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Nature communications, ISSN 2041-1723, 01/2019, Volume 10, Issue 1, pp. 155 - 155
Emmanuelle Souzeau, who contributed to analysis of data, was inadvertently omitted from the author list in the originally published version of this Article.... 
Association analysis | Eye diseases | Data processing | Cornea | Genomes
Journal Article
by Iglesias, Adriana I and Mishra, Aniket and Vitart, Veronique and Bykhovskaya, Yelena and Höhn, René and Springelkamp, Henriët and Cuellar-Partida, Gabriel and Gharahkhani, Puya and Bailey, Jessica N. Cooke and Willoughby, Colin E and Li, Xiaohui and Yazar, Seyhan and Nag, Abhishek and Khawaja, Anthony P and Polašek, Ozren and Siscovick, David and Mitchell, Paul and Tham, Yih Chung and Haines, Jonathan L and Kearns, Lisa S and Hayward, Caroline and Shi, Yuan and Van Leeuwen, Elisabeth M and Taylor, Kent D and Wang, Jie Jin and Rochtchina, Elena and Attia, John and Scott, Rodney and Holliday, Elizabeth G and Baird, Paul N and Xie, Jing and Inouye, Michael and Viswanathan, Ananth and Sim, Xueling and Bonnemaijer, Pieter and Rotter, Jerome I and Martin, Nicholas G and Zeller, Tanja and Mills, Richard A and Staffieri, Sandra E and Jonas, Jost B and Schmidtmann, Irene and Boutin, Thibaud and Kang, Jae H and Lucas, Sionne E. M and Wong, Tien Yin and Beutel, Manfred E and Wilson, James F and Allingham, R. Rand and Brilliant, Murray H and Budenz, Donald L and Christen, William G and Fingert, John and Friedman, David S and Gaasterland, Douglas and Gaasterland, Terry and Hauser, Michael A and Kraft, Peter and Lee, Richard K and Lichter, Paul R and Liu, Yutao and Loomis, Stephanie J and Moroi, Sayoko E and Pericak-Vance, Margaret A and Realini, Anthony and Richards, Julia E and Schuman, Joel S and Scott, William K and Singh, Kuldev and Sit, Arthur J and Vollrath, Douglas and Weinreb, Robert N and Wollstein, Gadi and Zack, Donald J and Zhang, Kang and Donnelly, Peter and Barroso, Ines and Blackwell, Jenefer M and Bramon, Elvira and Brown, Matthew A and Casas, Juan P and Corvin, Aiden and Deloukas, Panos and Duncanson, Audrey and Jankowski, Janusz and Markus, Hugh S and Mathew, Christopher G and Palmer, Colin N. A and Plomin, Robert and Rautanen, Anna and Sawcer, Stephen J and Trembath, Richard C and Wood, Nicholas W and Spencer, Chris C. A and Band, Gavin and Bellenguez, Céline and Freeman, Colin and Hellenthal, Garrett and Giannoulatou, Eleni and Pirinen, Matti and ... and Blue Mountains Eye Study-GWAS Grp and NEIGHBORHOOD Consortium and Wellcome Trust Case Control Consor and Blue Mountains Eye Study—GWAS group and Wellcome Trust Case Control Consortium 2 (WTCCC2)
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1 - 11
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide... 
DECORIN | CHROMATIN STATES | POLYMORPHISMS | RISK-FACTOR | MULTIDISCIPLINARY SCIENCES | MOUSE | GENE-EXPRESSION | MUTATIONS | HERITABILITY | LUMICAN | KERATOCONUS | Glaucoma | Cornea | Genes | Myopia | Association analysis | Genomes | Gene expression | Tissues | Connective tissues | Keratoconus | Collagen | Eye diseases | Extracellular matrix | Index Medicus
Journal Article
Nature communications, ISSN 2041-1723, 05/2018, Volume 9, Issue 1, p. 1864
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide... 
