Jonathan Pevsner - Publications

Affiliations: 
Neuroscience Johns Hopkins University School of Medicine, Baltimore, MD, United States 

62/142 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
2020 Thorpe J, Osei-Owusu IA, Avigdor BE, Tupler R, Pevsner J. Mosaicism in Human Health and Disease. Annual Review of Genetics. PMID 32916079 DOI: 10.1146/Annurev-Genet-041720-093403  0.351
2019 Sharim H, Grunwald A, Gabrieli T, Michaeli Y, Margalit S, Torchinsky D, Arielly R, Nifker G, Juhasz M, Gularek F, Almalvez M, Dufault B, Chandra SS, Liu A, Bhattacharya S, ... ... Pevsner J, et al. Long-read single-molecule maps of the functional methylome. Genome Research. PMID 30846530 DOI: 10.1101/Gr.240739.118  0.342
2017 McConnell MJ, Moran JV, Abyzov A, Akbarian S, Bae T, Cortes-Ciriano I, Erwin JA, Fasching L, Flasch DA, Freed D, Ganz J, Jaffe AE, Kwan KY, Kwon M, Lodato MA, ... ... Pevsner J, et al. Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network. Science (New York, N.Y.). 356. PMID 28450582 DOI: 10.1126/Science.Aal1641  0.354
2016 Horiuchi Y, Kondo MA, Okada K, Takayanagi Y, Tanaka T, Ho T, Varvaris M, Tajinda K, Hiyama H, Ni K, Colantuoni C, Schretlen D, Cascella NG, Pevsner J, Ishizuka K, et al. Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium. Translational Psychiatry. 6: e915. PMID 27727244 DOI: 10.1038/Tp.2016.154  0.607
2016 Shirley MD, Frelin L, López JS, Jedlicka A, Dziedzic A, Frank-Crawford MA, Silverman W, Hagopian L, Pevsner J. Copy Number Variants Associated with 14 Cases of Self-Injurious Behavior. Plos One. 11: e0149646. PMID 26933844 DOI: 10.1371/Journal.Pone.0149646  0.676
2015 Debeljak M, Freed DN, Welch JA, Haley L, Beierl K, Iglehart BS, Pallavajjala A, Gocke CD, Leffell MS, Lin M, Wood LD, Pevsner J, Wheelan SJ, Eshleman JR. Abstract 4270: NGS based microhaplotype counting for ultrasensitive human DNA detection Cancer Research. 75: 4270-4270. DOI: 10.1158/1538-7445.Am2015-4270  0.333
2014 Freed D, Stevens EL, Pevsner J. Somatic mosaicism in the human genome. Genes. 5: 1064-94. PMID 25513881 DOI: 10.3390/Genes5041064  0.66
2013 Horiuchi Y, Kano S, Ishizuka K, Cascella NG, Ishii S, Talbot CC, Jaffe AE, Okano H, Pevsner J, Colantuoni C, Sawa A. Olfactory cells via nasal biopsy reflect the developing brain in gene expression profiles: utility and limitation of the surrogate tissues in research for brain disorders. Neuroscience Research. 77: 247-50. PMID 24120685 DOI: 10.1016/J.Neures.2013.09.010  0.656
2013 Comi AM, Marchuk DA, Pevsner J. A needle in a haystack: Sturge-Weber syndrome gene discovery. Pediatric Neurology. 49: 391-2. PMID 24075845 DOI: 10.1016/J.Pediatrneurol.2013.07.009  0.332
2013 Baugher JD, Baugher BD, Shirley MD, Pevsner J. Sensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) method. Bmc Genomics. 14: 367. PMID 23724825 DOI: 10.1186/1471-2164-14-367  0.768
2013 Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B, North PE, Marchuk DA, Comi AM, Pevsner J. Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ. The New England Journal of Medicine. 368: 1971-9. PMID 23656586 DOI: 10.1056/Nejmoa1213507  0.761
2013 Kondo MA, Tajinda K, Colantuoni C, Hiyama H, Seshadri S, Huang B, Pou S, Furukori K, Hookway C, Jaaro-Peled H, Kano SI, Matsuoka N, Harada K, Ni K, Pevsner J, et al. Unique pharmacological actions of atypical neuroleptic quetiapine: possible role in cell cycle/fate control. Translational Psychiatry. 3: e243. PMID 23549417 DOI: 10.1038/Tp.2013.19  0.638
2012 Stevens EL, Baugher JD, Shirley MD, Frelin LP, Pevsner J. Unexpected relationships and inbreeding in HapMap phase III populations. Plos One. 7: e49575. PMID 23185369 DOI: 10.1371/Journal.Pone.0049575  0.746
2012 Shirley MD, Baugher JD, Stevens EL, Tang Z, Gerry N, Beiswanger CM, Berlin DS, Pevsner J. Chromosomal variation in lymphoblastoid cell lines. Human Mutation. 33: 1075-86. PMID 22374857 DOI: 10.1002/Humu.22062  0.753
2012 Stevens EL, Heckenberg G, Baugher JD, Roberson ED, Downey TJ, Pevsner J. Consanguinity in Centre d'Étude du Polymorphisme Humain (CEPH) pedigrees. European Journal of Human Genetics : Ejhg. 20: 657-67. PMID 22274586 DOI: 10.1038/Ejhg.2011.266  0.771
2011 Stevens EL, Heckenberg G, Roberson ED, Baugher JD, Downey TJ, Pevsner J. Inference of relationships in population data using identity-by-descent and identity-by-state. Plos Genetics. 7: e1002287. PMID 21966277 DOI: 10.1371/Journal.Pgen.1002287  0.768
