Browse by UCL people
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Number of items: 7.
Article
Catarino, CB;
Kasperaviciute, D;
Thom, M;
Cavalleri, GL;
Martinian, L;
Heinzen, EL;
Dorn, T;
... Sisodiya, SM; + view all
(2011)
Genomic microdeletions associated with epilepsy: Not a contraindication to resective surgery.
Epilepsia
, 52
(8)
1388 - 1392.
10.1111/j.1528-1167.2011.03087.x.
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Galizia, EC;
Srikantha, M;
Palmer, R;
Waters, JJ;
Lench, N;
Ogilvie, CM;
Kasperavičiūtė, D;
... Sisodiya, SM; + view all
(2012)
Array comparative genomic hybridization: results from an adult population with drug-resistant epilepsy and co-morbidities.
European Journal of Medical Genetics
, 55
(5)
342 - 348.
10.1016/j.ejmg.2011.12.011.
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Heinzen, EL;
Radtke, RA;
Urban, TJ;
Cavalleri, GL;
Depondt, C;
Need, AC;
Walley, NM;
... Goldstein, DB; + view all
(2010)
Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes.
The American Journal of Human Genetics
, 86
(5)
707 - 718.
10.1016/j.ajhg.2010.03.018.
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Kasperavičiute, D;
Catarino, CB;
Chinthapalli, K;
Clayton, LMS;
Thom, M;
Martinian, L;
Cohen, H;
... Sisodiya, SM; + view all
(2011)
Uncovering genomic causes of co-morbidity in epilepsy: Gene-driven phenotypic characterization of rare microdeletions.
PLoS ONE
, 6
(8)
, Article e23182. 10.1371/journal.pone.0023182.
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Liu, JY;
Kasperavičiūtė, D;
Martinian, L;
Thom, M;
Sisodiya, SM;
(2012)
Neuropathology of 16p13.11 deletion in epilepsy.
PLoS One
, 7
(4)
, Article e34813. 10.1371/journal.pone.0034813.
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McCormack, M;
Urban, TJ;
Shianna, KV;
Walley, N;
Pandolfo, M;
Depondt, C;
Chaila, E;
... Cavalleri, GL; + view all
(2012)
Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.
Pharmacogenomics
, 13
(4)
399 - 405.
10.2217/pgs.11.165.
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Need, AC;
Ge, DL;
Weale, ME;
Maia, J;
Feng, S;
Heinzen, EL;
Shianna, KV;
... Goldstein, DB; + view all
(2009)
A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia.
PLOS GENET
, 5
(2)
, Article e1000373. 10.1371/journal.pgen.1000373.
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