Faculty

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Oleg V Evgrafov, PhD
Associate Professor of Research Psychiatry
Psychiatry and The Behavioral Sciences
ZNI 401 1501 San Pablo Street Health Sciences Campus Los Angeles
+1 323 442 1167

Publications

Kim YJ, Ibrahim LA, Wang SZ, Yuan W, Evgrafov OV, Knowles JA, Wang K, Tao HW, Zhang LI. EphA7 regulates spiral ganglion innervation of cochlear hair cells. Dev Neurobiol. 2016 Apr; 76(4):452-69. View in: PubMed

Shi L, Guo Y, Dong C, Huddleston J, Yang H, Han X, Fu A, Li Q, Li N, Gong S, Lintner KE, Ding Q, Wang Z, Hu J, Wang D, Wang F, Wang L, Lyon GJ, Guan Y, Shen Y, Evgrafov OV, Knowles JA, Thibaud-Nissen F, Schneider V, Yu CY, Zhou L, Eichler EE, So KF, Wang K. Long-read sequencing and de novo assembly of a Chinese genome. Nat Commun. 2016; 7:12065. View in: PubMed

Sook Lee N, Evgrafov OV, Souaiaia T, Bonyad A, Herstein J, Yeun Lee J, Kim J, Ning Y, Sixto M, Weitz AC, Lenz HJ, Wang K, Knowles JA, Press MF, Salvaterra PM, Kirk Shung K, Chow RH. Non-coding RNAs derived from an alternatively spliced REST transcript (REST-003) regulate breast cancer invasiveness. Sci Rep. 2015; 5:11207. View in: PubMed

Wilkinson B, Grepo N, Thompson BL, Kim J, Wang K, Evgrafov OV, Lu W, Knowles JA, Campbell DB. The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes. Transl Psychiatry. 2015; 5:e568. View in: PubMed

Hodges LM, Fyer AJ, Weissman MM, Logue MW, Haghighi F, Evgrafov O, Rotondo A, Knowles JA, Hamilton SP. Evidence for Linkage and Association of GABRB3 and GABRA5 to Panic Disorder. Neuropsychopharmacology. 2014 Sep; 39(10):2423-31. View in: PubMed

Chen EA, Souaiaia T, Herstein JS, Evgrafov OV, Spitsyna VN, Rebolini DF, Knowles JA. Effect of RNA integrity on uniquely mapped reads in RNA-Seq. BMC Res Notes. 2014; 7:753. View in: PubMed

Staab TA, Egrafov O, Knowles JA, Sieburth D. Regulation of Synaptic nlg-1/Neuroligin Abundance by the skn-1/Nrf Stress Response Pathway Protects against Oxidative Stress. PLoS Genet. 2014 Jan; 10(1):e1004100. View in: PubMed

Staab TA, Griffen TC, Corcoran C, Evgrafov O, Knowles JA, Sieburth D. The conserved SKN-1/Nrf2 stress response pathway regulates synaptic function in Caenorhabditis elegans. PLoS Genet. 2013 Mar; 9(3):e1003354. View in: PubMed

Wrobel BB, Mazza JM, Evgrafov OV, Knowles JA. Assessing the efficacy of endoscopic office olfactory biopsy sites to produce neural progenitor cell cultures for the study of neuropsychiatric disorders. Int Forum Allergy Rhinol. 2013 Feb; 3(2):133-8. View in: PubMed

Plummer JT, Evgrafov OV, Bergman MY, Friez M, Haiman CA, Levitt P, Aldinger KA. Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome. Transl Psychiatry. 2013; 3:e316. View in: PubMed

Qiu S, Luo S, Evgrafov O, Li R, Schroth GP, Levitt P, Knowles JA, Wang K. Single-neuron RNA-Seq: technical feasibility and reproducibility. Front Genet. 2012; 3:124. View in: PubMed

Evgrafov OV, Wrobel BB, Kang X, Simpson G, Malaspina D, Knowles JA. Olfactory neuroepithelium-derived neural progenitor cells as a model system for investigating the molecular mechanisms of neuropsychiatric disorders. Psychiatr Genet. 2011 Oct; 21(5):217-28. View in: PubMed

