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by Barban, Nicola and Jansen, Rick and de Vlaming, Ronald and Vaez, Ahmad and Mandemakers, Jornt J and Tropf, Felix C and Shen, Xia and Wilson, James F and Chasman, Daniel I and Nolte, Ilja M and Tragante, Vinicius and van der Laan, Sander W and Perry, John R B and Kong, Augustine and Ahluwalia, Tarunveer S and Albrecht, Eva and Yerges-Armstrong, Laura and Atzmon, Gil and Auro, Kirsi and Ayers, Kristin and Bakshi, Andrew and Ben-Avraham, Danny and Berger, Klaus and Bergman, Aviv and Bertram, Lars and Bielak, Lawrence F and Bjornsdottir, Gyda and Bonder, Marc Jan and Broer, Linda and Bui, Minh and Barbieri, Caterina and Cavadino, Alana and Chavarro, Jorge E and Turman, Constance and Concas, Maria Pina and Cordell, Heather J and Davies, Gail and Eibich, Peter and Eriksson, Nicholas and Esko, Tõnu and Eriksson, Joel and Falahi, Fahimeh and Felix, Janine F and Fontana, Mark Alan and Franke, Lude and Gandin, Ilaria and Gaskins, Audrey J and Gieger, Christian and Gunderson, Erica P and Guo, Xiuqing and Hayward, Caroline and He, Chunyan and Hofer, Edith and Huang, Hongyan and Joshi, Peter K and Kanoni, Stavroula and Karlsson, Robert and Kiechl, Stefan and Kifley, Annette and Kluttig, Alexander and Kraft, Peter and Lagou, Vasiliki and Lecoeur, Cecile and Lahti, Jari and Li-Gao, Ruifang and Lind, Penelope A and Liu, Tian and Makalic, Enes and Mamasoula, Crysovalanto and Matteson, Lindsay and Mbarek, Hamdi and McArdle, Patrick F and McMahon, George and Meddens, S Fleur W and Mihailov, Evelin and Miller, Mike and Missmer, Stacey A and Monnereau, Claire and van der Most, Peter J and Myhre, Ronny and Nalls, Mike A and Nutile, Teresa and Kalafati, Ioanna Panagiota and Porcu, Eleonora and Prokopenko, Inga and Rajan, Kumar B and Rich-Edwards, Janet and Rietveld, Cornelius A and Robino, Antonietta and Rose, Lynda M and Rueedi, Rico and Ryan, Kathleen A and Saba, Yasaman and Schmidt, Daniel and Smith, Jennifer A and Stolk, Lisette and Streeten, Elizabeth and Tönjes, Anke and Thorleifsson, Gudmar and Ulivi, Sheila and ... and LifeLines Cohort Study and BIOS Consortium and Bios Consortium and Institutionen för kliniska vetenskaper, Avdelningen för obstetrik och gynekologi and Göteborgs universitet and Gothenburg University and Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition and Sahlgrenska Academy and Centre for Bone and Arthritis Research and Sahlgrenska akademin and Institute of Medicine, Department of Internal Medicine and Clinical Nutrition and Institute of Clinical Sciences, Department of Obstetrics and Gynecology
Nature genetics, ISSN 1546-1718, 10/2016, Volume 48, Issue 12, pp. 1462 - 1472
Journal Article
by Evangelou, Evangelos and Warren, Helen R and Mosen-Ansorena, David and Mifsud, Borbala and Pazoki, Raha and Gao, He and Ntritsos, Georgios and Dimou, Niki and Cabrera, Claudia P and Karaman, Ibrahim and Ng, Fu Liang and Evangelou, Marina and Witkowska, Katarzyna and Tzanis, Evan and Hellwege, Jacklyn N and Giri, Ayush and Velez Edwards, Digna R and Sun, Yan V and Cho, Kelly and Gaziano, J. Michael and Wilson, Peter W. F and Tsao, Philip S and Kovesdy, Csaba P and Esko, Tonu and Mägi, Reedik and Milani, Lili and Almgren, Peter and Boutin, Thibaud and Debette, Stéphanie and Ding, Jun