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Items: 1 to 20 of 252

1.

Amnion as a surrogate tissue reporter of the effects of maternal preeclampsia on the fetus.

Suzuki M, Maekawa R, Patterson NE, Reynolds DM, Calder BR, Reznik SE, Heo HJ, Einstein FH, Greally JM.

Clin Epigenetics. 2016 Jun 10;8:67. doi: 10.1186/s13148-016-0234-1. eCollection 2016.

2.

Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe.

Blauwendraat C, Francescatto M, Gibbs JR, Jansen IE, Simón-Sánchez J, Hernandez DG, Dillman AA, Singleton AB, Cookson MR, Rizzu P, Heutink P.

Genome Med. 2016 Jun 10;8(1):65. doi: 10.1186/s13073-016-0320-1.

3.

IGF1R as a Key Target in High Risk, Metastatic Medulloblastoma.

Svalina MN, Kikuchi K, Abraham J, Lal S, Davare MA, Settelmeyer TP, Young MC, Peckham JL, Cho YJ, Michalek JE, Hernandez BS, Berlow NE, Jackson M, Guillaume DJ, Selden NR, Bigner DD, Nazemi KJ, Green SC, Corless CL, Gultekin S, Mansoor A, Rubin BP, Woltjer R, Keller C.

Sci Rep. 2016 Jun 3;6:27012. doi: 10.1038/srep27012.

4.

Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease.

Sassi C, Ridge PG, Nalls MA, Gibbs R, Ding J, Lupton MK, Troakes C, Lunnon K, Al-Sarraj S, Brown KS, Medway C, Lord J, Turton J; ARUK Consortium, Morgan K, Powell JF, Kauwe JS, Cruchaga C, Bras J, Goate AM, Singleton AB, Guerreiro R, Hardy J.

PLoS One. 2016 Jun 1;11(6):e0150079. doi: 10.1371/journal.pone.0150079. eCollection 2016.

5.

Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation.

Do C, Lang CF, Lin J, Darbary H, Krupska I, Gaba A, Petukhova L, Vonsattel JP, Gallagher MP, Goland RS, Clynes RA, Dwork A, Kral JG, Monk C, Christiano AM, Tycko B.

Am J Hum Genet. 2016 May 5;98(5):934-55. doi: 10.1016/j.ajhg.2016.03.027.

PMID:
27153397
6.

Migration and DNA methylation: a comparison of methylation patterns in type 2 diabetes susceptibility genes between indians and europeans.

Elliott HR, Walia GK, Duggirala A, Groom A, Reddy SU, Chandak GR, Gupta V, Laakso M, Dekker JM; RISC Consortium, Walker M, Ebrahim S, Smith GD, Relton CL.

J Diabetes Res Clin Metab. 2013;2:6. Epub 2013 Feb 6.

7.

Allele-Skewed DNA Modification in the Brain: Relevance to a Schizophrenia GWAS.

Gagliano SA, Ptak C, Mak DY, Shamsi M, Oh G, Knight J, Boutros PC, Petronis A.

Am J Hum Genet. 2016 May 5;98(5):956-62. doi: 10.1016/j.ajhg.2016.03.006. Epub 2016 Apr 14.

PMID:
27087318
8.

Integrative Tissue-Specific Functional Annotations in the Human Genome Provide Novel Insights on Many Complex Traits and Improve Signal Prioritization in Genome Wide Association Studies.

Lu Q, Powles RL, Wang Q, He BJ, Zhao H.

PLoS Genet. 2016 Apr 8;12(4):e1005947. doi: 10.1371/journal.pgen.1005947. eCollection 2016 Apr.

9.

Shared genetic control of expression and methylation in peripheral blood.

Shakhbazov K, Powell JE, Hemani G, Henders AK, Martin NG, Visscher PM, Montgomery GW, McRae AF.

BMC Genomics. 2016 Apr 6;17(1):278. doi: 10.1186/s12864-016-2498-4.

10.

Systematic identification of genetic influences on methylation across the human life course.

Gaunt TR, Shihab HA, Hemani G, Min JL, Woodward G, Lyttleton O, Zheng J, Duggirala A, McArdle WL, Ho K, Ring SM, Evans DM, Davey Smith G, Relton CL.

Genome Biol. 2016 Mar 31;17(1):61. doi: 10.1186/s13059-016-0926-z.

11.

A Systematic Investigation into Aging Related Genes in Brain and Their Relationship with Alzheimer's Disease.

Meng G, Zhong X, Mei H.

PLoS One. 2016 Mar 3;11(3):e0150624. doi: 10.1371/journal.pone.0150624. eCollection 2016.

12.

Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci.

Karch CM, Ezerskiy LA, Bertelsen S; Alzheimer’s Disease Genetics Consortium (ADGC), Goate AM.

PLoS One. 2016 Feb 26;11(2):e0148717. doi: 10.1371/journal.pone.0148717. eCollection 2016.

13.

Genetic variants near MLST8 and DHX57 affect the epigenetic age of the cerebellum.

Lu AT, Hannon E, Levine ME, Hao K, Crimmins EM, Lunnon K, Kozlenkov A, Mill J, Dracheva S, Horvath S.

Nat Commun. 2016 Feb 2;7:10561. doi: 10.1038/ncomms10561.

14.

Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer's disease.

Watson CT, Roussos P, Garg P, Ho DJ, Azam N, Katsel PL, Haroutunian V, Sharp AJ.

Genome Med. 2016 Jan 19;8(1):5. doi: 10.1186/s13073-015-0258-8.

15.

Analysis of a four generation family reveals the widespread sequence-dependent maintenance of allelic DNA methylation in somatic and germ cells.

Tang A, Huang Y, Li Z, Wan S, Mou L, Yin G, Li N, Xie J, Xia Y, Li X, Luo L, Zhang J, Chen S, Wu S, Sun J, Sun X, Jiang Z, Chen J, Li Y, Wang J, Wang J, Cai Z, Gui Y.

Sci Rep. 2016 Jan 13;6:19260. doi: 10.1038/srep19260.

16.

Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brain.

Chen L, Tao Y, Song F, Yuan X, Wang J, Saffen D.

Sci Rep. 2016 Jan 8;6:19010. doi: 10.1038/srep19010.

17.

High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction.

McClay JL, Shabalin AA, Dozmorov MG, Adkins DE, Kumar G, Nerella S, Clark SL, Bergen SE; Swedish Schizophrenia Consortium, Hultman CM, Magnusson PK, Sullivan PF, Aberg KA, van den Oord EJ.

Genome Biol. 2015 Dec 23;16:291. doi: 10.1186/s13059-015-0842-7.

18.

HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease.

Ward LD, Kellis M.

Nucleic Acids Res. 2016 Jan 4;44(D1):D877-81. doi: 10.1093/nar/gkv1340. Epub 2015 Dec 10.

19.

The impact of genetic variation and cigarette smoke on DNA methylation in current and former smokers from the COPDGene study.

Qiu W, Wan E, Morrow J, Cho MH, Crapo JD, Silverman EK, DeMeo DL.

Epigenetics. 2015;10(11):1064-73. doi: 10.1080/15592294.2015.1106672.

PMID:
26646902
20.

Genome-wide methylation analysis identifies differentially methylated CpG loci associated with severe obesity in childhood.

Huang RC, Garratt ES, Pan H, Wu Y, Davis EA, Barton SJ, Burdge GC, Godfrey KM, Holbrook JD, Lillycrop KA.

Epigenetics. 2015;10(11):995-1005. doi: 10.1080/15592294.2015.1080411.

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