Valérie Layet

3.7k citations

22 papers · 925 indexed · h-index 13

Genetics top 5%
- Genomic variations and chromosomal abnormalities 4
- Genetic and Kidney Cyst Diseases 3
- BRCA gene mutations in cancer 2
Cancer Research top 10%
Molecular Biology
- Hedgehog Signaling Pathway Studies 2
- PI3K/AKT/mTOR signaling in cancer 2
Pathology and Forensic Medicine top 10%
Developmental Neuroscience
Cell Biology
- Skin and Cellular Biology Research 3
Rheumatology
- Glycogen Storage Diseases and Myoclonus 2
Pediatrics, Perinatology and Child Health
- Fetal and Pediatric Neurological Disorders 2

Co-authors: Catherine Dugast Thierry Frébourg Michel Longy Sophie Krieger Antoine Rousselin Pascaline Berthet Agnès Hardouin Brigitte Gilbert‐Dussardier
Cited by: Genetics Cancer Research Molecular Biology
Journals: The American Journal of Human Genetics (1 paper)Human Reproduction (1 paper)Journal of Medical Genetics (2 papers)
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

The 25 scholars most cited alongside Valérie Layet, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Valérie Layet Line = papers co-authored together Valérie Layet links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A novel insertion (c.1098dupT) in the albumin gene causes analbuminemia in a consanguineous family European Journal of Medical Genetics ·Gianluca Caridi,Francesca Lugani,Brigitte Rigat,Patrick Van den Abeele,Valérie Layet,Marie-Sophie Gavard,Monica Campagnoli,Monica Galliano,Lorenzo Minchiotti	2018	4
2	Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene 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	2017	23
3	BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer Familial Cancer ·Estelle Jamard,Bertrand Volard,Audrey Emmanuelle Dugué,Angélina Legros,Alexandra Leconte,Bénédicte Clarisse,Grégoire Davy,Florence Polycarpe,Catherine Dugast,Caroline Abadie,Thierry Frébourg,Julie Tinat,Isabelle Tennevet,Valérie Layet,Florence Joly,Laurent Castéra,Pascaline Berthet,Dominique Vaur,Sophie Krieger	2016	0
4	Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes European Journal of Human Genetics ·Laurent Castéra,Sophie Krieger,Antoine Rousselin,Angélina Legros,Jean-Jacques Baumann,Olivia Bruet,Baptiste Brault,Robin Fouillet,Nicolas Goardon,Olivier Letac,Stéphanie Baert‐Desurmont,Julie Tinat,Odile Béra,Catherine Dugast,Pascaline Berthet,Florence Polycarpe,Valérie Layet,Agnès Hardouin,Thierry Frébourg,Dominique Vaur	2014	175
5	CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study Orphanet Journal of Rare Diseases ·Ennio Del Giudice,Marina Macca,Floriana Imperati,Alessandra D’Amico,Philippe Parent,Laurent Pasquier,Valérie Layet,Stanislas Lyonnet,Veronique Stamboul-Darmency,Christel Thauvin‐Robinet,Brunella Franco,(unknown)	2014	29
6	High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome 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)	2013	225
7	Foetal presentation of cartilage hair hypoplasia with extensive granulomatous inflammation European Journal of Medical Genetics ·Marie Crahès,Pascale Saugier-Véber,Sophie Patrier,Moutaz Aziz,Nathalie Pirot,M. Brasseur‐Daudruy,Valérie Layet,Thierry Frébourg,Annie Laquerrière	2013	6
8	Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity 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	2013	25
9	Sirenomelia and caudal malformations in two families American Journal of Medical Genetics Part A ·Marion Gérard,Valérie Layet,Teresa Costa,Yves Roumazeilles,Pierre Chenal,Daniel Cailliez,Bénédicte Gérard	2012	9
10	Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndrome Human Reproduction ·Nicolas Gruchy,François Vialard,Matthieu Décamp,Agnès Choiset,Anderson Diniz Rossi,Nathalie Le Meur,Hélène Moirot,Catherine Yardin,M.N. Bonnet-Dupeyron,J. Lespinasse,M. Herbaut-Graux,Marianne Till,Valérie Layet,Nathalie Leporrier	2011	19
11	Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome The American Journal of Human Genetics ·Valérie Malan,Diana Rajan,Sophie Thomas,Adam Shaw,H. Louis Dit Picard,Valérie Layet,Marianne Till,Arie van Haeringen,Geert Mortier,Sheela Nampoothiri,Silvija Pušeljić,Laurence Legeai‐Mallet,Nigel P. Carter,Michel Vekemans,Arnold Münnich,Raoul C. M. Hennekam,Laurence Colleaux,Valérie Cormier‐Daire	2010	107
12	Mutational spectrum of CDKL5 in early‐onset encephalopathies: a study of a large collection of French patients and review of the literature Clinical Genetics ·Christophe Némos,Laëtitia Lambert,Fabienne Giuliano,Bérénice Doray,A. Roubertie,Alice Goldenberg,B Delobel,Valérie Layet,M Ange N'guyen,Aline Saunier,F. Verneau,Philippe Jonveaux,Christophe Philippe	2009	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 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	2008	89
14	High frequency of missense mutations in glycogen storage disease type VI 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	2007	31
15	Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation European Journal of Human Genetics ·Pascale Saugier-Véber,Alice Goldenberg,Valérie Drouin‐Garraud,Céline de La Rochebrochard,Valérie Layet,Nathalie Drouot,Nathalie Le Meur,Brigitte Gilbert‐Dussardier,Géraldine Joly‐Hélas,Hélène Moirot,Annick Rossi,Mario Tosi,Thierry Frébourg	2006	27
16	Early‐onset low‐grade papillary carcinoma of the bladder associated with Apert syndrome and a germline FGFR2 mutation (Pro253Arg) American Journal of Medical Genetics Part A ·Andreas Y. Andreou,Aude Lamy,Valérie Layet,Daniel Cailliez,Françoise Gobet,Christian Pfister,Michel Ménard,Thierry Frébourg	2006	13
17	Gorlin syndrome presenting as prenatal chylothorax in a girl Prenatal Diagnosis ·David Geneviève,R. Walter,Philippe Gorry,M-L Jacquemont,L. Dupic,Valérie Layet,Arnold Münnich,Valérie Cormier‐Daire,Marc Dommergues,Stanislas Lyonnet,Delphine Mitanchez	2005	8
18	Association between Cowden syndrome and Lhermitte-Duclos disease Surgical Neurology ·Stéphane Derrey,F. Proust,Bertrand Debono,Olivier Langlois,Antoine Layet,Valérie Layet,Michel Longy,P. Fréger,Annie Laquerrière	2004	33
19	Association d'une aplasie cutanée congénitale et d'une coarctation de l'aorte: association fortuite ? Archives de Pédiatrie ·H. Bruel,J. Poinsot,J.P. Chabrolle,Valérie Layet	1999	4
20	Encéphalopathie myoclonique précoce et hyperglycinémie sans cétose dans une même fratrie Archives de Pédiatrie ·H. Bruel,J. Boulloche,J.P. Chabrolle,Valérie Layet,J. Poinsot	1998	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), Genetic and Kidney Cyst Diseases (3 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Hedgehog Signaling Pathway Studies (2 papers), BRCA gene mutations in cancer (2 papers), PI3K/AKT/mTOR signaling in cancer (2 papers) and Fetal and Pediatric Neurological Disorders (2 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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