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Tytuł:
Japan PGx Data Science Consortium Database: SNPs and HLA genotype data from 2994 Japanese healthy individuals for pharmacogenomics studies.
Autorzy:
Kamitsuji S; StaGen, Tokyo, Japan.
Matsuda T; Astellas Pharma, Tokyo, Japan.
Nishimura K; Astellas Pharma, Tokyo, Japan.
Endo S; Daiichi Sankyo, Tokyo, Japan.
Wada C; Daiichi Sankyo, Tokyo, Japan.
Watanabe K; Daiichi Sankyo, Tokyo, Japan.
Hasegawa K; Otsuka Pharmaceutical, Tokyo, Japan.
Hishigaki H; Otsuka Pharmaceutical, Tokyo, Japan.
Masuda M; Otsuka Pharmaceutical, Tokyo, Japan.
Kuwahara Y; Taisho Pharmaceutical, Tokyo, Japan.
Tsuritani K; Taisho Pharmaceutical, Tokyo, Japan.
Sugiura K; Takeda Pharmaceutical Company Limited, Osaka, Japan.
Kubota T; Mitsubishi Tanabe Pharma Corporation, Osaka, Japan.
Miyoshi S; Mitsubishi Tanabe Pharma Corporation, Osaka, Japan.
Okada K; Mitsubishi Tanabe Pharma Corporation, Osaka, Japan.
Nakazono K; StaGen, Tokyo, Japan.
Sugaya Y; StaGen, Tokyo, Japan.
Yang W; StaGen, Tokyo, Japan.
Sawamoto T; Astellas Pharma, Tokyo, Japan.
Uchida W; Astellas Pharma, Tokyo, Japan.
Shinagawa A; Daiichi Sankyo, Tokyo, Japan.
Fujiwara T; Otsuka Pharmaceutical, Tokyo, Japan.
Yamada H; Taisho Pharmaceutical, Tokyo, Japan.
Suematsu K; Taisho Pharmaceutical, Tokyo, Japan.
Tsutsui N; Mitsubishi Tanabe Pharma Corporation, Osaka, Japan.
Kamatani N; StaGen, Tokyo, Japan.
Liou SY; Takeda Pharmaceutical Company Limited, Osaka, Japan.
Pokaż więcej
Corporate Authors:
Japan PGx Data Science Consortium (JPDSC)
Źródło:
Journal of human genetics [J Hum Genet] 2015 Jun; Vol. 60 (6), pp. 319-26. Date of Electronic Publication: 2015 Apr 09.
Typ publikacji:
Journal Article
MeSH Terms:
HLA Antigens/*genetics
Databases, Genetic ; Female ; Gene Frequency ; Genetic Association Studies ; Genotype ; Healthy Volunteers ; Humans ; Japan ; Male ; Pharmacogenetics ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Tytuł:
Systematic evaluation of personal genome services for Japanese individuals.
Autorzy:
Kido T; 1] Rikengenesis CO., LTD., Tokyo, Japan [2] JST, PRESTO, Tokyo, Japan.
Kawashima M
Nishino S
Swan M
Kamatani N
Butte AJ
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2013 Nov; Vol. 58 (11), pp. 734-41. Date of Electronic Publication: 2013 Sep 26.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Asian People*
Genome, Human*
Genetic Testing/*statistics & numerical data
Personal Health Services/*statistics & numerical data
Genetic Testing/trends ; Humans ; Personal Health Services/trends ; Polymorphism, Single Nucleotide ; Risk Assessment
Czasopismo naukowe
Tytuł:
Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis.
