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Maximizing the ability to detect modifying genetic factors of rare complex disorders – Fragile X-Associated Primary Ovarian Insufficiency and Down Syndrome - Congenital Heart Defects
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Roles of the SCN1A and SCN8A Voltage-Gated Sodium Channel Genes in Neurological Disease
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Identification of genetic modifiers of Fragile X-Associated Tremor/Ataxia Syndrome
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Statistical Methods for High-throughput Epigenomics Data
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Identification of Genetic and Epigenetic Factors regulating cell death and proliferation in cerebellum-related brain disorders
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