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The Journal of rheumatology, ISSN 0315-162X, 04/2019
The genetic component of ankylosing spondylitis (AS) development is ~90%. Of the known heritability, ~20% is explained by HLA-B27, and 113 identified... 
Journal Article
The Journal of Rheumatology, ISSN 0315-162X, 04/2019, p. jrheum.181209
Objective The genetic component of ankylosing spondylitis (AS) development is ~90%. Of the known heritability, ~20% is explained by HLA-B27, and 113 identified... 
Journal Article
by McCarthy, Shane and Das, Sayantan and Kretzschmar, Warren and Delaneau, Olivier and Wood, Anew R and Teumer, Alexander and Kang, Hyun Min and Fuchsberger, Christian and Danecek, Petr and Sharp, Kevin and Luo, Yang and Sidorel, Carlo and Kwong, Alan and Timpson, Nicholas and Koskinen, Seppo and Vrieze, Scott and Scott, Laura J and Zhang, He and Mahajan, Anubha and Veldink, Jan and Peters, Ulrike and Pato, Carlos and van Duijn, Cornelia M and Gillies, Christopher E and Gandin, Ilaria and Mezzavilla, Massimo and Gilly, Arthur and Cocca, Massimiliano and Traglia, Michela and Angius, Anea and Barrett, Jeffrey C and Boomsma, Dorrett and Branham, Kari and Breen, Gerome and Brummett, Chad M and Busonero, Fabio and Campbell, Harry and Chan, Anew and Che, Sai and Chew, Emily and Collins, Francis S and Corbin, Laura J and Smith, George Davey and Dedoussis, George and Dorr, Marcus and Farmaki, Aliki-Eleni and Ferrucci, Luigi and Forer, Lukas and Fraser, Ross M and Gabriel, Stacey and Levy, Shawn and Groop, Leif and Harrison, Tabitha and Hattersley, Anew and Holmen, Oddgeir L and Hveem, Kristian and Kretzler, Matthias and Lee, James C and McGue, Matt and Meitinger, Thomas and Melzer, David and Min, Josine L and Mohlke, Karen L and Vincent, John B and Nauck, Matthias and Nickerson, Deborah and Palotie, Aarno and Pato, Michele and Pirastu, Nicola and McInnis, Melvin and Richards, J. Brent and Sala, Cinzia and Salomaa, Veikko and Schlessinger, David and Schoenherr, Sebastian and Slagboom, P. Eline and Small, Kerrin and Spector, Timothy and Stambolian, Dwight and Tuke, Marcus and Tuomilehto, Jaakko and van den Berg, Leonard H and Van Rheenen, Wouter and Volker, Uwe and Wijmenga, Cisca and Toniolo, Daniela and Zeggini, Eleftheria and Gasparini, Paolo and Sampson, Matthew G and Wilson, James F and Frayling, Timothy and de Bakker, Paul I. W and Swertz, Morris A and McCarroll, Steven and Kooperberg, Charles and Dekker, Annelot and Altshuler, David and Willer, Cristen and Iacono, William and Ripatti, Samuli and ... and the Haplotype Reference Consortium and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1279 - 1283
We describe a reference panel of 64,976 human haplotypes at 39,235,157 SNPs constructed using whole-genome sequence data from 20 studies of predominantly... 
Studies | Datasets | Haplotypes | Consortia | Accuracy | Genealogy | Researchers | Genomics | Collaboration | Genomes | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
by Crosby, Jacy and Peloso, Gina M and Auer, Paul L and Crosslin, David R and Stitziel, Nathan O and Lange, Leslie A and Lu, Yingchang and Tang, Zheng-Zheng and Zhang, He and Hindy, George and Masca, Nicholas and Stirrups, Kathleen and Kanoni, Stavroula and Do, Ron and Jun, Goo and Hu, Youna and Kang, Hyun Min and Xue, Chenyi and Goel, Anuj and Farrall, Martin and Duga, Stefano and Merlini, Pier Angelica and Asselta, Rosanna and Girelli, Domenico and Olivieri, Oliviero and Martinelli, Nicola and Yin, Wu and Reilly, Dermot and Speliotes, Elizabeth and Fox, Caroline S and Hveem, Kristian and Holmen, Oddgeir L and Nikpay, Majid and Farlow, Deborah N and Assimes, Themistocles L and Franceschini, Nora and Robinson, Jennifer and North, Kari E and Martin, Lisa W and DePristo, Mark and Gupta, Namrata and Escher, Stefan A and Jansson, Jan-Håkan and Van Zuydam, Natalie and Palmer, Colin N. A and Wareham, Nicholas and Koch, Werner and Meitinger, Thomas and Peters, Annette and Lieb, Wolfgang and Erbel, Raimund and Konig, Inke R and Kruppa, Jochen and Degenhardt, Franziska and Gottesman, Omri and Bottinger, Erwin P and O'Donnell, Christopher J and Psaty, Bruce M and Ballantyne, Christie M and Abecasis, Goncalo and Ordovas, Jose M and Melander, Olle and Watkins, Hugh and Orho-Melander, Marju and Ardissino, Diego and Loos, Ruth J. F and McPherson, Ruth and Willer, Cristen J and Erdmann, Jeanette and Hall, Alistair S and Samani, Nilesh J and Deloukas, Panos and Schunkert, Heribert and Wilson, James G and Kooperberg, Charles and Rich, Stephen S and Tracy, Russell P and Lin, Dan-Yu and Altshuler, David and Gabriel, Stacey and Nickerson, Deborah A and Jarvik, Gail P and Cupples, L. Adrienne and Reiner, Alex P and Boerwinkle, Eric and Kathiresan, Sekar and The TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute and Natl Heart Lung Blood Inst and Exome Sequencing Project and TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
