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Items: 1 to 50 of 68

1.

Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.

Everett K, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley J, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis M, Guerrini R, Heils A, Kjeldsen M, Nabbout R, Sander T, Wirrell E, McKeigue P, Robinson R, Taske N, Gardiner M.

Epilepsy Res. 2007 Jul;75(2-3):145-53. Epub 2007 Jun 18.

PMID:
17580110
2.

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.

3.

Linkage and association analysis of CACNG3 in childhood absence epilepsy.

Everett KV, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dulac O, Eeg-Olofsson O, Feucht M, Friis M, Goutieres F, Guerrini R, Heils A, Kjeldsen M, Lehesjoki AE, Makoff A, Nabbout R, Olsson I, Sander T, Sirén A, McKeigue P, Robinson R, Taske N, Rees M, Gardiner M.

Eur J Hum Genet. 2007 Apr;15(4):463-72. Epub 2007 Jan 31. Erratum in: Eur J Hum Genet. 2008 May;16(5):659-60.

4.

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
5.

Exploration of the genetic architecture of idiopathic generalized epilepsies.

Hempelmann A, Taylor KP, Heils A, Lorenz S, Prud'homme JF, Nabbout R, Dulac O, Rudolf G, Zara F, Bianchi A, Robinson R, Gardiner RM, Covanis A, Lindhout D, Stephani U, Elger CE, Weber YG, Lerche H, Nürnberg P, Kron KL, Scheffer IE, Mulley JC, Berkovic SF, Sander T.

Epilepsia. 2006 Oct;47(10):1682-90.

6.

Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.

Lorenz S, Heils A, Kasper JM, Sander T.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):10-3.

PMID:
16958040
7.

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
8.

A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy.

Maljevic S, Krampfl K, Cobilanschi J, Tilgen N, Beyer S, Weber YG, Schlesinger F, Ursu D, Melzer W, Cossette P, Bufler J, Lerche H, Heils A.

Ann Neurol. 2006 Jun;59(6):983-7.

PMID:
16718694
9.

Evaluation of CACNA1H in European patients with childhood absence epilepsy.

Chioza B, Everett K, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis M, Heils A, Kjeldsen M, Larsson K, Lehesjoki AE, Nabbout R, Olsson I, Sander T, Sirén A, Robinson R, Rees M, Gardiner RM.

Epilepsy Res. 2006 May;69(2):177-81. Epub 2006 Feb 28.

PMID:
16504478
10.

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
11.

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.

12.

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
13.

Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy.

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

Epilepsy Res. 2005 Jun;65(1-2):53-7.

PMID:
16023832
14.

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
15.

Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy.

Lenzen KP, Heils A, Lorenz S, Hempelmann A, Höfels S, Lohoff FW, Schmitz B, Sander T.

Epilepsy Res. 2005 Feb;63(2-3):113-8.

PMID:
15725393
16.

CLCN2 and idiopathic generalized epilepsy.

Heils A.

Adv Neurol. 2005;95:265-71. No abstract available.

PMID:
15508929
17.

Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy.

Izzi C, Barbon A, Toliat MR, Heils A, Becker C, Nürnberg P, Sander T, Barlati S.

Am J Med Genet B Neuropsychiatr Genet. 2003 Nov 15;123B(1):59-63.

PMID:
14582146
18.
19.

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.

Haug K, Warnstedt M, Alekov AK, Sander T, Ramírez A, Poser B, Maljevic S, Hebeisen S, Kubisch C, Rebstock J, Horvath S, Hallmann K, Dullinger JS, Rau B, Haverkamp F, Beyenburg S, Schulz H, Janz D, Giese B, Müller-Newen G, Propping P, Elger CE, Fahlke C, Lerche H, Heils A.

Nat Genet. 2003 Apr;33(4):527-32. Epub 2003 Mar 3. Retraction in: Haug K, Warnstedt M, Alekov AK, Sander T, Ramírez A, Poser B, Maljevic S, Hebeisen S, Kubisch C, Rebstock J, Horvath S, Hallmann K, Dullinger JS, Rau B, Haverkamp F, Beyenburg S, Schulz H, Janz D, Giese B, Müller-Newen G, Propping P, Elger CE, Fahlke C,.

PMID:
12612585
20.

Polymorphic MAO-A and 5-HT-transporter genes: analysis of interactions in panic disorder.

