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المؤلفون: Adem Y Dawed, Andrea Mari, Andrew Brown, Timothy J McDonald, Lin Li, Shuaicheng Wang, Mun-Gwan Hong, Sapna Sharma, Neil R Robertson, Anubha Mahajan, Xuan Wang, Mark Walker, Stephen Gough, Leen M ‘t Hart, Kaixin Zhou, Ian Forgie, Hartmut Ruetten, Imre Pavo, Pallav Bhatnagar, Angus G Jones, Ewan R Pearson, L.M. 't Hart, M. Abdalla, J. Adam, J. Adamski, K. Adragni, K.H. Allin, M. Arumugam, N. Atabaki Pasdar, T. Baltauss, K.B. Banasik, P. Baum, J.D. Bell, M. Bergstrom, J.W. Beulens, S. Bianzano, R. Bizzotto, A. Bonneford, C.A.B. Brorsson, A.A. Brown, S.B. Brunak, L. Cabrelli, R. Caiazzo, M. Canouil, M. Dale, D. Davtian, A.Y. Dawed, F.M. De Masi, N. de Preville, K.F. Dekkers, E.T. Dermitzakis, H.A. Deshmukh, C. Dings, L. Donnelly, A. Dutta, B. Ehrhardt, P.J.M. Elders, C.E.T. Engel Thomas, L. Engelbrechtsen, R.G. Eriksen, R.E. Eriksen, Y. Fan, J. Fernandez, J. Ferrer, H. Fitipaldi, I.M. Forgie, A. Forman, P.W. Franks, F. Frau, A. Fritsche, P. Froguel, G. Frost, J. Gassenhuber, G.N. Giordano, T. Giorgino, S. Gough, U. Graefe-Mody, H. Grallert, R. Grempler, L. Groeneveld, L. Groop, V.G. Gudmundsdóttir, R.G. Gupta, M. Haid, T. Hansen, T.H. Hansen, A.T. Hattersley, R.S. Haussler, A.J. Heggie, A.M. Hennige, A.V. Hill, R.W. Holl, M.-G. Hong, M. Hudson, B. Jablonka, C. Jennison, J. Jiao, J.J. Johansen, A.G. Jones, A. Jonsson, T.K. Karaderi, J. Kaye, M. Klintenberg, R.W. Koivula, T. Kokkola, A.D.M. Koopman, A Kurbasic, T. Kuulasmaa, M. Laakso, T. Lehr, H. Loftus, R.L.A Lundbye Allesøe, A. Mahajan, A. Mari, G.M. Mazzoni, M.I. McCarthy, T.J. McDonald, D. McEvoy, N. McRobert, I. McVittie, M. Mourby, P. Musholt, P Mutie, R. Nice, C. Nicolay, A.M.N. Nielsen, B.N. Nilsson, C.N. Palmer, F. Pattou, I. Pavo, E.R. Pearson, O. Pedersen, H.K.P. Pedersen, M.H. Perry, H. Pomares-Millan, A. Ramisch, S.R. Rasmussen, V. Raverdi, M. Ridderstrale, N. Robertson, R.C. Roderick, M. Rodriquez, H. Ruetten, F. Rutters, W. Sackett, N. Scherer, J.M. Schwenk, N. Shah, S. Sharma, I. Sihinevich, N.B. Sondertoft, H. Staerfeldt, B. Steckel-Hamann, H. Teare, M.K. Thomas, E.L. Thomas, H.S. Thomsen, B. Thorand, C.E. Thorne, J. Tillner, A.T.L. Troen Lundgaard, M. Troll, K.D.T. Tsirigos, A. Tura, M. Uhlen, N. van Leeuwen, S. van Oort, H. Verkindt, H. Vestergaard, A. Viñuela, J.K Vogt, P.W.S Wad Sackett, D. Wake, M. Walker, A. Wesolowska-Andersen, B. Whitcher, M.W. White, H. Wu
المساهمون: Epidemiology and Data Science, ACS - Diabetes & metabolism, ACS - Heart failure & arrhythmias, APH - Health Behaviors & Chronic Diseases, General practice, APH - Aging & Later Life
المصدر: DIRECT consortium 2023, ' Pharmacogenomics of GLP-1 receptor agonists : a genome-wide analysis of observational data and large randomised controlled trials ', The Lancet Diabetes and Endocrinology, vol. 11, no. 1, pp. 33-41 . https://doi.org/10.1016/S2213-8587Test(22)00340-0
The Lancet Diabetes & Endocrinology, 11(1), 33-41. ELSEVIER SCIENCE INC
The Lancet Diabetes and Endocrinology, 11(1), 33-41. Elsevier BVمصطلحات موضوعية: Adult, Male, Blood Glucose, Adolescent, Endocrinology, Diabetes and Metabolism, Endocrinology and Diabetes, Glucagon-Like Peptide-1 Receptor, Endocrinology, Treatment Outcome, Diabetes Mellitus, Type 2, Pharmacogenetics, Endokrinologi och diabetes, Internal Medicine, Humans, Hypoglycemic Agents, Female, Genome-Wide Association Study, Randomized Controlled Trials as Topic
