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Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, ISSN 0931-0509, 07/2018
Cardiovascular mortality in patients receiving dialysis remains unacceptably high, with unexplained ancestry differences suggesting a genetic component. We... 
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 08/2010, Volume 6, Issue 8, p. e1001053
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 07/2018, Volume 14, Issue 7, pp. P1116 - P1116
Journal Article
by Tedja, Milly S and Wojciechowski, Robert and Hysi, Pirro G and Eriksson, Nicholas and Furlotte, Nicholas A and Verhoeven, Virginie J. M and Iglesias, Adriana I and Meester-Smoor, Magda A and Tompson, Stuart W and Fan, Qiao and Khawaja, Anthony P and Cheng, Ching-Yu and Höhn, René and Yamashiro, Kenji and Wenocur, Adam and Grazal, Clare and Haller, Toomas and Metspalu, Andres and Wedenoja, Juho and Jonas, Jost B and Wang, Ya Xing and Xie, Jing and Mitchell, Paul and Foster, Paul J and Klein, Barbara E. K and Klein, Ronald and Paterson, Andrew D and Hosseini, S. Mohsen and Shah, Rupal L and Williams, Cathy and Teo, Yik Ying and Tham, Yih Chung and Gupta, Preeti and Zhao, Wanting and Shi, Yuan and Saw, Woei-Yuh and Tai, E-Shyong and Sim, Xue Ling and Huffman, Jennifer E and Polašek, Ozren and Hayward, Caroline and Bencic, Goran and Rudan, Igor and Wilson, James F and Aung, Tin and Veluchamy, Amutha B and Burdon, Kathryn P and Campbell, Harry and Chen, Li Jia and Chen, Peng and Chen, Wei and Chew, Emily and Deangelis, Margaret M and Ding, Xiaohu and Döring, Angela and Evans, David M and Feng, Sheng and Fleck, Brian and Fogarty, Rhys D and Fondran, Jeremy R and Fossarello, Maurizio and Guo, Xiaobo and Haarman, Annet E. G and He, Mingguang and Howe, Laura D and Janmahasatian, Sarayut and Jhanji, Vishal and Kähönen, Mika and Kaprio, Jaakko and Kemp, John P and Khaw, Kay-Tee and Khor, Chiea-Chuen and Krapohl, Eva and Korobelnik, Jean-François and Lee, Kris and Li, Shi-Ming and Lu, Yi and Luben, Robert N and Mäkelä, Kari-Matti and McMahon, George and Meguro, Akira and Mihailov, Evelin and Miyake, Masahiro and Mizuki, Nobuhisa and Morrison, Margaux and Nangia, Vinay and Oexle, Konrad and Panda-Jonas, Songhomitra and Pang, Chi Pui and Pirastu, Mario and Plomin, Robert and Rantanen, Taina and Schache, Maria and Seppälä, Ilkka and Smith, George D and Pourcain, Beate St and Tam, Pancy O and Tideman, J. Willem L and Timpson, Nicholas J and Vaccargiu, Simona and ... and UK Biobank Eye Vis Consortium and CREAM and 23andMe Res Team and CREAM Consortium and 23andMe Research Team and UK Biobank Eye and Vision Consortium and The CREAM Consortium
Nature Genetics, ISSN 1061-4036, 06/2018, Volume 50, Issue 6, pp. 834 - 848
Journal Article
American Journal of Nephrology, ISSN 0250-8095, 02/2019, Volume 49, Issue 2, pp. 125 - 132
Background: Elevated serum concentrations of fibroblast growth factor 23 (FGF23) are associated with cardiovascular mortality in patients with chronic kidney... 