2011 Halper-Stromberg E, Frelin L, Ruczinski I, Scharpf R, Jie C, Carvalho B, Hao H, Hetrick K, Jedlicka A, Dziedzic A, Doheny K, Scott AF, Baylin S, Pevsner J, Spencer F, et al. Performance assessment of copy number microarray platforms using a spike-in experiment. Bioinformatics (Oxford, England). 27: 1052-60. PMID 21478196 DOI: 10.1093/Bioinformatics/Btr106  0.363
2011 Roberson ED, Wohler ES, Hoover-Fong JE, Lisi E, Stevens EL, Thomas GH, Leonard J, Hamosh A, Pevsner J. Genomic analysis of partial 21q monosomies with variable phenotypes. European Journal of Human Genetics : Ejhg. 19: 235-8. PMID 20823914 DOI: 10.1038/Ejhg.2010.150  0.768
2010 Sobreira NL, Cirulli ET, Avramopoulos D, Wohler E, Oswald GL, Stevens EL, Ge D, Shianna KV, Smith JP, Maia JM, Gumbs CE, Pevsner J, Thomas G, Valle D, Hoover-Fong JE, et al. Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene. Plos Genetics. 6: e1000991. PMID 20577567 DOI: 10.1371/Journal.Pgen.1000991  0.719
2009 Ting JC, Roberson ED, Currier DG, Pevsner J. Locations and patterns of meiotic recombination in two-generation pedigrees. Bmc Medical Genetics. 10: 93. PMID 19761602 DOI: 10.1186/1471-2350-10-93  0.635
2009 Roberson ED, Pevsner J. Visualization of shared genomic regions and meiotic recombination in high-density SNP data. Plos One. 4: e6711. PMID 19696932 DOI: 10.1371/Journal.Pone.0006711  0.668
2009 Pevsner J. Analysis of genomic DNA with the UCSC genome browser. Methods in Molecular Biology (Clifton, N.J.). 537: 277-301. PMID 19378150 DOI: 10.1007/978-1-59745-251-9_14  0.301
2009 Miller ND, Nance MA, Wohler ES, Hoover-Fong JE, Lisi E, Thomas GH, Pevsner J. Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function. American Journal of Medical Genetics. Part A. 149: 669-80. PMID 19253379 DOI: 10.1002/Ajmg.A.32705  0.326
2008 Scharpf RB, Parmigiani G, Pevsner J, Ruczinski I. Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays. The Annals of Applied Statistics. 2: 687-713. PMID 19609370 DOI: 10.1214/07-Aoas155  0.337
2007 Watkins PA, Maiguel D, Jia Z, Pevsner J. Evidence for 26 distinct acyl-coenzyme A synthetase genes in the human genome. Journal of Lipid Research. 48: 2736-50. PMID 17762044 DOI: 10.1194/Jlr.M700378-Jlr200  0.345
2007 Ting JC, Roberson ED, Miller ND, Lysholm-Bernacchi A, Stephan DA, Capone GT, Ruczinski I, Thomas GH, Pevsner J. Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio. Human Mutation. 28: 1225-35. PMID 17661425 DOI: 10.1002/Humu.20583  0.665
2007 Deng V, Matagne V, Banine F, Frerking M, Ohliger P, Budden S, Pevsner J, Dissen GA, Sherman LS, Ojeda SR. FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice. Human Molecular Genetics. 16: 640-50. PMID 17309881 DOI: 10.1093/Hmg/Ddm007  0.328
2007 Scharpf RB, Ting JC, Pevsner J, Ruczinski I. SNPchip: R classes and methods for SNP array data. Bioinformatics (Oxford, England). 23: 627-8. PMID 17204461 DOI: 10.1093/Bioinformatics/Btl638  0.313
2006 Ting JC, Ye Y, Thomas GH, Ruczinski I, Pevsner J. Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan. Bmc Bioinformatics. 7: 25. PMID 16420694 DOI: 10.1186/1471-2105-7-25  0.359
2005 Mao R, Wang X, Spitznagel EL, Frelin LP, Ting JC, Ding H, Kim JW, Ruczinski I, Downey TJ, Pevsner J. Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart. Genome Biology. 6: R107. PMID 16420667 DOI: 10.1186/Gb-2005-6-13-R107  0.526
2005 Mao R, Pevsner J. The use of genomic microarrays to study chromosomal abnormalities in mental retardation. Mental Retardation and Developmental Disabilities Research Reviews. 11: 279-85. PMID 16240409 DOI: 10.1002/Mrdd.20082  0.523
2005 Yan Q, Hunt PR, Frelin L, Vida TA, Pevsner J, Bean AJ. mVps24p functions in EGF receptor sorting/trafficking from the early endosome. Experimental Cell Research. 304: 265-73. PMID 15707591 DOI: 10.1016/J.Yexcr.2004.11.003  0.603
2004 Masayesva BG, Ha P, Garrett-Mayer E, Pilkington T, Mao R, Pevsner J, Speed T, Benoit N, Moon CS, Sidransky D, Westra WH, Califano J. Gene expression alterations over large chromosomal regions in cancers include multiple genes unrelated to malignant progression. Proceedings of the National Academy of Sciences of the United States of America. 101: 8715-20. PMID 15155901 DOI: 10.1073/Pnas.0400027101  0.554
2004 Mirnics K, Pevsner J. Progress in the use of microarray technology to study the neurobiology of disease. Nature Neuroscience. 7: 434-9. PMID 15114354 DOI: 10.1038/Nn1230  0.433
