17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status
- Creator: Adib-Samii, Poneh , Rost, Natalia , Gschwendtner, Andreas , Malik, Rainer , Richie, Alexa , Gamble, Dale , Segal, Helen , Parati, Eugenio A. , Ciusani, Emilio , Holliday, Elizabeth G. , Maguire, Jane , Wardlaw, Joanna , Traylor, Matthew , Worrall, Bradford , Bis, Joshua , Wiggins, Kerri L. , Longstreth, Will , Kittner, Steve J. , Cheng, Yu-Ching , Mosley, Thomas , Falcone, Guido J. , Furie, Karen L. , Leiva-Salinas, Carlos , Devan, William , Lau, Benison C. , Saleem Khan, Muhammed , Australian Stroke Genetics Collaborative , Wellcome Trust Case-Control Consortium-2 , METASTROKE , Sharma, Pankaj , Fornage, Miriam , Mitchell, Braxton D. , Psaty, Bruce M. , Sudlow, Cathie , Biffi, Alessandro , Levi, Christopher , Boncoraglio, Giorgio B. , Rothwell, Peter M. , Meschia, James , Dichgans, Martin , Rosand, Jonathan , Markus, Hugh S. , Lanfranconi, Silvia , Fitzpatrick, Kaitlin , Bevan, Steve , Kanakis, Allison , Valant, Valerie
- Resource Type: journal article
- Date: 2013
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis
- Creator: Mechelli, Rosella , Umeton, Renato , Wellcome Trust Case Control Consortium 2, , Romano, Silvia , Salvetti, Marco , Ristori, Giovanni , Cox, Mathew B. , Lechner-Scott, Jeannette S. , Scott, Rodney J. , Policano, Claudia , Annibali, Viviana , Coarelli, Giulia , Ricigliano, Vito A. G. , Vittori, Danila , Fornasiero, Arianna , Buscarinu, Maria Chiara , International Multiple Sclerosis Genetics Consortium,
- Resource Type: journal article
- Date: 2013
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis
- Creator: Ban, M. , McCauley, J. L. , Dudbridge, F. , Wason, J. , Robertson, N. P. , De Jager, P. L. , Hafler, D. A. , Barcellos, L. F. , Ivinson, A. J. , Sexton, D. , Oksenberg, J. R. , Hauser, S. L. , Zuvich, R. , Pericak-Vance, M. A. , Haines, J. , Compston, A. , Sawcer, S. , Baker, A. , Bergamaschi, L. , Cox, M. , Kemppinen, A. , D'Alfonso, S. , Guerini, F. R. , Lechner-Scott, J.
- Resource Type: journal article
- Date: 2010
A review on the genetics of aliphatic and aromatic hydrocarbon degradation
- Creator: Abbasian, Firouz , Lockington, Robin , Megharaj, Mallavarapu , Naidu, Ravi
- Resource Type: journal article
- Date: 2016
A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.
- Creator: Hungate, Eric A. , Vora, Sapana R. , Rudant, Jéremie , Orsi, Laurent , Clavel, Jacqueline , Milne, Elizabeth , Scott, Rodney J. , Pui, Ching-Hon , Cox, Nancy J. , Loh, Mignon L. , Yang, Jun J. , Skol, Andrew D. , Gamazon, Eric R. , Onel, Kenan , Moriyama, Takaya , Best, Timothy , Hulur, Imge , Lee, Younghee , Evans, Tiffany-Jane , Ellinghaus, Eva , Stanulla, Martin
- Resource Type: journal article
- Date: 2016
Adolescent females' assessment of and learning gains from researcher developed mouse genetics multimedia simulation (MouseGen) : A mixed methods analysis
- Creator: Terry, David William
- Resource Type: thesis
- Date: 2014
Altered expression of the plasminogen activation pathway in peripheral blood mononuclear cells in multiple sclerosis: possible pathomechanism of matrix metalloproteinase activation
- Creator: Cox, Mathew B. , Bowden, Nikola A. , Scott, Rodney J. , Lechner-Scott, Jeannette
- Resource Type: journal article
- Date: 2013
Are myocardial infarction-associated single-nucleotide polymorphisms associated with ischemic stroke?
- Creator: Cheng, Yu-Ching , Anderson, Christopher D. , Barlera, Simona , Biffi, Alessandro , Bookman, Ebony , Brott, Thomas G. , Brown, Robert D. , Chen, Fang , Chen, Wei-Min , Ciusani, Emilio , Cole, John W. , Cortellini, Lynelle , Bione, Silvia , Danesh, John , Doheny, Kimberley , Ferrucci, Luigi , Franzosi, Maria Grazia , Frossard, Philippe , Furie, Karen L. , Golledge, Jonathan , Hankey, Graeme J. , Hernandez, Dena , Holliday, Elizabeth G. , Keene, Keith , Hsu, Fang-Chi , Jannes, Jim , Kamal, Ayeesha , Khan, Muhammad Saleem , Kittner, Steven J. , Koblar, Simon A. , Lewis, Martin , Lincz, Lisa , Lisa, Antonella , Matarin, Mar , Maguire, Jane M. , Moscato, Pablo , Mychaleckyj, Josyf C. , Parati, Eugenio A. , Parolo, Silvia , Pugh, Elizabeth , Rost, Natalia S. , Schallert, Michael , Schmidt, Helena , Scott, Rodney J. , Sturm, Jonathan W. , Nalls, Michael , Yadav, Sunaina , Zaidi, Moazzam , Boncoraglio, Giorgio B. , Levi, Christopher Royce , Meschia, James F. , Rosand, Jonathan , Sale, Michele , Saleheen, Danish , Schmidt, Reinhold , Sharma, Pankaj , Rasheed, Asif , Worrall, Bradford , Mitchell, Branxton D. , Zeginigg, Marion , Attia, John , Baker, Ross
- Resource Type: journal article
- Date: 2012
Association analysis identifies 65 new breast cancer risk loci
- Creator: Michailidou, Kyriaki , Lindström, Sara , Bolla, Manjeet K. , Wang, Qin , Tyrer, Jonathan , Dicks, Ed , Lee, Andrew , Wang, Zhaoming , Allen, Jamie , Keeman, Renske , Eilber, Ursula , French, Juliet D. , Dennis, Joe , Scott, Rodney J. , Beesley, Jonathan , Hui, Shirley , Kar, Siddhartha , Lemaçon, Audrey , Soucy, Penny , Glubb, Dylan , Rostamianfar, Asha
- Resource Type: journal article
- Date: 2017
Association between apolipoprotein E polymorphisms and age-related macular degeneration: A HuGE review and meta-analysis
- Creator: Thakkinstian, Ammarin , Bowe, Steve , McEvoy, Mark , Smith, Wayne , Attia, John
- Resource Type: journal article
- Date: 2006
BCL-2 family isoforms in apoptosis and cancer
- Creator: Warren, Chloe F. A. , Wong-Brown, Michelle W. , Bowden, Nikola A.
