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genetics & heredity (3) 3
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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 and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1151 - 1161
textabstractHigh blood pressure is a major risk factor for cardiovascular disease and premature death. However, there is limited knowledge on specific causal... 
HEART | RISK-FACTORS | PLASMA-LEVELS | GENETICS & HEREDITY | CARDIOVASCULAR-DISEASE | GENE-CENTRIC ARRAY | AGING RESEARCH | LOCI | IDENTIFICATION | CHARGE | GENOME-WIDE ASSOCIATION | 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 | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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2. Full Text Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
by Wain, Louise V and Shrine, Nick R. G and Artigas, Maria Soler and Erzurumluoglu, A Mesut and Noyvert, Boris and Bossini-Castillo, Lara and Obeidat, Ma'en and Henrys, Amanda P and Portelli, Michael A and Hall, Robert J and Billington, Charlotte K and Rimington, Tracy L and Fenech, Anthony G and John, Catherine and Blake, Tineka and Jackson, Victoria E and Allen, Richard J and Prins, Bram P and Campbell, Archie and Porteous, David J and Jarvelin, Marjo-Riitta and Wielscher, Matthias and Jamess, Alan L and Hui, Jennie and Wareham, Nicholas J and Zhao, Jing Hua and Wilson, James F and Joshi, Peter K and Stubbe, Beate and Rawal, Rajesh and Schulz, Holger and Imboden, Medea and Probst-Hensch, Nicole M and Karrasch, Stefan and Gieger, Christian and Deary, Ian J and Harris, Sarah E and Marten, Jonathan and Rudan, Igor and Enroth, Stefan and Gyllensten, Ulf and Kerr, Shona M and Polasek, Ozren and Kahonen, Mika and Surakka, Ida and Vitart, Veronique and Hayward, Caroline and Lehtimaki, Terho and Raitakari, Olli T and Evans, David M and Henderson, A. John and Pennell, Craig E and Wang, Carol A and Sly, Peter D and Wan, Emily S and Busch, Robert and Hobbs, Brian D and Litonjua, Augusto and Sparrow, David W and Gulsvik, Amund and Bakke, Per S and Crapo, James D and Beaty, Terri H and Hansel, Nadia N and Mathias, Rasika A and Ruczinski, Ingo and Barnes, Kathleen C and Bosse, Yohan and Joubert, Philippe and van den Berge, Maarten and Brandsma, Corry-Anke and Pare, Peter D and Sin, Don and Nickle, David C and Hao, Ke and Gottesman, Omri and Dewey, Frederick E and Bruse, Shannon E and Carey, David J and Kirchner, H Lester and Jonsson, Stefan and Thorleifsson, Gudmar and Jonsdottir, Ingileif and Gislason, Thorarinn and Stefansson, Kari and Schurmann, Claudia and Nadkarni, Girish N and Bottinger, Erwin P and Loos, Ruth J. F and Walters, Robin G and Chen, Zhengming and Millwood, Iona Y and Vaucher, Julien and Kurmi, Om P and Li, Liming and Hansell, Anna L and Brightling, Chris and Zeggini, Eleftheria and Cho, Michael H and Silverman, Edwin K and ... and Geisinger-Regeneron DiscovEHR and Understanding Soc Sci Grp and Understanding Society Scientific Group and Geisinger-Regeneron DiscovEHR Collaboration and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 03/2017, Volume 49, Issue 3, pp. 416 - 425
Chronic obstructive pulmonary disease (COPD) is characterized by reduced lung function and is the third leading cause of death globally. Through genome-wide... 
