Audrey Briand‐Suleau

1.0k citations

16 papers · 437 indexed · h-index 11

Co-authors: Éric Pasmant Michel Goossens Dominique Vidaud Ingrid Laurendeau Armelle Luscan Sophie Brisset Gérard Tachdjian Michel Vidaud
Topics: Neurofibromatosis and Schwannoma Cases (5 papers)Genomic variations and chromosomal abnormalities (3 papers)Renal and related cancers (2 papers)
Cited by: Neurology Reproductive Medicine Genetics
Journals: PLoS ONE Human Molecular Genetics Human Reproduction
Partner nations: France Czechia United States

In The Last Decade

Audrey Briand‐Suleau

16 papers receiving 419 citations

Peers

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

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16 of 16 papers shown

#	Work	Indexed citations
1	Droplet Digital PCR for Fast and Accurate Characterization of NF1 Locus Deletions 2023 ·Journal of Molecular Diagnostics ·(unknown),(unknown),Juliette Nectoux,Ingrid Laurendeau,Audrey Briand‐Suleau,(unknown),(unknown),(unknown),(unknown),(unknown),Hélène Blanché,Béatrice Parfait,P. Wolkenstein,Michel Vidaud,Elisabeth Castellanos,Marinus J. Blok,Hilde Brems,Magdalena Koczkowska,(unknown),Katharina Wimmer,Dominique Vidaud,(unknown)	3
2	Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders 2021 ·Molecular Psychiatry ·Elma El Khouri,Jamal Ghoumid,Damien Haye,Fabienne Giuliano,(unknown),Audrey Briand‐Suleau,Pascal Grange,Valérie Nau,(unknown),Thierry Bienvenu,Hélène Jacquemin‐Sablon,Michel Goossens,Serge Amselem,Irina Giurgea	11
3	NF1-like optic pathway gliomas in children: clinical and molecular characterization of this specific presentation 2019 ·Neuro-Oncology Advances ·(unknown),Ingrid Laurendeau,Léa Guerrini‐Rousseau,Arnault Tauziède‐Espariat,Audrey Briand‐Suleau,Pascale Varlet,Dominique Vidaud,Michel Vidaud,Laurence Brugières,Jacques Grill,Éric Pasmant	7
4	Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis 2018 ·Neuro-Oncology ·Camille Louvrier,Éric Pasmant,Audrey Briand‐Suleau,(unknown),Patrick Nitschké,Juliette Nectoux,(unknown),Cécile Zordan,Cyril Goizet,Stéphane Goutagny,Dominique Lallemand,Michel Vidaud,Dominique Vidaud,Michel Kalamarides,Béatrice Parfait	49
5	Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome 2017 ·European Journal of Human Genetics ·Nicolas Lebrun,Irina Giurgea,Alice Goldenberg,Anne Dieux,Alexandra Afenjar,Jamal Ghoumid,(unknown),(unknown),Audrey Briand‐Suleau,Pierre Billuart,Thierry Bienvenu	25
6	Confirmation of mutation landscape of NF1‐associated malignant peripheral nerve sheath tumors 2017 ·Genes Chromosomes and Cancer ·Pierre Sohier,Armelle Luscan,Angharad Lloyd,Kevin E. Ashelford,Ingrid Laurendeau,Audrey Briand‐Suleau,Dominique Vidaud,Nicolás Ortonne,Éric Pasmant,Meena Upadhyaya	47
7	Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: A two-hit case with more severe clinical manifestations 2015 ·European Journal of Medical Genetics ·Sophie Brisset,Yline Capri,Audrey Briand‐Suleau,Lucie Tosca,Domitille Gras,(unknown),(unknown),Julien Saada,(unknown),Alain Verloès,Michel Goossens,Gérard Tachdjian,Corinne Métay	19
8	Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts 2015 ·European Journal of Medical Genetics ·Laure Raymond,Bruno Francou,François Petit,Lucie Tosca,Audrey Briand‐Suleau,Corinne Métay,Jelena Martinović,Anne‐Gaël Cordier,Alexandra Benachi,(unknown),Anne Guiochon‐Mantel,Michel Goossens,Gérard Tachdjian,Sophie Brisset	3
