152 related articles for article (PubMed ID: 34153138)
41. Genetic control of gene expression at novel and established chronic obstructive pulmonary disease loci.
Castaldi PJ; Cho MH; Zhou X; Qiu W; Mcgeachie M; Celli B; Bakke P; Gulsvik A; Lomas DA; Crapo JD; Beaty TH; Rennard S; Harshfield B; Lange C; Singh D; Tal-Singer R; Riley JH; Quackenbush J; Raby BA; Carey VJ; Silverman EK; Hersh CP
Hum Mol Genet; 2015 Feb; 24(4):1200-10. PubMed ID: 25315895
[TBL] [Abstract][Full Text] [Related]
42. Molecular Genetics and Functional Analysis Implicate
Rathi S; Danford I; Gudiseva HV; Verkuil L; Pistilli M; Vishwakarma S; Kaur I; Dave T; O'Brien JM; Chavali VRM
Cells; 2020 Aug; 9(9):. PubMed ID: 32825664
[TBL] [Abstract][Full Text] [Related]
43. The osteoporosis risk variant rs9820407 at 3p22.1 acts as an allele-specific enhancer to regulate CTNNB1 expression by long-range chromatin loop formation.
Wang Y; Lu L; Niu Y; Zhang Q; Cheng C; Huang H; Huang X; Huang Q
Bone; 2021 Dec; 153():116165. PubMed ID: 34461284
[TBL] [Abstract][Full Text] [Related]
44. Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal-tension glaucoma, and advanced glaucoma.
Burdon KP; Crawford A; Casson RJ; Hewitt AW; Landers J; Danoy P; Mackey DA; Mitchell P; Healey PR; Craig JE
Ophthalmology; 2012 Aug; 119(8):1539-45. PubMed ID: 22521085
[TBL] [Abstract][Full Text] [Related]
45. Association of cyclin-dependent kinase inhibitor 2B antisense RNA 1 gene expression and rs2383207 variant with breast cancer risk and survival.
Kattan SW; Hobani YH; Shaheen S; Mokhtar SH; Hussein MH; Toraih EA; Fawzy MS; Abdalla HA
Cell Mol Biol Lett; 2021 Apr; 26(1):14. PubMed ID: 33849428
[TBL] [Abstract][Full Text] [Related]
46. Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.
AbdulAzeez S; Al-Nafie AN; Al-Shehri A; Borgio JF; Baranova EV; Al-Madan MS; Al-Ali RA; Al-Muhanna F; Al-Ali A; Al-Mansori M; Ibrahim MF; Asselbergs FW; Keating B; Koeleman BP; Al-Ali AK
Int J Mol Sci; 2016 Mar; 17(3):395. PubMed ID: 26999117
[TBL] [Abstract][Full Text] [Related]
47. An Osteoporosis Risk SNP at 1p36.12 Acts as an Allele-Specific Enhancer to Modulate LINC00339 Expression via Long-Range Loop Formation.
Chen XF; Zhu DL; Yang M; Hu WX; Duan YY; Lu BJ; Rong Y; Dong SS; Hao RH; Chen JB; Chen YX; Yao S; Thynn HN; Guo Y; Yang TL
Am J Hum Genet; 2018 May; 102(5):776-793. PubMed ID: 29706346
[TBL] [Abstract][Full Text] [Related]
48. Risk single-nucleotide polymorphism-mediated enhancer-promoter interaction drives keloids through long noncoding RNA down expressed in keloids.
Deng CC; Zhang LX; Xu XY; Zhu DH; Cheng Q; Ma S; Rong Z; Yang B
Br J Dermatol; 2023 Jan; 188(1):84-93. PubMed ID: 36689521
[TBL] [Abstract][Full Text] [Related]
49. INFERNO: inferring the molecular mechanisms of noncoding genetic variants.
Amlie-Wolf A; Tang M; Mlynarski EE; Kuksa PP; Valladares O; Katanic Z; Tsuang D; Brown CD; Schellenberg GD; Wang LS
Nucleic Acids Res; 2018 Sep; 46(17):8740-8753. PubMed ID: 30113658
[TBL] [Abstract][Full Text] [Related]
50. Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma.
