SCOPUS 정보 검색 플랫폼

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 96, Issue 6, 2000, Pages 814-816

Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) and IGE

(7) Chioza, B a Goodwin, H a Blower, J b McCormick, D b Nashef, L b,c Asherson, P a Makoff, A J a

a KING'S COLLEGE LONDON (United Kingdom)

b KENT AND CANTERBURY HOSPITAL (United Kingdom)

c KING S COLLEGE HOSPITAL (United Kingdom)

Author keywords

Association study; CHRNA4; Idiopathic generalised epilepsy; Nicotinic acetylcholine receptor

Indexed keywords

NICOTINIC RECEPTOR; RECEPTOR SUBUNIT;

ADULT; ALLELE; ARTICLE; CAUCASIAN; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE REPLICATION; GENERALIZED EPILEPSY; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; IDIOPATHIC DISEASE; MALE; PRIORITY JOURNAL;

ADULT; ALLELES; DNA; EPILEPSY, GENERALIZED; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; MALE; POLYMORPHISM, GENETIC; RECEPTORS, NICOTINIC;

EID: 0034606323 PISSN: 15524841 EISSN: 1552485X Source Type: Journal
DOI: None Document Type: Article

Times cited : (13)

References (13)

1
- 0004963360
- Beck-Mannagetta G, Anderson VE, Doose H, Janz D, editors. Genetics of the epilepsy. Berlin: Springer-Verlag
- (1989) , pp. 119-126
- Beck-Mannagetta, G.¹ Janz, D.² Hoffmeister, U.³

2
- 0031748082
- Epilepsies in twins: Genetics of the major epilepsy syndromes
- (1998) Ann Neurol , vol.43 , pp. 435-445
- Berkovic, S.F.¹ Howell, R.A.² Hay, D.A.³ Hopper, J.L.⁴

3
- 0024317220
- Proposal for revised classification of epilepsy and epileptic syndromes
- (1989) Epilepsia , vol.30 , pp. 389-399

4
- 0015139734
- Essential isochronic epilepsy in MZ twin pairs
- (1971) Acta Genet Med Gemellol , vol.20 , pp. 380-383
- Gedda, L.¹ Tatarelli, R.²

5
- 0026846639
- Do idiopathic generalized epilepsies share a common susceptibility gene?
- (1992) Neurology , vol.42 , pp. 48-55
- Janz, D.¹ Beck Mannagetta, G.² Sander, T.³

6
- 0028811072
- Discordant patterns of linkage disequilibrium of the peptide-transporter loci within the HLA class II region
- (1995) Am J Hum Genet , vol.57 , pp. 1436-1444
- Klitz, W.¹ Stephens, J.C.² Grote, M.³ Carrington, M.⁴

7
- 17344372328
- A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
- (1998) Nat Genet , vol.18 , pp. 25-29
- Singh, N.A.¹ Charlier, C.² Stauffer, D.³ DuPont, B.R.⁴ Leach, R.J.⁵ Melis, R.⁶ Ronen, G.M.⁷ Bjere, I.⁸ Quattlebaum, T.⁹ Murphy, J.V.¹⁰ McHarg, M.L.¹¹ Gagnon, D.¹² Rosales, T.O.¹³ Peiffer, A.¹⁴ Anderson, V.E.¹⁵ Leppert, M.¹⁶

8
- 0028980028
- A missense mutation in the neuronal nicotinic acetylcholine receptor 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
- (1995) Nat Genet , vol.11 , pp. 201-203
- Steinlein, O.¹ Mulley, J.K.² Propping, P.³ Wallace, R.H.⁴ Phillips, H.A.⁵ Sutherland, G.R.⁶ Scheffer, I.E.⁷ Berkovic, S.F.⁸

9
- 0030916583
- An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy
- (1997) Hum Mol Genet , vol.6 , pp. 943-947
- Steinlein, O.¹ Magnusson, A.² Stoodt, J.³ Bertrand, S.⁴ Weiland, S.⁵ Berkovic, S.F.⁶ Nakken, K.O.⁷ Propping, P.⁸ Bertrand, D.⁹

10
- 0030749655
- Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit 4 with common idiopathic generalised epilepsies
- (1997) Am J Med Genet , vol.74 , pp. 445-449
- Steinlein, O.¹ Sander, T.² Stoodt, J.³ Kretz, R.⁴ Janz, D.⁵ Propping, P.⁶

11
- 0026494911
- A haplotype-based 'haplotype relative risk' approach to detecting allelic associations
- (1992) Hum Hered , vol.42 , pp. 337-346
- Terwilliger, J.¹ Ott, J.²

12
- 0003408938
- Baltimore: Johns Hopkins University Press
- (1994) Handbook of human genetic linkage
- Terwilliger, J.¹ Ott, J.²

13
- 0001200144
- Testing linkage disequilibrium between a disease gene and marker loci
- (1993) Am J Med Genet , vol.53 , pp. 1107
- Xie, X.¹ Ott, J.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.