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Items: 1 to 50 of 67

1.

Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.

Bigdeli TB, Genovese G, Georgakopoulos P, Meyers JL, Peterson RE, Iyegbe CO, Medeiros H, Valderrama J, Achtyes ED, Kotov R, Stahl EA, Abbott C, Azevedo MH, Belliveau RA, Bevilacqua E, Bromet EJ, Byerley W, Carvalho CB, Chapman SB, DeLisi LE, Dumont AL, O'Dushlaine C, Evgrafov OV, Fochtmann LJ, Gage D, Kennedy JL, Kinkead B, Macedo A, Moran JL, Morley CP, Dewan MJ, Nemesh J, Perkins DO, Purcell SM, Rakofsky JJ, Scolnick EM, Sklar BM, Sklar P, Smoller JW, Sullivan PF, Macciardi F, Marder SR, Gur RC, Gur RE, Braff DL; Consortium on the Genetics of Schizophrenia (COGS) Investigators, Nicolini H, Escamilla MA, Vawter MP, Sobell JL, Malaspina D, Lehrer DS, Buckley PF, Rapaport MH, Knowles JA; Genomic Psychiatry Cohort (GPC) Consortium, Fanous AH, Pato MT, McCarroll SA, Pato CN.

Mol Psychiatry. 2019 Oct 7. doi: 10.1038/s41380-019-0517-y. [Epub ahead of print]

PMID:
31591465
2.

Deconvolution of transcriptional networks identifies TCF4 as a master regulator in schizophrenia.

Doostparast Torshizi A, Armoskus C, Zhang H, Forrest MP, Zhang S, Souaiaia T, Evgrafov OV, Knowles JA, Duan J, Wang K.

Sci Adv. 2019 Sep 11;5(9):eaau4139. doi: 10.1126/sciadv.aau4139. eCollection 2019 Sep.

3.

Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation.

Rhie SK, Schreiner S, Witt H, Armoskus C, Lay FD, Camarena A, Spitsyna VN, Guo Y, Berman BP, Evgrafov OV, Knowles JA, Farnham PJ.

Sci Adv. 2018 Dec 13;4(12):eaav8550. doi: 10.1126/sciadv.aav8550. eCollection 2018 Dec.

4.

Integrative functional genomic analysis of human brain development and neuropsychiatric risks.

Li M, Santpere G, Imamura Kawasawa Y, Evgrafov OV, Gulden FO, Pochareddy S, Sunkin SM, Li Z, Shin Y, Zhu Y, Sousa AMM, Werling DM, Kitchen RR, Kang HJ, Pletikos M, Choi J, Muchnik S, Xu X, Wang D, Lorente-Galdos B, Liu S, Giusti-Rodríguez P, Won H, de Leeuw CA, Pardiñas AF; BrainSpan Consortium; PsychENCODE Consortium; PsychENCODE Developmental Subgroup, Hu M, Jin F, Li Y, Owen MJ, O'Donovan MC, Walters JTR, Posthuma D, Reimers MA, Levitt P, Weinberger DR, Hyde TM, Kleinman JE, Geschwind DH, Hawrylycz MJ, State MW, Sanders SJ, Sullivan PF, Gerstein MB, Lein ES, Knowles JA, Sestan N.

Science. 2018 Dec 14;362(6420). pii: eaat7615. doi: 10.1126/science.aat7615.

5.

Endogenous Cell Type-Specific Disrupted in Schizophrenia 1 Interactomes Reveal Protein Networks Associated With Neurodevelopmental Disorders.

Wilkinson B, Evgrafov OV, Zheng D, Hartel N, Knowles JA, Graham NA, Ichida JK, Coba MP.

Biol Psychiatry. 2019 Feb 15;85(4):305-316. doi: 10.1016/j.biopsych.2018.05.009. Epub 2018 May 23.

PMID:
29961565
6.

Analysis of Gene Expression Variance in Schizophrenia Using Structural Equation Modeling.

Igolkina AA, Armoskus C, Newman JRB, Evgrafov OV, McIntyre LM, Nuzhdin SV, Samsonova MG.

Front Mol Neurosci. 2018 Jun 11;11:192. doi: 10.3389/fnmol.2018.00192. eCollection 2018.

7.

Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders.

Li J, Zhang W, Yang H, Howrigan DP, Wilkinson B, Souaiaia T, Evgrafov OV, Genovese G, Clementel VA, Tudor JC, Abel T, Knowles JA, Neale BM, Wang K, Sun F, Coba MP.

