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by Anttila, Verneri and Winsvold, Bendik S and Gormley, Padhraig and Kurth, Tobias and Bettella, Francesco and McMahon, George and Kallela, Mikko and Malik, Rainer and de Vries, Boukje and Terwindt, Gisela and Medland, Sarah E and Todt, Unda and McArdle, Wendy L and Quaye, Lydia and Koiranen, Markku and Ikram, M Arfan and Lehtimäki, Terho and Stam, Anine H and Ligthart, Lannie and Wedenoja, Juho and Dunham, Ian and Neale, Benjamin M and Palta, Priit and Hamalainen, Eija and Schürks, Markus and Rose, Lynda M and Buring, Julie E and Ridker, Paul M and Steinberg, Stacy and Stefansson, Hreinn and Jakobsson, Finnbogi and Lawlor, Debbie A and Evans, David M and Ring, Susan M and Färkkilä, Markus and Artto, Ville and Kaunisto, Mari A and Freilinger, Tobias and Schoenen, Jean and Frants, Rune R and Pelzer, Nadine and Weller, Claudia M and Zielman, Ronald and Heath, Andrew C and Madden, Pamela A F and Montgomery, Grant W and Martin, Nicholas G and Borck, Guntram and Göbel, Hartmut and Heinze, Axel and Heinze-Kuhn, Katja and Williams, Frances M K and Hartikainen, Anna-Liisa and Pouta, Anneli and van den Ende, Joyce and Uitterlinden, Andre G and Hofman, Albert and Amin, Najaf and Hottenga, Jouke-Jan and Vink, Jacqueline M and Heikkilä, Kauko and Alexander, Michael and Muller-Myhsok, Bertram and Schreiber, Stefan and Meitinger, Thomas and Wichmann, Heinz Erich and Aromaa, Arpo and Eriksson, Johan G and Traynor, Bryan J and Trabzuni, Daniah and Rossin, Elizabeth and Lage, Kasper and Jacobs, Suzanne B R and Gibbs, J Raphael and Birney, Ewan and Kaprio, Jaakko and Penninx, Brenda W and Boomsma, Dorret I and van Duijn, Cornelia and Raitakari, Olli and Jarvelin, Marjo-Riitta and Zwart, John-Anker and Cherkas, Lynn and Strachan, David P and Kubisch, Christian and Ferrari, Michel D and van den Maagdenberg, Arn M J M and Dichgans, Martin and Wessman, Maija and Smith, George Davey and Stefansson, Kari and Daly, Mark J and UK Brain Expression Consortium and the International Headache Genetics Consortium and North American Brain Expression Consortium and Int Headache Genetics Consortium and North Amer Brain Expression
Nature genetics, ISSN 1546-1718, 2013, Volume 45, Issue 8, pp. 912 - 917
Migraine is the most common brain disorder, affecting approximately 14% of the adult population, but its molecular mechanisms are poorly understood. We report... 
POPULATION | HUMAN-DISEASE | PROTEIN | NEURITE OUTGROWTH | DOWN-REGULATION | TRANSFORMING-GROWTH-FACTOR | PROTEOLYSIS | ASSOCIATION | EXPRESSION | FAMILY | LEWIS(X) | GENES | GENETICS & HEREDITY | MUTATIONS | Genetic susceptibility | Genetic variation | Migraine | Physiological aspects | Genetic aspects | Research | Risk factors | Studies | Proteins | Signal transduction | Headaches | Population | Genomes | Meta-analysis
Journal Article
by Loos, Ruth J F and Lindgren, Cecilia M and Li, Shengxu and Wheeler, Eleanor and Zhao, Jing Hua and Prokopenko, Inga and Inouye, Michael and Freathy, Rachel M and Attwood, Antony P and Beckmann, Jacques S and Berndt, Sonja I and Bergmann, Sven and Bennett, Amanda J and Bingham, Sheila A and Bochud, Murielle and Brown, Morris and Cauchi, Stéphane and Connell, John M and Cooper, Cyrus and Smith, George Davey and Day, Ian and Dina, Christian and De, Subhajyoti and Dermitzakis, Emmanouil T and Doney, Alex S F and Elliott, Katherine S and Elliott, Paul and Evans, David M and Sadaf Farooqi, I and Froguel, Philippe and Ghori, Jilur and Groves, Christopher J and Gwilliam, Rhian and Hadley, David and Hall, Alistair S and Hattersley, Andrew T and Hebebrand, Johannes and Heid, Iris M and Herrera, Blanca and Hinney, Anke and Hunt, Sarah E and Jarvelin, Marjo-Riitta and Johnson, Toby and Jolley, Jennifer D M and Karpe, Fredrik and Keniry, Andrew and Khaw, Kay-Tee