نتائج البحث - "European continental ancestry group"

1

Learning the properties of adaptive regions with functional data analysis

المؤلفون: Jinguo Huang, Hillary Koch, Francesca Chiaromonte, Michael DeGiorgio, Mehreen R. Mughal

المصدر: PLoS Genetics, Vol 16, Iss 8, p e1008896 (2020)
PLoS Genetics

مصطلحات موضوعية: Cancer Research, Mutation rate, Heredity, Genomics Statistics, Introgression, Computer science, Population genetics, Animals, DNA-Binding Proteins, European Continental Ancestry Group, Genetic Variation, Humans, Membrane Transport Proteins, Neanderthals, Selection, Genetic, Software, Models, Genetic, Mutation Rate, QH426-470, Mathematical and Statistical Techniques, 0302 clinical medicine, Models, Genetics (clinical), 0303 health sciences, education.field_of_study, Natural selection, Simulation and Modeling, Statistics, Functional data analysis, Genomics, Genetic Mapping, Data point, Physical Sciences, Mutation (genetic algorithm), Research Article, Statistical Distributions, Evolutionary Processes, Population, Biology, Research and Analysis Methods, White People, Human Genomics, 03 medical and health sciences, Genetic, Genetics, Statistical Methods, education, Selection, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Selection (genetic algorithm), 030304 developmental biology, Evolutionary Biology, Genetic diversity, Biology and Life Sciences, Computational Biology, Probability Theory, Haplotypes, Evolutionary biology, Mathematics, 030217 neurology & neurosurgery, Forecasting

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a104563066e17f6ce7b29abb997722c0Test
https://doaj.org/article/9e4ac2c02d1a4fdeaf53aa3bdc0e84d5Test

2

European Roma groups show complex West Eurasian admixture footprints and a common South Asian genetic origin

المؤلفون: Erica Bianco, Laura R. Arauna, David Comas, Maria João Prata, Esther Rebato, Francesc Calafell, Alaitz Poveda, Neus Font-Porterias

المساهمون: Ministerio de Economía y Competitividad (España), European Commission, Generalitat de Catalunya, Instituto de Investigação e Inovação em Saúde

المصدر: PLoS Genetics, Vol 15, Iss 9, p e1008417 (2019)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Recercat. Dipósit de la Recerca de Catalunya
PLoS Genetics
Addi. Archivo Digital para la Docencia y la Investigación

مصطلحات موضوعية: Cancer Research, Heredity, Roma, Population genetics, Ethnic group, insights, QH426-470, migration, Geographical Locations, X chromosomes, 0302 clinical medicine, Peninsula, Ethnicity, Gene Flow / genetics, Ethnicities, identity, Minority Groups, Genetics (clinical), 0303 health sciences, education.field_of_study, Sex Chromosomes, geography.geographical_feature_category, Chromosome Biology, Human migration, Autosomes, Founder Effect, Gene flow, Europe, Roma / genetics, Ethnology, Asian Continental Ancestry Group / genetics, Genetic footprinting, Research Article, Asia, Demographic history, Human Migration, Population, Romani people, India, Genetic Fingerprinting and Footprinting, Biology, Research and Analysis Methods, isolate, Chromosomes, White People, diversity, 03 medical and health sciences, Asian People, Genetics, Humans, Molecular Biology Techniques, education, European Continental Ancestry Group / genetics, Molecular Biology, Comparative linguistics, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Evolutionary Biology, geography, Population Biology, business.industry, ancestry, Biology and Life Sciences, Genetic Variation, Cell Biology, Genetics, Population, Haplotypes, Genetic Variation / genetics, People and Places, Population Groupings, Haplotypes / genetics, genomes, business, Ethnic Groups / genetics, divergence, 030217 neurology & neurosurgery, population history, Founder effect

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::176050f82ea918879b01a70f5750c371Test
https://doaj.org/article/4341a5867c804738ad0a96b6338fcc0bTest

3

An approximate full-likelihood method for inferring selection and allele frequency trajectories from DNA sequence data

المؤلفون: Peter R. Wilton, Rasmus Nielsen, Aaron J. Stern

المساهمون: Hernandez, Ryan D

المصدر: PLoS Genetics
PLoS genetics, vol 15, iss 9
PLoS Genetics, Vol 15, Iss 9, p e1008384 (2019)

مصطلحات موضوعية: Cancer Research, Heredity, Computer science, Population Dynamics, Markov models, QH426-470, Geographical Locations, 0302 clinical medicine, Gene Frequency, Models, Natural Selection, Hidden Markov models, Genetics (clinical), Data Management, education.field_of_study, Likelihood Functions, 0303 health sciences, Natural selection, Edar Receptor, Pigmentation, Simulation and Modeling, Selection coefficient, Phylogenetic Analysis, Markov Chains, Asians, Phylogenetics, Physical sciences, Europe, Genetic Mapping, symbols, Likelihood function, Sequence Analysis, Monte Carlo Method, Algorithm, Research Article, Asian Continental Ancestry Group, Computer and Information Sciences, Evolutionary Processes, Population, European Continental Ancestry Group, Biology, Research and Analysis Methods, DNA sequencing, White People, Molecular Genetics, 03 medical and health sciences, symbols.namesake, Genetic, Asian People, Genetics, Humans, Evolutionary Systematics, Allele, education, Gene, Molecular Biology, Allele frequency, Alleles, Ecology, Evolution, Behavior and Systematics, Selection (genetic algorithm), Taxonomy, 030304 developmental biology, Evolutionary Biology, Base Sequence, Models, Genetic, Population Biology, Whites, Biology and Life Sciences, Probability theory, Markov chain Monte Carlo, DNA, Sequence Analysis, DNA, Minichromosome Maintenance Complex Component 6, Geographic Distribution, Haplotypes, People and Places, Generic health relevance, Selective sweep, Mathematics, 030217 neurology & neurosurgery, Importance sampling, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f500da5de53f97e4a5c185a55c1c4e33Test
https://doi.org/10.1371/journal.pgen.1008384Test

4

Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study

المؤلفون: Michael Boehnke, Narisu Narisu, Ryan P. Welch, Christian Fuchsberger, Pasi Soininen, Francis S. Collins, Adam E. Locke, Karen L. Mohlke, Peter S. Chines, Markku Laakso, Xueling Sim, Anne U. Jackson, James P. Davis, Antti J. Kangas, Tanya M. Teslovich, Johanna Kuusisto, Mika Ala-Korpela, Heather M. Stringham, Jeroen R. Huyghe

المساهمون: School of Medicine / Clinical Medicine

المصدر: PLoS Genetics
PLoS Genetics, Vol 13, Iss 10, p e1007079 (2017)
Davis, J P, Huyghe, J R, Locke, A E, Jackson, A U, Sim, X, Stringham, H M, Teslovich, T M, Welch, R P, Fuchsberger, C, Narisu, N, Chines, P S, Kangas, A J, Soininen, P, Ala-Korpela, M, Kuusisto, J, Collins, F S, Laakso, M, Boehnke, M & Mohlke, K L 2017, ' Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study ', PLoS Genetics, vol. 13, no. 10, e1007079 . https://doi.org/10.1371/journal.pgen.1007079Test

مصطلحات موضوعية: 0301 basic medicine, Exome/genetics, Male, Cancer Research, Principal Component Analysis/methods, Biochemistry, Subclass, chemistry.chemical_compound, Lipid Metabolism/genetics, Gene Frequency, Cell Signaling, Genotype, Exome, European Continental Ancestry Group/genetics, Genetics (clinical), Finland, Phospholipids, Genetics, Principal Component Analysis, Triglycerides/genetics, Middle Aged, Polymorphism, Single Nucleotide/genetics, Lipids, Cholesterol, Gene Frequency/genetics, Lipid Signaling, Genome-Wide Association Study/methods, Lipoproteins/genetics, Genomic Signal Processing, Research Article, Signal Transduction, lcsh:QH426-470, Lipoproteins, Quantitative Trait Loci, Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, White People, 03 medical and health sciences, medicine, Humans, Molecular Biology, Gene, Ecology, Evolution, Behavior and Systematics, Triglycerides, Cholesterol, HDL/genetics, Cholesterol, HDL, Biology and Life Sciences, Proteins, Cell Biology, medicine.disease, Lipid Metabolism, Minor allele frequency, lcsh:Genetics, 030104 developmental biology, chemistry, Lipids/genetics, Genetic Loci, Dyslipidemia, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef440e4f0d245ece68b724bb068765f0Test
https://pubmed.ncbi.nlm.nih.gov/29084231Test

5

Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies

المساهمون: Boston University School of Medicine (BUSM), Boston University [Boston] (BU), Institute of Genetics and Biophysics, Consiglio Nazionale delle Ricerche (CNR), Uppsala Universitet [Uppsala], Karolinska Institutet [Stockholm], Icelandic Heart Association, Heart Preventive Clinic and Research Institute, University of Iceland [Reykjavik], IRCCS San Raffaele Scientific Institute [Milan, Italie], Interactions Gène-Environnement en Physiopathologie Cardio-Vasculaire (IGE-PCV), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL), Faculté de Pharmacie [Nancy], Université de Lorraine (UL), The Wellcome Trust Centre for Human Genetics [Oxford], University of Oxford, Oxford Centre for Diabetes, Endocrinology and Metabolism (OCDEM), Department of Neurology [Boston], Harvard Medical School [Boston] (HMS)-Massachusetts General Hospital [Boston], Epidémiologie et Biostatistique [Bordeaux], Université Bordeaux Segalen - Bordeaux 2-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Universität Leipzig [Leipzig], Randox Laboratories, Epidémiologie des maladies chroniques : impact des interactions gène environnement sur la santé des populations, Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, Droit et Santé, Institut Universitaire d'Hématologie (IUH), Université Paris Diderot - Paris 7 (UPD7), UL, IGEPCV, Choi, Seung Hoan, Ruggiero, Daniela, Sorice, Rossella, Song, Ci, Nutile, Teresa, Vernon Smith, Albert, Concas, Maria Pina, Traglia, Michela, Barbieri, Caterina, Ndiaye, Ndeye Coumba, Stathopoulou, Maria G., Lagou, Vasiliki, Maestrale, Giovanni Battista, Sala, Cinzia, Debette, Stephanie, Kovacs, Peter, Lind, Lar, Lamont, John, Fitzgerald, Peter, Tönjes, Anke, Gudnason, Vilmundur, Toniolo, Daniela, Pirastu, Mario, Bellenguez, Celine, Vasan, Ramachandran S., Ingelsson, Erik, Leutenegger, Anne-Louise, Johnson, Andrew D., Destefano, Anita L., Visvikis-Siest, Sophie, Seshadri, Sudha, Ciullo, Marina, University of Oxford [Oxford]