Sand P, Lesch KP, Catalano M, Bosi M, Syagailo YV, Okladnova O, Di Bella D, Maffei P, Heils A, Friess F, Politi E, Nöthen MM, Franke P, Stöber G, Fritze J, Maier W, Propping P, Beckmann H, Bellodi L, Riederer P, Deckert J.

World J Biol Psychiatry. 2000 Jul;1(3):147-50.

PMID:
12607224
21.

Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12.

Sander T, Windemuth C, Schulz H, Saar K, Gennaro E, Riggio C, Bianchi A, Zara F, Rudolf G, Picard F, Bulteau C, Kaminska A, Cieuta C, Prud'homme JF, Dulac O, Bate L, Robinson R, Gardiner RM, Covanis A, de Haan GJ, Janssen GA, van Erp MG, Boezeman EH, Lindhout D, Heils A, Nürnberg P, Janz D; European Consortium on the Genetics of Idiopathic Generalized Epilepsy.

Epilepsia. 2003 Jan;44(1):32-9.

22.

Prodynorphin gene promoter polymorphism and temporal lobe epilepsy.

Tilgen N, Rebstock J, Horvath S, Propping P, Elger CE, Heils A.

Ann Neurol. 2003 Feb;53(2):280-1; author reply 281-2. No abstract available.

PMID:
12557303
23.

Association analysis between the human interleukin 1beta (-511) gene polymorphism and susceptibility to febrile convulsions.

Tilgen N, Pfeiffer H, Cobilanschi J, Rau B, Horvath S, Elger CE, Propping P, Heils A.

Neurosci Lett. 2002 Dec 6;334(1):68-70.

PMID:
12431777
24.

Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy.

Sander T, Toliat MR, Heils A, Leschik G, Becker C, Rüschendorf F, Rohde K, Mundlos S, Nürnberg P.

Epilepsy Res. 2002 Oct;51(3):249-55.

PMID:
12399075
25.

Metabolic consequences of a novel missense mutation of the mtDNA CO I gene.

Varlamov DA, Kudin AP, Vielhaber S, Schröder R, Sassen R, Becker A, Kunz D, Haug K, Rebstock J, Heils A, Elger CE, Kunz WS.

Hum Mol Genet. 2002 Aug 1;11(16):1797-805.

PMID:
12140182
26.

A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.

Kananura C, Haug K, Sander T, Runge U, Gu W, Hallmann K, Rebstock J, Heils A, Steinlein OK.

Arch Neurol. 2002 Jul;59(7):1137-41.

PMID:
12117362
28.

Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.

Robinson R, Taske N, Sander T, Heils A, Whitehouse W, Goutières F, Aicardi J, Lehesjoki AE, Siren A, Laue Friis M, Kjeldsen MJ, Panayiotopoulos C, Kennedy C, Ferrie C, Rees M, Gardiner RM.

Epilepsy Res. 2002 Feb;48(3):169-79.

PMID:
11904235
29.

Early experience and serotonin transporter gene variation interact to influence primate CNS function.

Bennett AJ, Lesch KP, Heils A, Long JC, Lorenz JG, Shoaf SE, Champoux M, Suomi SJ, Linnoila MV, Higley JD.

Mol Psychiatry. 2002;7(1):118-22.

30.

The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy.

Haug K, Hallmann K, Rebstock J, Dullinger J, Muth S, Haverkamp F, Pfeiffer H, Rau B, Elger CE, Propping P, Heils A.

Epilepsy Res. 2001 Dec;47(3):243-6.

PMID:
11738931
31.

Serotonergic gene transcriptional control regions: targets for antidepressant drug development?

Lesch KP, Heils A.

Int J Neuropsychopharmacol. 2000 Mar;3(1):67-79.

PMID:
11343581
32.

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. Epub 2001 Mar 14.

33.

Interleukin-1beta gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosis.

Heils A, Haug K, Kunz WS, Fernandez G, Horvath S, Rebstock J, Propping P, Elger CE.

Ann Neurol. 2000 Dec;48(6):948-50. No abstract available.

PMID:
11117556
35.

No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy.

Haug K, Hallmann K, Horvath S, Sander T, Kubisch C, Rau B, Dullinger J, Beyenburg S, Elger CE, Propping P, Heils A.

Epilepsy Res. 2000 Nov;42(1):57-62.

PMID:
10996506
36.

The voltage-gated sodium channel beta2-subunit gene and idiopathic generalized epilepsy.

Haug K, Sander T, Hallmann K, Rau B, Dullinger JS, Elger CE, Propping P, Heils A.

