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Genomic profiling identifies GATA6 as a candidate oncogene amplified in pancreatobiliary cancer.
Kwei KA, Bashyam MD, Kao J, Ratheesh R, Reddy EC, Kim YH, Montgomery K, Giacomini CP, Choi YL, Chatterjee S, Karikari CA, Salari K, Wang P, Hernandez-Boussard T, Swarnalata G, van de Rijn M, Maitra A, Pollack JR. Kwei KA, et al. Among authors: reddy ec. PLoS Genet. 2008 May 23;4(5):e1000081. doi: 10.1371/journal.pgen.1000081. PLoS Genet. 2008. PMID: 18535672 Free PMC article.
Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNA.
Bashyam MD, Chaudhary AK, Reddy EC, Devi AR, Savithri GR, Ratheesh R, Bashyam L, Mahesh E, Sen D, Puri R, Verma IC, Nampoothiri S, Vaidyanathan S, Chandrashekar MD, Kantheti P. Bashyam MD, et al. Among authors: reddy ec. Mol Genet Metab. 2010 May;100(1):96-9. doi: 10.1016/j.ymgme.2010.01.016. Epub 2010 Feb 2. Mol Genet Metab. 2010. PMID: 20188615
A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India.
Bashyam MD, Chaudhary AK, Reddy EC, Reddy V, Acharya V, Nagarajaram HA, Devi AR, Bashyam L, Dalal AB, Gupta N, Kabra M, Agarwal M, Phadke SR, Tainwala R, Kumar R, Hariharan SV. Bashyam MD, et al. Among authors: reddy ec. Br J Dermatol. 2012 Apr;166(4):819-29. doi: 10.1111/j.1365-2133.2011.10707.x. Epub 2012 Mar 5. Br J Dermatol. 2012. PMID: 22032522
Laboratory diagnosis of inherited platelet function disorders.
Rand ML, Reddy EC, Israels SJ. Rand ML, et al. Among authors: reddy ec. Transfus Apher Sci. 2018 Aug;57(4):485-493. doi: 10.1016/j.transci.2018.07.009. Epub 2018 Jul 24. Transfus Apher Sci. 2018. PMID: 30054199 Review.
14 results