يعرض 1 - 8 نتائج من 8 نتيجة بحث عن '"Ming-Huei Chen"', وقت الاستعلام: 2.22s تنقيح النتائج
  1. 1
    Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors

    المؤلفون: Nathan Pankratz, Peng Wei, Jennifer A Brody, Ming-Huei Chen, Paul S de Vries, Jennifer E Huffman, Mary Rachel Stimson, Paul L Auer, Eric Boerwinkle, Mary Cushman, Moniek P M de Maat, Aaron R Folsom, Oscar H Franco, Richard A Gibbs, Kelly K Haagenson, Albert Hofman, Jill M Johnsen, Christie L Kovar, Robert Kraaij, Barbara McKnight, Ginger A Metcalf, Donna Muzny, Bruce M Psaty, Weihong Tang, André G Uitterlinden, Jeroen G J van Rooij, Abbas Dehghan, Christopher J O'Donnell, Alex P Reiner, Alanna C Morrison, Nicholas L Smith

    المصدر: Hum Mol Genet

    مصطلحات موضوعية: Factor VIII, Exome Sequencing, von Willebrand Factor, Genetics, Fibrinogen, Humans, Original Article, General Medicine, Factor VII, Polymorphism, Single Nucleotide, Molecular Biology, Hemostatics, Genetics (clinical)

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02a7d75c79ba75f31f58b4ffc1eb8bf6Test
    https://doi.org/10.1093/hmg/ddac100Test


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  2. 2
    Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

    المؤلفون: Nauder Faraday, Brian D. Hobbs, Quan Sun, Michael Preuss, Ani Manichaikul, Eric Jorgenson, Ming-Huei Chen, Eric Boerwinkle, Florian Thibord, Arunoday Bhan, Alanna C. Morrison, Ramachandran S. Vasan, Nathan Pankratz, Charles Kooperberg, Deborah A. Nickerson, Joshua P. Lewis, Hélène Choquet, Jee-Young Moon, Jeffrey R. O'Connell, Marsha M. Wheeler, Albert V. Smith, Russell P. Tracy, Nathalie Chami, Ruth J. F. Loos, Alexander P. Reiner, Nicholas L. Smith, Gonçalo R. Abecasis, Laura M. Raffield, Amarise Little, Nancy L. Heard-Costa, Andrew D. Johnson, David C. Glahn, Rasika A. Mathias, Adam S. Butterworth, John Blangero, Joanne E. Curran, Timothy A. Thornton, Laura Almasy, Jerome I. Rotter, Nancy Min, Lisa R. Yanek, Donald M. Lloyd-Jones, Zhe Wang, Matthew P. Conomos, Myriam Fornage, Hua Tang, Lewis C. Becker, Lynette Ekunwe, Cecelia A. Laurie, Adolfo Correa, Jai G. Broome, Terri H. Beaty, Jennifer A. Brody, Caitlin P. McHugh, Yao Hu, Braxton D. Mitchell, Lifang Hou, Yun Li, Kathleen A. Ryan, Paul L. Auer, Stephen S. Rich, Kari E. North, Thomas W. Blackwell, Bruce M. Psaty, Deepti Jain, Paul S Vries, Praveen Surendran

    المساهمون: Butterworth, Adam [0000-0002-6915-9015], Apollo - University of Cambridge Repository

    المصدر: Human molecular genetics, vol 31, iss 3
    Hum Mol Genet

    مصطلحات موضوعية: Blood Platelets, Platelet disorder, Population, Genome-wide association study, Biology, Quantitative trait locus, Polymorphism, Single Nucleotide, Medical and Health Sciences, Genome, 03 medical and health sciences, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, 0302 clinical medicine, Clinical Research, and Blood Institute (U.S.), Genetics, Humans, 2.1 Biological and endogenous factors, Polymorphism, Precision Medicine, Aetiology, Mean platelet volume, education, Hemostatic function, Lung, Molecular Biology, Genetics (clinical), 030304 developmental biology, Blood Platelet Disorders, Genetics & Heredity, 0303 health sciences, education.field_of_study, Human Genome, Single Nucleotide, National Heart, Hematology, General Medicine, Biological Sciences, United States, 3. Good health, Phenotype, Good Health and Well Being, 030220 oncology & carcinogenesis, General Article, National Heart, Lung, and Blood Institute (U.S.), Genome-Wide Association Study, Biotechnology