المصدر: PLoS Genetics, Vol 12, Iss 2, p e1005874 (2016)
PLoS Genetics
PLoS Genetics, 2016, 12 (2), pp.e1005874. ⟨10.1371/journal.pgen.1005874⟩
PLoS Genetics, Public Library of Science, 2016, 12 (2), pp.e1005874. ⟨10.1371/journal.pgen.1005874⟩
PLOS genetics (Online) 12 (2016). doi:10.1371/journal.pgen.1005874
info:cnr-pdr/source/autori:Choi S.H.; Ruggiero D.; Sorice R.; Song C.; Nutile T.; Vernon Smith A.; Concas M.P.; Traglia M.; Barbieri C.; Ndiaye N.C.; Stathopoulou M.G.; Lagou V.; Maestrale G.B.; Sala C.; Debette S.; Kovacs P.; Lind L.; Lamont J.; Fitzgerald P.; Tonjes A.; Gudnason V.; Toniolo D.; Pirastu M.; Bellenguez C.; Vasan R.S.; Ingelsson E.; Leutenegger A.-L.; Johnson A.D.; DeStefano A.L.; Visvikis-Siest S.; Seshadri S.; Ciullo M./titolo:Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies/doi:10.1371%2Fjournal.pgen.1005874/rivista:PLOS genetics (Online)/anno:2016/pagina_da:/pagina_a:/intervallo_pagine:/volume:12

مصطلحات موضوعية: 0301 basic medicine, Vascular Endothelial Growth Factor A, Cell signaling, Medicin och hälsovetenskap, Cancer Research, Physiology, Angiogenesis, Gene Expression, Genome-wide association study, Signal transduction, Medical and Health Sciences, Database and Informatics Methods, chemistry.chemical_compound, Mathematical and Statistical Techniques, 0302 clinical medicine, Animal Cells, Medicine and Health Sciences, Chromosomes, Human, Genetics (clinical), ComputingMilieux_MISCELLANEOUS, Genetics, Ecology, Chromosome Biology, Genomics, Hematology, Single Nucleotide, VEGF signaling, Genomic Databases, VEGF, Phenotype, Body Fluids, 3. Good health, Vascular endothelial growth factor, Blood, 030220 oncology & carcinogenesis, Physical Sciences, Anatomy, Cellular Types, Statistics (Mathematics), Research Article, Human, Platelets, lcsh:QH426-470, Evolution, European Continental Ancestry Group, Single-nucleotide polymorphism, Biology, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Research and Analysis Methods, Genome Complexity, Chromosome, Polymorphism, Single Nucleotide, Chromosomes, White People, 03 medical and health sciences, Behavior and Systematics, Genetic, Genome-Wide Association Studies, Humans, Statistical Methods, 1000 Genomes Project, Polymorphism, Gene, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Genome-Wide Association Study, Genetic Loci, Blood Cells, Biology and Life Sciences, Computational Biology, Human Genetics, Cell Biology, Genome Analysis, Ecology, Evolution, Behavior and Systematic, Introns, lcsh:Genetics, Biological Databases, 030104 developmental biology, chemistry, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Expression quantitative trait loci, Mathematics, Meta-Analysis

وصف الملف: application/pdf; ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6b9455e6caa5145eaa899c1280a9fdcTest
http://europepmc.org/articles/PMC4766012?pdf=renderTest

6

ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy

المؤلفون: Norman Klopp, Sebastiaan Overeem, Birgit Frauscher, Guy A. Rouleau, Suna Onengut-Gumuscu, Alex Desautels, Susan D. Thompson, David Kemlink, Karel Sonka, Peter Geisler, Patrick Concannon, Poul Jennum, Birgit Högl, Maxime Breban, Patrice Bourgin, Geert Mayer, Panos Deloukas, Sirous Javidi, Fabio Pizza, Cisca Wijmenga, Michel Lecendreux, Juliette Faraco, Sona Nevsimalova, Rosa Peraita-Adrados, Isabelle Arnulf, Ling Lin, Mali Einen, Gosia Trynka, Joachim Hallmayer, Juliane Winkelmann, Vincent Damotte, Emmanuel Mignot, Laura Ehrmann, Stephen S. Rich, Tom Rico, Giuseppe Plazzi, Francesca Poli, Gert Jan Lammers, Peter Lichtner, Jacques Montplaisir, Bertrand Fontaine, Christian Gieger, Wei-Min Chen, Birgitte Rahbek Kornum, Alex Iranzo, Claudio L. Bassetti, Eimear E. Kenny, Yves Dauvilliers

المساهمون: Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), J. Faraco, L. Lin, B. R. Kornum, E. E. Kenny, G. Trynka, M. Einen, T. J. Rico, P. Lichtner, Y. Dauvillier, I. Arnulf, M. Lecendreux, S. Javidi, P. Geisler, G. Mayer, F. Pizza, F. Poli, G. Plazzi, S. Overeem, G. J. Lammer, D. Kemlink, K. Sonka, S. Nevsimalova, G. Rouleau, A. Desautel, J. Montplaisir, B. Frauscher, L. Ehrmann, B. Högl, P. Jennum, P. Bourgin, R. Peraita-Adrado, A. Iranzo, C. Bassetti, W. Chen, P. Concannon, S. D. Thompson, V. Damotte, B. Fontaine, M. Breban, C. Gieger, N. Klopp, P. Delouka, C. Wijmenga, J. Hallmayer, S. Onengut-Gumuscu, S. S. Rich, J. Winkelmann, E. Mignot

المصدر: PLoS Genetics
Plos Genetics, 9, 2, pp. e1003270
PLoS Genetics, Vol 9, Iss 2, p e1003270 (2013)
PLoS genetics, 9(2):e1003270. PUBLIC LIBRARY SCIENCE
Faraco, Juliette; Lin, Ling; Kornum, Birgitte Rahbek; Kenny, Eimear E; Trynka, Gosia; Einen, Mali; Rico, Tom J; Lichtner, Peter; Dauvilliers, Yves; Arnulf, Isabelle; Lecendreux, Michel; Javidi, Sirous; Geisler, Peter; Mayer, Geert; Pizza, Fabio; Poli, Francesca; Plazzi, Giuseppe; Overeem, Sebastiaan; Lammers, Gert Jan; Kemlink, David; ... (2013). ImmunoChip study implicates antigen presentation to T cells in narcolepsy. PLoS genetics, 9(2), e1003270. San Francisco, Calif.: Public Library of Science 10.1371/journal.pgen.1003270 <http://dx.doi.org/10.1371/journal.pgen.1003270Test>
PLoS Genetics, 9(2)
PLoS Genet. 9:e1003270 (2013)
Plos Genetics, 9, e1003270

مصطلحات موضوعية: Cancer Research, Receptors, Antigen, T-Cell, alpha-beta, genetics/metabolism, LOCI, 0302 clinical medicine, genetics/immunology/metabolism, Narcolepsy, HLA Antigens, CONFERS SUSCEPTIBILITY, Genetics (clinical), alpha-beta, Genetics, RISK, 0303 health sciences, Antigen Presentation, Intracellular Signaling Peptides and Proteins, genetics/immunology, Autoimmune Diseases, genetics/immunology/metabolism, European Continental Ancestry Group, Genetic Association Studies, Humans, Narcolepsy, genetics/immunology/physiopathology, Neuropeptides, Receptors, Antigen, T-Cell, OX40L, 3. Good health, medicine.anatomical_structure, DISEASES, Research Article, lcsh:QH426-470, T cell, DCN MP - Plasticity and memory, Antigen presentation, Immunology, HAPLOTYPE, Human leukocyte antigen, Biology, White People, genetics/immunology, Humans, Intracellular Signaling Peptides and Protein, 03 medical and health sciences, medicine, GENOME-WIDE ASSOCIATION, genetics/immunology/metabolism, Receptor, Molecular Biology, Ecology, Evolution, Behavior and Systematics, METAANALYSIS, 030304 developmental biology, genetics/immunology/physiopathology, Neuropeptide, Autoimmune disease, Orexins, T-cell receptor, medicine.disease, POLYMORPHISM, Orexin, lcsh:Genetics, genetics/immunology, Autoimmune Disease, genetics/immunology/metabolism, European Continental Ancestry Group, Genetic Association Studies, HLA Antigen, 030217 neurology & neurosurgery

وصف الملف: application/pdf; ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0fae51587df5287385af0ba8cd5399cTest
http://europepmc.org/articles/PMC3573113Test

