215 related articles for article (PubMed ID: 28334830)
1. Predicting the impact of non-coding variants on DNA methylation.
Zeng H; Gifford DK
Nucleic Acids Res; 2017 Jun; 45(11):e99. PubMed ID: 28334830
[TBL] [Abstract][Full Text] [Related]
2. Endometrial vezatin and its association with endometriosis risk.
Holdsworth-Carson SJ; Fung JN; Luong HT; Sapkota Y; Bowdler LM; Wallace L; Teh WT; Powell JE; Girling JE; Healey M; Montgomery GW; Rogers PA
Hum Reprod; 2016 May; 31(5):999-1013. PubMed ID: 27005890
[TBL] [Abstract][Full Text] [Related]
3. Polymorphisms involving gain or loss of CpG sites are significantly enriched in trait-associated SNPs.
Zhou D; Li Z; Yu D; Wan L; Zhu Y; Lai M; Zhang D
Oncotarget; 2015 Nov; 6(37):39995-40004. PubMed ID: 26503467
[TBL] [Abstract][Full Text] [Related]
4. Deep learning predicts DNA methylation regulatory variants in the human brain and elucidates the genetics of psychiatric disorders.
Zhou J; Chen Q; Braun PR; Perzel Mandell KA; Jaffe AE; Tan HY; Hyde TM; Kleinman JE; Potash JB; Shinozaki G; Weinberger DR; Han S
Proc Natl Acad Sci U S A; 2022 Aug; 119(34):e2206069119. PubMed ID: 35969790
[TBL] [Abstract][Full Text] [Related]
5. Quantifying functional impact of non-coding variants with multi-task Bayesian neural network.
Xu C; Liu Q; Zhou J; Xie M; Feng J; Jiang T
Bioinformatics; 2020 Mar; 36(5):1397-1404. PubMed ID: 31693090
[TBL] [Abstract][Full Text] [Related]
6. Mapping eQTL by leveraging multiple tissues and DNA methylation.
Acharya CR; Owzar K; Allen AS
BMC Bioinformatics; 2017 Oct; 18(1):455. PubMed ID: 29047346
[TBL] [Abstract][Full Text] [Related]
7. The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases.
Ahsan M; Ek WE; Rask-Andersen M; Karlsson T; Lind-Thomsen A; Enroth S; Gyllensten U; Johansson Å
PLoS Genet; 2017 Sep; 13(9):e1007005. PubMed ID: 28915241
[TBL] [Abstract][Full Text] [Related]
8. Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus.
Schulz H; Ruppert AK; Herms S; Wolf C; Mirza-Schreiber N; Stegle O; Czamara D; Forstner AJ; Sivalingam S; Schoch S; Moebus S; Pütz B; Hillmer A; Fricker N; Vatter H; Müller-Myhsok B; Nöthen MM; Becker AJ; Hoffmann P; Sander T; Cichon S
Nat Commun; 2017 Nov; 8(1):1511. PubMed ID: 29142228
[TBL] [Abstract][Full Text] [Related]
9. Comprehensive functional annotation of susceptibility SNPs prioritized 10 genes for schizophrenia.
Niu HM; Yang P; Chen HH; Hao RH; Dong SS; Yao S; Chen XF; Yan H; Zhang YJ; Chen YX; Jiang F; Yang TL; Guo Y
Transl Psychiatry; 2019 Jan; 9(1):56. PubMed ID: 30705251
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease.
Huan T; Joehanes R; Song C; Peng F; Guo Y; Mendelson M; Yao C; Liu C; Ma J; Richard M; Agha G; Guan W; Almli LM; Conneely KN; Keefe J; Hwang SJ; Johnson AD; Fornage M; Liang L; Levy D
Nat Commun; 2019 Sep; 10(1):4267. PubMed ID: 31537805
[TBL] [Abstract][Full Text] [Related]
11. The impact of methylation quantitative trait loci (mQTLs) on active smoking-related DNA methylation changes.
Gao X; Thomsen H; Zhang Y; Breitling LP; Brenner H
Clin Epigenetics; 2017; 9():87. PubMed ID: 28824732
[TBL] [Abstract][Full Text] [Related]
12. 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; ; Hultman CM; Magnusson PK; Sullivan PF; Aberg KA; van den Oord EJ
Genome Biol; 2015 Dec; 16():291. PubMed ID: 26699738
[TBL] [Abstract][Full Text] [Related]
13. Genetic-epigenetic interactions in cis: a major focus in the post-GWAS era.
Do C; Shearer A; Suzuki M; Terry MB; Gelernter J; Greally JM; Tycko B
Genome Biol; 2017 Jun; 18(1):120. PubMed ID: 28629478
[TBL] [Abstract][Full Text] [Related]
14. Epigenetic and genetic alterations and their influence on gene regulation in chronic lymphocytic leukemia.
Huang D; Ovcharenko I
BMC Genomics; 2017 Mar; 18(1):236. PubMed ID: 28302063
[TBL] [Abstract][Full Text] [Related]
15. Genetic control of individual differences in gene-specific methylation in human brain.
Zhang D; Cheng L; Badner JA; Chen C; Chen Q; Luo W; Craig DW; Redman M; Gershon ES; Liu C
Am J Hum Genet; 2010 Mar; 86(3):411-9. PubMed ID: 20215007
[TBL] [Abstract][Full Text] [Related]
16. Characterisation of non-coding genetic variation in histamine receptors using AnNCR-SNP.
Rojano E; Ranea JA; Perkins JR
Amino Acids; 2016 Oct; 48(10):2433-42. PubMed ID: 27270572
[TBL] [Abstract][Full Text] [Related]
17. Pancan-meQTL: a database to systematically evaluate the effects of genetic variants on methylation in human cancer.
Gong J; Wan H; Mei S; Ruan H; Zhang Z; Liu C; Guo AY; Diao L; Miao X; Han L
Nucleic Acids Res; 2019 Jan; 47(D1):D1066-D1072. PubMed ID: 30203047
[TBL] [Abstract][Full Text] [Related]
18. Characterization of cross-tissue genetic-epigenetic effects and their patterns in schizophrenia.
Lin D; Chen J; Perrone-Bizzozero N; Bustillo JR; Du Y; Calhoun VD; Liu J
Genome Med; 2018 Feb; 10(1):13. PubMed ID: 29482655
[TBL] [Abstract][Full Text] [Related]
19. A pooling-based approach to mapping genetic variants associated with DNA methylation.
Kaplow IM; MacIsaac JL; Mah SM; McEwen LM; Kobor MS; Fraser HB
Genome Res; 2015 Jun; 25(6):907-17. PubMed ID: 25910490
[TBL] [Abstract][Full Text] [Related]
20. SNPs located at CpG sites modulate genome-epigenome interaction.
Zhi D; Aslibekyan S; Irvin MR; Claas SA; Borecki IB; Ordovas JM; Absher DM; Arnett DK
Epigenetics; 2013 Aug; 8(8):802-6. PubMed ID: 23811543
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]