Original Report: Patient-Oriented, Translational Research | Cardiovascular disease | Chronic kidney disease-mineral bone disorder | Dialysis | Fibroblast growth factor-23 | Mortality | KIDNEY-DISEASE | CINACALCET | LEFT-VENTRICULAR HYPERTROPHY | GENE POLYMORPHISM | CHILDREN | GROWTH-FACTOR 23 | UROLOGY & NEPHROLOGY | EVENTS EVOLVE | FGF23 | ASSOCIATION
Journal Article
by Fan, Qiao and Verhoeven, Virginie and Wojciechowski, Robert and Barathi, Veluchamy and Hysi, Pirro and Guggenheim, Jean and Höhn, René and Vitart, Veronique and Khawaja, Anthony P and Yamashiro, Kenji and Hosseini, S Mohsen and Lehtimäki, Terho and Lu, Yi and Haller, Toomas and Xie, Jing and Delcourt, Cécile and Pirastu, Mario and Wedenoja, Juho and Gharahkhani, Puya and Venturini, Cristina and Miyake, Masahiro and Hewit, Alex and Guo, Xiaobo and Mazur, Johanna and Huffman, Jenifer E and Williams, Katie M and Polasek, Ozren and Campbell, Harry and Rudan, Igor and Vatavuk, Zoran and Wilson, James F and Joshi, Peter and Mcmahon, George and St Pourcain, Beate and Evans, David and Simpson, Claire and Schwantes-An, Tae-Hwi and Igo Jr., Robert and Mirshahi, Alireza and Cougnard-Grégoire, Auey and Bellenguez, Céline and Blettner, Maria and Raitakari, Olli and Kähönen, Mika and Seppälä, Ilkka and Zeller, Tanja and Meitinger, Thomas and Ried, Janina and Gieger, Christian and Portas, Laura and Leeuwen, Elisa and Amin, Najaf and Uitterlinden, Ané and Rivadeneira Ramirez, Fernando and Hofman, Albert and Vingerling, Hans and Wang, Ying and Wang, Xu and Tai-Hui Boh, Eileen and Ikram, Kamran and Sabanayagam, Charumathi and Gupta, Preeti and Tan, Vincent and Zhou, Lei and Ho, Candice E. H and Lim, Wan'E and Beuerman, Roger W and Siantar, Rosalynn and Tai, E-Shyong and Vithana, Eranga and Mihailov, Evelin and Khor, C.C and Hayward, Caroline and Luben, Robert and Foster, Paul and Klein, Barbara and Klein, Ronald and Wong, Hoi-Suen and Mitchell, Paul and Metspalu, Anes and Aung, Tin and Young, Terri L and He, Mingguang and Pärssinen, Olavi and Duijn, Cornelia and Jin Wang, Jie and Williams, Cathy and Jonas, Jost B and Teo, Yik Ying and Mackey, David and Oexle, Konrad and Yoshimura, N and Paterson, Anew D and Pfeiffer, Norbert and Wong, Tien Yin and Baird, Paul and Stambolian, Dwight and Wilson, Joan E. Bailey and Cheng, Ching-Yu and Hammond, Christopher J and ... and Consortium Refractive Error Myopia and Consortium for Refractive Error and Myopia and Consortium for Refractive Error and Myopia (CREAM)
Nature Communications, ISSN 2041-1723, 03/2016, Volume 7, Issue 1, pp. 11008 - 11008
Journal Article
Genetic Epidemiology, ISSN 0741-0395, 06/2018, Volume 42, Issue 4, pp. 405 - 414
Journal Article
by Schwantes-An, Tae-Hwi and Zhang, Juan and Chen, Li-Shiun and Hartz, Sarah M and Culverhouse, Robert C and Chen, Xiangning and Coon, Hilary and Frank, Josef and Kamens, Helen M and Konte, Bettina and Kovanen, Leena and Latvala, Antti and Legrand, Lisa N and Maher, Brion S and Melroy, Whitney E and Nelson, Elliot C and Reid, Mark W and Robinson, Jason D and Shen, Pei-Hong and Yang, Bao-Zhu and Andrews, Judy A and Aveyard, Paul and Beltcheva, Olga and Brown, Sandra A and Cannon, Dale S and Cichon, Sven and