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::090a81ca93ab346ddb1e6191899c14b3Test
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-496271Test -
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المؤلفون: the DIRECT Consortium, the MetGen Plus Consortium, Ewan R Pearson, Kathleen M. Giacomini, Leen M. ‘t Hart, Monique M. Hedderson, Jose C. Florez, Colin N A Palmer, Michiaki Kubo, Yukihide Momozawa, Yoichiro Kamatani, Ming Ta Michael Lee, John S. Witte, Varinderpal Kaur, Josep M. Mercader, Yu-Chuan Chang, Roderick C Slieker, Amber A van der Heijden, Joline W Beulens, Josephine H. Li, Fei Xu, Federico Innocenti, Amy Etheridge, Moneeza K Siddiqui, Yanfei Zhang, Nienke van Leeuwen, Kaixin Zhou, Sook Wah Yee, Adem Y Dawed
المصدر: Diabetes care, vol 44, iss 12
مصطلحات موضوعية: for the DIRECT Consortium, Blood Glucose, Glycated Hemoglobin, Likelihood Functions, [MetGen Plus investigators], Liver-Specific Organic Anion Transporter 1, Prevention, Diabetes, Human Genome, for MetGen Plus, Evaluation of treatments and therapeutic interventions, Medical and Health Sciences, Metformin, Endocrinology & Metabolism, Sulfonylurea Compounds, 6.1 Pharmaceuticals, Diabetes Mellitus, Genetics, Humans, Hypoglycemic Agents, Type 2, Metabolic and endocrine, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79b4f3c714497f38718331811cc93757Test
https://escholarship.org/uc/item/1pj67106Test -
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المؤلفون: Peter K. Joshi, Kaixin Zhou, Katharina E. Schraut, Emanuele Trucco, Mirna Kirin, Devanjali Relan, Alex S. F. Doney, Veronique Vitart, Ian J. Deary, Lucia Ballerini, Tom MacGillivray, Ellie Brown, James F. Wilson, Ozren Polasek, Colin N. A. Palmer, Caroline Hayward, Harry Campbell, Abirami Veluchamy, Sarah E. Harris, Suraj S. Vaidya, Ewan R. Pearson, Baljean Dhillon
المصدر: Veluchamy, A, Ballerini, L, Vitart, V, Schraut, K E, Kirin, M, Campbell, H, Joshi, P, Relan, D, Harris, S, Brown, E, Vaidya, S S, Dhillon, B, Zhou, K, Pearson, E R, Hayward, C, Polasek, O, Deary, I, MacGillivray, T, Wilson, J, Trucco, E, Palmer, C N A & Doney, A S F 2019, ' A novel genetic locus influencing retinal venular tortuosity is also associated with risk of coronary artery disease ', Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 39, no. 12, pp. 2542-2552 . https://doi.org/10.1161/ATVBAHA.119.312552Test
Arteriosclerosis, Thrombosis, and Vascular Biologyمصطلحات موضوعية: medicine.medical_specialty, retina, Cardiovascular health, Single-nucleotide polymorphism, Genome-wide association study, Coronary Artery Disease, 030204 cardiovascular system & hematology, Tortuosity, Coronary artery disease, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Retinal Diseases, Venules, Risk Factors, Internal medicine, medicine, heart rate, Humans, Genetic Predisposition to Disease, atrial fibrillation, 030304 developmental biology, 0303 health sciences, Retina, genome-wide association study, business.industry, Retinal Vessels, biomarkers, Retinal, Retinal vascular tortuosity, medicine.disease, 3. Good health, cardiovascular diseases, medicine.anatomical_structure, Phenotype, chemistry, Cardiology, ComputingMethodologies_DOCUMENTANDTEXTPROCESSING, Cardiology and Cardiovascular Medicine, business, Clinical and Population Studies
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc73e873d6828efcf3dcbe151f1f7b4cTest
