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1. Full Text Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
by Chambers, John C and Zhang, Weihua and Sehmi, Joban and Li, Xinzhong and Wass, Mark N and van der Harst, Pim and Holm, Hilma and Sanna, Serena and Kavousi, Maryam and Baumeister, Sebastian E and Coin, Lachlan J and Deng, Guohong and Gieger, Christian and Heard-Costa, Nancy L and Hottenga, Jouke-Jan and Kühnel, Brigitte and Kumar, Vinod and Lagou, Vasiliki and Liang, Liming and Luan, Jian'an and Vidal, Peo Marques and Mateo Leach, Irene and O'Reilly, Paul F and Peden, John F and Rahmioglu, Nilufer and Soininen, Pasi and Speliotes, Elizabeth K and Yuan, Xin and Thorleifsson, Gudmar and Alizadeh, Behrooz Z and Atwood, Larry D and Borecki, Ingrid B and Brown, Morris J and Charoen, Pimphen and Cucca, Francesco and Das, Debashish and de Geus, Eco J. C and Dixon, Anna L and Döring, Angela and Ehret, Georg and Eyjolfsson, Gudmundur I and Farrall, Martin and Forouhi, Nita G and Frieich, Nele and Goessling, Wolfram and Gudbjartsson, Daniel F and Harris, Tamara B and Hartikainen, Anna-Liisa and Heath, Simon and Hirschfield, Gideon M and Hofman, Albert and Homuth, Georg and Hyppönen, Elina and Janssen, Harry L. A and Johnson, Toby and Kangas, Antti J and Kema, Ido P and Kühn, Jens P and Lai, Sana and Lathrop, Mark and Lerch, Markus M and Li, Yun and Liang, T. Jake and Lin, Jing-Ping and Loos, Ruth J. F and Martin, Nicholas G and Moffatt, Miriam F and Montgomery, Grant W and Munroe, Patricia B and Musunuru, Kiran and Nakamura, Yusuke and O'Donnell, Christopher J and Olafsson, Isleifur and Penninx, Brenda W and Pouta, Anneli and Prins, Bram P and Prokopenko, Inga and Puls, Ralf and Ruokonen, Aimo and Savolainen, Markku J and Schlessinger, David and Schouten, Jeoffrey N. L and Seedorf, Udo and Sen-Chowdhry, Srijita and Siminovitch, Katherine A and Smit, Johannes H and Spector, Timothy D and Tan, Wenting and Teslovich, Tanya M and Tukiainen, Taru and Uitterlinden, Ane G and van der Klauw, Melanie M and Vasan, Ramachanan S and Wallace, Chris and Wallaschofski, Henri and Wichmann, H.-Erich and Willemsen, Gonneke and Würtz, Peter and Xu, Chun and Yerges-Armstrong, Laura M and ... and Meta-Anal Glucose Insulin-Related and Diabet Genetics Replication and Genetic Invest Anthropometric and Genetics Liver Dis GOLD Consortium and Global Lipids Genetics Consortium and Alcohol Genome-wide Assoc AlcGen and Int Consortium Blood Pressure ICBP and Meta-analyses of Glucose and Insulin-Related Traits Consortium (MAGIC) and Alcohol Genome-wide Association (AlcGen) Consortium and Genetic Investigation of Anthropometric Traits (GIANT) Consortium and Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study and International Consortium for Blood Pressure (ICBP-GWAS) and Genetics of Liver Disease (GOLD) Consortium
Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 11, pp. 1131 - U129
Concentrations of liver enzymes in plasma are widely used as indicators of liver disease. We carried out a genome-wide association study in 61,089 individuals,... 
