163 related articles for article (PubMed ID: 37022522)
1. Sub-region analysis of DMD gene in cases with idiopathic generalized epilepsy.
Lin ZJ; Huang BX; Su LF; Zhu SY; He JW; Chen GZ; Lin PX
Neurogenetics; 2023 Jul; 24(3):161-169. PubMed ID: 37022522
[TBL] [Abstract][Full Text] [Related]
2. Clinical application of trio-based whole-exome sequencing in idiopathic generalized epilepsy.
Lin ZJ; Li B; Lin PX; Song W; Yan LM; Meng H; He N
Seizure; 2024 Mar; 116():24-29. PubMed ID: 36842888
[TBL] [Abstract][Full Text] [Related]
3.
Bian WJ; Li ZJ; Wang J; Luo S; Li BM; Gao LD; He N; Yi YH
Front Mol Neurosci; 2022; 15():862480. PubMed ID: 35663265
[TBL] [Abstract][Full Text] [Related]
4. Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Heinzen EL; Depondt C; Cavalleri GL; Ruzzo EK; Walley NM; Need AC; Ge D; He M; Cirulli ET; Zhao Q; Cronin KD; Gumbs CE; Campbell CR; Hong LK; Maia JM; Shianna KV; McCormack M; Radtke RA; O'Conner GD; Mikati MA; Gallentine WB; Husain AM; Sinha SR; Chinthapalli K; Puranam RS; McNamara JO; Ottman R; Sisodiya SM; Delanty N; Goldstein DB
Am J Hum Genet; 2012 Aug; 91(2):293-302. PubMed ID: 22863189
[TBL] [Abstract][Full Text] [Related]
5. Revisiting the clinical impact of variants in EFHC1 in patients with different phenotypes of genetic generalized epilepsy.
Gonsales MC; Ribeiro PAO; Betting LE; Alvim MKM; Guerreiro CM; Yasuda CL; Gitaí DLG; Cendes F; Lopes-Cendes I
Epilepsy Behav; 2020 Nov; 112():107469. PubMed ID: 33181902
[TBL] [Abstract][Full Text] [Related]
6. Identification of potential disease-associated variants in idiopathic generalized epilepsy using targeted sequencing.
Gamirova R; Shagimardanova E; Sato T; Kannon T; Gamirova R; Tajima A
J Hum Genet; 2024 Feb; 69(2):59-67. PubMed ID: 37993639
[TBL] [Abstract][Full Text] [Related]
7. Gene-gene interaction network analysis indicates CNTN2 is a candidate gene for idiopathic generalized epilepsy.
Lin ZJ; He JW; Zhu SY; Xue LH; Zheng JF; Zheng LQ; Huang BX; Chen GZ; Lin PX
Neurogenetics; 2024 Apr; 25(2):131-139. PubMed ID: 38460076
[TBL] [Abstract][Full Text] [Related]
8. Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.
Sander T; Peters C; Kämmer G; Samochowiec J; Zirra M; Mischke D; Ziegler A; Kaupmann K; Bettler B; Epplen JT; Riess O
Am J Med Genet; 1999 Aug; 88(4):305-10. PubMed ID: 10402495
[TBL] [Abstract][Full Text] [Related]
9. Genetics of idiopathic generalized epilepsies.
Gardiner M
Epilepsia; 2005; 46 Suppl 9():15-20. PubMed ID: 16302872
[TBL] [Abstract][Full Text] [Related]
10. Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.
Marini C; Scheffer IE; Crossland KM; Grinton BE; Phillips FL; McMahon JM; Turner SJ; Dean JT; Kivity S; Mazarib A; Neufeld MY; Korczyn AD; Harkin LA; Dibbens LM; Wallace RH; Mulley JC; Berkovic SF
Epilepsia; 2004 May; 45(5):467-78. PubMed ID: 15101828
[TBL] [Abstract][Full Text] [Related]
11. Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes.
Lee CG; Lee J; Lee M
PLoS One; 2018; 13(6):e0199321. PubMed ID: 29924869
[TBL] [Abstract][Full Text] [Related]
12. Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies.