7

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

المؤلفون: Winkler, Thomas W, Justice, Anne E, Graff, Mariaelisa, Barata, Llilda, Feitosa, Mary F, Chu, Su, Czajkowski, Jacek, Esko, Tõnu, Fall, Tove, Kilpeläinen, Tuomas O, Lu, Yingchang, Mägi, Reedik, Mihailov, Evelin, Pers, Tune H, Rüeger, Sina, Teumer, Alexander, Ehret, Georg B, Ferreira, Teresa, Heard-Costa, Nancy L, Karjalainen, Juha, Lagou, Vasiliki, Mahajan, Anubha, Neinast, Michael D, Prokopenko, Inga, Simino, Jeannette, Teslovich, Tanya M, Jansen, Rick, Westra, Harm-Jan, White, Charles C, Absher, Devin, Ahluwalia, Tarunveer S, Ahmad, Shafqat, Albrecht, Eva, Alves, Alexessander Couto, Bragg-Gresham, Jennifer L, de Craen, Anton JM, Bis, Joshua C, Bonnefond, Amélie, Boucher, Gabrielle, Cadby, Gemma, Cheng, Yu-Ching, Chiang, Charleston WK, Delgado, Graciela, Demirkan, Ayse, Dueker, Nicole, Eklund, Niina, Eiriksdottir, Gudny, Eriksson, Joel, Feenstra, Bjarke, Fischer, Krista, Frau, Francesca, Galesloot, Tessel E, Geller, Frank, Goel, Anuj, Gorski, Mathias, Grammer, Tanja B, Gustafsson, Stefan, Haitjema, Saskia, Hottenga, Jouke-Jan, Huffman, Jennifer E, Jackson, Anne U, Jacobs, Kevin B, Johansson, Åsa, Kaakinen, Marika, Kleber, Marcus E, Lahti, Jari, Mateo Leach, Irene, Lehne, Benjamin, Liu, Youfang, Lo, Ken Sin, Lorentzon, Mattias, Luan, Jian'an, Madden, Pamela AF, Mangino, Massimo, McKnight, Barbara, Medina-Gomez, Carolina, Monda, Keri L, Montasser, May E, Müller, Gabriele, Müller-Nurasyid, Martina, Nolte, Ilja M, Panoutsopoulou, Kalliope, Pascoe, Laura, Paternoster, Lavinia, Rayner, Nigel W, Renström, Frida, Rizzi, Federica, Rose, Lynda M, Ryan, Kathy A, Salo, Perttu, Sanna, Serena, Scharnagl, Hubert, Shi, Jianxin, Smith, Albert Vernon, Southam, Lorraine, Stančáková, Alena, Steinthorsdottir, Valgerdur, Strawbridge, Rona J, Sung, Yun Ju, Tachmazidou, Ioanna, Tanaka, Toshiko, Thorleifsson, Gudmar, Trompet, Stella, Pervjakova, Natalia, Tyrer, Jonathan P, Vandenput, Liesbeth, van der Laan, Sander W, van der Velde, Nathalie, van Setten, Jessica, van Vliet-Ostaptchouk, Jana V, Verweij, Niek, Vlachopoulou, Efthymia, Waite, Lindsay L, Wang, Sophie R, Wang, Zhaoming, Wild, Sarah H, Willenborg, Christina, Wilson, James F, Wong, Andrew, Yang, Jian, Yengo, Loïc, Yerges-Armstrong, Laura M, Yu, Lei, Zhang, Weihua, Zhao, Jing Hua, Andersson, Ehm A, Bakker, Stephan JL, Baldassarre, Damiano, Banasik, Karina, Barcella, Matteo, Barlassina, Cristina, Bellis, Claire, Benaglio, Paola, Blangero, John, Blüher, Matthias, Bonnet, Fabrice, Bonnycastle, Lori L, Boyd, Heather A, Bruinenberg, Marcel, Buchman, Aron S, Campbell, Harry, Chen, Yii-Der Ida, Chines, Peter S, Claudi-Boehm, Simone, Cole, John, Collins, Francis S, de Geus, Eco JC, de Groot, Lisette CPGM, Dimitriou, Maria, Duan, Jubao, Enroth, Stefan, Eury, Elodie, Farmaki, Aliki-Eleni, Forouhi, Nita G, Friedrich, Nele, Gejman, Pablo V, Gigante, Bruna, Glorioso, Nicola, Go, Alan S, Gottesman, Omri, Gräßler, Jürgen, Grallert, Harald, Grarup, Niels, Gu, Yu-Mei, Broer, Linda, Ham, Annelies C, Hansen, Torben, Harris, Tamara B, Hartman, Catharina A, Hassinen, Maija, Hastie, Nicholas, Hattersley, Andrew T, Heath, Andrew C, Henders, Anjali K, Hernandez, Dena, Hillege, Hans, Holmen, Oddgeir, Hovingh, Kees G, Hui, Jennie, Husemoen, Lise L, Hutri-Kähönen, Nina, Hysi, Pirro G, Illig, Thomas, De Jager, Philip L, Jalilzadeh, Shapour, Jørgensen, Torben, Jukema, J Wouter, Juonala, Markus, Kanoni, Stavroula, Karaleftheri, Maria, Khaw, Kay Tee, Kinnunen, Leena, Kittner, Steven J, Koenig, Wolfgang, Kolcic, Ivana, Kovacs, Peter, Krarup, Nikolaj T, Kratzer, Wolfgang, Krüger, Janine, Kuh, Diana, Kumari, Meena, Kyriakou, Theodosios, Langenberg, Claudia, Lannfelt, Lars, Lanzani, Chiara, Lotay, Vaneet, Launer, Lenore J, Leander, Karin, Lindström, Jaana, Linneberg, Allan, Liu, Yan-Ping, Lobbens, Stéphane, Luben, Robert, Lyssenko, Valeriya, Männistö, Satu, Magnusson, Patrik K, McArdle, Wendy L, Menni, Cristina, Merger, Sigrun, Milani, Lili, Montgomery, Grant W, Morris, Andrew P, Narisu, Narisu, Nelis, Mari, Ong, Ken K, Palotie, Aarno, Pérusse, Louis, Pichler, Irene, Pilia, Maria G, Pouta, Anneli, Rheinberger, Myriam, Ribel-Madsen, Rasmus, Richards, Marcus, Rice, Kenneth M, Rice, Treva K, Rivolta, Carlo, Salomaa, Veikko, Sanders, Alan R, Sarzynski, Mark A, Scholtens, Salome, Scott, Robert A, Scott, William R, Sebert, Sylvain, Sengupta, Sebanti, Sennblad, Bengt, Seufferlein, Thomas, Silveira, Angela, Slagboom, P Eline, Smit, Jan H, Sparsø, Thomas H, Stirrups, Kathleen, Stolk, Ronald P, Stringham, Heather M, Swertz, Morris A, Swift, Amy J, Syvänen, Ann-Christine, Tan, Sian-Tsung, Thorand, Barbara, Tönjes, Anke, Tremblay, Angelo, Tsafantakis, Emmanouil, van der Most, Peter J, Völker, Uwe, Vohl, Marie-Claude, Vonk, Judith M, Waldenberger, Melanie, Walker, Ryan W, Wennauer, Roman, Widén, Elisabeth, Willemsen, Gonneke, Wilsgaard, Tom, Wright, Alan F, Zillikens, M Carola, van Dijk, Suzanne C, van Schoor, Natasja M, Asselbergs, Folkert W, de Bakker, Paul IW, Beckmann, Jacques S, Beilby, John, Bennett, David A, Bergman, Richard N, Bergmann, Sven, Böger, Carsten A, Boehm, Bernhard O, Boerwinkle, Eric, Boomsma, Dorret I, Bornstein, Stefan R, Bottinger, Erwin P, Bouchard, Claude, Chambers, John C, Chanock, Stephen J, Chasman, Daniel I, Cucca, Francesco, Cusi, Daniele, Dedoussis, George, Erdmann, Jeanette, Eriksson, Johan G, Evans, Denis A, de Faire, Ulf, Farrall, Martin, Ferrucci, Luigi, Ford, Ian, Franke, Lude, Franks, Paul W, Froguel, Philippe, Gansevoort, Ron T, Gieger, Christian, Grönberg, Henrik, Gudnason, Vilmundur, Gyllensten, Ulf, Hall, Per, Hamsten, Anders, van der Harst, Pim, Hayward, Caroline, Heliövaara, Markku, Hengstenberg, Christian, Hicks, Andrew A, Hingorani, Aroon, Hofman, Albert, Hu, Frank, Huikuri, Heikki V, Hveem, Kristian, James, Alan L, Jordan, Joanne M, Jula, Antti, Kähönen, Mika, Kajantie, Eero, Kathiresan, Sekar, Kiemeney, Lambertus ALM, Kivimaki, Mika, Knekt, Paul B, Koistinen, Heikki A, Kooner, Jaspal S, Koskinen, Seppo, Kuusisto, Johanna, Maerz, Winfried, Martin, Nicholas G, Laakso, Markku, Lakka, Timo A, Lehtimäki, Terho, Lettre, Guillaume, Levinson, Douglas F, Lind, Lars, Lokki, Marja-Liisa, Mäntyselkä, Pekka, Melbye, Mads, Metspalu, Andres, Mitchell, Braxton D, Moll, Frans L, Murray, Jeffrey C, Musk, Arthur W, Nieminen, Markku S, Njølstad, Inger, Ohlsson, Claes, Oldehinkel, Albertine J, Oostra, Ben A, Palmer, Lyle J, Pankow, James S, Pasterkamp, Gerard, Pedersen, Nancy L, Pedersen, Oluf, Penninx, Brenda W, Perola, Markus, Peters, Annette, Polašek, Ozren, Pramstaller, Peter P, Psaty, Bruce M, Qi, Lu, Quertermous, Thomas, Raitakari, Olli T, Rankinen, Tuomo, Rauramaa, Rainer, Ridker, Paul M, Rioux, John D, Rivadeneira, Fernando, Rotter, Jerome I, Rudan, Igor, den Ruijter, Hester M, Saltevo, Juha, Sattar, Naveed, Schunkert, Heribert, Schwarz, Peter EH, Shuldiner, Alan R, Sinisalo, Juha, Snieder, Harold, Sørensen, Thorkild IA, Spector, Tim D, Staessen, Jan A, Stefania, Bandinelli, Thorsteinsdottir, Unnur, Stumvoll, Michael, Tardif, Jean-Claude, Tremoli, Elena, Tuomilehto, Jaakko, Uitterlinden, André G, Uusitupa, Matti, Verbeek, André LM, Vermeulen, Sita H, Viikari, Jorma S, Vitart, Veronique, Völzke, Henry, Vollenweider, Peter, Waeber, Gérard, Walker, Mark, Wallaschofski, Henri, Wareham, Nicholas J, Watkins, Hugh, Zeggini, Eleftheria, arcOGEN Consortium, CHARGE Consortium, DIAGRAM Consortium, GLGC Consortium, Global-BPGen Consortium, ICBP Consortium, MAGIC Consortium, Chakravarti, Aravinda, Clegg, Deborah J, Cupples, L Adrienne, Gordon-Larsen, Penny, Jaquish, Cashell E, Rao, DC, Abecasis, Goncalo R, Assimes, Themistocles L, Barroso, Inês, Berndt, Sonja I, Boehnke, Michael, Deloukas, Panos, Fox, Caroline S, Groop, Leif C, Hunter, David J, Ingelsson, Erik, Kaplan, Robert C, McCarthy, Mark I, Mohlke, Karen L, O'Connell, Jeffrey R, Schlessinger, David, Strachan, David P, Stefansson, Kari, van Duijn, Cornelia M, Hirschhorn, Joel N, Lindgren, Cecilia M, Heid, Iris M, North, Kari E, Borecki, Ingrid B, Kutalik, Zoltán, Loos, Ruth JF

