Concepedia

NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy

Yuwu Jiang, Yuehua Zhang, Tian Sang, Feng Zhang, Taoyun Ji, Qionghui Huang, Han Xie, Renqian Du, Bin Cai, Haijuan Zhao,

Human Genetics · 2012 · 41 citations · 24 references

DOI

Concepts

References

24

Strong Association of De Novo Copy Number Mutations with Autism

Jonathan Sebat, B. Lakshmi, Dheeraj Malhotra et al. · Science · 2007 · 2.8K citations · Full text

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Association between Microdeletion and Microduplication at 16p11.2 and Autism

Lauren A. Weiss, Yiping Shen, Joshua M. Korn et al. · New England Journal of Medicine · 2008 · 1.7K citations · Full text

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Rare chromosomal deletions and duplications increase risk of schizophrenia

Nature · 2008 · 1.5K citations · Full text

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Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

Heather C. Mefford, Andrew J. Sharp, Carl Baker et al. · New England Journal of Medicine · 2008 · 811 citations · Full text

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Association Between Microdeletion and Microduplication at 16p11.2 and Autism

Lauren A. Weiss, Yiping Shen, Joshua M. Korn et al. · Obstetrical & Gynecological Survey · 2008 · 654 citations

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