2004 Petrova PS, Raibekas A, Pevsner J, Vigo N, Anafi M, Moore MK, Peaire A, Shridhar V, Smith DI, Kelly J, Durocher Y, Commissiong JW. Discovering novel phenotype-selective neurotrophic factors to treat neurodegenerative diseases. Progress in Brain Research. 146: 168-83. PMID 14699964 DOI: 10.1016/S0079-6123(03)46012-3  0.319
2003 Bouton CM, Pevsner J. DRAGON and DRAGON view: information annotation and visualization tools for large-scale expression data. Current Protocols in Bioinformatics / Editoral Board, Andreas D. Baxevanis ... [Et Al.]. Unit 7.4. PMID 18428707 DOI: 10.1002/0471250953.Bi0704S02  0.78
2003 Cohen DR, Matarazzo V, Palmer AM, Tu Y, Jeon OH, Pevsner J, Ronnett GV. Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis. Molecular and Cellular Neurosciences. 22: 417-29. PMID 12727440 DOI: 10.1016/S1044-7431(03)00026-5  0.34
2003 Mao R, Zielke CL, Zielke HR, Pevsner J. Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain. Genomics. 81: 457-67. PMID 12706104 DOI: 10.1016/S0888-7543(03)00035-1  0.555
2003 Comi AM, Hunt P, Vawter MP, Pardo CA, Becker KG, Pevsner J. Increased fibronectin expression in sturge-weber syndrome fibroblasts and brain tissue. Pediatric Research. 53: 762-9. PMID 12621118 DOI: 10.1203/01.Pdr.0000058921.54071.19  0.705
2002 Colantuoni C, Henry G, Zeger S, Pevsner J. SNOMAD (Standardization and NOrmalization of MicroArray Data): web-accessible gene expression data analysis. Bioinformatics (Oxford, England). 18: 1540-1. PMID 12424128 DOI: 10.1093/Bioinformatics/18.11.1540  0.662
2002 Colantuoni C, Henry G, Zeger S, Pevsner J. Local mean normalization of microarray element signal intensities across an array surface: quality control and correction of spatially systematic artifacts. Biotechniques. 32: 1316-20. PMID 12074162 DOI: 10.2144/02326Mt02  0.637
2002 Bouton CM, Pevsner J. DRAGON View: information visualization for annotated microarray data. Bioinformatics (Oxford, England). 18: 323-4. PMID 11847082  0.746
2002 Sung YK, Moon C, Yoo JY, Moon C, Pearse D, Pevsner J, Ronnett GV. Plunc, a member of the secretory gland protein family, is up-regulated in nasal respiratory epithelium after olfactory bulbectomy. The Journal of Biological Chemistry. 277: 12762-9. PMID 11821380 DOI: 10.1074/Jbc.M106208200  0.314
2002 Colantuoni C, Comi A, Purcell AE, Pevsner J. The use of microarrays to study childhood developmental brain disorders Current Genomics. 3: 21-31. DOI: 10.2174/1389202023350660  0.751
2001 Purcell AE, Jeon OH, Pevsner J. The abnormal regulation of gene expression in autistic brain tissue. Journal of Autism and Developmental Disorders. 31: 545-9. PMID 11814264 DOI: 10.1023/A:1013290826504  0.728
2001 Johnston MV, Jeon OH, Pevsner J, Blue ME, Naidu S. Neurobiology of Rett syndrome: a genetic disorder of synapse development. Brain & Development. 23: S206-13. PMID 11738874 DOI: 10.1016/S0387-7604(01)00351-5  0.347
2001 Purcell AE, Jeon OH, Zimmerman AW, Blue ME, Pevsner J. Postmortem brain abnormalities of the glutamate neurotransmitter system in autism. Neurology. 57: 1618-28. PMID 11706102 DOI: 10.1212/Wnl.57.9.1618  0.697
2001 Colantuoni C, Jeon OH, Hyder K, Chenchik A, Khimani AH, Narayanan V, Hoffman EP, Kaufmann WE, Naidu S, Pevsner J. Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification. Neurobiology of Disease. 8: 847-65. PMID 11592853 DOI: 10.1006/Nbdi.2001.0428  0.706
2001 Bouton CM, Hossain MA, Frelin LP, Laterra J, Pevsner J. Microarray analysis of differential gene expression in lead-exposed astrocytes. Toxicology and Applied Pharmacology. 176: 34-53. PMID 11578147 DOI: 10.1006/Taap.2001.9274  0.784
2001 Purcell AE, Rocco MM, Lenhart JA, Hyder K, Zimmerman AW, Pevsner J. Assessment of neural cell adhesion molecule (NCAM) in autistic serum and postmortem brain. Journal of Autism and Developmental Disorders. 31: 183-94. PMID 11450817 DOI: 10.1023/A:1010751232295  0.686
2001 Johnston-Wilson NL, Bouton CM, Pevsner J, Breen JJ, Torrey EF, Yolken RH. Emerging technologies for large-scale screening of human tissues and fluids in the study of severe psychiatric disease. The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (Cinp). 4: 83-92. PMID 11343633 DOI: 10.1017/S1461145701002255  0.77
2001 Bouton CM, Frelin LP, Forde CE, Arnold Godwin H, Pevsner J. Synaptotagmin I is a molecular target for lead. Journal of Neurochemistry. 76: 1724-35. PMID 11259490 DOI: 10.1046/J.1471-4159.2001.00168.X  0.726
2000 Bouton CM, Pevsner J. Effects of lead on gene expression. Neurotoxicology. 21: 1045-55. PMID 11233751  0.767
2000 Bouton CM, Pevsner J. DRAGON: Database Referencing of Array Genes Online. Bioinformatics (Oxford, England). 16: 1038-9. PMID 11159315  0.762