https://www.pure.ed.ac.uk/ws/files/124475783/VeluchamyATAVB2019NovelGeneticLocusInfluencing.pdfTest -
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المؤلفون: Michael Boehnke, Anke R. Hammerschlag, Stavroula Kanoni, Nilesh J. Samani, Stefan Blankenberg, Arpana Agrawal, Ersin Yavas, Chris Hsu, Dominique Arveiler, Giovanni Veronesi, Sarah E. Harris, Guillaume Lettre, Leah Wetherill, Helen R. Warren, M Samuel, Manav Kapoor, Praveen Surendran, Mengzhen Liu, Massimo Mangino, Abdulla Al Shafi Majumder, Chiara Batini, Jeff Haessler, Anton J. M. De Craen, Matt McGue, Laura J. Bierut, Yi Ling Chou, Markku Laakso, Ian J. Deary, Rebecca Rohde, Nhung Le, David Schlessinger, J. Dylan Weissenkampen, Claudia Langenberg, Tim D. Spector, Paul W. Franks, John P. Rice, Philippe M. Frossard, Hanieh Yaghootkar, Janie Corley, Frank Kee, J. Wouter Jukema, Pim van der Harst, Dermot F. Reily, Jenny Chang-Claude, Nicholas G. Martin, Tatiana Foroud, Sune F. Nielsen, Charles Kooperberg, Rudolf A. de Boer, Francesco Cucca, Paul D.P. Pharoah, Alex P. Reiner, Daniel R. Barnes, Anders Mälarstig, Jonathan Marten, Henry Völzke, Yu Jiang, Jukka Kontto, J Danesh, Antonis C. Antoniou, Andrew C. Heath, Nicholas J. Wareham, Joanna M. M. Howson, Alison Goate, Olov Rolandsson, Frida Renström, Chu Chen, Vinicius Tragante, Matt J. Neville, Kathleen Stirrups, Clemens Baumbach, Colin N. A. Palmer, Adam S. Butterworth, William G. Iacono, Naveed Sattar, Ian P. Hall, Daniel O. Stram, Giorgio Pistis, Jan-Håkan Jansson, Jaakko Kaprio, David R. Weir, David P. Strachan, Martin D. Tobin, Folkert W. Asselbergs, John M. Starr, Stefan Weiss, Thomas F. Vogt, Riccardo E. Marioni, Maarten Hoek, Jessica Tyrrell, Hilary A. Tindle, Alison M. Dunning, Anu Loukola, Joe Dennis, Victoria E. Jackson, Louise V. Wain, Eleftheria Zeggini, Weihua Zhang, Yaming Shao, Kari Kuulasmaa, Elisabeth Altmaier, Jean-Claude Tardif, Jian Gong, A. Mesut Erzurumluoglu, Andries R. van der Leij, Kari E. North, Anna F. Dominiczak, Martina Müller-Nurasyid, Scott I. Vrieze, Sarah Bertelsen, Markus Perola, Evangelos Evangelou, Chris J. Packard, Gonçalo R. Abecasis, Robert A. Scott, S. Trompet, Jennifer A. Smith, H. Steven Scholte, Timothy M. Frayling, Danielle Posthuma, Ian Ford, Douglas F. Easton, Børge Grønne Nordestgaard, Michiel L. Bots, Charles B. Eaton, Sharon L.R. Kardia, Dewan S. Alam, Xiaowei Zhan, Sean P. David, Maria Uria-Nickelsen, Dongbing Lai, Ilonca Vaartjes, Mark J. Caulfield, Valérie Turcot, Jean Ferrières, Emanuele Di Angelantonio, Robin Young, Pamela A. F. Madden, Tibor V. Varga, Asif Rasheed, Peter van der Meer, Dajiang J. Liu, Ioanna Tachmazidou, Panos Deloukas, Danish Saleheen, Evelin Mihailov, Caroline Hayward, Patricia B. Munroe, Beenish Qaiser, Jessica D. Faul, John C. Chambers, Matthias Nauck, Niek Verweij, Jordan M. Hughey, Christopher A. Haiman, Hans J. Grabe, Muriel Caslake, Saima Afaq, Jaspal S. Kooner, Tinca J. C. Polderman, Philippe Amouyel, Wei Zhao, Göran Hallmans, Andres Metspalu, Jarmo Virtamo, Carl A. Melbourne, Kaixin Zhou, Christiaan de Leeuw, Peter S. Sever, Eirini Marouli, Neil Poulter, Rajiv Chowdhury, Jian'an Luan, Deborah J. Thompson, F Karpe, Kyriaki Michailidou, David M. Brazel, Heather M. Stringham