المساهمون: Division of Statistical Genomics, Washington University School of Medicine, Institut Pasteur du Cambodge, Réseau International des Instituts Pasteur (RIIP), Estonian Genome and Medicine, University of Tartu, Institute of Molecular and Cell Biology, Department of Medical Epidemiology and Biostatistics (MEB), Karolinska Institutet [Stockholm], Institute of Metabolic Science, MRC, Brown University, Center for Biological Sequence Analysis [Lyngby], Technical University of Denmark [Lyngby] (DTU), King‘s College London, Groningen Bioinformatics Centre, GBB, University of Groningen [Groningen], University of Queensland [Brisbane], National Institut of Food Science and Technology, University of Agriculture, Department of Biostatistics and Center for Statistical Genetics, University of Michigan [Ann Arbor], University of Michigan System-University of Michigan System, Department of neurology, Leiden University Medical Center (LUMC), University of Washington [Seattle], Metabolic functional (epi)genomics and molecular mechanisms involved in type 2 diabetes and related diseases - UMR 8199 - UMR 1283 (GI3M), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Genetic Epidemiology Unit, Erasmus University Medical Center [Rotterdam] (Erasmus MC), Deptartment of Medical Biochemistry and Microbiology, Uppsala University, Infectious diseases division, Department of internal medicine, Washington University in Saint Louis (WUSTL), Limnology, Ecology, Department of Ecology and Evolutionary Biology, University of California, Core Genotyping Facility, National Cancer Institute [Bethesda] (NCI-NIH), National Institutes of Health [Bethesda] (NIH)-National Institutes of Health [Bethesda] (NIH), Division of Cancer Epidemiology and Genetics, Institute of Health Sciences and Biocenter Oulu, University of Oulu, Department of Chemical Engineering Taiwan (DCET - NTHU), National Tsing Hua University [Hsinchu] (NTHU), University of Oxford [Oxford], Department of Epidemiology, University of North Carolina [Chapel Hill] (UNC), University of North Carolina System (UNC)-University of North Carolina System (UNC), Human Genetics, The Wellcome Trust Sanger Institute [Cambridge], Departments of Epidemiology and Nutrition, Harvard School of Public Health, Department of Clinical Sciences, Lund University [Lund]-Lund University Diabetes Centre, Genetic Epidemiology and Clinical Research Group, Umea University Hospital, Department of Medicine, University of Eastern Finland-Kuopio University Hospital, Department of Medical Sciences, Department of Educational Psychology and Counseling, National Taiwan Normal University (NTNU), Laboratory for Cardiovascular Genomics and Informatics [Yokohama] (RIKEN IMS), RIKEN Center for Integrative Medical Sciences [Yokohama] (RIKEN IMS), RIKEN - Institute of Physical and Chemical Research [Japon] (RIKEN)-RIKEN - Institute of Physical and Chemical Research [Japon] (RIKEN), deCODE Genetics, deCODE genetics [Reykjavik], Interuniversity Cardiology Institute Netherlands, Molecular Genetics Section, University of Groningen [Groningen]-University Medical Centre Groningen, Kidney Center, University Medical Center Groningen [Groningen] (UMCG), The University of Texas Health Science Center at Houston (UTHealth), Texas Biomedical Research Institute [San Antonio, TX], Medical Department III, Universität Leipzig [Leipzig], Foie, métabolismes et cancer, Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Dept. of Epidemiology Research, Statens Serum Institut [Copenhagen], GNS Science, Blackett Laboratory, Imperial College London, Medstar Research Institute, University of Rochester [USA], MRC Epidemiology Unit, University of Cambridge [UK] (CAM)-Institute of Metabolic Science, Institute of Epidemiology [Neuherberg] (EPI), German Research Center for Environmental Health - Helmholtz Center München (GmbH), Novo Nordisk Foundation Center for Basic Metabolic Research (CBMR), Faculty of Health and Medical Sciences, University of Copenhagen = Københavns Universitet (KU)-University of Copenhagen = Københavns Universitet (KU), Dept Biochem & Mol Biol, Pennsylvania State University (Penn State), Penn State System-Penn State System, Genomic Research Laboratory, Service of Infectious Disease, Hôpitaux Universitaires de Genève (HUG), Epidemiology, University Medical Centre Groningen, Unit for Molecular Epidemiology, German Research Center for Environmental Health-Helmholtz-Zentrum München (HZM), Program in Translational NeuroPsychiatric Genomics, Brigham and Women's Hospital [Boston], Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, USA, Broad Institute of MIT and Harvard (BROAD INSTITUTE), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston]-Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], Harvard Medical School [Boston] (HMS), Research Centre for Prevention and Health (RCPH), Department of Public Health [Copenhagen], University of Copenhagen = Københavns Universitet (KU)-University of Copenhagen = Københavns Universitet (KU)-Faculty of Health and Medical Sciences, University of Copenhagen = Københavns Universitet (KU)-University of Copenhagen = Københavns Universitet (KU)-Capital Region of Denmark, University of Copenhagen = Københavns Universitet (KU), Faculty of Medicine, Institute of Public Health, Aalborg University [Denmark] (AAU), Department of Nutrition-Dietetics, Harokopio University of Athens, Department of Medical Statistics, Epidemiology and Medical Informatics, University of Zagreb, MRC National Survey of Health and Development, MRC Unit for Lifelong Health and Ageing, Department of Epidemiology and Public Health, University College of London [London] (UCL), Department of Public health and Caring Sciences, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden, Research Center for Prevention and Health, Glostrup Hospital, Génétique des maladies multifactorielles (GMM), Université de Lille, Droit et Santé-Centre National de la Recherche Scientifique (CNRS), Cambridge Institute of Public Health, University of Cambridge [UK] (CAM), Chronic Disease Epidemiology and Prevention Unit, National Institute for Health and Welfare [Helsinki], Queensland Institute of Medical Research, Medical Research Council Epidemiology Unit, Institute of Metabolic Science, Addenbrooke's Hospital, Head of Medical Sequencing, Department of Biostatistics, University of Washington, Department of Chronic Disease Prevention, Molecular Epidemiology, Department of Genetics, Université Laval [Québec] (ULaval), Interfaculty Institute for Genetics and Functional Genomics, Universität Greifswald - University of Greifswald, Netherlands Genomics Initiative, Netherlands Consortium for Healthy Aging [Leiden, Netherlands] (NCHA), Department of Internal Medicine, Université de Lausanne (UNIL), Carl Gustav Carus University Hospital, Loughborough University, Genomics and Bioinformatics Platform, Fondazione Filarete, Department of Medicine, Surgery, and Dentistry, University of Milano, Medizinische Klinik II, Universität zu Lübeck [Lübeck], Department of Genomic Medicine, University of Manchester [Manchester], The Wellcome Trust Centre for Human Genetics [Oxford], National Institutes of Health [Bethesda] (NIH), Department of Nephrology, University Medical Center, University of Groningen, Helmholtz-Zentrum München (HZM), Icelandic Heart Association, Kopavogur, Iceland., Faculty of Medicine, University of Iceland [Reykjavik], Genetics and Pathology, Department of child and adolescent psychiatry, Universität Duisburg-Essen [Essen], Department of Internal Medicine II, Division of Respirology, University of Regensburg, Regensburg, Germany, Universität Regensburg (UR), Franz-Volhard-Centrum für Klinische Forschung, ECRC, Department of Clinical Physiology, University of Tampere [Finland]-Tampere University Hospital, Finnish Institute of Occupational Health of Helsinki, Department of Clinical Chemistry, Faculty of Medecine [Helsinki], University of Helsinki-University of Helsinki, Department of Oncology, University of Tampere Medical School, University of Tampere, Department of Physiology, University of Eastern Finland-Institute of Biomedicine, Department of Medicine, Montreal, Developmental Brain and Behaviour Unit, University of Southampton, Division of Gastroenterology and Hepatology, Department of Immunology, Mayo Clinic, Centre for Bone and Arthritis Research, Institute of Medicine-University of Gothenburg (GU), Interdisciplinary Center for Psychiatric Epidemiology, Experimental Cardiology Laboratory, University Medical Center [Utrecht], Peter MacCallum Cancer Center, Faculty of Health Sciences, Aarhus University [Aarhus], Institute for Molecular Medicine Finland [Helsinki] (FIMM), Helsinki Institute of Life Science (HiLIFE), Department of Health Services, University of Washington, Group Health Research Institute, Group Health Cooperative, Department of Epidemiology, University of Washington, Department of Medicine, University of Washington, Cardiovascular Health Research Unit, University of Washington, The Research Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku University Hospital (TYKS), Erasmus Medical Centre, Cedars-Sinai Medical Center, Department of Pathological Biochemistry, Royal Infirmary, Unit of Genetic Epidemiology and Bioinformatics, Department of Epidemiology, University Medical Center Groningen, Department of Pediatrics, Augusta University - Medical College of Georgia, University System of Georgia (USG)-University System of Georgia (USG), Institute of Preventive Medicine, Copenhagen University Hospital-Bispebjerg and Frederiksberg Hospitals, Maastricht University [Maastricht], Department of Public Health, South Ostrobothnia Central Hospital, Department of Clinical and Preventive Medicine, Danube-University Krems, Netherlands Consortium for Healthy Ageing, Leiden, The Netherlands, Institute of Public Health and Clinical Nutrition, University of Eastern Finland, Department of Epidemiology & Biostatistics, Radboud University Medical Center [Nijmegen], Institute for Community Medicine, Centre Hospitalier Universitaire Vaudois [Lausanne] (CHUV), MRC epidemiology Unit, Framingham Heart Study, National Heart, Lung, and Blood Institute [Bethesda] (NHLBI)-Boston University [Boston] (BU), Metabolic Disease Group, University of Cambridge Metabolic Research Laboratories, Department of Genetics and Biotechnology, Wellcome Trust, Divisions of Genetics and Endocrinology and Program in Genomics, Boston Children's Hospital, Metabolism Initiative and Program in Medical and Population Genetics, Endocrinology and Metabolism, The Churchill Hospital-Oxford Centre for Diabetes, Department of Epidemiology and Preventive Medicine, Regensburg University Medical Center, University of North Carolina System (UNC)-University of North Carolina System (UNC)-UNC Gillings School of Global Public Health-Carolina Center for Genome Sciences, Department of Medical Genetics, Epidemiology Unit, Addenbrooke's Hospital-Medical Research Council (MRC), P30 AG010161/AG/NIA NIH HHS/United States, Psychiatry, Epidemiology and Data Science, NCA - Neurobiology of mental health, EMGO - Lifestyle, overweight and diabetes, APH - Amsterdam Public Health, AMS - Amsterdam Movement Sciences, Geriatrics, ACS - Amsterdam Cardiovascular Sciences, Vascular Medicine, Other departments, Biological Psychology, Neuroscience Campus Amsterdam - Neurobiology of Mental Health, EMGO+ - Lifestyle, Overweight and Diabetes, RS: CARIM - R3 - Vascular biology, MUMC+: DA BV AIOS Radiologie (9), Epidemiologie, Orthopedie, Institute for Molecular Medicine Finland, Helsinki Collegium for Advanced Studies, Behavioural Sciences, University of Helsinki, Transplantation Laboratory, Medicum, Research Programs Unit, Research Programme of Molecular Medicine, Aarno Palotie / Principal Investigator, Elisabeth Ingrid Maria Widen / Principal Investigator, Clinicum, Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Children's Hospital, Lastentautien yksikkö, Marja-Liisa Lokki / Principal Investigator, Kardiologian yksikkö, Leif Groop Research Group, Quantitative Genetics, Developmental Psychology Research Group, Genomics of Neurological and Neuropsychiatric Disorders, Genomic Discoveries and Clinical Translation, Ehret, Georg Benedikt, Danmarks Tekniske Universitet = Technical University of Denmark (DTU), Universiteit Leiden-Universiteit Leiden, Metabolic functional (epi)genomics and molecular mechanisms involved in type 2 diabetes and related diseases - UMR 8199 - UMR 1283 (EGENODIA (GI3M)), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), University of California (UC), University of Oxford, Lund University [Lund], Universität Leipzig, Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), University of Copenhagen = Københavns Universitet (UCPH)-University of Copenhagen = Københavns Universitet (UCPH), Helmholtz Zentrum München = German Research Center for Environmental Health, University of Copenhagen = Københavns Universitet (UCPH)-University of Copenhagen = Københavns Universitet (UCPH)-Faculty of Health and Medical Sciences, University of Copenhagen = Københavns Universitet (UCPH)-University of Copenhagen = Københavns Universitet (UCPH)-Capital Region of Denmark, University of Copenhagen = Københavns Universitet (UCPH), Université de Lausanne = University of Lausanne (UNIL), Universität zu Lübeck = University of Lübeck [Lübeck], Universität Duisburg-Essen = University of Duisburg-Essen [Essen], Helsingin yliopisto = Helsingfors universitet = University of Helsinki-Helsingin yliopisto = Helsingfors universitet = University of Helsinki, University of Gothenburg (GU)-Institute of Medicine, Boston University [Boston] (BU)-National Heart, Lung, and Blood Institute [Bethesda] (NHLBI), Luan, Jian'an [0000-0003-3137-6337], Tyrer, Jonathan [0000-0003-3724-4757], Forouhi, Nita [0000-0002-5041-248X], Khaw, Kay-Tee [0000-0002-8802-2903], Langenberg, Claudia [0000-0002-5017-7344], Luben, Robert [0000-0002-5088-6343], Ong, Kenneth [0000-0003-4689-7530], Johnson, Kathleen [0000-0002-6823-3252], Wareham, Nicholas [0000-0003-1422-2993], Barroso, Ines [0000-0001-5800-4520], Apollo - University of Cambridge Repository, CHARGE Consortium, DIAGRAM Consortium, GLGC Consortium, Global-BPGen Consortium, ICBP Consortium, MAGIC Consortium, Biochemistry, Surgery, Internal Medicine, Public Health, Medical Oncology, Pathology, Erasmus MC other, Child and Adolescent Psychiatry / Psychology, Clinical Genetics

