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Armin Heils

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Kate Everett; Barry Chioza; Jean Aicardi; Harald N Aschauer; Oebele Brouwer; Petra M.C. Callenbach; Athanasios Covanis; Joseph Dooley; Olivier Dulac; Martina Durner; Orvar Eeg-Olofsson; Martha Feucht; Mogens Laue Friis; Renzo Guerrini; Armin Heils; Marianne Juel Kjeldsen; Rima Nabbout; Thomas Sander; Elaine Wirrell; Paul M McKeigue; Robert Robinson; Nichole Taske; Mark Gardiner
Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.
Gianpiero L Cavalleri; Nicole M Walley; Nicole Soranzo; John Mulley; Colin Doherty; Ashish Kapoor; Chantal Depondt; John M Lynch; Ingrid E Scheffer; Armin Heils; Anne Gehrmann; Peter Kinirons; Sonia Gandhi; Parthasarathy Satishchandra; Nicholas W Wood; Anuranjan Anand; Thomas Sander; Samuel F Berkovic; Norman Delanty; David B Goldstein; Sanjay M Sisodiya
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy.
Kate Everett; Barry Chioza; Jean Aicardi; Harald N Aschauer; Oebele Brouwer; Petra M.C. Callenbach; Athanasios Covanis; Olivier Dulac; Orvar Eeg-Olofsson; Martha Feucht; Mogens Laue Friis; Françoise Goutieres; Renzo Guerrini; Armin Heils; Marianne Juel Kjeldsen; Anna-Elina Lehesjoki; Andrew Makoff; Rima Nabbout; Ingrid Olsson; Thomas Sander; Auli Sirén; Paul M McKeigue; Robert Robinson; Nichole Taske; Michele Rees; Mark Gardiner
Linkage and association analysis of CACNG3 in childhood absence epilepsy.

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All Publications

2007: Kate Everett; Barry Chioza; Jean Aicardi; Harald N Aschauer; Oebele Brouwer; Petra M.C. Callenbach; Athanasios Covanis; Joseph Dooley; Olivier Dulac; Martina Durner; Orvar Eeg-Olofsson; Martha Feucht; Mogens Laue Friis; Renzo Guerrini; Armin Heils; Marianne Juel Kjeldsen; Rima Nabbout; Thomas Sander; Elaine Wirrell; Paul M McKeigue; Robert Robinson; Nichole Taske; Mark Gardiner
Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.
Epilepsy research 2007;75(2-3):145-53.
2007: Gianpiero L Cavalleri; Nicole M Walley; Nicole Soranzo; John Mulley; Colin Doherty; Ashish Kapoor; Chantal Depondt; John M Lynch; Ingrid E Scheffer; Armin Heils; Anne Gehrmann; Peter Kinirons; Sonia Gandhi; Parthasarathy Satishchandra; Nicholas W Wood; Anuranjan Anand; Thomas Sander; Samuel F Berkovic; Norman Delanty; David B Goldstein; Sanjay M Sisodiya
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy.
Epilepsia 2007;48(4):706-12.
2007: Kate Everett; Barry Chioza; Jean Aicardi; Harald N Aschauer; Oebele Brouwer; Petra M.C. Callenbach; Athanasios Covanis; Olivier Dulac; Orvar Eeg-Olofsson; Martha Feucht; Mogens Laue Friis; Françoise Goutieres; Renzo Guerrini; Armin Heils; Marianne Juel Kjeldsen; Anna-Elina Lehesjoki; Andrew Makoff; Rima Nabbout; Ingrid Olsson; Thomas Sander; Auli Sirén; Paul M McKeigue; Robert Robinson; Nichole Taske; Michele Rees; Mark Gardiner
Linkage and association analysis of CACNG3 in childhood absence epilepsy.
European journal of human genetics : EJHG 2007;15(4):463-72.
2007: Anne Hempelmann; Joana Cobilanschi; Armin Heils; Hiltrud Muhle; Ulrich Stephani; Yvonne G Weber; Holger Lerche; Thomas Sander
Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.
Epilepsy research 2007;74(1):28-32.
2007: Susanne Lorenz; Armin Heils; Johannes M Kasper; Thomas Sander
Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(1):10-3.
2006: Anne Hempelmann; Kirsten P Taylor; Armin Heils; Susanne Lorenz; Jean-François Prud'homme; Rima Nabbout; Olivier Dulac; Gabrielle Rudolf; Federico Zara; Amedeo Bianchi; Robert Robinson; R Mark Gardiner; Athanasios Covanis; Dick Lindhout; Ulrich Stephani; Christian E Elger; Yvonne G Weber; Holger Lerche; Peter Nürnberg; Katherine L Kron; Ingrid E Scheffer; John C Mulley; Samuel F Berkovic; Thomas Sander
Exploration of the genetic architecture of idiopathic generalized epilepsies.
