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. 2012 May 29;53(8):1457–1467. doi: 10.1111/j.1528-1167.2012.03511.x

Table 1.

Epi4K patient cohorts

Cohort Patient types (numbers) References
The Epilepsy Phenome/Genome Project (EPGP) First-degree relative pairs with IGE or NFE (n = 1,500) Trios with IS (n = 250), LGS (n = 250) or malformations of cortical development (n = 250) EPGP (2007)
Epilepsy Family Study of Columbia University Multiplex families with three or more affected patients with IGE or NFE (n = 32) Ottman et al. (2005); Ottman and Susser (1992)
The Epilepsy Research Centre, University of Melbourne Multiplex families with three or more affected patients with IGE or NFE (n = 250) Marini et al. (2004)
Quebec Familial Epilepsy Study Multiplex families with three or more affected patients with IGE or NFE (n = 47) Kinirons et al. (2008)
Childhood Absence Epilepsy Study (CAE) Singletons with CAE (n = 446) Glauser et al. (2010)
SANAD and University of Melbourne Newly diagnosed singletons with 716 IGE (n = 716) or focal epilepsy (n = 1,721) prospectively followed for seizure outcome Bleck (2007); Marson et al. (2007)
EPIGEN Singletons with IGE (n = 700) or NFE (n > 3,000) EPIGEN (2008)

IGE, idiopathic generalized epilepsy; NFE, nonlesional focal epilepsy; IS, infantile spasms; LGS, Lennox-Gastaut syndrome; CAE, childhood absence epilepsy.