C-REACTIVE PROTEIN | COMMON VARIANTS | METABOLIC SYNDROME | HEPATOCELLULAR-CARCINOMA | RISK-FACTORS | SALT EXPORT PUMP | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | GENETIC-VARIANTS | HEREDITARY CHOLESTASIS | CORONARY-HEART-DISEASE | Genome-Wide Association Study | Polymorphism, Single Nucleotide | Liver - enzymology | Enzymes - blood | Enzymes - genetics | Humans | Enzymes | Weight control | Data collection | Genetics | Gene loci | Genomes | Gene expression | Autoimmune diseases | Metabolic disorders | Index Medicus
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2. Full Text New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism
by Horikoshi, Momoko and Yaghootkar, Hanieh and Mook-Kanamori, Dennis O and Sovio, Ulla and Taal, H. Rob and Hennig, Branwen J and Bradfield, Jonathan P and St Pourcain, Beate and Evans, David M and Charoen, Pimphen and Kaakinen, Marika and Cousminer, Diana L and Lehtimaki, Terho and Kreiner-Moller, Eskil and Warrington, Nicole M and Bustamante, Mariona and Feenstra, Bjarke and Berry, Diane J and Thiering, Elisabeth and Pfab, Thiemo and Barton, Sheila J and Shields, Beverley M and Kerkhof, Marjan and van Leeuwen, Elisa and Fulford, Anthony J and Kutalik, Zoltan and Zhao, Jing Hua and den Hoed, Marcel and Mahajan, Anubha and Lindi, Virpi and Goh, Liang-Kee and Hottenga, Jouke-Jan and Wu, Ying and Raitakari, Olli T and Harder, Marie N and Meirhaeghe, Aline and Ntalla, Ioanna and Salem, Rany M and Jameson, Karen A and Zhou, Kaixin and Monies, Dorota M and Lagou, Vasiliki and Kirin, Mirna and Heikkinen, Jani and Adair, Linda S and Alkuraya, Fowzan S and Al-Odaib, Ali and Amouyel, Philippe and Andersson, Ehm Astrid and Bennett, Amanda J and Blakemore, Alexana I. F and Buxton, Jessica L and Dallongeville, Jean and Das, Shikta and de Geus, Eco J. C and Estivill, Xavier and Flexeder, Claudia and Froguel, Philippe and Geller, Frank and Godfrey, Keith M and Gottrand, Frederic and Groves, Christopher J and Hansen, Torben and Hirschhorn, Joel N and Hofman, Albert and Hollegaard, Mads V and Hougaard, David M and Hyppoenen, Elina and Inskip, Hazel M and Isaacs, Aaron and Jorgensen, Torben and Kanaka-Gantenbein, Christina and Kemp, John P and Kiess, Wieland and Kilpelainen, Tuomas O and Klopp, Norman and Knight, Bridget A and Kuzawa, Christopher W and McMahon, George and Newnham, John P and Niinikoski, Harri and Oostra, Ben A and Pedersen, Louise and Postma, Dirkje S and Ring, Susan M and Rivadeneira, Fernando and Robertson, Neil R and Sebert, Sylvain and Simell, Olli and Slowinski, Torsten and Tiesler, Carla M. T and Toenjes, Anke and Vaag, Allan and Viikari, Jorma S and Vink, Jacqueline M and Vissing, Nadja Hawwa and Wareham, Nicholas J and Willemsen, Gonneke and Witte, Daniel R and Zhang, Haitao and ... and Early Growth Genetics EGG and MAGIC and Early Growth Genetics (EGG) Consortium and Meta-Analyses of Glucose- and Insulin-related traits Consortium (MAGIC) and The Meta-Analyses of Glucose- and Insulin-related traits Consortium (MAGIC)
Nature Genetics, ISSN 1061-4036, 01/2013, Volume 45, Issue 1, pp. 76 - 82
Birth weight within the normal range is associated with a variety of adult-onset diseases, but the mechanisms behind these associations are poorly... 
