Akihiro Sekine


Ontology type: schema:Person     


Person Info

NAME

Akihiro

SURNAME

Sekine

Publications in SciGraph latest 50 shown

  • 2017-12 Evolution of multi-drug resistant HCV clones from pre-existing resistant-associated variants during direct-acting antiviral therapy determined by third-generation sequencing in SCIENTIFIC REPORTS
  • 2015-12 Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels in NATURE COMMUNICATIONS
  • 2015-12 Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia in NATURE COMMUNICATIONS
  • 2014-05 Targeted next-generation sequencing and fine linkage disequilibrium mapping reveals association of PNPLA3 and PARVB with the severity of nonalcoholic fatty liver disease in JOURNAL OF HUMAN GENETICS
  • 2013-07 Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan in HUMAN GENETICS
  • 2012-05 Association between type 2 diabetes genetic susceptibility loci and visceral and subcutaneous fat area as determined by computed tomography in JOURNAL OF HUMAN GENETICS
  • 2012-04 Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians in DIABETOLOGIA
  • 2012-01 Genetic variations in the CYP17A1 and NT5C2 genes are associated with a reduction in visceral and subcutaneous fat areas in Japanese women in JOURNAL OF HUMAN GENETICS
  • 2011-10 Computed tomography analysis of the association between the SH2B1 rs7498665 single-nucleotide polymorphism and visceral fat area in JOURNAL OF HUMAN GENETICS
  • 2011-09 Association of variations in the FTO, SCG3 and MTMR9 genes with metabolic syndrome in a Japanese population in JOURNAL OF HUMAN GENETICS
  • 2010-12 Association of the rs738409 polymorphism in PNPLA3 with liver damage and the development of nonalcoholic fatty liver disease in BMC MEDICAL GENETICS
  • 2006-12 Linkage disequilibrium of evolutionarily conserved regions in the human genome in BMC GENOMICS
  • 2005-07 Single nucleotide polymorphisms in the gene encoding Krüppel-like factor 7 are associated with type 2 diabetes in DIABETOLOGIA
  • 2005-06 Erratum: A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities in NATURE GENETICS
  • 2005-05 CUL1, a component of E3 ubiquitin ligase, alters lymphocyte signal transduction with possible effect on rheumatoid arthritis in GENES & IMMUNITY
  • 2005-05 A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities in NATURE GENETICS
  • 2004-10 Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 109 drug-related genes in four Asian populations in JOURNAL OF HUMAN GENETICS
  • 2004-08 Identification of 20 novel SNPs in the guanine nucleotide binding protein alpha 12 gene locus in JOURNAL OF HUMAN GENETICS
  • 2004-05 Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-α secretion in vitro in NATURE
  • 2004-04-01 Catalog of 300 SNPs in 23 genes encoding G-protein coupled receptors in JOURNAL OF HUMAN GENETICS
  • 2003-12 An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis in NATURE GENETICS
  • 2003-09-01 Catalog of 178 variations in the Japanese population among eight human genes encoding G protein-coupled receptors (GPCRs) in JOURNAL OF HUMAN GENETICS
  • 2003-08 Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis in NATURE GENETICS
  • 2003-05-01 Catalog of 680 variations among eight cytochrome P450 (CYP) genes, nine esterase genes, and two other genes in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2003-01-01 Catalog of 668 SNPs detected among 31 genes encoding potential drug targets on the cell surface in JOURNAL OF HUMAN GENETICS
  • 2002-11 Catalog of 238 variations among six human genes encoding solute carriers (hSLCs) in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2002-10-01 Catalog of 86 single-nucleotide polymorphisms (SNPs) in three uridine diphosphate glycosyltransferase genes: UGT2A1, UGT2B15, and UGT8 in JOURNAL OF HUMAN GENETICS
  • 2002-08 906 variations among 27 genes encoding cytochrome P450 (CYP) enzymes and aldehyde dehydrogenases (ALDHs) in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2002-06-01 Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4 , ABCA7 , ABCA8 , ABCD1 , ABCD3 , ABCD4 , ABCE1 , ABCF1 , ABCG1 , ABCG2 , ABCG4 , ABCG5 , and ABCG8 in JOURNAL OF HUMAN GENETICS
  • 2002-04 Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C ( ABCC/MRP/CFTR ) in JOURNAL OF HUMAN GENETICS
  • 2002-02 Thirteen single-nucleotide polymorphisms (SNPs) in the alcohol dehydrogenase 4 (ADH4) gene locus in JOURNAL OF HUMAN GENETICS
  • 2002-01-01 Catalog of 77 single-nucleotide polymorphisms (SNPs) in the carbohydrate sulfotransferase 1 ( CHST1 ) and carbohydrate sulfotransferase 3 ( CHST3 ) genes in JOURNAL OF HUMAN GENETICS
  • 2002-01-01 Three hundred twenty-six genetic variations in genes encoding nine members of ATP-binding cassette, subfamily B (ABCB/MDR/TAP), in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2001-11-01 Catalog of 258 single-nucleotide polymorphisms (SNPs) in genes encoding three organic anion transporters, three organic anion-transporting polypeptides, and three NADH:ubiquinone oxidoreductase flavoproteins in JOURNAL OF HUMAN GENETICS
  • 2001-10 Catalog of 46 single-nucleotide polymorphisms (SNPs) in the microsomal glutathione S-transferase 1 ( MGST1 ) gene in JOURNAL OF HUMAN GENETICS
  • 2001-09-01 Identification of 197 genetic variations in six human methyltransferase genes in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2001-09-01 High-density single-nucleotide polymorphism (SNP) map of the 150-kb region corresponding to the human ATP-binding cassette transporter A1 ( ABCA1 ) gene in JOURNAL OF HUMAN GENETICS
  • 2001-06-01 Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase families in JOURNAL OF HUMAN GENETICS
  • 2001-05-18 Identification of single-nucleotide polymorphisms (SNPs) of human N-acetyltransferase genes NAT1, NAT2, AANAT, ARD1, and L1CAM in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2001-05-18 Seventy genetic variations in human microsomal and soluble epoxide hydrolase genes (EPHX1 and EPHX2) in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2001-04-03 Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes in JOURNAL OF HUMAN GENETICS
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