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The American Journal of Human Genetics, ISSN 0002-9297, 11/2011, Volume 89, Issue 5, pp. 619 - 627
Journal Article
by Altshuler, David M and Gibbs, Richard A and Peltonen, Leena and Schaffner, Stephen F and Yu, Fuli and Dermitzakis, Emmanouil and Bonnen, Penelope E and De Bakker, Paul I. W and Deloukas, Panos and Gabriel, Stacey B and Gwilliam, Rhian and Hunt, Sarah and Inouye, Michael and Jia, Xiaoming and Aarno Palotie, Palotie and Parkin, Melissa and Whittaker, Pamela and Chang, Kyle and Hawes, Alicia and Lewis, Lora R and Ren, Yanru and Wheeler, David and Muzny, Donna Marie and Barnes, Chris and Darvishi, Katayoon and Hurles, Matthew and Korn, Joshua M and Kristiansson, Kati and Lee, Charles and McCarroll, Steven A and Nemesh, James and Keinan, Alon and Montgomery, Stephen B and Samuela Pollack, Pollack and Price, Alkes L and Soranzo, Nicole and Gonzaga-Jauregui, Claudia and Anttila, Verneri and Brodeur, Wendy and Daly, Mark J and Leslie, Stephen and McVean, Gil and Moutsianas, Loukas and Nguyen, Huy and Zhang, Qingrun and Ghori, Mohammed J. R and McGinnis, Ralph and McLaren, William and Pollack, Samuela and Takeuchi, Fumihiko and Grossman, Sharon R and Shlyakhter, Ilya and Hostetter, Elizabeth B and Sabeti, Pardis C and Adebamowo, Clement A and Foster, Morris W and Gordon, Deborah R and Licinio, Julio and Manca, Maria Cristina and Marshall, Patricia A and Matsuda, Ichiro and Ngare, Duncan and Wang, Vivian Ota and Reddy, Deepa and Rotimi, Charles N and Royal, Charmaine D and Sharp, Richard R and Zeng, Changqing and Brooks, D.B and McEwen, Jean E and Int HapMap 3 Consortium and International HapMap 3 Consortium and The International HapMap 3 Consortium
Nature, ISSN 0028-0836, 09/2010, Volume 467, Issue 7311, pp. 52 - 58
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
by Ripke, Stephan and O'Dushlaine, Colm and Chambert, Kimberly and Moran, Jennifer L and Kähler, Anna K and Akterin, Susanne and Bergen, Sarah E and Collins, Ann L and Crowley, James J and Fromer, Menachem and Kim, Yunjung and Lee, Sang Hong and Magnusson, Patrik K. E and Sanchez, Nick and Stahl, Eli A and Williams, Stephanie and Wray, Naomi R and Xia, Kai and Bettella, Francesco and Borglum, Anders D and Bulik-Sullivan, Brendan K and Cormican, Paul and Craddock, Nick and de Leeuw, Christiaan and Durmishi, Naser and Gill, Michael and Golimbet, Vera and Hamshere, Marian L and Holmans, Peter and Hougaard, David M and Kendler, Kenneth S and Lin, Kuang and Morris, Derek W and Mors, Ole and Mortensen, Preben B and Neale, Benjamin M and O'Neill, Francis A and Owen, Michael J and Milovancevic, Milica Pejovic and Posthuma, Danielle and Powell, John and Richards, Alexander L and Riley, Brien P and Ruderfer, Douglas and Rujescu, Dan and Sigurdsson, Engilbert and Silagadze, Teimuraz and Smit, August B and Stefansson, Hreinn and Steinberg, Stacy and Suvisaari, Jaana and Tosato, Sarah and Verhage, Matthijs and Walters, James T and Levinson, Douglas F and Gejman, Pablo V and Laurent, Claudine and Mowry, Bryan J and O'Donovan, Michael C and Pulver, Ann E and Schwab, Sibylle G and Wildenauer, Dieter B and Dudbridge, Frank and Shi, Jianxin and Albus, Margot and Alexander, Madeline and Campion, Dominique and Cohen, David and Dikeos, Dimitris and Duan, Jubao and Eichhammer, Peter and Godard, Stephanie and Hansen, Mark and Lerer, F. Bernard