and Luben, Robert N and Mangino, Massimo and Marchini, Jonathan and McArdle, Wendy L and McGinnis, Ralph and Meyre, David and Munroe, Patricia B and Morris, Andrew D and Ness, Andrew R and Neville, Matthew J and Nica, Alexandra C and Ong, Ken K and O'Rahilly, Stephen and Owen, Katharine R and Palmer, Colin N A and Papadakis, Konstantinos and Potter, Simon and Pouta, Anneli and Qi, Lu and Randall, Joshua C and Rayner, Nigel W and Ring, Susan M and Sandhu, Manjinder S and Scherag, André and Sims, Matthew A and Song, Kijoung and Soranzo, Nicole and Speliotes, Elizabeth K and Syddall, Holly E and Teichmann, Sarah A and Timpson, Nicholas J and Tobias, Jonathan H and Uda, Manuela and Ganz Vogel, Carla I and Wallace, Chris and Waterworth, Dawn M and Weedon, Michael N and Willer, Cristen J and Wraight, Vicki L and Yuan, Xin and Zeggini, Eleftheria and Hirschhorn, Joel N and Strachan, David P and Ouwehand, Willem H and Caulfield, Mark J and Samani, Nilesh J and Frayling, Timothy M and Vollenweider, Peter and Waeber, Gerard and Mooser, Vincent and Deloukas, Panos and McCarthy, Mark I and Wareham, Nicholas J and ... and Diabetes Genetics Initiative and The Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial and FUSION and The Wellcome Trust Case Control Consortium and KORA and The SardiNIA Study and Nurses' Health Study and SardiNIA Study and Prostate Lung Colorectal Ovarian and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial
Nature genetics, ISSN 1546-1718, 2008, Volume 40, Issue 6, pp. 768 - 775
To identify common variants influencing body mass index (BMI), we analyzed genome-wide association data from 16,876 individuals of European descent. After... 
FTO GENE | GENETICS & HEREDITY | MELANOCORTIN-4 RECEPTOR GENE | EARLY-ONSET OBESITY | FRAMESHIFT MUTATION | DOMINANT | ADULT OBESITY | EXPRESSION | CHILDHOOD | DEFICIENCY | GENOME-WIDE ASSOCIATION | Meta-Analysis as Topic | Humans | Middle Aged | Alpha-Ketoglutarate-Dependent Dioxygenase FTO | Male | Body Weight - genetics | Obesity - genetics | Case-Control Studies | Genetic Variation | Proteins | Adult | Female | Child | Body Mass Index | Genetic Predisposition to Disease | Cross-Sectional Studies | Receptor, Melanocortin, Type 4 - genetics | Adiposity - genetics | Linkage Disequilibrium | Obesity - pathology | Randomized Controlled Trials as Topic | Obesity - epidemiology | Adolescent | Alleles | Aged | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 18 - genetics | Genome, Human | Quantitative Trait Loci | Cohort Studies | Obesity | Body mass index | Genetic variation | Physiological aspects | Genetic aspects | Diagnosis | Research | Risk factors | Medical research | Biomedical research | Body fat | Health services | Genetics | Birth weight | Adults | Progeny | Integration | Pedigree | Data processing | Melanocortin MC4 receptors | Single-nucleotide polymorphism | Children | Mutation | Population levels | Clinical Medicine | Näringslära | Hälsovetenskap | Endokrinologi och diabetes | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Nutrition and Dietetics | Endocrinology and Diabetes | Health Sciences
Journal Article
by Gormley, Padhraig and Anttila, Verneri and Winsvold, Bendik S and Palta, Priit and Esko, Tonu and Pers, Tune H and Farh, Kai-How and Cuenca-Leon, Ester and Muona, Mikko and Furlotte, Nicholas A and Kurth, Tobias and Ingason, Andres and McMahon, George and Ligthart, Lannie and Terwindt, Gisela M and Kallela, Mikko and Freilinger, Tobias M and Ran, Caroline and Gordon, Scott G and Stam, Anine H and Steinberg, Stacy and Borck, Guntram and Koiranen, Markku and Quaye, Lydia and Adams, Hieab H H and Lehtimäki, Terho and Sarin, Antti-Pekka and Wedenoja, Juho and Hinds, David A and Buring, Julie E and Schürks, Markus and Ridker, Paul M and Hrafnsdottir, Maria Gudlaug and Stefansson, Hreinn and