-
1
-
-
0007961081
-
Sixty-six twin pairs affected by seizures
-
Lennox WG. Sixty-six twin pairs affected by seizures. Res Publ Assoc Res Nerv Ment Dis 1947;26:11-34.
-
(1947)
Res Publ Assoc Res Nerv Ment Dis
, vol.26
, pp. 11-34
-
-
Lennox, W.G.1
-
3
-
-
0031882602
-
Univariate genetic analyses of epilepsy and seizures in a population-based twin study: The Virginia twin registry
-
Miller LL, Pellock JM, DeLorenzo RJ, Meyer JM, Corey LA. Univariate genetic analyses of epilepsy and seizures in a population-based twin study: the Virginia twin registry. Genet Epidemiol 1998;15:33-49.
-
(1998)
Genet Epidemiol
, vol.15
, pp. 33-49
-
-
Miller, L.L.1
Pellock, J.M.2
Delorenzo, R.J.3
Meyer, J.M.4
Corey, L.A.5
-
4
-
-
0026339811
-
Genetic factors in epileptic seizures: Evidence from a large twin population
-
Sillanpaa M, Koskenvuo M, Romanov K, Kaprio J. Genetic factors in epileptic seizures: evidence from a large twin population. Acta Neurol Scand 1991;84:523-526.
-
(1991)
Acta Neurol Scand
, vol.84
, pp. 523-526
-
-
Sillanpaa, M.1
Koskenvuo, M.2
Romanov, K.3
Kaprio, J.4
-
5
-
-
0025989275
-
The occurrence of epilepsy and febrile seizures in Virginian and Norwegian twins
-
Corey LA, Pellock JM, Solaas MH, Nance WE, DeLorenzo RJ. The occurrence of epilepsy and febrile seizures in Virginian and Norwegian twins. Neurology 1991;41:1433-1436.
-
(1991)
Neurology
, vol.41
, pp. 1433-1436
-
-
Corey, L.A.1
Pellock, J.M.2
Solaas, M.H.3
Nance, W.E.4
Delorenzo, R.J.5
-
6
-
-
0035014077
-
Genetic and environmental factors in epilepsy: A population-based study of 11,900 Danish twin pairs
-
Kjeldsen MJ, Kyvik KO, Christensen K, Friis ML. Genetic and environmental factors in epilepsy: a population-based study of 11,900 Danish twin pairs. Epilepsy Res 2001;44:167-178.
-
(2001)
Epilepsy Res
, vol.44
, pp. 167-178
-
-
Kjeldsen, M.J.1
Kyvik, K.O.2
Christensen, K.3
Friis, M.L.4
-
7
-
-
0032892015
-
Epilepsy and seizure occurrence in a population-based sample of Virginian twins and their families
-
Miller LL, Pellock JM, Boggs JG, DeLorenzo RJ, Meyer JM, Corey LA. Epilepsy and seizure occurrence in a population-based sample of Virginian twins and their families. Epilepsy Res 1999;34:135-143.
-
(1999)
Epilepsy Res
, vol.34
, pp. 135-143
-
-
Miller, L.L.1
Pellock, J.M.2
Boggs, J.G.3
Delorenzo, R.J.4
Meyer, J.M.5
Corey, L.A.6
-
8
-
-
0024317220
-
Proposal for revised classification of epilepsies and epileptic syndromes
-
Commission on Classification and Terminology of the International League Against Epilepsies
-
Commission on Classification and Terminology of the International League Against Epilepsies. Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 1989;30:389-399.
-
(1989)
Epilepsia
, vol.30
, pp. 389-399
-
-
-
9
-
-
0042932513
-
Epileptic seizures and syndromes in twins: The importance of genetic factors
-
Kjeldsen MJ, Corey LA, Christensen K, Friis ML. Epileptic seizures and syndromes in twins: the importance of genetic factors. Epilepsy Res 2003;55:137-146.