المصدر: PLoS Genetics
e1006166
PLoS Genetics, Public Library of Science, 2015, 11 (10), pp.e1005378. ⟨10.1371/journal.pgen.1005378⟩
PLoS Genetics, 11(10):e1005378. Public Library of Science
PLOS genetics (Online) 11 (2015): e1005378. doi:10.1371/journal.pgen.1005378
info:cnr-pdr/source/autori:Winkler, Thomas W; Justice, Anne E; Graff, Mariaelisa; Barata, Llilda; Feitosa, Mary F; Chu, Su; Czajkowski, Jacek; Esko, Tonu; Fall, Tove; Kilpelainen, Tuomas O; Lu, Yingchang; Magi, Reedik; Mihailov, Evelin; Pers, Tune H; Rueger, Sina; Teumer, Alexander; Ehret, Georg B; Ferreira, Teresa; Heard-Costa, Nancy L; Karjalainen, Juha; Lagou, Vasiliki; Mahajan, Anubha; Neinast, Michael D; Prokopenko, Inga; Simino, Jeannette; Teslovich, Tanya M; Jansen, Rick; Westra, Harm-Jan; White, Charles C; Absher, Devin; Ahluwalia, Tarunveer S; Ahmad, Shafqat; Albrecht, Eva; Alves, Alexessander Couto; Bragg-Gresham, Jennifer L; de Craen, Anton J M; Bis, Joshua C; Bonnefond, Amelie; Boucher, Gabrielle; Cadby, Gemma; Cheng, Yu-Ching; Chiang, Charleston W K; Delgado, Graciela; Demirkan, Ayse; Dueker, Nicole; Eklund, Niina; Eiriksdottir, Gudny; Eriksson, Joel; Feenstra, Bjarke; Fischer, Krista; Frau, Francesca; Galesloot, Tessel E; Geller, Frank; Goel, Anuj; Gorski, Mathias; Grammer, Tanja B; Gustafsson, Stefan; Haitjema, Saskia; Hottenga, Jouke-Jan; Huffman, Jennifer E; Jackson, Anne U; Jacobs, Kevin B; Johansson, Asa; Kaakinen, Marika; Kleber, Marcus E; Lahti, Jari; Mateo Leach, Irene; Lehne, Benjamin; Liu, Youfang; Lo, Ken Sin; Lorentzon, Mattias; Luan, Jian'an; Madden, Pamela A F; Mangino, Massimo; McKnight, Barbara; Medina-Gomez, Carolina; Monda, Keri L; Montasser, May E; Muller, Gabriele; Muller-Nurasyid, Martina; Nolte, Ilja M; Panoutsopoulou, Kalliope; Pascoe, Laura; Paternoster, Lavinia; Rayner, Nigel W; Renstrom, Frida; Rizzi, Federica; Rose, Lynda M; Ryan, Kathy A; Salo, Perttu; Sanna, Serena; Scharnagl, Hubert; Shi, Jianxin; Smith, Albert Vernon; Southam, Lorraine; Stancakova, Alena; Steinthorsdottir, Valgerdur; Strawbridge, Rona J; Sung, Yun Ju; Tachmazidou, Ioanna; Tanaka, Toshiko; Thorleifsson, Gudmar; Trompet, Stella; Pervjakova, Natalia; Tyrer, Jonathan P; Vandenput, Liesbeth; van der Laan, Sander W; van der Velde, Nathalie; van Setten, Jessica; van Vliet-Ostaptchouk, Jana V; Verweij, Niek; Vlachopoulou, Efthymia; Waite, Lindsay L; Wang, Sophie R; Wang, Zhaoming; Wild, Sarah H; Willenborg, Christina; Wilson, James F; Wong, Andrew; Yang, Jian; Yengo, Loic; Yerges-Armstrong, Laura M; Yu, Lei; Zhang, Weihua; Zhao, Jing Hua; Andersson, Ehm A; Bakker, Stephan J L; Baldassarre, Damiano; Banasik, Karina; Barcella, Matteo; Barlassina, Cristina; Bellis, Claire; Benaglio, Paola; Blangero, John; Bluher, Matthias; Bonnet, Fabrice; Bonnycastle, Lori L; Boyd, Heather A; Bruinenberg, Marcel; Buchman, Aron S; Campbell, Harry; Chen, Yii-Der Ida; Chines, Peter S; Claudi-Boehm, Simone; Cole, John; Collins, Francis S; de Geus, Eco J C; de Groot, Lisette C P G M; Dimitriou, Maria; Duan, Jubao; Enroth, Stefan; Eury, Elodie; Farmaki, Aliki-Eleni; Forouhi, Nita G; Friedrich, Nele; Gejman, Pablo V; Gigante, Bruna; Glorioso, Nicola; Go, Alan S; Gottesman, Omri; GraSSler, Jurgen; Grallert, Harald; Grarup, Niels; Gu, Yu-Mei; Broer, Linda; Ham, Annelies C; Hansen, Torben; Harris, Tamara B; Hartman, Catharina A; Hassinen, Maija; Hastie, Nicholas; Hattersley, Andrew T; Heath, Andrew C; Henders, Anjali K; Hernandez, Dena; Hillege, Hans; Holmen, Oddgeir; Hovingh, Kees G; Hui, Jennie; Husemoen, Lise L; Hutri-Kahonen, Nina; Hysi, Pirro G; Illig, Thomas; De Jager, Philip L; Jalilzadeh, Shapour; Jorgensen, Torben; Jukema, J Wouter; Juonala, Markus; Kanoni, Stavroula; Karaleftheri, Maria; Khaw, Kay Tee; Kinnunen, Leena; Kittner, Steven J; Koenig, Wolfgang; Kolcic, Ivana; Kovacs, Peter; Krarup, Nikolaj T; Kratzer, Wolfgang; Kruger, Janine; Kuh, Diana; Kumari, Meena; Kyriakou, Theodosios; Langenberg, Claudia; Lannfelt, Lars; Lanzani, Chiara; Lotay, Vaneet; Launer, Lenore J; Leander, Karin; Lindstrom, Jaana; Linneberg, Allan; Liu, Yan-Ping; Lobbens, Stephane; Luben, Robert; Lyssenko, Valeriya; Mannisto, Satu; Magnusson, Patrik K; McArdle, Wendy L; Menni, Cristina; Merger, Sigrun; Milani, Lili; Montgomery, Grant W; Morris, Andrew P; Narisu, Narisu; Nelis, Mari; Ong, Ken K; Palotie, Aarno; Perusse, Louis; Pichler, Irene; Pilia, Maria G; Pouta, Anneli; Rheinberger, Myriam; Ribel-Madsen, Rasmus; Richards, Marcus; Rice, Kenneth M; Rice, Treva K; Rivolta, Carlo; Salomaa, Veikko; Sanders, Alan R; Sarzynski, Mark A; Scholtens, Salome; Scott, Robert A; Scott, William R; Sebert, Sylvain; Sengupta, Sebanti; Sennblad, Bengt; Seufferlein, Thomas; Silveira, Angela; Slagboom, P Eline; Smit, Jan H; Sparso, Thomas H; Stirrups, Kathleen; Stolk, Ronald P; Stringham, Heather M; Swertz, Morris A; Swift, Amy J; Syvanen, Ann-Christine; Tan, Sian-Tsung; Thorand, Barbara; Tonjes, Anke; Tremblay, Angelo; Tsafantakis, Emmanouil; van der Most, Peter J; Volker, Uwe; Vohl, Marie-Claude; Vonk, Judith M; Waldenberger, Melanie; Walker, Ryan W; Wennauer, Roman; Widen, Elisabeth; Willemsen, Gonneke; Wilsgaard, Tom; Wright, Alan F; Zillikens, M Carola; van Dijk, Suzanne C; van Schoor, Natasja M; Asselbergs, Folkert W; de Bakker, Paul I W; Beckmann, Jacques S; Beilby, John; Bennett, David A; Bergman, Richard N; Bergmann, Sven; Boger, Carsten A; Boehm, Bernhard O; Boerwinkle, Eric; Boomsma, Dorret I; Bornstein, Stefan R; Bottinger, Erwin P; Bouchard, Claude; Chambers, John C; Chanock, Stephen J; Chasman, Daniel I; Cucca, Francesco; Cusi, Daniele; Dedoussis, George; Erdmann, Jeanette; Eriksson, Johan G; Evans, Denis A; de Faire, Ulf; Farrall, Martin; Ferrucci, Luigi; Ford, Ian; Franke, Lude; Franks, Paul W; Froguel, Philippe; Gansevoort, Ron T; Gieger, Christian; Gronberg, Henrik; Gudnason, Vilmundur; Gyllensten, Ulf; Hall, Per; Hamsten, Anders; van der Harst, Pim; Hayward, Caroline; Heliovaara, Markku; Hengstenberg, Christian; Hicks, Andrew A; Hingorani, Aroon; Hofman, Albert; Hu, Frank; Huikuri, Heikki V; Hveem, Kristian; James, Alan L; Jordan, Joanne M; Jula, Antti; Kahonen, Mika; Kajantie, Eero; Kathiresan, Sekar; Kiemeney, Lambertus A L M; Kivimaki, Mika; Knekt, Paul B; Koistinen, Heikki A; Kooner, Jaspal S; Koskinen, Seppo; Kuusisto, Johanna; Maerz, Winfried; Martin, Nicholas G; Laakso, Markku; Lakka, Timo A; Lehtimaki, Terho; Lettre, Guillaume; Levinson, Douglas F; Lind, Lars; Lokki, Marja-Liisa; Mantyselka, Pekka; Melbye, Mads; Metspalu, Andres; Mitchell, Braxton D; Moll, Frans L; Murray, Jeffrey C; Musk, Arthur W; Nieminen, Markku S; Njolstad, Inger; Ohlsson, Claes; Oldehinkel, Albertine J; Oostra, Ben A; Palmer, Lyle J; Pankow, James S; Pasterkamp, Gerard; Pedersen, Nancy L; Pedersen, Oluf; Penninx, Brenda W; Perola, Markus; Peters, Annette; Polasek, Ozren; Pramstaller, Peter P; Psaty, Bruce M; Qi, Lu; Quertermous, Thomas; Raitakari, Olli T; Rankinen, Tuomo; Rauramaa, Rainer; Ridker, Paul M; Rioux, John D; Rivadeneira, Fernando; Rotter, Jerome I; Rudan, Igor; den Ruijter, Hester M; Saltevo, Juha; Sattar, Naveed; Schunkert, Heribert; Schwarz, Peter E H; Shuldiner, Alan R; Sinisalo, Juha; Snieder, Harold; Sorensen, Thorkild I A; Spector, Tim D; Staessen, Jan A; Stefania, Bandinelli; Thorsteinsdottir, Unnur; Stumvoll, Michael; Tardif, Jean-Claude; Tremoli, Elena; Tuomilehto, Jaakko; Uitterlinden, Andre G; Uusitupa, Matti; Verbeek, Andre L M; Vermeulen, Sita H; Viikari, Jorma S; Vitart, Veronique; Volzke, Henry; Vollenweider, Peter; Waeber, Gerard; Walker, Mark; Wallaschofski, Henri; Wareham, Nicholas J; Watkins, Hugh; Zeggini, Eleftheria; Chakravarti, Aravinda; Clegg, Deborah J; Cupples, L Adrienne; Gordon-Larsen, Penny; Jaquish, Cashell E; Rao, D C; Abecasis, Goncalo R; Assimes, Themistocles L; Barroso, Ines; Berndt, Sonja I; Boehnke, Michael; Deloukas, Panos; Fox, Caroline S; Groop, Leif C; Hunter, David J; Ingelsson, Erik; Kaplan, Robert C; McCarthy, Mark I; Mohlke, Karen L; O'Connell, Jeffrey R; Schlessinger, David; Strachan, David P; Stefansson, Kari; van Duijn, Cornelia M; Hirschhorn, Joel N; Lindgren, Cecilia M; Heid, Iris M; North, Kari E; Borecki, Ingrid B; Kutalik, Zoltan; Loos, Ruth J F/titolo:The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study./doi:10.1371%2Fjournal.pgen.1005378/rivista:PLOS genetics (Online)/anno:2015/pagina_da:e1005378/pagina_a:/intervallo_pagine:e1005378/volume:11
