المؤلفون: Keller MF; Laboratory of Neurogenetics Department of Biological Anthropology, Temple University, Philadelphia, PA, USA., Reiner AP; Department of Epidemiology Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA., Okada Y; Laboratory for Statistical Analysis Department of Human Genetics and Disease Diversity, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan., van Rooij FJ; Department of Epidemiology Consortium for Healthy Aging (NGI-NCHA), The Netherlands Genomics Initiative, Leiden, The Netherlands., Johnson AD; Cardiovascular Epidemiology and Human Genomics Branch, NHLBI Division of Intramural Research, Bethesda, MD, USA NHLBI Framingham Heart Study, Bethesda, MD, USA., Chen MH; Department of Neurology, Boston University School of Medicine, Boston, MA, USA NHLBI Framingham Heart Study, Bethesda, MD, USA., Smith AV; Icelandic Heart Association, Kopavogur, Iceland University of Iceland, Reykjavik, Iceland., Morris AP; Genetic and Genomic Epidemiology Unit, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK Department of Biostatistics, University of Liverpool, Liverpool, UK., Tanaka T; Longitudinal Studies Section, Clinical Research Branch., Ferrucci L; Longitudinal Studies Section, Clinical Research Branch., Zonderman AB; Behavioral Epidemiology Section, Laboratory of Epidemiology & Population Sciences, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD, USA., Lettre G; Montreal Heart Institute, Montréal, Canada Département de Médecine, Université de Montréal, Montréal, Canada., Harris T; Laboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA., Garcia M; Laboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA., Bandinelli S; Geriatric Rehabilitation Unit, Azienda Sanitaria Firenze (ASF), Florence, Italy., Qayyum R; GeneSTAR Research Program, Division of General Internal Medicine., Yanek LR; GeneSTAR Research Program, Division of General Internal Medicine., Becker DM; GeneSTAR Research Program, Division of General Internal Medicine., Becker LC; GeneSTAR Research Program, Division of General Internal Medicine Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA., Kooperberg C; Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA., Keating B; Center for Applied Genomics, Children's Hospital of Philadelphia, PA, USA Department of Pediatrics, University of Pennsylvania, PA, USA., Reis J; Division of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, Bethesda, MD, USA., Tang H; Stanford University School of Medicine, Stanford, CA 94305, USA., Boerwinkle E; The Brown Foundation, Institute of Molecular Medicine for the Prevention of Human Diseases, University of Texas, Houston, TX, USA., Kamatani Y; Laboratory for Statistical Analysis., Matsuda K; Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan., Kamatani N; Laboratory for Statistical Analysis., Nakamura Y; Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan Department of Medicine Department of Surgery, Center for Personalized Therapeutics, The University of Chicago, Chicago, IL, USA., Kubo M; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan., Liu S; Department of Epidemiology Department of Medicine, Brown University, Providence, RI, USA., Dehghan A; Department of Epidemiology Consortium for Healthy Aging (NGI-NCHA), The Netherlands Genomics Initiative, Leiden, The Netherlands., Felix JF; Department of Epidemiology Consortium for Healthy Aging (NGI-NCHA), The Netherlands Genomics Initiative, Leiden, The Netherlands., Hofman A; Department of Epidemiology Consortium for Healthy Aging (NGI-NCHA), The Netherlands Genomics Initiative, Leiden, The Netherlands., Uitterlinden AG; Department of Epidemiology Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands Consortium for Healthy Aging (NGI-NCHA), The Netherlands Genomics Initiative, Leiden, The Netherlands., van Duijn CM; Department of Epidemiology Consortium for Healthy Aging (NGI-NCHA), The Netherlands Genomics Initiative, Leiden, The Netherlands., Franco OH; Department of Epidemiology ErasmusAGE, Department of Epidemiology Consortium for Healthy Aging (NGI-NCHA), The Netherlands Genomics Initiative, Leiden, The Netherlands., Longo DL; Laboratory of Genetics., Singleton AB; Laboratory of Neurogenetics., Psaty BM; Cardiovascular Health Research Unit Department of Medicine Department of Epidemiology and Health Services, University of Washington, Seattle, WA, USA Group Health Research Institute, Group Health Cooperative, Seattle, WA, USA., Evans MK; Health Disparities Research Section, Clinical Research Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA., Cupples LA; NHLBI Framingham Heart Study, Bethesda, MD, USA Boston University Department of Statistics, Boston, MA, USA., Rotter JI; Institute for Translational Genomics and Population Sciences, Los Angeles BioMedical Research Institute at Harbor-UCLA Medical Center, Torrance, CA, USA Division of Genetic Outcomes, Department of Pediatrics, Harbor-UCLA Medical Center, Torrance, CA, USA., O'Donnell CJ; Cardiovascular Epidemiology and Human Genomics Branch, NHLBI Division of Intramural Research, Bethesda, MD, USA NHLBI Framingham Heart Study, Bethesda, MD, USA., Takahashi A; Laboratory for Statistical Analysis., Wilson JG; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, MS, USA., Ganesh SK; Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA Department of Human Genetics, University of Michigan, Ann Arbor, MI, USA sganesh@med.umich.edu nallsm@mail.nih.gov., Nalls MA; Laboratory of Neurogenetics sganesh@med.umich.edu nallsm@mail.nih.gov.