    وصف الملف: application/pdf; application/octet-stream

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fc9557e325812482460ef4586ad1a77Test
    https://doi.org/10.1093/hmg/ddab252Test


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  3. 3
    Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium

    المؤلفون: Melissa E. Garcia, Majken K. Jensen, Margaux F. Keller, Joachim H. Ix, Richard A. Jensen, Vasan S. Ramachandran, Jie Yao, Kenneth J. Mukamal, Anne B. Newman, Tamara B. Harris, Frank B. Hu, Ming-Huei Chen, Jorge R. Kizer, Bruce M. Psaty, Alice M. Arnold, James S. Pankow, Jerome I. Rotter, Ronit Katz, Luc Djoussé, David S. Siscovick, Xiuqing Guo, Mike A. Nalls, Ida Chen, Yongmei Liu, Ron C. Hoogeveen, Qi Sun, Eric B. Rimm, Mark O. Goodarzi, Marilyn C. Cornelis, Joseph M. Zmuda, Kathryn M. Rexrode

    المصدر: Human molecular genetics, vol 26, iss 11

    مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Genotype, alpha-2-HS-Glycoprotein, Population, 030209 endocrinology & metabolism, Locus (genetics), Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Medical and Health Sciences, White People, 03 medical and health sciences, Exon, 0302 clinical medicine, Diabetes Mellitus, Genetics, Humans, 2.1 Biological and endogenous factors, SNP, Polymorphism, Aetiology, education, Molecular Biology, Gene, Metabolic and endocrine, Genetics (clinical), Aged, Metabolic Syndrome, Genetics & Heredity, education.field_of_study, Association Studies Articles, Human Genome, Single Nucleotide, General Medicine, Middle Aged, Biological Sciences, Black or African American, 030104 developmental biology, Diabetes Mellitus, Type 2, Genetic Loci, Female, Type 2, Genome-Wide Association Study

    وصف الملف: application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fb5b598bf38b9e518ce5be416e1c53fTest
    https://doi.org/10.1093/hmg/ddx091Test


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  4. 4
    RVFam: an R package for rare variant association analysis with family data

    المؤلفون: Ming-Huei Chen, Qiong Yang

    المصدر: Bioinformatics. 32:624-626

    مصطلحات موضوعية: 0301 basic medicine, Statistics and Probability, Computer science, Genetic Variation, Genome-wide association study, Computational biology, Applications Notes, Biochemistry, Rare variant association, Computer Science Applications, 03 medical and health sciences, Computational Mathematics, R package, 030104 developmental biology, Computational Theory and Mathematics, Genetic variation, Humans, Family, Molecular Biology, Software, Genome-Wide Association Study, Genetic association

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2881f7c3bf1ca951b4842068069cb992Test
    https://doi.org/10.1093/bioinformatics/btv609Test


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  5. 5
    Clinical and Genetic Correlates of Growth Differentiation Factor 15 in the Community

    المؤلفون: James L. Januzzi, Kai C. Wollert, Lars Lind, Erik Ingelsson, Thomas J. Wang, Cecilia M. Lindgren, Elizabeth L. McCabe, Jennifer E. Ho, Andrew P. Morris, Susan Cheng, Tibor Kempf, Anahita Ghorbani, Anubha Mahajan, Ming-Huei Chen, Martin G. Larson, Andrew D. Johnson, Ramachandran S. Vasan

    المصدر: Clinical Chemistry. 58:1582-1591

    مصطلحات موضوعية: Male, medicine.medical_specialty, Growth Differentiation Factor 15, Offspring, Quantitative Trait Loci, Clinical Biochemistry, Locus (genetics), Genome-wide association study, 030204 cardiovascular system & hematology, Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, Article, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Internal medicine, Diabetes mellitus, medicine, Humans, Genetic Predisposition to Disease, Aged, 030304 developmental biology, 0303 health sciences, Framingham Risk Score, Cholesterol, HDL, Biochemistry (medical), Middle Aged, medicine.disease, 3. Good health, Endocrinology, Cardiovascular Diseases, Multivariate Analysis, Female, GDF15, Genome-Wide Association Study, Cohort study

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daec179300e15edf27ffd800174ac971Test
    https://doi.org/10.1373/clinchem.2012.190322Test