المساهمون: Brein en Cognitie (Psychologie, FMG), Psychology Other Research (FMG), Human genetics, Amsterdam Neuroscience - Compulsivity, Impulsivity & Attention, Amsterdam Reproduction & Development (AR&D), Cardiovascular Centre (CVC), Restoring Organ Function by Means of Regenerative Medicine (REGENERATE), Graduate School, Experimental Vascular Medicine, ACS - Diabetes & metabolism, Amsterdam Cardiovascular Sciences, ACS - Atherosclerosis & ischemic syndromes, AGEM - Digestive immunity, AGEM - Endocrinology, metabolism and nutrition, Laboratory Genetic Metabolic Diseases, Gastroenterology and Hepatology, Experimental Immunology, Radiotherapy, Cardiology, HUSLAB, Institute for Molecular Medicine Finland, Department of Public Health, Genetic Epidemiology, Barnes, Daniel [0000-0002-3781-7570], Erzurumluoglu, Mesut [0000-0003-1322-8138], Apollo - University of Cambridge Repository, Biological Psychology, Complex Trait Genetics
المصدر: Biological Psychiatry, 85(11), 946-955. Elsevier
Biological Psychiatry, 85(11), 946-955. Elsevier USA
Biological Psychiatry, 85(11), 946-955. ELSEVIER SCIENCE INC
Brazel, D M, Jiang, Y, Hughey, J M, Turcot, V, Zhan, X, Gong, J, Batini, C, Weissenkampen, J D, Liu, M, Barnes, D R, Bertelsen, S, Chou, Y-L, Erzurumluoglu, A M, Faul, J D, Haessler, J, Hammerschlag, A R, Hsu, C, Kapoor, M, Lai, D, Le, N, de Leeuw, C A, Loukola, A, Mangino, M, Melbourne, C A, Pistis, G, Qaiser, B, Rohde, R, Shao, Y, Stringham, H, Wetherill, L, Zhao, W, Agrawal, A, Bierut, L, Chen, C, Eaton, C B, Goate, A, Haiman, C, Heath, A, Iacono, W G, Martin, N G, Polderman, T J, Reiner, A, Rice, J, Schlessinger, D, Scholte, H S, Smith, J A, Tardif, J-C, Tindle, H A, van der Leij, A R, Boehnke, M, Chang-Claude, J, Cucca, F, David, S P, Foroud, T, Howson, J M M, Kardia, S L R, Kooperberg, C, Laakso, M, Lettre, G, Madden, P, Mcgue, M, North, K, Posthuma, D, Spector, T, Stram, D, Tobin, M D, Weir, D R, Kaprio, J, Abecasis, G R, Liu, D J, Vrieze, S, Surendran, P, Young, R, Barnes, D R, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Kontto, J, Perola, M, Caslake, M, de Craen, A J M, Trompet, S, Uria-Nickelsen, M, Malarstig, A, Reily, D F, Hoek, M, Vogt, T, Jukema, J W, Sattar, N, Ford, I, Packard, C J, Alam, D S, Majumder, A A S, Di Ange-Lantonio, E, Chowdhury, R, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrieres, J, Kee, F, Kuulasmaa, K, Mueller-Nurasyid, M, Veronesi, G, Virtamo, J, Frossard, P, Nordestgaard, B G, Saleheen, D, Danesh, J, Butterworth, A S, Howson, J M M, Erzurumluoglu, A M, Jackson, V E, Melbourne, C A, Varga, T V, Warren, H R, Tragante, V, Tachmazidou, I, Harris, S E, Evangelou, E, Marten, J, Zhang, W, Altmaier, E, Luan, J, Langenberg, C, Scott, R A, Yaghootkar, H, Stirrups, K, Kanoni, S, Marouli, E, Karpe, F, Dominiczak, A F, Sever, P, Poulter, N, Rolandsson, O, Baumbach, C, Afaq, S, Chambers, J C, Kooner, J S, Wareham, N J, Renstrom, F, Hallmans, G, Marioni, R E, Corley, J, Starr, J M, Verweij, N, de Boer, R A, van der Meer, P, Yavas, E, Vaartjes, I, Bots, M L, Asselbergs, F W, Grabe, H J, Volzke, H, Nauck, M, Weiss, S, Pharoah, P D P, Dunning, A M, Dennis, J G, Thompson, D J, Michailidou, K, Easton, D F, Antoniou, A C, Tyrrell, J, Mihailov, E, Samani, N J, Zhou, K, Neville, M J, Metspalu, A, Palmer, C N A, Hall, I P, Strachan, D P, Deary, I J, Frayling, T M, Hayward, C, van der Harst, P, Zeggini, E, Munroe, P B, Jansson, J-H, Franks, P W, Deloukas, P, Caulfield, M J, Wain, L V & Tobin, M D 2019, ' Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ', Biological Psychiatry, vol. 85, no. 11, pp. 946-955 . https://doi.org/10.1016/j.biopsych.2018.11.024Test
Biological Psychiatry, 85(11), 946. Elsevier USA