Ring, Susan M and Hottenga, Jouke-Jan and Penninx, Brenda W J H and Färkkilä, Markus and Artto, Ville and Kaunisto, Mari and Vepsäläinen, Salli and Malik, Rainer and Heath, Andrew C and Madden, Pamela A F and Martin, Nicholas G and Montgomery, Grant W and Kurki, Mitja I and Kals, Mart and Mägi, Reedik and Pärn, Kalle and Hämäläinen, Eija and Huang, Hailiang and Byrnes, Andrea E and Franke, Lude and Huang, Jie and Stergiakouli, Evie and Lee, Phil H and Sandor, Cynthia and Webber, Caleb and Cader, Zameel and Muller-Myhsok, Bertram and Schreiber, Stefan and Meitinger, Thomas and Eriksson, Johan G and Salomaa, Veikko and Heikkilä, Kauko and Loehrer, Elizabeth and Uitterlinden, Andre G and Hofman, Albert and van Duijn, Cornelia M and Cherkas, Lynn and Pedersen, Linda M and Stubhaug, Audun and Nielsen, Christopher S and Männikkö, Minna and Mihailov, Evelin and Milani, Lili and Göbel, Hartmut and Esserlind, Ann-Louise and Christensen, Anne Francke and Hansen, Thomas Folkmann and Werge, Thomas and Kaprio, Jaakko and Aromaa, Arpo J and Raitakari, Olli and Ikram, M Arfan and Spector, Tim and Järvelin, Marjo-Riitta and Metspalu, Andres and Kubisch, Christian and Strachan, David P and Ferrari, Michel D and Belin, Andrea C and Dichgans, Martin and Wessman, Maija and van den Maagdenberg, Arn M J M and Zwart, John-Anker and Boomsma, Dorret I and Smith, George Davey and Stefansson, Kari and ... and International Headache Genetics Consortium and Int Headache Genetics Consortium
Nature genetics, ISSN 1546-1718, 2016, Volume 48, Issue 8, pp. 856 - 866
Journal Article
by Middeldorp, Christel M and Hammerschlag, Anke R and Ouwens, Klaasjan G and Groen-Blokhuis, Maria M and St. Pourcain, Beate and Greven, Corina U and Pappa, Irene and Tiesler, Carla M.T and Ang, Wei and Nolte, Ilja M and Vilor-Tejedor, Natalia and Bacelis, Jonas and Ebejer, Jane L and Zhao, Huiying and Davies, Gareth E and Ehli, Erik A and Evans, David M and Fedko, Iryna O and Guxens, Mònica and Hottenga, Jouke-Jan and Hudziak, James J and Jugessur, Astanand and Kemp, John P and Krapohl, Eva and Martin, Nicholas G and Murcia, Mario and Myhre, Ronny and Ormel, Johan and Ring, Susan M and Standl, Marie and Stergiakouli, Evie and Stoltenberg, Camilla and Thiering, Elisabeth and Timpson, Nicholas J and Trzaskowski, Maciej and van der Most, Peter J and Wang, Carol and Nyholt, Dale R and Medland, Sarah E and Neale, Benjamin and Jacobsson, Bo and Sunyer, Jordi and Hartman, Catharina A and Whitehouse, Andrew J.O and Pennell, Craig E and Heinrich, Joachim and Plomin, Robert and Davey Smith, George and Tiemeier, Henning and Posthuma, Danielle and Boomsma, Dorret I and EArly Genetics and Lifecourse Epidemiology (EAGLE) Consortium, Psychiatric Genomics Consortium ADHD Working Group and EArly Genetics Lifecourse and Psychiatric Genomics Consortium and EArly Genetics and Lifecourse Epidemiology (EAGLE) Consortium and Psychiatric Genomics Consortium ADHD Working Group and Institutionen för kliniska vetenskaper, Avdelningen för obstetrik och gynekologi and Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy and Sahlgrenska akademin and Institute of Clinical Sciences, Department of Obstetrics and Gynecology
Journal of the American Academy of Child and Adolescent Psychiatry, ISSN 0890-8567, 2016, Volume 55, Issue 10, pp. 896 - 905.e6
Journal Article
