PubRank

Akira Hata

Author PubWeight™ 78.00‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms. Nat Genet 2007 2.77
2 Fbxw7 acts as a critical fail-safe against premature loss of hematopoietic stem cells and development of T-ALL. Genes Dev 2008 2.12
3 A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. J Hum Genet 2010 1.97
4 Susceptibility loci for intracranial aneurysm in European and Japanese populations. Nat Genet 2008 1.90
5 Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet 2010 1.86
6 Identification of hypertension-susceptibility genes and pathways by a systemic multiple candidate gene approach: the millennium genome project for hypertension. Hypertens Res 2008 1.72
7 Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms. J Hum Genet 2010 1.61
8 A genome-wide association study identifies three new risk loci for Kawasaki disease. Nat Genet 2012 1.58
9 Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients. J Hum Genet 2007 1.55
10 Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies. J Hum Genet 2010 1.49
11 High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project. Hum Mol Genet 2007 1.44
12 A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12. J Hum Genet 2006 1.30
13 Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium Genome Project. Hypertension 2010 1.26
14 Common variants in CASP3 confer susceptibility to Kawasaki disease. Hum Mol Genet 2010 1.20
15 Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease. J Hum Genet 2004 1.20
16 Identification of functional polymorphisms in the promoter region of the human PICK1 gene and their association with methamphetamine psychosis. Am J Psychiatry 2007 1.17
17 Development of a nomogram to predict probability of positive initial prostate biopsy among Japanese patients. Urology 2006 1.13
18 The galanin signaling cascade is a candidate pathway regulating oncogenesis in human squamous cell carcinoma. Genes Chromosomes Cancer 2009 1.09
19 Linkage and association analyses of the osteoprotegerin gene locus with human osteoporosis. J Hum Genet 2002 1.08
20 Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk. Proc Natl Acad Sci U S A 2011 1.08
21 Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans. Hum Mol Genet 2011 1.03
22 TRIC-A channels in vascular smooth muscle contribute to blood pressure maintenance. Cell Metab 2011 1.02
23 An intronic variable number of tandem repeat polymorphisms of the cold-induced autoinflammatory syndrome 1 (CIAS1) gene modifies gene expression and is associated with essential hypertension. Eur J Hum Genet 2006 1.02
24 The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation. Am J Med Genet A 2008 1.01
25 The GSTP1 gene is a susceptibility gene for childhood asthma and the GSTM1 gene is a modifier of the GSTP1 gene. Int Arch Allergy Immunol 2007 0.98
26 CD14 -550 C/T, which is related to the serum level of soluble CD14, is associated with the development of respiratory syncytial virus bronchiolitis in the Japanese population. J Infect Dis 2007 0.97
27 Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion. J Hum Genet 2012 0.94
28 Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH). Hum Genet 2011 0.93
29 topors, a p53 and topoisomerase I-binding RING finger protein, is a coactivator of p53 in growth suppression induced by DNA damage. Oncogene 2005 0.92
30 Lower frequency of daily teeth brushing is related to high prevalence of cardiovascular risk factors. Exp Biol Med (Maywood) 2009 0.92
31 Replication of genetic association studies in asthma and related phenotypes. J Hum Genet 2010 0.91
32 Cyclosporin A treatment for Kawasaki disease refractory to initial and additional intravenous immunoglobulin. Pediatr Infect Dis J 2011 0.91
33 A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms. Hum Mol Genet 2006 0.91
34 Spatial accessibility to pediatric services. J Community Health 2008 0.91
35 Mutation of the follicle-stimulating hormone receptor gene 5'-untranslated region associated with female hypertension. Hypertension 2006 0.91
36 Differential effects of chromosome 9p21 variation on subphenotypes of intracranial aneurysm: site distribution. Stroke 2010 0.89
37 Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms. Hum Genet 2007 0.88
38 Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly. Am J Med Genet A 2008 0.87
39 AtObgC, a plant ortholog of bacterial Obg, is a chloroplast-targeting GTPase essential for early embryogenesis. Plant Mol Biol 2009 0.87
40 The male/female ratio of spontaneous fetal deaths and low birthweight in Japan. Pediatr Int 2008 0.87
41 Evaluation of clinical usefulness of second-generation HCV core antigen assay: comparison with COBAS AMPLICOR HCV MONITOR assay version 2.0. Liver Int 2005 0.86
42 CD40 ligand gene and Kawasaki disease. Eur J Hum Genet 2004 0.85
43 Effect of obesity on incidence of type 2 diabetes declines with age among Japanese women. Exp Biol Med (Maywood) 2009 0.85
44 An association between maternal smoking and preeclampsia in Japanese women. Semin Thromb Hemost 2002 0.84
45 Association of gamma-glutamyltransferase with incidence of type 2 diabetes in Japan. Exp Biol Med (Maywood) 2010 0.84