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  6. 6
    A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3

    المؤلفون: Ramachandran S. Vasan, Heyo K. Kroemer, Henri Wallaschofski, Nele Friedrich, Florian Ernst, Mark O. Goodarzi, Jenny Manolopoulou, Henry Völzke, Lisa S. Sullivan, Martina Müller, Carolyn S.P. Lam, Ariadni Spyroglou, Norman Klopp, Christian Gieger, Jerome I. Rotter, Howard D. Strickler, Matthias Nauck, H.-Erich Wichmann, Martin Bidlingmaier, Robert C. Kaplan, Reiner Biffar, Anne B. Newman, Qiong Yang, Ming-Huei Chen, Kenneth Rice, Alexander Teumer, Anne R. Cappola, Angela Döring, Georg Homuth, Michael Pollak, Ann-Kristin Petersen, Nicole L. Glazer, Holly Smith, Douglas B. Sawyer, Y.-D. Ida Chen, Martin Reincke, Bruce M. Psaty

    المصدر: Hum. Mol. Genet. 20, 1241-1251 (2011)

    مصطلحات موضوعية: Male, IGFBP3, Locus (genetics), Genome-wide association study, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, White People, Cohort Studies, Genetics, Humans, Insulin-Like Growth Factor I, Molecular Biology, Gene, Genetics (clinical), Aged, Carbohydrate homeostasis, Cell growth, Association Studies Articles, Chromosome, General Medicine, Insulin-Like Growth Factor Binding Protein 3, Growth-factor-I, Factor-binding protein-3, Breast-cancer risk, Genetic-variation, Factor (IGF)-I, Mortality, Disease, Polymorphism, Deficiency, Hormone, Female, Chromosomes, Human, Pair 7, Genome-Wide Association Study

    وصف الملف: application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef4e6ae3d67c9e17bd8600b233f948eaTest
    https://doi.org/10.1093/hmg/ddq560Test


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  7. 7
    Genome-wide association meta-analysis for total serum bilirubin levels

    المؤلفون: Fernando Rivadeneira, Albert Hofman, Qiong Yang, Cornelia M. van Duijn, Tamara B. Harris, Vilmundur Gudnason, Abbas Dehghan, André G. Uitterlinden, L. Adrienne Cupples, Jing-Ping Lin, Lenore J. Launer, Christopher J. O'Donnell, Ming-Huei Chen, Maryam Kavousi, Andrew D. Johnson, Jacqueline C.M. Witteman, Albert V. Smith, Thor Aspelund, Bruno H. Stricker

    المساهمون: Epidemiology, Internal Medicine

    المصدر: Human Molecular Genetics, 18(14), 2700-2710. Oxford University Press

    مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Bilirubin, Organic Anion Transporters, Genome-wide association study, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, White People, chemistry.chemical_compound, Framingham Heart Study, SDG 3 - Good Health and Well-being, Internal medicine, Genetic variation, Genetics, medicine, Humans, Prospective Studies, Glucuronosyltransferase, Allele, Molecular Biology, Genetics (clinical), Aged, Netherlands, Genetic association, biology, Liver-Specific Organic Anion Transporter 1, Association Studies Articles, Genetic Variation, General Medicine, Middle Aged, Endocrinology, chemistry, biology.protein, SLCO1B1, Genome-Wide Association Study

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::022ec2cbc5e54c0da166908ad8b12053Test
    https://doi.org/10.1093/hmg/ddp202Test


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  8. 8
    GWAF: an R package for genome-wide association analyses with family data

    المؤلفون: Qiong Yang, Ming-Huei Chen

    المصدر: Bioinformatics. 26:580-581

    مصطلحات موضوعية: Statistics and Probability, Genotype, Single-nucleotide polymorphism, Genome-wide association study, Genomics, Computational biology, Biology, Polymorphism, Single Nucleotide, Biochemistry, Genome, Framingham Heart Study, Genetic model, Humans, SNP, Genetic Predisposition to Disease, Molecular Biology, Genetics, Genome, Human, Computer Science Applications, Applications Note, Computational Mathematics, Computational Theory and Mathematics, Human genome, Software, Genome-Wide Association Study

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0a0ddeab337026cd8ac40c69483c82fTest
    https://doi.org/10.1093/bioinformatics/btp710Test


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