409 related articles for article (PubMed ID: 31537805)
1. 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]
2. Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms.
Zhang T; Choi J; Dilshat R; Einarsdóttir BÓ; Kovacs MA; Xu M; Malasky M; Chowdhury S; Jones K; Bishop DT; Goldstein AM; Iles MM; Landi MT; Law MH; Shi J; Steingrímsson E; Brown KM
Am J Hum Genet; 2021 Sep; 108(9):1631-1646. PubMed ID: 34293285
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Genetic impacts on DNA methylation help elucidate regulatory genomic processes.
Villicaña S; Castillo-Fernandez J; Hannon E; Christiansen C; Tsai PC; Maddock J; Kuh D; Suderman M; Power C; Relton C; Ploubidis G; Wong A; Hardy R; Goodman A; Ong KK; Bell JT
Genome Biol; 2023 Jul; 24(1):176. PubMed ID: 37525248
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. meQTL mapping in the GENOA study reveals genetic determinants of DNA methylation in African Americans.
Shang L; Zhao W; Wang YZ; Li Z; Choi JJ; Kho M; Mosley TH; Kardia SLR; Smith JA; Zhou X
Nat Commun; 2023 May; 14(1):2711. PubMed ID: 37169753
[TBL] [Abstract][Full Text] [Related]
7. Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose.
Chung RH; Chiu YF; Wang WC; Hwu CM; Hung YJ; Lee IT; Chuang LM; Quertermous T; Rotter JI; Chen YI; Chang IS; Hsiung CA
Diabetologia; 2021 Jul; 64(7):1613-1625. PubMed ID: 33842983
[TBL] [Abstract][Full Text] [Related]
8. Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on disease.
Richardson TG; Haycock PC; Zheng J; Timpson NJ; Gaunt TR; Davey Smith G; Relton CL; Hemani G
Hum Mol Genet; 2018 Sep; 27(18):3293-3304. PubMed ID: 29893838
[TBL] [Abstract][Full Text] [Related]
9. Genome- and epigenome-wide association studies identify susceptibility of CpG sites and regions for metabolic syndrome in a Korean population.
Lee HS; Kim B; Park T
Clin Epigenetics; 2024 Apr; 16(1):60. PubMed ID: 38685121
[TBL] [Abstract][Full Text] [Related]
10. Identification of novel functional CpG-SNPs associated with Type 2 diabetes and birth weight.
Liu RK; Lin X; Wang Z; Greenbaum J; Qiu C; Zeng CP; Zhu YY; Shen J; Deng HW
Aging (Albany NY); 2021 Apr; 13(7):10619-10658. PubMed ID: 33835050
[TBL] [Abstract][Full Text] [Related]
11. Genome-wide sequencing-based identification of methylation quantitative trait loci and their role in schizophrenia risk.
Perzel Mandell KA; Eagles NJ; Wilton R; Price AJ; Semick SA; Collado-Torres L; Ulrich WS; Tao R; Han S; Szalay AS; Hyde TM; Kleinman JE; Weinberger DR; Jaffe AE
Nat Commun; 2021 Sep; 12(1):5251. PubMed ID: 34475392
[TBL] [Abstract][Full Text] [Related]
12. Mendelian randomization integrating GWAS and mQTL data identified novel pleiotropic DNA methylation loci for neuropathology of Alzheimer's disease.
Liu D; Wang Y; Jing H; Meng Q; Yang J
Neurobiol Aging; 2021 Jan; 97():18-27. PubMed ID: 33120085
[TBL] [Abstract][Full Text] [Related]
13. Elucidating the genetic architecture of DNA methylation to identify promising molecular mechanisms of disease.
Ma J; Joehanes R; Liu C; Keshawarz A; Hwang SJ; Bui H; Tejada B; Sooda M; Munson PJ; Demirkale CY; Courchesne P; Heard-Costa NL; Pitsillides AN; Feolo M; Sharopova N; Vasan RS; Huan T; Levy D
Sci Rep; 2022 Nov; 12(1):19564. PubMed ID: 36380121
[TBL] [Abstract][Full Text] [Related]
14. Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease.
Yao C; Chen G; Song C; Keefe J; Mendelson M; Huan T; Sun BB; Laser A; Maranville JC; Wu H; Ho JE; Courchesne P; Lyass A; Larson MG; Gieger C; Graumann J; Johnson AD; Danesh J; Runz H; Hwang SJ; Liu C; Butterworth AS; Suhre K; Levy D
Nat Commun; 2018 Aug; 9(1):3268. PubMed ID: 30111768
[TBL] [Abstract][Full Text] [Related]
15. Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: the Framingham Heart Study.
Keshawarz A; Bui H; Joehanes R; Ma J; Liu C; Huan T; Hwang SJ; Tejada B; Sooda M; Courchesne P; Munson PJ; Demirkale CY; Yao C; Heard-Costa NL; Pitsillides AN; Lin H; Liu CT; Wang Y; Peloso GM; Lundin J; Haessler J; Du Z; Cho M; Hersh CP; Castaldi P; Raffield LM; Wen J; Li Y; Reiner AP; Feolo M; Sharopova N; Vasan RS; DeMeo DL; Carson AP; Kooperberg C; Levy D
Sci Rep; 2023 Aug; 13(1):12952. PubMed ID: 37563237
[TBL] [Abstract][Full Text] [Related]
16. An alternative approach to multiple testing for methylation QTL mapping reduces the proportion of falsely identified CpGs.
Luijk R; Goeman JJ; Slagboom EP; Heijmans BT; van Zwet EW
Bioinformatics; 2015 Feb; 31(3):340-5. PubMed ID: 25282645
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue.
Shi J; Marconett CN; Duan J; Hyland PL; Li P; Wang Z; Wheeler W; Zhou B; Campan M; Lee DS; Huang J; Zhou W; Triche T; Amundadottir L; Warner A; Hutchinson A; Chen PH; Chung BS; Pesatori AC; Consonni D; Bertazzi PA; Bergen AW; Freedman M; Siegmund KD; Berman BP; Borok Z; Chatterjee N; Tucker MA; Caporaso NE; Chanock SJ; Laird-Offringa IA; Landi MT
Nat Commun; 2014 Feb; 5():3365. PubMed ID: 24572595
[TBL] [Abstract][Full Text] [Related]
20. Epigenome-wide association study of whole blood gene expression in Framingham Heart Study participants provides molecular insight into the potential role of CHRNA5 in cigarette smoking-related lung diseases.
Yao C; Joehanes R; Wilson R; Tanaka T; Ferrucci L; Kretschmer A; Prokisch H; Schramm K; Gieger C; Peters A; Waldenberger M; Marzi C; Herder C; Levy D
Clin Epigenetics; 2021 Mar; 13(1):60. PubMed ID: 33752734
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
