Rajini R. Haraksingh, Ph.D.

Affiliations: 
2012 Yale University, New Haven, CT 
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"Rajini Haraksingh"

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Michael Snyder grad student 2012 Yale
 (Genome-wide mapping and functional analysis of copy number variation in the human genome.)
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Publications

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Sahadeo NSD, Nicholls S, Moreira FRR, et al. (2023) Implementation of genomic surveillance of SARS-CoV-2 in the Caribbean: Lessons learned for sustainability in resource-limited settings. Plos Global Public Health. 3: e0001455
Zhou B, Ho SS, Greer SU, et al. (2019) Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562. Genome Research
Zhou B, Ho SS, Zhang X, et al. (2018) Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis. Journal of Medical Genetics
Haraksingh RR, Abyzov A, Urban AE. (2017) Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans. Bmc Genomics. 18: 321
Haraksingh RR, Jahanbani F, Rodriguez-Paris J, et al. (2014) Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss. Bmc Genomics. 15: 1155
Enns GM, Shashi V, Bainbridge M, et al. (2014) Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 751-8
Haraksingh RR, Snyder MP. (2013) Impacts of variation in the human genome on gene regulation. Journal of Molecular Biology. 425: 3970-7
Dolled-Filhart MP, Lee M, Ou-Yang CW, et al. (2013) Computational and bioinformatics frameworks for next-generation whole exome and genome sequencing. Thescientificworldjournal. 2013: 730210
Zhang Y, Haraksingh R, Grubert F, et al. (2013) Child development and structural variation in the human genome. Child Development. 84: 34-48
Dolled-Filhart MP, Lordemann A, Dahl W, et al. (2012) Personalizing rare disease research: how genomics is revolutionizing the diagnosis and treatment of rare disease. Personalized Medicine. 9: 805-819
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