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Explores the genetic mechanisms of retinoblastoma and their clinical implications, shedding light on tumor suppression, DNA repair, and genetic recombination.
Focuses on large-scale inference for detecting QTL hotspots in sparse regression models, emphasizing the need to use genomics to understand variation in phenotypes and disease susceptibility.
Explores the opportunities and challenges of genomics in biotechnologies and biomedicine, focusing on the human genome, personalized medicine, and the genomics of sudden cardiac death.
Explores genetic traits inheritance, family tree analysis, and various modes of genetic trait transmission in humans, including specific genetic disorders.
