The CoLaus study: a population-based study to investigate the epidemiology and genetic determinants of cardiovascular risk factors and metabolic syndrome von Firmann, Mathieu, Mayor, Vladimir, Vidal, Pedro Marques, Bochud, Murielle, Pécoud, Alain, Hayoz, Daniel, Paccaud, Fred, Preisig, Martin, Song, Kijoung S, Yuan, Xin, Danoff, Theodore M, Stirnadel, Heide A, Waterworth, Dawn, Mooser, Vincent, Waeber, Gérard, Vollenweider, Peter

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An 18-kDa Translocator Protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28 von Owen, David R, Yeo, Astrid J, Gunn, Roger N, Song, Kijoung, Wadsworth, Graham, Lewis, Andrew, Rhodes, Chris, Pulford, David J, Bennacef, Idriss, Parker, Christine A, StJean, Pamela L, Cardon, Lon R, Mooser, Vincent E, Matthews, Paul M, Rabiner, Eugenii A, Rubio, Justin P

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Population-Based Genome-wide Association Studies Reveal Six Loci Influencing Plasma Levels of Liver Enzymes von Yuan, Xin, Waterworth, Dawn, Perry, John R.B., Lim, Noha, Song, Kijoung, Chambers, John C., Zhang, Weihua, Vollenweider, Peter, Stirnadel, Heide, Johnson, Toby, Bergmann, Sven, Beckmann, Noam D., Li, Yun, Ferrucci, Luigi, Melzer, David, Hernandez, Dena, Singleton, Andrew, Scott, James, Elliott, Paul, Waeber, Gerard, Cardon, Lon, Frayling, Timothy M., Kooner, Jaspal S., Mooser, Vincent

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A powerful method of combining measures of association and Hardy-Weinberg disequilibrium for fine-mapping in case-control studies von Song, Kijoung, Elston, Robert C.

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Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank von Fawcett, Katherine A., Song, Kijoung, Qian, Guoqing, Farmaki, Aliki-Eleni, Packer, Richard, John, Catherine, Shrine, Nick, Granell, Raquel, Ring, Sue, Timpson, Nicholas J., Yerges-Armstrong, Laura M., Eastell, Richard, Wain, Louise, Scott, Robert A., Tobin, Martin D., Hall, Ian P.

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Carriage of the V279F null allele within the gene encoding Lp-PLA₂ is protective from coronary artery disease in South Korean males von Jang, Yangsoo, Waterworth, Dawn, Lee, Jong-Eun, Song, Kijoung, Kim, Sujin, Kim, Hyo-Soo, Park, Kyung Woo, Cho, Hyun-Jai, Oh, Il-Young, Park, Jeong Euy, Lee, Bok-Soo, Ku, Hyo Jeong, Shin, Dong-Jik, Lee, Jong Ho, Jee, Sun Ha, Han, Bok-Ghee, Jang, Hye-Yoon, Cho, Eun-Young, Vallance, Patrick, Whittaker, John, Cardon, Lon, Mooser, Vincent

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Urotensin-II system in genetic control of blood pressure and renal function von Debiec, Radoslaw, Christofidou, Paraskevi, Denniff, Matthew, Bloomer, Lisa D, Bogdanski, Pawel, Wojnar, Lukasz, Musialik, Katarzyna, Charchar, Fadi J, Thompson, John R, Waterworth, Dawn, Song, Kijoung, Vollenweider, Peter, Waeber, Gerard, Zukowska-Szczechowska, Ewa, Samani, Nilesh J, Lambert, David, Tomaszewski, Maciej

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Higher Offspring Survival among Tibetan Women with High Oxygen Saturation Genotypes Residing at 4,000 m von Beall, Cynthia M., Song, Kijoung, Elston, Robert C., Goldstein, Melvyn C.