Wang Y, Mehta G, Mayani R, Lu J, Souaiaia T, Chen Y, Clark A, Yoon HJ, Wan L, Evgrafov OV, Knowles JA, Deelman E, Chen T. RseqFlow: workflows for RNA-Seq data analysis. Bioinformatics. 2011 Sep 15; 27(18):2598-600. View in: PubMed

Hodges LM, Weissman MM, Haghighi F, Costa R, Bravo O, Evgrafov O, Knowles JA, Fyer AJ, Hamilton SP. Association and linkage analysis of candidate genes GRP, GRPR, CRHR1, and TACR1 in panic disorder. Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5; 150B(1):65-73. View in: PubMed

Verma R, Holmans P, Knowles JA, Grover D, Evgrafov OV, Crowe RR, Scheftner WA, Weissman MM, DePaulo JR, Potash JB, Levinson DF. Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3. Biol Psychiatry. 2008 Jun 15; 63(12):1185-9. View in: PubMed

Lachman HM, Fann CS, Bartzis M, Evgrafov OV, Rosenthal RN, Nunes EV, Miner C, Santana M, Gaffney J, Riddick A, Hsu CL, Knowles JA. Genomewide suggestive linkage of opioid dependence to chromosome 14q. Hum Mol Genet. 2007 Jun 1; 16(11):1327-34. View in: PubMed

Levinson DF, Evgrafov OV, Knowles JA, Potash JB, Weissman MM, Scheftner WA, Depaulo JR, Crowe RR, Murphy-Eberenz K, Marta DH, McInnis MG, Adams P, Gladis M, Miller EB, Thomas J, Holmans P. Genetics of recurrent early-onset major depression (GenRED): significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers. Am J Psychiatry. 2007 Feb; 164(2):259-64. View in: PubMed

Fofanova OV, Evgrafov OV, Polyakov AV, Peterkova VA, Dedov II. A novel splicing mutation in exon 4 (456G>A) of the GH1 gene in a patient with congenital isolated growth hormone deficiency. Hormones (Athens). 2006 Oct-Dec; 5(4):288-94. View in: PubMed

Fyer AJ, Hamilton SP, Durner M, Haghighi F, Heiman GA, Costa R, Evgrafov O, Adams P, de Leon AB, Taveras N, Klein DF, Hodge SE, Weissman MM, Knowles JA. A third-pass genome scan in panic disorder: evidence for multiple susceptibility loci. Biol Psychiatry. 2006 Aug 15; 60(4):388-401. View in: PubMed

Fofanova OV, Evgrafov OV, Polyakov AV, Peterkova VA, Dedov II. GH-1 gene splicing mutations: molecular basis of hereditary isolated growth hormone deficiency in children. Bull Exp Biol Med. 2006 Mar; 141(3):347-52. View in: PubMed

Evgrafov OV, Mersiyanova I, Irobi J, Van Den Bosch L, Dierick I, Leung CL, Schagina O, Verpoorten N, Van Impe K, Fedotov V, Dadali E, Auer-Grumbach M, Windpassinger C, Wagner K, Mitrovic Z, Hilton-Jones D, Talbot K, Martin JJ, Vasserman N, Tverskaya S, Polyakov A, Liem RK, Gettemans J, Robberecht W, De Jonghe P, Timmerman V. Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. Nat Genet. 2004 Jun; 36(6):602-6. View in: PubMed

Tang BS, Luo W, Xia K, Xiao JF, Jiang H, Shen L, Tang JG, Zhao GH, Cai F, Pan Q, Dai HP, Yang QD, Xia JH, Evgrafov OV. A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24. Hum Genet. 2004 May; 114(6):527-33. View in: PubMed

Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, Rochelle J, Dadali EL, Zappia M, Nelis E, Patitucci A, Senderek J, Parman Y, Evgrafov O, Jonghe PD, Takahashi Y, Tsuji S, Pericak-Vance MA, Quattrone A, Battaloglu E, Polyakov AV, Timmerman V, Schröder JM, Vance JM, Battologlu E. Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A. Nat Genet. 2004 May; 36(5):449-51. View in: PubMed

