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Ranjit K. Thirumaran

Researcher at St. Jude Children's Research Hospital

Publications -  28
Citations -  1380

Ranjit K. Thirumaran is an academic researcher from St. Jude Children's Research Hospital. The author has contributed to research in topics: Single-nucleotide polymorphism & Odds ratio. The author has an hindex of 20, co-authored 27 publications receiving 1245 citations. Previous affiliations of Ranjit K. Thirumaran include German Cancer Research Center.

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Metabolism of low-dose inorganic arsenic in a central European population: influence of sex and genetic polymorphisms.

TL;DR: The results show that the M287T (T→C) polymorphism in the AS3MT gene, the A222V (C→T) polymorphisms in the MTHFR gene, body mass index, and sex are major factors that influence arsenic metabolism in this population, with a median of 8.0 μg/L arsenic in urine.
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Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations for Test Result Reporting

TL;DR: This article provides nomenclature recommendations developed by an international workgroup to increase transparency and standardization of pharmacogenetic (PGx) result reporting.
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B-RAF and N-RAS mutations are preserved during short time in vitro propagation and differentially impact prognosis.

TL;DR: It is demonstrated that B-RAF and N-RAS mutations are well preserved during short term in vitro propagation and, most importantly, differentially impact the outcome of melanoma patients.
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Clinical impact of pharmacogenetic profiling with a clinical decision support tool in polypharmacy home health patients: A prospective pilot randomized controlled trial.

TL;DR: Pharmacogenetic testing of polypharmacy patients aged 50 and older, supported by an appropriate CDST, considerably reduced re-hospitalizations and ED visits at 60 days following enrollment resulting in potential health resource utilization savings and improved healthcare.
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Polymorphisms in the DNA repair genes XRCC1, APEX1, XRCC3 and NBS1, and the risk for lung cancer in never- and ever-smokers.

TL;DR: The results show that the genetic variation in XR CC1, XRCC3 and NBS1 influence lung cancer susceptibility among women, and that combinations of risk alleles in the two HR genes can enhance the effects.