240 related articles for article (PubMed ID: 35649373)
1. Mapping cis-regulatory elements in human neurons links psychiatric disease heritability and activity-regulated transcriptional programs.
Sanchez-Priego C; Hu R; Boshans LL; Lalli M; Janas JA; Williams SE; Dong Z; Yang N
Cell Rep; 2022 May; 39(9):110877. PubMed ID: 35649373
[TBL] [Abstract][Full Text] [Related]
2. Illuminating links between cis-regulators and trans-acting variants in the human prefrontal cortex.
Liu S; Won H; Clarke D; Matoba N; Khullar S; Mu Y; Wang D; Gerstein M
Genome Med; 2022 Nov; 14(1):133. PubMed ID: 36424644
[TBL] [Abstract][Full Text] [Related]
3. Tissue-specific and tissue-agnostic effects of genome sequence variation modulating blood pressure.
Lee D; Han SK; Yaacov O; Berk-Rauch H; Mathiyalagan P; Ganesh SK; Chakravarti A
Cell Rep; 2023 Nov; 42(11):113351. PubMed ID: 37910504
[TBL] [Abstract][Full Text] [Related]
4. Integrative modeling of eQTLs and cis-regulatory elements suggests mechanisms underlying cell type specificity of eQTLs.
Brown CD; Mangravite LM; Engelhardt BE
PLoS Genet; 2013; 9(8):e1003649. PubMed ID: 23935528
[TBL] [Abstract][Full Text] [Related]
5. Convolutional neural network model to predict causal risk factors that share complex regulatory features.
Lee T; Sung MK; Lee S; Yang W; Oh J; Kim JY; Hwang S; Ban HJ; Choi JK
Nucleic Acids Res; 2019 Dec; 47(22):e146. PubMed ID: 31598692
[TBL] [Abstract][Full Text] [Related]
6. Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes.
Song M; Yang X; Ren X; Maliskova L; Li B; Jones IR; Wang C; Jacob F; Wu K; Traglia M; Tam TW; Jamieson K; Lu SY; Ming GL; Li Y; Yao J; Weiss LA; Dixon JR; Judge LM; Conklin BR; Song H; Gan L; Shen Y
Nat Genet; 2019 Aug; 51(8):1252-1262. PubMed ID: 31367015
[TBL] [Abstract][Full Text] [Related]
7. Integrative analysis of liver-specific non-coding regulatory SNPs associated with the risk of coronary artery disease.
Selvarajan I; Toropainen A; Garske KM; López Rodríguez M; Ko A; Miao Z; Kaminska D; Õunap K; Örd T; Ravindran A; Liu OH; Moreau PR; Jawahar Deen A; Männistö V; Pan C; Levonen AL; Lusis AJ; Heikkinen S; Romanoski CE; Pihlajamäki J; Pajukanta P; Kaikkonen MU
Am J Hum Genet; 2021 Mar; 108(3):411-430. PubMed ID: 33626337
[TBL] [Abstract][Full Text] [Related]
8. The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine.
Yang Z; Zhou D; Li H; Cai X; Liu W; Wang L; Chang H; Li M; Xiao X
Mol Psychiatry; 2020 Jan; 25(1):48-66. PubMed ID: 31723243
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Enhancer variants associated with Alzheimer's disease affect gene expression via chromatin looping.
Kikuchi M; Hara N; Hasegawa M; Miyashita A; Kuwano R; Ikeuchi T; Nakaya A
BMC Med Genomics; 2019 Sep; 12(1):128. PubMed ID: 31500627
[TBL] [Abstract][Full Text] [Related]
11. Multifaceted genome-wide study identifies novel regulatory loci in SLC22A11 and ZNF45 for body mass index in Indians.
Giri AK; Prasad G; Bandesh K; Parekatt V; Mahajan A; Banerjee P; Kauser Y; Chakraborty S; Rajashekar D; ; Sharma A; Mathur SK; Basu A; McCarthy MI; Tandon N; Bharadwaj D
Mol Genet Genomics; 2020 Jul; 295(4):1013-1026. PubMed ID: 32363570
[TBL] [Abstract][Full Text] [Related]
12. Comprehensive evaluation of disease- and trait-specific enrichment for eight functional elements among GWAS-identified variants.
Markunas CA; Johnson EO; Hancock DB
Hum Genet; 2017 Jul; 136(7):911-919. PubMed ID: 28567521
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide enhancer maps link risk variants to disease genes.
Nasser J; Bergman DT; Fulco CP; Guckelberger P; Doughty BR; Patwardhan TA; Jones TR; Nguyen TH; Ulirsch JC; Lekschas F; Mualim K; Natri HM; Weeks EM; Munson G; Kane M; Kang HY; Cui A; Ray JP; Eisenhaure TM; Collins RL; Dey K; Pfister H; Price AL; Epstein CB; Kundaje A; Xavier RJ; Daly MJ; Huang H; Finucane HK; Hacohen N; Lander ES; Engreitz JM
Nature; 2021 May; 593(7858):238-243. PubMed ID: 33828297
[TBL] [Abstract][Full Text] [Related]
14. Novel disease syndromes unveiled by integrative multiscale network analysis of diseases sharing molecular effectors and comorbidities.
Li H; Fan J; Vitali F; Berghout J; Aberasturi D; Li J; Wilson L; Chiu W; Pumarejo M; Han J; Kenost C; Koripella PC; Pouladi N; Billheimer D; Bedrick EJ; Lussier YA
BMC Med Genomics; 2018 Dec; 11(Suppl 6):112. PubMed ID: 30598089
[TBL] [Abstract][Full Text] [Related]
15. Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants.
Narahara M; Higasa K; Nakamura S; Tabara Y; Kawaguchi T; Ishii M; Matsubara K; Matsuda F; Yamada R
PLoS One; 2014; 9(6):e100924. PubMed ID: 24956270
[TBL] [Abstract][Full Text] [Related]
16. Prefrontal cortex eQTLs/mQTLs enriched in genetic variants associated with alcohol use disorder and other diseases.
Lin H; Wang F; Rosato AJ; Farrer LA; Henderson DC; Zhang H
Epigenomics; 2020 May; 12(9):789-800. PubMed ID: 32496132
[No Abstract] [Full Text] [Related]
17. Integrated analysis of genome-wide association studies and 3D epigenomic characteristics reveal the BMP2 gene regulating loin muscle depth in Yorkshire pigs.
Miao Y; Zhao Y; Wan S; Mei Q; Wang H; Fu C; Li X; Zhao S; Xu X; Xiang T
PLoS Genet; 2023 Jun; 19(6):e1010820. PubMed ID: 37339141
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A Dementia-Associated Risk Variant near TMEM106B Alters Chromatin Architecture and Gene Expression.
Gallagher MD; Posavi M; Huang P; Unger TL; Berlyand Y; Gruenewald AL; Chesi A; Manduchi E; Wells AD; Grant SFA; Blobel GA; Brown CD; Chen-Plotkin AS
Am J Hum Genet; 2017 Nov; 101(5):643-663. PubMed ID: 29056226
[TBL] [Abstract][Full Text] [Related]
20. Functional Characterization of Genetic Variant Effects on Expression.
Flynn ED; Lappalainen T
Annu Rev Biomed Data Sci; 2022 Aug; 5():119-139. PubMed ID: 35483347
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
