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B M C Bioinformatics, ISSN 1471-2105, 03/2010, Volume 11, Issue 1, pp. 134 - 134
Journal Article
by Gunter Schumann and Lachlan J. Coin and Anbarasu Lourdusamy and Pimphen Charoen and Karen H. Berger and David Stacey and Sylvane Desrivières and Fazil A. Aliev and Anokhi A. Khan and Najaf Amin and Yurii S. Aulchenko and Georgy Bakalkin and Stephan J. Bakker and Beverley Balkau and Joline W. Beulens and Ainhoa Bilbao and Rudolf A. de Boer and Delphine Beury and Michiel L. Bots and Elemi J. Breetvelt and Stéphane Cauchi and Christine Cavalcanti-Proença and John C. Chambers and Toni-Kim Clarke and Norbert Dahmen and Eco J. de Geus and Danielle Dick and Francesca Ducci and Alanna Easton and Howard J. Edenberg and Tõnu Esk and Alberto Fernández-Medarde and Tatiana Foroud and Nelson B. Freimer and Jean-Antoine Girault and Diederick E. Grobbee and Simonetta Guarrera and Daniel F. Gudbjartsson and Anna-Liisa Hartikainen and Andrew C. Heath and Victor Hesselbrock and Albert Hofman and Jouke-Jan Hottenga and Matti K. Isohanni and Jaakko Kaprio and Kay-Tee Khaw and Brigitte Kuehnel and Jaana Laitinen and Stéphane Lobbens and Jian'an Luan and Massimo Mangino and Matthieu Maroteaux and Giuseppe Matullo and Mark I. McCarthy and Christian Mueller and Gerjan Navis and Mattijs E. Numans and Alejandro Núñez and Dale R. Nyholt and Charlotte N. Onland-Moret and Ben A. Oostra and Paul F. O'Reilly and Miklos Palkovits and Brenda W. Penninx and Silvia Polidoro and Anneli Pouta and Inga Prokopenko and Fulvio Ricceri and Eugenio Santos and Johannes H. Smit and Nicole Soranzo and Kijoung Song and Ulla Sovio and Michael Stumvoll and Ida Surakk and Thorgeir E. Thorgeirsson and Unnur Thorsteinsdottir and Claire Troakes and Thorarinn Tyrfingsson and Anke Tönjes and Cuno S. Uiterwaal and Andre G. Uitterlinden and Pim van der Harst and Yvonne T. van der Schouw and Oliver Staehlin and Nicole Vogelzangs and Peter Vollenweider and Gerard Waeber and Nicholas J. Wareham and Dawn M. Waterworth and John B. Whitfield and Erich H. Wichmann and Gonneke Willemsen and Jacqueline C. Witteman and Xin Yuan and Guangju Zhai and Jing H. Zhao and Weihua Zhang and Nicholas G. Martin and Andres Metspalu and ... and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för farmaceutisk biovetenskap and Uppsala universitet and Farmaceutiska fakulteten
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 04/2011, Volume 108, Issue 17, pp. 7119 - 7124
Alcohol consumption is a moderately heritable trait, but the genetic basis in humans is largely unknown, despite its clinical and societal importance. We... 
