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PloS one, ISSN 1932-6203, 08/2012, Volume 7, Issue 8, p. e41730
Journal Article
by Williams, Frances M. K and Carter, Angela M and Hysi, Pirro G and Surdulescu, Gabriela and Hodgkiss, Dylan and Soranzo, Nicole and Traylor, Matthew and Bevan, Steve and Dichgans, Martin and Rothwell, Peter M. W and Sudlow, Cathie and Farrall, Martin and Silander, Kaisa and Kaunisto, Mari and Wagner, Peter and Saarela, Olli and Kuulasmaa, Kari and Virtamo, Jarmo and Salomaa, Veikko and Amouyel, Philippe and Arveiler, Dominique and Ferrieres, Jean and Wiklund, Per-Gunnar and Arfan Ikram, M and Hofman, Albert and Boncoraglio, Giorgio B and Parati, Eugenio A and Helgadottir, Anna and Gretarsdottir, Solveig and Thorsteinsdottir, Unnur and Thorleifsson, Gudmar and Stefansson, Kari and Seshadri, Sudha and DeStefano, Anita and Gschwendtner, Andreas and Psaty, Bruce and Longstreth, Will and Mitchell, Braxton D and Cheng, Yu-Ching and Clarke, Robert and Ferrario, Marco and Bis, Joshua C and Levi, Christopher and Attia, John and Holliday, Elizabeth G and Scott, Rodney J and Fornage, Myriam and Sharma, Pankaj and Furie, Karen L and Rosand, Jonathan and Nalls, Mike and Meschia, James and Mosely, Thomas H and Evans, Alun and Palotie, Aarno and Markus, Hugh S and Grant, Peter J and Spector, Tim D and on Behalf of the EuroCLOT Investigators the Wellcome Trust Case Control Consortium 2 MOnica Risk, Genetics, Archiving and Monograph MetaStroke and the International Stroke Genetics Consortium and EuroCLOT Investigators and Wellcome Trust Case Control Consor and Int Stroke Genetics Consortium and MOnica Risk, Genetics, Archiving and Monograph and MetaStroke and International Stroke Genetics Consortium and Wellcome Trust Case Control Consortium 2
Annals of neurology, ISSN 0364-5134, 01/2013, Volume 73, Issue 1, pp. 16 - 31
Journal Article
PloS one, ISSN 1932-6203, 2011, Volume 6, Issue 9, p. e24220
Journal Article
PloS one, ISSN 1932-6203, 2008, Volume 3, Issue 8, p. e2986
Background: Rare mutations of the low-density lipoprotein receptor gene (LDLR) cause familial hypercholesterolemia, which increases the risk for coronary... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Receptors, LDL - genetics | Oligonucleotide Array Sequence Analysis | Risk Assessment | Humans | Risk Factors | Cholesterol, LDL - drug effects | Chromosome Mapping | Random Allocation | Case-Control Studies | Genetic Variation | Cholesterol, LDL - genetics | Coronary Disease - prevention & control | Anticholesteremic Agents - therapeutic use | Coronary Disease - genetics | Cholesterol, LDL - blood | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 10 | Medical research | Hypercholesterolemia | Blood cholesterol | Low density lipoproteins | Genes | Medicine, Experimental | Genetic research | Genetics | Genetic aspects | Single nucleotide polymorphisms | Coronary heart disease | Risk factors | Lipoproteins (low density) | Risk | Lipids | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Gene polymorphism | Epidemiology | Consortia | Confidence intervals | Randomization | Population | Lipoprotein (low density) receptors | Children | Heart diseases | Statistical analysis | Mortality | Coronary artery | Health risks | Environmental health | Genetic diversity | Regression analysis | Metabolism | LDLR gene | Apolipoproteins | Coronary artery disease | Low density lipoprotein | Cholesterol | Studies | Genetic variance | Hospitals | Coronary vessels | Alleles | Biomarkers | Receptor density | Adults | Mutation | Polymorphism
Journal Article
by Leone, Maurizio A and Barizzone, Nadia and Esposito, Federica and Lucenti, Ausiliatrice and Harbo, Hanne F and Goris, An and Kockum, Ingrid and Oturai, Annette Bang and Celius, Elisabeth Gulowsen and Mero, Inger L and Dubois, Bénédicte and Olsson, Tomas and Søndergaard, Helle Bach and Cusi, Daniele and Lupoli, Sara and Andreassen, Bettina Kulle and Barcellos, L and Booth, D and Comabella, M and Compston, A and D'Alfonso, Sandra and De Jager, P and Fontaine, B and Hafler, D and Haines, J and Hauser, S.L and Hawkins, C and Hemmer, B and Hillert, J and Ivinson, A and Martin, R and Martinelli Boneschi, F and McCauley, J.L and Oksenberg, J and Oturai, A and Patsopoulos, N and Pericak-Vance, M and Saarela, J and Sawcer, S and Spurkland, A and Stewart, G and Zipp, F and Myhr, Kjell-Morten and Guerini, Franca R and Naldi, Paola and Galimberti, Daniela and Scarpini, Elio and Bergamaschi, Roberto and Di Sapio, Antonella and Caputo, Domenico and Rosso, Gabriella and Cordera, Susanna and Cavalla, Paola and Cavallo, Roberto and Benedetti, Maria D and Salvetti, Marco and Capra, Ruggero and Ghezzi, Angelo and Annovazzi, Pietro and Coniglio, Gabriella and Liberatore, Giuseppe and Rodegher, Mariaemma and Moiola, Lucia and Colombo, Bruno and Radaelli, Marta and Rossi, Paolo and Martinelli, Vittorio and Comi, Giancarlo and Martinelli-Boneschi, Filippo and International Multiple Sclerosis G and PROGRESSO Group and Wellcome Trust Case Control Consortium 2 and International Multiple Sclerosis Genetics Consortium and PROGEMUS Group and the International Multiple Sclerosis Genetics Consortium and the PROGEMUS Group and the Wellcome Trust Case Control Consortium 2 and the PROGRESSO Group
PloS one, ISSN 1932-6203, 06/2013, Volume 8, Issue 6, p. e64408
Journal Article
PloS one, ISSN 1932-6203, 07/2009, Volume 4, Issue 7, pp. e6138 - e6138
Journal Article
by Mechelli, Rosella and Umeton, Renato and Policano, Claudia and Annibali, Viviana and Coarelli, Giulia and Ricigliano, Vito A. G and Vittori, Danila and Fornasiero, Arianna and Buscarinu, Maria Chiara and Romano, Silvia and Salvetti, Marco and Ristori, Giovanni and 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 ... and Int Multiple Sclerosis Genetics and Wellcome Trust Case Control and International Multiple Sclerosis Genetics Consortium and Wellcome Trust Case Control Consortium,2
PloS one, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, p. e63300
Journal Article