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consortia (2) 2
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1. Full Text Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
by Surenan, P and nos, Fotios and Young, Robin and Warren, Helen and Cook, J.P and Manning, Alisa and Grarup, Niels and Sim, Xueling and Barnes, Daniel and Witkowska, Ewa and Staley, James R and Tragante, Vinicius and Tukiainen, Taru and Yaghootkar, Hanieh and Masca, N and Freitag, Christine and Ferreira, Teresa and Giannakopoulou, Olga and Tinker, A and Harakalova, Magdalena and Mihailov, Evelin and Liu, C and Kraja, Aldi and Nielsen, Sune and Rasheed, Asif and Samuel, Maria and Zhao, Wei and Bonnycastle, Lori and Jackson, Anne and Narisu, Narisu and Swift, Amy and Southam, Lorraine and Marten, Jonathan and Huyghe, Jeroen R and Stancáková, Alena and Fava, Cristiano and Ohlsson, T and Matchan, Angela and Stirrups, Kathy and Bork-Jensen, Jette and Gjesing, Anette and Kontto, J and Perola, Markus and Shaw-Hawkins, Sue and Havulinna, Aki and Zhang, H and Donnelly, Louise and Groves, Christopher and Rayner, Nigel William and Neville, Matthew and Robertson, Neil and Yiorkas, A.M and Herzig, K.H and Kajantie, Eero and Zhang, Weihua and Willems, Sara and Lannfelt, Lars and Malerba, Giovanni and Soranzo, Nicole and Trabetti, Elisabetta and Verweij, Niek and Evangelou, Evangelos and Moayyeri, Alireza and Vergnaud, A.-C and Nelson, Christopher P and Poveda, A and Varga, Tibor V and Caslake, Muriel and De Craen, Anton J. M and Trompet, Stella and Luan, Jian'An and Scott, Robert and Harris, Sarah and Liewald, David C and Marioni, Riccardo and Menni, Cristina and Farmaki, Aliki-Eleni and Hallmans, Göran and Renström, Frida and Huffman, Jennifer and Hassinen, M and Burgess, Stephen and Vasan, R.S and Felix, Janine and Uria-Nickelsen, M and Mälarstig, Anders and Reilly, D.F and Hoek, M and Vogt, T.F and Lin, Honghuang and Lieb, Wolfgang and Traylor, Matthew and Markus, Hugh and Highland, Heather and Justice, Anne and Marouli, Eirini and Lindström, Jaana and Uusitupa, Matti and Komulainen, Pirjo and Lakka, Timo and ... and Understanding Soc Sci Grp and Wellcome Trust Case Control Consor and GoT2DGenes Consortium and ExomeBP Consortium and CHD Exome Consortium and Giant Consortiumm and CHARGE Exome Chip Blood Pressure C and EPIC-CVD Consortium and CHARGE Heart Failure Consortiumm and EchoGen Consortiumm and EPIC-InterAct Consortium and Lifelines Cohort Study and Metastroke Consortiumm and T2D-GENES Consortium and Wellcome Trust Case Control Consortium and Understanding Society Scientific Group and EchoGen Consortium and CHD Exome+ Consortium and CHARGE+ Exome Chip Blood Pressure Consortium and CHARGE-Heart Failure Consortium and METASTROKE Consortium and GIANT Consortium
Nature genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1151 - 1161
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Variation | Genetic Predisposition to Disease | Genome-Wide Association Study | Blood Pressure - genetics | Humans | Genotype | Hypertension - genetics | Studies | Hypertension | Consortia | Datasets | Genealogy | Quality control | Cardiovascular disease | Blood pressure | Genomes | Meta-analysis | Index Medicus | Kardiologi | Medicinsk genetik | Basic Medicine | Medical Genetics | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin
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2. Full Text New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
by Shrine, Nick and Guyatt, Anna L and Erzurumluoglu, A. Mesut and Jackson, Victoria E and Hobbs, Brian D and Melbourne, Carl A and Batini, Chiara and Fawcett, Katherine A and Song, Kijoung and Sakornsakolpat, Phuwanat and Li, Xingnan and Boxall, Ruth and Reeve, Nicola F and Obeidat, Ma’en and Zhao, Jing Hua and Wielscher, Matthias and Weiss, Stefan and Kentistou, Katherine A and Cook, James P and Sun, Benjamin B and Zhou, Jian and Hui, Jennie and Karrasch, Stefan and Imboden, Medea and Harris, Sarah E and Marten, Jonathan and Enroth, Stefan and Kerr, Shona M and Surakka, Ida and Vitart, Veronique and Lehtimäki, Terho and Allen, Richard J and Bakke, Per S and Beaty, Terri H and Bleecker, Eugene R and Bossé, Yohan and Brandsma, Corry-Anke and Chen, Zhengming and Crapo, James D and Danesh, John and DeMeo, Dawn L and Dudbridge, Frank and Ewert, Ralf and Gieger, Christian and Gulsvik, Amund and Hansell, Anna L and Hao, Ke and Hoffman, Joshua D and Hokanson, John E and Homuth, Georg and Joshi, Peter K and Joubert, Philippe and Langenberg, Claudia and Li, Xuan and Li, Liming and Lin, Kuang and Lind, Lars and Locantore, Nicholas and Luan, Jian’an and Mahajan, Anubha and Maranville, Joseph C and Murray, Alison and Nickle, David C and Packer, Richard and Parker, Margaret M and Paynton, Megan L and Porteous, David J and Prokopenko, Dmitry and Qiao, Dandi and Rawal, Rajesh and Runz, Heiko and Sayers, Ian and Sin, Don D and Smith, Blair H and Soler Artigas, María and Sparrow, David and Tal-Singer, Ruth and Timmers, Paul R. H. J and Van den Berge, Maarten and Whittaker, John C and Woodruff, Prescott G and Yerges-Armstrong, Laura M and Troyanskaya, Olga G and Raitakari, Olli T and Kähönen, Mika and Polašek, Ozren and Gyllensten, Ulf and Rudan, Igor and Deary, Ian J and Probst-Hensch, Nicole M and Schulz, Holger and James, Alan L and Wilson, James F and Stubbe, Beate and Zeggini, Eleftheria and Jarvelin, Marjo-Riitta and Wareham, Nick and Silverman, Edwin K and Hayward, Caroline and Morris, Andrew P and ... and Understanding Soc Sci Grp and Understanding Society Scientific Group
Nature genetics, ISSN 1061-4036, 03/2019, Volume 51, Issue 3, pp. 481 - 493
LOCI | GWAS | VARIANTS | HERITABILITY | GENOME-WIDE ASSOCIATION | COPD | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Risk Factors | Male | Smoking - genetics | Lung - physiopathology | Case-Control Studies | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Female | Aged | Genome-Wide Association Study - methods | Pulmonary Disease, Chronic Obstructive - genetics | Respiratory function | Lung diseases | Genomes | Gene expression | Studies | Consortia | Pathways | Obstructive lung disease | New combinations | Quality control | Chronic obstructive pulmonary disease | Health risk assessment | Smoking | Index Medicus
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