Browse by UCL people
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Number of items: 4.
Article
Kasperaviciute, D;
Catarino, CB;
Matarin, M;
Leu, C;
Novy, J;
Tostevin, A;
Leal, B;
... Sisodiya, SM; + view all
(2013)
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Brain: A Journal of Neurology
, 136
(10)
pp. 3140-3150.
10.1093/brain/awt233.
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Meschia, JF;
Singleton, A;
Nalls, MA;
Rich, SS;
Sharma, P;
Ferrucci, L;
Matarin, M;
... Worrall, BB; + view all
(2011)
Genomic Risk Profiling of Ischemic Stroke: Results of an International Genome-Wide Association Meta-Analysis.
PLOS ONE
, 6
(9)
, Article e23161. 10.1371/journal.pone.0023161.
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Nalls, MA;
Simon-Sanchez, J;
Gibbs, JR;
Paisan-Ruiz, C;
Bras, JT;
Tanaka, T;
Matarin, M;
... Singleton, AB; + view all
(2009)
Measures of Autozygosity in Decline: Globalization, Urbanization, and Its Implications for Medical Genetics.
PLoS Genetics
, 5
(3)
, Article e1000415. 10.1371/journal.pgen.1000415.
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Webb, TR;
Matarin, M;
Gardner, JC;
Kelberman, D;
Hassan, H;
Ang, W;
Michaelides, M;
... Hardcastle, AJ; + view all
(2012)
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development.
The American Journal of Human Genetics
, 90
(2)
247 - 259.
10.1016/j.ajhg.2011.12.019.
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