Valérie Layet

3.7k citations

22 papers · 925 indexed · h-index 13

Co-authors: Catherine Dugast Thierry Frébourg Michel Longy Sophie Krieger Antoine Rousselin Pascaline Berthet Agnès Hardouin Brigitte Gilbert‐Dussardier
Topics: Genomic variations and chromosomal abnormalities (4 papers)Skin and Cellular Biology Research (3 papers)Genetic and Kidney Cyst Diseases (3 papers)
Cited by: Genetics Cancer Research Molecular Biology
Journals: The American Journal of Human Genetics Human Reproduction Journal of Medical Genetics
Partner nations: France Netherlands Belgium

In The Last Decade

Valérie Layet

21 papers receiving 914 citations

Peers

Countries citing papers authored by Valérie Layet

Since Specialization

Citations

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

Fields of papers citing papers by Valérie Layet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valérie Layet

This figure shows the co-authorship network connecting the top 25 collaborators of Valérie Layet. A scholar is included among the top collaborators of Valérie Layet 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 Valérie Layet. Valérie Layet 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	A novel insertion (c.1098dupT) in the albumin gene causes analbuminemia in a consanguineous family 2018 ·European Journal of Medical Genetics ·Gianluca Caridi,Francesca Lugani,Brigitte Rigat,(unknown),Valérie Layet,(unknown),Monica Campagnoli,Monica Galliano,Lorenzo Minchiotti	4
2	Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene 2017 ·Acta Neuropathologica Communications ·Pascale Saugier-Véber,Florent Marguet,François Lecoquierre,Homa Adle‐Biassette,Fabien Guimiot,Sara Cipriani,Sophie Patrier,M. Brasseur‐Daudruy,Alice Goldenberg,Valérie Layet,Yline Capri,Marion Gérard,Thierry Frébourg,Annie Laquerrière	23
3	BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer 2016 ·Familial Cancer ·(unknown),(unknown),Audrey Emmanuelle Dugué,Angélina Legros,Alexandra Leconte,Bénédicte Clarisse,(unknown),(unknown),Catherine Dugast,Caroline Abadie,Thierry Frébourg,Julie Tinat,Isabelle Tennevet,Valérie Layet,Florence Joly,Laurent Castéra,Pascaline Berthet,Dominique Vaur,Sophie Krieger	0
4	Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes 2014 ·European Journal of Human Genetics ·Laurent Castéra,Sophie Krieger,Antoine Rousselin,Angélina Legros,(unknown),(unknown),Baptiste Brault,(unknown),Nicolas Goardon,(unknown),Stéphanie Baert‐Desurmont,Julie Tinat,Odile Béra,Catherine Dugast,Pascaline Berthet,(unknown),Valérie Layet,Agnès Hardouin,Thierry Frébourg,Dominique Vaur	175
5	CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study 2014 ·Orphanet Journal of Rare Diseases ·Ennio Del Giudice,(unknown),(unknown),Alessandra D’Amico,Philippe Parent,Laurent Pasquier,Valérie Layet,Stanislas Lyonnet,(unknown),Christel Thauvin‐Robinet,Brunella Franco,(unknown)	29
6	High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome 2013 ·Journal of Medical Genetics ·Virginie Bubien,Françoise Bonnet,Véronique Brouste,Stéphanie Hoppe,Emmanuelle Barouk-Simonet,Albert David,Patrick Edery,Armand Bottani,Valérie Layet,Olivier Caron,Brigitte Gilbert‐Dussardier,Capucine Delnatte,Catherine Dugast,Jean‐Pierre Fricker,Dominique Bonneau,Nicolas Sévenet,Michel Longy,F. Caux,(unknown)	225
7	Foetal presentation of cartilage hair hypoplasia with extensive granulomatous inflammation 2013 ·European Journal of Medical Genetics ·Marie Crahès,Pascale Saugier-Véber,Sophie Patrier,Moutaz Aziz,(unknown),M. Brasseur‐Daudruy,Valérie Layet,Thierry Frébourg,Annie Laquerrière	6
8	Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity 2013 ·Orphanet Journal of Rare Diseases ·S. Hadj‐Rabia,Bert Callewaert,E. Bourrat,Marlies Kempers,Astrid S. Plomp,Valérie Layet,Deborah Bartholdi,Marjolijn Renard,Julie De Backer,Fransiska Malfait,Olivier Vanakker,Paul Coucke,Anne M. De Paepe,Christine Bodemer	25
9	Sirenomelia and caudal malformations in two families 2012 ·American Journal of Medical Genetics Part A ·Marion Gérard,Valérie Layet,(unknown),(unknown),(unknown),(unknown),Bénédicte Gérard	9
