289 related articles for article (PubMed ID: 27861577)
1. Identifying Causal Genes at the Multiple Sclerosis Associated Region 6q23 Using Capture Hi-C.
Martin P; McGovern A; Massey J; Schoenfelder S; Duffus K; Yarwood A; Barton A; Worthington J; Fraser P; Eyre S; Orozco G
PLoS One; 2016; 11(11):e0166923. PubMed ID: 27861577
[TBL] [Abstract][Full Text] [Related]
2. Capture Hi-C identifies a novel causal gene, IL20RA, in the pan-autoimmune genetic susceptibility region 6q23.
McGovern A; Schoenfelder S; Martin P; Massey J; Duffus K; Plant D; Yarwood A; Pratt AG; Anderson AE; Isaacs JD; Diboll J; Thalayasingam N; Ospelt C; Barton A; Worthington J; Fraser P; Eyre S; Orozco G
Genome Biol; 2016 Nov; 17(1):212. PubMed ID: 27799070
[TBL] [Abstract][Full Text] [Related]
3. Functional relevance for multiple sclerosis-associated genetic variants.
Lin X; Deng FY; Mo XB; Wu LF; Lei SF
Immunogenetics; 2015 Jan; 67(1):7-14. PubMed ID: 25308886
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis.
Alcina A; Fedetz M; Fernández O; Saiz A; Izquierdo G; Lucas M; Leyva L; García-León JA; Abad-Grau Mdel M; Alloza I; Antigüedad A; Garcia-Barcina MJ; Vandenbroeck K; Varadé J; de la Hera B; Arroyo R; Comabella M; Montalban X; Petit-Marty N; Navarro A; Otaegui D; Olascoaga J; Blanco Y; Urcelay E; Matesanz F
J Med Genet; 2013 Jan; 50(1):25-33. PubMed ID: 23160276
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Analysis of TNFAIP3, a feedback inhibitor of nuclear factor-kappaB and the neighbor intergenic 6q23 region in rheumatoid arthritis susceptibility.
Dieguez-Gonzalez R; Calaza M; Perez-Pampin E; Balsa A; Blanco FJ; Cañete JD; Caliz R; Carreño L; de la Serna AR; Fernandez-Gutierrez B; Ortiz AM; Herrero-Beaumont G; Pablos JL; Narvaez J; Navarro F; Marenco JL; Gomez-Reino JJ; Gonzalez A
Arthritis Res Ther; 2009; 11(2):R42. PubMed ID: 19292917
[TBL] [Abstract][Full Text] [Related]
9. Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms.
Shepard CJ; Cline SG; Hinds D; Jahanbakhsh S; Prokop JW
Physiol Genomics; 2019 Nov; 51(11):562-577. PubMed ID: 31482761
[TBL] [Abstract][Full Text] [Related]
10. Epigenomic and Transcriptomic Prioritization of Candidate Obesity-Risk Regulatory GWAS SNPs.
Zhang X; Li TY; Xiao HM; Ehrlich KC; Shen H; Deng HW; Ehrlich M
Int J Mol Sci; 2022 Jan; 23(3):. PubMed ID: 35163195
[TBL] [Abstract][Full Text] [Related]
11. Unbiased analysis of potential targets of breast cancer susceptibility loci by Capture Hi-C.
Dryden NH; Broome LR; Dudbridge F; Johnson N; Orr N; Schoenfelder S; Nagano T; Andrews S; Wingett S; Kozarewa I; Assiotis I; Fenwick K; Maguire SL; Campbell J; Natrajan R; Lambros M; Perrakis E; Ashworth A; Fraser P; Fletcher O
Genome Res; 2014 Nov; 24(11):1854-68. PubMed ID: 25122612
[TBL] [Abstract][Full Text] [Related]
12. Gene, pathway and network frameworks to identify epistatic interactions of single nucleotide polymorphisms derived from GWAS data.
Liu Y; Maxwell S; Feng T; Zhu X; Elston RC; Koyutürk M; Chance MR
BMC Syst Biol; 2012; 6 Suppl 3(Suppl 3):S15. PubMed ID: 23281810
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Dissection of the Major Hematopoietic Quantitative Trait Locus in Chromosome 6q23.3 Identifies miR-3662 as a Player in Hematopoiesis and Acute Myeloid Leukemia.
Maharry SE; Walker CJ; Liyanarachchi S; Mehta S; Patel M; Bainazar MA; Huang X; Lankenau MA; Hoag KW; Ranganathan P; Garzon R; Blachly JS; Guttridge DC; Bloomfield CD; de la Chapelle A; Eisfeld AK
Cancer Discov; 2016 Sep; 6(9):1036-51. PubMed ID: 27354268
[TBL] [Abstract][Full Text] [Related]
15. Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs.
Ricaño-Ponce I; Zhernakova DV; Deelen P; Luo O; Li X; Isaacs A; Karjalainen J; Di Tommaso J; Borek ZA; Zorro MM; Gutierrez-Achury J; Uitterlinden AG; Hofman A; van Meurs J; ; ; Netea MG; Jonkers IH; Withoff S; van Duijn CM; Li Y; Ruan Y; Franke L; Wijmenga C; Kumar V
J Autoimmun; 2016 Apr; 68():62-74. PubMed ID: 26898941
[TBL] [Abstract][Full Text] [Related]
16. Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis.
Lill CM; Schilling M; Ansaloni S; Schröder J; Jaedicke M; Luessi F; Schjeide BM; Mashychev A; Graetz C; Akkad DA; Gerdes LA; Kroner A; Blaschke P; Hoffjan S; Winkelmann A; Dörner T; Rieckmann P; Steinhagen-Thiessen E; Lindenberger U; Chan A; Hartung HP; Aktas O; Lohse P; Buttmann M; Kümpfel T; Kubisch C; Zettl UK; Epplen JT; Zipp F; Bertram L
Neurogenetics; 2014 May; 15(2):129-34. PubMed ID: 24638856
[TBL] [Abstract][Full Text] [Related]
17. Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adults.
Close J; Game L; Clark B; Bergounioux J; Gerovassili A; Thein SL
BMC Genomics; 2004 May; 5(1):33. PubMed ID: 15169551
[TBL] [Abstract][Full Text] [Related]
18. Predicting causal variants affecting expression by using whole-genome sequencing and RNA-seq from multiple human tissues.
Brown AA; Viñuela A; Delaneau O; Spector TD; Small KS; Dermitzakis ET
Nat Genet; 2017 Dec; 49(12):1747-1751. PubMed ID: 29058714
[TBL] [Abstract][Full Text] [Related]
19. Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis.
Ragnedda G; Disanto G; Giovannoni G; Ebers GC; Sotgiu S; Ramagopalan SV
PLoS One; 2012; 7(10):e46730. PubMed ID: 23094030
[TBL] [Abstract][Full Text] [Related]
20. Quantifying missing heritability at known GWAS loci.
Gusev A; Bhatia G; Zaitlen N; Vilhjalmsson BJ; Diogo D; Stahl EA; Gregersen PK; Worthington J; Klareskog L; Raychaudhuri S; Plenge RM; Pasaniuc B; Price AL
PLoS Genet; 2013; 9(12):e1003993. PubMed ID: 24385918
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]