- Resource Type: journal article
- Date: 2019
Candidate gene association studies in stroke
- Creator: Holliday, Elizabeth G. , Oldmeadow, Christopher J. , Maguire, Jane M. , Attia, John
- Resource Type: book chapter
- Date: 2013
Catechol-O-methyltransferase (COMT) genotype moderates the effects of childhood trauma on cognition and symptoms in schizophrenia
- Creator: Green, Melissa J. , Chia, T.-Yunn , Cairns, Murray J. , Wu, Jingqin , Tooney, Paul A. , Scott, Rodney J. , Carr, Vaughan J.
- Resource Type: journal article
- Date: 2014
Characterising the genetic risk for type 2 diabetes in a Malaysian multi-ethnic cohort
- Creator: Abdullah, N. , Abdul Murad, N. , Scott, R. J. , Holliday, E. G. , Attia, J. , Oldmeadow, C. , Mohd Haniff, E. A. , Syafruddin, S. E. , Abd Jalal, N. , Ismail, N. , Ishak, M. , Jamal, R.
- Resource Type: journal article
- Date: 2015
Clinical use of SNP-microarrays for the detection of genome-wide changes in haematological malignancies with a focus on B-cell neoplasms
- Creator: Berry, Nadine Kaye
- Resource Type: thesis
- Date: 2020
Combined analysis of exon splicing and genome wide polymorphism data predict schizophrenia risk loci.
- Creator: Oldmeadow, Christopher , Mossman, David , Evans, Tiffany-Jane , Holliday, Elizabeth G. , Tooney, Paul A. , Cairns, Murray J. , Wu, Jingqin , Carr, Vaughan , Attia, John R. , Scott, Rodney J.
- Resource Type: journal article
- Date: 2014
Combined effects of complement factor H genotypes, fish consumption, and inflammatory markers on long-term risk for age-related macular degeneration in a cohort
- Creator: Wang, Jie Jin , Rochtchina, Elena , Smith, Wayne , Klein, Ronald , Klein, Barbara E. K. , Joshi, Tripti , Sivakumaran, Theru A. , Iyengar, Sudha , Mitchell, Paul
- Resource Type: journal article
- Date: 2009
Common coding variant in SERPINA1 increases the risk for large artery stroke
- Creator: Malik, Rainer , Cardenas, IF , Rothwell, PM , Levi, C , Attia, J , Sudlow, CLM , Braun, D , Markus, HS , Wintrode, PL , Berger, K , Jenne, DE , Dichgans, M , Dau, Therese , Seixas, Susana , Bevan, Steve , Lincz, Lisa F. , Holliday, Elizabeth G. , Burgess, Annette I. , Rannikmäe, Kristiina , Minnerup, Jens , Kriebel, Jennifer , Waldenberger, Melanie , Müller-Nurasyid, Martina , Gonik, Maria , Levi, Christopher , Attia, John , Maguire, Jane , Sivakumar, Anirudh , Deredge, Daniel J. , Edeleva, Evgeniia V. , Götzfried, Jessica , van der Laan, Sander W. , Pasterkamp, Gerard , Beaufort, Nathalie
- Resource Type: journal article
- Date: 2017
Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome
- Creator: Xavier, Alexandre , Olsen, Maren Fridtjofsen , Lavik, Liss A. , Johansen, Jostein , Singh, Ashish Kumar , Sjursen, Wenche , Scott, Rodney J. , Talseth-Palmer, Bente A.
- Resource Type: journal article
- Date: 2019
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
- Creator: Marshall, Christian R. , Howrigan, Daniel P. , Gujral, Madhusudan , Brandler, William M. , Malhotra, Dheeraj , Wang, Zhouzhi , Fuentes Fajarado, Karin V. , Maile, Michelle S. , Ripke, Stephan , Agartz, Ingrud , Albus, Margot , Alexander, Madeline , Merico, Daniele , Atkins, Joshua , Cairns, Murray J. , Carr, Vaughan J. , Henskens, Frans A. , Kelly, Brian J. , Loughland, Carmel L. , Michie, Patricia T. , Schall, Ulrich , Scott, Rodney J. , Tooney, Paul A. , Thiruvahindrapuram, Bhooma , Wu, Jing Qin , Wu, Wenting , Greer, Douglas S. , Antaki, Douglas , Shetty, Aniket , Holmans, Peter A. , Pinto, Dalila
- Resource Type: journal article
- Date: 2017