مؤلفون مشاركون: CHARGE Hematology, COGENT, BioBank Japan Project (RIKEN) Working Groups

المصدر: Human molecular genetics [Hum Mol Genet] 2014 Dec 20; Vol. 23 (25), pp. 6944-60. Date of Electronic Publication: 2014 Aug 05.

نوع المنشور: Journal Article; Meta-Analysis; Research Support, American Recovery and Reinvestment Act; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genome, Human* , Phenotype* , Polymorphism, Single Nucleotide* , Quantitative Trait Loci*, Leukocytes/*metabolism, Black or African American ; Asian People ; Bayes Theorem ; Genome-Wide Association Study ; Genotype ; Humans ; Leukocyte Count ; Leukocytes/cytology ; Linkage Disequilibrium ; White People

المؤلفون: Sano M; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan, msano@a8.keio.jp., Kamitsuji S; StaGen Co. Ltd., Tokyo, Japan., Kamatani N; StaGen Co. Ltd., Tokyo, Japan., Hong KW; Center for Genome Science, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongwon 363-951, Korea and., Han BG; Center for Genome Science, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongwon 363-951, Korea and., Kim Y; Center for Genome Science, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongwon 363-951, Korea and., Kim JW; Department of Internal Medicine, Inje University Ilsan Paik Hospital, Goyang, Korea., Aizawa Y; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan., Fukuda K; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.

مؤلفون مشاركون: Japan Pharmacogenomics Data Science Consortium (JPDSC)

المصدر: Human molecular genetics [Hum Mol Genet] 2014 Dec 15; Vol. 23 (24), pp. 6668-76. Date of Electronic Publication: 2014 Jul 23.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide* , Quantitative Trait Loci*, Heart Conduction System/*physiology , Sodium-Calcium Exchanger/*genetics, Adult ; Aged ; Alleles ; Animals ; Asian People ; Electrocardiography ; Female ; Gene Deletion ; Gene Frequency ; Genome-Wide Association Study ; Humans ; Male ; Mice ; Mice, Knockout ; Middle Aged ; Sodium-Calcium Exchanger/metabolism

المؤلفون: Hara K; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8655, Japan., Fujita H, Johnson TA, Yamauchi T, Yasuda K, Horikoshi M, Peng C, Hu C, Ma RC, Imamura M, Iwata M, Tsunoda T, Morizono T, Shojima N, So WY, Leung TF, Kwan P, Zhang R, Wang J, Yu W, Maegawa H, Hirose H, Kaku K, Ito C, Watada H, Tanaka Y, Tobe K, Kashiwagi A, Kawamori R, Jia W, Chan JC, Teo YY, Shyong TE, Kamatani N, Kubo M, Maeda S, Kadowaki T

