Audrey Briand‐Suleau

1.0k total citations
16 papers, 437 citations indexed

About

Audrey Briand‐Suleau is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Audrey Briand‐Suleau has authored 16 papers receiving a total of 437 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in Audrey Briand‐Suleau's work include Neurofibromatosis and Schwannoma Cases (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Renal and related cancers (2 papers). Audrey Briand‐Suleau is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Renal and related cancers (2 papers). Audrey Briand‐Suleau collaborates with scholars based in France, United States and Lebanon. Audrey Briand‐Suleau's co-authors include Dominique Vidaud, Michel Goossens, Éric Pasmant, Ingrid Laurendeau, Armelle Luscan, Gérard Tachdjian, Sophie Brisset, Lucie Tosca, Michel Vidaud and Béatrice Parfait and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Human Reproduction.

In The Last Decade

Audrey Briand‐Suleau

16 papers receiving 419 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Audrey Briand‐Suleau France 11 168 151 122 69 64 16 437
Khawar Siddique United States 8 65 0.4× 35 0.2× 78 0.6× 18 0.3× 56 0.9× 12 365
Virginia C. Thurston United States 12 297 1.8× 50 0.3× 224 1.8× 56 0.8× 36 0.6× 17 599
Reema L. Habiby United States 13 569 3.4× 125 0.8× 491 4.0× 51 0.7× 261 4.1× 23 932
Olga Dratviman‐Storobinsky Israel 15 214 1.3× 32 0.2× 82 0.7× 28 0.4× 66 1.0× 31 509
Marylène Rousseau Canada 8 106 0.6× 111 0.7× 125 1.0× 26 0.4× 6 0.1× 9 345
Tadeusz Mazurczak Poland 17 299 1.8× 29 0.2× 444 3.6× 60 0.9× 16 0.3× 57 763
Guoqing Wang China 11 57 0.3× 111 0.7× 17 0.1× 40 0.6× 41 0.6× 23 403
Oronzo Scarciolla Italy 10 222 1.3× 54 0.4× 71 0.6× 8 0.1× 25 0.4× 12 386
Goran Brajušković Serbia 13 343 2.0× 51 0.3× 45 0.4× 42 0.6× 13 0.2× 68 511
Louise Gregory United Kingdom 14 224 1.3× 31 0.2× 171 1.4× 25 0.4× 35 0.5× 25 520

Countries citing papers authored by Audrey Briand‐Suleau

Since Specialization
Citations

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

Fields of papers citing papers by Audrey Briand‐Suleau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Audrey Briand‐Suleau. 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 Audrey Briand‐Suleau. The network helps show where Audrey Briand‐Suleau may publish in the future.

Co-authorship network of co-authors of Audrey Briand‐Suleau

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

All Works

16 of 16 papers shown
1.
Nectoux, Juliette, Ingrid Laurendeau, Audrey Briand‐Suleau, et al.. (2023). Droplet Digital PCR for Fast and Accurate Characterization of NF1 Locus Deletions. Journal of Molecular Diagnostics. 26(2). 150–157. 3 indexed citations
2.
Khouri, Elma El, Jamal Ghoumid, Damien Haye, et al.. (2021). Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders. Molecular Psychiatry. 26(7). 3572–3585. 11 indexed citations
3.
Laurendeau, Ingrid, Léa Guerrini‐Rousseau, Arnault Tauziède‐Espariat, et al.. (2019). NF1-like optic pathway gliomas in children: clinical and molecular characterization of this specific presentation. Neuro-Oncology Advances. 2(Supplement_1). i98–i106. 7 indexed citations
4.
Louvrier, Camille, Éric Pasmant, Audrey Briand‐Suleau, et al.. (2018). Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis. Neuro-Oncology. 20(7). 917–929. 49 indexed citations
5.
Lebrun, Nicolas, Irina Giurgea, Alice Goldenberg, et al.. (2017). Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome. European Journal of Human Genetics. 26(1). 107–116. 25 indexed citations
6.
Sohier, Pierre, Armelle Luscan, Angharad Lloyd, et al.. (2017). Confirmation of mutation landscape of NF1‐associated malignant peripheral nerve sheath tumors. Genes Chromosomes and Cancer. 56(5). 421–426. 47 indexed citations
7.
Raymond, Laure, Bruno Francou, François Petit, et al.. (2015). Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts. European Journal of Medical Genetics. 58(11). 591–596. 3 indexed citations
8.
Brisset, Sophie, Yline Capri, Audrey Briand‐Suleau, et al.. (2015). Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: A two-hit case with more severe clinical manifestations. European Journal of Medical Genetics. 58(9). 497–501. 19 indexed citations
9.
Pasmant, Éric, Béatrice Parfait, Armelle Luscan, et al.. (2014). Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations?. European Journal of Human Genetics. 23(5). 596–601. 75 indexed citations
10.
Acker, Joël, et al.. (2014). Sub1 and Maf1, Two Effectors of RNA Polymerase III, Are Involved in the Yeast Quiescence Cycle. PLoS ONE. 9(12). e114587–e114587. 11 indexed citations
11.
Briand‐Suleau, Audrey, Jelena Martinović, Lucie Tosca, et al.. (2014). SALL4 and NFATC2: Two major actors of interstitial 20q13.2 duplication. European Journal of Medical Genetics. 57(4). 174–180. 2 indexed citations
12.
Brisset, Sophie, Petra Dušátková, Audrey Briand‐Suleau, et al.. (2014). Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23. Molecular Cytogenetics. 7(1). 17–17. 11 indexed citations
13.
Mégarbané, André, Bénédicte Demeer, Paule Bénit, et al.. (2013). KBP–cytoskeleton interactions underlie developmental anomalies in Goldberg–Shprintzen syndrome. Human Molecular Genetics. 22(12). 2387–2399. 24 indexed citations
14.
Ghoumid, Jamal, Nadège Bondurand, Marlène Rio, et al.. (2013). ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat–Wilson syndrome. Human Molecular Genetics. 22(13). 2652–2661. 41 indexed citations
15.
Young, Jacques, Corinne Métay, Jérôme Bouligand, et al.. (2012). SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development. Human Reproduction. 27(5). 1460–1465. 99 indexed citations
16.
Tosca, Lucie, Cécile Bas, Laure Lecerf, et al.. (2011). Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility. Reproductive BioMedicine Online. 24(1). 72–82. 10 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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