2000 Hossain MA, Bouton CM, Pevsner J, Laterra J. Induction of vascular endothelial growth factor in human astrocytes by lead. Involvement of a protein kinase C/activator protein-1 complex-dependent and hypoxia-inducible factor 1-independent signaling pathway. The Journal of Biological Chemistry. 275: 27874-82. PMID 10882716 DOI: 10.1074/Jbc.M002185200  0.744
2000 Colantuoni C, Purcell AE, Bouton CM, Pevsner J. High throughput analysis of gene expression in the human brain. Journal of Neuroscience Research. 59: 1-10. PMID 10658179 DOI: 10.1002/(Sici)1097-4547(20000101)59:1<1::Aid-Jnr1>3.0.Co;2-2  0.784
2000 Pevsner J. 194. Abnormal regulation of expressed genes in human brain diseases revealed using cDNA microarrays Biological Psychiatry. 47: S59. DOI: 10.1016/S0006-3223(00)00458-3  0.402
2000 Colantuoni C, Jeon O, Bouton C, Purcell A, Hyder K, Chenchik A, Khimani A, Yolken R, Zeger S, Kaufmann W, Naidu S, Pevsner J. 29. Differential gene expression in human postmortem Rett syndrome brain revealed by cDNA microarray Biological Psychiatry. 47: S8-S9. DOI: 10.1016/S0006-3223(00)00287-0  0.785
1999 Smith KD, Kemp S, Braiterman LT, Lu JF, Wei HM, Geraghty M, Stetten G, Bergin JS, Pevsner J, Watkins PA. X-linked adrenoleukodystrophy: genes, mutations, and phenotypes. Neurochemical Research. 24: 521-35. PMID 10227685 DOI: 10.1023/A:1022535930009  0.307
1999 Khimani AH, Colantuoni C, Pevsner J, Garlick RK, Killian JB. MICROMAX™ microarray system I: a complete system for high throughput gene expression analysis and drug discovery Nature Genetics. 23: 55-55. DOI: 10.1038/14340  0.703
1999 Pevsner J. Analysis of gene expression in human brain diseases using high density microarrays Nature Genetics. 23: 15-15. DOI: 10.1038/14228  0.387
1996 Pevsner J, Hsu SC, Hyde PS, Scheller RH. Mammalian homologues of yeast vacuolar protein sorting (vps) genes implicated in Golgi-to-lysosome trafficking. Gene. 183: 7-14. PMID 8996080 DOI: 10.1016/S0378-1119(96)00367-8  0.317
Low-probability matches (unlikely to be authored by this person)
2003 Naidu S, Bibat G, Kratz L, Kelley RI, Pevsner J, Hoffman E, Cuffari C, Rohde C, Blue ME, Johnston MV. Clinical variability in Rett syndrome. Journal of Child Neurology. 18: 662-8. PMID 14649546 DOI: 10.1177/08830738030180100801  0.297
2014 Srivastava S, Cohen J, Pevsner J, Aradhya S, McKnight D, Butler E, Johnston M, Fatemi A. A novel variant in GABRB2 associated with intellectual disability and epilepsy. American Journal of Medical Genetics. Part A. 164: 2914-21. PMID 25124326 DOI: 10.1002/Ajmg.A.36714  0.293
2003 Petrova P, Raibekas A, Pevsner J, Vigo N, Anafi M, Moore MK, Peaire AE, Shridhar V, Smith DI, Kelly J, Durocher Y, Commissiong JW. MANF: a new mesencephalic, astrocyte-derived neurotrophic factor with selectivity for dopaminergic neurons. Journal of Molecular Neuroscience : Mn. 20: 173-88. PMID 12794311 DOI: 10.1385/Jmn:20:2:173  0.291
2019 Guo H, Li Y, Shen L, Wang T, Jia X, Liu L, Xu T, Ou M, Hoekzema K, Wu H, Gillentine MA, Liu C, Ni H, Peng P, Zhao R, ... ... Pevsner J, et al. Disruptive variants of associate with autism and interfere with neuronal development and synaptic transmission. Science Advances. 5: eaax2166. PMID 31579823 DOI: 10.1126/Sciadv.Aax2166  0.288
2002 Pevsner J. Leonardo da Vinci's contributions to neuroscience. Trends in Neurosciences. 25: 217-20. PMID 11998691 DOI: 10.1016/S0166-2236(00)02121-4  0.288
2018 Day AM, McCulloch CE, Hammill AM, Juhász C, Lo WD, Pinto AL, Miles DK, Fisher BJ, Ball KL, Wilfong AA, Levin AV, Thau AJ, Comi AM, Koenig JI, ... ... Pevsner J, et al. Physical and Family History Variables Associated With Neurological and Cognitive Development in Sturge-Weber Syndrome. Pediatric Neurology. PMID 30853154 DOI: 10.1016/J.Pediatrneurol.2018.12.002  0.288
2014 Debeljak M, Freed DN, Welch JA, Haley L, Beierl K, Iglehart BS, Pallavajjala A, Gocke CD, Leffell MS, Lin MT, Pevsner J, Wheelan SJ, Eshleman JR. Haplotype counting by next-generation sequencing for ultrasensitive human DNA detection. The Journal of Molecular Diagnostics : Jmd. 16: 495-503. PMID 25132481 DOI: 10.1016/J.Jmoldx.2014.04.003  0.287
2018 Jouroukhin Y, Zhu X, Shevelkin AV, Hasegawa Y, Abazyan B, Saito A, Pevsner J, Kamiya A, Pletnikov MV. Adolescent Δ-Tetrahydrocannabinol Exposure and Astrocyte-Specific Genetic Vulnerability Converge on Nuclear Factor-κB-Cyclooxygenase-2 Signaling to Impair Memory in Adulthood. Biological Psychiatry. PMID 30219209 DOI: 10.1016/J.Biopsych.2018.07.024  0.278