Autorzy:
Mahasirimongkol S; Medical Genetics Section, National Institute of Health, Department of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand. />Yanai H
Mushiroda T
Promphittayarat W
Wattanapokayakit S
Phromjai J
Yuliwulandari R
Wichukchinda N
Yowang A
Yamada N
Kantipong P
Takahashi A
Kubo M
Sawanpanyalert P
Kamatani N
Nakamura Y
Tokunaga K
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2012 Jun; Vol. 57 (6), pp. 363-7. Date of Electronic Publication: 2012 May 03.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Loci*
Genome-Wide Association Study*
Asian People/*genetics
Tuberculosis/*genetics
Age Factors ; Case-Control Studies ; Genetic Predisposition to Disease ; Genotype ; Humans ; Japan ; Meta-Analysis as Topic ; Polymorphism, Single Nucleotide ; Quality Control ; Thailand
Czasopismo naukowe
Tytuł:
Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes.
Autorzy:
Yamaguchi-Kabata Y; Laboratory for Medical Informatics, Center for Genomic Medicine, The Institute of Physical and Chemical Research (RIKEN), Yokohama, Japan. />Tsunoda T
Kumasaka N
Takahashi A
Hosono N
Kubo M
Nakamura Y
Kamatani N
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2012 May; Vol. 57 (5), pp. 326-34. Date of Electronic Publication: 2012 Mar 29.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Mapping*
Genetic Variation*
Asian People/*genetics
Haplotypes/*genetics
Polymorphism, Single Nucleotide/*genetics
Population Groups/*genetics
Gene Frequency ; Genome-Wide Association Study ; Genotype ; Homozygote ; Humans
Czasopismo naukowe
Tytuł:
A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.
Autorzy:
Jongjaroenprasert W; Endocrine and Metabolism Unit, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Rama 6 Road, Mahidol University, Bangkok, Thailand. />Phusantisampan T
Mahasirimongkol S
Mushiroda T
Hirankarn N
Snabboon T
Chanprasertyotin S
Tantiwong P
Soonthornpun S
Rattanapichart P
Mamanasiri S
Himathongkam T
Ongphiphadhanakul B
Takahashi A
Kamatani N
Kubo M
Nakamura Y
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2012 May; Vol. 57 (5), pp. 301-4. Date of Electronic Publication: 2012 Mar 08.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Genetic Variation*
Genome-Wide Association Study*
Chromosomes, Human, Pair 17/*genetics
Hyperthyroidism/*genetics
Paralysis, Hyperkalemic Periodic/*genetics
Asian People/genetics ; Case-Control Studies ; Genotype ; Humans ; Linkage Disequilibrium ; Male ; Polymorphism, Single Nucleotide ; Potassium Channels, Inwardly Rectifying/genetics ; Thailand
Czasopismo naukowe
Tytuł:
A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population.
Autorzy:
Cha PC; Institute of Medical Science, Laboratory of Molecular Medicine, Human Genome Center, The University of Tokyo, Tokyo, Japan.
Zembutsu H
Takahashi A
Kubo M
Kamatani N
Nakamura Y
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2012 Apr; Vol. 57 (4), pp. 235-7. Date of Electronic Publication: 2012 Feb 09.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genome-Wide Association Study*
Polymorphism, Single Nucleotide*
Asian People/*genetics
Gallbladder Neoplasms/*genetics
Receptors, Cell Surface/*genetics
Tumor Suppressor Proteins/*genetics
Aged ; Case-Control Studies ; DCC Receptor ; Female ; Gallbladder Neoplasms/diagnosis ; Gene Frequency ; Genetic Predisposition to Disease ; Genetics, Population ; Genome, Human ; Humans ; Logistic Models ; Loss of Heterozygosity ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
Autorzy:
Nakabayashi K; Department of Cell Biology, Fukuoka University, Fukuoka, Japan. />Tajima A
Yamamoto K
Takahashi A
Hata K
Takashima Y
Koyanagi M
Nakaoka H
Akamizu T
Ishikawa N
Kubota S
Maeda S
Tsunoda T
Kubo M
Kamatani N
Nakamura Y
Sasazuki T
Shirasawa S
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2011 Nov; Vol. 56 (11), pp. 772-8. Date of Electronic Publication: 2011 Sep 08.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Loci*
Graves Disease/*genetics
Major Histocompatibility Complex/*genetics
Alleles ; Asian People/genetics ; Case-Control Studies ; Gene Frequency ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Genotype ; Humans ; Japan/ethnology ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Tytuł:
Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility.
