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Smoking + BMI in heart disease
WGS for cardiovascular outcomes
RNA-Seq in pancreatic cancer
Genetic analysis of patients with Inherited Retinal Dystrophies (IRDs) using next generation sequencing to identify the causative variants
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Selected Publications (3)
Variables (30)
Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencing.
K. Branham, H. Matsui, P. Biswas, et al. (2016). Physiological genomics. Cited 38 times.
https://doi.org/10.1152/physiolgenomics.00101.2016
IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis
Anil Chekuri, Aditya A. Guru, P. Biswas, et al. (2018). Human Genetics. Cited 21 times.
https://doi.org/10.1007/s00439-018-1897-9
Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree
Kevin M Gustafson, J. Duncan, P. Biswas, et al. (2017). Genes. Cited 17 times.
https://doi.org/10.3390/genes8090210