2016 Lee BJ, Marchionni L, Andrews CE, Norris AL, Nucifora LG, Wu YC, Wright RA, Pevsner J, Ross CA, Margolis RL, Sawa A, Nucifora FC. Analysis of differential gene expression mediated by clozapine in human postmortem brains. Schizophrenia Research. PMID 28038920 DOI: 10.1016/J.Schres.2016.12.017  0.277
2007 Gao P, Zhang H, Dinavahi R, Li F, Xiang Y, Raman V, Bhujwalla ZM, Felsher DW, Cheng L, Pevsner J, Lee LA, Semenza GL, Dang CV. HIF-dependent antitumorigenic effect of antioxidants in vivo. Cancer Cell. 12: 230-8. PMID 17785204 DOI: 10.1016/J.Ccr.2007.08.004  0.266
2001 Fisher RJ, Pevsner J, Burgoyne RD. Control of fusion pore dynamics during exocytosis by Munc18. Science (New York, N.Y.). 291: 875-8. PMID 11157167 DOI: 10.1126/Science.291.5505.875  0.265
2004 Polster BM, Pevsner J, Hardwick JM. Viral Bcl-2 homologs and their role in virus replication and associated diseases. Biochimica Et Biophysica Acta. 1644: 211-27. PMID 14996505 DOI: 10.1016/J.Bbamcr.2003.11.001  0.263
2019 Pevsner J. Leonardo da Vinci's studies of the brain. Lancet (London, England). 393: 1465-1472. PMID 30967217 DOI: 10.1016/S0140-6736(19)30302-2  0.262
1998 Lo NW, Shaper JH, Pevsner J, Shaper NL. The expanding beta 4-galactosyltransferase gene family: messages from the databanks. Glycobiology. 8: 517-26. PMID 9597550 DOI: 10.1093/Glycob/8.5.517  0.262
2005 Pevsner J. Gene expression in Autism The Neurobiology of Autism. 207-216.  0.26
1999 Kadkol SS, Brody JR, Pevsner J, Bai J, Pasternack GR. Correction to "Modulation of oncogenic potential by alternative gene use in human prostate cancer" Nature Medicine. 5: 1087. PMID 10471270 DOI: 10.1038/12530  0.257
2020 Thorpe J, Frelin LP, McCann M, Pardo CA, Cohen BA, Comi AM, Pevsner J. Identification of a mosaic activating mutation in GNA11 in atypical Sturge-Weber Syndrome. The Journal of Investigative Dermatology. PMID 32771470 DOI: 10.1016/J.Jid.2020.03.978  0.251
2019 Nucifora L, MacDonald M, Lee B, Peters M, Norris A, Orsburn BO, Gleason K, Yang K, Margolis R, Pevsner J, Tamminga C, Sweet R, Ross C, Sawa A, Nucifora F. O2.3. Increased Protein Insolubility In Brains From A Subset Of Patients With Schizophrenia Schizophrenia Bulletin. 45. DOI: 10.1093/Schbul/Sbz021.187  0.251
2019 Yang K, Kondo MA, Jaaro-Peled H, Cash-Padgett T, Kano SI, Ishizuka K, Pevsner J, Tomoda T, Sawa A, Niwa M. The transcriptome landscape associated with Disrupted-in-Schizophrenia-1 locus impairment in early development and adulthood. Schizophrenia Research. PMID 31204062 DOI: 10.1016/J.Schres.2019.05.032  0.248
2019 Nucifora L, MacDonald M, Lee B, Peters M, Norris A, Orsburn B, Yang K, Gleason K, Margolis R, Pevsner J, Tamminga C, Sweet R, Ross C, Sawa A, Nucifora F. F168. Increased Protein Insolubility in Brains From a Subset of Patients With Schizophrenia Biological Psychiatry. 85. DOI: 10.1016/J.Biopsych.2019.03.705  0.247
2019 Nucifora LG, MacDonald ML, Lee BJ, Peters ME, Norris AL, Orsburn BC, Yang K, Gleason K, Margolis RL, Pevsner J, Tamminga CA, Sweet RA, Ross CA, Sawa A, Nucifora FC. Increased Protein Insolubility in Brains From a Subset of Patients With Schizophrenia. The American Journal of Psychiatry. appiajp201918070864. PMID 31055969 DOI: 10.1176/Appi.Ajp.2019.18070864  0.246
2019 Cho S, Maharathi B, Ball KL, Loeb JA, Pevsner J. Sturge-Weber Syndrome Patient Registry: Delayed Diagnosis and Poor Seizure Control. The Journal of Pediatrics. PMID 31587863 DOI: 10.1016/J.Jpeds.2019.08.025  0.243
2008 Wang W, Carvalho B, Miller ND, Pevsner J, Chakravarti A, Irizarry RA. Estimating genome-wide copy number using allele-specific mixture models. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 15: 857-66. PMID 18707534 DOI: 10.1089/Cmb.2007.0148  0.237
1985 Pevsner J, Trifiletti RR, Strittmatter SM, Snyder SH. Isolation and characterization of an olfactory receptor protein for odorant pyrazines. Proceedings of the National Academy of Sciences of the United States of America. 82: 3050-4. PMID 2986147 DOI: 10.1073/Pnas.82.9.3050  0.235
2004 Fannjiang Y, Cheng WC, Lee SJ, Qi B, Pevsner J, McCaffery JM, Hill RB, Basañez G, Hardwick JM. Mitochondrial fission proteins regulate programmed cell death in yeast. Genes & Development. 18: 2785-97. PMID 15520274 DOI: 10.1101/Gad.1247904  0.231
1989 Snyder SH, Sklar PB, Hwang PM, Pevsner J. Molecular mechanisms of olfaction. Trends in Neurosciences. 12: 35-8. PMID 2471337 DOI: 10.1016/0166-2236(89)90154-9  0.227