Autorzy:
Kumar V; Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University of Tokyo, Tokyo, Japan.
Matsuo K
Takahashi A
Hosono N
Tsunoda T
Kamatani N
Kong SY
Nakagawa H
Cui R
Tanikawa C
Seto M
Morishima Y
Kubo M
Nakamura Y
Matsuda K
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2011 Jun; Vol. 56 (6), pp. 436-9. Date of Electronic Publication: 2011 Apr 07.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Genetic Variation*
Chromosomes, Human, Pair 13/*genetics
Chromosomes, Human, Pair 14/*genetics
Lymphoma, Large B-Cell, Diffuse/*genetics
Polymorphism, Single Nucleotide/*genetics
Adult ; Aged ; Female ; Genome-Wide Association Study ; Humans ; Male ; Middle Aged ; Myotonin-Protein Kinase ; Protein-Tyrosine Kinases/genetics
Czasopismo naukowe
Tytuł:
A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia.
Autorzy:
Dai J; Laboratory of Bone and Joint Diseases, Center for Genomic Medicine, RIKEN, Tokyo, Japan.
Kim OH
Cho TJ
Miyake N
Song HR
Karasugi T
Sakazume S
Ikema M
Matsui Y
Nagai T
Matsumoto N
Ohashi H
Kamatani N
Nishimura G
Furuichi T
Takahashi A
Ikegawa S
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2011 May; Vol. 56 (5), pp. 398-400. Date of Electronic Publication: 2011 Mar 17.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Founder Effect*
Bone Diseases, Developmental/*genetics
Mutation/*genetics
Nucleotidases/*genetics
Haplotypes ; Humans ; Japan ; Korea ; Polymorphism, Single Nucleotide/genetics
Czasopismo naukowe
Tytuł:
Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population.
Autorzy:
Low SK; Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan. />Zembutsu H
Takahashi A
Kamatani N
Cha PC
Hosono N
Kubo M
Matsuda K
Nakamura Y
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2011 Mar; Vol. 56 (3), pp. 211-6. Date of Electronic Publication: 2011 Jan 13.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
Intracranial Aneurysm/*genetics
Lim Kinases/*genetics
Matrix Metalloproteinase 2/*genetics
Tumor Necrosis Factor-alpha/*genetics
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Asian People/genetics ; Case-Control Studies ; Female ; Humans ; Male ; Middle Aged ; Sex Factors ; Young Adult
Czasopismo naukowe
Tytuł:
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
Autorzy:
Aoki A; Laboratory for Cardiovascular Disease, Center for Genomic Medicine, RIKEN, Yokohama, Japan.
Ozaki K
Sato H
Takahashi A
Kubo M
Sakata Y
Onouchi Y
Kawaguchi T
Lin TH
Takano H
Yasutake M
Hsu PC
Ikegawa S
Kamatani N
Tsunoda T
Juo SH
Hori M
Komuro I
Mizuno K
Nakamura Y
Tanaka T
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2011 Jan; Vol. 56 (1), pp. 47-51. Date of Electronic Publication: 2010 Nov 25.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 5*/genetics
Polymorphism, Single Nucleotide*
Asian People/*genetics
Myocardial Infarction/*genetics
Algorithms ; Female ; Gene Frequency ; Genetic Predisposition to Disease ; Genetics, Population ; Genome-Wide Association Study ; Genotype ; Humans ; Linkage Disequilibrium ; Male ; Validation Studies as Topic
Czasopismo naukowe
Tytuł:
Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese population.