and Giulianini, Franco and Holliday, Elizabeth G and Jackson, Anne U and Li-Gao, Ruifang and Lin, Wei-Yu and Luan, Jian’an and Mangino, Massimo and Oldmeadow, Christopher and Prins, Bram Peter and Qian, Yong and Sargurupremraj, Muralidharan and Shah, Nabi and Surendran, Praveen and Thériault, Sébastien and Verweij, Niek and Willems, Sara M and Zhao, Jing-Hua and Amouyel, Philippe and Connell, John and de Mutsert, Renée and Doney, Alex S. F and Farrall, Martin and Menni, Cristina and Morris, Andrew D and Noordam, Raymond and Paré, Guillaume and Poulter, Neil R and Shields, Denis C and Stanton, Alice and Thom, Simon and Abecasis, Gonçalo and Amin, Najaf and Arking, Dan E and Ayers, Kristin L and Barbieri, Caterina M and Batini, Chiara and Bis, Joshua C and Blake, Tineka and Bochud, Murielle and Boehnke, Michael and Boerwinkle, Eric and Boomsma, Dorret I and Bottinger, Erwin P and Braund, Peter S and Brumat, Marco and Campbell, Archie and Campbell, Harry and Chakravarti, Aravinda and Chambers, John C and Chauhan, Ganesh and Ciullo, Marina and Cocca, Massimiliano and Collins, Francis and Cordell, Heather J and Davies, Gail and de Borst, Martin H and de Geus, Eco J and Deary, Ian J and Deelen, Joris and Del Greco M, Fabiola and Demirkale, Cumhur Yusuf and Dörr, Marcus and Ehret, Georg B and Elosua, Roberto and Enroth, Stefan and Erzurumluoglu, A. Mesut and Ferreira, Teresa and Frånberg, Mattias and Franco, Oscar H and Gandin, Ilaria and ... and the Million Veteran Program and Million Vet Program and Million Veteran Program and The Million Veteran Program
Nature genetics, ISSN 1546-1718, 09/2018, Volume 50, Issue 10, pp. 1412 - 1425
Journal Article
by van den Berg, Stéphanie M and de Moor, Marleen H. M and Verweij, Karin J. H and Krueger, Robert F and Luciano, Michelle and Arias Vasquez, Alejandro and Matteson, Lindsay K and Derringer, Jaime and Esko, Tõnu and Amin, Najaf and Gordon, Scott D and Hansell, Narelle K and Hart, Amy B and Seppälä, Ilkka and Huffman, Jennifer E and Konte, Bettina and Lahti, Jari and Lee, Minyoung and Miller, Mike and Nutile, Teresa and Tanaka, Toshiko and Teumer, Alexander and Viktorin, Alexander and Wedenoja, Juho and Abdellaoui, Abdel and Abecasis, Goncalo R and Adkins, Daniel E and Agrawal, Arpana and Allik, Jüri and Appel, Katja and Bigdeli, Timothy B and Busonero, Fabio and Campbell, Harry and Costa, Paul T and Smith, George Davey and Davies, Gail and de Wit, Harriet and Ding, Jun and Engelhardt, Barbara E and Eriksson, Johan G and Fedko, Iryna O and Ferrucci, Luigi and Franke, Barbara and Giegling, Ina and Grucza, Richard and Hartmann, Annette M and Heath, Andrew C and Heinonen, Kati and Henders, Anjali K and Homuth, Georg and Hottenga, Jouke-Jan and Iacono, William G and Janzing, Joost and Jokela, Markus and Karlsson, Robert and Kemp, John P and Kirkpatrick, Matthew G and Latvala, Antti and Lehtimäki, Terho and Liewald, David C and Madden, Pamela A. F and Magri, Chiara and Magnusson, Patrik K. E and Marten, Jonathan and Maschio, Andrea and Mbarek, Hamdi and Medland, Sarah E and Mihailov, Evelin and Milaneschi, Yuri and Montgomery, Grant W and Nauck, Matthias and Nivard, Michel G and Ouwens, Klaasjan G and Palotie, Aarno and Pettersson, Erik and Polasek, Ozren and Qian, Yong and Pulkki-Råback, Laura and Raitakari, Olli T and Realo, Anu and Rose, Richard J and Ruggiero, Daniela and Schmidt, Carsten O and Slutske, Wendy S and Sorice, Rossella and Starr, John M and St Pourcain, Beate and Sutin, Angelina R and Timpson, Nicholas J and Trochet, Holly and Vermeulen, Sita and Vuoksimaa, Eero and Widen, Elisabeth and Wouda, Jasper and Wright, Margaret J and Zgaga, Lina and Porteous, David and Minelli, Alessandra and Palmer, Abraham A and Rujescu, Dan and ... and Generation Scotland