-
(2003)
Epilepsy Res
, vol.55
, pp. 137-146
-
-
Kjeldsen, M.J.1
Corey, L.A.2
Christensen, K.3
Friis, M.L.4
-
11
-
-
1842580622
-
Epilepsy in twins: Insights from unique historical data of William Lennox
-
Vadlamudi L, Andermann E, Lombroso CT, et al. Epilepsy in twins: insights from unique historical data of William Lennox. Neurology 2004;62:1127-1133.
-
(2004)
Neurology
, vol.62
, pp. 1127-1133
-
-
Vadlamudi, L.1
Andermann, E.2
Lombroso, C.T.3
-
12
-
-
77950857874
-
Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009
-
Berg AT, Berkovic SF, Brodie MJ, et al. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009. Epilepsia 2010;51:676-685.
-
(2010)
Epilepsia
, vol.51
, pp. 676-685
-
-
Berg, A.T.1
Berkovic, S.F.2
Brodie, M.J.3
-
13
-
-
79957603217
-
Epilepsy genetics: Past, present, and future
-
Poduri A, Lowenstein D. Epilepsy genetics: past, present, and future. Curr Opin Genet Dev 2011;21:325-332.
-
(2011)
Curr Opin Genet Dev
, vol.21
, pp. 325-332
-
-
Poduri, A.1
Lowenstein, D.2
-
14
-
-
33947492441
-
Channelopathies in idiopathic epilepsy
-
Heron SE, Scheffer IE, Berkovic SF, Dibbens LM, Mulley JC. Channelopathies in idiopathic epilepsy. Neurotherapeutics 2007;4:295-304.
-
(2007)
Neurotherapeutics
, vol.4
, pp. 295-304
-
-
Heron, S.E.1
Scheffer, I.E.2
Berkovic, S.F.3
Dibbens, L.M.4
Mulley, J.C.5
-
15
-
-
84878877916
-
Recent advances in the molecular genetics of epilepsy
-
Hildebrand MS, Dahl HH, Damiano JA, Smith RJ, Scheffer IE, Berkovic SF. Recent advances in the molecular genetics of epilepsy. J Med Genet 2013;50:271-279.
-
(2013)
J Med Genet
, vol.50
, pp. 271-279
-
-
Hildebrand, M.S.1
Dahl, H.H.2
Damiano, J.A.3
Smith, R.J.4
Scheffer, I.E.5
Berkovic, S.F.6
-
17
-
-
18544376557
-
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
-
Kalachikov S, Evgrafov O, Ross B, et al. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet 2002;30:335-341.
-
(2002)
Nat Genet
, vol.30
, pp. 335-341
-
-
Kalachikov, S.1
Evgrafov, O.2
Ross, B.3
-
18
-
-
84871978529
-
Glucose transporter 1 deficiency in the idiopathic generalized epilepsies
-
Arsov T, Mullen SA, Rogers S, et al. Glucose transporter 1 deficiency in the idiopathic generalized epilepsies. Ann Neurol 2012;72:807-815.
-
(2012)
Ann Neurol
, vol.72
, pp. 807-815
-
-
Arsov, T.1
Mullen, S.A.2
Rogers, S.3
-
19
-
-
84858143942
-
GLUT1 deficiency: A glut of epilepsy phenotypes
-
Scheffer IE. GLUT1 deficiency: a glut of epilepsy phenotypes. Neurology 2012;78:524-525.
-
(2012)
Neurology
, vol.78
, pp. 524-525
-
-
Scheffer, I.E.1
-
20
-
-
84878352545
-
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
-
Dibbens LM, de Vries B, Donatello S, et al. Mutations in DEPDC5 cause familial focal epilepsy with variable foci. Nat Genet 2013;45:546-551.
-
(2013)
Nat Genet
, vol.45
, pp. 546-551
-
-
Dibbens, L.M.1
De Vries, B.2
Donatello, S.3
-
21
-
-
59149096726
-
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
-
Helbig I, Mefford HC, Sharp AJ, et al. 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Nat Genet 2009;41:160-162.
-
(2009)
Nat Genet
, vol.41
, pp. 160-162
-
-
Helbig, I.1
Mefford, H.C.2
Sharp, A.J.3
-
22
-
-
37849011324
-
Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants
-
Heron SE, Khosravani H, Varela D, et al. Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants. Ann Neurol 2007;62: 560-568.
