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Creators: Springelkamp, Henriët | Höhn, René | Luo, Xiaoyan | Deloukas, Panos | Duncanson, Audrey | Jankowski, Janusz | Markus, Hugh S. | Mathew, Christopher G. | Palmer, Colin N. A. | Plomin, Robert | Rautanen, Anna | Sawcer, Stephen J. | Trembath, Richard C. | Ramdas, Wishal D. | Viswanathan, Ananth C. | Wood, Nicholas W. | Spencer, Chris C. A. | Band, Gavin | Bellenguez, Céline | Freeman, Colin | Hellenthal, Garrett | Giannoulatou, Eleni | Pirinen, Matti | Pearson, Richard | Vithana, Eranga | Strange, Amy | Su, Zhan | Vukcevic, Damjan | Donnelly, Peter | Langford, Cordelia | Hunt, Sarah E. | Edkins, Sarah | Gwilliam, Rhian | Blackburn, Hannah | Bumpstead, Suzannah J. | Nongpiur, Monisha E. | Droniv, Serge | Gillman, Matthew | Gray, Emma | Hammond, Naomi | Jayakumar, Alagurevathi | McCann, Owen T. | Liddle, Jennifer | Potter, Simon C. | Ravindrarajah, Alagurevathi | Rocketts, Michelle | Montgomery, Grant W. | Waller, Matthew | Weston, Paul | Widaa, Sara | Whittaker, Pamela | Barroso, Ines | Blackwell, Jenefer M. | Brown , Matthew A. | Corvin, Aiden | Xu, Liang | Spencer , Chris C. A. | Spector, Timothy D. | Mirshahi, Alireza | Saw, Seang-Mei | Vingerling, Johannes R. | Teo, Yik-Ying | Haines, Jonathan L. | Wolfs, Roger C. W. | Lemij, Hans G. | Tai, E-Shyong | Mountain, Jenny E. | Jansonius, Nomdo M. | Jonas, Jost B. | Hammond, CJ | Gharahkhani, Puya | Lu, Yi | Amin, Najaf | Mishra, Aniket | Karssen, Lennart C. | Sim, Kar-seng | van Leeuwen, Elisabeth M. | Iglesias, Adriana I. | Verhoeven, Virginie J. M. | Hauser, Michael A. | Loon, Seng-Chee | Despriet, Dominiek D. G. | Nag, Abhishek | Venturini, Cristina | Hysi, Pirro G. | Sanfilippo, Paul G. | Schillert, Arne | Kang, Jae H. | Landers, John | Jonasson, Fridbert | Cree, Angela J. | van Koolwijk, Leonieke M. E. | Rivadeneira, Fernando | Souzeau, Emmanuelle | Jonsson, Vesteinn | Khor, Chiea-Cheun | Menon, Geeta | Mitchell, Paul | Wang, Jie Jin | Rochtchina, Elena | Attia, John | Scott, Rodney | Holliday, Elizabeth G. | Wong, Tien-Yin | Baird, Paul N. | Xie, Jing | Loomis, Stephanie J. | Inouye, Michael | Viswanathan, Ananth | Sim, Xueling | Weinreb, Robert N. | de Jong, Paulus T. V. M. | Oostra, Ben A. | Uitterlinden, André G. | Hofman, Albert | Ennis, Sarah | Thorsteinsdottir, Unnu | Bailey, Jessica N. Cooke | Burdon, Kathryn | Allingham, R. Band | Brilliant, Murray H. | Budenz, Donald L. | Christen, William G. | Fingert, John | Friedman, David S. | Gaasterland, Douglas | Gaasterland, Terry | Gibson, Jane | Hauder, Michael A. | Kang, Jae Hee | Kraft, Peter | Lee, Richard K. | Lichter, Paul R. | Liu, Yutao | Moroi, Sayoko E. | Pasquale, Louis R. | Thorleifsson, Gudmar | Pericak-Vance, Margaret A. | Realini, Anthony | Richards, Julia E. | Schuman, Joel S. | Scott, William K. | Singh, Kuldev | Sit, Arthur J. | Vollrath, Douglas | Wiggs, Janey L. | Janssen, Sarah F. | Wollstein, Gadi | Zack, Donald J. | Zhang, Kang | Bramon, Elvira | Brown, Matthew A. | Casas, Juan P.
