From CDC Information Database
This database includes general CDC public health information on specific diseases and health related topics. When available, the database displays genomic information from various CDC web pages. Users are also encouraged to conduct searches of CDC website for additional information.
- Causes of developmental disabilities include genetics
- Developmental disabilities are a group of conditions due to an impairment in physical, learning, language, or behavior areas.
About one in six children in the U.S. have one or more developmental disabilities or other developmental delays
From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports.
American journal of medical genetics. Part A 2016 Feb .
Brownstein Catherine A, Kleiman Robin J, Engle Elizabeth C, Towne Meghan C, D'Angelo Eugene J, Yu Timothy W, Beggs Alan H, Picker Jonathan, Fogler Jason M, Carroll Devon, Schmitt Rachel C O, Wolff Robert R, Shen Yiping, Lip Va, Bilguvar Kaya, Kim April, Tembulkar Sahil, O'Donnell Kyle, Gonzalez-Heydrich Jose - RYR2, PTDSS1 and AREG genes are implicated in a Lebanese population-based study of copy number variation in autism.
Scientific reports 2016 6 19088.
Soueid Jihane, Kourtian Silva, Makhoul Nadine J, Makoukji Joelle, Haddad Sariah, Ghanem Simona S, Kobeissy Firas, Boustany Rose-Ma - Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
JAMA psychiatry 2015 Dec 1-11.
D'Angelo Debra, Lebon Sébastien, Chen Qixuan, Martin-Brevet Sandra, Snyder LeeAnne Green, Hippolyte Loyse, Hanson Ellen, Maillard Anne M, Faucett W Andrew, Macé Aurélien, Pain Aurélie, Bernier Raphael, Chawner Samuel J R A, David Albert, Andrieux Joris, Aylward Elizabeth, Baujat Genevieve, Caldeira Ines, Conus Philippe, Ferrari Carrina, Forzano Francesca, Gérard Marion, Goin-Kochel Robin P, Grant Ellen, Hunter Jill V, Isidor Bertrand, Jacquette Aurélia, Jønch Aia E, Keren Boris, Lacombe Didier, Le Caignec Cédric, Martin Christa Lese, Männik Katrin, Metspalu Andres, Mignot Cyril, Mukherjee Pratik, Owen Michael J, Passeggeri Marzia, Rooryck-Thambo Caroline, Rosenfeld Jill A, Spence Sarah J, Steinman Kyle J, Tjernagel Jennifer, Van Haelst Mieke, Shen Yiping, Draganski Bogdan, Sherr Elliott H, Ledbetter David H, van den Bree Marianne B M, Beckmann Jacques S, Spiro John E, Reymond Alexandre, Jacquemont Sébastien, Chung Wendy K, - Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease.
Nature neuroscience 2015 Dec .
Johnson Michael R, Shkura Kirill, Langley Sarah R, Delahaye-Duriez Andree, Srivastava Prashant, Hill W David, Rackham Owen J L, Davies Gail, Harris Sarah E, Moreno-Moral Aida, Rotival Maxime, Speed Doug, Petrovski Slavé, Katz Anaïs, Hayward Caroline, Porteous David J, Smith Blair H, Padmanabhan Sandosh, Hocking Lynne J, Starr John M, Liewald David C, Visconti Alessia, Falchi Mario, Bottolo Leonardo, Rossetti Tiziana, Danis Bénédicte, Mazzuferi Manuela, Foerch Patrik, Grote Alexander, Helmstaedter Christoph, Becker Albert J, Kaminski Rafal M, Deary Ian J, Petretto Enri - 1q21.1 microduplication in a patient with mental impairment and congenital heart defect.
Molecular medicine reports 2015 Oct 12 (4): 5655-8.
Sun Guowen, Tan Zhiping, Fan Liangliang, Wang Jian, Yang Yifeng, Zhang Weiz
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