Lumican - metabolism | Glaucoma, Open-Angle - genetics | Humans | Corneal Diseases - metabolism | Corneal Dystrophies, Hereditary - ethnology | Corneal Diseases - genetics | Ehlers-Danlos Syndrome - genetics | Corneal Dystrophies, Hereditary - pathology | Loeys-Dietz Syndrome - metabolism | Mendelian Randomization Analysis | Fibrillin-1 - metabolism | Cornea - pathology | Keratoconus - pathology | Corneal Diseases - pathology | Decorin - genetics | Gene Expression | Eye Diseases, Hereditary - pathology | Lumican - genetics | ADAMTS Proteins - metabolism | Proteoglycans - metabolism | Ehlers-Danlos Syndrome - ethnology | European Continental Ancestry Group | Myopia - pathology | Cornea - metabolism | Myopia - ethnology | Loeys-Dietz Syndrome - pathology | Corneal Diseases - ethnology | Marfan Syndrome - metabolism | Marfan Syndrome - pathology | Cornea - abnormalities | Quantitative Trait Loci | Proteoglycans - genetics | ADAMTS Proteins - genetics | Transforming Growth Factor beta2 - metabolism | Corneal Dystrophies, Hereditary - genetics | Glaucoma, Open-Angle - pathology | Keratoconus - metabolism | Loeys-Dietz Syndrome - ethnology | Glaucoma, Open-Angle - ethnology | Myopia - metabolism | Ehlers-Danlos Syndrome - pathology | Marfan Syndrome - ethnology | Keratoconus - genetics | Glaucoma, Open-Angle - metabolism | Fibrillin-1 - genetics | Eye Diseases, Hereditary - ethnology | Genome-Wide Association Study | Quantitative Trait, Heritable | Corneal Dystrophies, Hereditary - metabolism | Marfan Syndrome - genetics | Eye Diseases, Hereditary - genetics | Myopia - genetics | Asian Continental Ancestry Group | Keratoconus - ethnology | Ehlers-Danlos Syndrome - metabolism | Loeys-Dietz Syndrome - genetics | Polymorphism, Single Nucleotide | Transforming Growth Factor beta2 - genetics | Genome, Human | Decorin - metabolism | Eye Diseases, Hereditary - metabolism | Cornea | Decorin | Corneal Dystrophies, Hereditary | Myopia | Corneal Diseases | Marfan Syndrome | Keratoconus | ADAMTS Proteins | Lumican | Transforming Growth Factor beta2 | Ehlers-Danlos Syndrome | Glaucoma, Open-Angle | Fibrillin-1 | Eye Diseases, Hereditary | Proteoglycans | Wellcome Trust Case Control Consortium 2 (WTCCC2) | Blue Mountains Eye Study—GWAS group | Loeys-Dietz Syndrome | NEIGHBORHOOD Consortium
Journal Article
by Webb, Thomas R and Erdmann, Jeanette and Stirrups, Kathleen E and Stitziel, Nathan O and Masca, Nicholas G D and Jansen, Henning and Kanoni, Stavroula and Nelson, Christopher P and Ferrario, Paola G and König, Inke R and Eicher, John D and Johnson, Anew D and Hamby, Stephen E and Betsholtz, Christer and Ruusalepp, Arno and Franzén, Oscar and Schadt, Eric E and Björkegren, Johan L M and Weeke, Peter E 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 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, Pier A and Duga, Stefano and Marziliano, Nicola and Denny, Josh C and Shaffer, Christian and El-Mokhtari, Nour Eddine and Franke, Ane 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 Virtamo, Jarma and Nikpay, Majid and Olivieri, Oliviero and Provost, Sylvie and AlQarawi, Alaa and Robertson, Neil R and Akinsansya, 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 Müller-Nurasyid, Martina and Strauch, Konstantin and Varga, Tibor V and Waldenberger, Melanie and Zeng, Lingyao and Chowdhury, Rajiv and Salomaa, Veikko and Ford, Ian and Jukema, J Wouter and Amouyel, Philippe and Kontto, Jukka and Nordestgaard, Børge G and Ferrières, Jean and Saleheen, Danish and Sattar, Naveed and Surenan, Praveen and Wagner, Aline and Young, Robin and Howson, Joanna M M and ... and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet and Vaskulärbiologi
Journal of the American College of Cardiology, ISSN 0735-1097, 02/2017, Volume 69, Issue 7, p. 823
BACKGROUND: Genome-wide association studies have so far identified 56 loci associated with risk of coronary artery disease (CAD). Many CAD loci show... 