Nat Neurosci. 2017 Aug;20(8):1150-1161. doi: 10.1038/nn.4594. Epub 2017 Jun 26.

8.

Transcriptional Gene Silencing of the Autism-Associated Long Noncoding RNA MSNP1AS in Human Neural Progenitor Cells.

DeWitt JJ, Hecht PM, Grepo N, Wilkinson B, Evgrafov OV, Morris KV, Knowles JA, Campbell DB.

Dev Neurosci. 2016;38(5):375-383. doi: 10.1159/000453258. Epub 2016 Dec 29.

9.

Assessing characteristics of RNA amplification methods for single cell RNA sequencing.

Dueck HR, Ai R, Camarena A, Ding B, Dominguez R, Evgrafov OV, Fan JB, Fisher SA, Herstein JS, Kim TK, Kim JM, Lin MY, Liu R, Mack WJ, McGroty S, Nguyen JD, Salathia N, Shallcross J, Souaiaia T, Spaethling JM, Walker CP, Wang J, Wang K, Wang W, Wildberg A, Zheng L, Chow RH, Eberwine J, Knowles JA, Zhang K, Kim J.

BMC Genomics. 2016 Nov 24;17(1):966.

10.

Impact of the Autism-Associated Long Noncoding RNA MSNP1AS on Neuronal Architecture and Gene Expression in Human Neural Progenitor Cells.

DeWitt JJ, Grepo N, Wilkinson B, Evgrafov OV, Knowles JA, Campbell DB.

Genes (Basel). 2016 Sep 28;7(10). pii: E76.

11.

Long-read sequencing and de novo assembly of a Chinese genome.

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.

Nat Commun. 2016 Jun 30;7:12065. doi: 10.1038/ncomms12065.

12.

EphA7 regulates spiral ganglion innervation of cochlear hair cells.

Kim YJ, Ibrahim LA, Wang SZ, Yuan W, Evgrafov OV, Knowles JA, Wang K, Tao HW, Zhang LI.

Dev Neurobiol. 2016 Apr;76(4):452-69. doi: 10.1002/dneu.22326. Epub 2015 Jul 27.

13.

Non-coding RNAs derived from an alternatively spliced REST transcript (REST-003) regulate breast cancer invasiveness.

Lee NS, Evgrafov OV, Souaiaia T, Bonyad A, Herstein J, Lee JY, Kim J, Ning Y, Sixto M, Weitz AC, Lenz HJ, Wang K, Knowles JA, Press MF, Salvaterra PM, Shung KK, Chow RH.

Sci Rep. 2015 Jun 8;5:11207. doi: 10.1038/srep11207.

14.

The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes.

Wilkinson B, Grepo N, Thompson BL, Kim J, Wang K, Evgrafov OV, Lu W, Knowles JA, Campbell DB.

Transl Psychiatry. 2015 May 19;5:e568. doi: 10.1038/tp.2015.62.

15.

Effect of RNA integrity on uniquely mapped reads in RNA-Seq.

Chen EA, Souaiaia T, Herstein JS, Evgrafov OV, Spitsyna VN, Rebolini DF, Knowles JA.

BMC Res Notes. 2014 Oct 23;7:753. doi: 10.1186/1756-0500-7-753.

16.

Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.

Plummer JT, Evgrafov OV, Bergman MY, Friez M, Haiman CA, Levitt P, Aldinger KA.

Transl Psychiatry. 2013 Oct 22;3:e316. doi: 10.1038/tp.2013.91.

17.

Assessing the efficacy of endoscopic office olfactory biopsy sites to produce neural progenitor cell cultures for the study of neuropsychiatric disorders.

Wrobel BB, Mazza JM, Evgrafov OV, Knowles JA.

Int Forum Allergy Rhinol. 2013 Feb;3(2):133-8. doi: 10.1002/alr.21080. Epub 2012 Nov 28.

18.

RseqFlow: workflows for RNA-Seq data analysis.

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.

Bioinformatics. 2011 Sep 15;27(18):2598-600. doi: 10.1093/bioinformatics/btr441. Epub 2011 Jul 27.

19.

Olfactory neuroepithelium-derived neural progenitor cells as a model system for investigating the molecular mechanisms of neuropsychiatric disorders.

Evgrafov OV, Wrobel BB, Kang X, Simpson G, Malaspina D, Knowles JA.

Psychiatr Genet. 2011 Oct;21(5):217-28. doi: 10.1097/YPG.0b013e328341a2f0.

