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Bishakha Roy

Researcher at Griffith University

Publications -  15
Citations -  408

Bishakha Roy is an academic researcher from Griffith University. The author has contributed to research in topics: Familial hemiplegic migraine & Gene. The author has an hindex of 9, co-authored 15 publications receiving 372 citations. Previous affiliations of Bishakha Roy include Queensland University of Technology.

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Functional analysis of missense variants in the TRESK ( KCNK18 ) K + channel

TL;DR: The functional characterisation of additional TRESK channel missense variants identified in unrelated patients indicates that a single non-functional TResK variant is not alone sufficient to cause typical migraine and highlights the genetic complexity of this disorder.
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Review: Alternative Splicing (AS) of Genes As An Approach for Generating Protein Complexity.

TL;DR: The ability to determine and predict AS is important as disorders in splicing patterns may lead to abnormal splice variants resulting in genetic diseases and the diversity of proteins produced by AS poses a challenge for successful drug discovery and therefore a greater understanding of AS would be beneficial.
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Genotypes of the MTHFR C677T and MTRR A66G genes act independently to reduce migraine disability in response to vitamin supplementation

TL;DR: In this paper, the genotypic effects of methylenetetetrahydrofolate reductase (MTHFR) and methionine synthase reductases (MTRR) gene variants on the occurrence of migraine in response to vitamin supplementation were examined.
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Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine.

TL;DR: The results of this study showed no significant association between the intronic 16bp deletion in the CALCA gene and migraine in the tested Australian Caucasian population, however, given the evidence linking CGRP and migraine, further investigation of variants with this gene may be warranted.
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The human μ-opioid receptor gene polymorphism (A118G) is associated with head pain severity in a clinical cohort of female migraine with aura patients

TL;DR: In this paper, a preliminary study was conducted to determine whether genotypes of the OPRM1 A118G SNP are associated with head pain severity in a clinical cohort of female migraineurs.