FASTING GLUCOSE | INDIVIDUALS | COMMON VARIANTS | METAANALYSIS | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | TYPE-2 DIABETES RISK | BLOOD-PRESSURE | HEAD CIRCUMFERENCE | GLUCOKINASE GENE | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Blood Pressure - genetics | Diabetes Mellitus, Type 2 - genetics | Humans | Male | Birth Weight - genetics | Body Height - genetics | Adult | Female | Fetal Development - genetics | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Infant, Newborn | Genetic Linkage | Quantitative trait loci | Type 2 diabetes | Birth size | Physiological aspects | Birth weight | Genetic aspects | Research | Single nucleotide polymorphisms | Diagnosis | Genotype & phenotype | Prenatal development | Blood pressure | Diabetes | Insulin | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap
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3. Full Text Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
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
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4. Full Text Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
by Freathy, Rachel and Mook-Kanamori, Dennis and Sovio, Ulla and Prokopenko, Inga and Timpson, Nicholas and Berry, Diane and Warrington, Nicole and Widen, Elisabeth and Hottenga, Jouke Jan and Kaakinen, Marika and Lange, Leslie and Bradfield, Jonathan and Kerkhof, Marjan and Marsh, Julie and Mägi, Reedik and Chen, Chao and Lyon, Helen and Kirin, Mirna and Adair, Linda and Aulchenko, Yurii and Bennett, Amanda and Borja, Judith and Bouatia-Naji, Nabila and Charoen, Pimphen and Coin, Lachlan and Cousminer, Diana and Geus, Eco and Deloukas, Panagiotis and Elliott, Paul and Evans, David and Froguel, Philippe and Glaser, Beate and Groves, Christopher and Hartikainen, A.L and Hassanali, Neelam and Hirschhorn, Joel and Hofman, Albert and Holly, Jeff and Hyppönen, Elina and Kanoni, Stavroula and Knight, Bridget and Laitinen, Jaana and Lindgren, Cecilia and McArdle, Wendy and O'Reilly, Paul and Pennell, Craig and Postma, Dirkje and Pouta, Anneli and Ramasamy, Adaikalavan and Rayner, Nigel William and Ring, Susan and Rivadeneira Ramirez, Fernando and Shields, Beverley and Strachan, David and Surakka, Ida and Taanila, Anja and Tiesler, Carla and Uitterlinden, Ané and Tikka-Kleemola, Päivi and Wijga, Alet and Willemsen, Gonneke and Zhang, Haitao and Zhao, Jing Hua and Wilson, James and Steegers-Theunissen, Régine and Hattersley, Anew and Hagen, Knut and Peltonen, Leena Johanna and Mohlke, Karen and Grant, Struan and Hakonarson, Hakon and Koppelman, Gerard and Dedoussis, George and Heinrich, Joachim and Gillman, Matthew W and Palmer, Cameron and Frayling, Timothy and Boomsma, Dorret and Smith, G.D and Power, Christopher and Jaddoe, Vincent and Jarvelin, Marjo-Riitta and McCarthy, Mark and EGG Consortium and MAGIC and WTCCC and GIANT Consortium and Wellcome Trust Case Control Consortium and Meta-Analyses of Glucose and Insulin-related traits Consortium and Early Growth Genetics (EGG) Consortium and Genetic Investigation of ANthropometric Traits (GIANT) Consortium and The Wellcome Trust Case Control Consortium (WTCCC) and the Early Growth Genetics (EGG) Consortium and The Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) and The Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature Genetics, ISSN 1061-4036, 05/2010, Volume 42, Issue 5, pp. 430 - 435
textabstractTo identify genetic variants associated with birth weight, we meta-analyzed six genome-wide association (GWA) studies (n = 10,623 Europeans from... 
