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Alain Verloes
Researcher at University of Paris
Publications - 464
Citations - 21574
Alain Verloes is an academic researcher from University of Paris. The author has contributed to research in topics: Microcephaly & Noonan syndrome. The author has an hindex of 73, co-authored 450 publications receiving 19231 citations. Previous affiliations of Alain Verloes include Institut Universitaire de France & Max Planck Society.
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Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French setting
A.-L. Soilly,Charley Robert-Viard,Céline Besse,Bénédicte Gérard,Anne Boland,Amélie Piton,Yannis Duffourd,Jacques Muller,Charlotte Pöe,Thibaut Jouan,Laurence Faivre,Delphine Bacq-Daian,Bertand Isidor,David Geneviève,Sylvie Odent,Nicole Philip,Martine Doco-Fenzy,Didier Lacombe,JF Deleuze,Christine Binquet,Stéphanie Arpin,Patricia Blanchet,Sophie Blesson,Odile Boute-Benejean,Tiffany Busa,Estelle Colin,Christine Coubes,Françoise Devillard,Patrick Edery,Salima El Chehadeh,Mélanie Fradin,Alice Goldenberg,Anne-Marie Guerrot,Yvan Herenger,Nada Houcinat,Nolwenn Jean-Marçais,Pierre-Simon Jouk,Laetitia Lambert,Alinoë Lavillaureix,Marie Legendre,Bruno Leheup,Sylvie Manouvrier,Sandra Mercier,Sébastien Moutton,Mathilde Nizon,Laurent Pasquier,Florence Petit,Lucile Pinson,Céline Poirsier,Linda Pons,Audrey Putoux,Chloé Quélin,M. Renaud,Mari Rossi,Arthur Sorlin,Marta Spodenkiewicz,Julien Thevenon,Annick Toutain,Julien Van-Gils,Clémence Vanlerberghe,Alain Verloes,Marie Vincent,Caroline Vincent-Delorme,Marjorie Willems,AG Ziegler,Christel Thauvin-Robinet,Clara Lejeune +66 more
TL;DR: In this article , a micro-costing bottom-up approach was conducted for the year 2018 in a French setting as part of the DISSEQ study, a cost-effectiveness study funded by the Ministry of Health and performed in collaboration with the GAD (Génétique des Anomalies du Développement) , a genetic team from the Dijon University Hospital, and a public sequencing platform, the Centre National de Recherche en Génomique Humaine (CNRGH).
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L'isolation des cellules fœtales en circulation dans le sang maternel: mise au point*
TL;DR: Les perspectives d'avenir sont cependant prometteuses, sans qu'on puisse encore prevoir le moment ou le diagnostic d'une affection genetique du foetus pourra etre pose en routine a partir d'un simple prise de sang maternelle.
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Bloom syndrome in children: unusual case of early onset lung damage.
H. Ajmi,I. Trabelsi,khouloud Rjiba,Sameh Mabrouk,N. Zouari,Soumaya Mougou-Zerelli,Alain Verloes,S. Abroug +7 more
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New dysostosis showing multilevel absence of vertebral pedicles: unique developmental anomaly of vertebral arches?
TL;DR: An apparently normal child who shows hypopaplasia of the vertebral pedicles and posterior arches of several cervical, thoracic, and lumbar vertebrae with normally fused spinous apophyses, hypoplastic sacrum,Lumbar epidural lipomatosis, synostoses of some cervical vertebral disks, and sacral spina bifida is reported.
New Syndrome A New Syndrome of Congenital Generalized Osteosclerosis and Bilateral Polymicrogyria
Luigi Titomanlio,Clarisse Baumann,Gheorghe Bonyhay,Edith Vuillard,Catherine Garel,Patricia Terdjman,Alain Verloes,Anne-Lise Delezoide +7 more
TL;DR: In this paper, a 29-week male fetus with healthy con-sanguineous parents showed a severe scleros-ing bone disorder affecting all skeletal elements,resulting in insufficient modeling, generalized densification, and fragility of the skeleton.