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Year | Number of Results |
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Page 1
Genomic Study of Cardiovascular Continuum Comorbidity.
Acta Naturae. 2015 Jul-Sep;7(3):89-99.
Acta Naturae. 2015.
PMID: 26483964
Free PMC article.
Study of Alzheimer family case reveals hemochromotosis-associated HFE mutation.
Artemov AV, Boulygina ES, Tsygankova SV, Nedoluzhko AV, Chekanov NN, Gruzdeva NM, Selezneva ND, Roshchina IF, Gavrilova SI, Velichkovsky BB, Skryabin KG, Prokhortchouk EB.
Artemov AV, et al. Among authors: chekanov nn.
Hum Genome Var. 2014 Jul 31;1:14004. doi: 10.1038/hgv.2014.4. eCollection 2014.
Hum Genome Var. 2014.
PMID: 27081498
Free PMC article.
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Combining two technologies for full genome sequencing of human.
Skryabin KG, Prokhortchouk EB, Mazur AM, Boulygina ES, Tsygankova SV, Nedoluzhko AV, Rastorguev SM, Matveev VB, Chekanov NN, D A G, Teslyuk AB, Gruzdeva NM, Velikhov VE, Zaridze DG, Kovalchuk MV.
Skryabin KG, et al. Among authors: chekanov nn.
Acta Naturae. 2009 Oct;1(3):102-7.
Acta Naturae. 2009.
PMID: 22649622
Free PMC article.
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Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.
Purdue MP, Johansson M, Zelenika D, Toro JR, Scelo G, Moore LE, Prokhortchouk E, Wu X, Kiemeney LA, Gaborieau V, Jacobs KB, Chow WH, Zaridze D, Matveev V, Lubinski J, Trubicka J, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Bucur A, Bencko V, Foretova L, Janout V, Boffetta P, Colt JS, Davis FG, Schwartz KL, Banks RE, Selby PJ, Harnden P, Berg CD, Hsing AW, Grubb RL 3rd, Boeing H, Vineis P, Clavel-Chapelon F, Palli D, Tumino R, Krogh V, Panico S, Duell EJ, Quirós JR, Sanchez MJ, Navarro C, Ardanaz E, Dorronsoro M, Khaw KT, Allen NE, Bueno-de-Mesquita HB, Peeters PH, Trichopoulos D, Linseisen J, Ljungberg B, Overvad K, Tjønneland A, Romieu I, Riboli E, Mukeria A, Shangina O, Stevens VL, Thun MJ, Diver WR, Gapstur SM, Pharoah PD, Easton DF, Albanes D, Weinstein SJ, Virtamo J, Vatten L, Hveem K, Njølstad I, Tell GS, Stoltenberg C, Kumar R, Koppova K, Cussenot O, Benhamou S, Oosterwijk E, Vermeulen SH, Aben KK, van der Marel SL, Ye Y, Wood CG, Pu X, Mazur AM, Boulygina ES, Chekanov NN, Foglio M, Lechner D, Gut I, Heath S, Blanche H, Hutchinson A, Thomas G, Wang Z, Yeager M, Fraumeni JF Jr, Skryabin KG, McKay JD, Rothman N, Chanock SJ, Lathrop M, Brennan P.
Purdue MP, et al. Among authors: chekanov nn.
Nat Genet. 2011 Jan;43(1):60-5. doi: 10.1038/ng.723. Epub 2010 Dec 5.
Nat Genet. 2011.
PMID: 21131975
Free PMC article.
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Report on noninvasive prenatal testing: classical and alternative approaches.
Pantiukh KS, Chekanov NN, Zaigrin IV, Zotov AM, Mazur AM, Prokhortchouk EB.
Pantiukh KS, et al. Among authors: chekanov nn.
F1000Res. 2016 Apr 22;5:722. doi: 10.12688/f1000research.8243.1. eCollection 2016.
F1000Res. 2016.
PMID: 27781087
Free PMC article.
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Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP.
Cheng TH, Gorman M, Martin L, Barclay E, Casey G; Colon Cancer Family Registry; CGEMS; Saunders B, Thomas H, Clark S, Tomlinson I.
Cheng TH, et al.
Eur J Hum Genet. 2015 Feb;23(2):260-3. doi: 10.1038/ejhg.2014.74. Epub 2014 May 7.
Eur J Hum Genet. 2015.
PMID: 24801760
Free PMC article.
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Individual Genome of the Russian Male: SNP Calling and a de novo Assembly of Unmapped Reads.
Chekanov NN, Boulygina ES, Beletskiy AV, Prokhortchouk EB, Skryabin KG.
Chekanov NN, et al.
Acta Naturae. 2010 Jul;2(3):122-6.
Acta Naturae. 2010.
PMID: 22649659
Free PMC article.
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