524 related articles for article (PubMed ID: 31500627)
1. 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]
2. 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]
3. CRISPR-mediated deletion of prostate cancer risk-associated CTCF loop anchors identifies repressive chromatin loops.
Guo Y; Perez AA; Hazelett DJ; Coetzee GA; Rhie SK; Farnham PJ
Genome Biol; 2018 Oct; 19(1):160. PubMed ID: 30296942
[TBL] [Abstract][Full Text] [Related]
4. Bridging between Mouse and Human Enhancer-Promoter Long-Range Interactions in Neural Stem Cells, to Understand Enhancer Function in Neurodevelopmental Disease.
D'Aurizio R; Catona O; Pitasi M; Li YE; Ren B; Nicolis SK
Int J Mol Sci; 2022 Jul; 23(14):. PubMed ID: 35887306
[TBL] [Abstract][Full Text] [Related]
5. Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci.
Karch CM; Ezerskiy LA; Bertelsen S; ; Goate AM
PLoS One; 2016; 11(2):e0148717. PubMed ID: 26919393
[TBL] [Abstract][Full Text] [Related]
6. Genetic risk for Alzheimer's disease is concentrated in specific macrophage and microglial transcriptional networks.
Tansey KE; Cameron D; Hill MJ
Genome Med; 2018 Feb; 10(1):14. PubMed ID: 29482603
[TBL] [Abstract][Full Text] [Related]
7. Multiple CTCF sites cooperate with each other to maintain a TAD for enhancer-promoter interaction in the β-globin locus.
Kang J; Kim YW; Park S; Kang Y; Kim A
FASEB J; 2021 Aug; 35(8):e21768. PubMed ID: 34245617
[TBL] [Abstract][Full Text] [Related]
8. Multiple Functional Variants at 13q14 Risk Locus for Osteoporosis Regulate RANKL Expression Through Long-Range Super-Enhancer.
Zhu DL; Chen XF; Hu WX; Dong SS; Lu BJ; Rong Y; Chen YX; Chen H; Thynn HN; Wang NN; Guo Y; Yang TL
J Bone Miner Res; 2018 Jul; 33(7):1335-1346. PubMed ID: 29528523
[TBL] [Abstract][Full Text] [Related]
9. Translating Alzheimer's disease-associated polymorphisms into functional candidates: a survey of IGAP genes and SNPs.
Katsumata Y; Nelson PT; Estus S; ; Fardo DW
Neurobiol Aging; 2019 Feb; 74():135-146. PubMed ID: 30448613
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. On the identification of potential regulatory variants within genome wide association candidate SNP sets.
Chen CY; Chang IS; Hsiung CA; Wasserman WW
BMC Med Genomics; 2014 Jun; 7():34. PubMed ID: 24920305
[TBL] [Abstract][Full Text] [Related]
12. Bayesian genome-wide TWAS with reference transcriptomic data of brain and blood tissues identified 141 risk genes for Alzheimer's disease dementia.
Guo S; Yang J
Alzheimers Res Ther; 2024 Jun; 16(1):120. PubMed ID: 38824563
[TBL] [Abstract][Full Text] [Related]
13. Three-dimensional genome architectural CCCTC-binding factor makes choice in duplicated enhancers at Pcdhα locus.
Wu Y; Jia Z; Ge X; Wu Q
Sci China Life Sci; 2020 Jun; 63(6):835-844. PubMed ID: 32249388
[TBL] [Abstract][Full Text] [Related]
14. Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation.
Croteau-Chonka DC; Rogers AJ; Raj T; McGeachie MJ; Qiu W; Ziniti JP; Stubbs BJ; Liang L; Martinez FD; Strunk RC; Lemanske RF; Liu AH; Stranger BE; Carey VJ; Raby BA
PLoS One; 2015; 10(10):e0140758. PubMed ID: 26474488
[TBL] [Abstract][Full Text] [Related]
15. Convergent lines of evidence support BIN1 as a risk gene of Alzheimer's disease.
Zhu J; Liu X; Yin H; Gao Y; Yu H
Hum Genomics; 2021 Jan; 15(1):9. PubMed ID: 33516273
[TBL] [Abstract][Full Text] [Related]
16. Bioinformatics pipeline to guide late-onset Alzheimer's disease (LOAD) post-GWAS studies: Prioritizing transcription regulatory variants within LOAD-associated regions.
Lutz MW; Chiba-Falek O
Alzheimers Dement (N Y); 2022; 8(1):e12244. PubMed ID: 35229021
[TBL] [Abstract][Full Text] [Related]
17. Comparative and Functional Genomic Resource for Mechanistic Studies of Human Blood Pressure-Associated Single Nucleotide Polymorphisms.
Mishra MK; Liang EY; Geurts AM; Auer PWL; Liu P; Rao S; Greene AS; Liang M; Liu Y
Hypertension; 2020 Mar; 75(3):859-868. PubMed ID: 31902252
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Conserved epigenomic signals in mice and humans reveal immune basis of Alzheimer's disease.
Gjoneska E; Pfenning AR; Mathys H; Quon G; Kundaje A; Tsai LH; Kellis M
Nature; 2015 Feb; 518(7539):365-9. PubMed ID: 25693568
[TBL] [Abstract][Full Text] [Related]
20. Identification of Key Long Non-Coding RNAs in the Pathology of Alzheimer's Disease and their Functions Based on Genome-Wide Associations Study, Microarray, and RNA-seq Data.
Han Z; Xue W; Tao L; Zhu F
J Alzheimers Dis; 2019; 68(1):339-355. PubMed ID: 30776002
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