46 Association study of the C3 gene with adult and childhood asthma. J Hum Genet 2008 0.84
47 IL-10 gene polymorphism, but not TGF-beta1 gene polymorphisms, is associated with food allergy in a Japanese population. Pediatr Allergy Immunol 2008 0.84
48 Functional polymorphisms of the FPR1 gene and aggressive periodontitis in Japanese. Biochem Biophys Res Commun 2007 0.84
49 FokI variant of vitamin D receptor gene and factors related to atherosclerosis associated with ossification of the posterior longitudinal ligament of the spine: a multi-hospital case-control study. Spine (Phila Pa 1976) 2008 0.84
50 Association of CCR2-CCR5 haplotypes and CCL3L1 copy number with Kawasaki Disease, coronary artery lesions, and IVIG responses in Japanese children. PLoS One 2010 0.84
51 Fas polymorphisms influence susceptibility to autoimmune hepatitis. Am J Gastroenterol 2005 0.84
52 Post-traumatic stress disorder in pre-school aged children after a gas explosion. Eur J Pediatr 2002 0.83
53 BMI mediates the association between low educational level and higher blood pressure during pregnancy in Japan. BMC Public Health 2013 0.83
54 Insertion/deletion polymorphism of the angiotensin-converting enzyme gene and preeclampsia in Japanese patients. Semin Thromb Hemost 2005 0.83
55 High-resolution mapping for essential hypertension using microsatellite markers. Hypertension 2007 0.82
56 4G/5G variant of plasminogen activator inhibitor-1 gene and severe pregnancy-induced hypertension: subgroup analyses of variants of angiotensinogen and endothelial nitric oxide synthase. J Epidemiol 2009 0.82
57 No association of polymorphisms in the 5' region of the CD14 gene and food allergy in a Japanese population. Allergol Int 2007 0.82
58 Spine and rib abnormalities and stature in spondylocostal dysostosis. Spine (Phila Pa 1976) 2006 0.82
59 Inflammatory cytokine profiles during Cyclosporin treatment for immunoglobulin-resistant Kawasaki disease. Cytokine 2012 0.81
60 The egogram is a potent, independent risk factor for hypertension in pregnancy. Semin Thromb Hemost 2005 0.81
61 Association analysis of genes involved in the maintenance of the integrity of the extracellular matrix with intracranial aneurysms in a Japanese cohort. Cerebrovasc Dis 2009 0.81
62 Association between a variant of the glutathione S-transferase P1 gene (GSTP1) and hypertension in pregnancy in Japanese: interaction with parity, age, and genetic factors. Semin Thromb Hemost 2003 0.81
63 A1166C variant of angiotensin II type 1 receptor gene is associated with severe hypertension in pregnancy independently of T235 variant of angiotensinogen gene. J Hum Genet 2004 0.80
64 Integrated analysis of expression and genome alteration reveals putative amplified target genes in esophageal cancer. Oncol Rep 2007 0.80
65 CD14 and IL4R gene polymorphisms modify the effect of day care attendance on serum IgE levels. J Allergy Clin Immunol 2009 0.80
66 Association of TNFRSF4 gene polymorphisms with essential hypertension. J Hypertens 2008 0.80
67 Evaluation of contrast visual acuity in patients with retinitis pigmentosa. Clin Ophthalmol 2011 0.78
68 [Contribution of socioeconomic status to smoking behavior of parents of 4th grade elementary school students in Japan]. Nihon Koshu Eisei Zasshi 2011 0.78
69 Association of SLC6A9 gene variants with human essential hypertension. J Atheroscler Thromb 2009 0.78
70 Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis. J Hum Genet 2012 0.77
71 Diabetes Mellitus is Associated With Low Secretion Rates of Immunoglobulin A in Saliva. J Epidemiol 2015 0.77
72 Association of the GABRB3 gene with nonsyndromic oral clefts. Cleft Palate Craniofac J 2008 0.77
73 Association between fatty acid binding protein 3 gene variants and essential hypertension in humans. Am J Hypertens 2008 0.77
74 The M235T variant of the angiotensinogen gene and the body mass index are useful markers for prevention of hypertension in pregnancy: a tree-based analysis of gene-environment interaction. Semin Thromb Hemost 2002 0.77
75 Haplotype analysis of the human collectin placenta 1 (hCL-P1) gene. J Hum Genet 2003 0.76
76 International web-based survey of informed consent procedures in genetic epidemiological studies: towards the establishment of a research coordinator accreditation system. J Hum Genet 2009 0.76
77 Relationship between RANTES polymorphisms and respiratory syncytial virus bronchiolitis in a Japanese infant population. Jpn J Infect Dis 2011 0.75
78 A commentary on for what am i participating? The need for communication after receiving consent from biobanking project participants: experience in Japan. J Hum Genet 2011 0.75
79 Further analysis of microsatellite marker in the BDNF gene. Am J Med Genet B Neuropsychiatr Genet 2005 0.75
80 Association study of matrix metalloproteinase-12 gene polymorphisms and asthma in a Japanese population. Int Arch Allergy Immunol 2012 0.75
81 [Susceptibility genes for Kawasaki disease]. Nihon Rinsho 2008 0.75
82 Methylenetetrahydrofolate reductase genotype, vitamin B12, and folate influence plasma homocysteine in hemodialysis patients. Am J Kidney Dis 2002 0.75