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Items: 1 to 20 of 95

1.

Association of BRD2 polymorphisms with photoparoxysmal response.

Lorenz S, Taylor KP, Gehrmann A, Becker T, Muhle H, Gresch M, Tauer U, Sander T, Stephani U.

Neurosci Lett. 2006 May 29;400(1-2):135-9. Epub 2006 Mar 3.

PMID:
16516380
2.

Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity.

Lorenz S, Heils A, Taylor KP, Gehrmann A, Muhle H, Gresch M, Becker T, Tauer U, Stephani U, Sander T.

Neurosci Lett. 2006 Apr 24;397(3):234-9. Epub 2006 Jan 6.

PMID:
16406321
3.

A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.

Gu W, Sander T, Heils A, Lenzen KP, Steinlein OK.

Epilepsy Res. 2005 Aug-Sep;66(1-3):91-8.

PMID:
16112844
4.

BRD2 and TAP-1 genes and juvenile myoclonic epilepsy.

Layouni S, Buresi C, Thomas P, Malafosse A, Dogui M.

Neurol Sci. 2010 Feb;31(1):53-6. doi: 10.1007/s10072-009-0190-z. Epub 2009 Dec 2.

PMID:
19953286
5.

Association analysis of malic enzyme 2 gene polymorphisms with idiopathic generalized epilepsy.

Lenzen KP, Heils A, Lorenz S, Hempelmann A, Sander T.

Epilepsia. 2005 Oct;46(10):1637-41.

6.

Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13.

Pinto D, Westland B, de Haan GJ, Rudolf G, da Silva BM, Hirsch E, Lindhout D, Trenité DG, Koeleman BP.

Hum Mol Genet. 2005 Jan 1;14(1):171-8. Epub 2004 Nov 17.

PMID:
15548544
7.

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. Epub 2003 Jun 25.

8.

Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy.

Hempelmann A, Heils A, Sander T.

Epilepsy Res. 2006 Oct;71(2-3):223-8. Epub 2006 Jul 28.

PMID:
16876983
9.

Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy.

Tauer U, Lorenz S, Lenzen KP, Heils A, Muhle H, Gresch M, Neubauer BA, Waltz S, Rudolf G, Mattheisen M, Strauch K, Nürnberg P, Schmitz B, Stephani U, Sander T.

Ann Neurol. 2005 Jun;57(6):866-73.

PMID:
15929039
10.

A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy.

Cavalleri GL, Walley NM, Soranzo N, Mulley J, Doherty CP, Kapoor A, Depondt C, Lynch JM, Scheffer IE, Heils A, Gehrmann A, Kinirons P, Gandhi S, Satishchandra P, Wood NW, Anand A, Sander T, Berkovic SF, Delanty N, Goldstein DB, Sisodiya SM.

Epilepsia. 2007 Apr;48(4):706-12.

11.

Association analysis of BRD2 (RING3) and epilepsy in a Dutch population.

de Kovel CG, Pinto D, de Haan GJ, Kasteleijn-Nolst Trenité DG, Lindhout D, Koeleman BP.

Epilepsia. 2007 Nov;48(11):2191-2. No abstract available.

12.

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. Epub 2007 Jan 9.

PMID:
17215107
13.

No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.

Durner M, Shinnar S, Resor SR, Moshe SL, Rosenbaum D, Cohen J, Harden C, Kang H, Hertz S, Wallace S, Luciano D, Ballaban-Gil K, Greenberg DA.

Am J Med Genet. 2000 Feb 7;96(1):49-52.

PMID:
10686551
14.

Genetics of photosensitivity (photoparoxysmal response): a review.

Stephani U, Tauer U, Koeleman B, Pinto D, Neubauer BA, Lindhout D.

Epilepsia. 2004;45 Suppl 1:19-23. Review.

15.

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 20;88(4):305-10.

PMID:
10402495
16.

Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis.

Muhle H, von Spiczak S, Gaus V, Kara S, Helbig I, Hampe J, Franke A, Weber Y, Lerche H, Kleefuss-Lie AA, Elger CE, Schreiber S, Stephani U, Sander T.

Epilepsy Res. 2010 May;89(2-3):319-26. doi: 10.1016/j.eplepsyres.2010.02.004. Epub 2010 Mar 24.

PMID:
20338729
17.

Mapping, genomic structure, and polymorphisms of the human GABABR1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsy.

Peters HC, Kämmer G, Volz A, Kaupmann K, Ziegler A, Bettler B, Epplen JT, Sander T, Riess O.

Neurogenetics. 1998 Dec;2(1):47-54.

PMID:
9933300
18.

Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene.

Puri V, McQuillin A, Choudhury K, Datta S, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Moorey H, Morgan J, Punukollu B, Kandasami G, Curtis D, Gurling H.

Biol Psychiatry. 2007 Apr 1;61(7):873-9. Epub 2006 Sep 15.

PMID:
16978587
19.

Association of functional polymorphisms of the human tryptophan hydroxylase 2 gene with risk for bipolar disorder in Han Chinese.

Lin YM, Chao SC, Chen TM, Lai TJ, Chen JS, Sun HS.

Arch Gen Psychiatry. 2007 Sep;64(9):1015-24.

PMID:
17768266
20.

Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14.

Sander T, Schulz H, Vieira-Saeker AM, Bianchi A, Sailer U, Bauer G, Scaramelli A, Wienker TF, Saar K, Reis A, Janz D, Epplen JT, Riess O.

Am J Med Genet. 1999 Apr 16;88(2):182-7.

PMID:
10206240

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