Epilepsia 2006;47(10):1682-90.
2006: Anne Hempelmann; Armin Heils; Thomas Sander
Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy.
Epilepsy research 2006;71(2-3):223-8.
2006: Snezana Maljevic; Klaus Krampfl; Joana Cobilanschi; Nikola Tilgen; Susanne Beyer; Yvonne G Weber; Friedrich Schlesinger; Daniel Ursu; Werner Melzer; Patrick Cossette; Johannes Bufler; Holger Lerche; Armin Heils
A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy.
Annals of neurology 2006;59(6):983-7.
2006: Barry Chioza; Kate Everett; Harald N Aschauer; Oebele Brouwer; Petra M.C. Callenbach; Athanasios Covanis; Olivier Dulac; Martina Durner; Orvar Eeg-Olofsson; Martha Feucht; Mogens Laue Friis; Armin Heils; Marianne Juel Kjeldsen; Katrin Larsson; Anna-Elina Lehesjoki; Rima Nabbout; Ingrid Olsson; Thomas Sander; Auli Sirén; Robert Robinson; Michele Rees; R Mark Gardiner
Evaluation of CACNA1H in European patients with childhood absence epilepsy.
Epilepsy research 2006;69(2):177-81.
2006: Susanne Lorenz; Armin Heils; Kirsten P Taylor; Anne Gehrmann; Hiltrud Muhle; Meike Gresch; Tim Becker; Ulrike Tauer; Ulrich Stephani; Thomas Sander
Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity.
Neuroscience letters 2006;397(3):234-9.
2005: Kirsten P Lenzen; Armin Heils; Susanne Lorenz; Anne Hempelmann; Thomas Sander
Association analysis of malic enzyme 2 gene polymorphisms with idiopathic generalized epilepsy.
Epilepsia 2005;46(10):1637-41.
2005: Wenli Gu; Thomas Sander; Armin Heils; Kirsten P Lenzen; Ortrud K Steinlein
A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.
Epilepsy research 2005;66(1-3):91-8.
2005: Kirsten P Lenzen; Armin Heils; Susanne Lorenz; Anne Hempelmann; Thomas Sander
Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy.
Epilepsy research 2005;65(1-2):53-7.
2005: Ulrike Tauer; Susanne Lorenz; Kirsten P Lenzen; Armin Heils; Hiltrud Muhle; Meike Gresch; Bernd A Neubauer; Stephan Waltz; Gabrielle Rudolf; Manuel Mattheisen; Konstantin Strauch; Peter Nürnberg; Bettina Schmitz; Ulrich Stephani; Thomas Sander
Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy.
Annals of neurology 2005;57(6):866-73.
2005: Kirsten P Lenzen; Armin Heils; Susanne Lorenz; Anne Hempelmann; S Höfels; F W Lohoff; Bettina Schmitz; Thomas Sander
Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy.
Epilepsy research 2005;63(2-3):113-8.
2005: Armin Heils
CLCN2 and idiopathic generalized epilepsy.
Advances in neurology 2005;95():265-71.
2003: Claudia Izzi; Alessandro Barbon; Mohammad R Toliat; Armin Heils; Christian Becker; Peter Nürnberg; Thomas Sander; Sergio Barlati
Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;123B(1):59-63.
2003: Karsten Haug; Maike Warnstedt; Alexi K. Alekov; Thomas Sander; Alfredo Ramírez; Barbara Poser; Snezana Maljevic; Simon Hebeisen; Christian Kubisch; Johannes Rebstock; Steve Horvath; Kerstin Hallmann; Joern S Dullinger; Birgit Rau; Fritz Haverkamp; Stefan Beyenburg; Herbert Schulz; Dieter Janz; Bernd Giese; Gerhard Müller-Newen; Peter Propping; Christian E Elger; Christoph Fahlke; Holger Lerche; Armin Heils
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.
Nature genetics 2003;33(4):527-32.
2003: Nikola Tilgen; Johannes Rebstock; Steve Horvath; Peter Propping; Christian Erich Elger; Armin Heils
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy.
Annals of neurology 2003;53(2):280-1; author reply 281-2.
