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Thomas Sander

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Katharina Pernhorst; Lutz Priebe; Thomas Sander; Susanne Schoch; Karen van Loo; Marec von Lehe; Sven Cichon; Christoph Helmstaedter; Stefan Herms; Per Hoffmann; Albert J Becker
Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue.
Tomislav Majic; Johannes Rentzsch; Yehonala Gudlowski; Stefan Ehrlich; Georg Juckel; Thomas Sander; Undine E Lang; Georg Winterer; Jürgen Gallinat
COMT Val108/158Met genotype modulates human sensory gating.
Ortrud K Steinlein; Holger Trucks; Eric Aichinger; Thomas Sander
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta.

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All Publications

2013: Katharina Pernhorst; Lutz Priebe; Thomas Sander; Susanne Schoch; Karen van Loo; Marec von Lehe; Sven Cichon; Christoph Helmstaedter; Stefan Herms; Per Hoffmann; Albert J Becker
Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue.
Brain research 2013;1499():136-44.
2011: Tomislav Majic; Johannes Rentzsch; Yehonala Gudlowski; Stefan Ehrlich; Georg Juckel; Thomas Sander; Undine E Lang; Georg Winterer; Jürgen Gallinat
COMT Val108/158Met genotype modulates human sensory gating.
NeuroImage 2011;55(2):818-24.
2011: Ortrud K Steinlein; Holger Trucks; Eric Aichinger; Thomas Sander
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta.
BMC medical genetics 2011;12():152.
2010: Carolin Opgen-Rhein; Eva Janina Brandl; Daniel J Müller; Andres H Neuhaus; Arun K Tiwari; Thomas Sander; Michael Dettling
Association of HTR2C, but not LEP or INSIG2, genes with antipsychotic-induced weight gain in a German sample.
Pharmacogenomics 2010;11(6):773-80.
2010: Michael Steffens; Tim Becker; Thomas Sander; Rolf Fimmers; Christine Herold; Daniela A Holler; Costin Leu; Stefan Herms; Sven Cichon; Bastian Bohn; Thomas Gerstner; Michael Griebel; Markus M Nöthen; Thomas F Wienker; Max P Baur
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests.
Human heredity 2010;69(4):268-84.
2010: Henning Budde; Thomas Sander; Catrin Wernicke; Anett Müller; Jürgen Gallinat; Lutz G Schmidt; Michael N Smolka
Serotonin transporter promoter polymorphism and dopaminergic sensitivity in alcoholics.
Journal of neural transmission (Vienna, Austria : 1996) 2010;117(1):133-8.
2009: Barry A Chioza; Jean Aicardi; Harald N Aschauer; Oebele Brouwer; Petra M.C. Callenbach; Athanasios Covanis; Joseph M Dooley; Olivier Dulac; Martina Durner; Orvar Eeg-Olofsson; Martha Feucht; Mogens Laue Friis; Renzo Guerrini; Marianne Juel Kjeldsen; Rima Nabbout; Lina Nashef; Thomas Sander; Auli Sirén; Elaine Wirrell; Paul M McKeigue; Robert Robinson; R Mark Gardiner; Kate V Everett
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.
Epilepsy research 2009;87(2-3):247-55.
2009: 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
Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.
Nature genetics 2009;41(9):1043.
2009: Ailing Kleefuss-Lie; Waltraut Friedl; Sven Cichon; Karsten Haug; Maike Warnstedt; Alexi Alekov; Thomas Sander; Alfredo Ramirez; Barbara Poser; Snezana Maljevic; Simon Hebeisen; Christian Kubisch; Johannes Rebstock; Steve Horvath; Kerstin Hallmann; Jörn 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
CLCN2 variants in idiopathic generalized epilepsy.
Nature genetics 2009;41(9):954-5.