Autorzy:
Hotta K; Laboratory for Endocrinology and Metabolism, Center for Genomic Medicine, RIKEN, Yokohama, Japan. />Nakamura M
Nakamura T
Matsuo T
Nakata Y
Kamohara S
Miyatake N
Kotani K
Komatsu R
Itoh N
Mineo I
Wada J
Yoneda M
Nakajima A
Funahashi T
Miyazaki S
Tokunaga K
Kawamoto M
Masuzaki H
Ueno T
Hamaguchi K
Tanaka K
Yamada K
Hanafusa T
Oikawa S
Yoshimatsu H
Nakao K
Sakata T
Matsuzawa Y
Nakamura Y
Kamatani N
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2010 Nov; Vol. 55 (11), pp. 738-42. Date of Electronic Publication: 2010 Aug 12.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Body Mass Index*
Asian People/*genetics
Intra-Abdominal Fat/*diagnostic imaging
Polymorphism, Single Nucleotide/*genetics
Proteins/*genetics
Adult ; Alpha-Ketoglutarate-Dependent Dioxygenase FTO ; Female ; Humans ; Male ; Methionine Sulfoxide Reductases/genetics ; Middle Aged ; Nerve Tissue Proteins/genetics ; Radiography ; Receptor, Melanocortin, Type 4/genetics ; Transcription Factor AP-2/genetics ; Waist Circumference ; Waist-Hip Ratio
Czasopismo naukowe
Tytuł:
Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes.
Autorzy:
Kumasaka N; Laboratory for Statistical Analysis, Research Group for Medical Informatics, Center for Genomic Medicine, RIKEN, Tokyo, Japan. />Yamaguchi-Kabata Y
Takahashi A
Kubo M
Nakamura Y
Kamatani N
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2010 Aug; Vol. 55 (8), pp. 525-33. Date of Electronic Publication: 2010 Jun 17.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Algorithms*
Principal Component Analysis*
Polymorphism, Single Nucleotide/*genetics
Genetics, Population ; Genome, Human ; Genome-Wide Association Study ; Genotype ; Humans ; Sample Size
Czasopismo naukowe
Tytuł:
Making a haplotype catalog with estimated frequencies based on SNP homozygotes.
Autorzy:
Yamaguchi-Kabata Y; Laboratory for Statistical Analysis, Center for Genomic Medicine, The Institute of Physical and Chemical Research (RIKEN), Minato-ku, Tokyo, Japan. />Tsunoda T
Takahashi A
Hosono N
Kubo M
Nakamura Y
Kamatani N
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2010 Aug; Vol. 55 (8), pp. 500-6. Date of Electronic Publication: 2010 May 20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Homozygote*
Asian People/*genetics
Haplotypes/*genetics
Polymorphism, Single Nucleotide/*genetics
Gene Frequency ; Genome, Human ; Genome-Wide Association Study ; Genotype ; Humans ; Linkage Disequilibrium ; Mathematical Computing ; Phenotype
Czasopismo naukowe
Tytuł:
pHCR: a parallel haplotype configuration reduction algorithm for haplotype interaction analysis.
Autorzy:
Makarasara W; Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Kumasaka N
Assawamakin A
Takahashi A
Intarapanich A
Ngamphiw C
Kulawonganunchai S
Ruangrit U
Fucharoen S
Kamatani N
Tongsima S
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2009 Nov; Vol. 54 (11), pp. 634-41. Date of Electronic Publication: 2009 Nov 20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Algorithms*
Haplotypes*
Computational Biology/*methods
Alleles ; Genetic Association Studies/methods ; Genetic Predisposition to Disease ; Hemoglobin E/genetics ; Humans ; Reproducibility of Results ; beta-Thalassemia/genetics
Czasopismo naukowe
Tytuł:
A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma.
