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.