نتائج البحث - "Louise Wain"

المساهمون: Internal Medicine, Epidemiology, Dermatology, Esko, Tõnu [0000-0003-1982-6569], Pilling, Luke C [0000-0002-3332-8454], Schurmann, Claudia [0000-0003-4158-9192], Milani, Lili [0000-0002-5323-3102], Wang, Richard [0000-0003-4063-6508], Dehghan, Abbas [0000-0001-6403-016X], Melzer, David [0000-0002-0170-3838], Meitinger, Thomas [0000-0002-8838-8403], Dörr, Marcus [0000-0001-7471-475X], Zeller, Tanja [0000-0003-3379-2641], Prokisch, Holger [0000-0003-2379-6286], Völker, Uwe [0000-0002-5689-3448], Levy, Daniel [0000-0003-1843-8724], Apollo - University of Cambridge Repository, McCarthy, Mark I, Department of Neuroscience and Biomedical Engineering, Aalto-yliopisto, Aalto University

المصدر: PLOS Genetics
PLoS Genetics (print), 11(3). Public Library of Science
PLoS Genetics
PLoS genetics, vol 11, iss 3
PLoS Genetics, 11(3):e1005035
Europe PubMed Central
PLoS Genetics, Vol 11, Iss 3, p e1005035 (2015)

مصطلحات موضوعية: Aging, Cancer Research, Genome-wide association study, Blood Pressure, 030204 cardiovascular system & hematology, Cardiovascular, 0302 clinical medicine, Clinical genetics, Medicine and health sciences, Drug research and development, Genome-wide association studies, Gene expression, Research laboratories, Cardiology, Genetic epidemiology, 2.1 Biological and endogenous factors, Aetiology, Genetics (clinical), Genetics, Regulation of gene expression, Genetics & Heredity, 0303 health sciences, International Consortium for Blood Pressure GWAS (ICBP), Single Nucleotide, Phenotype, POTASSIUM, 3. Good health, ddc, TRIALS, Hypertension, Life Sciences & Biomedicine, Biotechnology, Research Article, International Consortium for Blood Pressure GWAS, lcsh:QH426-470, Genotype, Single-nucleotide polymorphism, Biology, PERIPHERAL-BLOOD, PROFILE, Polymorphism, Single Nucleotide, 03 medical and health sciences, MICROARRAY ANALYSIS, Humans, Genetic Predisposition to Disease, Polymorphism, GENOME-WIDE ASSOCIATION, Molecular Biology, Gene, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Genetic association, 0604 Genetics, Science & Technology, Prevention, Human Genome, ta1182, PREVENTION, gene expression, blood pressure, hypertension, SODIUM, lcsh:Genetics, MICE, Gene Expression Regulation, CELLS, Transcriptome, Developmental Biology, Genome-Wide Association Study

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e3028d1ff016d4aed76f7dc2775add7

Find this article in full text from ProQuest

9

Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease

المؤلفون: Mark Caulfield, Alexander Mentzer, Eleftheria Zeggini, Michael Weedon, Eleni Giannoulatou, Samuel Charles Robson, Christopher Nelson, Paul Martin, Patricia Munroe, Detelina Grozeva, John Isaacs, Stephen Eyre, Clare Turnbull, Amanda Bennett, James Lee, Andrew Hattersley, Chris Wallace, David Evans, Joanna Howson, Jan Aerts, Julian Maller, Christine Albert, Lisa Jones, Michael O'Donovan, Willem Ouwehand, Sara Pulit, Gerome Breen, Hana Lango Allen, Ann Morgan, Panos Deloukas, Chris Barnes, Pille Harrison, Allan Young, Gareth Evans, Martin Tobin, Simon Myers, Natalie Prescott, Lynne J Hocking, Oliver Burren, Louise Wain, Ian Bruce, William Newman, Miles Parkes, Anna Dominiczak, Mark McCarthy, Cecilia Lindgren, Oliver Brand, Alistair Hall

المساهمون: Kronenberg, Florian, Nelson, Christopher P [0000-0001-8025-2897], Pulit, Sara L [0000-0002-2502-3669], Albert, Christine M [0000-0002-2081-1121], Apollo - University of Cambridge Repository