Corley, Robin P and Dahmen, Norbert and Degenhardt, Louisa and Foroud, Tatiana and Gaebel, Wolfgang and Giegling, Ina and Glatt, Stephen J and Grucza, Richard A and Hardin, Jill and Hartmann, Annette M and Heath, Andrew C and Herms, Stefan and Hodgkinson, Colin A and Hoffmann, Per and Hops, Hyman and Huizinga, David and Ising, Marcus and Johnson, Eric O and Johnstone, Elaine and Kaneva, Radka P and Kendler, Kenneth S and Kiefer, Falk and Kranzler, Henry R and Krauter, Ken S and Levran, Orna and Lucae, Susanne and Lynskey, Michael T and Maier, Wolfgang and Mann, Karl and Martin, Nicholas G and Mattheisen, Manuel and Montgomery, Grant W and Müller-Myhsok, Bertram and Murphy, Michael F and Neale, Michael C and Nikolov, Momchil A and Nishita, Denise and Nöthen, Markus M and Nurnberger, John and Partonen, Timo and Pergadia, Michele L and Reynolds, Maureen and Ridinger, Monika and Rose, Richard J and Rouvinen-Lagerström, Noora and Scherbaum, Norbert and Schmäl, Christine and Soyka, Michael and Stallings, Michael C and Steffens, Michael and Treutlein, Jens and Tsuang, Ming and Wall, Tamara L and Wodarz, Norbert and Yuferov, Vadim and Zill, Peter and Bergen, Andrew W and Chen, Jingchun and Cinciripini, Paul M and Edenberg, Howard J and Ehringer, Marissa A and Ferrell, Robert E and Gelernter, Joel and Goldman, David and Hewitt, John K and Hopfer, Christian J and Iacono, William G and Kaprio, Jaakko and Kreek, Mary Jeanne and Kremensky, Ivo M and Madden, Pamela A.F and McGue, Matt and Munafò, Marcus R and Philibert, Robert A and ...
Behavior Genetics, ISSN 0001-8244, 3/2016, Volume 46, Issue 2, pp. 151 - 169
The mu1 opioid receptor gene, OPRM1, has long been a high-priority candidate for human genetic studies of addiction. Because of its potential functional... 
Public Health | Addiction | Psychology | Opioid receptor | Clinical Psychology | Health Psychology | Substance dependence | OPRM1 | Genetic association | Single nucleotide polymorphism (SNP) | DRUG-DEPENDENCE | HEROIN DEPENDENCE | SINGLE-NUCLEOTIDE POLYMORPHISM | QUANTITATIVE TRAIT LOCI | NICOTINE DEPENDENCE | PSYCHOLOGY, MULTIDISCIPLINARY | MU-OPIOID-RECEPTOR | GENETICS & HEREDITY | GENE OPRM1 | BEHAVIORAL SCIENCES | USE DISORDERS | ALCOHOL DEPENDENCE | GENOME-WIDE ASSOCIATION | European Continental Ancestry Group - genetics | Gene Frequency - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Male | Substance-Related Disorders - genetics | Case-Control Studies | Sample Size | Adolescent | Alleles | Polymorphism, Single Nucleotide - genetics | Adult | Receptors, Opioid, mu - genetics | Child | Cohort Studies | Liability (Law) | Analysis | Substance abuse | Candidates | Drug dependency | Mental health | Alcohol dependence | Alcohol | Genomes | Addictive behaviour | Cannabis | Analgesics | Substance dependency | Addictive behaviors | Genetics | Genetic factors | Statistical analysis | Narcotics | Opioid receptors | Data processing | Cigarettes | Addictions | Medicine | Liability | Brain research | Collaboration | Cocaine | Drug dependence | Psychiatry | Power | Nicotine | Smoking | Index Medicus | opioid receptor | genetic association | single nucleotide polymorphism (SNP) | substance dependence
Journal Article