Brazel, D M, Jiang, Y, Hughey, J M, Turcot, V, Zhan, X, Gong, J, Batini, C, Weissenkampen, J D, Liu, M, Surendran, P, Young, R, Barnes, D R, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Kontto, J, Perola, M, Caslake, M, de Craen, A J M, Trompet, S, Uria-Nickelsen, M, Malarstig, A, Reily, D F, Hoek, M, Vogt, T, Jukema, J W, Sattar, N, Ford, I, Packard, C J, Alam, D S, Majumder, A A S, di Angelantonio, E, Chowdhury, R, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrières, J, Kee, F, Kuulasmaa, K, Müller-Nurasyid, M, Veronesi, G, Virtamo, J, EPIC-CVD Consortium, Frossard, P, Nordestgaard, B R G, Saleheen, D, Danesh, J, Hammerschlag, A R, Posthuma, D, Spector, T, Stram, D O, Tobin, M D, Weir, D R, Kaprio, J, Abecasis, G R, Liu, D J, Vrieze, S & CHD Exome+ Consortium 2019, ' Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ', Biological Psychiatry, vol. 85, no. 11, pp. 946-955 . https://doi.org/10.1016/j.biopsych.2018.11.024Test
Biological psychiatry. Elsevier USA
CHD Exome+ Consortium & Consortium for Genetics of Smoking Behaviour 2019, ' Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ', Biological Psychiatry, vol. 85, no. 11, pp. 946-955 . https://doi.org/10.1016/j.biopsych.2018.11.024Testمصطلحات موضوعية: 0301 basic medicine, Nonsynonymous substitution, Genome-wide association study, 3124 Neurology and psychiatry, 0302 clinical medicine, DEPENDENCE, Genotype, Databases, Genetic, SEQUENCE VARIANTS, GWAS, Exome, Non-U.S. Gov't, Oligonucleotide Array Sequence Analysis, Genetics, RISK, HERITABILITY, Research Support, Non-U.S. Gov't, Smoking, ASSOCIATION, 3. Good health, ADH1B, Phenotype, Behavioral genetics, LOW-FREQUENCY, Alcohol, Heritability, Nicotine, Tobacco, Alcohol Drinking, Non-P.H.S, Single-nucleotide polymorphism, Biology, Research Support, Polymorphism, Single Nucleotide, N.I.H, 03 medical and health sciences, Research Support, N.I.H., Extramural, SDG 3 - Good Health and Well-being, Genetic variation, Journal Article, Humans, Genetic Predisposition to Disease, COMMON, Biological Psychiatry, 3112 Neurosciences, Genetic Variation, Extramural, MISSENSE VARIANTS, R1, Genetic architecture, 030104 developmental biology, U.S. Gov't, 030217 neurology & neurosurgery, Research Support, U.S. Gov't, Non-P.H.S, Genome-Wide Association Study
وصف الملف: application/pdf; text/plain; application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c4c6686918e3fb0cec91a0a7423b4f4Test
https://dare.uva.nl/personal/pure/en/publications/exome-chip-metaanalysis-fine-maps-causal-variants-and-elucidates-the-genetic-architecture-of-rare-coding-variants-in-smoking-and-alcohol-useTest(5b2dcbfd-0c32-47f3-869f-1ff60f676314).html -
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المؤلفون: Daniel R. Witte, Vanessa C. Guy, Hakon Hakonarson, Ivan Brandslund, Henrik Vestergaard, Rajashree Mishra, Olle Melander, Torben Hansen, Benjamin F. Voight, Annemari Käräjämäki, Fernando Ovalle, Asa Davis, R. David Leslie, Kenyaita M. Hodge, Stanley Schwartz, Lars G. Fritsche, Emma Ahlqvist, David J. Brillon, Didac Mauricio, Mette K. Andersen, Stephen Varvel, Kaixin Zhou, Bjørn Olav Åsvold, Mikael Åkerlund, Niels Grarup, Leif Groop, Philippe Froguel, Diana L. Cousminer, Alessandra Chesi, Adrian Vella, Jonathan P. Bradfield, Tiinamaija Tuomi, Ronald I. Harris, Elin Pettersen Sørgjerd, James Snyder, Carla J. Greenbaum, M. I. Hawa, Michael R. Rickels, Kurt Højlund, Allan Linneberg, Bernhard O. Boehm, Ewan R. Pearson, Oluf Pedersen, Richard E. Pratley, Nanette C. Schloot, Kamlesh Khunti, Henning Beck-Nielsen, Cecilia E. Kim, Valdemar Grill, Mette Wod, John T. Lonsdale, Knud Bonnet Yderstræde, Struan F.A. Grant
