Janz D - Search Results

1

Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism.

Sander T, Hildmann T, Kretz R, Fürst R, Sailer U, Bauer G, Schmitz B, Beck-Mannagetta G, Wienker TF, Janz D. Sander T, et al. Among authors: janz d. Am J Med Genet. 1997 Jul 25;74(4):416-21. Am J Med Genet. 1997. PMID: 9259378

2

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.

Sander T, Windemuth C, Schulz H, Saar K, Gennaro E, Bianchi A, Zara F, Bulteau C, Kaminska A, Ville D, Cieuta C, Prud'homme JF, Dulac O, Bate L, Gardiner RM, de Haan GJ, Janssen GA, Witte J, Halley DJ, Lindhout D, Wienker TF, Janz D; European Consortium on the Genetics of Idiopathic Generalized Epilepsy. Sander T, et al. Among authors: janz d. Am J Med Genet. 2002 Aug 8;114(6):673-8. doi: 10.1002/ajmg.10645. Am J Med Genet. 2002. PMID: 12210286

3

Do idiopathic generalized epilepsies share a common susceptibility gene?

Janz D, Beck-Mannagetta G, Sander T. Janz D, et al. Neurology. 1992 Apr;42(4 Suppl 5):48-55. Neurology. 1992. PMID: 1574176

4

Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients.

Durner M, Sander T, Greenberg DA, Johnson K, Beck-Mannagetta G, Janz D. Durner M, et al. Among authors: janz d. Neurology. 1991 Oct;41(10):1651-5. doi: 10.1212/wnl.41.10.1651. Neurology. 1991. PMID: 1922810

5

The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1".

Sander T, Hildmann T, Janz D, Wienker TF, Neitzel H, Bianchi A, Bauer G, Sailer U, Berek K, Schmitz B, et al. Sander T, et al. Among authors: janz d. Ann Neurol. 1995 Aug;38(2):210-7. doi: 10.1002/ana.410380213. Ann Neurol. 1995. PMID: 7654068

6

Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies.

Sander T, Janz D, Ramel C, Ross CA, Paschen W, Hildmann T, Wienker TF, Bianchi A, Bauer G, Sailer U, et al. Sander T, et al. Among authors: janz d. Neurology. 1995 Sep;45(9):1713-20. doi: 10.1212/wnl.45.9.1713. Neurology. 1995. PMID: 7675232

7

Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.

Sander T, Hildmann T, Wienker TF, Ramel C, Beck-Mannagetta G, Bianchi A, Sailer U, Berek K, Bauer G, Neitzel H, Schmitz B, Durner M, Johnson KJ, Janz D. Sander T, et al. Among authors: janz d. Am J Med Genet. 1996 Feb 16;67(1):31-9. doi: 10.1002/(SICI)1096-8628(19960216)67:1<31::AID-AJMG5>3.0.CO;2-V. Am J Med Genet. 1996. PMID: 8678111

8

Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.

Sander T, Hildmann T, Janz D, Wienker TF, Bianchi A, Bauer G, Sailer U, Scaramelli A, Neitzel H, Schmitz B, Bailey ME, Beck-Mannagetta G, Johnson KJ, Darlison MG. Sander T, et al. Among authors: janz d. Epilepsy Res. 1996 Apr;23(3):235-44. doi: 10.1016/0920-1211(95)00098-4. Epilepsy Res. 1996. PMID: 8739126

9

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. Steinlein O, et al. Among authors: janz d. Am J Med Genet. 1997 Jul 25;74(4):445-9. doi: 10.1002/(sici)1096-8628(19970725)74:4<445::aid-ajmg18>3.0.co;2-i. Am J Med Genet. 1997. PMID: 9259383

10

Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15.

Sander T, Kretz R, Williamson MP, Elmslie FV, Rees M, Hildmann T, Bianchi A, Bauer G, Sailer U, Scaramelli A, Schmitz B, Gardiner RM, Janz D, Beck-Mannagetta G. Sander T, et al. Among authors: janz d. Acta Neurol Scand. 1997 Jul;96(1):1-7. Acta Neurol Scand. 1997. PMID: 9262125

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