PLoS Genetics, 11(10)
PLoS genetics, 11(10). Public Library of Science
Plos Genetics, 11(10):e1005378. Public Library of Science
Winkler, T W, Justice, A E, Graff, M, Barata, L, Feitosa, M F, Chu, S, Czajkowski, J, Esko, T, Fall, T, Kilpelainen, T O, Lu, Y, Magi, R, Mihailov, E, Pers, T H, Rueeger, S, Teumer, A, Ehret, G B, Ferreira, T, Heard-Costa, N L, Karjalainen, J, Lagou, V, Mahajan, A, Neinast, M D, Prokopenko, I, Simino, J, Teslovich, T M, Jansen, R, Westra, H, White, C C, Absher, D, Ahluwalia, T S, Ahmad, S, Albrecht, E, Alves, A C, Bragg-Gresham, J L, Craen, A J M, Bis, J C, Bonnefond, A, Boucher, G, Cadby, G, Cheng, Y, Chiang, C W K, Delgado, G, Demirkan, A, Dueker, N, Eklund, N, Eiriksdottir, G, Eriksson, J, Feenstra, B, Fischer, K, Frau, F, Galesloot, T E, Geller, F, Goel, A, Gorski, M, Grammer, T B, Gustafsson, S, Haitjema, S, Hottenga, J J, Huffman, J E, Jackson, A U, Jacobs, K B, Johansson, A, Kaakinen, M, Kleber, M E, Lahti, J, Leach, I M, Lehne, B, Lo, K S, Lorentzon, M, Luan, J, Madden, P A F, Mangino, M, McKnight, B, Medina-Gomez, C, Monda, K L, Montasser, M E, Mueller, G, Mueller-Nurasyid, M, Nolte, I M, Panoutsopoulou, K, Pascoe, L, Paternoster, L, Rayner, N W, Renstrom, F, Rizzi, F, Rose, L M, Ryan, K A, Salo, P, Sanna, S, Scharnagl, H, Shi, J, Smith, A V, Southam, L, Stancakova, A, Steinthorsdottir, V, Strawbridge, R J, Sung, Y J, Tachmazidou, I, Tanaka, T, Thorleifsson, G, Trompet, S, Pervjakova, N, Tyrer, J P, Vandenput, L, van der Laan, S W, van der Velde, N, van Setten, J, van Vliet-Ostaptchouk, J V, Verweij, N, Vlachopoulou, E, Waite, L L, Wang, S R, Wang, Z, Wild, S H, Willenborg, C, Wilson, J F, Wong, A, Yang, J, Yengo, L, Yerges-Armstrong, L M, Yu, L, Zhang, W, Zhao, J H, Andersson, E A, Bakker, S J L, Baldassarre, D, Banasik, K, Barcella, M, Barlassina, C, Bellis, C, Benaglio, P, Blangero, J, Blueher, M, Bonnet, F, Bonnycastle, L L, Boyd, H A, Bruinenberg, M, Buchman, A S, Campbell, H, Chen, Y I, Chines, P S, Claudi-Boehm, S, Cole, J, Collins, F S, de Geus, E J C, de Groot, L C P G M, Dimitriou, M, Duan, J, Enroth, S, Eury, E, Farmaki, A, Forouhi, N G, Friedrich, N, Gejman, P V, Gigante, B, Glorioso, N, Go, A S, Gottesman, O, Graessler, J, Grallert, H, Grarup, N, Gu, Y, Broer, L, van der Ham, A C, Hansen, T, Harris, T B, Hartman, C A, Hassinen, M, Hastie, N, Hattersley, A T, Heath, A C, Henders, A K, Hernandez, D, Hillege, H, Holmen, O, Hovingh, K G, Hui, J, Husemoen, L L, Hutri-Kahonen, N, Hysi, P G, Illig, T, de Jager, P L, Jalilzadeh, S, Jorgensen, T, Jukema, J W, Juonala, M, Kanoni, S, Karaleftheri, M, Khaw, K T, Kinnunen, L, Kittner, S J, Koenig, W, Kolcic, I, Kovacs, P, Krarup, N T, Kratzer, W, Krueger, J, Kuh, D, Kumari, M, Kyriakou, T, Langenberg, C, Lannfelt, L, Lanzani, C, Lotay, V, Launer, L J, Leander, K, Lindstrom, J, Linneberg, A, Liu, Y, Lobbens, S, Luben, R, Lyssenko, V, Mannisto, S, Magnusson, P K, McArdle, W L, Menni, C, Merger, S, Milani, L, Montgomery, G W, Morris, A P, Narisu, N, Nelis, M, Ong, K K, Palotie, A, Perusse, L, Pichler, I, Pilia, M G, Pouta, A, Rheinberger, M, Ribel-Madsen, R, Richards, M, Rice, K M, Rice, T K, Rivolta, C, Salomaa, V, Sanders, A R, Sarzynski, M A, Scholtens, S, Scott, R A, Scott, W R, Sebert, S, Sengupta, S, Sennblad, B, Seufferlein, T, Silveira, A, Slagboom, P E, Smit, J H, Sparso, T H, Stirrups, K, Stolk, R P, Stringham, H M, Swertz, M A, Swift, A J, Syvanen, A, Tan, S, Thorand, B, Toenjes, A, Tremblay, A, Tsafantakis, E, van der Most, P J, Voelker, U, Vohl, M, Vonk, J M, Waldenberger, M, Walker, R W, Wennauer, R, Widen, E, Willemsen, G, Wilsgaard, T, Wright, A F, Zillikens, M C, van Dijk, S C, van Schoor, N M, Asselbergs, F W, Bakker, P I W, Beckmann, J S, Beilby, J, Bennett, D A, Bergman, R N, Bergmann, S, Boeger, C A, Boehm, B O, Boerwinkle, E, Boomsma, D I, Bornstein, S R, Bottinger, E P, Bouchard, C, Chambers, J C, Chanock, S J, Chasman, D I, Cucca, F, Cusi, D, Dedoussis, G, Erdmann, J, Eriksson, J G, Evans, D A, de Faire, U, Farrall, M, Ferrucci, L, Ford, I, Franke, L, Franks, P W, Froguel, P, Gansevoort, R T, Gieger, C, Gronberg, H, Gudnason, V, Gyllensten, U, Hall, P, Hamsten, A, van der Harst, P, Hayward, C, Heliovaara, M, Hengstenberg, C, Hicks, A A, Hingorani, A, Hofman, A, Hu, F, Huikuri, H V, Hveem, K, James, A L, Jordan, J M, Jula, A, Kaehoenen, M, Kajantie, E, Kathiresan, S, Kiemeney, L A L M, Kivimaki, M, Knekt, P B, Koistinen, H A, Kooner, J S, Koskinen, S, Kuusisto, J, Maerz, W, Martin, N G, Laakso, M, Lakka, T A, Lehtimaki, T, Lettre, G, Levinson, D F, Lind, L, Lokki, M, Mantyselka, P, Melbye, M, Metspalu, A, Mitchell, B D, Moll, F L, Murray, J C, Musk, A W, Nieminen, M S, Njolstad, I, Ohlsson, C, Oldehinkel, A J, Oostra, B A, Palmer, L J, Pankow, J S, Pasterkamp, G, Pedersen, N L, Pedersen, O, Penninx, B W J H, Perola, M, Peters, A, Polasek, O, Pramstaller, P P, Psaty, B M, Qi, L, Quertermous, T, Raitakari, O T, Rankinen, T, Rauramaa, R, Ridker, P M, Rioux, J D, Rivadeneira, F, Rotter, J I, Rudan, I, den Ruijter, H M, Saltevo, J, Sattar, N, Schunkert, H, Schwarz, P E H, Shuldiner, A R, Sinisalo, J, Snieder, H, Sorensen, T I A, Spector, T D, Staessen, J A, Stefania, B, Thorsteinsdottir, U, Stumvoll, M, Tardif, J, Tremoli, E, Tuomilehto, J, Uitterlinden, A G, Uusitupa, M, Verbeek, A L M, Vermeulen, S H, Viikari, J S, Vitart, V, Voelzke, H, Vollenweider, P, Waeber, G, Walker, M, Wallaschofski, H, Wareham, N J, Watkins, H, Zeggini, E, Chakravarti, A, Clegg, D J, Cupples, L A, Gordon-Larsen, P, Jaquish, C E, Rao, D C, Abecasis, G R, Assimes, T L, Barroso, I, Berndt, S I, Boehnke, M, Deloukas, P, Fox, C S, Groop, L C, Hunter, D J, Ingelsson, E, Kaplan, R C, McCarthy, M I, Mohlke, K L, O'Connell, J R, Schlessinger, D, Strachan, D P, Stefansson, K, van Duijn, C M, Hirschhorn, J N, Lindgren, C M, Heid, I M, North, K E, Borecki, I B, Kutalik, Z & Loos, R J F 2015, ' The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study ', PLoS Genetics, vol. 11, no. 10, e1005378 . https://doi.org/10.1371/journal.pgen.1005378Test
PLOS Genetics, Vol. 11, No 10 (2015) P. e1005378
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
PLoS Genetics, 2015, 11 (10), pp.e1005378. ⟨10.1371/journal.pgen.1005378⟩
PLoS Genetics, Vol 12, Iss 6, p e1006166 (2016)
Plos Genetics, vol. 11, no. 10, pp. e1005378
PLoS Genetics; 11(10), no e1005378 (2015)
PLoS Genetics (online), 11(10). Public Library of Science
PLoS Genetics, Vol 11, Iss 10, p e1005378 (2015)