المساهمون: Centre of Excellence in Complex Disease Genetics, Institute for Molecular Medicine Finland, Diabetes and Obesity Research Program, Research Programs Unit, Department of Medicine, Clinicum, Endokrinologian yksikkö, University of Helsinki, HUS Abdominal Center, Lee Kong Chian School of Medicine (LKCMedicine)
المصدر: Groop, L C, Leslie, R D, Grant, S F A & Bone Mineral Density in Childhood Study 2018, ' First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes ', Diabetes Care, vol. 41, no. 11, pp. 2396-2403 . https://doi.org/10.2337/dc18-1032Test
Diabetes Care
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Cousminer, D L, Ahlqvist, E, Mishra, R, Andersen, M K, Chesi, A, Hawa, M I, Davis, A, Hodge, K M, Bradfield, J P, Zhou, K, Guy, V C, Akerlund, M, Wod, M, Fritsche, L G, Vestergaard, H, Snyder, J, Højlund, K, Linneberg, A, Käräjämäki, A, Brandslund, I, Kim, C E, Witte, D, Sørgjerd, E P, Brillon, D J, Pedersen, O, Beck-Nielsen, H, Grarup, N, Pratley, R E, Rickels, M R, Vella, A, Ovalle, F, Melander, O, Harris, R I, Varvel, S, Grill, V E R, Bone Mineral Density in Childhood Study, Hakonarson, H, Froguel, P, Lonsdale, J T, Mauricio, D, Schloot, N C, Khunti, K, Greenbaum, C J, Asvold, B O, Yderstræde, K B, Pearson, E R, Schwartz, S, Voight, B F, Hansen, T, Tuomi, T & Boehm, B O 2018, ' First genome-wide association study of latent autoimmune diabetes in adults reveals novel insights linking immune and metabolic diabetes ', Diabetes Care, vol. 41, no. 11, pp. 2396-2403 . https://doi.org/10.2337/dc18-1032Testمصطلحات موضوعية: Male, 0301 basic medicine, Research design, Endocrinology, Diabetes and Metabolism, Latent Autoimmune Diabetes in Adults/genetics, LOCI, Genome-wide association study, Type 2 diabetes, VARIANTS, PHENOTYPE, LADA, Glucose Intolerance/genetics, INDUCIBLE 6-PHOSPHOFRUCTO-2-KINASE, 0302 clinical medicine, Diabetes Mellitus, Type 1/genetics, INSULIN-RESISTANCE, Latent Autoimmune Diabetes, Middle Aged, 3. Good health, Diabetes Mellitus, Type 2/genetics, Female, Adult, Insulin/metabolism, 030209 endocrinology & metabolism, FREQUENCY, GENETIC ARCHITECTURE, Young Adult, 03 medical and health sciences, Insulin resistance, Genetic, Diabetes mellitus, Internal Medicine, medicine, Humans, Medicine [Science], Immune System Phenomena/genetics, Pathophysiology/Complications, TYPE-1, Aged, Advanced and Specialized Nursing, Autoimmune disease, Type 1 diabetes, business.industry, Case-control study, medicine.disease, 030104 developmental biology, Haplotypes, Case-Control Studies, 3121 General medicine, internal medicine and other clinical medicine, Immunology, ONSET, business, Genome-Wide Association Study
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http://hdl.handle.net/10138/306614Test -
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المؤلفون: Ewan R. Pearson, Adem Y. Dawed, Kaixin Zhou, Helle Krogh Pedersen
المصدر: Zhou, K, Pedersen, H K, Dawed, A Y & Pearson, E R 2016, ' Pharmacogenomics in diabetes mellitus : insights into drug action and drug discovery ', Nature Reviews. Endocrinology, vol. 12, no. 6, pp. 337-346 . https://doi.org/10.1038/nrendo.2016.51Test
