46 related articles for article (PubMed ID: 15009221)
1. Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy.
Greenberg DA; Durner M; Keddache M; Shinnar S; Resor SR; Moshe SL; Rosenbaum D; Cohen J; Harden C; Kang H; Wallace S; Luciano D; Ballaban-Gil K; Tomasini L; Zhou G; Klotz I; Dicker E
Am J Hum Genet; 2000 Feb; 66(2):508-16. PubMed ID: 10677311
[TBL] [Abstract][Full Text] [Related]
2. BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy.
Pal DK; Evgrafov OV; Tabares P; Zhang F; Durner M; Greenberg DA
Am J Hum Genet; 2003 Aug; 73(2):261-70. PubMed ID: 12830434
[TBL] [Abstract][Full Text] [Related]
3. Association of variants in the ABCB1, CYP2C19 and CYP2C9 genes for Juvenile Myoclonic Epilepsy.
Jara-Prado A; Guerrero-Camacho JL; Ángeles-López QD; Ochoa-Morales A; Dávila-Ortiz de Montellano DJ; Ramírez-García MÁ; Breda-Yepes M; Durón RM; Delgado-Escueta AV; Barrios-González DA; Martínez-Juárez IE
Neurol Sci; 2024 Apr; 45(4):1635-1643. PubMed ID: 37875597
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. EFHC1 gene mutation profile of Turkish JME patients and its association with disease risk.
Aslan-Kara K; Dündar-Yenilmez E; Ateş E; Alparslan MM; Peköz T; Bozdemir H; Tuli A
Seizure; 2024 Jan; 114():79-83. PubMed ID: 38088014
[TBL] [Abstract][Full Text] [Related]
6. Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation.
Grigorenko EL; Wood FB; Meyer MS; Pauls DL
Am J Hum Genet; 2000 Feb; 66(2):715-23. PubMed ID: 10677331
[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. Blinders, phenotype, and fashionable genetic analysis: a critical examination of the current state of epilepsy genetic studies.
Greenberg DA; Subaran R
Epilepsia; 2011 Jan; 52(1):1-9. PubMed ID: 21219301
[TBL] [Abstract][Full Text] [Related]
9. Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry.
Subaran RL; Conte JM; Stewart WC; Greenberg DA
Epilepsia; 2015 Feb; 56(2):188-94. PubMed ID: 25489633
[TBL] [Abstract][Full Text] [Related]
10. The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness.
Charlesworth J; Kramer PL; Dyer T; Diego V; Samples JR; Craig JE; Mackey DA; Hewitt AW; Blangero J; Wirtz MK
Invest Ophthalmol Vis Sci; 2010 Jul; 51(7):3509-14. PubMed ID: 20237253
[TBL] [Abstract][Full Text] [Related]
11. DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
Bai D; Bailey JN; Durón RM; Alonso ME; Medina MT; Martínez-Juárez IE; Suzuki T; Machado-Salas J; Ramos-Ramírez R; Tanaka M; Ortega RH; López-Ruiz M; Rasmussen A; Ochoa A; Jara-Prado A; Yamakawa K; Delgado-Escueta AV
Epilepsia; 2009 May; 50(5):1184-90. PubMed ID: 18823326
[TBL] [Abstract][Full Text] [Related]
12. Phenotypic concordance in 70 families with IGE-implications for genetic studies of epilepsy.
Kinirons P; Rabinowitz D; Gravel M; Long J; Winawer M; Sénéchal G; Ottman R; Cossette P
Epilepsy Res; 2008 Nov; 82(1):21-28. PubMed ID: 18723325
[TBL] [Abstract][Full Text] [Related]
13. Evaluating candidate genes in common epilepsies and the nature of evidence.
Pal DK; Strug LJ; Greenberg DA
Epilepsia; 2008 Mar; 49(3):386-92. PubMed ID: 18028406
[TBL] [Abstract][Full Text] [Related]
14. The state of the art in the genetic analysis of the epilepsies.
Greenberg DA; Pal DK
Curr Neurol Neurosci Rep; 2007 Jul; 7(4):320-8. PubMed ID: 17618539
[TBL] [Abstract][Full Text] [Related]
15. Evidence for linkage between juvenile myoclonic epilepsy-related idiopathic generalized epilepsy and 6p11-12 in Dutch families.
Pinto D; de Haan GJ; Janssen GA; Boezeman EH; van Erp MG; Westland B; Witte J; Bader A; Halley DJ; Kasteleijn-Nolst Trenité DG; Lindhout D; Koeleman BP
Epilepsia; 2004 Mar; 45(3):211-7. PubMed ID: 15009221
[TBL] [Abstract][Full Text] [Related]
16. Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.
Whitehouse WP; Rees M; Curtis D; Sundqvist A; Parker K; Chung E; Baralle D; Gardiner RM
Am J Hum Genet; 1993 Sep; 53(3):652-62. PubMed ID: 8352275
[TBL] [Abstract][Full Text] [Related]
17. Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families.
Bai D; Alonso ME; Medina MT; Bailey JN; Morita R; Cordova S; Rasmussen A; Ramos-Peek J; Ochoa A; Jara A; Donnadieu FR; Cadena G; Yamakawa K; Delgado-Escueta AV
Am J Med Genet; 2002 Dec; 113(3):268-74. PubMed ID: 12439895
[TBL] [Abstract][Full Text] [Related]
18. Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.
Delgado-Escueta AV; Medina MT; Serratosa JM; Castroviejo IP; Gee MN; Weissbecker K; Westling BW; Fong CY; Alonso ME; Cordova S; Shah P; Khan S; Sainz J; Rubio-Donnadieu F; Sparkes RS
Adv Neurol; 1999; 79():351-74. PubMed ID: 10514826
[TBL] [Abstract][Full Text] [Related]
19. Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy.
Delgado-Escueta AV; Greenberg D; Weissbecker K; Liu A; Treiman L; Sparkes R; Park MS; Barbetti A; Terasaki PI
Epilepsia; 1990; 31 Suppl 3():S19-29. PubMed ID: 2121470
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