مؤلفون مشاركون: DIAGRAM consortium

المصدر: Human molecular genetics [Hum Mol Genet] 2014 Jan 01; Vol. 23 (1), pp. 239-46. Date of Electronic Publication: 2013 Aug 14.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genome-Wide Association Study*, Diabetes Mellitus, Type 2/*genetics , Guanine Nucleotide Dissociation Inhibitors/*genetics , Monocarboxylic Acid Transporters/*genetics, Genetic Loci ; Genetic Predisposition to Disease ; Genetic Variation ; Genome, Human ; Haplotypes ; Humans ; Leptin/genetics ; MicroRNAs/genetics ; Polymorphism, Single Nucleotide

المؤلفون: Imamura M; Laboratory for Endocrinology and Metabolism, RIKEN Center for Genomic Medicine, Yokohama, Kanagawa, Japan., Maeda S, Yamauchi T, Hara K, Yasuda K, Morizono T, Takahashi A, Horikoshi M, Nakamura M, Fujita H, Tsunoda T, Kubo M, Watada H, Maegawa H, Okada-Iwabu M, Iwabu M, Shojima N, Ohshige T, Omori S, Iwata M, Hirose H, Kaku K, Ito C, Tanaka Y, Tobe K, Kashiwagi A, Kawamori R, Kasuga M, Kamatani N, Nakamura Y, Kadowaki T

مؤلفون مشاركون: Diabetes Genetics Replication and Meta-analysis (DIAGRAM) Consortium

المصدر: Human molecular genetics [Hum Mol Genet] 2012 Jul 01; Vol. 21 (13), pp. 3042-9. Date of Electronic Publication: 2012 Mar 28.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, Ankyrins/*genetics , Asian People/*genetics , Diabetes Mellitus, Type 2/*ethnology , Diabetes Mellitus, Type 2/*genetics, Cells, Cultured ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Genotype ; Humans ; Japan

المؤلفون: Low SK; Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan., Takahashi A, Cha PC, Zembutsu H, Kamatani N, Kubo M, Nakamura Y

المصدر: Human molecular genetics [Hum Mol Genet] 2012 May 01; Vol. 21 (9), pp. 2102-10. Date of Electronic Publication: 2012 Jan 27.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Intracranial Aneurysm/*genetics , Receptor, Endothelin A/*genetics, Asian People/genetics ; Case-Control Studies ; Chromosomes, Human, Pair 4/genetics ; Chromosomes, Human, Pair 9/genetics ; Cyclin-Dependent Kinase Inhibitor p15/genetics ; Genetic Predisposition to Disease ; Genetic Variation ; Genome-Wide Association Study ; Humans ; Japan ; Polymorphism, Single Nucleotide

المؤلفون: Nguyen HH; Laboratory for Biomarker Development, Center for Genome Medicine, RIKEN, Tokyo, Japan., Takata R, Akamatsu S, Shigemizu D, Tsunoda T, Furihata M, Takahashi A, Kubo M, Kamatani N, Ogawa O, Fujioka T, Nakamura Y, Nakagawa H

المصدر: Human molecular genetics [Hum Mol Genet] 2012 May 01; Vol. 21 (9), pp. 2076-85. Date of Electronic Publication: 2012 Feb 08.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 5/*genetics , Homeodomain Proteins/*genetics , Homeodomain Proteins/*metabolism , Prostatic Neoplasms/*genetics , Prostatic Neoplasms/*metabolism , Receptors, Calcitriol/*metabolism, 5' Untranslated Regions ; Base Sequence ; Case-Control Studies ; Cell Line, Tumor ; Cell Proliferation ; Chromosome Mapping ; Cloning, Molecular ; Exons ; Gene Frequency ; Genetic Predisposition to Disease ; Homeodomain Proteins/antagonists & inhibitors ; Humans ; Male ; Prostatic Neoplasms/etiology ; Prostatic Neoplasms/pathology ; RNA, Small Interfering/genetics