مصطلحات موضوعية: 0301 basic medicine, Drug-Related Side Effects and Adverse Reactions, Pharmacogenomic Variants, endocrine system diseases, Gastrointestinal Diseases, Endocrinology, Diabetes and Metabolism, Drug development, 030209 endocrinology & metabolism, Type 2 diabetes, Pharmacology, Bioinformatics, Genome-wide association studies, Genomic analysis, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, SDG 3 - Good Health and Well-being, Diabetes mellitus, Drug Discovery, medicine, Edema, Humans, Hypoglycemic Agents, Hepatocyte Nuclear Factor 1-alpha, Heart Failure, Molecular medicine, business.industry, Systems Biology, nutritional and metabolic diseases, Type 2 Diabetes Mellitus, medicine.disease, Hypoglycemia, Metformin, HNF1A, Sulfonylurea Compounds, 030104 developmental biology, Diabetes Mellitus, Type 2, Pharmacogenetics, Pharmacogenomics, Thiazolidinediones, Chemical and Drug Induced Liver Injury, business, Genome-Wide Association Study
وصف الملف: application/pdf
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https://doi.org/10.1038/nrendo.2016.51Test -
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المؤلفون: Daniel M, Rotroff, Sook Wah, Yee, Kaixin, Zhou, Skylar W, Marvel, Hetal S, Shah, John R, Jack, Tammy M, Havener, Monique M, Hedderson, Michiaki, Kubo, Mark A, Herman, He, Gao, Josyf C, Mychaleckyi, Howard L, McLeod, Alessandro, Doria, Kathleen M, Giacomini, Ewan R, Pearson, Michael J, Wagner, John B, Buse, Alison A, Motsinger-Reif
المصدر: Diabetes. 67(7)
مصطلحات موضوعية: Male, STAT3 Transcription Factor, endocrine system diseases, Carboxypeptidases A, Pharmacogenomic Variants, nutritional and metabolic diseases, Genetics/Genomes/Proteomics/Metabolomics, Middle Aged, Polymorphism, Single Nucleotide, Metformin, Cohort Studies, Treatment Outcome, Diabetes Mellitus, Type 2, Double-Blind Method, Humans, Female, Eye Proteins, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::73a9fa6cc28c8b0d2d07ade13cc9bf57Test
https://pubmed.ncbi.nlm.nih.gov/29650774Test -
8
المؤلفون: Ian J. Deary, James Wilson, Caroline Hayward, Emanuele Trucco, Ozren Polasek, Abirami Veluchamy, Ellie Brown, Harry Campbell, Ewan R. Pearson, Alex S. F. Doney, Colin N. A. Palmer, Kaixin Zhou, Mirna Kirin, Peter K. Joshi, Devanjali Relan, Lucia Ballerini, Suraj S. Vaidya, Veronique Vitart, Bal Dhillon, Tom MacGillivray, Sarah E. Harris, Katherine Schraut
مصطلحات موضوعية: 0303 health sciences, medicine.medical_specialty, Locus (genetics), Genome-wide association study, Retinal, Anatomy, 030204 cardiovascular system & hematology, Biology, medicine.disease, Tortuosity, 3. Good health, Coronary artery disease, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, chemistry, Internal medicine, medicine, Cardiology, Retinal arteriolar tortuosity, SNP, 030304 developmental biology, Genetic association
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6b8809595e7aa72ae1e79db517895a1Test
https://doi.org/10.1101/121012Test -
9
المؤلفون: Kaixin Zhou, Adem Y. Dawed, Ewan R. Pearson, Adnan Ali, Paul W. Franks
المصدر: Diabetologia