1985 Sanberg PR, Pevsner J, Autuono PG, Coyle JT. Fetal methylazoxymethanol acetate-induced lesions cause reductions in dopamine receptor-mediated catalepsy and stereotypy. Neuropharmacology. 24: 1057-62. PMID 4080104 DOI: 10.1016/0028-3908(85)90191-1  0.219
2002 Poole LJ, Yu Y, Kim PS, Zheng QZ, Pevsner J, Hayward GS. Altered patterns of cellular gene expression in dermal microvascular endothelial cells infected with Kaposi's sarcoma-associated herpesvirus. Journal of Virology. 76: 3395-420. PMID 11884566 DOI: 10.1128/Jvi.76.7.3395-3420.2002  0.218
2003 Matsushita K, Morrell CN, Cambien B, Yang SX, Yamakuchi M, Bao C, Hara MR, Quick RA, Cao W, O'Rourke B, Lowenstein JM, Pevsner J, Wagner DD, Lowenstein CJ. Nitric oxide regulates exocytosis by S-nitrosylation of N-ethylmaleimide-sensitive factor. Cell. 115: 139-50. PMID 14567912 DOI: 10.1016/S0092-8674(03)00803-1  0.218
1988 Pevsner J, Hwang PM, Sklar PB, Venable JC, Snyder SH. Odorant-binding protein and its mRNA are localized to lateral nasal gland implying a carrier function. Proceedings of the National Academy of Sciences of the United States of America. 85: 2383-7. PMID 3353387 DOI: 10.1073/Pnas.85.7.2383  0.218
2003 Ha PK, Benoit NE, Yochem R, Sciubba J, Zahurak M, Sidransky D, Pevsner J, Westra WH, Califano J. A transcriptional progression model for head and neck cancer. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 9: 3058-64. PMID 12912957  0.216
1986 Pevsner J, Sklar PB, Snyder SH. Odorant-binding protein: localization to nasal glands and secretions. Proceedings of the National Academy of Sciences of the United States of America. 83: 4942-6. PMID 3523479 DOI: 10.1073/Pnas.83.13.4942  0.213
2007 Ladd-Acosta C, Pevsner J, Sabunciyan S, Yolken RH, Webster MJ, Dinkins T, Callinan PA, Fan JB, Potash JB, Feinberg AP. DNA methylation signatures within the human brain. American Journal of Human Genetics. 81: 1304-15. PMID 17999367 DOI: 10.1086/524110  0.212
1987 PEVSNER J, SKLAR PB, SNYDER SH. Isolation and Characterization of an Odorant-Binding Protein Annals of the New York Academy of Sciences. 510: 547-549. DOI: 10.1111/J.1749-6632.1987.Tb43621.X  0.21
2008 Miller RA, Christoforou N, Pevsner J, McCallion AS, Gearhart JD. Efficient array-based identification of novel cardiac genes through differentiation of mouse ESCs. Plos One. 3: e2176. PMID 18478100 DOI: 10.1371/Journal.Pone.0002176  0.206
2022 Kondo M, Norris A, Yang K, Cheshire M, Newkirk I, Chen X, Ishizuka K, Jaffe AE, Sawa A, Pevsner J. Dysfunction of mitochondria and GABAergic interneurons in the anterior cingulate cortex of individuals with schizophrenia. Neuroscience Research. PMID 36162734 DOI: 10.1016/j.neures.2022.09.011  0.204
1990 Pevsner J, Snyder SH. Odorant-binding protein: Odorant transport function in the vertebrate nasal epithelium Chemical Senses. 15: 217-222. DOI: 10.1093/Chemse/15.2.217  0.202
2020 Osei-Owusu IA, Norris AL, Joynt AT, Thorpe J, Cho S, Tierney E, Schmidt J, Hagopian L, Harris J, Pevsner J. Characterization of an unbalanced translocation causing 3q28qter duplication and 10q26.2qter deletion in a patient with global developmental delay and self-injury. Cold Spring Harbor Molecular Case Studies. 6. PMID 33335013 DOI: 10.1101/mcs.a005884  0.191
2018 Krishnan V, Park SA, Shin SS, Alon L, Tressler CM, Stokes W, Banerjee J, Sorrell ME, Tian Y, Fridman GY, Celnik P, Pevsner J, Guggino WB, Gilad AA, Pelled G. Wireless control of cellular function by activation of a novel protein responsive to electromagnetic fields. Scientific Reports. 8: 8764. PMID 29884813 DOI: 10.1038/S41598-018-27087-9  0.183
2016 Freed D, Pevsner J. The Contribution of Mosaic Variants to Autism Spectrum Disorder. Plos Genetics. 12: e1006245. PMID 27632392 DOI: 10.1371/journal.pgen.1006245  0.179
2021 Huang L, Bichsel C, Norris A, Thorpe J, Pevsner J, Alexandrescu S, Pinto A, Zurakowski D, Kleiman RJ, Sahin M, Greene AK, Bischoff J. Endothelial p.R183Q Increases ANGPT2 (Angiopoietin-2) and Drives Formation of Enlarged Blood Vessels. Arteriosclerosis, Thrombosis, and Vascular Biology. ATVBAHA121316651. PMID 34670408 DOI: 10.1161/ATVBAHA.121.316651  0.176
2021 Fjær R, Marciniak K, Sundnes O, Hjorthaug H, Sheng Y, Hammarström C, Sitek JC, Vigeland MD, Backe PH, Øye AM, Fosse JH, Stav-Noraas TE, Uchiyama Y, Matsumoto N, Comi A, ... Pevsner J, et al. A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-weber syndrome. Human Molecular Genetics. PMID 34124757 DOI: 10.1093/hmg/ddab144  0.173
