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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: Sook Wah Yee, Skylar W. Marvel, Hetal Shah, Tammy M. Havener, Michiaki Kubo, MetGen Investigators, John B. Buse, Accord, He Gao, Alessandro Doria, Kaixin Zhou, Monique M. Hedderson, Ewan R. Pearson, Mark A. Herman, ACCORDion Investigators, John Jack, Josyf C. Mychaleckyi, Kathleen M. Giacomini, Howard L. McLeod, Michael J. Wagner, Alison A. Motsinger-Reif, Daniel M. Rotroff
المصدر: Diabetes. 67:1428-1440
مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, PRPF31, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Type 2 diabetes, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Diabetes mellitus, Internal Medicine, Medicine, business.industry, Genetic variants, nutritional and metabolic diseases, Total body, medicine.disease, 3. Good health, Metformin, Clinical trial, 030104 developmental biology, Endocrinology, 030220 oncology & carcinogenesis, Knockout mouse, business, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::a0f29570193e2168220a458852d8f26bTest
https://doi.org/10.2337/db17-1164Test -
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المؤلفون: Ewan R. Pearson, Christopher Jennison, Kaixin Zhou, Louise A. Donnelly, Paul W. Franks, Alex S. F. Doney
المصدر: Diabetologia
Donnelly, L A, Zhou, K, Doney, A S F, Jennison, C, Franks, P W & Pearson, E R 2018, ' Rates of glycaemic deterioration in a real-world population with type 2 diabetes ', Diabetologia, vol. 61, no. 3, pp. 607-615 . https://doi.org/10.1007/s00125-017-4519-5Testمصطلحات موضوعية: Blood Glucose, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, 030209 endocrinology & metabolism, Type 2 diabetes, Endocrinology and Diabetes, 030204 cardiovascular system & hematology, Coefficient of failure, Article, Body Mass Index, Cohort Studies, 03 medical and health sciences, Elderly, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Diabetes mellitus, Internal Medicine, Electronic Health Records, Humans, Hypoglycemic Agents, Insulin, Medicine, Intensive care medicine, Electronic medical records, Observational, Aged, Glycated Hemoglobin, business.industry, Human physiology, World population, Middle Aged, medicine.disease, 3. Good health, Diabetes Mellitus, Type 2, Endokrinologi och diabetes, Female, Observational study, business, Glycaemic deterioration
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07ef5f028b627c4c07e9149ce119369cTest
https://doi.org/10.1007/s00125-017-4519-5Test -
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المؤلفون: Roger Tavendale, Colin N. A. Palmer, Ewan R. Pearson, Kaixin Zhou, Tanja Dujic
المصدر: Diabetes Care. 39:1896-1901
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Serotonin uptake, Genotype, Gastrointestinal Diseases, Endocrinology, Diabetes and Metabolism, 030209 endocrinology & metabolism, Article, Intestinal absorption, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Diabetes mellitus, Internal Medicine, medicine, Humans, Hypoglycemic Agents, Alleles, Serotonin transporter, Aged, Serotonin Plasma Membrane Transport Proteins, Advanced and Specialized Nursing, Polymorphism, Genetic, biology, business.industry, Odds ratio, Middle Aged, medicine.disease, Metformin, 3. Good health, 030104 developmental biology, Endocrinology, Diabetes Mellitus, Type 2, biology.protein, Female, Serotonin, business, Octamer Transcription Factor-1, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a7bbd70935d75cc2165f29d3b5a1d79Test
https://doi.org/10.2337/dc16-0706Test -
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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
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a67a805e834eac5811cf022a2340e8eTest
http://hdl.handle.net/10138/306614Test -
7
المؤلفون: Simone P. Rauh, Julia C. Stingl, Neil Robertson, Leen M 't Hart, Adem Y. Dawed, Anubha Mahajan, Petra J. M. Elders, Paul W. Franks, Nienke van Leeuwen, Mark I. McCarthy, Reinhard W. Holl, Ewan R. Pearson, Robert W. Koivula, Angus G. Jones, Kaixin Zhou
مصطلحات موضوعية: 0303 health sciences, medicine.medical_specialty, Organic cation transport proteins, biology, business.industry, Patient characteristics, 030209 endocrinology & metabolism, Type 2 diabetes, medicine.disease, 3. Good health, Metformin, Discontinuation, 03 medical and health sciences, Plasma membrane monoamine transporter, 0302 clinical medicine, Endocrinology, Internal medicine, Concomitant, medicine, biology.protein, business, 030304 developmental biology, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e38473521fa34cd838e9bd6b882f89aTest
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المؤلفون: Rajesh V. Thakker, Paul J. Newey, Jonathan Berg, Kaixin Zhou, Colin N. A. Palmer
المصدر: Journal of the Endocrine Society
مصطلحات موضوعية: 0301 basic medicine, Nonsynonymous substitution, Parathyroid, Bone, and Mineral Metabolism, Endocrinology, Diabetes and Metabolism, Population, 030209 endocrinology & metabolism, Context (language use), Disease, Biology, germline, ExAC, genetic testing, 03 medical and health sciences, 0302 clinical medicine, medicine, single nucleotide variant, penetrance, education, Exome, Clinical Research Articles, Genetic testing, Genetics, education.field_of_study, Endocrine disease, medicine.diagnostic_test, medicine.disease, Penetrance, 3. Good health, 030104 developmental biology, mutation
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e41e8fa2e8c5f832ee310742f28b38eTest
https://pubmed.ncbi.nlm.nih.gov/29308445Test -
9
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 -
10
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