Pal DK, Evgrafov OV, Tabares P, Zhang F, Durner M, Greenberg DA. BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy. Am J Hum Genet. 2003 Aug; 73(2):261-70. View in: PubMed

Resnick IB, Kondratenko I, Pashanov E, Maschan AA, Karachunsky A, Togoev O, Timakov A, Polyakov A, Tverskaya S, Evgrafov O, Roumiantsev AG. 657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls. Am J Med Genet A. 2003 Jul 15; 120A(2):174-9. View in: PubMed

Fofanova OV, Evgrafov OV, Polyakov AV, Poltaraus AB, Peterkova VA, Dedov II. A novel IVS2 -2A>T splicing mutation in the GH-1 gene in familial isolated growth hormone deficiency type II in the spectrum of other splicing mutations in the Russian population. J Clin Endocrinol Metab. 2003 Feb; 88(2):820-6. View in: PubMed

Kalachikov S, Evgrafov O, Ross B, Winawer M, Barker-Cummings C, Martinelli Boneschi F, Choi C, Morozov P, Das K, Teplitskaya E, Yu A, Cayanis E, Penchaszadeh G, Kottmann AH, Pedley TA, Hauser WA, Ottman R, Gilliam TC. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet. 2002 Mar; 30(3):335-41. View in: PubMed

Resnick IB, Kondratenko I, Togoev O, Vasserman N, Shagina I, Evgrafov O, Tverskaya S, Cerosaletti KM, Gatti RA, Concannon P. Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian families. J Pediatr. 2002 Mar; 140(3):355-61. View in: PubMed

Polyakov AV, Shagina IA, Khlebnikova OV, Evgrafov OV. Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract. Clin Genet. 2001 Dec; 60(6):476-8. View in: PubMed

Ismailov SM, Fedotov VP, Dadali EL, Polyakov AV, Van Broeckhoven C, Ivanov VI, De Jonghe P, Timmerman V, Evgrafov OV. A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21. Eur J Hum Genet. 2001 Aug; 9(8):646-50. View in: PubMed

Viktorova TV, Vermisheva MA, Shagina IV, Evgrafov OV, Khsnutdinova EK. [Polymorphism of microsatellite loci DYS19, DYS393, and frequency of the T-C transition of the RBF5 locus on the Y-chromosome in inhabitants of the Volga-Ural region]. Genetika. 2000 Aug; 36(8):1150-6. View in: PubMed

Karunas AS, Mersiianova IV, Poliakov AV, Evgrafov OV, Khusnutdinova EK. [Analysis of mutations and haplotypes of polymorphic markers in patients with Wilson-Konovalov disease from Bashkir]. Genetika. 2000 Jul; 36(7):972-9. View in: PubMed

Mersiyanova IV, Perepelov AV, Polyakov AV, Sitnikov VF, Dadali EL, Oparin RB, Petrin AN, Evgrafov OV. A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene. Am J Hum Genet. 2000 Jul; 67(1):37-46. View in: PubMed

Mersiyanova IV, Ismailov SM, Polyakov AV, Dadali EL, Fedotov VP, Nelis E, Löfgren A, Timmerman V, van Broeckhoven C, Evgrafov OV. Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients. Hum Mutat. 2000; 15(4):340-7. View in: PubMed

Vasserman NN, Karzakova LM, Tverskaya SM, Saperov VN, Muchukova OM, Pavlova GP, Efimova NK, Vankina NN, Evgrafov OV. Localization of the gene responsible for familial benign polycythemia to chromosome 11q23. Hum Hered. 1999 Jun; 49(3):129-32. View in: PubMed

Fofanova OV, Takamura N, Kinoshita E, Meerson EM, Iljina VK, Nechvolodova OL, Evgrafov OV, Peterkova VA, Yamashita S. A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia. Endocr J. 1998 Dec; 45(6):791-5. View in: PubMed

