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Damiano, JA, Do, H, Ozturk, E, Burgess, R, Kalnins, R, Jones, NC, Dobrovic, A, Berkovic, SF, Hildebrand, MS.
Sensitive quantitative detection of somatic mosaic mutation in "double cortex" syndrome..
Epileptic Disord
19(4)
:
450 -455
2017
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Zhang, Y-H, Burgess, R, Malone, JP, Glubb, GC, Helbig, KL, Vadlamudi, L, Kivity, S, Afawi, Z, Bleasel, A, Grattan-Smith, P, et al.
Genetic epilepsy with febrile seizures plus: Refining the spectrum..
Neurology
89(12)
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1210 -1219
2017
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Freytag, S, Burgess, R, Oliver, KL, Bahlo, M.
brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasets..
Genome Med
9(1)
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55
2017
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Damiano, JA, Burgess, R, Kivity, S, Lerman-Sagie, T, Afawi, Z, Scheffer, IE, Berkovic, SF, Hildebrand, MS.
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrum..
Epilepsia
58(3)
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e40 -e43
2017
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Epi4K consortium, Epilepsy Phenome/Genome Project.
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study..
Lancet Neurol
16(2)
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135 -143
2017
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