Rajini R. Haraksingh, Ph.D. - Publications

Affiliations: 
2012 Yale University, New Haven, CT 

8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
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  0.56
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  0.56
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  0.56
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  0.56
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  0.56
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  0.56
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  0.56
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  0.56
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