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FGF21 signalling pathway and metabolic traits - genetic association analysis von KAESS, Bernhard M, BARNES, Timothy A, ZUKOWSKA-SZCZECHOWSKA, Ewa, SAMANI, Nilesh J, HENGSTENBERG, Christian, TOMASZEWSKI, Maciej, STARK, Klaus, CHARCHAR, Fadi J, WATERWORTH, Dawn, KIJOUNG SONG, WANG, William Ys, VOLLENWEIDER, Peter, WAEBER, Gerard, MOOSER, Vincent

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Abstract 1284: Identification of potential cancer regulatory germline single-nucleotide polymorphisms in the non-coding genome von Kulkarni, Diptee A., Song, Kijoung, Guo, Karl

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New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries von Shrine, Nick, Guyatt, Anna L., Erzurumluoglu, A. Mesut, Jackson, Victoria E., Hobbs, Brian D., Melbourne, Carl A., Batini, Chiara, Fawcett, Katherine A., Song, Kijoung, Sakornsakolpat, Phuwanat, Boxall, Ruth, Reeve, Nicola F., Obeidat, Ma’en, Zhao, Jing Hua, Wielscher, Matthias, Weiss, Stefan, Kentistou, Katherine A., Cook, James P., Sun, Benjamin B., Zhou, Jian, Hui, Jennie, Karrasch, Stefan, Imboden, Medea, Harris, Sarah E, Marten, Jonathan, Enroth, Stefan, Kerr, Shona M., Surakka, Ida, Vitart, Veronique, Lehtimäki, Terho, Bakke, Per S., Beaty, Terri H., Bossé, Yohan, Brandsma, Corry-Anke, Chen, Zhengming, Crapo, James D., Danesh, John, DeMeo, Dawn L., Dudbridge, Frank, Gieger, Christian, Gulsvik, Amund, Hansell, Anna L., Hao, Ke, Hoffman, Joshua D., Hokanson, John E., Homuth, Georg, Joshi, Peter K., Joubert, Philippe, Langenberg, Claudia, Li, Xuan, Li, Liming, Lin, Kuang, Lind, Lars, Locantore, Nicholas, Luan, Jian’an, Mahajan, Anubha, Maranville, Joseph C., Murray, Alison, Packer, Richard, Parker, Margaret M., Paynton, Megan L., Porteous, David J., Prokopenko, Dmitry, Runz, Heiko, Sin, Don D, Smith, Blair H, Soler Artigas, María, Sparrow, David, Tal-Singer, Ruth, Timmers, Paul R. H. J., Whittaker, John C., Woodruff, Prescott G., Yerges-Armstrong, Laura M., Troyanskaya, Olga G., Raitakari, Olli T., Kähönen, Mika, Polašek, Ozren, Gyllensten, Ulf, Rudan, Igor, Deary, Ian J., Probst-Hensch, Nicole M., Schulz, Holger, James, Alan L, Wilson, James F., Stubbe, Beate, Zeggini, Eleftheria, Jarvelin, Marjo-Riitta, Wareham, Nick, Silverman, Edwin K., Hayward, Caroline, Morris, Andrew P., Butterworth, Adam S., Scott, Robert A., Walters, Robin G., Meyers, Deborah A., Cho, Michael H., Strachan, David P., Hall, Ian P., Tobin, Martin D., Wain, Louise V.

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Effect of case and control definitions on genome‐wide association study (GWAS) findings von Isgut, Monica, Song, Kijoung, Ehm, Margaret G., Wang, May Dongmei, Davitte, Jonathan

