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1. Full Text New genetic loci link adipose and insulin biology to body fat distribution
by Shungin, Dmitry and Winkler, Thomas W and Croteau-Chonka, Damien C and Ferreira, Teresa and Locke, Adam E and Mägi, Reedik and Strawbridge, Rona J and Pers, Tune H and Fischer, Krista and Justice, Anne E and Workalemahu, Tsegaselassie and Wu, Joseph M. W and Buchkovich, Martin L and Heard-Costa, Nancy L and Roman, Tamara S and ng, Alexander W and Song, Ci and Gustafsson, Stefan and Day, Felix R and Esko, Tonu and Fall, Tove and Kutalik, Zoltán and Luan, Jian'an and Randall, Joshua C and Scherag, Ané and Vedantam, Sailaja and Wood, Anew R and Chen, Jin and Fehrmann, Rudolf and Karjalainen, Juha and Kahali, Bratati and Liu, Ching-Ti and Schmidt, Ellen M and Absher, Devin and Amin, Najaf and Anderson, Denise and Beekman, Marian and Bragg-Gresham, Jennifer L and Buyske, Steven and Demirkan, Ayse and Ehret, Georg B and Feitosa, Mary F and Goel, Anuj and Jackson, Anne U and Johnson, Toby and Kleber, Marcus E and PAGE Consortium and LifeLines Cohort Study and CARDIOGRAMplusC4D Consortium and MuTHER Consortium and ICBP and ADIPOGEN Consortium and CKDGen Consortium and GEFOS Consortium and Int Endogene Consortium and GENIE Consortium and MAGIC Investigators and ReproGen Consortium and GLGC and ADIPOGen Consortium and International Endogene Consortium and The PAGE Consortium and The International Endogene Consortium and The MAGIC Investigators and The ReproGen Consortium and The CKDGen Consortium and The ADIPOGen Consortium and The ICBP and The CARDIOGRAMplusC4D Consortium and The GENIE Consortium and The GLGC and The GEFOS Consortium and The MuTHER Consortium and The LifeLines Cohort Study and Göteborgs universitet and Gothenburg University and Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition and Sahlgrenska Academy and Centre for Bone and Arthritis Research and Sahlgrenska akademin and Institute of Medicine, Department of Internal Medicine and Clinical Nutrition
Nature (London), ISSN 0028-0836, 2015, Volume 518, Issue 7538, pp. 187 - U378
no | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Body Mass Index | Genome-Wide Association Study | Age Factors | Neovascularization, Physiologic - genetics | Epigenesis, Genetic | Humans | Male | Continental Population Groups - genetics | Sex Characteristics | Obesity - genetics | Europe - ethnology | Genome, Human - genetics | Adipose Tissue - metabolism | Insulin - metabolism | Models, Biological | Adipocytes - metabolism | Insulin Resistance - genetics | Polymorphism, Single Nucleotide - genetics | Female | Body Fat Distribution | Transcription, Genetic - genetics | Adipogenesis - genetics | Waist-Hip Ratio | Quantitative Trait Loci - genetics | Adipose tissues | Quantitative trait loci | Genetic research | Genetic aspects | Research | Metabolism | Health aspects | Studies | Body mass index | Genealogy | Body fat | Insulin resistance | Genetics | Genomes | Abdomen | Meta-analysis | Index Medicus | Life Sciences | Adipocytes/metabolism Adipogenesis/genetics Adipose Tissue/metabolism Age Factors Body Fat Distribution Body Mass Index Continental Population Groups/genetics Epigenesis, Genetic Europe/ethnology Female Genome, Human/genetics Genome-Wide Association Study Humans Insulin/metabolism Insulin Resistance/genetics Male Models, Biological Neovascularization, Physiologic/genetics Obesity/genetics Polymorphism, Single Nucleotide/genetics Quantitative Trait Loci/genetics Sex Characteristics Transcription, Genetic/genetics Waist-Hip Ratio | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Endokrinologi och diabetes | Public Health, Global Health, Social Medicine and Epidemiology | Endocrinology and Diabetes | Genetic: genetics | Insulin Resistance: genetics | Adipocytes: metabolism | Transcription | Medical and Health Sciences | Physiologic: genetics | Insulin: metabolism | Medicin och hälsovetenskap | Human: genetics | Obesity: genetics | Europe: ethnology | Adipose Tissue: metabolism | Single Nucleotide: genetics | Klinisk medicin | Clinical Medicine | Quantitative Trait Loci: genetics | Neovascularization | Genome | Adipogenesis: genetics | Continental Population Groups: genetics | Polymorphism