Behavior genetics, ISSN 1573-3297, 09/2015, Volume 46, Issue 2, pp. 170 - 182
Journal Article
by Warren, Helen R and Evangelou, Evangelos and Cabrera, Claudia P and Gao, He and Ren, Meixia and Mifsud, Borbala and Ntalla, Ioanna and Surendran, Praveen and Liu, Chunyu and Cook, James P and Kraja, Aldi T and Drenos, Fotios and Loh, Marie and Verweij, Niek and Marten, Jonathan and Karaman, Ibrahim and Lepe, Marcelo P Segura and O'Reilly, Paul F and Knight, Joanne and Snieder, Harold and Kato, Norihiro and He, Jiang and Tai, E Shyong and Said, M Abdullah and Porteous, David and Alver, Maris and Poulter, Neil and Farrall, Martin and Gansevoort, Ron T and Padmanabhan, Sandosh and Mägi, Reedik and Stanton, Alice and Connell, John and Bakker, Stephan J L and Metspalu, Andres and Shields, Denis C and Thom, Simon and Brown, Morris and Sever, Peter and Esko, Tõnu and Hayward, Caroline and van der Harst, Pim and Saleheen, Danish and Chowdhury, Rajiv and Chambers, John C and Chasman, Daniel I and Chakravarti, Aravinda and Newton-Cheh, Christopher and Lindgren, Cecilia M and Levy, Daniel and Kooner, Jaspal S and Keavney, Bernard and Tomaszewski, Maciej and Samani, Nilesh J and Howson, Joanna M M and Tobin, Martin D and Munroe, Patricia B and Ehret, Georg B and Wain, Louise V and The CHD Exome+ Consortium and The International Consortium of Blood Pressure (ICBP) 1000G Analyses and The International Genomics of Blood Pressure (iGEN-BP) Consortium and The UK Biobank CardioMetabolic Consortium BP working group and The Cohorts for Heart and Ageing Research in Genome Epidemiology (CHARGE) BP Exome Consortium and The GoT2DGenes Consortium and The ExomeBP Consortium and The T2D-GENES Consortium and CHARGE BP Exome Consortium and UK Biobank CardioMetab Consortium and GoT2D Genes Consortium and Understanding Soc Sci Grp and Lifelines Cohort Study and Int Consortium Blood Pressure ICBP and BIOS Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-GENES Consortium and iGEN-BP Consortium and International Consortium of Blood Pressure (ICBP) 1000G Analyses and Understanding Society Scientific group and CHD Exome+ Consortium and Cohorts for Heart and Ageing Research in Genome Epidemiology (CHARGE) BP Exome Consortium and International Genomics of Blood Pressure (iGEN-BP) Consortium and UK Biobank CardioMetabolic Consortium BP working group and GoT2DGenes Consortium
Nature genetics, ISSN 1546-1718, 01/2017, Volume 49, Issue 3, pp. 403 - 415
Journal Article