VARIANTS | GENETICS | SUSCEPTIBILITY | FAM13A | GENETICS & HEREDITY | RISK | EPIDEMIOLOGY | HISTORY | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Risk Factors | Genetic Loci - genetics | Male | Lung - physiopathology | Asthma - genetics | Epigenesis, Genetic - genetics | Alleles | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | Genome-Wide Association Study - methods | Pulmonary Disease, Chronic Obstructive - genetics | Quantitative trait loci | Molecular targeted therapy | Lung diseases, Obstructive | Care and treatment | Innovations | Development and progression | Genetic aspects | Health aspects | Studies | Chronic obstructive pulmonary disease | Genomes | Health risk assessment | Medical and Health Sciences | Medicin och hälsovetenskap
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3. Full Text Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
by Turcot, Valérie and Lu, Yingchang and Highland, Heather M and Schurmann, Claudia and Justice, Anne E and Fine, Rebecca S and Bradfield, Jonathan P and Esko, Tõnu and Giri, Ayush and Graff, Mariaelisa and Guo, Xiuqing and Hendricks, Audrey E and Karaderi, Tugce and Lempradl, Adelheid and Locke, Adam E and Mahajan, Anubha and Marouli, Eirini and Sivapalaratnam, Suthesh and Young, Kristin L and Alfred, Tamuno and Feitosa, Mary F and Masca, Nicholas G. D and Manning, Alisa K and Medina-Gomez, Carolina and Mudgal, Poorva and Ng, Maggie C. Y and Reiner, Alex P and Vedantam, Sailaja and Willems, Sara M and Winkler, Thomas W and Abecasis, Gonçalo and Aben, Katja K and Alam, Dewan S and Alharthi, Sameer E and Allison, Matthew and Amouyel, Philippe and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Bang, Lia E and Barroso, Inês and Bastarache, Lisa and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boehnke, Michael and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Brumat, Marco and Burt, Amber A and Butterworth, Adam S and Campbell, Peter T and Cappellani, Stefania and Carey, David J and Catamo, Eulalia and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der I and Chowdhury, Rajiv and Christensen, Cramer and Chu, Audrey Y and Cocca, Massimiliano and Cook, James P and Corley, Janie and Corominas Galbany, Jordi and Cox, Amanda J and Crosslin, David S and Cuellar-Partida, Gabriel and D'Eustacchio, Angela and Danesh, John and Davies, Gail and Bakker, Paul I. W and Groot, Mark C. H and Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and Heijer, Martin and Hollander, Anneke I and Ruijter, Hester M and Dennis, Joe G and Denny, Josh C and Angelantonio, Emanuele and Drenos, Fotios and Du, Mengmeng and Dubé, Marie-Pierre and Dunning, Alison M and Easton, Douglas F and Edwards, Todd L and ... and Chd Exome Consortium and EPIC InterAct Consortium and Global Lipids Genetic Consortium and GoT2D Genes Consortium and MAGIC Investigators and Understanding Soc Sci Grp and ReproGen Consortium and Interval Study and Epic-Cvd Consortium and ExomeBP Consortium and T2D-Genes Consortium and INTERVAL Study and EPIC-CVD Consortium and EPIC InterAct Consortium and CHD Exome+ Consortium and Understanding Society Scientific Group and The MAGIC Investigators and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Nature Genetics, ISSN 1061-4036, 01/2018, Volume 50, Issue 1, pp. 26 - 35
Genome-wide association studies (GWAS) have identified >250 loci for body mass index (BMI), implicating pathways related to neuronal biology. Most GWAS loci... 
GLUCOSE-HOMEOSTASIS | DONEPEZIL 23 MG | AMP ISOFORM 1 | SEVERE ALZHEIMERS-DISEASE | GENETICS & HEREDITY | HYPOTHALAMIC AMPK | MELANOCORTIN-4 RECEPTOR GENE | FRAMESHIFT MUTATION | INSULIN SENSITIVITY | CODING VARIANTS | GENOME-WIDE ASSOCIATION | Energy intake | Obesity | Therapeutic applications | Genes | Energy expenditure | Melanocortin MC4 receptors | Stop codon | Genomes | Biology | Gene expression | Loci | Meta-analysis | Carriers | Proteins | Body mass index | Pathways | Gene frequency | Body mass | Coding | Body size | Bioinformatics | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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