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2. Full Text Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci
by Jones, G.T and Tromp, G and Kuivaniemi, H and Gretarsdottir, S and Baas, A.F and Giusti, B and Strauss, E and Hof, F.N. van 't and Webb, T.R and Erdman, R and Ritchie, M.D and Elmore, J.R and Verma, A and Pendergrass, S and Kullo, I.J and Ye, Z and Peissig, P.L and Gottesman, O and Verma, S.S and Malinowski, J and Rasmussen-Torvik, L.J and Smelser, D.T and Crosslin, D.R and Anade, M. de and Ryer, E.J and McCarty, C.A and Bottinger, E.P and Pacheco, J.A and Crawford, D.C and Carrell, D.S and Gerhard, G.S and Franklin, D.P and Carey, D.J and Phillips, V.L and Williams, M.J and Wei, W and Blair, R and Hill, A.A and Vasudevan, T.M and Lewis, D.R and Thomson, I.A and Krysa, J and Hill, G.B and Roake, J and Merriman, T.R and Oszkinis, G and Galora, S and Saracini, C and Abbate, R and Pulli, R and Pratesi, C and Saratzis, A and Verissimo, A.R and Bumpstead, S and Badger, S.A and Clough, R.E and Cockerill, G and Hafez, H and Scott, D.J and Futers, T.S and Romaine, S.P and Bridge, K and Griffin, K.J and Bailey, M.A and Smith, A and Thompson, M.M and Bockxmeer, F.M. van and Matthiasson, S.E and Thorleifsson, G and Thorsteinsdottir, U and Blankensteijn, J.D and Teijink, J.A and Wijmenga, C and Graaf, J. de and Kiemeney, L.A.L.M and Lindholt, J.S and Hughes, A and Bradley, D.T and Stirrups, K and Golledge, J and Norman, P.E and Powell, J.T and Humphries, S.E and Hamby, S.E and Goodall, A.H and Nelson, C.P and Sakalihasan, N and Courtois, A and Ferrell, R.E and Eriksson, P and Folkersen, L and Franco-Cereceda, A and Eicher, J.D and Johnson, A.D and Betsholtz, C and Ruusalepp, A and Franzen, O and Schadt, E.E and Bjorkegren, J.L and et al and Cardiogenics Consortium and Int Consortium Blood Pressure
Circulation research, ISSN 0009-7330, 2017, Volume 120, Issue 2, pp. 341 - 353
computational biology | meta-analysis | genetics | aortic aneurysm abdominal | matrix metalloproteinases | genome-wide association study | Cardiac & Cardiovascular Systems | Peripheral Vascular Disease | Life Sciences & Biomedicine | Hematology | Cardiovascular System & Cardiology | Science & Technology | Aortic Aneurysm, Abdominal - diagnosis | Genetic Predisposition to Disease - genetics | Humans | Genetic Loci - genetics | Genome-Wide Association Study - trends | Aortic Aneurysm, Abdominal - genetics | Genetic Variation - genetics | Aortic Aneurysm, Abdominal - epidemiology | Genetic Predisposition to Disease - epidemiology | Genome-Wide Association Study - methods | Diabetes mellitus | Coronary artery | Aneurysm | Aneurysms | Lipids | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Risk factors | Gelatinase B | Chromosome 1 | Interleukin 6 | Interleukin 6 receptors | Aorta | Lipoprotein (low density) receptors | Blood pressure | Chromosome 13 | Heritability | Cardiovascular diseases | Heart diseases | Index Medicus | 10082 | Clinical Track | 10084 | 10185 | 10195 | aortic aneurysm, abdominal | 10014 | Medicin och hälsovetenskap
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3. Full Text Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