Steinlein O; Sander T; Stoodt J; Kretz R; Janz D; Propping P
Am J Med Genet; 1997 Jul; 74(4):445-9. PubMed ID: 9259383
[TBL] [Abstract][Full Text] [Related]
13. A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.
Escayg A; Heils A; MacDonald BT; Haug K; Sander T; Meisler MH
Am J Hum Genet; 2001 Apr; 68(4):866-73. PubMed ID: 11254445
[TBL] [Abstract][Full Text] [Related]
14. HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond.
Marini C; Porro A; Rastetter A; Dalle C; Rivolta I; Bauer D; Oegema R; Nava C; Parrini E; Mei D; Mercer C; Dhamija R; Chambers C; Coubes C; Thévenon J; Kuentz P; Julia S; Pasquier L; Dubourg C; Carré W; Rosati A; Melani F; Pisano T; Giardino M; Innes AM; Alembik Y; Scheidecker S; Santos M; Figueiroa S; Garrido C; Fusco C; Frattini D; Spagnoli C; Binda A; Granata T; Ragona F; Freri E; Franceschetti S; Canafoglia L; Castellotti B; Gellera C; Milanesi R; Mancardi MM; Clark DR; Kok F; Helbig KL; Ichikawa S; Sadler L; Neupauerová J; Laššuthova P; Šterbová K; Laridon A; Brilstra E; Koeleman B; Lemke JR; Zara F; Striano P; Soblet J; Smits G; Deconinck N; Barbuti A; DiFrancesco D; LeGuern E; Guerrini R; Santoro B; Hamacher K; Thiel G; Moroni A; DiFrancesco JC; Depienne C
Brain; 2018 Nov; 141(11):3160-3178. PubMed ID: 30351409
[TBL] [Abstract][Full Text] [Related]
15. Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.
Hempelmann A; Cobilanschi J; Heils A; Muhle H; Stephani U; Weber Y; Lerche H; Sander T
Epilepsy Res; 2007 Apr; 74(1):28-32. PubMed ID: 17215107
[TBL] [Abstract][Full Text] [Related]
16. Leu226Trp CACNA1A variant associated with juvenile myoclonic epilepsy with and without intellectual disability.
Alehabib E; Kokotović T; Ranji-Burachaloo S; Tafakhori A; Ramshe SM; Esmaeilizadeh Z; Darvish H; Movafagh A; Nagy V
Clin Neurol Neurosurg; 2022 Feb; 213():107108. PubMed ID: 34995834
[TBL] [Abstract][Full Text] [Related]
17. Linkage analysis of idiopathic generalised epilepsy in families of probands with Juvenile Myoclonic Epilepsy and marker loci in the region of EPM 1 on chromosome 21 q: Unverricht-Lundborg disease and JME are not allelic variants.
Rees M; Curtis D; Parker K; Sundqvist A; Baralle D; Bespalova IN; Burmeister M; Chung E; Gardiner RM; Whitehouse WP
Neuropediatrics; 1994 Feb; 25(1):20-5. PubMed ID: 8208346
[TBL] [Abstract][Full Text] [Related]
18. Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.
Heron SE; Khosravani H; Varela D; Bladen C; Williams TC; Newman MR; Scheffer IE; Berkovic SF; Mulley JC; Zamponi GW
Ann Neurol; 2007 Dec; 62(6):560-8. PubMed ID: 17696120
[TBL] [Abstract][Full Text] [Related]
19. The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy.
Sander T; Peters C; Janz D; Bianchi A; Bauer G; Wienker TF; Hildmann T; Epplen JT; Riess O
Epilepsy Res; 1998 Jan; 29(2):115-22. PubMed ID: 9477143
[TBL] [Abstract][Full Text] [Related]
20. Phenotypic expansion of KCNH1-associated disorders to include isolated epilepsy and its associations with genotypes and molecular sub-regional locations.
Tian MQ; Li RK; Yang F; Shu XM; Li J; Chen J; Peng LY; Yu XH; Yang CJ
CNS Neurosci Ther; 2023 Jan; 29(1):270-281. PubMed ID: 36285361
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]