and Liang, Kung-Yee and Maier, Wolfgang and Mallet, Jacques and Nertney, Deborah A and Nestadt, Gerald and Norton, Nadine and Papadimitriou, George N and Ribble, Robert and Sanders, Alan R and Silverman, Jeremy M and Walsh, Dermot and Williams, Nigel M and Wormley, Brandon and Arranz, Maria J and Bakker, Steven and Bender, Stephan and Bramon, Elvira and Collier, David and Crespo-Facorro, Benedicto and Hall, Jeremy and Iyegbe, Conrad and Jablensky, Assen and Kahn, Rene S and Kalaydjieva, Luba and Lawrie, Stephen and Lewis, Cathryn M and ... and Multictr Genetic Studies Schizophr and Wellcome Trust Case Control Consor and Psychosis Endophenotypes Int Conso and Wellcome Trust Case Control Consortium 2 and Multicenter Genetic Studies of Schizophrenia Consortium and Psychosis Endophenotypes International Consortium
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 10, pp. 1150 - 1159
Journal Article
by Jostins, Luke and Ripke, Stephan and Weersma, Rinse K and Duerr, Richard H and McGovern, Dermot P and Hui, Ken Y and Lee, James C and Schumm, L. Philip and Sharma, Yashoda and Anderson, Carl A and Essers, Jonah and Mitrovic, Mitja and Ning, Kaida and Cleynen, Isabelle and Theatre, Emilie and Spain, Sarah L and Raychaudhuri, Soumya and Goyette, Philippe and Wei, Zhi and Abraham, Clara and Achkar, Jean-Paul and Ahmad, Tariq and Amininejad, Leila and Ananthakrishnan, Ashwin N and Andersen, Vibeke and Anews, Jane M and Baidoo, Leonard and Balschun, Tobias and Bampton, Peter A and Bitton, Alain and Boucher, Gabrielle and Brand, Stephan and Büning, Carsten and Cohain, Ariella and Cichon, Sven and D'Amato, Mauro and de Jong, Dirk and Devaney, Kathy L and Dubinsky, Marla and Edwards, Cathryn and Ellinghaus, David and Ferguson, Lynnette R and Franchimont, Denis and Fransen, Karin and Gearry, Richard and Georges, Michel and Gieger, Christian and Glas, Jürgen and Haritunians, Talin and Hart, Ailsa and Hawkey, Chris and Hedl, Matija and Hu, Xinli and Karlsen, Tom H and Kupcinskas, Limas and Kugathasan, Subra and Latiano, Anna and Laukens, Debby and Lawrance, Ian C and Lees, Charlie W and Louis, Edouard and Mahy, Gillian and Mansfield, John and Morgan, Angharad R and Mowat, Craig and Newman, William and Palmieri, Orazio and Ponsioen, Cyriel Y and Potocnik, Uros and Prescott, Natalie J and Regueiro, Miguel and Rotter, Jerome I and Russell, Richard K and Sanderson, Jeremy D and Sans, Miquel and Satsangi, Jack and Schreiber, Stefan and Simms, Lisa A and Sventoraityte, Jurgita and Targan, Stephan R and Taylor, Kent D and Tremelling, Mark and Verspaget, Hein W and de Vos, Martine and Wijmenga, Cisca and Wilson, David C and Winkelmann, Juliane and Xavier, Ramnik J and Zeissig, Sebastian and Zhang, Bin and Zhang, Clarence K and Zhao, Hongyu and Silverberg, Mark S and Annese, Vito and Hakonarson, Hakon and Brant, Steven R and Radford-Smith, Graham and Mathew, Christopher G and Rioux, John D and Schadt, Eric E and ... and Int IBD Genetics Consortium IIBDGC and International IBD Genetics Consortium (IIBDGC) and The International IBD Genetics Consortium (IIBDGC) and Region Örebro län and Örebro universitet and Institutionen för medicinska vetenskaper
Nature, ISSN 0028-0836, 2012, Volume 491, Issue 7422, pp. 119 - 124
Crohn's disease and ulcerative colitis, the two common forms of inflammatory bowel disease (IBD), affect over 2.5 million people of European ancestry, with... 