2009: Andres H Neuhaus; Carolin Opgen-Rhein; C Urbanek; Eckhart Hahn; T M T Ta; M Seidelsohn; S Strathmann; F Kley; N Wieseke; Thomas Sander; Michael Dettling
COMT Val 158 Met polymorphism is associated with cognitive flexibility in a signal discrimination task in schizophrenia.
Pharmacopsychiatry 2009;42(4):141-4.
2009: Undine E Lang; Rainer Hellweg; Thomas Sander; Jürgen Gallinat
The Met allele of the BDNF Val66Met polymorphism is associated with increased BDNF serum concentrations.
Molecular psychiatry 2009;14(2):120-2.
2008: Katharina Schmack; Florian Schlagenhauf; Philipp Sterzer; Jana Wrase; Anne Beck; Theresa Dembler; Peter Kalus; Imke Puls; Thomas Sander; Andreas Heinz; Jürgen Gallinat
Catechol-O-methyltransferase val158met genotype influences neural processing of reward anticipation.
NeuroImage 2008;42(4):1631-8.
2008: Bin Tang; Thomas Sander; Kimberley Craven; Anne Hempelmann; Andrew Escayg
Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy.
Neurobiology of disease 2008;29(1):59-70.
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.
2007: Jürgen Gallinat; Thomas Götz; Peter Kalus; Malek Bajbouj; Thomas Sander; Georg Winterer
Genetic variations of the NR3A subunit of the NMDA receptor modulate prefrontal cerebral activity in humans.
Journal of cognitive neuroscience 2007;19(1):59-68.
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: Anne Hempelmann; Santosh Kumar; Shanmugakonar Muralitharan; Thomas Sander
Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia.
Neuroscience letters 2006;402(1-2):118-20.
2006: Michael von Brevern; Nga Ta; Anupama Shankar; Anna Wiste; Anne Siegel; Andrea Radtke; Thomas Sander; Andrew Escayg
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.
Headache 2006;46(7):1136-41.
2006: Susanne Lorenz; Kirsten P Taylor; Anne Gehrmann; Tim Becker; Hiltrud Muhle; Meike Gresch; Ulrike Tauer; Thomas Sander; Ulrich Stephani
Association of BRD2 polymorphisms with photoparoxysmal response.
Neuroscience letters 2006;400(1-2):135-9.
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: Undine E Lang; Rainer Hellweg; Peter Kalus; Malek Bajbouj; Kirsten P Lenzen; Thomas Sander; Dieter Kunz; Jürgen Gallinat
Association of a functional BDNF polymorphism and anxiety-related personality traits.
Psychopharmacology 2005;180(1):95-9.
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: Bernd A Neubauer; Stephan Waltz; M Grothe; Andreas Hahn; I Tuxhorn; Thomas Sander; Gerhard Kurlemann; Ulrich Stephani
Photosensitivity: genetics and clinical significance.
Advances in neurology 2005;95():217-26.
2004: Wenli Gu; Thomas Sander; Tim Becker; Ortrud K Steinlein
Genotypic association of exonic LGI4 polymorphisms and childhood absence epilepsy.
Neurogenetics 2004;5(1):41-4.
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: Jürgen Gallinat; Daniel Senkowski; Catrin Wernicke; Georg Juckel; Isabell Becker; Thomas Sander; Michael N Smolka; Victor Perez; Hans Rommelspacher; Georg Winterer; Werner M Herrmann
Allelic variants of the functional promoter polymorphism of the human serotonin transporter gene is associated with auditory cortical stimulus processing.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2003;28(3):530-2.
2003: Georg Winterer; Michael N Smolka; Jerzy Samochowiec; Mario Ziller; Richard Mahlberg; Jürgen Gallinat; Hans Rommelspacher; Werner M Herrmann; Thomas Sander
Association of EEG coherence and an exonic GABA(B)R1 gene polymorphism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;117B(1):51-6.
2003: Georg Winterer; Richard Mahlberg; Michael N Smolka; Jerzy Samochowiec; Mario Ziller; Hans Rommelspacher; Werner M Herrmann; Lutz G Schmidt; Thomas Sander
Association analysis of exonic variants of the GABA(B)-receptor gene and alpha electroencephalogram voltage in normal subjects and alcohol-dependent patients.