Medical research | Ethanol | Medical genetics | Alleles | Alcohol drinking | Epidemiology | Human genetics | Research universities | Behavioral genetics | Alcohols | Transcriptional expression analysis | Epidemiologic | Genome-wide analysis | GENOTYPES | genome-wide analysis | MULTIDISCIPLINARY SCIENCES | MEN | transcriptional expression analysis | ADDICTIVE BEHAVIOR | DROSOPHILA | epidemiologic | DEPENDENCE | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Quantitative Trait, Heritable | Gene Expression Regulation - genetics | Humans | Genotype | Male | Drosophila melanogaster - genetics | Alcohol Drinking - genetics | Drosophila melanogaster - metabolism | Proteins - genetics | Animals | Proteins - metabolism | Nuclear Proteins - biosynthesis | Female | Mice | Polymorphism, Single Nucleotide | Nuclear Proteins - genetics | Alcohol Drinking - metabolism | Autism | Development and progression | Genetics | Genetic aspects | Genomes | Disease susceptibility | Research | Drinking of alcoholic beverages | Health aspects | Genotype & phenotype | Brain | Rodents | Gene expression | Alcohol use | Index Medicus | Cortex (prefrontal) | Genotyping | Drinking behavior | Body weight | Replication | Single-nucleotide polymorphism | Biological Sciences | Medical and Health Sciences | Medicin och hälsovetenskap | MEDICIN | MEDICINE
Journal Article
by Estrada Gil, Karol and Styrkarsdottir, Unnur and Evangelou, Evangelos and Hsu, Yi-Hsiang and Duncan, Emma and Ntzani, Evangelia and Oei, Ling and Albagha, Omar M and Amin, Najaf and Kemp, John and Koller, Daniel and Li, Guo and Liu, Ching-Ti and Minster, Ryan and Moayyeri, Alireza and Vandenput, Liesbeth and Willner, Dana and Xiao, Su-Mei and Yerges-Armstrong, Laura and Zheng, Hou-Feng and Alonso, Nerea and Eriksson, Joel and Kammerer, Candace and Kaptoge, Stephen and Leo, Paul and Thorleifsson, Gudmar and Wilson, Scott and Wilson, James and Aalto, Ville and Alen, Theo and Aragaki, Aaron and Aspelund, Thor and Center, Jacqueline and Dailiana, Zoe and Duggan, C and Garcia, Melissa and Garcia-Giralt, Natàlia and Giroux, Sylvie and Hallmans, Göran and Hocking, Lynne and Husted, Lise Bjerre and Jameson, Karen and Khusainova, Rita and Kim, Ghi Su and Kooperberg, Charles and Koromila, Theodora and Kruk, Marcin and Laaksonen, Marika and LaCroix, Anea and Lee, Seung and Leung, Ping and Lewis, Joshua and Masi, Laura and Mencej-Beac, Simona and Nguyen, Tuan and Nogues, Xavier and Patel, Millan and Prezelj, Janez and Rose, Lynda and Scollen, Serena and Siggeirsdottir, Kristin and Smith, G.D and Svensson, Olle and Trompet, Stella and Trummer, Olivia and Schoor, Natasja and Woo, Margaret M and Zhu, Kun and Balcells, Susana and Brandi, M.L and Buckley, Brendan M and Cheng, Sulin and Christiansen, C and Cooper, Charles and Dedoussis, George and Ford, Ian and Frost, Morten and Goltzman, David and González-Macías, Jesús and Kähönen, Mika and Karlsson, Magnus and Khusnutdinova, Elza and Koh, Jung-Min and Kollia, Panagoula and Langdahl, Bente and Leslie, William and Lips, Paul and Ljunggren, Östen and Lorenc, Roman and Marc, Janja and Mellström, Dan and Obermayer-Pietsch, Barbara and Olmos, David and Pettersson-Kymmer, Ulrika and Reid, David and Riancho, José and Ridker, Paul and Rousseau, Francois and Lagboom, P Eline and Tang, Nelson L and ... and Medicinska fakulteten and Umeå universitet and Institutionen för folkhälsa och klinisk medicin and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk farmakologi and Näringsforskning and Institutionen för kirurgisk och perioperativ vetenskap
Nature Genetics, ISSN 1061-4036, 05/2012, Volume 44, Issue 5, pp. 491 - 501
textabstractBone mineral density (BMD) is the most widely used predictor of fracture risk. We performed the largest meta-analysis to date on lumbar spine and... 
