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Nature reviews. Genetics, ISSN 1471-0064, 01/2005, Volume 6, Issue 1, pp. 75 - 79
Genetic research has moved from Mendelian genetics to sequence maps to the study of natural human genetic variation at the level of the genome... 
Ethics, Medical | Genetics, Population | Confidentiality - ethics | Choice Behavior | Computational Biology - ethics | Humans | Databases as Topic - ethics | Genetic Research - ethics | Genome, Human | Insurance, Health | Index Medicus | Bioethics
Journal Article
Nature reviews. Genetics, ISSN 1471-0064, 05/2008, Volume 9, Issue 5, pp. 406 - 411
Recent advances in high-throughput genomic technologies are showing concrete results in the form of an increasing number of genome-wide association studies and... 
Bioethics - trends | Databases, Nucleic Acid - ethics | Humans | Databases, Nucleic Acid - trends | Genome, Human | Genomics - trends | Genomics - ethics | Genetic research | Usage | Genetic discrimination | Methods | Index Medicus
Journal Article
Journal Article
PloS one, ISSN 1932-6203, 03/2009, Volume 4, Issue 3, pp. e4906 - e4906
Journal Article
by Traylor, Matthew and Farrall, Martin and Holliday, Elizabeth G and Sudlow, Cathie and Hopewell, Jemma C and Cheng, Yu-Ching and Fornage, Myriam and Ikram, M Arfan and Malik, Rainer and Bevan, Steve and Thorsteinsdottir, Unnur and Nalls, Mike A and Longstreth, WT and Wiggins, Kerri L and Yadav, Sunaina and Parati, Eugenio A and DeStefano, Anita L and Worrall, Bradford B and Kittner, Steven J and Khan, Muhammad Saleem and Reiner, Alex P and Helgadottir, Anna and Achterberg, Sefanja and Fernandez-Cadenas, Israel and Abboud, Sherine and Schmidt, Reinhold and Walters, Matthew and Chen, Wei-Min and Ringelstein, E Bernd and O'Donnell, Martin and Ho, Weang Kee and Pera, Joanna and Lemmens, Robin and Norrving, Bo and Higgins, Peter and Benn, Marianne and Sale, Michele and Kuhlenbäumer, Gregor and Doney, Alexander S F and Vicente, Astrid M and Delavaran, Hossein and Algra, Ale and Davies, Gail and Oliveira, Sofia A and Palmer, Colin N A and Deary, Ian and Schmidt, Helena and Pandolfo, Massimo and Montaner, Joan and Carty, Cara and de Bakker, Paul I W and Kostulas, Konstantinos and Ferro, Jose M and van Zuydam, Natalie R and Valdimarsson, Einar and Nordestgaard, Børge G and Lindgren, Arne and Thijs, Vincent and Slowik, Agnieszka and Saleheen, Danish and Paré, Guillaume and Berger, Klaus and Thorleifsson, Gudmar and Hofman, Albert and Mosley, Thomas H and Mitchell, Braxton D and Furie, Karen and Clarke, Robert and Levi, Christopher and Seshadri, Sudha and Gschwendtner, Andreas and Boncoraglio, Giorgio B and Sharma, Pankaj and Bis, Joshua C and Gretarsdottir, Solveig and Psaty, Bruce M and Rothwell, Peter M and Rosand, Jonathan and Meschia, James F and Stefansson, Kari and Dichgans, Martin and Markus, Hugh S and The Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and on behalf of the International Stroke Genetics Consortium and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2)
Lancet neurology, ISSN 1474-4422, 11/2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
PloS one, ISSN 1932-6203, 05/2010, Volume 5, Issue 5, pp. e10780 - e10780
Journal Article