☰

Rajini R. Haraksingh, Ph.D. - Publications

Affiliations: 
2012 Yale University, New Haven, CT 
Tree Info Similar researchers PubMed Report error

14 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Sahadeo NSD, Nicholls S, Moreira FRR, O'Toole Á, Ramkissoon V, Whittaker C, Hill V, McCrone JT, Mohammed N, Ramjag A, Brown Jordan A, Hill SC, Singh R, Nathaniel-Girdharrie SM, Hinds A, ... ... Haraksingh R, et al. 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. PMID 36963002 DOI: 10.1371/journal.pgph.0001455  0.401
2019 Zhou B, Ho SS, Greer SU, Zhu X, Bell JM, Arthur JG, Spies N, Zhang X, Byeon S, Pattni R, Ben-Efraim N, Haney MS, Haraksingh RR, Song G, Ji HP, et al. Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562. Genome Research. PMID 30737237 DOI: 10.1101/Gr.234948.118  0.684
2018 Zhou B, Ho SS, Zhang X, Pattni R, Haraksingh RR, Urban AE. 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. PMID 30061371 DOI: 10.1136/Jmedgenet-2018-105272  0.546
2017 Haraksingh RR, Abyzov A, Urban AE. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans. Bmc Genomics. 18: 321. PMID 28438122 DOI: 10.1186/S12864-017-3658-X  0.576
2014 Haraksingh RR, Jahanbani F, Rodriguez-Paris J, Gelernter J, Nadeau KC, Oghalai JS, Schrijver I, Snyder MP. Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss. Bmc Genomics. 15: 1155. PMID 25528277 DOI: 10.1186/1471-2164-15-1155  0.515
2014 Enns GM, Shashi V, Bainbridge M, Gambello MJ, Zahir FR, Bast T, Crimian R, Schoch K, Platt J, Cox R, Bernstein JA, Scavina M, Walter RS, Bibb A, Jones M, ... ... Haraksingh R, et al. 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. PMID 24651605 DOI: 10.1038/Gim.2014.22  0.437
2013 Haraksingh RR, Snyder MP. Impacts of variation in the human genome on gene regulation. Journal of Molecular Biology. 425: 3970-7. PMID 23871684 DOI: 10.1016/J.Jmb.2013.07.015  0.649
2013 Dolled-Filhart MP, Lee M, Ou-Yang CW, Haraksingh RR, Lin JC. Computational and bioinformatics frameworks for next-generation whole exome and genome sequencing. Thescientificworldjournal. 2013: 730210. PMID 23365548 DOI: 10.1155/2013/730210  0.477
2013 Zhang Y, Haraksingh R, Grubert F, Abyzov A, Gerstein M, Weissman S, Urban AE. Child development and structural variation in the human genome. Child Development. 84: 34-48. PMID 23311762 DOI: 10.1111/Cdev.12051  0.727
2012 Dolled-Filhart MP, Lordemann A, Dahl W, Haraksingh RR, Ou-Yang CW, Lin JC. Personalizing rare disease research: how genomics is revolutionizing the diagnosis and treatment of rare disease. Personalized Medicine. 9: 805-819. PMID 29776237 DOI: 10.2217/Pme.12.97  0.492
2012 Chen R, Mias GI, Li-Pook-Than J, Jiang L, Lam HY, Chen R, Miriami E, Karczewski KJ, Hariharan M, Dewey FE, Cheng Y, Clark MJ, Im H, Habegger L, Balasubramanian S, ... ... Haraksingh R, et al. Personal omics profiling reveals dynamic molecular and medical phenotypes. Cell. 148: 1293-307. PMID 22424236 DOI: 10.1016/J.Cell.2012.02.009  0.4
2012 Lam HY, Pan C, Clark MJ, Lacroute P, Chen R, Haraksingh R, O'Huallachain M, Gerstein MB, Kidd JM, Bustamante CD, Snyder M. Detecting and annotating genetic variations using the HugeSeq pipeline. Nature Biotechnology. 30: 226-9. PMID 22398614 DOI: 10.1038/Nbt.2134  0.649
2012 Dolled-Filhart MP, Lordemann A, Dahl W, Haraksingh RR, Ou-Yang CW, Lin JCH. Personalizing rare disease research: How genomics is revolutionizing the diagnosis and treatment of rare disease Personalized Medicine. 9: 805-819. DOI: 10.2217/pme.12.97  0.338
2011 Haraksingh RR, Abyzov A, Gerstein M, Urban AE, Snyder M. Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms. Plos One. 6: e27859. PMID 22140474 DOI: 10.1371/Journal.Pone.0027859  0.625
Show low-probability matches.