Behavior genetics 2003;33(1):7-15.
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: Christine Windemuth; Herbert Schulz; Kathrin Saar; Elena Gennaro; Amedeo Bianchi; Federico Zara; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; R Nabbout-Tarantino; Jean-François Prud'homme; Olivier Dulac; Louise Bate; R Mark Gardiner; Dick Lindhout; Thomas F Wienker; Dieter Janz; Thomas Sander
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures.
Epilepsy research 2002;51(1-2):23-9.
2002: Thomas Sander; Christine Windemuth; Herbert Schulz; Kathrin Saar; Elena Gennaro; Amedeo Bianchi; Federico Zara; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; Jean-François Prud'homme; Olivier Dulac; Louise Bate; R Mark Gardiner; Gerrit-Jan de Haan; Guus A M A J Janssen; Jorine Witte; D J J Halley; Dick Lindhout; Thomas F Wienker; Dieter Janz
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.
American journal of medical genetics 2002;114(6):673-8.
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: Colette Kananura; Thomas Sander; Sindhu Rajan; Regina Preisig-Müller; Karl-Heinz Grzeschik; Jürgen Daut; Christian Derst; Ortrud K Steinlein
Tandem pore domain K(+)-channel TASK-3 (KCNK9) and idiopathic absence epilepsies.
American journal of medical genetics 2002;114(2):227-9.
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: Ortrud K Steinlein; B A Neubauer; Thomas Sander; L Song; J Stoodt; D B Mount
Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy.
Epilepsy research 2001;44(2-3):191-5.
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: Georg Winterer; Michael N Smolka; Jerzy Samochowiec; Christoph Mulert; Mario Ziller; Richard Mahlberg; Yvonne Wuebben; Jürgen Gallinat; Hans Rommelspacher; W M Herrman; Thomas Sander
Association analysis of GABAAbeta2 and gamma2 gene polymorphisms with event-related prefrontal activity in man.
Human genetics 2000;107(5):513-8.
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: Thomas Sander; Agata Ostapowicz; Jerzy Samochowiec; Michael N Smolka; Georg Winterer; Lutz G Schmidt
Genetic variation of the glutamate transporter EAAT2 gene and vulnerability to alcohol dependence.
Psychiatric genetics 2000;10(3):103-7.
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: Thomas Sander; W Berlin; Agata Ostapowicz; Jerzy Samochowiec; N Gscheidel; Margret R Hoehe
Variation of the genes encoding the human glutamate EAAT2, serotonin and dopamine transporters and Susceptibility to idiopathic generalized epilepsy.
Epilepsy research 2000;41(1):75-81.
2000: Petra Franke; T Wang; M M Möthen; Michael Knapp; H Neith; Dirk Lichtermann; K M Capellen; Thomas Sander; Peter Propping; Wolfgang Maier
Susceptibility for alcoholism: DRD4 exon III polymorphism: a case-control and a family-based association approach.
Addiction biology 2000;5(3):289-95.
2000: Thomas Sander; Herbert Schulz; Kathrin Saar; Elena Gennaro; M C Riggio; Amedeo Bianchi; Federico Zara; D Luna; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; F Picard; Jean-François Prud'homme; Louise Bate; A Sundquist; R Mark Gardiner; Guus A M A J Janssen; Gerrit-Jan de Haan; Dorothée G A Kasteleijn-Nolst Trenité; Adri Bader; Dick Lindhout; Olaf Riess; Thomas F Wienker; Dieter Janz; A Reis
Genome search for susceptibility loci of common idiopathic generalised epilepsies.
Human molecular genetics 2000;9(10):1465-72.
2000: Andrew Escayg; M De Waard; D D Lee; D Bichet; P Wolf; T Mayer; J Johnston; Robert W Baloh; Thomas Sander; Miriam H Meisler
Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.