by Wuttke, Matthias and Li, Yong and Li, Man and Sieber, Karsten B and Feitosa, Mary F and Gorski, Mathias and Tin, Adrienne and Wang, Lihua and Chu, Audrey Y and Hoppmann, Anselm and Kirsten, Holger and Giri, Ayush and Chai, Jin-Fang and Sveinbjornsson, Gardar and Tayo, Bamidele O and Nutile, Teresa and Fuchsberger, Christian and Marten, Jonathan and Cocca, Massimiliano and Ghasemi, Sahar and Xu, Yizhe and Horn, Katrin and Noce, Damia and van der Most, Peter J and Sedaghat, Sanaz and Yu, Zhi and Akiyama, Masato and Afaq, Saima and Ahluwalia, Tarunveer S and Almgren, Peter and Amin, Najaf and Ärnlöv, Johan and Bakker, Stephan J. L and Bansal, Nisha and Baptista, Daniela and Bergmann, Sven and Biggs, Mary L and Biino, Ginevra and Boehnke, Michael and Boerwinkle, Eric and Boissel, Mathilde and Bottinger, Erwin P and Boutin, Thibaud S and Brenner, Hermann and Brumat, Marco and Burkhardt, Ralph and Butterworth, Adam S and Campana, Eric and Campbell, Archie and Campbell, Harry and Canouil, Mickaël and Carroll, Robert J and Catamo, Eulalia and Chambers, John C and Chee, Miao-Ling and Chee, Miao-Li and Chen, Xu and Cheng, Ching-Yu and Cheng, Yurong and Christensen, Kaare and Cifkova, Renata and Ciullo, Marina and Concas, Maria Pina and Cook, James P and Coresh, Josef and Corre, Tanguy and Sala, Cinzia Felicita and Cusi, Daniele and Danesh, John and Daw, E. Warwick and de Borst, Martin H and De Grandi, Alessandro and de Mutsert, Renée and de Vries, Aiko P. J and Degenhardt, Frauke and Delgado, Graciela and Demirkan, Ayse and Di Angelantonio, Emanuele and Dittrich, Katalin and Divers, Jasmin and Dorajoo, Rajkumar and Eckardt, Kai-Uwe and Ehret, Georg and Elliott, Paul and Endlich, Karlhans and Evans, Michele K and Felix, Janine F and Foo, Valencia Hui Xian and Franco, Oscar H and Franke, Andre and Freedman, Barry I and Freitag-Wolf, Sandra and Friedlander, Yechiel and Froguel, Philippe and Gansevoort, Ron T and Gao, He and Gasparini, Paolo and Gaziano, J. Michael and Giedraitis, Vilmantas and Gieger, Christian and ... and V. A. Million Veteran Program and Lifelines Cohort Study and Lifelines COHort Study
Nature genetics, ISSN 1546-1718, 05/2019, Volume 51, Issue 6, pp. 957 - 972
Chronic kidney disease (CKD) is responsible for a public health burden with multi-systemic complications. Through transancestry meta-analysis of genome-wide... 
COMMON VARIANTS | METAANALYSIS | TRANSPORTER | TRANS-EQTLS | INTEGRATION | DISEASE | RENAL-FUNCTION | CLASSIFICATION | HERITABILITY | GENOME-WIDE ASSOCIATION | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Glomerular Filtration Rate | Quantitative Trait, Heritable | Humans | Genetic Association Studies - methods | European Continental Ancestry Group | Chromosome Mapping | Renal Insufficiency, Chronic - physiopathology | Kidney Function Tests | Inheritance Patterns | Phenotype | Renal Insufficiency, Chronic - genetics | Uromodulin - urine | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Renal Insufficiency, Chronic - urine | Quantitative trait loci | Genetic markers | Chronic kidney failure | Analysis | Genetic aspects | Diagnosis | Identification and classification | Glomerular filtration rate | Phenotypes | Animal models | Kidneys | Epidermal growth factor receptors | Complications | Genes | Cardiovascular disease | Mapping | Genomes | Metabolism | Gene expression | Loci | Human tissues | Meta-analysis | Studies | Urea | Population | Genetics | Gene loci | Kidney diseases | Gene mapping | Bioinformatics | Public health | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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