Browse by UCL people
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Number of items: 14.
Article
(2014)
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.
The Lancet Neurology
, 13
(9)
893 - 903.
10.1016/S1474-4422(14)70171-1.
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Abou-Khalil, B;
Auce, P;
Avbersek, A;
Bahlo, M;
Balding, DJ;
Bast, T;
Baum, L;
... Zimprich, F; + view all
(2018)
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
Nature Communications
, 9
, Article 5269. 10.1038/s41467-018-07524-z.
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Berghuis, B;
Stapleton, C;
Sonsma, ACM;
Hulst, J;
de Haan, GJ;
Lindhout, D;
Demurtas, R;
... McCormack, M; + view all
(2019)
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.
Epilepsia Open
, 4
(1)
pp. 102-109.
10.1002/epi4.12297.
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International League Against Epilepsy Consortium on Complex Epil;
(2014)
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.
Lancet Neurology
, 13
(9)
pp. 893-903.
10.1016/S1474-4422(14)70171-1.
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Jeffares, DC;
Jolly, C;
Hoti, M;
Speed, D;
Shaw, L;
Rallis, C;
Balloux, F;
... Sedlazeck, FJ; + view all
(2017)
Transient structural variations have strong effects on quantitative traits and reproductive isolation in fission yeast.
Nature Communications
, 8
, Article 14061. 10.1038/ncomms14061.
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Jeffares, DC;
Rallis, C;
Rieux, A;
Speed, D;
Převorovský, M;
Mourier, T;
Marsellach, FX;
... Bähler, J; + view all
(2015)
The genomic and phenotypic diversity of Schizosaccharomyces pombe.
Nat Genet
, 47
(3)
235 - 241.
10.1038/ng.3215.
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Kia, DA;
Noyce, AJ;
White, J;
Speed, D;
Nicolas, A;
IPDGC collaborators, .;
Burgess, S;
... Wood, NW; + view all
(2018)
Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease.
Annals of Neurology
, 84
(2)
pp. 191-199.
10.1002/ana.25294.
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Krohn, J;
Speed, D;
Palme, R;
Touma, C;
Mott, R;
Flint, J;
(2014)
Genetic interactions with sex make a relatively small contribution to the heritability of complex traits in mice.
PLOS One
, 9
(5)
, Article e96450. 10.1371/journal.pone.0096450.
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Levine, AP;
Pontikos, N;
Schiff, ER;
Jostins, L;
Speed, D;
NIDDK Inflammatory Bowel Disease Genetics Consortium, .;
Lovat, LB;
... Segal, AW; + view all
(2016)
Genetic Complexity of Crohn’s Disease in Two Large Ashkenazi Jewish Families.
Gastroenterology
, 151
(4)
pp. 698-709.
10.1053/j.gastro.2016.06.040.
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McCormack, M;
Gui, H;
Ingason, A;
Speed, D;
Wright, GEB;
Zhang, EJ;
Secolin, R;
... Cavalleri, GL; + view all
(2018)
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.
Neurology
, 90
(4)
e332-e341.
10.1212/WNL.0000000000004853.
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Speed, D;
Balding, DJ;
(2014)
MultiBLUP: improved SNP-based prediction for complex traits.
Genome Research
, 24
(9)
pp. 1550-1557.
10.1101/gr.169375.113.
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Speed, D;
Cai, N;
Johnson, MR;
Nejentsev, S;
Balding, DJ;
(2017)
Reevaluation of SNP heritability in complex human traits.
Nature Genetics
, 49
(7)
pp. 986-992.
10.1038/ng.3865.
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Speed, D;
Hemani, G;
Johnson, MR;
Balding, DJ;
(2012)
Improved heritability estimation from genome-wide SNPs.
The American Journal of Human Genetics
, 91
(6)
1011 - 1021.
10.1016/j.ajhg.2012.10.010.
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Speed, D;
O'Brien, TJ;
Palotie, A;
Shkura, K;
Marson, AG;
Balding, DJ;
Johnson, MR;
(2014)
Describing the genetic architecture of epilepsy through heritability analysis.
Brain
, 137
(10)
pp. 2680-2689.
10.1093/brain/awu206.
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