METAANALYSIS | ISOFORMS | GESTATIONAL-AGE | GENE | ADENYLYL-CYCLASE | GENETICS & HEREDITY | TYPE-2 DIABETES RISK | COHORT | EXPRESSION | HEAD CIRCUMFERENCE | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Isoenzymes - genetics | Diabetes Mellitus, Type 2 - genetics | Humans | Cyclins - genetics | Genotype | Male | Pregnancy | Birth Weight | Ethnic Groups | Alleles | Glucose - metabolism | Female | Models, Genetic | Adenylyl Cyclases - genetics | Cohort Studies | Type 2 diabetes | Genetic susceptibility | Genetic aspects | Research | Birth weight, Low | Single nucleotide polymorphisms | Health aspects | Risk factors | Studies | Medical research | Genotype & phenotype | Birth weight | Index Medicus
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5. Full Text Whole-genome sequence-based analysis of thyroid function
by Taylor, Peter N and Porcu, Eleonora and Chew, Shelby and Campbell, Purdey J and Traglia, Michela and Brown, Suzanne J and Mullin, Benjamin H and Shihab, Hashem A and Min, Josine and Walter, Klaudia and Memari, Yasin and Huang, Jie and Barnes, Michael R and Beilby, John P and Charoen, Pimphen and Danecek, Petr and Dudbridge, Frank and Forgetta, Vincenzo and Greenwood, Celia and Grundberg, Elin and Johnson, Andrew D and Hui, Jennie and Lim, Ee M and McCarthy, Shane and Muddyman, Dawn and Panicker, Vijay and Perry, John R. B and Bell, Jordana T and Yuan, Wei and Relton, Caroline and Gaunt, Tom and Schlessinger, David and Abecasis, Goncalo and Cucca, Francesco and Surdulescu, Gabriela L and Woltersdorf, Wolfram and Zeggini, Eleftheria and Zheng, Hou-Feng and Toniolo, Daniela and Dayan, Colin M and Naitza, Silvia and Walsh, John P and Spector, Tim and Smith, George Davey and Durbin, Richard and Richards, J. Brent and Sanna, Serena and Soranzo, Nicole and Timpson, Nicholas J and Wilson, Scott G and Turki, Saeed Al and Anderson, Carl and Anney, Richard and Antony, Dinu and Artigas, Maria Soler and Ayub, Muhammad and Balasubramaniam, Senduran and Barrett, Jeffrey C and Barroso, Inês and Beales, Phil and Bentham, Jamie and Bhattacharya, Shoumo and Birney, Ewan and Blackwood, Douglas and Bobrow, Martin and Bochukova, Elena and Bolton, Patrick and Bounds, Rebecca and Boustred, Chris and Breen, Gerome and Calissano, Mattia and Carss, Keren and Chatterjee, Krishna and Chen, Lu and Ciampi, Antonio and Cirak, Sebhattin and Clapham, Peter and Clement, Gail and Coates, Guy and Collier, David and Cosgrove, Catherine and Cox, Tony and Craddock, Nick and Crooks, Lucy and Curran, Sarah and Curtis, David and Daly, Allan and Day-Williams, Aaron and Day, Ian N. M and Down, Thomas and Du, Yuanping and Dunham, Ian and Edkins, Sarah and Ellis, Peter and Evans, David and Faroogi, Sadaf and Fatemifar, Ghazaleh and Fitzpatrick, David R and Flicek, Paul and Flyod, James and ... and UK10K Consortium and UK0K Consortium and The UK10K Consortium
Nature Communications, ISSN 2041-1723, 2015, Volume 6, Issue 1, pp. 5681 - 5681
Normal thyroid function is essential for health, but its genetic architecture remains poorly understood. Here, for the heritable thyroid traits thyrotropin... 
IMPUTATION | HORMONE | VARIANTS | TRANSTHYRETIN | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | SERUM TSH | COMMON | WIDE ASSOCIATION | MAP | THYROXINE-BINDING | 3',5'-Cyclic-AMP Phosphodiesterases - metabolism | Thyrotropin - genetics | Genetic Association Studies | Humans | United Kingdom | DNA Methylation - genetics | 3',5'-Cyclic-AMP Phosphodiesterases - genetics | Thyrotropin - metabolism | Synapsins - genetics | Synapsins - metabolism | Thyroid Gland - physiology | Thyroxine - metabolism | Thyroxine - genetics | Genomics - methods | Thyroid Gland - metabolism | Cohort Studies | Index Medicus
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