مصطلحات موضوعية: 0301 basic medicine, Netherlands Twin Register (NTR), Male, Cancer Research, endocrine system diseases, Biological pathways, QH426-470, Genome, Body Mass Index, Body Size, Genetics (clinical), ddc:616, Genetics & Heredity, Sex Characteristics, Loci, MAGIC Consortium, Mass index, Age Factors, Chromosome Mapping, Middle Aged, Genealogy, Self-reported height, Peripheral-blood, Scale (social sciences), ICBP Consortium, Female, Life Sciences & Biomedicine, Medical Genetics, Research Article, arcOGEN Consortium, musculoskeletal diseases, Adult, European Continental Ancestry Group, Natural menopause, Aged, Body Size/genetics, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide, Waist-Hip Ratio, Biology, Body size, DIAGRAM Consortium, Age and sex, White People, Fat distribution, GLGC Consortium, 03 medical and health sciences, Life-course, Genetics, Weight-gain, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Medicinsk genetik, [SDV.GEN]Life Sciences [q-bio]/Genetics, 0604 Genetics, Science & Technology, nutritional and metabolic diseases, Correction, 030104 developmental biology, GWAS meta-analysis, Global-BPGen Consortium, Common SNPS, CHARGE Consortium, 3111 Biomedicine, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48d6f5f932496e7163246968cbc949bcTest
https://pubmed.ncbi.nlm.nih.gov/27355579Test