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Variants in MTNR1B influence fasting glucose levels von Ahmadi, Kourosh, Mooser, Vincent, Wichmann, H-Erich, Sandhu, Manjinder, Saramies, Jouko, Palmer, Colin N A, Isomaa, Bo, Peltonen, Leena, Schlessinger, David, Thorsteinsdottir, Unnur, Hottenga, Jouke-Jan, Jarvelin, Marjo Riitta, McCann, Owen T, Dupuis, Josée, Manning, Alisa K, Cervino, Alessandra, Zeggini, Eleftheria, Boomsma, Dorret I, Soranzo, Nicole, Sijbrands, Eric, Crisponi, Laura, Willemsen, Gonneke, Van Duijn, Cornelia, Stefansson, Kari, Scuteri, Angelo, Watanabe, Richard M, Potter, Simon C, Groop, Leif C, Zhao, Jing Hua, Deloukas, Panos, Freimer, Nelson, Beckmann, Jacques S, Boehnke, Michael, Smit, Jan H, Kong, Augustine, Fox, Caroline S, Bergman, Richard N, Chen, Wei-Min, Cupples, L Adrienne, Florez, Jose C, Erdos, Michael R, Hunt, Sarah, Song, Kijoung, Bochud, Murielle, Kuusisto, Johanna, Dehghan, Abbas, Lindblad, Ulf, Altshuler, David, Sharp, Stephen, Yuan, Xin, Tuomi, Tiinamaija, Vollenweider, Peter, Penninx, Brenda WJH, Aulchenko, Yurii, Saxena, Richa, Voight, Benjamin F, McCarthy, Mark I, Lim, Noha, Lakatta, Edward, Mohlke, Karen L, Uitterlinden, André G, Illig, Thomas, Elliott, Paul, Naitza, Silvia, Randall, Joshua, Krestyaninova, Maria, Morris, Andrew D, Lindgren, Cecilia M, Collins, Francis S, Abecasis, Gonçalo R, Buchanan, Thomas A, Scott, Laura J, Gateva, Vesela, Sanna, Serena, Johnson, Toby, Doney, Alex S F, Spector, Tim D, Waeber, Gerard, Uda, Manuela, Orrù, Marco, Laakso, Markku, Barroso, Inês, Rathmann, Wolfgang, de Geus, Eco J C, Bonnycastle, Lori L, Thorleifsson, Gudmar, Stringham, Heather M, Waterworth, Dawn, Meigs, James B, Wheeler, Eleanor, Witteman, Jacqueline C M, Loos, Ruth J F, Kaakinen, Marika, Lyssenko, Valeriya, Wareham, Nicholas J, Prokopenko, Inga, Cao, Antonio, Scheet, Paul, Hughes, Thomas E, Langenberg, Claudia

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Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption von Schumann, Gunter, Coin, Lachlan J, Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H, Stacey, David, Desrivières, Sylvane, Aliev, Fazil A, Khan, Anokhi A, Aulchenko, Yurii S, Bakalkin, Georgy, Bakker, Stephan J, Balkau, Beverley, Beulens, Joline W, Bilbao, Ainhoa, de Boer, Rudolf A, Beury, Delphine, Bots, Michiel L, Cauchi, Stéphane, Cavalcanti-Proença, Christine, Chambers, John C, Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J, Dick, Danielle, Ducci, Francesca, Easton, Alanna, Esk, Tõnu, Foroud, Tatiana, Freimer, Nelson B, Girault, Jean-Antoine, Grobbee, Diederick E, Guarrera, Simonetta, Gudbjartsson, Daniel F, Hartikainen, Anna-Liisa, Heath, Andrew C, Hesselbrock, Victor, Hottenga, Jouke-Jan, Kaprio, Jaakko, Khaw, Kay-Tee, Kuehnel, Brigitte, Laitinen, Jaana, Luan, Jian'an, Mangino, Massimo, Maroteaux, Matthieu, Matullo, Giuseppe, Mueller, Christian, Navis, Gerjan, Numans, Mattijs E, Núñez, Alejandro, Nyholt, Dale R, Onland-Moret, Charlotte N, Oostra, Ben A, O'Reilly, Paul F, Palkovits, Miklos, Penninx, Brenda W, Polidoro, Silvia, Pouta, Anneli, Prokopenko, Inga, Ricceri, Fulvio, Santos, Eugenio, Smit, Johannes H, Soranzo, Nicole, Song, Kijoung, Sovio, Ulla, Stumvoll, Michael, Surakk, Ida, Thorgeirsson, Thorgeir E, Thorsteinsdottir, Unnur, Troakes, Claire, Tyrfingsson, Thorarinn, Tönjes, Anke, Uiterwaal, Cuno S, Uitterlinden, Andre G, van der Harst, Pim, van der Schouw, Yvonne T, Staehlin, Oliver, Waeber, Gerard, Wareham, Nicholas J, Wichmann, Erich H, Witteman, Jacqueline C, Yuan, Xin, Zhai, Guangju, Zhao, Jing H, Zhang, Weihua, Martin, Nicholas G, Metspalu, Andres, Doering, Angela, Scott, James, Spector, Tim D, Loos, Ruth J, Boomsma, Dorret I, Peltonen, Leena, van Duijn, Cornelia M, Vineis, Paolo, Kooner, Jaspal S, Spanagel, Rainer, Heberlein, Ulrike A, Jarvelin, Marjo-Riitta, Elliott, Paul