1999 Wang H, Pevsner J. Detection of endogenous biotin in various tissues: novel functions in the hippocampus and implications for its use in avidin-biotin technology. Cell and Tissue Research. 296: 511-6. PMID 10370137 DOI: 10.1007/s004410051311  0.169
2003 Peri S, Navarro JD, Amanchy R, Kristiansen TZ, Jonnalagadda CK, Surendranath V, Niranjan V, Muthusamy B, Gandhi TK, Gronborg M, Ibarrola N, Deshpande N, Shanker K, Shivashankar HN, Rashmi BP, ... ... Pevsner J, et al. Development of human protein reference database as an initial platform for approaching systems biology in humans. Genome Research. 13: 2363-71. PMID 14525934 DOI: 10.1101/Gr.1680803  0.168
2007 Wang W, Carvalho B, Miller N, Pevsner J, Chakravarti A, Irizarry RA. Estimating genome-wide copy number using allele specific mixture models Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 4453: 137-150.  0.161
2018 Scheinfeldt LB, Hodges K, Pevsner J, Berlin D, Turan N, Gerry NP. Genetic and genomic stability across lymphoblastoid cell line expansions. Bmc Research Notes. 11: 558. PMID 30075799 DOI: 10.1186/s13104-018-3664-3  0.16
2021 Wang Y, Bae T, Thorpe J, Sherman MA, Jones AG, Cho S, Daily K, Dou Y, Ganz J, Galor A, Lobon I, Pattni R, Rosenbluh C, Tomasi S, Tomasini L, ... ... Pevsner J, et al. Comprehensive identification of somatic nucleotide variants in human brain tissue. Genome Biology. 22: 92. PMID 33781308 DOI: 10.1186/s13059-021-02285-3  0.159
2016 Goodwin CR, Woodard CL, Zhou X, Pan J, Olivi A, Xia S, Bettegowda C, Sciubba DM, Pevsner J, Zhu H, Laterra J. Microarray-Based Phospho-Proteomic Profiling of Complex Biological Systems. Translational Oncology. 9: 124-9. PMID 27084428 DOI: 10.1016/J.Tranon.2016.02.001  0.156
2000 Dang DT, Pevsner J, Yang VW. The biology of the mammalian Krüppel-like family of transcription factors. The International Journal of Biochemistry & Cell Biology. 32: 1103-21. PMID 11137451 DOI: 10.1016/S1357-2725(00)00059-5  0.156
1991 Volknandt W, Pevsner J, Elferink LA, Schilling J, Scheller RH. A synaptic vesicle specific GTP-binding protein from ray electric organ. Brain Research. Molecular Brain Research. 11: 283-90. PMID 1721993 DOI: 10.1016/0169-328X(91)90037-X  0.155
2007 Goin-Kochel RP, Abbacchi A, Constantino JN, Geschwind DH, Brown WT, Bucan M, Buxbaum J, Gilliam TC, Greenberg DA, Ledbetter DH, Miller B, Nelson SF, Pevsner J, Schellenberg GD, Smango-Sprouse CA, et al. Lack of evidence for increased genetic loading for autism among families of affected females: A replication from family history data in two large samples Autism. 11: 279-286. PMID 17478580 DOI: 10.1177/1362361307076857  0.154
1999 Watkins PA, Pevsner J, Steinberg SJ. Human very long-chain acyl-CoA synthetase and two human homologs: initial characterization and relationship to fatty acid transport protein. Prostaglandins, Leukotrienes, and Essential Fatty Acids. 60: 323-8. PMID 10471116 DOI: 10.1016/S0952-3278(99)80007-6  0.132
1997 Wang H, Frelin L, Pevsner J. Human syntaxin 7: a Pep12p/Vps6p homologue implicated in vesicle trafficking to lysosomes. Gene. 199: 39-48. PMID 9358037 DOI: 10.1016/S0378-1119(97)00343-0  0.128
1997 Naren AP, Nelson DJ, Xie W, Jovov B, Pevsner J, Bennett MK, Benos DJ, Quick MW, Kirk KL. Regulation of CFTR chloride channels by syntaxin and Munc18 isoforms. Nature. 390: 302-5. PMID 9384384 DOI: 10.1038/36882  0.126
2009 Pevsner J. Bioinformatics and Functional Genomics: Second Edition Bioinformatics and Functional Genomics: Second Edition. 1-951. DOI: 10.1002/9780470451496  0.123
1994 Pevsner J, Hsu SC, Scheller RH. n-Sec1: a neural-specific syntaxin-binding protein. Proceedings of the National Academy of Sciences of the United States of America. 91: 1445-9. PMID 8108429  0.12
1999 Kadkol SS, Brody JR, Pevsner J, Bai J, Pasternack GR. Modulation of oncogenic potential by alternative gene use in human prostate cancer. Nature Medicine. 5: 275-9. PMID 10086381 DOI: 10.1038/6488  0.114
1994 Pevsner J, Volknandt W, Wong BR, Scheller RH. Two rat homologs of clathrin-associated adaptor proteins. Gene. 146: 279-83. PMID 8076832 DOI: 10.1016/0378-1119(94)90306-9  0.112
2000 Ward DM, Pevsner J, Scullion MA, Vaughn M, Kaplan J. Syntaxin 7 and VAMP-7 are soluble N-ethylmaleimide-sensitive factor attachment protein receptors required for late endosome-lysosome and homotypic lysosome fusion in alveolar macrophages. Molecular Biology of the Cell. 11: 2327-33. PMID 10888671 DOI: 10.1091/Mbc.11.7.2327  0.111