PMID:
21451437
20.

Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3.

Verma R, Holmans P, Knowles JA, Grover D, Evgrafov OV, Crowe RR, Scheftner WA, Weissman MM, DePaulo JR Jr, Potash JB, Levinson DF.

Biol Psychiatry. 2008 Jun 15;63(12):1185-9. doi: 10.1016/j.biopsych.2008.02.005. Epub 2008 Mar 25.

21.

Genomewide suggestive linkage of opioid dependence to chromosome 14q.

Lachman HM, Fann CS, Bartzis M, Evgrafov OV, Rosenthal RN, Nunes EV, Miner C, Santana M, Gaffney J, Riddick A, Hsu CL, Knowles JA.

Hum Mol Genet. 2007 Jun 1;16(11):1327-34. Epub 2007 Apr 4.

PMID:
17409192
22.

Genetics of recurrent early-onset major depression (GenRED): significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers.

Levinson DF, Evgrafov OV, Knowles JA, Potash JB, Weissman MM, Scheftner WA, Depaulo JR Jr, Crowe RR, Murphy-Eberenz K, Marta DH, McInnis MG, Adams P, Gladis M, Miller EB, Thomas J, Holmans P.

Am J Psychiatry. 2007 Feb;164(2):259-64.

PMID:
17267788
23.

A novel splicing mutation in exon 4 (456G>A) of the GH1 gene in a patient with congenital isolated growth hormone deficiency.

Fofanova OV, Evgrafov OV, Polyakov AV, Peterkova VA, Dedov II.

Hormones (Athens). 2006 Oct-Dec;5(4):288-94.

24.

GH-1 gene splicing mutations: molecular basis of hereditary isolated growth hormone deficiency in children.

Fofanova OV, Evgrafov OV, Polyakov AV, Peterkova VA, Dedov II.

Bull Exp Biol Med. 2006 Mar;141(3):347-52.

PMID:
17073157
25.

Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.

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.

Nat Genet. 2004 Jun;36(6):602-6. Epub 2004 May 2.

PMID:
15122254
26.

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.

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.

Hum Genet. 2004 May;114(6):527-33. Epub 2004 Mar 12.

PMID:
15021985
27.

[Proximal autosomal recessive types of spinal muscular atrophy].

Kolokolov OV, Iudina GK, Solovykh NN, Evgrafov OV.

Zh Nevrol Psikhiatr Im S S Korsakova. 2003;103(8):66-8. Russian.

PMID:
14564781
28.

BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy.

Pal DK, Evgrafov OV, Tabares P, Zhang F, Durner M, Greenberg DA.

Am J Hum Genet. 2003 Aug;73(2):261-70. Epub 2003 Jun 25.

29.

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.

Fofanova OV, Evgrafov OV, Polyakov AV, Poltaraus AB, Peterkova VA, Dedov II.

J Clin Endocrinol Metab. 2003 Feb;88(2):820-6.

PMID:
12574219
30.

Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract.

Polyakov AV, Shagina IA, Khlebnikova OV, Evgrafov OV.

Clin Genet. 2001 Dec;60(6):476-8. No abstract available.

PMID:
11846744
31.

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21.

Ismailov SM, Fedotov VP, Dadali EL, Polyakov AV, Van Broeckhoven C, Ivanov VI, De Jonghe P, Timmerman V, Evgrafov OV.

Eur J Hum Genet. 2001 Aug;9(8):646-50.

32.

A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency.

Fofanova OV, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S.

Pituitary. 1998 Apr;1(1):45-9.

PMID:
11081182
33.

[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].

Viktorova TV, Vermisheva MA, Shagina IV, Evgrafov OV, Khsnutdinova EK.

Genetika. 2000 Aug;36(8):1150-6. Russian.

PMID:
11033788
34.

[Analysis of mutations and haplotypes of polymorphic markers in patients with Wilson-Konovalov disease from Bashkir].

Karunas AS, Mersiianova IV, Poliakov AV, Evgrafov OV, Khusnutdinova EK.

Genetika. 2000 Jul;36(7):972-9. Russian.

PMID:
10994503
35.

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene.

Mersiyanova IV, Perepelov AV, Polyakov AV, Sitnikov VF, Dadali EL, Oparin RB, Petrin AN, Evgrafov OV.

Am J Hum Genet. 2000 Jul;67(1):37-46. Epub 2000 Jun 7.

36.

Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients.