by Willer, Cristen and Speliotes, Elizabeth and Loos, Ruth and Li, Shengxu and Lindgren, Cecilia and Heid, Iris and Berndt, Sonja and Elliott, Amanda and Jackson, Anne and Lamina, Claudia and Lettre, Guillaume and Lim, Noha and Lyon, Helen and McCarroll, Steven and Papadakis, Konstantinos and Qi, Lu and Randall, Joshua and Roccasecca, R.M and Sanna, Serena and Scheet, Paul and Weedon, Michael and Wheeler, Eleanor and Zhao, Jing Hua and Jacobs, Leonie and Prokopenko, Inga and Soranzo, Nicole and Tanaka, Toshiko and Timpson, Nicholas and Almgren, Peter and Bennett, Amanda and Bergman, Richard and Bingham, Sheila and Bonnycastle, Lori and Brown, Morris and Burtt, Noël and Chines, Peter and Coin, Lachlan and Collins, Francis and Connell, John and Cooper, Charles and Smith, Davey and Dennison, Elaine and Deodhar, Parimal and Erdos, Michael and Estrada Gil, Karol and Evans, David and Gianniny, Lauren and Gieger, Christian and Gillson, Christopher and Guiducci, Candace and Hackett, Rachel and Hadley, David and Hall, Alistair and Havulinna, Aki and Hebebrand, Johannes and Hofman, Albert and Isomaa, Bo and Johnson, Toby and Jousilahti, Pekka and Jovanovic, Zorica and Khaw, Kay-Tee and Kraft, Peter and Kuokkanen, Mikko and Kuusisto, Johanna and Laitinen, Jaana and Lakatta, Edward and Luan, J and Luben, Robert and Mangino, Massimo and McArdle, Wendy and Meitinger, Thomas and Mulas, Antonella and Munroe, Patricia and Narisu, Narisu and Ness, Anew and Northstone, Kate and O'Rahilly, Stephen and Purmann, Carolin and Rees, Matthew and Ridderstråle, Martin and Ring, Susan and Rivadeneira Ramirez, Fernando and Ruokonen, Aimo and Sandhu, Manjinder and Saramies, Jouko and Scott, Laura and Scuteri, Angelo and Silander, Kaisa and Sims, Matthew and Song, Kijoung and Stephens, Jonathan and Stevens, Suzanne and Stringham, Heather and Tung, Loraine and Valle, Timo and Tikka-Kleemola, Päivi and Vimaleswaran, Karani and Vollenweider, Peter and Waeber, Gérard and Wallace, Chris and ... and the GIANT Consortium and Wellcome Trust Case Control and Giant Consortium and Wellcome Trust Case Control Consortium and Genetic Investigation of ANthropometric Traits Consortium
Nature genetics, ISSN 1546-1718, 2008, Volume 41, Issue 1, pp. 25 - 34
Journal Article
by Elks, Cathy and Perry, John and Sulem, Patrick and Chasman, Daniel and Franceschini, Nora and He, Chunyan and Lunetta, Kathryn and Visser, Jenny and Byrne, Enda and Cousminer, Diana and Gudbjartsson, Daniel and Esko, Tõnu and Feenstra, Bjarke and Hottenga, Jouke Jan and Koller, Daniel and Kutalik, Zoltán and Lin, Peng and Mangino, Massimo and Marongiu, Mara and McArdle, Patrick and Smith, Albert Vernon and Stolk, Lisette and Wingerden, Sophie and Zhao, Jing Hua and Albrecht, Eva and Corre, Tanguy and Ingelsson, Erik and Hayward, Caroline and Magnusson, Patrik and Ulivi, Shelia and Warrington, Nicole and Zgaga, Lina and Alavere, Helene and Amin, Najaf and Aspelund, Thor and Bandinelli, Stefania and Barroso, Inês and Berenson, Gerald and Bergmann, Sven and Blackburn, Hannah and Boerwinkle, Eric and Buring, Julie and Busonero, F and Campbell, Harry and Chanock, Stephen and Chen, Wei and Cornelis, Marilyn and Couper, David and Coviello, Anea and Adamo, Pio and Faire, Ulf and Geus, Eco and Deloukas, Panagiotis and Döring, Angela and Easton, Douglas and Eiriksdottir, Gudny and Emilsson, Valur and Eriksson, Johan and Ferrucci, Luigi and Folsom, Aaron and Foroud, Tatiana and Garcia, Melissa and Gasparini, Paolo and Geller, Frank and Gieger, Christian and Gudnason, Vilmundur and Hall, Alistair and Hankinson, Susan and Ferreli, Liana and Heath, Anew and Hernandez, Dena and Hofman, Albert and Hu, Frank and Illig, Thomas and Järvelin, M.R and Johnson, Anew and Karasik, David and Khaw, Kay-Tee and Kiel, Douglas and Kilpelänen, Tuomas and Kolcic, Ivana and Kraft, Peter and Launer, Lenore and Laven, Joop and Li, Shengxu and Liu, Jianjun and Levy, Daniel and Martin, Nicholas and Melbye, Mads and Mooser, Vincent and Murray, Jeffrey and Nalls, Michael and Navarro, Pau and Nelis, Mari and Ness, Anew and Northstone, Kate and Oostra, Ben and Peacock, Munro and Palmer, Cameron and Palotie, Aarno and ... and GIANT Consortium and The GIANT Consortium
Nature genetics, ISSN 1061-4036, 12/2010, Volume 42, Issue 12, pp. 1077 - 1085
Journal Article