Baranov VS, Tarasenko OV, Baranov VS, Tarasenko OV, Baranov AN, Kiselev AV, Ivashchenko TE, Evgrafov OV, Mikhailov V, Dickson G. [Expression of the human dystrophin gene in mdx mouse muscle fibers after transfection using liposomes and synthetic oligopeptides]. Genetika. 1998 Jul; 34(7):876-82. View in: PubMed

Fofanova O, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S. Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency. J Clin Endocrinol Metab. 1998 Jul; 83(7):2601-4. View in: PubMed

Fofanova OV, Takamura N, Kinoshita E, Yoshimoto M, Tsuji Y, Peterkova VA, Evgrafov OV, Dedov II, Goncharov NP, Yamashita S. Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiency. Am J Med Genet. 1998 Jun 5; 77(5):360-5. View in: PubMed

Zelenin AV, Tarasenko OV, Kolesnikov VA, Mikhailov VM, Kiselev AV, Baranov AN, Zelenina IA, Shafei RA, Ivashchenko TE, Evgrafov OV. [Expression of the human dystrophin gene in mdx mouse skeletal muscles after ballistic transfection]. Genetika. 1998 Jun; 34(6):730-6. View in: PubMed

Fofanova OV, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S. A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency. Pituitary. 1998 Apr; 1(1):45-9. View in: PubMed

Mukhin KIu, Evgrafov OV, Petrukhin AS, Khomiakova SP. [Genetic aspects of juvenile myoclonic epilepsy]. Zh Nevrol Psikhiatr Im S S Korsakova. 1998; 98(7):48-52. View in: PubMed

Polyakov AV, Dzenis IG, Baharev VA, Evgrafov OV. High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect. Hum Mutat. 1998; Suppl 1:S53-4. View in: PubMed

Tverskaya SM, Dadali EL, Evgrafov OV. Prenatal DNA diagnosis on demand--a possible new approach to DNA service provision. Prenat Diagn. 1997 Oct; 17(10):989-90. View in: PubMed

Zerjal T, Dashnyam B, Pandya A, Kayser M, Roewer L, Santos FR, Schiefenhövel W, Fretwell N, Jobling MA, Harihara S, Shimizu K, Semjidmaa D, Sajantila A, Salo P, Crawford MH, Ginter EK, Evgrafov OV, Tyler-Smith C. Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis. Am J Hum Genet. 1997 May; 60(5):1174-83. View in: PubMed

Petrukhin AS, Zavadenko NN, Petrukhin AA, Evgrafov OV. [The DNA diagnosis of a familial case of Kennedy's spinal and bulbar amyotrophy]. Zh Nevrol Psikhiatr Im S S Korsakova. 1997; 97(3):45-8. View in: PubMed

Evgrafov OV, Polyakov AV, Dzenis IG, Baharev VA. Preliminary investigation of mutations in 21-hydroxylase gene in patients with congenital adrenal hyperplasia in Russia. Hum Mutat. 1995; 5(2):131-6. View in: PubMed

Shagina I, Dadali HL, Sitnikov VP, Pugachev VV, Malygina NA, Evgrafov OV. Prenatal diagnosis of spinal muscular atrophy in Russia. Prenat Diagn. 1995 Jan; 15(1):27-34. View in: PubMed

Chukhrova AL, Malygina NA, Poliakov AV, Zaitseva SP, Sitnikov VF, Dadali EL, Kamennykh LN, Khrennikov VIu, Badalian LO, Evgrafov OV. [Screening for deletion in patients with Duchenne's myodystrophy by multiplex amplification]. Tsitol Genet. 1994 Jul-Aug; 28(4):80-3. View in: PubMed

Baranov VS, Gorbunova VN, Malysheva OV, Artemyeva OV, Kascheeva TK, Evgrafov OV, Polyakov AV, Lebedev VM, Kuznetzova TV, Shlykova SN, et al. Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia. Prenat Diagn. 1993 May; 13(5):323-33. View in: PubMed

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