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by Tang, Lichun
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Large recurrent microdeletions associated with schizophrenia
by Stefansson, Hreinn
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Parental origin of sequence variants associated with complex diseases
by Gudjonsson, Sigurjon A
Nature (London), 2009-12-17, Vol.462 (7275), p.868-874
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A genome-wide association study identifies novel risk loci for type 2 diabetes
by Meyre, David
Nature (London), 2007-02-22, Vol.445 (7130), p.881-885
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Rare chromosomal deletions and duplications increase risk of schizophrenia
by Stone, JL
Nature (London), 2008-09-11, Vol.455 (7210), p.237-241
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Human Genome Sequencing in Health and Disease
by Gonzaga-Jauregui, Claudia
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DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome
by Joshi, Ricky S
American journal of human genetics, 2016-09-01, Vol.99 (3), p.555-566
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Reconstructing Indian population history
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Nature, 2009-09-24, Vol.461 (7263), p.489-494
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Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis
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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
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