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LDL-cholesterol concentrations: a genome-wide association study von Sandhu, Manjinder S, Dr, Waterworth, Dawn M, PhD, Debenham, Sally L, PhD, Wheeler, Eleanor, PhD, Papadakis, Konstantinos, MSc, Zhao, Jing Hua, PhD, Song, Kijoung, PhD, Yuan, Xin, PhD, Johnson, Toby, PhD, Ashford, Sofie, BSc, Inouye, Michael, MSc, Luben, Robert, BSc, Sims, Matthew, BSc, Hadley, David, MSc, McArdle, Wendy, PhD, Barter, Philip, Prof, Kesäniemi, Y Antero, Prof, Mahley, Robert W, Prof, McPherson, Ruth, Prof, Grundy, Scott M, Prof, Bingham, Sheila A, Prof, Khaw, Kay-Tee, Prof, Loos, Ruth JF, PhD, Waeber, Gérard, Prof, Barroso, Inês, PhD, Strachan, David P, Prof, Deloukas, Panagiotis, PhD, Vollenweider, Peter, MD, Wareham, Nicholas J, Prof, Mooser, Vincent, MD

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Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases von Li, Rui, Brockschmidt, Felix F, Kiefer, Amy K, Stefansson, Hreinn, Nyholt, Dale R, Song, Kijoung, Vermeulen, Sita H, Kanoni, Stavroula, Glass, Daniel, Medland, Sarah E, Dimitriou, Maria, Waterworth, Dawn, Tung, Joyce Y, Geller, Frank, Heilmann, Stefanie, Hillmer, Axel M, Bataille, Veronique, Eigelshoven, Sibylle, Hanneken, Sandra, Moebus, Susanne, Herold, Christine, den Heijer, Martin, Montgomery, Grant W, Deloukas, Panos, Eriksson, Nicholas, Heath, Andrew C, Becker, Tim, Sulem, Patrick, Mangino, Massimo, Vollenweider, Peter, Spector, Tim D, Dedoussis, George, Martin, Nicholas G, Kiemeney, Lambertus A, Mooser, Vincent, Stefansson, Kari, Hinds, David A, Nöthen, Markus M, Richards, J Brent

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Influence of CRTC1 Polymorphisms on Body Mass Index and Fat Mass in Psychiatric Patients and the General Adult Population von Choong, Eva, Quteineh, Lina, Cardinaux, Jean-René, Gholam-Rezaee, Mehdi, Vandenberghe, Frederik, Dobrinas, Maria, Bondolfi, Guido, Etter, Manuela, Holzer, Laurent, Magistretti, Pierre, von Gunten, Armin, Preisig, Martin, Vollenweider, Peter, Beckmann, Jacques S, Pralong, François P, Waeber, Gerard, Kutalik, Zoltan, Conus, Philippe, Bochud, Murielle, Eap, Chin B

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Pyrexia in dabrafenib-treated melanoma patients is not associated with common genetic variation or von Kulkarni, Diptee, Song, Kijoung, Briley, Linda, King, Karen, Dabrowski, Christine, Mookerjee, Bijoyesh, Legos, Jeff, Spraggs, Colin

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Genetic Architecture of Ambulatory Blood Pressure in the General Population: Insights From Cardiovascular Gene-Centric Array von Tomaszewski, Maciej, Debiec, Radoslaw, Braund, Peter S, Nelson, Christopher P, Hardwick, Robert, Christofidou, Paraskevi, Denniff, Matthew, Codd, Veryan, Rafelt, Suzanne, van der Harst, Pim, Waterworth, Dawn, Song, Kijoung, Vollenweider, Peter, Waeber, Gerard, Zukowska-Szczechowska, Ewa, Burton, Paul R, Mooser, Vincent, Charchar, Fadi J, Thompson, John R, Tobin, Martin D, Samani, Nilesh J

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Pharmacogenetic investigation of pyrexia in patients treated with dabrafenib alone or in combination with trametinib from five melanoma studies von Kulkarni, Diptee A, Song, Kijoung, Briley, Linda P, King, Karen S, Dabrowski, Christine Ellen, Del Buono, Heather Lynn, Mookerjee, Bijoyesh, Legos, Jeffrey J., Spraggs, Colin F.

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