8

Selection on a Variant Associated with Improved Viral Clearance Drives Local, Adaptive Pseudogenization of Interferon Lambda 4 (IFNL4)

المؤلفون: Key, F., https://orcid.org/0000-0003-2812-6636Test, Peter, B., https://orcid.org/0000-0003-2526-8081Test, Dennis, M., Huerta-Sanchez, E., Tang, W., Prokunina-Olsson, L., Nielsen, R., Andrés, A., https://orcid.org/0000-0002-8590-9672Test

المساهمون: Pritchard, Jonathan K

المصدر: PLoS Genetics
PLoS genetics, vol 10, iss 10
PLoS Genetics, Vol 10, Iss 10, p e1004681 (2014)

مصطلحات موضوعية: Asian Continental Ancestry Group, lcsh:QH426-470, Far East, Population, European Continental Ancestry Group, Polymorphism, Single Nucleotide, White People, Hepatitis, Genetic, Asian People, Gene Frequency, Models, Genetics, Animals, Humans, Genetic Predisposition to Disease, Polymorphism, Selection, Genetic, Selection, Conserved Sequence, Mammals, Evolutionary Biology, Genome, Base Sequence, Models, Genetic, Whites, Asia, Eastern, Genome, Human, Liver Disease, Interleukins, Human Genome, Biology and Life Sciences, Bayes Theorem, Single Nucleotide, Hepatitis C, Asians, lcsh:Genetics, Emerging Infectious Diseases, Infectious Diseases, Genetics, Population, Haplotypes, Africa, Digestive Diseases, Infection, Pseudogenes, Human, Developmental Biology, Research Article

وصف الملف: application/pdf; application/zip

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::54adee89438dbc1393efec8d109a7832Test
http://europepmc.org/articles/PMC4199494Test

9

Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations

المؤلفون: Andrew A. Hicks, Irina V. Zorkoltseva, Christopher S. Franklin, Thomas Meitinger, Michael Preuss, Cristian Pattaro, Lennart C. Karssen, Veronique Vitart, Sarah H. Wild, Fernando Rivadeneira, Åsa Johansson, James F. Wilson, Anatoly V. Kirichenko, Ghazal Zaboli, Ozren Polasek, Wilmar Igl, Tatiana I. Axenovich, Christopher J. O'Donnell, Jacqueline C. M. Witteman, James A B Floyd, Linda Broer, Arne Pfeufer, Lude Franke, Igor Rudan, Zrinka Biloglav, Christopher P. Nelson, Nora Franceschini, Ivana Kolcic, Aaron Isaacs, Yurii S. Aulchenko, Harry Campbell, Nicholas D. Hastie, Cornelia M. van Duijn, Ritsert C. Jansen, Irene Pichler, Alan F. Wright, Caroline Hayward, Albert Hofman, Ben A. Oostra, Jennifer E. Huffman, Ulf Gyllensten, Gerd Schmitz, Carsten Gnewuch, Inger Jonasson, Francisco S. Domingues, Ayse Demirkan, André G. Uitterlinden, Gerhard Liebisch, A. Cecile J.W. Janssens, Peter Ugocsai, Peter P. Pramstaller, Joshua C. Bis, Susan Campbell, Maksim Struchalin

المساهمون: Epidemiology, Internal Medicine, Clinical Genetics, Groningen Biomolecular Sciences and Biotechnology, Bioinformatics, Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Stem Cell Aging Leukemia and Lymphoma (SALL)

المصدر: PLoS Genetics
PLoS Genetics, Vol 8, Iss 2, p e1002490 (2012)
PLoS Genetics (print), 8(2). Public Library of Science
Plos Genetics, 8(2). Public Library of Science
PLoS genetics, 8(2):e1002490. PUBLIC LIBRARY SCIENCE
Demirkan, A, van Duijn, C M, Ugocsai, P, Isaacs, A, Pramstaller, P P, Liebisch, G, Wilson, J F, Johansson, Å, Rudan, I, Aulchenko, Y S, Kirichenko, A V, Janssens, A C J W, Jansen, R C, Gnewuch, C, Domingues, F S, Pattaro, C, Wild, S H, Jonasson, I, Polasek, O, Zorkoltseva, I V, Hofman, A, Karssen, L C, Struchalin, M, Floyd, J, Igl, W, Biloglav, Z, Broer, L, Pfeufer, A, Pichler, I, Campbell, S, Zaboli, G, Kolcic, I, Rivadeneira, F, Huffman, J, Hastie, N D, Uitterlinden, A, Franke, L, Franklin, C S, Vitart, V, Nelson, C P, Preuss, M, Bis, J C, O'Donnell, C J, Franceschini, N, Witteman, J C M, Axenovich, T, Oostra, B A, Hayward, C & Wright, A F & Campbell, H 2012, ' Genome-wide association study identifies novel loci associated with circulating phospho-and sphingolipid concentrations ', PLoS Genetics, vol. 8, no. 2, pp. e1002490 . https://doi.org/10.1371/journal.pgen.1002490Test
PLoS Genetics; Vol 8

مصطلحات موضوعية: Apolipoprotein E, Cancer Research, Medicin och hälsovetenskap, Epidemiology, Medical and Health Sciences, Biochemistry, Carotid Intima-Media Thickness, DISEASE, chemistry.chemical_compound, 0302 clinical medicine, Delta-5 Fatty Acid Desaturase, PHOSPHATIDYLCHOLINE, Databases, Genetic, Phospholipids/blood, CARDIoGRAM Consortium, European Continental Ancestry Group/genetics, Genetics (clinical), Phospholipids, chemistry.chemical_classification, 0303 health sciences, Genome, Sphingolipids/blood, Single Nucleotide, LYSOPHOSPHATIDYLCHOLINE, Lipids, HIGH-THROUGHPUT QUANTIFICATION, 3. Good health, Lysophosphatidylcholine, Glycerophospholipid, Fatty acid elongation, Medicine, lipids (amino acids, peptides, and proteins), FATTY-ACIDS, Sphingomyelin, Diabetes Mellitus, Type 2/blood, Human, Research Article, SUSCEPTIBILITY LOCI, lcsh:QH426-470, Membrane lipids, European Continental Ancestry Group, Biology, DIAGRAM Consortium, Polymorphism, Single Nucleotide, White People, HUMAN PLATELETS, 03 medical and health sciences, Databases, SDG 3 - Good Health and Well-being, Genetic, Diabetes Mellitus, Genetics, Humans, ddc:610, TANDEM MASS-SPECTROMETRY, Polymorphism, Molecular Biology, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Type 2/blood, 0604 Genetics, Sphingolipids, Population Biology, Genome, Human, MEMBRANE-LIPIDS, Fatty acid, Human Genetics, Sphingolipid, lcsh:Genetics, Metabolism, chemistry, ATHEROSCLEROSIS, Diabetes Mellitus, Type 2, Genetic Loci, CHARGE Consortium, 030217 neurology & neurosurgery, EUROSPAN consortium, Developmental Biology, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85b5f973d174b07a0fa63145fbd6d3bfTest
http://europepmc.org/articles/PMC3280968Test

10

Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene

المساهمون: Medical Research Council (MRC)

المصدر: PLoS genetics
Scopus-Elsevier
PLoS Genetics, Vol 6, Iss 7, p e1001035 (2010)
PLoS genetics, vol. 6, no. 7, pp. e1001035
PLoS Genetics

مصطلحات موضوعية: Cancer Research, Candidate gene, Linkage disequilibrium, CARDIOVASCULAR MORTALITY, LOCI, Genome-wide association study, 0302 clinical medicine, PRIMARY HYPERPARATHYROIDISM, Genetics (clinical), Genetics, Genetics & Heredity, 0303 health sciences, education.field_of_study, A986S POLYMORPHISM, 030220 oncology & carcinogenesis, Calcium-sensing receptor, BONE-MINERAL DENSITY, Life Sciences & Biomedicine, Research Article, medicine.medical_specialty, lcsh:QH426-470, Population, European Continental Ancestry Group, Public Health and Epidemiology, chemistry.chemical_element, Single-nucleotide polymorphism, Biology, Calcium, HYPOCALCIURIC HYPERCALCEMIA, Polymorphism, Single Nucleotide, White People, 03 medical and health sciences, ADULT, Internal medicine, medicine, Humans, CORONARY-HEART-DISEASE, education, Molecular Biology, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Calcium metabolism, 0604 Genetics, Science & Technology, Genome, Human, Genetics and Genomics, Calcium/blood, European Continental Ancestry Group/statistics & numerical data, Genome-Wide Association Study/statistics & numerical data, Receptors, Calcium-Sensing/genetics, COMMON VARIANT, lcsh:Genetics, Endocrinology, chemistry, MYOCARDIAL-INFARCTION, Computational Biology/Population Genetics, Receptors, Calcium-Sensing, Computational Biology/Genomics, Genome-Wide Association Study, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6b83bcefb08e4afe756a5322c7e91f4Test

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