1. Vlak MH, Algra A, Brandenburg R, Rinkel GJ. Prevalence of unruptured intracranial aneurysms, with emphasis on sex, age, comorbidity, country, and time period: a systematic review and meta-analysis. Lancet Neurol. 2011; 10:626–636.
Article
2. Li MH, Chen SW, Li YD, Chen YC, Cheng YS, Hu DJ, et al. Prevalence of unruptured cerebral aneurysms in Chinese adults aged 35 to 75 years: a cross-sectional study. Ann Intern Med. 2013; 159:514–521.
Article
3. Hitchcock E, Gibson WT. A review of the genetics of intracranial berry aneurysms and implications for genetic counseling. J Genet Couns. 2017; 26:21–31.
Article
4. Darsaut TE, Findlay JM, Magro E, Kotowski M, Roy D, Weill A, et al. Surgical clipping or endovascular coiling for unruptured intracranial aneurysms: a pragmatic randomised trial. J Neurol Neurosurg Psychiatry. 2017; 88:663–668.
Article
5. Backes D, Rinkel GJ, Laban KG, Algra A, Vergouwen MD. Patient- and aneurysm-specific risk factors for intracranial aneurysm growth: a systematic review and meta-analysis. Stroke. 2016; 47:951–957.
Article
6. Bourcier R, Redon R, Desal H. Genetic investigations on intracranial aneurysm: update and perspectives. J Neuroradiol. 2015; 42:67–71.
Article
7. Tromp G, Weinsheimer S, Ronkainen A, Kuivaniemi H. Molecular basis and genetic predisposition to intracranial aneurysm. Ann Med. 2014; 46:597–606.
Article
8. Alg VS, Sofat R, Houlden H, Werring DJ. Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals. Neurology. 2013; 80:2154–2165.
Article
9. Yasuno K, Bakırcıoğlu M, Low SK, Bilgüvar K, Gaál E, Ruigrok YM, et al. Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk. Proc Natl Acad Sci U S A. 2011; 108:19707–19712.
Article
10. Yasuno K, Bilguvar K, Bijlenga P, Low SK, Krischek B, Auburger G, et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet. 2010; 42:420–425.
Article
11. Hashikata H, Liu W, Inoue K, Mineharu Y, Yamada S, Nanayakkara S, et al. Confirmation of an association of single-nucleotide polymorphism rs1333040 on 9p21 with familial and sporadic intracranial aneurysms in Japanese patients. Stroke. 2010; 41:1138–1144.
Article
12. Liu L, Huang X, Cai Y, Feng K, DU J, Lu H, et al. [Correlation between endothelin receptor type A gene polymorphism and sporadic intracranial aneurysms]. Nan Fang Yi Ke Da Xue Xue Bao. 2014; 34:60–64.
13. Chen Y, Li G, Fan H, Guo S, Li R, Yin J, et al. CDKN2BAS gene polymorphisms and the risk of intracranial aneurysm in the Chinese population. BMC Neurol. 2017; 17:214.
Article
14. Low SK, Takahashi A, Cha PC, Zembutsu H, Kamatani N, Kubo M, et al. Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA. Hum Mol Genet. 2012; 21:2102–2110.
Article
15. Bilguvar K, Yasuno K, Niemelä M, Ruigrok YM, von Und Zu Fraunberg M, van Duijn CM, et al. Susceptibility loci for intracranial aneurysm in European and Japanese populations. Nat Genet. 2008; 40:1472–1477.
Article
16. Foroud T, Koller DL, Lai D, Sauerbeck L, Anderson C, Ko N, et al. Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk. Stroke. 2012; 43:2846–2852.
Article
17. Foroud T, Lai D, Koller D, Van't Hof F, Kurki MI, Anderson CS, et al. Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7. Stroke. 2014; 45:3194–3199.
Article
18. Kurki MI, Gaál EI, Kettunen J, Lappalainen T, Menelaou A, Anttila V, et al. High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms. PLoS Genet. 2014; 10:e1004134.
Article
19. Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005; 21:263–265.
Article
20. Mueller JC. Linkage disequilibrium for different scales and applications. Brief Bioinform. 2004; 5:355–364.
Article
21. Olsson S, Csajbok LZ, Jood K, Nylén K, Nellgård B, Jern C. Association between genetic variation on chromosome 9p21 and aneurysmal subarachnoid haemorrhage. J Neurol Neurosurg Psychiatry. 2011; 82:384–388.