مصطلحات موضوعية: 0301 basic medicine, Blood Glucose, medicine.medical_specialty, G6PC, Evidence-based practice, endocrine system diseases, Genotype, SLC2A4, Endocrinology, Diabetes and Metabolism, Type 2 diabetes, Endocrinology and Diabetes, Bioinformatics, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, Internal Medicine, Medicine, Humans, Gene, Glucose Transporter Type 4, business.industry, nutritional and metabolic diseases, Human physiology, medicine.disease, Text-mining, Metformin, 3. Good health, 030104 developmental biology, Diabetes Mellitus, Type 2, 030220 oncology & carcinogenesis, Gene-set enrichment, Endokrinologi och diabetes, Medical genetics, business, Algorithms, medicine.drug, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2dce77c41d355dc5942e1fd6d17eeceTest
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-142907Test -
10
المؤلفون: Kathleen M. Giacomini, Adriaan Kooy, Coen D.A. Stehouwer, MetGen Investigators, Valdis Pirags, Daniel M. Rotroff, Ivan Tkáč, Huan-Chieh Chien, Michael J. Wagner, Shiro Maeda, Federico Innocenti, Joline W.J. Beulens, Monique M. Hedderson, Eric L. Seiser, Sook Wah Yee, Bruno H. Stricker, Accord Investigators, Jozef Židzik, Leen M 't Hart, Rury R. Holman, Alison A. Motsinger-Reif, Jose C. Florez, Albert Hofman, Mattijs Out, Albert M. Levin, Christopher J. Groves, Michiaki Kubo, Longyang Wu, Catherine E. de Keyser, Ewan R. Pearson, Lisa Logie, Calum Sutherland, Sabina Semiz, Tanja Dujic, John S. Witte, Amanda J. Bennett, Kathleen A. Jablonski, Linda Zaharenko, Nienke van Leeuwen, Ling Chen, Dpp Investigators, Roger Tavendale, Ruth L. Coleman, Amber A. van der Heijden, Colin N. A. Palmer, Janis Klovins, Martin Javorský, Ron H.N. van Schaik, Mark I. McCarthy, L. Keoki Williams, Kaixin Zhou
المساهمون: Epidemiology, Clinical Chemistry, General practice, EMGO - Lifestyle, overweight and diabetes, Epidemiology and Data Science, MUMC+: HVC Pieken Maastricht Studie (9), RS: CARIM - R3.01 - Vascular complications of diabetes and the metabolic syndrome, Interne Geneeskunde, MUMC+: MA Interne Geneeskunde (3)
المصدر: Nature Genetics, 48(9), 1055
Nature Genetics, 48(9), 1055-+. Nature Publishing Group
Nature Genetics, 48(9), 1055-1059. Nature Publishing Group
Zhou, K, Yee, S W, Seiser, E L, van Leeuwen, N, Tavendalel, R, Bennett, A J, Groves, C J, Coleman, R L, van der Heijden, A A, Beulens, J W, de Keyser, C E, Zaharenkoll, L, Rotroff', D M, Out, M, Jablonski, K A, Chen, L, Javorsky, M, Zidzik, J, Levin, A M, Williams, L K, Dujic, T, Semiz, S, Kubo, M, Chien, H-C, Maeda, S, Witte, J S, Wu, L, Tkac, I, Kooy, A, van Schaik, R H N, Stehouwer, C D A, Logie, L, Sutherland, C, Klovins, J, Pirags, V, Hofman, A, Stricker, B H, Motsinger-Reif, A A, Wagner, M J, Innocenti, F, Hart, L M, Holman, R R, McCarthy, M I, Hedderson, M M, Palmer, C N A, Florez, J C, Giacomini, K M & Pearson, E R 2016, ' Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin ', Nature Genetics, vol. 48, no. 9, pp. 1055-1059 . https://doi.org/10.1038/ng.3632Testمصطلحات موضوعية: Blood Glucose, 0301 basic medicine, medicine.medical_specialty, endocrine system diseases, Genome-wide association study, Type 2 diabetes, Polymorphism, Single Nucleotide, White People, Body Mass Index, 03 medical and health sciences, Quantitative Trait, Heritable, Internal medicine, Diabetes mellitus, Genetics, medicine, Humans, Hypoglycemic Agents, Allele, Glycemic, Glucose Transporter Type 2, Glycated Hemoglobin, biology, Glucose transporter, nutritional and metabolic diseases, medicine.disease, Metformin, 3. Good health, 030104 developmental biology, Endocrinology, Diabetes Mellitus, Type 2, biology.protein, GLUT2, Genome-Wide Association Study, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92d8e457d5e17ebbdb7b48c533893063Test
https://hdl.handle.net/1887/96245Test