9	Sub1 and Maf1, Two Effectors of RNA Polymerase III, Are Involved in the Yeast Quiescence Cycle 2014 ·PLoS ONE ·Joël Acker,(unknown),Marie Vandamme,(unknown),Audrey Briand‐Suleau,Christine Conesa	11
10	SALL4 and NFATC2: Two major actors of interstitial 20q13.2 duplication 2014 ·European Journal of Medical Genetics ·Audrey Briand‐Suleau,Jelena Martinović,Lucie Tosca,(unknown),Sophie Brisset,Jérôme Bouligand,(unknown),Irina Giurgea,(unknown),(unknown),Carole Goumy,Christine Francannet,Anne Guiochon‐Mantel,Alexandra Benachi,Joris Vermeesch,Gérard Tachdjian,Philippe Vago,Michel Goossens,Corinne Métay	2
11	Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations? 2014 ·European Journal of Human Genetics ·Éric Pasmant,Béatrice Parfait,Armelle Luscan,P. Goussard,Audrey Briand‐Suleau,Ingrid Laurendeau,Corinne Fouveaut,Chrystel Leroy,(unknown),P. Wolkenstein,Michel Vidaud,Dominique Vidaud	75
12	Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23 2014 ·Molecular Cytogenetics ·Sophie Brisset,(unknown),Petra Dušátková,Audrey Briand‐Suleau,Karen Milcent,Corinne Métay,(unknown),Zdenĕk Šumnı́k,Lucie Tosca,Michel Goossens,Philippe Labrune,(unknown),Jan Lebl,Gérard Tachdjian,Zdeněk Sedláček	11
13	KBP–cytoskeleton interactions underlie developmental anomalies in Goldberg–Shprintzen syndrome 2013 ·Human Molecular Genetics ·(unknown),André Mégarbané,Bénédicte Demeer,(unknown),Paule Bénit,Audrey Briand‐Suleau,(unknown),Jamal Ghoumid,(unknown),Xavier Decrouy,Martine Doco‐Fenzy,Pierre Rustin,Dominique Gaillard,Michel Goossens,Irina Giurgea	24
14	ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat–Wilson syndrome 2013 ·Human Molecular Genetics ·Jamal Ghoumid,(unknown),(unknown),Nadège Bondurand,Marlène Rio,Audrey Briand‐Suleau,(unknown),Linda Goodwin,(unknown),Constantin Yanicostas,Michel Goossens,Stanislas Lyonnet,David Mowat,Jeanne Amiel,Nadia Soussi‐Yanicostas,Irina Giurgea	41
15	SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development 2012 ·Human Reproduction ·Jacques Young,Corinne Métay,Jérôme Bouligand,(unknown),Bruno Francou,Luigi Maione,Lucie Tosca,Julie Sarfati,Frédéric Brioude,Blandine Esteva,Audrey Briand‐Suleau,Sophie Brisset,Michel Goossens,Gérard Tachdjian,Anne Guiochon‐Mantel	99
16	Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility 2011 ·Reproductive BioMedicine Online ·(unknown),Lucie Tosca,(unknown),Cécile Bas,Laure Lecerf,Jacques Young,Audrey Briand‐Suleau,(unknown),Jérôme Bouligand,Sophie Brisset,Micheline Misrahi,Anne Guiochon‐Mantel,Michel Goossens,Gérard Tachdjian	10

About Audrey Briand‐Suleau

Audrey Briand‐Suleau is a scholar working on Aging, Genetics and Neurology, having authored 16 papers that have together received 437 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Renal and related cancers (2 papers). The work is most often cited by research in Neurology (151 citations), Reproductive Medicine (64 citations) and Genetics (122 citations). Audrey Briand‐Suleau has collaborated with scholars based in France, Czechia and United States. Frequent co-authors include Éric Pasmant, Michel Goossens, Dominique Vidaud, Ingrid Laurendeau, Armelle Luscan, Sophie Brisset, Gérard Tachdjian, Michel Vidaud, Béatrice Parfait and Lucie Tosca. Their work appears in journals such as PLoS ONE, Human Molecular Genetics and Human Reproduction.

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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