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2020
Mark Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids with Aortic Stenosis
Chen, Hao Yu ; Cairns, Benjamin J. ; Small, Aeron M. ; Burr, Hannah A. ; Ambikkumar, Athithan ; Martinsson, Andreas ^LU ; Thériault, Sébastien ; Munter, Hans Markus ; Steffen, Brian and Zhang, Richard , et al. (2020) In JAMA Cardiology 5(6). p.694-702
- Contribution to journal › Article
2018
Mark Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke
Cole, John W. ; Xu, Huichun ; Ryan, Kathleen ; Jaworek, Thomas ; Dueker, Nicole ; McArdle, Patrick ; Gaynor, Brady ; Cheng, Yu Ching ; O'Connell, Jeffrey and Bevan, Steve , et al. (2018) In PLoS ONE 13(11).
- Contribution to journal › Article
2017
Mark Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans
Heinz, Lisa ; Kim, Gwang Jin ; Marrakchi, Slaheddine ; Christiansen, Julie ; Turki, Hamida ; Rauschendorf, Marc Alexander ; Lathrop, Mark ; Hausser, Ingrid ; Zimmer, Andreas D. and Fischer, Judith (2017) In American Journal of Human Genetics 100(6). p.926-939
- Contribution to journal › Article
2016
Mark Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
Cheng, Yu-Ching ; Stanne, Tara M ; Giese, Anne-Katrin ; Ho, Weang Kee ; Traylor, Matthew ; Amouyel, Philippe ; Holliday, Elizabeth G ; Malik, Rainer ; Xu, Huichun and Kittner, Steven J , et al. (2016) In Stroke: a journal of cerebral circulation 47(2). p.307-316
- Contribution to journal › Article
2014
Mark Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.
Leblond, Claire S ; Nava, Caroline ; Polge, Anne ; Gauthier, Julie ; Huguet, Guillaume ; Lumbroso, Serge ; Giuliano, Fabienne ; Stordeur, Coline ; Depienne, Christel and Mouzat, Kevin , et al. (2014) In PLoS Genetics 10(9).
- Contribution to journal › Article
2013
Mark Common Polymorphisms in the CYP11B1 and CYP11B2 Genes: Evidence for a Digenic Influence on Hypertension
Alvarez-Madrazo, Samantha ; MacKenzie, Scott M. ; Davies, Eleanor ; Fraser, Robert ; Lee, Wai-Kwong ; Brown, Morris ; Caulfield, Mark J. ; Dominiczak, Anna F. ; Farrall, Martin and Lathrop, Mark , et al. (2013) In Hypertension 61(1). p.232-239
- Contribution to journal › Article
Mark Deciphering the 8q24.21 association for glioma
Enciso-Mora, Victor ; Hosking, Fay J. ; Kinnersley, Ben ; Wang, Yufei ; Shete, Sanjay ; Zelenika, Diana ; Broderick, Peter ; Idbaih, Ahmed ; Delattre, Jean-Yves and Hoang-Xuan, Khe , et al. (2013) In Human Molecular Genetics 22(11). p.2293-2302
- Contribution to journal › Article
Mark Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Beecham, Ashley H. ; Patsopoulos, Nikolaos A. ; Xifara, Dionysia K. ; Davis, Mary F. ; Kemppinen, Anu ; Cotsapas, Chris ; Shah, Tejas S. ; Spencer, Chris ; Booth, David and Goris, An , et al. (2013) In Nature Genetics 45(11). p.1353-1353
- Contribution to journal › Article
2012
Mark SHANK1 Deletions in Males with Autism Spectrum Disorder
Sato, Daisuke ; Lionel, Anath C. ; Leblond, Claire S. ; Prasad, Aparna ; Pinto, Dalila ; Walker, Susan ; O'Connor, Irene ; Russell, Carolyn ; Drmic, Irene E. and Hamdan, Fadi F. , et al. (2012) In American Journal of Human Genetics 90(5). p.879-887
- Contribution to journal › Article
Mark Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Leblond, Claire S. ; Heinrich, Jutta ; Delorme, Richard ; Proepper, Christian ; Betancur, Catalina ; Huguet, Guillaume ; Konyukh, Marina ; Chaste, Pauline ; Ey, Elodie and Råstam, Maria ^LU , et al. (2012) In PLoS Genetics 8(2).
- Contribution to journal › Article

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