WOMEN | POPULATION | IMPUTATION | VARIANTS | DISEASE | GENETICS & HEREDITY | OSTEOPOROTIC FRACTURES | GENE-EXPRESSION | LRP5 | PATTERNS | IMPUTED DATA | Glycoproteins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Low Density Lipoprotein Receptor-Related Protein-5 - genetics | Extracellular Matrix Proteins - genetics | Humans | Risk Factors | Computational Biology | Intercellular Signaling Peptides and Proteins - genetics | European Continental Ancestry Group | Genotype | Male | Bone Density - genetics | Gene Expression Profiling | Phosphoproteins - genetics | Fractures, Bone - genetics | Mitochondrial Membrane Transport Proteins - genetics | Polymorphism, Single Nucleotide - genetics | Female | Femur Neck - physiopathology | Osteoporosis - genetics | Spectrin - genetics | Quantitative Trait Loci | Lumbar Vertebrae - physiopathology | Quantitative trait loci | Measurement | Fractures | Bones | Genetic aspects | Identification and classification | Density | Risk factors | Medical research | Osteoporosis | Genomics | Bone density | Gene loci | Index Medicus | Vèrtebres lumbars | Gens | Femur | Genes | Bone densitometry | Densitometria òssia | Fèmur | Lumbar vertebrae | Basic Medicine | Medical Genetics | Medicinsk genetik | ortopedi | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | genetik | Genetics | Orthopaedics
Journal Article
by Voight, Benjamin and Scott, Laura and Steinthorsdottir, Valgerdur and Morris, Anew and Dina, Christian and Welch, Ryan and Zeggini, Eleftheria and Huth, Cornelia and Aulchenko, Yurii and Thorleifsson, Gudmar and McCulloch, Laura and Ferreira, Teresa and Grallert, Harald and Amin, Najaf and Wu, Guanming and Willer, Cristen and Raychaudhuri, Soumya and McCarroll, Steven and Langenberg, Claudia and Hofmann, Oliver and Dupuis, Josée and Qi, Lu and Segrè, Ayellet and Hoek, Mandy and Navarro, Pau and Ardlie, Kristin and Balkau, Beverley and Benediktsson, Rafn and Bennett, Amanda and Blagieva, Roza and Boerwinkle, Eric and Bonnycastle, Lori and Boström, Kristina Bengtsson and Bravenboer, Bert and Bumpstead, Suzannah and Burtt, Noël and Charpentier, Guillaume and Chines, Peter and Cornelis, Marilyn and Couper, David and Crawford, Gabe and Doney, Alex and Elliott, Katherine and Erdos, Michael and Fox, Caroline and Franklin, Christopher and Ganser, Martha and Gieger, Christian and Grarup, Niels and Green, Todd and Griffin, Simon and Groves, Christopher and Guiducci, Candace and Hadjadj, Samy and Hassanali, Neelam and Herder, Christian and Isomaa, Bo and Jackson, Anne and Johnson, Paul and Jørgensen, Torben and Kao, Wen and Klopp, Norman and Kong, Augustine and Kraft, Peter and Kuusisto, Johanna and Lauritzen, Torsten and Li, Man and Lieverse, Aloysius and Lindgren, Cecilia and Lyssenko, Valeriya and Marre, Michel and Meitinger, Thomas and Midthjell, Kristian and Morken, Mario and Narisu, Narisu and Nilsson, Peter and Owen, Katharine and Payne, Felicity and Perry, John and Petersen, A.K and Platou, Carl and Proença, Christine and Prokopenko, Inga and Rathmann, Wolfgang and Rayner, Nigel William and Robertson, Neil and Rocheleau, Ghislain and Roden, Michael and Sampson, Michael and Saxena, Richa and Shields, Beverley and Shrader, Peter and Sigurdsson, Gunnar and Sparsø, Thomas and Strassburger, Klaus and Stringham, Heather and Sun, Qi and Swift, Amy and Thorand, Barbara and Tichet, Jean and ... and GIANT Consortium and MAGIC Investigators and MAGIC investigators and The GIANT Consortium and The MAGIC investigators and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 07/2010, Volume 42, Issue 7, pp. 579 - 589
Journal Article