10	Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndrome 2011 ·Human Reproduction ·Nicolas Gruchy,François Vialard,Matthieu Décamp,Agnès Choiset,(unknown),Nathalie Le Meur,Hélène Moirot,Catherine Yardin,(unknown),J. Lespinasse,(unknown),Marianne Till,Valérie Layet,Nathalie Leporrier	19
11	Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome 2010 ·The American Journal of Human Genetics ·Valérie Malan,Diana Rajan,Sophie Thomas,Adam Shaw,(unknown),Valérie Layet,Marianne Till,Arie van Haeringen,Geert Mortier,Sheela Nampoothiri,Silvija Pušeljić,Laurence Legeai‐Mallet,(unknown),Michel Vekemans,Arnold Münnich,Raoul C. M. Hennekam,Laurence Colleaux,Valérie Cormier‐Daire	107
12	Mutational spectrum of CDKL5 in early‐onset encephalopathies: a study of a large collection of French patients and review of the literature 2009 ·Clinical Genetics ·Christophe Némos,Laëtitia Lambert,Fabienne Giuliano,Bérénice Doray,(unknown),Alice Goldenberg,B Delobel,Valérie Layet,(unknown),(unknown),(unknown),Philippe Jonveaux,Christophe Philippe	83
13	Screening BRCA1 and BRCA2 unclassified variants for splicing mutations using reverse transcription PCR on patient RNA and an ex vivo assay based on a splicing reporter minigene 2008 ·Journal of Medical Genetics ·Céline Bonnet,Sophie Krieger,Myriam Vézain,Antoine Rousselin,Isabelle Tournier,Alexandra Martins,Pascaline Berthet,Annie Chevrier,Catherine Dugast,Valérie Layet,Anita De Rossi,Rosette Lidereau,Thierry Frébourg,Agnès Hardouin,Mario Tosi	89
14	High frequency of missense mutations in glycogen storage disease type VI 2007 ·Journal of Inherited Metabolic Disease ·Nicholas Beauchamp,Joanna Taybert,M. P. Champion,Valérie Layet,Peter Heinz‐Erian,A. Dalton,M S Tanner,Ewa Pronicka,Mark Sharrard	31
15	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
16	Early‐onset low‐grade papillary carcinoma of the bladder associated with Apert syndrome and a germline FGFR2 mutation (Pro253Arg) 2006 ·American Journal of Medical Genetics Part A ·Andreas Y. Andreou,Aude Lamy,Valérie Layet,(unknown),Françoise Gobet,Christian Pfister,Michel Ménard,Thierry Frébourg	13
17	Gorlin syndrome presenting as prenatal chylothorax in a girl 2005 ·Prenatal Diagnosis ·David Geneviève,R. Walter,Philippe Gorry,(unknown),(unknown),Valérie Layet,Arnold Münnich,Valérie Cormier‐Daire,Marc Dommergues,Stanislas Lyonnet,Delphine Mitanchez	8
18	Association between Cowden syndrome and Lhermitte-Duclos disease 2004 ·Surgical Neurology ·Stéphane Derrey,F. Proust,Bertrand Debono,Olivier Langlois,(unknown),Valérie Layet,Michel Longy,P. Fréger,Annie Laquerrière	33
19	Association d'une aplasie cutanée congénitale et d'une coarctation de l'aorte: association fortuite ? 1999 ·Archives de Pédiatrie ·H. Bruel,(unknown),(unknown),Valérie Layet	4
20	Encéphalopathie myoclonique précoce et hyperglycinémie sans cétose dans une même fratrie 1998 ·Archives de Pédiatrie ·H. Bruel,(unknown),(unknown),Valérie Layet,(unknown)	3

About Valérie Layet

Valérie Layet is a scholar working on Genetics, Cell Biology and Molecular Biology, having authored 22 papers that have together received 925 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Skin and Cellular Biology Research (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). The work is most often cited by research in Genetics (513 citations), Cancer Research (165 citations) and Molecular Biology (506 citations). Valérie Layet has collaborated with scholars based in France, Netherlands and Belgium. Frequent co-authors include Catherine Dugast, Thierry Frébourg, Michel Longy, Sophie Krieger, Antoine Rousselin, Pascaline Berthet, Agnès Hardouin, Brigitte Gilbert‐Dussardier, Albert David and Emmanuelle Barouk-Simonet. Their work appears in journals such as The American Journal of Human Genetics, Human Reproduction and Journal of Medical Genetics.

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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