HYPER-IGE SYNDROME | RISK LOCI | NETWORK | NUMBER | METAANALYSIS | TUBERCULOSIS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | MUTATIONS | EXPRESSION | Crohn Disease - genetics | Humans | Inflammatory Bowel Diseases - immunology | Colitis, Ulcerative - genetics | Mycobacterium tuberculosis - immunology | Inflammatory Bowel Diseases - physiopathology | Colitis, Ulcerative - immunology | Host-Pathogen Interactions - immunology | Mycobacterium tuberculosis - pathogenicity | Haplotypes - genetics | Mycobacterium - pathogenicity | Mycobacterium Infections - genetics | Inflammatory Bowel Diseases - genetics | Crohn Disease - microbiology | Mycobacterium Infections - microbiology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Reproducibility of Results | Mycobacterium - immunology | Crohn Disease - immunology | Genome, Human - genetics | Phenotype | Colitis, Ulcerative - microbiology | Host-Pathogen Interactions - genetics | Polymorphism, Single Nucleotide - genetics | Inflammatory Bowel Diseases - microbiology | Crohn Disease - physiopathology | Colitis, Ulcerative - physiopathology | Inflammatory bowel disease | Candidates | Tuberculosis | Architecture | Genetics | Genomes | Diabetes | Gene expression | Health risk assessment | Immune system | Index Medicus | Rheumatology and Autoimmunity | Basic Medicine | Medical Genetics | Medicinsk genetik | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Reumatologi och inflammation | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin
Journal Article
by Sawcer, Stephen and Hellenthal, Garrett and Pirinen, Matti and Spencer, Chris C.A and Patsopoulos, Nikolaos A and Moutsianas, Loukas and Dilthey, Alexander and Su, Zhan and Freeman, Colin and Hunt, Sarah E and Edkins, Sarah and Gray, Emma and Booth, David R and Potter, Simon C and Goris, An and Band, Gavin and Oturai, Annette Bang and Strange, Amy and Saarela, Janna and Bellenguez, Céline and Fontaine, Bertrand and Gillman, Matthew and Hemmer, Bernhard and Gwilliam, Rhian and Zipp, Frauke and Jayakumar, Alagurevathi and Martin, Roland and Leslie, Stephen and Hawkins, Stanley and Giannoulatou, Eleni and D'Alfonso, Sandra and Blackburn, Hannah and Boneschi, Filippo Martinelli and Liddle, Jennifer and Harbo, Hanne F and Perez, Marc L and Spurkland, Anne and Waller, Matthew J and Mycko, Marcin P and Ricketts, Michelle and Comabella, Manuel and Hammond, Naomi and Kockum, Ingrid and McCann, Owen T and Ban, Maria and Whittaker, Pamela and Kemppinen, Anu and Weston, Paul and Hawkins, Clive and Widaa, Sara and Zajicek, John and Dronov, Serge and Robertson, Neil and Bumpstead, Suzannah J and Barcellos, Lisa F and Ravindrarajah, Rathi and Abraham, Roby and Alfredsson, Lars and Ardlie, Kristin and Aubin, Cristin and Baker, Amie and Baker, Katharine and Baranzini, Sergio E and Bergamaschi, Laura and Bergamaschi, Roberto and Bernstein, Allan and Berthele, Achim and Boggild, Mike and Bradfield, Jonathan P and Brassat, David and Broadley, Simon A and Buck, Dorothea and Butzkueven, Helmut and Capra, Ruggero and Carroll, William M and Cavalla, Paola and Celius, Elisabeth G and Cepok, Sabine and Chiavacci, Rosetta and Clerget-Darpoux, Françoise and Clysters, Katleen and Comi, Giancarlo and Cossburn, Mark and Cournu-Rebeix, Isabelle and Cox, Mathew B and Cozen, Wendy and Cree, Bruce A.C and Cross, Anne H and Cusi, Daniele and Daly, Mark J and Davis, Emma and De Bakker, Paul I.W and Debouverie, Marc and D'Hooghe, Marie Beatrice and Dixon, Katherine and Dobosi, Rita and Dubois, Bénédicte and Ellinghaus, David and Elovaara, Irina and Esposito, Federica and ... and Wellcome Trust Case Control Consor and Int Multiple Sclerosis Genetics Co and Wellcome Trust Case Control Consortium 2 and International Multiple Sclerosis Genetics Consortium and The International Multiple Sclerosis Genetics Consortium & The Wellcome Trust Case Control Consortium 2 and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Nature, ISSN 0028-0836, 08/2011, Volume 476, Issue 7359, pp. 214 - 219
Journal Article