-
(2007)
Ann Neurol
, vol.62
, pp. 560-568
-
-
Heron, S.E.1
Khosravani, H.2
Varela, D.3
-
23
-
-
0020573145
-
Predicting zygosity in Norwegian twin pairs born 1915-1960
-
Magnus P, Berg K, Nance WE. Predicting zygosity in Norwegian twin pairs born 1915-1960. Clin Genet 1983;24:103-112.
-
(1983)
Clin Genet
, vol.24
, pp. 103-112
-
-
Magnus, P.1
Berg, K.2
Nance, W.E.3
-
24
-
-
0034850563
-
Severe myoclonic epilepsy of infancy: Extended spectrum of GEFS1?
-
Singh R, Andermann E, Whitehouse WP, et al. Severe myoclonic epilepsy of infancy: extended spectrum of GEFS1? Epilepsia 2001;42:837-844.
-
(2001)
Epilepsia
, vol.42
, pp. 837-844
-
-
Singh, R.1
Andermann, E.2
Whitehouse, W.P.3
-
25
-
-
78049485650
-
Familial mesial temporal lobe epilepsy: A benign epilepsy syndrome showing complex inheritance
-
Crompton DE, Scheffer IE, Taylor I, et al. Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance. Brain 2010;133:3221-3231.
-
(2010)
Brain
, vol.133
, pp. 3221-3231
-
-
Crompton, D.E.1
Scheffer, I.E.2
Taylor, I.3
-
26
-
-
0033006825
-
Likelihood-based approach to estimating twin concordance for dichotomous traits
-
Witte JS, Carlin JB, Hopper JL. Likelihood-based approach to estimating twin concordance for dichotomous traits. Genet Epidemiol 1999;16:290-304.
-
(1999)
Genet Epidemiol
, vol.16
, pp. 290-304
-
-
Witte, J.S.1
Carlin, J.B.2
Hopper, J.L.3
-
27
-
-
3042801131
-
Is benign rolandic epilepsy genetically determined?
-
Vadlamudi L, Harvey AS, Connellan MM, et al. Is benign rolandic epilepsy genetically determined? Ann Neurol 2004;56:129-132.
-
(2004)
Ann Neurol
, vol.56
, pp. 129-132
-
-
Vadlamudi, L.1
Harvey, A.S.2
Connellan, M.M.3
-
28
-
-
33644789372
-
Analyzing the etiology of benign rolandic epilepsy: A multicenter twin collaboration
-
Vadlamudi L, Kjeldsen MJ, Corey LA, et al. Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaboration. Epilepsia 2006;47:550-555.
-
(2006)
Epilepsia
, vol.47
, pp. 550-555
-
-
Vadlamudi, L.1
Kjeldsen, M.J.2
Corey, L.A.3
-
29
-
-
0001836892
-
Familial temporal lobe epilepsy: A new syndrome with adolescent/adult onset and a benign course
-
In: Wolf P, ed. London: John Libbey
-
Berkovic SF, Howell RA, Hopper J. Familial temporal lobe epilepsy: a new syndrome with adolescent/adult onset and a benign course. In: Wolf P, ed. Epileptic Seizures and Syndromes. London: John Libbey; 1994:257-263.
-
(1994)
Epileptic Seizures and Syndromes
, pp. 257-263
-
-
Berkovic, S.F.1
Howell, R.A.2
Hopper, J.3
-
30
-
-
0029834204
-
Familial temporal lobe epilepsy: A common disorder identified in twins
-
Berkovic SF, McIntosh A, Howell RA, Mitchell A, Sheffield LJ, Hopper JL. Familial temporal lobe epilepsy: a common disorder identified in twins. Ann Neurol 1996; 40:227-235.
