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Genes, 2022
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Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants.
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Frontiers in Cardiovascular Medicine, 2022
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Whole genome mapping and identification of single nucleotide polymorphisms of four Bangladeshi individuals and their functional significance.
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A synergetic effect of BARD1 mutations on tumorigenesis.
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A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment.
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Effect of a poly(ADP-ribose) polymerase-1 inhibitor against esophageal squamous cell carcinoma cell lines.
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A population-specific uncommon variant in GRIN3A associated with schizophrenia.
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Biological Psychiatry, 2013
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