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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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LSD1 regulates marginal zone B cell development, B cell proliferation, and plasmablast differentiation
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Identifying the Genetic Drivers of 3q29 Deletion-Associated Phenotypes
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Genetic Characterization of the Anaerobic β-lactamase of Clostridioides difficile
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The Taiman transcriptional coactivator engages Toll signals to promote apoptosis and inter-tissue invasion in Drosophila
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Chromatin Accessibility and Transcription Dynamics During In Vitro Astrocyte Differentiation of Huntington’s Disease Monkey Pluripotent Stem Cells
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A new high-throughput variant annotation and classification method and its implementation in the investigation of schizophrenia-associated copy number regions
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Arl13b is a Target for the Treatment of Medulloblastoma
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High Resolution X Chromosome Copy Number Variation in Autism
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Regulation of Base Excision Repair in Response to Genotoxic Stress
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