Ng SK; Burdon KP; Fitzgerald JT; Zhou T; Fogarty R; Souzeau E; Landers J; Mills RA; Casson RJ; Ridge B; Graham SL; Hewitt AW; Mackey DA; Healey PR; Wang JJ; Mitchell P; MacGregor S; Craig JE
Invest Ophthalmol Vis Sci; 2016 Jun; 57(7):3416-21. PubMed ID: 27367510
[TBL] [Abstract][Full Text] [Related]
51. A Genome-wide Association Study Identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1, and KRT80 As Risk Loci Contributing to Cutaneous Leishmaniasis in Brazil.
Castellucci LC; Almeida L; Cherlin S; Fakiola M; Francis RW; Carvalho EM; Santos da Hora A; do Lago TS; Figueiredo AB; Cavalcanti CM; Alves NS; Morais KLP; Teixeira-Carvalho A; Dutra WO; Gollob KJ; Cordell HJ; Blackwell JM
Clin Infect Dis; 2021 May; 72(10):e515-e525. PubMed ID: 32830257
[TBL] [Abstract][Full Text] [Related]
52. Genome-wide association study on coronary artery disease in type 1 diabetes suggests beta-defensin 127 as a risk locus.
Antikainen AAV; Sandholm N; Trégouët DA; Charmet R; McKnight AJ; Ahluwalia TS; Syreeni A; Valo E; Forsblom C; Gordin D; Harjutsalo V; Hadjadj S; Maxwell AP; Rossing P; Groop PH
Cardiovasc Res; 2021 Jan; 117(2):600-612. PubMed ID: 32077919
[TBL] [Abstract][Full Text] [Related]
53. Investigation of established genetic risk variants for glioma in prediagnostic samples from a population-based nested case-control study.
Wibom C; Späth F; Dahlin AM; Langseth H; Hovig E; Rajaraman P; Johannesen TB; Andersson U; Melin B
Cancer Epidemiol Biomarkers Prev; 2015 May; 24(5):810-6. PubMed ID: 25713050
[TBL] [Abstract][Full Text] [Related]
54. Risk SNP-Mediated Enhancer-Promoter Interaction Drives Colorectal Cancer through Both
Tian J; Lou J; Cai Y; Rao M; Lu Z; Zhu Y; Zou D; Peng X; Wang H; Zhang M; Niu S; Li Y; Zhong R; Chang J; Miao X
Cancer Res; 2020 May; 80(9):1804-1818. PubMed ID: 32127356
[TBL] [Abstract][Full Text] [Related]
55. Discovery and Functional Characterization of Two Regulatory Variants Underlying Lupus Susceptibility at 2p13.1.
Fazel-Najafabadi M; Rallabandi HR; Singh MK; Maiti GP; Morris J; Looger LL; Nath SK
Genes (Basel); 2022 Jun; 13(6):. PubMed ID: 35741778
[TBL] [Abstract][Full Text] [Related]
56. Transcriptome-Wide Association Study Identifies New Candidate Susceptibility Genes for Glioma.
Atkins I; Kinnersley B; Ostrom QT; Labreche K; Il'yasova D; Armstrong GN; Eckel-Passow JE; Schoemaker MJ; Nöthen MM; Barnholtz-Sloan JS; Swerdlow AJ; Simon M; Rajaraman P; Chanock SJ; Shildkraut J; Bernstein JL; Hoffmann P; Jöckel KH; Lai RK; Claus EB; Olson SH; Johansen C; Wrensch MR; Melin B; Jenkins RB; Sanson M; Bondy ML; Houlston RS
Cancer Res; 2019 Apr; 79(8):2065-2071. PubMed ID: 30709929
[TBL] [Abstract][Full Text] [Related]
57. Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer.
He H; Li W; Liyanarachchi S; Srinivas M; Wang Y; Akagi K; Wang Y; Wu D; Wang Q; Jin V; Symer DE; Shen R; Phay J; Nagy R; de la Chapelle A
Proc Natl Acad Sci U S A; 2015 May; 112(19):6128-33. PubMed ID: 25918370
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. Regulating of cell cycle progression by the lncRNA CDKN2B-AS1/miR-324-5p/ROCK1 axis in laryngeal squamous cell cancer.
Liu F; Xiao Y; Ma L; Wang J
Int J Biol Markers; 2020 Mar; 35(1):47-56. PubMed ID: 31960744
[TBL] [Abstract][Full Text] [Related]
60. CDKN2B-AS1: An Indispensable Long Non-coding RNA in Multiple Diseases.
Song C; Qi Y; Zhang J; Guo C; Yuan C
Curr Pharm Des; 2020; 26(41):5335-5346. PubMed ID: 32767927
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