The New England Journal of Medicine, ISSN 0028-4793, 07/2014, Volume 371, Issue 1, pp. 22 - 31
Journal Article
by Morris, Andrew P and Voight, Benjamin F and Teslovich, Tanya M and Ferreira, Teresa and Segrè, Ayellet V and Steinthorsdottir, Valgerdur and Strawbridge, Rona J and Khan, Hassan and Grallert, Harald and Mahajan, Anubha and Prokopenko, Inga and Kang, Hyun Min and Dina, Christian and Esko, Tonu and Fraser, Ross M and Kanoni, Stavroula and Kumar, Ashish and Lagou, Vasiliki and Langenberg, Claudia and Luan, Jian'An and Lindgren, Cecilia M and Müller-Nurasyid, Martina and Pechlivanis, Sonali and Rayner, N. William and Scott, Laura J and Wiltshire, Steven and Yengo, Loic and Kinnunen, Leena and Rossin, Elizabeth J and Raychaudhuri, Soumya and Johnson, Andrew D and Dimas, Antigone S and Loos, Ruth J.F and Vedantam, Sailaja and Chen, Han and Florez, Jose C and Fox, Caroline and Liu, Ching-Ti and Rybin, Denis and Couper, David J and Kao, Wen Hong L and Li, Man and Cornelis, Marilyn C and Kraft, Peter and Sun, Qi and Van Dam, Rob M and Stringham, Heather M and Chines, Peter S and Fischer, Krista and Fontanillas, Pierre and Holmen, Oddgeir L and Hunt, Sarah E and Jackson, Anne U and Kong, Augustine and Lawrence, Robert and Meyer, Julia and Perry, John R.B and Platou, Carl G.P and Potter, Simon and Rehnberg, Emil and Robertson, Neil and Sivapalaratnam, Suthesh and Stančáková, Alena and Stirrups, Kathleen and Thorleifsson, Gudmar and Tikkanen, Emmi and Wood, Andrew R and Almgren, Peter and Atalay, Mustafa and Benediktsson, Rafn and Bonnycastle, Lori L and Burtt, Noël and Carey, Jason and Charpentier, Guillaume and Crenshaw, Andrew T and Doney, Alex S.F and Dorkhan, Mozhgan and Edkins, Sarah and Emilsson, Valur and Eury, Elodie and Forsen, Tom and Gertow, Karl and Gigante, Bruna and Grant, George B and Groves, Christopher J and Guiducci, Candace and Herder, Christian and Hreidarsson, Astradur B and Hui, Jennie and James, Alan and Jonsson, Anna and Rathmann, Wolfgang and Klopp, Norman and Kravic, Jasmina and Krjutškov, Kaarel and Langford, Cordelia and Leander, Karin and Lindholm, Eero and Lobbens, Stéphane and MäNnistö, Satu and ... and Meta-Anal Glucose Insulin-Related and Genetic Invest ANthropometric and Wellcome Trust Case Control and Asian Genetic Epidemiology and S Asian Type 2 Diabet SAT2D and DIAbet Genetics Replication and the DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Lund University and Genomics, Diabetes and Endocrinology and Internmedicin - epidemiologi and EpiHealth: Epidemiology for Health and Genomik, diabetes och endokrinologi and Internal Medicine - Epidemiology and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Nature Genetics, ISSN 1061-4036, 09/2012, Volume 44, Issue 9, pp. 981 - 990
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 4, pp. 345 - 351
Journal Article
by Mahajan, Anubha and Go, Min Jin and Zhang, Weihua and Below, Jennifer E and Gaulton, Kyle J and Ferreira, Teresa and Horikoshi, Momoko and Johnson, Anew D and Ng, Maggie C. Y and Prokopenko, Inga and Saleheen, Danish and Wang, Xu and Zeggini, Eleftheria and Abecasis, Goncalo R and Adair, Linda S and Almgren, Peter and Atalay, Mustafa and Aung, Tin and Baldassarre, Damiano and Balkau, Beverley and Bao, Yuqian and Barnett, Anthony H and Barroso, Ines and Basit, Abdul and Been, Latonya F and Beilby, John and Bell, Graeme I and Benediktsson, Rafn and Bergman, Richard N and Boehm, Bernhard O and Boerwinkle, Eric and Bonnycastle, Lori L and Burtt, Noël and Cai, Qiuyin and Campbell, Harry and Carey, Jason and Cauchi, Stephane and Caulfield, Mark and Chan, Juliana C. N and Chang, Li-Ching and