Vijaykrishnan Narayanan - Publications

Pennsylvania State University, State College, PA, United States 
Computer Science

18 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
2016 Lemke JR, Geider K, Helbig KL, Heyne HO, Schütz H, Hentschel J, Courage C, Depienne C, Nava C, Heron D, Møller RS, Hjalgrim H, Lal D, Neubauer BA, Nürnberg P, ... ... Narayanan V, et al. Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. Neurology. PMID 27164704 DOI: 10.1212/WNL.0000000000002740  0.44
2015 Narayanan MJ, Rangasamy S, Narayanan V. Incontinentia pigmenti (Bloch-Sulzberger syndrome). Handbook of Clinical Neurology. 132: 271-80. PMID 26564087 DOI: 10.1016/B978-0-444-62702-5.00020-2  0.44
2015 Rojnueangnit K, Xie J, Gomes A, Sharp A, Callens T, Chen Y, Liu Y, Cochran M, Abbott MA, Atkin J, Babovic-Vuksanovic D, Barnett CP, Crenshaw M, Bartholomew DW, Basel L, ... ... Narayanan V, et al. High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation. Human Mutation. PMID 26178382 DOI: 10.1002/humu.22832  0.44
2015 Schrauwen I, Szelinger S, Siniard AL, Kurdoglu A, Corneveaux JJ, Malenica I, Richholt R, Van Camp G, De Both M, Swaminathan S, Turk M, Ramsey K, Craig DW, Narayanan V, Huentelman MJ. A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome. Plos One. 10: e0131797. PMID 26176221 DOI: 10.1371/journal.pone.0131797  0.44
2015 Schrauwen I, Szelinger S, Siniard AL, Corneveaux JJ, Kurdoglu A, Richholt R, De Both M, Malenica I, Swaminathan S, Rangasamy S, Kulkarni N, Bernes S, Buchhalter J, Ramsey K, Craig DW, ... Narayanan V, et al. A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi Syndrome. Investigative Ophthalmology & Visual Science. 56: 3896-904. PMID 26091538 DOI: 10.1167/iovs.14-16261  0.44
2014 Szelinger S, Malenica I, Corneveaux JJ, Siniard AL, Kurdoglu AA, Ramsey KM, Schrauwen I, Trent JM, Narayanan V, Huentelman MJ, Craig DW. Characterization of x chromosome inactivation using integrated analysis of whole-exome and mRNA sequencing. Plos One. 9: e113036. PMID 25503791 DOI: 10.1371/journal.pone.0113036  0.44
2014 Ma LY, Wu C, Jin Y, Gao M, Li GH, Turner D, Shen JX, Zhang SJ, Narayanan V, Jentarra G, Wu J. Electrophysiological phenotypes of MeCP2 A140V mutant mouse model. Cns Neuroscience & Therapeutics. 20: 420-8. PMID 24750778 DOI: 10.1111/cns.12229  0.44
2013 Rangasamy S, D'Mello SR, Narayanan V. Epigenetics, autism spectrum, and neurodevelopmental disorders. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 10: 742-56. PMID 24104594 DOI: 10.1007/s13311-013-0227-0  0.44
2013 McCamy MB, Collins N, Otero-Millan J, Al-Kalbani M, Macknik SL, Coakley D, Troncoso XG, Boyle G, Narayanan V, Wolf TR, Martinez-Conde S. Simultaneous recordings of ocular microtremor and microsaccades with a piezoelectric sensor and a video-oculography system. Peerj. 1: e14. PMID 23638348 DOI: 10.7717/peerj.14  0.44
2012 Dastidar SG, Bardai FH, Ma C, Price V, Rawat V, Verma P, Narayanan V, D'Mello SR. Isoform-specific toxicity of Mecp2 in postmitotic neurons: suppression of neurotoxicity by FoxG1. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 2846-55. PMID 22357867 DOI: 10.1523/JNEUROSCI.5841-11.2012  0.44
2012 Jentarra GM, Rice SG, Olfers S, Rajan C, Saffen DM, Narayanan V. Skewed allele-specific expression of the NF1 gene in normal subjects: a possible mechanism for phenotypic variability in neurofibromatosis type 1. Journal of Child Neurology. 27: 695-702. PMID 22068829 DOI: 10.1177/0883073811423439  0.44
2011 Narayanan V. Genetics and child neurology: what every trainee/resident should know. Seminars in Pediatric Neurology. 18: 81-4. PMID 22036485 DOI: 10.1016/j.spen.2011.05.012  0.44
2011 Choi C, Narayanan V. Millisecond flash annealing as a flatband voltage shift enabler for p-type metal-oxide-semiconductor devices with high-k/metal gate Electrochemical and Solid-State Letters. 14: H241-H243. DOI: 10.1149/1.3566073  0.6
2009 Mangalagiri P, Narayanan V. Lifetime reliability aware design flow techniques for dual-vdd based platform FPGAs Proceedings of the 2009 Ieee Computer Society Annual Symposium On Vlsi, Isvlsi 2009. 61-66. DOI: 10.1109/ISVLSI.2009.42  1
2008 Liu W, Narayanan V. Ataxia With Oculomotor Apraxia Seminars in Pediatric Neurology. 15: 216-220. PMID 19073331 DOI: 10.1016/j.spen.2008.10.014  0.32
2007 Narayanan V, Kan EC. A madelung fluid based density gradient model for large barrier tunneling calculations International Conference On Simulation of Semiconductor Processes and Devices, Sispad. 318-321. DOI: 10.1109/SISPAD.2006.282899  0.96
2006 Narayanan V, Xie Y. Reliability concerns in embedded system designs Computer. 39: 118-120. DOI: 10.1109/MC.2006.31  0.44
2004 Narayanan V, Kan EC. A critical examination of the basis of macroscopic quantum transport approaches 2004 10th International Workshop On Computational Electronics, Ieee Iwce-10 2004, Abstracts. 233-234.  0.96
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