المصدر: PloS one, vol 8, iss 4
PLoS ONE
Huertas-Vazquez, A, Nelson, C P, Guo, X, Reinier, K, Uy-Evanado, A, Teodorescu, C, Ayala, J, Jerger, K, Chugh, H, Lees, C, Satsangi, J, Braund, P S, Deloukas, P, Hall, A S, Balmforth, A J, Jones, M, Taylor, K D, Pulit, S L, Newton-Cheh, C, Gunson, K, Jui, J, Rotter, J I, Albert, C M & Samani, N J & Chugh, S S 2013, ' Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease ', PLoS ONE, vol. 8, no. 4, pp. e59905 . https://doi.org/10.1371/journal.pone.0059905
PLoS ONE, Vol 8, Iss 4, p e59905 (2013)

مصطلحات موضوعية: Male, Candidate gene, WTCCC+, Epidemiology, rab3 GTP-Binding Proteins, lcsh:Medicine, Genome-wide association study, Coronary Artery Disease, 030204 cardiovascular system & hematology, Arrhythmias, Bioinformatics, Cardiovascular, Sudden cardiac death, Coronary artery disease, 0302 clinical medicine, hemic and lymphatic diseases, 2.1 Biological and endogenous factors, Aetiology, lcsh:Science, 0303 health sciences, education.field_of_study, Multidisciplinary, Single Nucleotide, Middle Aged, 3. Good health, Death, DNA-Binding Proteins, Heart Disease, Genetic Epidemiology, Medicine, Female, Cardiac, Research Article, Risk, Adult, congenital, hereditary, and neonatal diseases and abnormalities, Clinical Research Design, General Science & Technology, Population, Context (language use), Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Clinical Research, medicine, Genetics, Humans, Genetic Predisposition to Disease, cardiovascular diseases, Polymorphism, education, Genetic Association Studies, Heart Disease - Coronary Heart Disease, 030304 developmental biology, Aged, Population Biology, Prevention, lcsh:R, Human Genome, Case-control study, Human Genetics, medicine.disease, Atherosclerosis, Sudden, Introns, Death, Sudden, Cardiac, Genetic epidemiology, Genetic Loci, Case-Control Studies, Genetics of Disease, Genetic Polymorphism, lcsh:Q, Population Genetics, Transcription Factors

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413b69ecd88503df6e2e916b1d80a494
https://escholarship.org/uc/item/2rp0q03x

10

Seven newly identified loci for autoimmune thyroid disease

المؤلفون: Mark Caulfield, Alexander Mentzer, Eleftheria Zeggini, Hui Guo, Michael Weedon, Eleni Giannoulatou, Samuel Charles Robson, Paul Martin, Patricia Munroe, Detelina Grozeva, John Isaacs, Stephen Eyre, Clare Turnbull, James Lee, Andrew Hattersley, Diana M Eccles, Chris Wallace, David Evans, Neil Walker, Joanna Howson, Jan Aerts, Julian Maller, Lisa Jones, Matt Simmonds, Willem Ouwehand, Gerome Breen, Hana Lango Allen, Ann Morgan, John Todd, Christopher George Mathew, Chris Barnes, Pille Harrison, Allan Young, Gareth Evans, Martin Tobin, Simon Myers, Natalie Prescott, Lynne J Hocking, Oliver Burren, Louise Wain, Ian Bruce, William Newman, Miles Parkes, Sarah Hunt, Anna Dominiczak, Mark McCarthy, Cecilia Lindgren, Oliver Brand, Alistair Hall

المصدر: Human Molecular Genetics
Human Molecular Genetics; Vol 21

مصطلحات موضوعية: Male, Graves' disease, 030209 endocrinology & metabolism, Single-nucleotide polymorphism, Genome-wide association study, Hashimoto Disease, Biology, Polymorphism, Single Nucleotide, Thyroiditis, Autoimmune Diseases, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, Molecular Biology, Allele frequency, Genetics (clinical), 030304 developmental biology, Genetics & Heredity, 0303 health sciences, Association Studies Articles, Chromosome Mapping, 11 Medical And Health Sciences, General Medicine, 06 Biological Sciences, medicine.disease, Thyroid Diseases, C420 Human Genetics, Graves Disease, 3. Good health, Chromosome Banding, Minor allele frequency, Genetic Loci, Case-Control Studies, Wellcome Trust Case Control Consortium, Female, SNP array

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72f244472105de8353b7b3cd404e3409
https://pubmed.ncbi.nlm.nih.gov/22922229

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