المؤلفون: Mbarek H; Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato, Tokyo., Ochi H, Urabe Y, Kumar V, Kubo M, Hosono N, Takahashi A, Kamatani Y, Miki D, Abe H, Tsunoda T, Kamatani N, Chayama K, Nakamura Y, Matsuda K

المصدر: Human molecular genetics [Hum Mol Genet] 2011 Oct 01; Vol. 20 (19), pp. 3884-92. Date of Electronic Publication: 2011 Jul 12.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease* , Genome-Wide Association Study*, Asian People/*genetics , HLA-DP Antigens/*genetics , HLA-DQ Antigens/*genetics , Hepatitis B, Chronic/*genetics, Case-Control Studies ; Humans ; Polymorphism, Single Nucleotide ; Risk Factors

المؤلفون: Iida A; Laboratory for Bone and Joint Diseases, Center for Genomic Medicine, RIKEN, Tokyo 108-8639, Japan., Takahashi A, Kubo M, Saito S, Hosono N, Ohnishi Y, Kiyotani K, Mushiroda T, Nakajima M, Ozaki K, Tanaka T, Tsunoda T, Oshima S, Sano M, Kamei T, Tokuda T, Aoki M, Hasegawa K, Mizoguchi K, Morita M, Takahashi Y, Katsuno M, Atsuta N, Watanabe H, Tanaka F, Kaji R, Nakano I, Kamatani N, Tsuji S, Sobue G, Nakamura Y, Ikegawa S

المصدر: Human molecular genetics [Hum Mol Genet] 2011 Sep 15; Vol. 20 (18), pp. 3684-92. Date of Electronic Publication: 2011 Jun 10.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease*, Amyotrophic Lateral Sclerosis/*genetics , Asian People/*genetics , Carrier Proteins/*genetics , Carrier Proteins/*metabolism, Adult ; Aged ; Aged, 80 and over ; Amyotrophic Lateral Sclerosis/metabolism ; Case-Control Studies ; Female ; Genetic Association Studies ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide ; Signal Transduction ; Spinal Cord/metabolism ; Transforming Growth Factor beta/metabolism ; Young Adult

المؤلفون: Okada Y; Laboratory for Statistical Analysis, Center for Genomic Medicine, RIKEN, Yokohama, Japan. yokada@src.riken.jp, Takahashi A, Ohmiya H, Kumasaka N, Kamatani Y, Hosono N, Tsunoda T, Matsuda K, Tanaka T, Kubo M, Nakamura Y, Yamamoto K, Kamatani N

المصدر: Human molecular genetics [Hum Mol Genet] 2011 Mar 15; Vol. 20 (6), pp. 1224-31. Date of Electronic Publication: 2010 Dec 31.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genome-Wide Association Study* , Polymorphism, Single Nucleotide*, Asian People/*genetics , C-Reactive Protein/*metabolism , Inflammation/*genetics , Interleukin-6/*genetics, Adult ; Aged ; Case-Control Studies ; Female ; Genotype ; Humans ; Inflammation/blood ; Male ; Middle Aged

المؤلفون: Ozeki T; Research Group for Pharmacogenomics, RIKEN Center for Genomic Medicine, Yokohama 230-0045, Japan., Mushiroda T, Yowang A, Takahashi A, Kubo M, Shirakata Y, Ikezawa Z, Iijima M, Shiohara T, Hashimoto K, Kamatani N, Nakamura Y

المصدر: Human molecular genetics [Hum Mol Genet] 2011 Mar 01; Vol. 20 (5), pp. 1034-41. Date of Electronic Publication: 2010 Dec 10.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease*/etiology , Genome-Wide Association Study*, Anticonvulsants/*adverse effects , Asian People/*genetics , Carbamazepine/*adverse effects , Drug-Related Side Effects and Adverse Reactions/*genetics , HLA-A Antigens/*genetics, Adolescent ; Adult ; Aged ; Aged, 80 and over ; Alleles ; Child ; Child, Preschool ; Cohort Studies ; Drug-Related Side Effects and Adverse Reactions/etiology ; Female ; Genotype ; Humans ; Infant ; Japan ; Male ; Middle Aged ; Young Adult