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| De novo mutations in epileptic encephalopathies Nature 501 (7466), 217-221, 2013 | 1514 | 2013 |
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| HLA-A* 3101 and carbamazepine-induced hypersensitivity reactions in Europeans M McCormack, A Alfirevic, S Bourgeois, JJ Farrell, D Kasperavičiūtė, ... New England Journal of Medicine 364 (12), 1134-1143, 2011 | 1109 | 2011 |
| Genic intolerance to functional variation and the interpretation of personal genomes S Petrovski, Q Wang, EL Heinzen, AS Allen, DB Goldstein PLoS genetics 9 (8), e1003709, 2013 | 1034 | 2013 |
| A genome-wide investigation of SNPs and CNVs in schizophrenia AC Need, D Ge, ME Weale, J Maia, S Feng, EL Heinzen, KV Shianna, ... PLoS genetics 5 (2), e1000373, 2009 | 573 | 2009 |
| Somatic activation of AKT3 causes hemispheric developmental brain malformations A Poduri, GD Evrony, X Cai, PC Elhosary, R Beroukhim, MK Lehtinen, ... Neuron 74 (1), 41-48, 2012 | 507 | 2012 |
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| Rare deletions at 16p13. 11 predispose to a diverse spectrum of sporadic epilepsy syndromes EL Heinzen, RA Radtke, TJ Urban, GL Cavalleri, C Depondt, AC Need, ... The American Journal of Human Genetics 86 (5), 707-718, 2010 | 286 | 2010 |
| De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies CT Myers, JM McMahon, AL Schneider, S Petrovski, AS Allen, GL Carvill, ... The American Journal of Human Genetics 99 (2), 287-298, 2016 | 264 | 2016 |
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| A roadmap for precision medicine in the epilepsies EpiPM Consortium The Lancet Neurology 14 (12), 1219-1228, 2015 | 215 | 2015 |
| Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome MC Manzini, DE Tambunan, RS Hill, WY Tim, TM Maynard, EL Heinzen, ... The American Journal of Human Genetics 91 (3), 541-547, 2012 | 213 | 2012 |
| The copy number variation landscape of congenital anomalies of the kidney and urinary tract M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ... Nature genetics 51 (1), 117-127, 2019 | 209 | 2019 |
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| Genome-wide mRNA expression correlates of viral control in CD4+ T-cells from HIV-1-infected individuals M Rotger, KK Dang, J Fellay, EL Heinzen, S Feng, P Descombes, ... PLoS pathogens 6 (2), e1000781, 2010 | 193 | 2010 |
| Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study D Kasperavičiūtė, CB Catarino, EL Heinzen, C Depondt, GL Cavalleri, ... Brain 133 (7), 2136-2147, 2010 | 184 | 2010 |
Anna NeedImperial College LondonVerified email at imperial.ac.uk
