini,Henri Plauchu	157
15	Germinal mosaicism and familial recurrence of a SOX2 mutation with highly variable phenotypic expression extending from AEG syndrome to absence of ocular involvement 2007 ·American Journal of Medical Genetics Part A ·Nicolas Chassaing,Brigitte Gilbert‐Dussardier,Florence Nicot,V. Fermeaux,Férechté Encha‐Razavi,(unknown),Annick Toutain,Patrick Calvas	38
16	Syndrome d’Oguchi ou cécité nocturne congénitale stationnaire : à propos d’un cas 2007 ·Journal Français d Ophtalmologie ·M Boissonnot,(unknown),Brigitte Gilbert‐Dussardier,P. Dighiero	2
17	Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation 2006 ·European Journal of Human Genetics ·Pascale Saugier-Véber,Alice Goldenberg,Valérie Drouin‐Garraud,(unknown),Valérie Layet,Nathalie Drouot,Nathalie Le Meur,Brigitte Gilbert‐Dussardier,Géraldine Joly‐Hélas,Hélène Moirot,Annick Rossi,Mario Tosi,Thierry Frébourg	27
18	Screening of ARX in mental retardation families: consequences for the strategy of molecular diagnosis 2005 ·Neurogenetics ·Karine Poirier,Didier Lacombe,Brigitte Gilbert‐Dussardier,Martine Raynaud,Vincent Desportes,Arjan P.M. de Brouwer,Claude Moraine,J P Fryns,Hans‐Hilger Ropers,C. Beldjord,Jamel Chelly,Thierry Bienvenu	32
19	X-linked dominant chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia 2005 ·American Journal of Medical Genetics Part A ·Nicolas Chassaing,(unknown),Dominique Carles,Anne Lise Delezoïde,(unknown),Jacques Battin,Jean‐François Chateil,Brigitte Gilbert‐Dussardier,Isabelle Coupry,Benoı̂t Arveiler,Robert Saura,Didier Lacombe	11
20	A novel arginine (245) to glutamine change in exon 8 of the ornithine carbamoyl transferase gene in two unrelated children presenting with late onset deficiency and showing the same enzymatic pattern 1994 ·Human Molecular Genetics ·Brigitte Gilbert‐Dussardier,Daniel Rabier,Sandra Strautnieks,(unknown),Jean‐Paul Bonnefont,(unknown)	5

About Brigitte Gilbert‐Dussardier

Brigitte Gilbert‐Dussardier is a scholar working on Genetics, Clinical Biochemistry and Genetics, having authored 48 papers that have together received 1.4k indexed citations. Recurring topics across this work include Tracheal and airway disorders (11 papers), Genomic variations and chromosomal abnormalities (9 papers) and Vascular Anomalies and Treatments (7 papers). The work is most often cited by research in Genetics (444 citations), Sensory Systems (75 citations) and Genetics (369 citations). Brigitte Gilbert‐Dussardier has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Dominique Bonneau, Patrick Edery, Albert David, Valérie Layet, Nicolas Sévenet, Françoise Bonnet, Michel Longy, F. Caux, Gaëtan Lesca and Alain Calender. Their work appears in journals such as JAMA, PLoS ONE and Annals of Neurology.

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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