Výsledky vyhledávání - "Valérie, Layet"

Akademický článek

Outcomes of 4 years of molecular genetic diagnosis on a panel of genes involved in premature aging syndromes, including laminopathies and related disorders

Publikováno v: Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-16 (2019)

Abstract Background Segmental progeroid syndromes are a heterogeneous group of rare and often severe genetic disorders that have been studied since the twentieth century. These progeroid syndromes are defined as segmental because only some of the fea

Externí odkaz: https://doaj.org/article/5b8ec6fec4c7421196987198b3d889a0

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Akademický článek

Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene

Autor: Pascale Saugier-Veber, Florent Marguet, François Lecoquierre, Homa Adle-Biassette, Fabien Guimiot, Sara Cipriani, Sophie Patrier, Marie Brasseur-Daudruy, Alice Goldenberg, Valérie Layet, Yline Capri, Marion Gérard, Thierry Frébourg, Annie Laquerrière

Publikováno v: Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-12 (2017)

Abstract Congenital hydrocephalus is considered as either acquired due to haemorrhage, infection or neoplasia or as of developmental nature and is divided into two subgroups, communicating and obstructive. Congenital hydrocephalus is either syndromic

Externí odkaz: https://doaj.org/article/8adcfada33254a5ea2c7dbc4263f1ac2

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Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder

Autor: Marjolaine Willems, Benjamin Durand, Boris Keren, Kristina Pilekær Sørensen, Rosanna Weksberg, Magalie Barth, Christina Fagerberg, Cyril Mignot, Laurence Perrin, Lucas Bronicki, Nathalie Drouot, Imene Boujelbene, Marc Abramowicz, Maria Kibaek, Bertrand Isidor, Thierry Bienvenu, Mathilde Nizon, Perrine Charles, Laurent Pasquier, Yann Herault, Marie Christine Birling, Bruno Delobel, Michel Guipponi, Lydie Burglen, Mélanie Fradin, Anne Sophie Denommé, Florence Demurger, Benjamin Cogné, Sébastien Moutton, Allan Bayat, Frederic Tran Mau Them, Christèle Dubourg, Alice Goldenberg, Christine Francannet, Jean-Louis Mandel, Laurence Faivre, Jérémie Courraud, Anne Marie Guerrot, Julia Metreau, Loréline Genschik, Bénédicte Demeer, Marie Vincent, Mathilde Renaud, Julien Thevenon, Sandrine Passemard, Christine Coubes, Amélie Piton, David Geneviève, Maria del Mar Muniz Moreno, Bénédicte Gérard, Estelle Colin, Valérie Layet, Michèle Mathieu-Dramard, Salima El Chehadeh, Katrine M Johannesen, Julie D. Thompson, Cathrine Elisabeth Tronhjem, Pascale Saugier, Elise Schaefer, Eric Chater-Diehl, Séverine Drunat, Rikke S. Møller, Paul Kuentz, Claire Feger, Albert David, Antonio Vitobello, Marlène Rio, Khaoula Khachnaoui, Joane Svane, Stéphane Auvin

Publikováno v: Genetics in Medicine
Genetics in Medicine, Nature Publishing Group, 2021, 23 (11), pp.2150-2159. ⟨10.1038/s41436-021-01263-1⟩
Courraud, J, Chater-Diehl, E, Durand, B, Vincent, M, del Mar Muniz Moreno, M, Boujelbene, I, Drouot, N, Genschik, L, Schaefer, E, Nizon, M, Gerard, B, Abramowicz, M, Cogné, B, Bronicki, L, Burglen, L, Barth, M, Charles, P, Colin, E, Coubes, C, David, A, Delobel, B, Demurger, F, Passemard, S, Denommé, A S, Faivre, L, Feger, C, Fradin, M, Francannet, C, Genevieve, D, Goldenberg, A, Guerrot, A M, Isidor, B, Johannesen, K M, Keren, B, Kibæk, M, Kuentz, P, Mathieu-Dramard, M, Demeer, B, Metreau, J, Steensbjerre Møller, R, Moutton, S, Pasquier, L, Pilekær Sørensen, K, Perrin, L, Renaud, M, Saugier, P, Rio, M, Svane, J, Thevenon, J, Tran Mau Them, F, Tronhjem, C E, Vitobello, A, Layet, V, Auvin, S, Khachnaoui, K, Birling, M C, Drunat, S, Bayat, A, Dubourg, C, El Chehadeh, S, Fagerberg, C, Mignot, C, Guipponi, M, Bienvenu, T, Herault, Y, Thompson, J, Willems, M, Mandel, J L, Weksberg, R & Piton, A 2021, ' Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder ', Genetics in Medicine, vol. 23, no. 11, pp. 2150-2159 . https://doi.org/10.1038/s41436-021-01263-1
Genetics in Medicine, 2021, 23 (11), pp.2150-2159. ⟨10.1038/s41436-021-01263-1⟩

Purpose: DYRK1A syndrome is among the most frequent monogenic forms of intellectual disability (ID). We refined the molecular and clinical description of this disorder and developed tools to improve interpretation of missense variants, which remains

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdfaa53f4998959df49373b2281d53db
https://doi.org/10.1038/s41436-021-01263-1

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Heterozygous HTRA1 nonsense or frameshift mutations are pathogenic

Publikováno v: Brain. 144:2616-2624

Heterozygous missense HTRA1 mutations have been associated with an autosomal dominant cerebral small vessel disease (CSVD) whereas the pathogenicity of heterozygous HTRA1 stop codon variants is unclear. We performed a targeted high throughput sequenc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::212ce227b61b00e5447fe3e027ce0276
https://doi.org/10.1093/brain/awab271

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Exome sequencing identifies the first genetic determinants of sirenomelia in humans

Publikováno v: Human Mutation
Human Mutation, 2020, 41 (5), pp.926-933. ⟨10.1002/humu.23998⟩
Human Mutation, 41(5), 926-933. Wiley
Human Mutation, Wiley, 2020, 41 (5), pp.926-933. ⟨10.1002/humu.23998⟩

Full access; International audience; Sirenomelia is a rare severe malformation sequence of unknown cause characterized by fused legs and severe visceral abnormalities. We present a series of nine families including two rare familial aggregations of s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4f4809cccfe22a8f8d876db3d7e0573
https://hdl.handle.net/11370/0ac3ca3a-6458-40da-92ae-b9d82ef21217

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