Mersiyanova IV, Ismailov SM, Polyakov AV, Dadali EL, Fedotov VP, Nelis E, Löfgren A, Timmerman V, van Broeckhoven C, Evgrafov OV.

Hum Mutat. 2000;15(4):340-7. Erratum in: Hum Mutat 2000;16(2):175.

PMID:
10737979
37.

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

Fofanova OV, Takamura N, Kinoshita E, Meerson EM, Iljina VK, Nechvolodova OL, Evgrafov OV, Peterkova VA, Yamashita S.

Endocr J. 1998 Dec;45(6):791-5.

38.

Localization of the gene responsible for familial benign polycythemia to chromosome 11q23.

Vasserman NN, Karzakova LM, Tverskaya SM, Saperov VN, Muchukova OM, Pavlova GP, Efimova NK, Vankina NN, Evgrafov OV.

Hum Hered. 1999 Jun;49(3):129-32.

PMID:
10364675
39.

[Expression of the human dystrophin gene in mdx mouse muscle fibers after transfection using liposomes and synthetic oligopeptides].

Baranov VS, Tarasenko OV, Baranov VS, Tarasenko OV, Baranov AN, Kiselev AV, Ivashchenko TE, Evgrafov OV, Mikhailov Vm, Dickson G.

Genetika. 1998 Jul;34(7):876-82. Russian.

PMID:
9749328
40.

[Genetic aspects of juvenile myoclonic epilepsy].

Mukhin KIu, Evgrafov OV, Petrukhin AS, Khomiakova SP.

Zh Nevrol Psikhiatr Im S S Korsakova. 1998;98(7):48-52. Review. Russian. No abstract available.

PMID:
9721380
41.

[Expression of the human dystrophin gene in mdx mouse skeletal muscles after ballistic transfection].

Zelenin AV, Tarasenko OV, Kolesnikov VA, Mikhaĭlov VM, Kiselev AV, Baranov AN, Zelenina IA, Shafei RA, Ivashchenko TE, Evgrafov OV.

Genetika. 1998 Jun;34(6):730-6. Russian.

PMID:
9719921
42.

Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency.

Fofanova O, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S.

J Clin Endocrinol Metab. 1998 Jul;83(7):2601-4.

PMID:
9661653
43.

Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiency.

Fofanova OV, Takamura N, Kinoshita E, Yoshimoto M, Tsuji Y, Peterkova VA, Evgrafov OV, Dedov II, Goncharov NP, Yamashita S.

Am J Med Genet. 1998 Jun 5;77(5):360-5. Review.

PMID:
9632165
44.

PCR detection of Y-specific sequences in patients with Ullrich-Turner syndrome: clinical implications and limitations.

Osipova GR, Karmanov ME, Kozlova SI, Evgrafov OV.

Am J Med Genet. 1998 Apr 1;76(4):283-7.

PMID:
9545090
45.

High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect.

Polyakov AV, Dzenis IG, Baharev VA, Evgrafov OV.

Hum Mutat. 1998;Suppl 1:S53-4. No abstract available.

PMID:
9452039
46.

Prenatal DNA diagnosis on demand--a possible new approach to DNA service provision.

Tverskaya SM, Dadali EL, Evgrafov OV.

Prenat Diagn. 1997 Oct;17(10):989-90. No abstract available.

PMID:
9358582
47.

Bacterial beta-galactosidase and human dystrophin genes are expressed in mouse skeletal muscle fibers after ballistic transfection.

Zelenin AV, Kolesnikov VA, Tarasenko OA, Shafei RA, Zelenina IA, Mikhailov VV, Semenova ML, Kovalenko DV, Artemyeva OV, Ivaschenko TE, Evgrafov OV, Dickson G, Baranovand VS.

FEBS Lett. 1997 Sep 8;414(2):319-22.

48.

[A new member of the MER2 repeat family is detected in the promoter region of the human X11 gene].

Gel'fand MS, Pugachev VV, Evgrafov OV.

Dokl Akad Nauk. 1997 Jun;354(5):690-5. Russian. No abstract available.

PMID:
9289283
49.

Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis.

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.

Am J Hum Genet. 1997 May;60(5):1174-83.

50.

[The DNA diagnosis of a familial case of Kennedy's spinal and bulbar amyotrophy].

Petrukhin AS, Zavadenko NN, Petrukhin AA, Evgrafov OV.

Zh Nevrol Psikhiatr Im S S Korsakova. 1997;97(3):45-8. Russian.

PMID:
9157759

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