2017 Theisen BE, Rumyantseva A, Cohen JS, Alcaraz WA, Shinde DN, Tang S, Srivastava S, Pevsner J, Trifunovic A, Fatemi A. Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy. American Journal of Medical Genetics. Part A. PMID 28650581 DOI: 10.1002/Ajmg.A.38339  0.109
1993 Volknandt W, Pevsner J, Elferink LA, Scheller RH. Association of three small GTP-binding proteins with cholinergic synaptic vesicles. Febs Letters. 317: 53-6. PMID 8428634 DOI: 10.1016/0014-5793(93)81490-Q  0.096
1996 Pevsner J. The role of Sec1p-related proteins in vesicle trafficking in the nerve terminal. Journal of Neuroscience Research. 45: 89-95. PMID 8843026 DOI: 10.1002/(SICI)1097-4547(19960715)45:2<89::AID-JNR1>3.0.CO;2-B  0.095
1988 Pevsner J, Reed RR, Feinstein PG, Snyder SH. Molecular cloning of odorant-binding protein: member of a ligand carrier family. Science (New York, N.Y.). 241: 336-9. PMID 3388043 DOI: 10.1126/SCIENCE.3388043  0.086
2000 Wang H, Wolosker H, Pevsner J, Snyder SH, Selkoe DJ. Regulation of rat magnocellular neurosecretory system by D-aspartate: evidence for biological role(s) of a naturally occurring free D-amino acid in mammals. The Journal of Endocrinology. 167: 247-52. PMID 11054638 DOI: 10.1677/Joe.0.1670247  0.086
2020 Rubinstein YR, Robinson PN, Gahl WA, Avillach P, Baynam G, Cederroth H, Goodwin RM, Groft SC, Hansson MG, Harris NL, Huser V, Mascalzoni D, McMurry JA, Might M, Nellaker C, ... ... Pevsner J, et al. The case for open science: rare diseases. Jamia Open. 3: 472-486. PMID 33426479 DOI: 10.1093/jamiaopen/ooaa030  0.086
1991 Volknandt W, Vogel M, Pevsner J, Misumi Y, Ikehara Y, Zimmermann H. 5'-nucleotidase from the electric ray electric lobe. Primary structure and relation to mammalian and procaryotic enzymes. European Journal of Biochemistry / Febs. 202: 855-61. PMID 1765099 DOI: 10.1111/J.1432-1033.1991.TB16443.X  0.08
1998 Shuang R, Zhang L, Fletcher A, Groblewski GE, Pevsner J, Stuenkel EL. Regulation of Munc-18/syntaxin 1A interaction by cyclin-dependent kinase 5 in nerve endings. The Journal of Biological Chemistry. 273: 4957-66. PMID 9478941 DOI: 10.1074/Jbc.273.9.4957  0.078
1994 Pevsner J, Scheller RH. Mechanisms of vesicle docking and fusion: insights from the nervous system. Current Opinion in Cell Biology. 6: 555-60. PMID 7986533 DOI: 10.1016/0955-0674(94)90076-0  0.073
1994 Pevsner J, Hsu SC, Braun JE, Calakos N, Ting AE, Bennett MK, Scheller RH. Specificity and regulation of a synaptic vesicle docking complex. Neuron. 13: 353-61. PMID 8060616 DOI: 10.1016/0896-6273(94)90352-2  0.073
2002 Wang H, Wolosker H, Morris JF, Pevsner J, Snyder SH, Selkoe DJ. Naturally occurring free D-aspartate is a nuclear component of cells in the mammalian hypothalamo-neurohypophyseal system. Neuroscience. 109: 1-4. PMID 11784695 DOI: 10.1016/S0306-4522(01)00545-0  0.062
1987 Pevsner J, Sklar PB, Snyder SH. Isolation and characterization of an odorant-binding protein Annals of the New York Academy of Sciences. 510: 547-549.  0.054
1996 Bianchet MA, Bains G, Pelosi P, Pevsner J, Snyder SH, Monaco HL, Amzel LM. The three-dimensional structure of bovine odorant binding protein and its mechanism of odor recognition. Nature Structural Biology. 3: 934-9. PMID 8901871 DOI: 10.1038/nsb1196-934  0.045
1984 Sanberg PR, Pevsner J, Coyle JT. Parametric influences on catalepsy. Psychopharmacology. 82: 406-8. PMID 6427835 DOI: 10.1007/Bf00427696  0.045
1990 Pevsner J, Hou V, Snowman AM, Snyder SH. Odorant-binding protein. Characterization of ligand binding. The Journal of Biological Chemistry. 265: 6118-25. PMID 2318850  0.041
1989 Glikman L, Glicksman A, Pevsner J, Levin I. Abnormal renal mobility--an indication for surgical intervention. Urologia Internationalis. 44: 166-8. PMID 2749932  0.034
1988 Snyder SH, Sklar PB, Pevsner J. Molecular mechanisms of olfaction. The Journal of Biological Chemistry. 263: 13971-4. PMID 2459115  0.028
2013 Pevsner J. Leonardo da Vinci, Neuroscientist Scientific American. 23: 48-55. DOI: 10.1038/SCIENTIFICAMERICANCREATIVITY1213-48  0.01
2007 Pevsner J. Removal of cerumen from ear canal using lighted curettes. American Family Physician. 76: 32. PMID 17668838  0.01
2005 Pevsner J. Leonardo da Vinci, Neuroscientist Scientific American Mind. 16: 84-91. DOI: 10.1038/SCIENTIFICAMERICANMIND0405-84  0.01
1994 Pevsner J. Concerns about universal hepatitis B immunization. American Family Physician. 49: 47; author reply 48,. PMID 8273721  0.01
Hide low-probability matches.