Neuroreport. 2000 Aug 21;11(12):2687-9.

PMID:
10976944
37.

Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.

Haug K, Kremerskothen J, Hallmann K, Sander T, Dullinger J, Rau B, Beyenburg S, Lentze MJ, Barnekow A, Elger CE, Propping P, Heils A.

Mol Cell Probes. 2000 Aug;14(4):255-60.

PMID:
10970730
38.

Effect of 1-trichloromethyl-1,2,3,4-tetrahydro-beta-carboline (TaClo) on human serotonergic cells.

Bringmann G, Brückner R, Mössner R, Feineis D, Heils A, Lesch KP.

Neurochem Res. 2000 Jun;25(6):837-43.

PMID:
10944002
39.

Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy.

Haug K, Sander T, Hallmann K, Lentze MJ, Propping P, Elger CE, Heils A.

Epilepsy Res. 2000 Apr;39(2):127-32.

PMID:
10759301
40.

Serotonin transporter function is modulated by brain-derived neurotrophic factor (BDNF) but not nerve growth factor (NGF).

Mössner R, Daniel S, Albert D, Heils A, Okladnova O, Schmitt A, Lesch KP.

Neurochem Int. 2000 Mar;36(3):197-202.

PMID:
10676853
41.

Reduction of 5-hydroxytryptamine (5-HT)(1A)-mediated temperature and neuroendocrine responses and 5-HT(1A) binding sites in 5-HT transporter knockout mice.

Li Q, Wichems C, Heils A, Van De Kar LD, Lesch KP, Murphy DL.

J Pharmacol Exp Ther. 1999 Dec;291(3):999-1007.

PMID:
10565817
42.

Association of the serotonin transporter promoter regulatory region polymorphism and obsessive-compulsive disorder.

Bengel D, Greenberg BD, Corá-Locatelli G, Altemus M, Heils A, Li Q, Murphy DL.

Mol Psychiatry. 1999 Sep;4(5):463-6.

43.

Isolated absence of the septum pellucidum.

Supprian T, Sian J, Heils A, Hofmann E, Warmuth-Metz M, Solymosi L.

Neuroradiology. 1999 Aug;41(8):563-6.

PMID:
10447564
44.

Molecular manipulations as tools for enhancing our understanding of 5-HT neurotransmission.

Murphy DL, Wichems C, Li Q, Heils A.

Trends Pharmacol Sci. 1999 Jun;20(6):246-52. Review.

PMID:
10366867
45.

[Agenesis septum pellucidum in a schizophrenic patient].

Supprian T, Heils A, Hofmann E, Warmuth-Metz M, Stöber G, Franzek E.

Nervenarzt. 1999 Mar;70(3):269-75. German.

PMID:
10231816
46.

The appetite suppressant d-fenfluramine induces apoptosis in human serotonergic cells.

Bengel D, Isaacs KR, Heils A, Lesch KP, Murphy DL.

Neuroreport. 1998 Sep 14;9(13):2989-93.

PMID:
9804303
47.

Enhancement of serotonin transporter function by tumor necrosis factor alpha but not by interleukin-6.

Mössner R, Heils A, Stöber G, Okladnova O, Daniel S, Lesch KP.

Neurochem Int. 1998 Sep;33(3):251-4.

PMID:
9759920
48.

Susceptibility for schizophrenia is not influenced by a functional insertion/deletion variant in the promoter of the serotonin transporter gene.

Stöber G, Jatzke S, Heils A, Jungkunz G, Fuchs E, Knapp M, Riederer P, Lesch KP.

Eur Arch Psychiatry Clin Neurosci. 1998;248(2):82-6.

PMID:
9684917
49.

Distribution of the B33 CTG repeat polymorphism in a subtype of schizophrenia.

Bengel D, Balling U, Stöber G, Heils A, Li SH, Ross CA, Jungkunz G, Franzek E, Beckmann H, Riederer P, Lesch KP.

Eur Arch Psychiatry Clin Neurosci. 1998;248(2):78-81.

PMID:
9684916
50.

Insertion/deletion variant (-141C Ins/Del) in the 5' regulatory region of the dopamine D2 receptor gene: lack of association with schizophrenia and bipolar affective disorder. Short communication.

Stöber G, Jatzke S, Heils A, Jungkunz G, Knapp M, Mössner R, Riederer P, Lesch KP.

J Neural Transm (Vienna). 1998;105(1):101-9.

PMID:
9588764

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