by Okbay, Aysu and Baselmans, B.M.L and Neve, Jan-Emmanuel and Turley, Patrick and Nivard, Michel and Fontana, M.A and Meddens, Fleur and Karlsson Linner, Richard and Rietveld, Niels and Derringer, J and Gratten, Jacob and Lee, James J and Liu, J.Z and Vlaming, Ronald and SAhluwalia, T and Buchwald, J and Cavadino, Alana and Frazier-Wood, Alexis C and Furlotte, N.A and Garfield, V and Geisel, M.H and Gonzalez, Juan R and Haitjema, S and Karlsson, Robert and Der Laan, S.W and Ladwig, Karl-Heinz and Lahti, Jari and Lee, Sven and Lind, Penelope and Liu, T and Matteson, L and Mihailov, Evelin and Miller, Mike and CMinica, C and MNolte, I and Mook-Kanamori, Dennis and Most, Peter and Oldmeadow, Christopher and Qian, Yong and Raitakari, Olli and Rawal, Rajesh and Realo, Anu and Rueedi, R and Schmidt, B and Smith, Albert Vernon and Stergiakouli, Evangelia and Tanaka, Toshiko and Taylor, Kent and Wedenoja, J and Wellmann, J and Westra, Harm-Jan and MWillems, S and Zhao, W and LifeLines Cohort Study
Nature genetics, ISSN 1061-4036, 06/2016, Volume 48, Issue 6, pp. 624 - 633
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Neuroticism | Genome-Wide Association Study | Phenotype | Humans | Bayes Theorem | Anxiety Disorders - genetics | Polymorphism, Single Nucleotide | Depression - genetics | Genome-wide association studies | Genetic variation | Depression, Mental | Genetic aspects | Identification and classification | Methods | Risk factors | Studies | Psychological aspects | Consortia | Social sciences | Quality control | Personality | Genomes | Behavior | Mental depression | Statistics | Epidemiology | Meta-analysis | Index Medicus | Quantitative Finance | Medicin och hälsovetenskap
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4. Full Text Defining the role of common variation in the genomic and biological architecture of adult human height
by Wood, Anew R and Esko, Tonu and Yang, Jian and Vedantam, Sailaja and Pers, Tune H and Gustafsson, Stefan and Chu, Auey Y and Estrada, Karol and Luan, Jian'an and Kutalik, Zoltán and Amin, Najaf and Buchkovich, Martin L and Croteau-Chonka, Damien C and Day, Felix R and Duan, Yanan and Fall, Tove and Fehrmann, Rudolf and Ferreira, Teresa and Jackson, Anne U and Karjalainen, Juha and Lo, Ken Sin and Locke, Adam E and Mägi, Reedik and Mihailov, Evelin and Porcu, Eleonora and Randall, Joshua C and Scherag, Ané and Vinkhuyzen, Anna A. E and Westra, Harm-Jan and Winkler, Thomas W and Workalemahu, Tsegaselassie and Zhao, Jing Hua and Absher, Devin and Albrecht, Eva and Anderson, Denise and Baron, Jeffrey and Beekman, Marian and Demirkan, Ayse and Ehret, Georg B and Feenstra, Bjarke and Feitosa, Mary F and Fischer, Krista and Fraser, Ross M and Goel, Anuj and Gong, Jian and Justice, Anne E and Kanoni, Stavroula and van der Velde, Nathalie and Hovingh, G. Kees and Kastelein, John J. P and PAGE Consortium and MIGen Consortium and LifeLines Cohort Study and Elect Med Records & Genom eMERGE C and Electronic Medical Records and Genomics (eMEMERGEGE) Consortium and PAGEGE Consortium and The MIGen Consortium and The PAGE Consortium and The Electronic Medical Records and Genomics (eMERGE) Consortium and The LifeLines Cohort Study and Göteborgs universitet and Gothenburg University and Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition and Sahlgrenska Academy and Centre for Bone and Arthritis Research and Sahlgrenska akademin and Institute of Medicine, Department of Internal Medicine and Clinical Nutrition
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 11, pp. 1173 - 1186
no | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetics, Population | European Continental Ancestry Group - genetics | Analysis of Variance | Oligonucleotide Array Sequence Analysis | Humans | Polymorphism, Single Nucleotide - genetics | Adult | Genetic Variation - genetics | Genome-Wide Association Study - methods | Body Height - genetics | Stature | Genome-wide association studies | Genetic variation | Genes | Genetic aspects | Research | Identification and classification | Studies | Genomes | Genealogy | Architecture | Statistics | Index Medicus | Medicinsk genetik | Medical Genetics | GENETIC-VARIATION | SNPS | MUTATIONS | COMPLEX TRAITS | HERITABILITY | Clinical Medicine | Endokrinologi och diabetes | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes | complex traits | mutations | snps | genetic-variation | heritability
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5. Full Text Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
by Willems, Sara M and Zhao, Wei and Robertson, Neil R and Kitajima, Hidetoshi and Taliun, Daniel and Rayner, N. William and Guo, Xiuqing and Lu, Yingchang and Hu, Yao and Huo, Shaofeng and Cook, James P and Flannick, Jason and Grarup, Niels and Trubetskoy, Vassily Vladimirovich and Marten, Jonathan and An, Ping and Ligthart, Symen and Malerba, Giovanni and Tajes, Juan Fernandez and Lecoeur, Cecile and Bielak, Lawrence F and Graff, Marielisa and Highland, Heather M and Liu, Dajiang J and Warren, Helen R and Brody, Jennifer A and Chen, Yii-Der Ida and Christensen, Cramer and Eastwood, Sophie V and Giedraitis, Vilmantas and Grove, Megan L and de Haan, Hugoline G and Tybjaerg-Hansen, Anne and Jorgensen, Marit E and Jorgensen, Torben and Kim, Sung Soo and Kriebel, Jennifer and Lall, Kristi and Lehne, Benjamin and Li, Huaixing and Mamakou, Vasiliki and McKean-Cowdin, Roberta and Nadkarni, Girish and Peyser, Patricia A and Rathmann, Wolfgang and Rich, Stephen S and Rolandsson, Olov and Schonherr, Sebastian and Taylor, Kent D and Teslovich, Tanya M and Tin, Adrienne and Yao, Jie and Amouyel, Philippe and Collins, Francis S and Deloukas, Panos and Florez, Jose C and Heckbert, Susan R and Howson, Joanna M. M and Ingelsson, Martin and Kathiresan, Sekar and Kuusisto, Johanna and Langenberg, Claudia and Meitinger, Thomas and Melander, Olle and Morris, Andrew D and Orho-Melander, Marju and Owen, Katharine R and Province, Michael A and Ridker, Paul M and Sheu, Wayne H. -H and Sladek, Rob and Smith, Blair H and Willer, Cristen J and Butterworth, Adam S and Chambers, John Campbell and Chasman, Daniel I and Danesh, John and van Duijn, Cornelia and Franco, Oscar H and Hattersley, Andrew T and Hayward, Caroline and Ingelsson, Erik and Karpe, Fredrik and Kooner, Jaspal Singh and Kuulasmaa, Kari and Lin, Xu and Loos, Ruth J. F and Palmer, Colin N. A and Rauramaa, Rainer and Soranzo, Nicole and Stefansson, Kari and Thorsteinsdottir, Unnur and Tuomi, Tiinamaija and Wilson, James G and Zeggini, Eleftheria and Goodarzi, Mark O and Meigs, James B and Saleheen, Danish and Morris, Andrew P and McCarthy, Mark I and MAGIC Consortium and ExomeBP Consortium and GIANT Consortium
Nature genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 559 - 571
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Diabetes Mellitus, Type 2 - classification | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Diabetes Mellitus, Type 2 - genetics | Humans | Male | Genome-Wide Association Study - statistics & numerical data | Genetic Variation | Diabetes Mellitus, Type 2 - physiopathology | Alleles | Female | Chromosome Mapping - statistics & numerical data | Whole Exome Sequencing - statistics & numerical data | Type 2 diabetes | Genome-wide association studies | Usage | Genetic aspects | Risk factors | Exome sequencing | Index Medicus
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