Article
22. Zholdybayeva EV, Medetov YZ, Aitkulova AM, Makhambetov YT, Akshulakov SK, Kaliyev AB, et al. Genetic risk factors for intracranial aneurysm in the Kazakh population. J Mol Neurosci. 2018; 66:135–145.
Article
23. Abrantes P, Santos MM, Sousa I, Xavier JM, Francisco V, Krug T, et al. Genetic variants underlying risk of intracranial aneurysms: insights from a GWAS in Portugal. PLoS One. 2015; 10:e0133422.
Article
24. Nakaoka H, Takahashi T, Akiyama K, Cui T, Tajima A, Krischek B, et al. Differential effects of chromosome 9p21 variation on subphenotypes of intracranial aneurysm: site distribution. Stroke. 2010; 41:1593–1598.
Article
25. Deka R, Koller DL, Lai D, Indugula SR, Sun G, Woo D, et al. The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm. Stroke. 2010; 41:1132–1137.
Article
26. Visel A, Zhu Y, May D, Afzal V, Gong E, Attanasio C, et al. Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice. Nature. 2010; 464:409–412.
Article
27. Jarinova O, Stewart AF, Roberts R, Wells G, Lau P, Naing T, et al. Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus. Arterioscler Thromb Vasc Biol. 2009; 29:1671–1677.
Article
28. Burd CE, Jeck WR, Liu Y, Sanoff HK, Wang Z, Sharpless NE. Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk. PLoS Genet. 2010; 6:e1001233.
Article
29. Kabir F, Ullah I, Ali S, Gottsch AD, Naeem MA, Assir MZ, et al. Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases. Mol Vis. 2016; 22:610–625.
30. Hong EP, Kim BJ, Kim C, Choi HJ, Jeon JP. Association of SOX17 gene polymorphisms and intracranial aneurysm: a case-control study and meta-analysis. World Neurosurg. 2018; 110:e823–e829.
Article
31. Han X, Han X, Wang Z, Shen J, Dong Q. HDAC9 regulates ox-LDL-induced endothelial cell apoptosis by participating in inflammatory reactions. Front Biosci (Landmark Ed). 2016; 21:907–917.
Article
32. Ding H, Xu Y, Bao X, Wang X, Cui G, Wang W, et al. Confirmation of genomewide association signals in Chinese Han population reveals risk loci for ischemic stroke. Stroke. 2010; 41:177–180.
Article
33. Traylor M, Farrall M, Holliday EG, Sudlow C, Hopewell JC, Cheng YC, et al. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies. Lancet Neurol. 2012; 11:951–962.
Article
34. Dichgans M, Malik R, König IR, Rosand J, Clarke R, Gretarsdottir S, et al. Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. Stroke. 2014; 45:24–36.
Article
35. Shroff N, Ander BP, Zhan X, Stamova B, Liu D, Hull H, et al. HDAC9 polymorphism alters blood gene expression in patients with large vessel atherosclerotic stroke. Transl Stroke Res. 2019; 10:19–25.
Article
36. Mikhail M, Vachon PH, D'Orléans-Juste P, Jacques D, Bkaily G. Role of endothelin-1 and its receptors, ETA and ETB, in the survival of human vascular endothelial cells. Can J Physiol Pharmacol. 2017; 95:1298–1305.
Article
37. Hong EP, Kim BJ, Cho SS, Yang JS, Choi HJ, Kang SH, et al. Genomic variations in susceptibility to intracranial aneurysm in the Korean population. J Clin Med. 2019; 8:E275.
Article
38. Hirate Y, Suzuki H, Kawasumi M, Takase HM, Igarashi H, Naquet P, et al. Mouse Sox17 haploinsufficiency leads to female subfertility due to impaired implantation. Sci Rep. 2016; 6:24171.
Article
39. Miao WJ, Yuan DJ, Zhang GZ, Liu Q, Ma HM, Jin QQ. lncRNA CASC2/miR18a5p axis regulates the malignant potential of nasopharyngeal carcinoma by targeting RBBP8. Oncol Rep. 2019; 41:1797–1806.
Article
40. Zhou S, Dion PA, Rouleau GA. Genetics of intracranial aneurysms. Stroke. 2018; 49:780–787.
Article