Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

Author:

Levy Dan,Ronemus Michael,Yamrom Boris,Lee Yoon-ha,Leotta Anthony,Kendall Jude,Marks Steven,Lakshmi B.,Pai Deepa,Ye Kenny,Buja Andreas,Krieger Abba,Yoon Seungtai,Troge Jennifer,Rodgers Linda,Iossifov Ivan,Wigler Michael

Publisher

Elsevier BV

Subject

General Neuroscience

Reference47 articles.

1. Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals;Bijlsma;Eur. J. Med. Genet.,2009

2. Genetic advances in autism: heterogeneity and convergence on shared pathways;Bill;Curr. Opin. Genet. Dev.,2009

3. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders;Ching;Am. J. Med. Genet. B. Neuropsychiatr. Genet.,2010

4. Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies;de Kovel;Brain,2010

5. Eating disorders;Fairburn;Lancet,2003

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