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Items: 1 to 20 of 125

1.

Deep sequencing reveals variations in somatic cell mosaic mutations between monozygotic twins with discordant psychiatric disease.

Morimoto Y, Ono S, Imamura A, Okazaki Y, Kinoshita A, Mishima H, Nakane H, Ozawa H, Yoshiura KI, Kurotaki N.

Hum Genome Var. 2017 Jul 27;4:17032. doi: 10.1038/hgv.2017.32. eCollection 2017.

2.

One thousand somatic SNVs per skin fibroblast cell set baseline of mosaic mutational load with patterns that suggest proliferative origin.

Abyzov A, Tomasini L, Zhou B, Vasmatzis N, Coppola G, Amenduni M, Pattni R, Wilson M, Gerstein M, Weissman S, Urban AE, Vaccarino FM.

Genome Res. 2017 Apr;27(4):512-523. doi: 10.1101/gr.215517.116. Epub 2017 Feb 24.

PMID:
28235832
3.

Somatically acquired structural genetic differences: a longitudinal study of elderly Danish twins.

Magaard Koldby K, Nygaard M, Christensen K, Christiansen L.

Eur J Hum Genet. 2016 Oct;24(10):1506-10. doi: 10.1038/ejhg.2016.34. Epub 2016 Apr 20.

PMID:
27094753
4.

An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.

Huang MC, Chuang TP, Chen CH, Wu JY, Chen YT, Li LH, Yang HC.

BMC Genomics. 2016 Mar 31;17:266. doi: 10.1186/s12864-016-2478-8.

5.

Failure to Identify Somatic Mutations in Monozygotic Twins Discordant for Schizophrenia by Whole Exome Sequencing.

Lyu N, Guan LL, Ma H, Wang XJ, Wu BM, Shang FH, Wang D, Wen H, Yu X.

Chin Med J (Engl). 2016 Mar 20;129(6):690-5. doi: 10.4103/0366-6999.178009.

6.

Extensive Hidden Genomic Mosaicism Revealed in Normal Tissue.

Vattathil S, Scheet P.

Am J Hum Genet. 2016 Mar 3;98(3):571-8. doi: 10.1016/j.ajhg.2016.02.003.

7.

The Constitution of the Human Embryo as Substantial Change.

Alvargonzález D.

J Med Philos. 2016 Apr;41(2):172-91. doi: 10.1093/jmp/jhv062. Epub 2016 Feb 4.

8.
9.

Unrevealed mosaicism in the next-generation sequencing era.

Gajecka M.

Mol Genet Genomics. 2016 Apr;291(2):513-30. doi: 10.1007/s00438-015-1130-7. Epub 2015 Oct 19. Review.

10.

Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome.

Žilina O, Koltšina M, Raid R, Kurg A, Tõnisson N, Salumets A.

BMC Genomics. 2015 Sep 16;16:703. doi: 10.1186/s12864-015-1916-3.

11.

Chromosomal Rearrangements in Cancer: Detection and potential causal mechanisms.

Hasty P, Montagna C.

Mol Cell Oncol. 2014 Jul;1(1). pii: e29904.

12.

DNA methylation differences in monozygotic twin pairs discordant for schizophrenia identifies psychosis related genes and networks.

Castellani CA, Laufer BI, Melka MG, Diehl EJ, O'Reilly RL, Singh SM.

BMC Med Genomics. 2015 May 6;8:17. doi: 10.1186/s12920-015-0093-1.

13.

Characterization of large structural genetic mosaicism in human autosomes.