-
(1996)
Ann Neurol
, vol.40
, pp. 227-235
-
-
Berkovic, S.F.1
McIntosh, A.2
Howell, R.A.3
Mitchell, A.4
Sheffield, L.J.5
Hopper, J.L.6
-
31
-
-
1842580632
-
LGI1 mutations in autosomal dominant partial epilepsy with auditory features
-
Ottman R, Winawer M, Kalachikov S, et al. LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology 2004;62:1120-1126.
-
(2004)
Neurology
, vol.62
, pp. 1120-1126
-
-
Ottman, R.1
Winawer, M.2
Kalachikov, S.3
-
32
-
-
0030943313
-
Generalized epilepsy with febrile seizures plus: A genetic disorder with heterogeneous clinical phenotypes
-
Scheffer I, Berkovic SF. Generalized epilepsy with febrile seizures plus: a genetic disorder with heterogeneous clinical phenotypes. Brain 1997;120:479-490.
-
(1997)
Brain
, vol.120
, pp. 479-490
-
-
Scheffer, I.1
Berkovic, S.F.2
-
33
-
-
0032953159
-
Generalized epilepsy with febrile seizures plus: A common childhood-onset genetic epilepsy syndrome
-
Singh R, Scheffer I, Crossland K, Berkovic SF. Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome. Ann Neurol 1999;45:75-81.
-
(1999)
Ann Neurol
, vol.45
, pp. 75-81
-
-
Singh, R.1
Scheffer, I.2
Crossland, K.3
Berkovic, S.F.4
-
34
-
-
84878438110
-
Genetics of febrile seizure subtypes and syndromes: A twin study
-
Eckhaus J, Lawrence KM, Helbig I, et al. Genetics of febrile seizure subtypes and syndromes: a twin study. Epilepsy Res 2013;105:103-109.
-
(2013)
Epilepsy Res
, vol.105
, pp. 103-109
-
-
Eckhaus, J.1
Lawrence, K.M.2
Helbig, I.3
-
35
-
-
84876384938
-
Genetics of epilepsy syndromes in families with photosensitivity
-
Taylor I, Berkovic SF, Scheffer IE. Genetics of epilepsy syndromes in families with photosensitivity. Neurology 2013;80:1322-1329.
-
(2013)
Neurology
, vol.80
, pp. 1322-1329
-
-
Taylor, I.1
Berkovic, S.F.2
Scheffer, I.E.3
-
36
-
-
84869088193
-
Sodium channels and the neurobiology of epilepsy
-
Oliva M, Berkovic SF, Petrou S. Sodium channels and the neurobiology of epilepsy. Epilepsia 2012;53:1849-1859.
-
(2012)
Epilepsia
, vol.53
, pp. 1849-1859
-
-
Oliva, M.1
Berkovic, S.F.2
Petrou, S.3
-
37
-
-
33947123754
-
The spectrum of SCN1A-related infantile epileptic encephalopathies
-
Harkin LA, McMahon JM, Iona X, et al. The spectrum of SCN1A-related infantile epileptic encephalopathies. Brain 2007;130:843-852.
-
(2007)
Brain
, vol.130
, pp. 843-852
-
-
Harkin, L.A.1
McMahon, J.M.2
Iona, X.3
-
38
-
-
84879684377
-
Targeted resequencing in epileptic encephalopathies identifies recurrent de novo mutations in CHD2 and SYNGAP1
-
Carvill GL, Heavin SB, Yendle SC, et al. Targeted resequencing in epileptic encephalopathies identifies recurrent de novo mutations in CHD2 and SYNGAP1. Nat Genet 2013;45:825-830.
-
(2013)
Nat Genet
, vol.45
, pp. 825-830
-
-
Carvill, G.L.1
Heavin, S.B.2
Yendle, S.C.3
-
39
-
-
84865020270
-
Targeted next generation sequencing as a diagnostic tool in epileptic disorders
-
Lemke JR, Riesch E, Scheurenbrand T, et al. Targeted next generation sequencing as a diagnostic tool in epileptic disorders. Epilepsia 2012;53:1387-1398.
-
(2012)
Epilepsia
, vol.53
, pp. 1387-1398
-
-
Lemke, J.R.1
Riesch, E.2
Scheurenbrand, T.3
|