2003: Thomas Sander; Christine Windemuth; Herbert Schulz; Kathrin Saar; Elena Gennaro; Concetta Riggio; Amedeo Bianchi; Federico Zara; Gabrielle Rudolf; Fabienne Picard; Christine Bulteau; Anna Kaminska; Cécile Cieuta; Jean-François Prud'homme; Olivier Dulac; Louise Bate; Robert Robinson; R Mark Gardiner; Athanasios Covanis; Gerrit-Jan de Haan; Guus A M A J Janssen; M Gerard van Erp; Eduard H J F Boezeman; Dick Lindhout; Armin Heils; Peter Nürnberg; Dieter Janz
Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12.
Epilepsia 2003;44(1):32-9.
2002: Nikola Tilgen; Heike Pfeiffer; Joana Cobilanschi; Birgit Rau; Steve Horvath; Christian E Elger; Peter Propping; Armin Heils
Association analysis between the human interleukin 1beta (-511) gene polymorphism and susceptibility to febrile convulsions.
Neuroscience letters 2002;334(1):68-70.
2002: Thomas Sander; Mohammad R Toliat; Armin Heils; Gundula Leschik; Christian Becker; Franz Rüschendorf; Klaus Rohde; Stefan Mundlos; Peter Nürnberg
Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy.
Epilepsy research 2002;51(3):249-55.
2002: Dmitry A Varlamov; Alexei P Kudin; Stefan Vielhaber; Rolf Schröder; Robert Sassen; Albert Becker; Dagmar Kunz; Karsten Haug; Johannes Rebstock; Armin Heils; Christian E Elger; Wolfram S Kunz
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene.
Human molecular genetics 2002;11(16):1797-805.
2002: Colette Kananura; Karsten Haug; Thomas Sander; Uwe Runge; Wenli Gu; Kerstin Hallmann; Johannes Rebstock; Armin Heils; Ortrud K Steinlein
A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.
Archives of neurology 2002;59(7):1137-41.
2002: Thomas Sander; Mohammad R Toliat; Armin Heils; Christian Becker; Peter Nürnberg
Failure to replicate an allelic association between an exon 8 polymorphism of the human alpha(1A) calcium channel gene and common syndromes of idiopathic generalized epilepsy.
Epilepsy research 2002;49(2):173-7.
2002: Robert Robinson; Nichole Taske; Thomas Sander; Armin Heils; William P Whitehouse; Françoise Goutières; Jean Aicardi; Anna-Elina Lehesjoki; Auli Siren; Mogens Laue Friis; Marianne Juel Kjeldsen; Chrysostomos P Panayiotopoulos; Colin Kennedy; Colin D Ferrie; Michele Rees; R Mark Gardiner
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.
Epilepsy research 2002;48(3):169-79.
2001: Karsten Haug; Kerstin Hallmann; Johannes Rebstock; Joern S Dullinger; S Muth; Fritz Haverkamp; H Pfeiffer; Birgit Rau; Christian E Elger; Peter Propping; Armin Heils
The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy.
Epilepsy research 2001;47(3):243-6.
2001: Andrew Escayg; Armin Heils; Bryan T MacDonald; Karsten Haug; Thomas Sander; Miriam H Meisler
A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.
American journal of human genetics 2001;68(4):866-73.
2000: Armin Heils; K Haug; Wolfram S Kunz; G Fernandez; Steve Horvath; Johannes Rebstock; Peter Propping; Christian E Elger
Interleukin-1beta gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosis.
Annals of neurology 2000;48(6):948-50.
2000: Karsten Haug; Kerstin Hallmann; Steve Horvath; Thomas Sander; Christian Kubisch; Birgit Rau; Joern S Dullinger; Stefan Beyenburg; Christian E Elger; Peter Propping; Armin Heils
No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy.
Epilepsy research 2000;42(1):57-62.
2000: Karsten Haug; Thomas Sander; Kerstin Hallmann; Birgit Rau; Joern S Dullinger; Christian E Elger; Peter Propping; Armin Heils
The voltage-gated sodium channel beta2-subunit gene and idiopathic generalized epilepsy.
Neuroreport 2000;11(12):2687-9.
2000: Karsten Haug; Joachim Kremerskothen; Kerstin Hallmann; Thomas Sander; Joern S Dullinger; Birgit Rau; Stefan Beyenburg; M J Lentze; Angelika Barnekow; Christian E Elger; Peter Propping; Armin Heils
Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.
Molecular and cellular probes 2000;14(4):255-60.
2000: Karsten Haug; Thomas Sander; Kerstin Hallmann; M J Lentze; Peter Propping; Christian E Elger; Armin Heils
Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy.
Epilepsy research 2000;39(2):127-32.