Date: 2014
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/1302885
Description: Glaucoma is characterized by irreversible optic nerve degeneration and is the most frequent cause of irreversible blindness worldwide. Here, the International Glaucoma Genetics Consortium conducts a m... More
Full Text: Full Text
Reviewed: Reviewed
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Creators: Bellenguez, Céline | Bevan, Steve | Band, Gavin | Syme, Paul D. | Malik, Rainer | Pera, Joanna | Norrving, Bo | Lemmens, Robin | Freeman, Colin | Schanz, Renata | James, Tom | Poole, Deborah | Gschwendtner, Andreas | Murphy, Lee | Segal, Helen | Cortellini, Lynelle | Cheng, Yu-Ching | Woo, Daniel | Nalls, Michael A. | Müller-Myhsok, Bertram | Meisinger, Christa | Seedorf, Udo | Ross-Adams, Helen | Spencer, Chris C. A. | Boonen, Steven | Wloch-Kopec, Dorota | Valant, Valerie | Slark, Julia | Furie, Karen | Delavaran, Hossein | Langford, Cordelia | Deloukas, Panos | Edkins, Sarah | Hunt, Sarah | Burgess, Annette I. | Gray, Emma | Dronov, Serge | Peltonen, Leena | Gretarsdottir, Solveig | Thorleifsson, Gudmar | Thorsteinsdottir, Unnur | Stefansson, Kari | Boncoraglio, Giorgio B. | Parati, Eugenio A. | Attia, John | Pirinen, Matti | Holliday, Elizabeth | Levi, Chris | Franzosi, Maria-Grazia | Goel, Anuj | Helgadottir, Anna | Blackwell, Jenefer M. | Bramon, Elvira | Brown, Matthew A. | Casas, Juan P. | Corvin, Aiden | Jackson, Caroline A. | Duncanson, Audrey | Jankowski, Janusz | Mathew, Christopher G. | Palmer, Colin N. A. | Plomin, Robert | Rautanen, Anna | Sawcer, Stephen J. | Trembath, Richard C. | Viswanathan, Ananth C. | Wood, Nicholas W. | Traylor, Matthew | Worrall, Bradford B. | Kittner, Steven J. | Mitchell, Braxton D. | Kissela, Brett | Meschia, James F. | Thijs, Vincent | Lindgren, Arne | Macleod, Mary Joan | Slowik, Agnieszka | Walters, Matthew | Strange, Amy | Rosand, Jonathan | Sharma, Pankaj | Farrall, Martin | Sudlow, Cathie L. M. | Rothwell, Peter M. | Dichgans, Martin | Donnelly, Peter | Markus, Hugh S. | Su, Zhan
Date: 2012
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/1325463
Description: Genetic factors have been implicated in stroke risk, but few replicated associations have been reported. We conducted a genome-wide association study (GWAS) for ischemic stroke and its subtypes in 3,5... More
Reviewed: Reviewed
Date: 2010
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/928717
Description: Mental retardation (MR) is characterized by cognitive impairment with an IQ <70. Many of the major causes are genetically determined and the ~30% male excess suggests that mutations in genes carried o... More
Reviewed: Reviewed
Date: 2009
Resource Type: journal article
Identifier: uon:7942
Description: Large-scale systematic resequencing has been proposed as the key future strategy for the discovery of rare, disease-causing sequence variants across the spectrum of human complex disease. We have sequ... More
Reviewed: Reviewed
Date: 2008
Resource Type: journal article
Identifier: uon:5122
Description: Mental retardation (MR) is the most frequent handicap among children and young adults. Although a large proportion of X-linked MR genes have been identified, only four genes responsible for autosomal-... More
Reviewed: Reviewed
Date: 2008
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/43193
Description: Linkage analysis and DNA sequencing in a family exhibiting an X-linked mental retardation (XLMR) syndrome, characterized by microcephaly, epilepsy, ataxia, and absent speech and resembling Angelman sy... More
Reviewed: Reviewed
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