Autorzy:
Ng CC; Laboratory for International Alliance, RIKEN Center for Genomic Medicine, Tsurumi-ku, Yokohama, Japan. />Yew PY
Puah SM
Krishnan G
Yap LF
Teo SH
Lim PV
Govindaraju S
Ratnavelu K
Sam CK
Takahashi A
Kubo M
Kamatani N
Nakamura Y
Mushiroda T
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2009 Jul; Vol. 54 (7), pp. 392-7. Date of Electronic Publication: 2009 May 29.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Genome-Wide Association Study*
Asian People/*genetics
Integrins/*genetics
Nasopharyngeal Neoplasms/*genetics
Adolescent ; Adult ; Aged ; Alleles ; Case-Control Studies ; Female ; Humans ; Linkage Disequilibrium/genetics ; Malaysia ; Male ; Middle Aged ; Polymorphism, Single Nucleotide/genetics ; Reproducibility of Results ; Young Adult
Czasopismo naukowe
Tytuł:
Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects.
Autorzy:
Saito A; Division of Genomic Medicine, Department of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan. />Kawamoto M
Kamatani N
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2009 Jun; Vol. 54 (6), pp. 317-23. Date of Electronic Publication: 2009 Apr 03.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genome-Wide Association Study*
Quantitative Trait Loci*
Bilirubin/*blood
Glucuronosyltransferase/*genetics
Haplotypes/*genetics
Polymorphism, Single Nucleotide/*genetics
Adult ; Asian People/genetics ; Female ; Gene Frequency ; Genotype ; Glucuronosyltransferase/metabolism ; Humans ; Linkage Disequilibrium ; Male
Czasopismo naukowe
Tytuł:
Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association.
Autorzy:
Miyake K; Division of Diabetes, Metabolism and Endocrinology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Yang W
Hara K
Yasuda K
Horikawa Y
Osawa H
Furuta H
Ng MC
Hirota Y
Mori H
Ido K
Yamagata K
Hinokio Y
Oka Y
Iwasaki N
Iwamoto Y
Yamada Y
Seino Y
Maegawa H
Kashiwagi A
Wang HY
Tanahashi T
Nakamura N
Takeda J
Maeda E
Yamamoto K
Tokunaga K
Ma RC
So WY
Chan JC
Kamatani N
Makino H
Nanjo K
Kadowaki T
Kasuga M
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2009 Apr; Vol. 54 (4), pp. 236-41. Date of Electronic Publication: 2009 Feb 27.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Models, Genetic*
Asian People/*genetics
Diabetes Mellitus, Type 2/*genetics
Alleles ; Genetic Testing ; Genome-Wide Association Study ; Humans ; Japan ; Odds Ratio ; ROC Curve ; Reproducibility of Results ; Risk Assessment
Czasopismo naukowe
Tytuł:
Screening of 336 single-nucleotide polymorphisms in 85 obesity-related genes revealed McKusick-Kaufman syndrome gene variants are associated with metabolic syndrome.
Autorzy:
Hotta K; Laboratory for Endocrinology and Metabolism, Center for Genomic Medicine, RIKEN, Kanagawa, Japan. />Nakamura T
Takasaki J
Takahashi H
Takahashi A
Nakata Y
Kamohara S
Kotani K
Komatsu R
Itoh N
Mineo I
Wada J
Masuzaki H
Yoneda M
Nakajima A
Funahashi T
Miyazaki S
Tokunaga K
Hamaguchi K
Tanaka K
Yamada K
Hanafusa T
Oikawa S
Yoshimatsu H
Nakao K
Sakata T
Matsuzawa Y
Kamatani N
Nakamura Y
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2009 Apr; Vol. 54 (4), pp. 230-5. Date of Electronic Publication: 2009 Feb 27.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Genetic Testing*
Abnormalities, Multiple/*genetics
Metabolic Syndrome/*genetics
Obesity/*genetics
Polymorphism, Single Nucleotide/*genetics
Female ; Gene Frequency ; Group II Chaperonins/genetics ; Haplotypes ; Humans ; Linkage Disequilibrium/genetics ; Male ; Middle Aged ; Regression Analysis ; Reproducibility of Results ; Syndrome
Czasopismo naukowe

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