expression quantitative trait loci | genetics | genome-wide association | single nucleotide polymorphism | cholesteryl ester transfer protein | Medical and Health Sciences | Medicin och hälsovetenskap
Journal Article
by Gharahkhani, Puya and Fitzgerald, Rebecca Clare and Vaughan, Thomas L and Palles, Claire and Gockel, Ines and Tomlinson, Ian and Buas, Matthew F and May, Andrea and Gerges, Christian and Anders, Mario and Becker, Jessica and Kreuser, Nicole and Noder, Tania and Venerito, Marino and Veits, Lothar and Schmidt, Thomas and Manner, Hendrik and Schmidt, Claudia and Hess, Timo and Böhmer, Anne C and Izbicki, Jakob R and Hölscher, Arnulf H and Lang, Hauke and Lorenz, Dietmar and Schumacher, Brigitte and Hackelsberger, Andreas and Mayershofer, Rupert and Pech, Oliver and Vashist, Yogesh and Ott, Katja and Vieth, Michael and Weismüller, Josef and Nöthen, Markus M and Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) and Esophageal Adenocarcinoma GenEtics Consortium (EAGLE) and Wellcome Trust Case Control Consortium 2 (WTCCC2) and Attwood, Stephen and Barr, Hugh and Chegwidden, Laura and de Caestecker, John and Harrison, Rebecca and Love, Sharon B and MacDonald, David and Moayyedi, Paul and Prenen, Hans and Watson, RG Peter and Iyer, Prasad G and Anderson, Lesley A and Bernstein, Leslie and Chow, Wong-Ho and Hardie, Laura J and Lagergren, Jesper and Liu, Geoffrey and Risch, Harvey A and Wu, Anna H and Ye, Weimin and Bird, Nigel C and Shaheen, Nicholas J and Gammon, Marilie D and Corley, Douglas A and Caldas, Carlos Manuel and Moebus, Susanne and Knapp, Michael and Peters, Wilbert HM and Neuhaus, Horst and Rösch, Thomas and Ell, Christian and MacGregor, Stuart and Pharoah, Paul David and Whiteman, David C and Jankowski, Janusz and Schumacher, Johannes
ISSN 1470-2045, 2016
Journal Article
by Surenan, Praveen and nos, Fotios and Young, Robin and Warren, Helen and Cook, James P and Manning, Alisa K and Grarup, Niels and Sim, Xueling and Barnes, Daniel R and Witkowska, Kate and Staley, James R and Tragante, Vinicius and Tukiainen, Taru and Yaghootkar, Hanieh and Masca, Nicholas and Freitag, Daniel F and Ferreira, Teresa and Giannakopoulou, Olga and Tinker, Anew and Harakalova, Magdalena and Mihailov, Evelin and Liu, Chunyu and Kraja, Aldi T and Nielsen, Sune Fallgaard and Rasheed, Asif and Samue, Maria and Zhao, Wei and Bonnycastle, Lori L and Jackson, Anne U and Narisu, Narisu and Swift, Amy J and Southam, Lorraine and Marten, Jonathan and Huyghe, Jeroen R and Stancakova, Alena and Fava, Cristiano and Ohlsson, Therese and Matchan, Angela and Stirrups, Kathleen E and Bork-Jensen, Jette and Gjesing, Anette P and Kontto, Jukka and Perola, Markus and Shaw-Hawkins, Susan and Havulinna, Aki S and Zhang, He and Donnelly, Louise A and Groves, Christopher J and Rayner, N. William and Neville, Matt J and Robertson, Neil R and Yiorkas, Anianos M and Herzig, Karl-Heinz and Kajantie, Eero and Zhang, Weihua and Willems, Sara M and Lannfelt, Lars and Malerba, Giovanni and Soranzo, Nicole and Trabetti, Elisabetta and Verweij, Niek and Evangelou, Evangelos and Moayyeri, Alireza and Vergnaud, Anne-Claire and Nelson, Christopher P and Poveda, Alaitz and Varga, Tibor V and Caslake, Muriel and de Craen, Anton J. M and Trompet, Stella and Luan, Jian'an and Scott, Robert A and Harris, Sarah E and Liewald, David C. M and Marioni, Riccardo and Menni, Cristina and Farmaki, Aliki-Eleni and Hallmans, Goran and Renstrom, Frida and Huffman, Jennifer E and Hassinen, Maija and Burgess, Stephen and Vasan, Ramachanan S and Felix, Janine F and Uria-Nickelsen, Maria and Malarstign, Anders and Reilly, Dermot F and Hoek, Maarten and Vogt, Thomas F and Lin, Honghuang and Lieb, Wolfgang and Traylor, Matthew and Markus, Hugh S and Highland, Heather M and Justice, Anne E and Marouli, Eirini and Lindstrom, Jaana and Uusitupa, Matti and Komulainen, Pirjo and Lakka, Timo A and ... and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Geriatrik and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1151 - 1161
High blood pressure is a major risk factor for cardiovascular disease and premature death. However, there is limited knowledge on specific causal genes and... 
Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
by Ehret, Georg and Ferreira, Teresa and Chasman, Daniel and Jackson, Anne and Schmidt, Ellen and Johnson, Toby and Thorleifsson, Gudmar and Luan, Jian'An and Donnelly, Louise and Kanoni, Stavroula and Petersen, A.K and Pihur, Vasyl and Strawbridge, Rona and Shungin, Dmitry and Hughes, M.F and Meirelles, O and Kaakinen, Marika and Bouatia-Naji, Nabila and Kristiansson, Kati and Shah, Sonia and Kleber, Marcus and Guo, Xiuqing and Lyytikäinen, Leo-Pekka and Fava, Cristiano and Eriksson, Niclas and Nolte, Ilja and Magnusson, Patrik and Salfati, Elias and Rallidis, Loukianos and Theusch, E and Smith, A.J.P and Folkersen, Lasse and Witkowska, Ewa and Pers, Tune and Joehanes, Roby and Kim, S.K and Lataniotis, Lazaros and Jansen, R and Johnson, Anew and Warren, Helen and Kim, Y.J and Zhao, W and Wu, Ying and Tayo, Bamidele and Bochud, Murielle and Absher, Devin and Adair, Linda and Amin, Najaf and Arking, Dan and Axelsson, Tomas and Baldassarre, Damiano and Balkau, Beverley and Bandinelli, Stefania and Barnes, Michael and Barroso, Inês and Bevan, S and Bis, Joshua and Bjornsdottir, G and Boehnke, Michael and Boerwinkle, Eric and Bonnycastle, Lori and Boomsma, Dorret and Bornstein, Stefan and Brown, Morris and Burnier, Michel and Cabrera, C.P and Chambers, John and Chang, I.-S and Cheng, C.-Y and Chines, Peter and Chung, R.-H and Collins, Francis and Connell, J.M and Döring, Angela and Dallongeville, J and Danesh, John and Faire, Ulf and Delgado, G and Dominiczak, Anna and Doney, Alex and nos, Fotios and Edkins, Ted and Eicher, J.D and Elosua, Roberto and Enroth, Stefan and Erdmann, Jeanette and Eriksson, Per and Esko, Tõnu and Evangelou, Evangelos and Evans, Alun and Fall, Magnus and Farrall, Martin and Felix, Janine and Ferrieres, Jean and Ferrucci, Luigi and Fornage, Myriam and Forrester, Terrence and Franceschini, Nora and Franco, Oscar and Franco-Cereceda, Anders and ... and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Kardiologi and Molekylär medicin and Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Uppsala kliniska forskningscentrum (UCR)
Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1171 - 1184
Journal Article
by Kanoni, Stavroula and Masca, Nicholas G D and Stirrups, Kathleen E and Varga, Tibor V and Warren, Helen R and Scott, Robert A and Southam, Lorraine and Zhang, Weihua and Yaghootkar, Hanieh and Müller-Nurasyid, Martina and Alves, Alexessander Couto and Strawbridge, Rona J and Lataniotis, Lazaros and Hashim, Nikman An and Besse, Céline and Boland, Anne and Braund, Peter S and Connell, John M and Dominiczak, Anna and Farmaki, Aliki-Eleni and Franks, Stephen and Grallert, Harald and Jansson, Jan-Håkan and Karaleftheri, Maria and Keinänen-Kiukaanniemi, Sirkka and Matchan, Angela and Pasko, Dorota and Peters, Annette and Poulter, Neil and Rayner, Nigel W and Renström, Frida and Rolandsson, Olov and Sabater-Lleal, Maria and Sennblad, Bengt and Sever, Peter and Shields, Denis C and Silveira, Angela and Stanton, Alice V and Strauch, Konstantin and Tomaszewski, Maciej and Tsafantakis, Emmanouil and Waldenberger, Melanie and Blakemore, Alexandra I. F and Dedoussis, George and Escher, Stefan A and Kooner, Jaspal S and McCarthy, Mark I and Palmer, Colin N. A and Hamsten, Anders and Caulfield, Mark J and Frayling, Timothy M and Tobin, Martin D and Jarvelin, Marjo Riitta and Zeggini, Eleftheria and Gieger, Christian and Chambers, John C and Wareham, Nick J and Munroe, Patricia B and Franks, Paul W and Samani, Nilesh J and Deloukas, Panos and EpiHealth: Epidemiology for Health and Lund University and Genetic and Molecular Epidemiology and Genetisk och molekylär epidemiologi and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Human Molecular Genetics, ISSN 0964-6906, 2016, Volume 25, Issue 18, p. 4094
It has been hypothesized that low frequency (1-5% minor allele frequency (MAF)) and rare (<1% MAF) variants with large effect sizes may contribute to the... 
Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
by Ripke, Stephan and Neale, Benjamin M and Corvin, Aiden and Walters, James T. R and Farh, Kai-How and Holmans, Peter A and Lee, Phil and Bulik-Sullivan, Brendan and Collier, David A and Huang, Hailiang and Pers, Tune H and Agartz, Ingrid and Agerbo, Esben and Albus, Margot and Alexander, Madeline and Amin, Farooq and Bacanu, Silviu A and Begemann, Martin and Belliveau, Richard A and Bene, Judit and Bergen, Sarah E and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberly D and Chan, Raymond C. K and Chen, Ronald Y. L and Chen, Eric Y. H and Cheng, Wei and Cheung, Eric F. C and Chong, Siow Ann and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Cormican, Paul and Craddock, Nick and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and del Favero, Jurgen and Demontis, Ditte and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Durmishi, Naser and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedl, Marion and Friedman, Joseph I and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Golimbet, Vera and Gopal, Srihari and Gratten, Jacob and de Haan, Lieuwe and Hammer, Christian and Hamshere, Marian L and Hansen, Mark and Hansen, Thomas and Haroutunian, Vahram and Hartmann, Annette M and Henskens, Frans A and Herms, Stefan and Hirschhorn, Joel N and Hoffmann, Per and Hofman, Anea and Hollegaard, Mads V and Hougaard, David M and Ikeda, Masashi and Joa, Inge and ... and Psychiat Genomics Consortium and Wellcome Trust Case-Control Consor and Psychosis Endophenotypes Int Conso and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature, ISSN 0028-0836, 2014, Volume 511, Issue 7510, pp. 421 - 427
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be... 
COMMON VARIANTS | MUTATIONS | MULTIDISCIPLINARY SCIENCES | CONFERRING RISK | GENOME-WIDE ASSOCIATION | Schizophrenia | Genetic research | Research | Health aspects | Analysis | Studies | Confidence intervals | Hypotheses | Genealogy | Sample size | Genomics | Genetics | Trends | Index Medicus | Clinical Medicine | Psykiatri | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Psychiatry
Journal Article
by Sabater-Lleal, Maria and Huang, Jie and Chasman, Daniel and Naitza, Silvia and Dehghan, Abbas and Johnson, Andrew D and Teumer, Alexander and Reiner, Alex P and Folkersen, Lasse and Basu, Saonli and Rudnicka, Alicja R and Trompet, Stella and Mälarstig, Anders and Baumert, Jens and Bis, Joshua C and Guo, Xiuqing and Hottenga, Jouke J and Shin, So-Youn and Lopez, Lorna M and Lahti, Jari and Tanaka, Toshiko and Yanek, Lisa R and Oudot-Mellakh, Tiphaine and Wilson, James F and Navarro, Pau and Huffman, Jennifer E and Zemunik, Tatijana and Redline, Susan and Mehra, Reena and Pulanic, Drazen and Rudan, Igor and Wright, Alan F and Kolcic, Ivana and Polasek, Ozren and Wild, Sarah H and Campbell, Harry and Curb, J David and Wallace, Robert and Liu, Simin and Eaton, Charles B and Becker, Diane M and Becker, Lewis C and Bandinelli, Stefania and Räikkönen, Katri and Widen, Elisabeth and Palotie, Aarno and Fornage, Myriam and Green, David and Gross, Myron and Davies, Gail and Harris, Sarah E and Liewald, David C and Starr, John M and Williams, Frances M.K and Grant, P.J and Spector, Timothy D and Strawbridge, Rona J and Silveira, Angela and Sennblad, Bengt and Rivadeneira, Fernando and Uitterlinden, Andre G and Franco, Oscar H and Hofman, Albert and van Dongen, Jenny and Willemsen, G and Boomsma, Dorret I and Yao, Jie and Jenny, Nancy Swords and Haritunians, Talin and McKnight, Barbara and Lumley, Thomas and Taylor, Kent D and Rotter, Jerome I and Psaty, Bruce M and Peters, Annette and Gieger, Christian and Illig, Thomas and Grotevendt, Anne and Homuth, Georg and Völzke, Henry and Kocher, Thomas and Goel, Anuj and Franzosi, Maria Grazia and Seedorf, Udo and Clarke, Robert and Steri, Maristella and Tarasov, Kirill V and Sanna, Serena and Schlessinger, David and Stott, David J and Sattar, Naveed and Buckley, Brendan M and Rumley, Ann and Lowe, Gordon D and McArdle, Wendy L and Chen, Ming-Huei and Tofler, Geoffrey H and Song, Jaejoon and Boerwinkle, Eric and Folsom, Aaron R and ...
Circulation, ISSN 0009-7322, 9/2013, Volume 128, Issue 12
Journal Article
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PLoS ONE, ISSN 1932-6203, 06/2013, Volume 8, Issue 6, pp. e64408 - e64408
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