Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.
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Yusuke Nakamura | M. Kubo | A. Takahashi | N. Kamatani | H. Zembutsu | Siew-Kee Low | P. Cha | M. Kubo
[1] Andrew D. Johnson,et al. Association of Single Nucleotide Polymorphisms on Chromosome 9p21.3 With Platelet Reactivity: A Potential Mechanism for Increased Vascular Disease , 2010, Circulation. Cardiovascular genetics.
[2] Katsuhito Yasuno,et al. Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms , 2010, Journal of Human Genetics.
[3] K. Furie,et al. Chromosome 9p21 in Ischemic Stroke: Population Structure and Meta-Analysis , 2010, Stroke.
[4] R. McPherson. Chromosome 9p21 and coronary artery disease. , 2010, The New England journal of medicine.
[5] Alejandro F. Frangi,et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci , 2010, Nature genetics.
[6] R. Gibson,et al. EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity. , 2010, Physiological genomics.
[7] T. Inagawa. Risk factors for the formation and rupture of intracranial saccular aneurysms in Shimane, Japan. , 2010, World neurosurgery.
[8] Jonathan C. Cohen,et al. Targeted Deletion of the 9p21 Noncoding Coronary Artery Disease Risk Interval in Mice , 2010, Nature.
[9] H. Yoshida,et al. Association of genetic variants with myocardial infarction in Japanese individuals with metabolic syndrome. , 2009, Atherosclerosis.
[10] Benjamin J. Wright,et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3 , 2009, Nature Genetics.
[11] Murim Choi,et al. Susceptibility loci for intracranial aneurysm in European and Japanese populations , 2008, Nature Genetics.
[12] Michelle R. Campbell,et al. Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: current and developing technologies. , 2008, Mutation research.
[13] H. Stefánsson,et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm , 2008, Nature Genetics.
[14] A. Gylfason,et al. A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction , 2007, Science.
[15] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.
[16] J. Okamoto,et al. Down-regulation of an inhibitor of cell growth, transmembrane protein 34 (TMEM34), in anaplastic thyroid cancer , 2007, Journal of Cancer Research and Clinical Oncology.
[17] T. Kirino,et al. Risk of rupture associated with intact cerebral aneurysms in the Japanese population: a systematic review of the literature from Japan. , 2005, Journal of neurosurgery.
[18] Mark Daly,et al. Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..
[19] T. Inagawa. Trends in Surgical and Management Outcomes in Patients with Aneurysmal Subarachnoid Hemorrhage in Izumo City, Japan, between 1980–1989 and 1990–1998 , 2005, Cerebrovascular Diseases.
[20] C. C. McCarthy,et al. Identification and Characterization of PS-GAP as a Novel Regulator of Caspase-activated PAK-2* , 2004, Journal of Biological Chemistry.
[21] K. Nozaki,et al. Genome-Wide Scan for Japanese Familial Intracranial Aneurysms: Linkage to Several Chromosomal Regions , 2004, Circulation.
[22] B. Morris,et al. Association of EDNRA, but not WNK4 or FKBP1B, polymorphisms with essential hypertension , 2003, Clinical genetics.
[23] D. Altman,et al. Measuring inconsistency in meta-analyses , 2003, BMJ : British Medical Journal.
[24] H. Kuivaniemi,et al. Search for intracranial aneurysm susceptibility gene(s) using Finnish families , 2002, BMC Medical Genetics.
[25] H. Ohkuma,et al. Incidence of Aneurysmal Subarachnoid Hemorrhage in Shimokita, Japan, From 1989 to 1998 , 2002, Stroke.
[26] Yusuke Nakamura,et al. A high-throughput SNP typing system for genome-wide association studies , 2001, Journal of Human Genetics.
[27] C. Tzourio,et al. Association between migraine and endothelin type A receptor (ETA −231 A/G) gene polymorphism , 2001, Neurology.
[28] J. Mocco,et al. Influence of Smoking, Hypertension, and Sex on the Phenotypic Expression of Familial Intracranial Aneurysms in Siblings , 2001, Neurosurgery.
[29] M. Hennerici,et al. Endothelin-1 in Subarachnoid Hemorrhage: An Acute-Phase Reactant Produced by Cerebrospinal Fluid Leukocytes , 2000, Stroke.
[30] T. Ingall,et al. A multinational comparison of subarachnoid hemorrhage epidemiology in the WHO MONICA stroke study. , 2000, Stroke.
[31] S. Juvela. Plasma endothelin concentrations after aneurysmal subarachnoid hemorrhage. , 2000, Journal of neurosurgery.
[32] K. Roeder,et al. Genomic Control for Association Studies , 1999, Biometrics.
[33] D. Arveiler,et al. Polymorphisms of the endothelin-A and -B receptor genes in relation to blood pressure and myocardial infarction: the Etude Cas-Témoins sur l'Infarctus du Myocarde (ECTIM) Study. , 1999, American journal of hypertension.
[34] R. Vanninen,et al. Risk of harboring an unruptured intracranial aneurysm. , 1998, Stroke.
[35] W. Schievink,et al. Genetics of intracranial aneurysms. , 1997, Neurosurgery.
[36] A. Algra,et al. Risk Factors for Subarachnoid Hemorrhage A Systematic Review , 1996 .
[37] J. Pickard,et al. Endothelin ETA receptor expression in human cerebrovascular smooth muscle cells , 1995, British journal of pharmacology.
[38] D. Schaid,et al. Familial aneurysmal subarachnoid hemorrhage: a community-based study. , 1995, Journal of neurosurgery.
[39] T. Koepsell,et al. Subarachnoid hemorrhage and family history. A population-based case-control study. , 1995, Archives of neurology.
[40] D. Chauveau,et al. Intracranial aneurysms in autosomal dominant polycystic kidney disease. , 1994, Kidney international.
[41] S. Sasayama,et al. Endothelin-1-selective receptor in the arterial intima of patients with hypertension. , 1994, Hypertension.
[42] M. Ryynänen,et al. Familial subarachnoid hemorrhage in east Finland, 1977-1990. , 1993, Neurosurgery.
[43] J. Figge,et al. Endothelin-1 stimulates DNA synthesis and proliferation of pulmonary artery smooth muscle cells. , 1992, The American journal of physiology.
[44] V. Salomaa,et al. Epidemiology of subarachnoid hemorrhage in Finland from 1983 to 1985. , 1991, Stroke.
[45] Murat Gunel,et al. Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13. , 2005, American journal of human genetics.
[46] 恩田 英明. Genomewide-linkage and haplotype-association studies map intracranial aneurysm to chromosome 7q11 , 2002 .
[47] HirokiOhkuma,et al. Incidence of Aneurysmal Subarachnoid Hemorrhage in Shimokita, Japan, From 1989 to 1998 , 2002 .