Chang, Tien-Jyun and Chang, Yi-Cheng and Charpentier, Guillaume and Chen, Chien-Hsiun and Chen, Han and Chen, Yuan-Tsong and Chia, Kee-Seng and Chidambaram, Manickam and Chines, Peter S and Cho, Nam H and Cho, Young Min and Chuang, Lee-Ming and Collins, Francis S and Cornelis, Marilyn C and Couper, David J and Crenshaw, Anew T and van Dam, Rob M and Danesh, John and Das, Debashish and de Faire, Ulf and Dedoussis, George and Deloukas, Panos and Dimas, Antigone S and Dina, Christian and Doney, Alex S. F and Donnelly, Peter J and Dorkhan, Mozhgan and van Duijn, Cornelia and Dupuis, Josée and Edkins, Sarah and Elliott, Paul and Emilsson, Valur and Erbel, Raimund and Eriksson, Johan G and Escobedo, Jorge and Esko, Tonu and Eury, Elodie and Florez, Jose C and Fontanillas, Pierre and Forouhi, Nita G and Forsen, Tom and Fox, Caroline and Fraser, Ross M and Frayling, Timothy M and Froguel, Philippe and Frossard, Philippe and Gao, Yutang and Gertow, Karl and Gieger, Christian and Gigante, Bruna and Grallert, Harald and Grant, George B and Groop, Leif C and Groves, Christopher J and Grundberg, Elin and Guiducci, Candace and Hamsten, Anders and Han, Bok-Ghee and Hara, Kazuo and Hassanali, Neelam and ... and South Asian Type Diabet SAT2D Cons and DIAbet Genetics Replication & Meta and Mexican Amer Type 2 Diabet MAT2D C and Asian Genetic Epidemiology Network and Type 2 Diabet Genetic Exploration and South Asian Type 2 Diabetes (SAT2D) Consortium and Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and Type 2 Diabetes Genetic Exploration by Nex-generation sequencing in muylti-Ethnic Samples (T2D-GENES) Consortium and DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium and Mexican American Type 2 Diabetes (MAT2D) Consortium and Type 2 Diabetes Genetic Exploration by Next-generation sequencing in multi-Ethnic Samples (T2D-GENES) Consortium and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 3, pp. 234 - 244
Journal Article
by Stitziel, Nathan O and Stirrups, Kathleen E and Masca, Nicholas G. D and Erdmann, Jeanette and Ferrario, Paola G and König, Inke R and Weeke, Peter E and Webb, Thomas R and Auer, Paul L and Schick, Ursula M and Lu, Yingchang and Zhang, He and Dube, Marie-Pierre and Goel, Anuj and Farrall, Martin and Peloso, Gina M and Won, Hong-Hee and Do, Ron and van Iperen, Erik and Kanoni, Stavroula and Kruppa, Jochen and Mahajan, Anubha and Scott, Robert A and Willenborg, Christina and Braund, Peter S and van Capelleveen, Julian C and Doney, Alex S. F and Donnelly, Louise A and Asselta, Rosanna and Merlini, Piera A and Duga, Stefano and Marziliano, Nicola and Denny, Josh C and Shaffer, Christian M and El-Mokhtari, Nour Eddine and Franke, Ane and Gottesman, Omri and Heilmann, Stefanie and Hengstenberg, Christian and Hoffmann, Per and Holmen, Oddgeir L and Hveem, Kristian and Jansson, Jan-Håkan and Jöckel, Karl-Heinz and Kessler, Thorsten and Kriebel, Jennifer and Laugwitz, Karl L and Marouli, Eirini and Martinelli, Nicola and McCarthy, Mark I and van Zuydam, Natalie R and Meisinger, Christa and Esko, Tõnu and Mihailov, Evelin and Escher, Stefan A and Alver, Maris and Moebus, Susanne and Morris, Anew D and Müller-Nurasyid, Martina and Nikpay, Majid and Olivieri, Oliviero and Perreault, Louis-Philippe Lemieux and AlQarawi, Alaa and Robertson, Neil R and Akinsanya, Karen O and Reilly, Dermot F and Vogt, Thomas F and Yin, Wu and Asselbergs, Folkert W and Kooperberg, Charles and Jackson, Rebecca D and Stahl, Eli and Strauch, Konstantin and Varga, Tibor V and Waldenberger, Melanie and Zeng, Lingyao and Kraja, Aldi T and Liu, Chunyu and Ehret, Georg B and Newton-Cheh, Christopher and Chasman, Daniel I and Chowdhury, Rajiv and Ferrario, Marco and Ford, Ian and Jukema, J. Wouter and Kee, Frank and Kuulasmaa, Kari and Nordestgaard, Børge G and Perola, Markus and Saleheen, Danish and Sattar, Naveed and Surenan, Praveen and Tregouet, David and Young, Robin and Howson, Joanna M. M and Butterworth, Adam S and Danesh, John and Ardissino, Diego and Bottinger, Erwin P and Erbel, Raimund and ... and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
The New England Journal of Medicine, ISSN 0028-4793, 03/2016, Volume 374, Issue 12, pp. 1134 - 1144
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 2, pp. 200 - 204
Journal Article