Machiela MJ, Zhou W, Sampson JN, Dean MC, Jacobs KB, Black A, Brinton LA, Chang IS, Chen C, Chen C, Chen K, Cook LS, Crous Bou M, De Vivo I, Doherty J, Friedenreich CM, Gaudet MM, Haiman CA, Hankinson SE, Hartge P, Henderson BE, Hong YC, Hosgood HD 3rd, Hsiung CA, Hu W, Hunter DJ, Jessop L, Kim HN, Kim YH, Kim YT, Klein R, Kraft P, Lan Q, Lin D, Liu J, Le Marchand L, Liang X, Lissowska J, Lu L, Magliocco AM, Matsuo K, Olson SH, Orlow I, Park JY, Pooler L, Prescott J, Rastogi R, Risch HA, Schumacher F, Seow A, Setiawan VW, Shen H, Sheng X, Shin MH, Shu XO, VanDen Berg D, Wang JC, Wentzensen N, Wong MP, Wu C, Wu T, Wu YL, Xia L, Yang HP, Yang PC, Zheng W, Zhou B, Abnet CC, Albanes D, Aldrich MC, Amos C, Amundadottir LT, Berndt SI, Blot WJ, Bock CH, Bracci PM, Burdett L, Buring JE, Butler MA, Carreón T, Chatterjee N, Chung CC, Cook MB, Cullen M, Davis FG, Ding T, Duell EJ, Epstein CG, Fan JH, Figueroa JD, Fraumeni JF Jr, Freedman ND, Fuchs CS, Gao YT, Gapstur SM, Patiño-Garcia A, Garcia-Closas M, Gaziano JM, Giles GG, Gillanders EM, Giovannucci EL, Goldin L, Goldstein AM, Greene MH, Hallmans G, Harris CC, Henriksson R, Holly EA, Hoover RN, Hu N, Hutchinson A, Jenab M, Johansen C, Khaw KT, Koh WP, Kolonel LN, Kooperberg C, Krogh V, Kurtz RC, LaCroix A, Landgren A, Landi MT, Li D, Liao LM, Malats N, McGlynn KA, McNeill LH, McWilliams RR, Melin BS, Mirabello L, Peplonska B, Peters U, Petersen GM, Prokunina-Olsson L, Purdue M, Qiao YL, Rabe KG, Rajaraman P, Real FX, Riboli E, Rodríguez-Santiago B, Rothman N, Ruder AM, Savage SA, Schwartz AG, Schwartz KL, Sesso HD, Severi G, Silverman DT, Spitz MR, Stevens VL, Stolzenberg-Solomon R, Stram D, Tang ZZ, Taylor PR, Teras LR, Tobias GS, Viswanathan K, Wacholder S, Wang Z, Weinstein SJ, Wheeler W, White E, Wiencke JK, Wolpin BM, Wu X, Wunder JS, Yu K, Zanetti KA, Zeleniuch-Jacquotte A, Ziegler RG, de Andrade M, Barnes KC, Beaty TH, Bierut LJ, Desch KC, Doheny KF, Feenstra B, Ginsburg D, Heit JA, Kang JH, Laurie CA, Li JZ, Lowe WL, Marazita ML, Melbye M, Mirel DB, Murray JC, Nelson SC, Pasquale LR, Rice K, Wiggs JL, Wise A, Tucker M, Pérez-Jurado LA, Laurie CC, Caporaso NE, Yeager M, Chanock SJ.

Am J Hum Genet. 2015 Mar 5;96(3):487-97. doi: 10.1016/j.ajhg.2015.01.011.

14.

Multiple system atrophy: the application of genetics in understanding etiology.

Federoff M, Schottlaender LV, Houlden H, Singleton A.

Clin Auton Res. 2015 Feb;25(1):19-36. doi: 10.1007/s10286-014-0267-5. Epub 2015 Feb 17. Review.

15.

Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease.

Yang HJ, Ratnapriya R, Cogliati T, Kim JW, Swaroop A.

Prog Retin Eye Res. 2015 May;46:1-30. doi: 10.1016/j.preteyeres.2015.01.005. Epub 2015 Feb 7. Review.

16.

Identification of structural DNA variations in human cell cultures after long-term passage.

Pavlova GV, Vergun AA, Rybalkina EY, Butovskaya PR, Ryskov AP.

Cell Cycle. 2015;14(2):200-5. doi: 10.4161/15384101.2014.974427.

17.

Epigenetics of discordant monozygotic twins: implications for disease.

Castillo-Fernandez JE, Spector TD, Bell JT.

Genome Med. 2014 Jul 31;6(7):60. doi: 10.1186/s13073-014-0060-z. eCollection 2014. Review.

18.

Epigenetic signature of birth weight discordance in adult twins.

Tan Q, Frost M, Heijmans BT, von Bornemann Hjelmborg J, Tobi EW, Christensen K, Christiansen L.

BMC Genomics. 2014 Dec 4;15:1062. doi: 10.1186/1471-2164-15-1062.

19.

Somatic mutations, genome mosaicism, cancer and aging.

Vijg J.

Curr Opin Genet Dev. 2014 Jun;26:141-9. doi: 10.1016/j.gde.2014.04.002. Epub 2014 Oct 2. Review.

20.

Ecological and evolutionary implications of genomic structural variations.

Chain FJ, Feulner PG.

Front Genet. 2014 Sep 16;5:326. doi: 10.3389/fgene.2014.00326. eCollection 2014. No abstract available.

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