American journal of human genetics 2000;66(5):1531-9.
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.
2000: Thomas Sander; W Berlin; N Gscheidel; Birgit Wendel; Dieter Janz; Margret R Hoehe
Genetic variation of the human mu-opioid receptor and susceptibility to idiopathic absence epilepsy.
Epilepsy research 2000;39(1):57-61.
2000: Kerstin Hallmann; M Durner; Thomas Sander; Ortrud K Steinlein
Mutation analysis of the inwardly rectifying K(+) channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy.
American journal of medical genetics 2000;96(1):8-11.
2000: N Gscheidel; Thomas Sander; Birgit Wendel; Petra Heere; Lutz G Schmidt; Hans Rommelspacher; Margret R Hoehe; Jerzy Samochowiec
Five exon 1 variants of mu opioid receptor and vulnerability to alcohol dependence.
Polish journal of pharmacology 2000;52(1):27-31.
2000: Lutz G Schmidt; Thomas Sander; S Kuhn; Michael N Smolka; Hans Rommelspacher; Jerzy Samochowiec; Klaus-Peter Lesch
Different allele distribution of a regulatory MAOA gene promoter polymorphism in antisocial and anxious-depressive alcoholics.
Journal of neural transmission (Vienna, Austria : 1996) 2000;107(6):681-9.
2000: Petra Franke; Markus M Nöthen; T Wang; Michael Knapp; Dirk Lichtermann; Helge Neidt; Thomas Sander; Peter Propping; Wolfgang Maier
DRD4 exon III VNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach.
Molecular psychiatry 2000;5(1):101-4.
1999: Thomas Sander; C Peters; G Kämmer; Jerzy Samochowiec; M Zirra; Dietmar Mischke; Andreas Ziegler; Klemens Kaupmann; B Bettler; JT Epplen; Olaf Riess
Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.
American journal of medical genetics 1999;88(4):305-10.
1999: Thomas Sander; Yana V Syagailo; Jerzy Samochowiec; Olga Okladnova; Klaus-Peter Lesch; Dieter Janz
Association analysis of a regulatory promoter polymorphism of the PAX-6 gene with idiopathic generalized epilepsy.
Epilepsy research 1999;36(1):61-7.
1999: Michael N Smolka; Thomas Sander; Lutz G Schmidt; Jerzy Samochowiec; Hans Rommelspacher; N Gscheidel; Birgit Wendel; Margret R Hoehe
mu-opioid receptor variants and dopaminergic sensitivity in alcohol withdrawal.
Psychoneuroendocrinology 1999;24(6):629-38.
1999: Jerzy Samochowiec; M Rottmann; Olga Okladnova; Yana V Syagailo; Gerald Stöber; Thomas Sander; E Mühlbauer; Michael N Smolka; M Tranitz; Georg Winterer; Hans Rommelspacher; Lutz G Schmidt; Klaus-Peter Lesch
Association analysis of a PAX-6 gene promoter-associated polymorphic repeat with alcohol dependence.
Addiction biology 1999;4(3):323-8.
1999: Thomas Sander; Jerzy Samochowiec; M Ladehoff; Michael N Smolka; C Peters; Olaf Riess; Hans Rommelspacher; Lutz G Schmidt
Association analysis of exonic variants of the gene encoding the GABAB receptor and alcohol dependence.
Psychiatric genetics 1999;9(2):69-73.
1999: Ortrud K Steinlein; J Stoodt; C Biervert; Dieter Janz; Thomas Sander
The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy.
Neuroreport 1999;10(6):1163-6.
1999: Jerzy Samochowiec; Klaus-Peter Lesch; M Rottmann; Michael N Smolka; Yana V Syagailo; Olga Okladnova; Hans Rommelspacher; Georg Winterer; Lutz G Schmidt; Thomas Sander
Association of a regulatory polymorphism in the promoter region of the monoamine oxidase A gene with antisocial alcoholism.
Psychiatry research 1999;86(1):67-72.
1999: Thomas Sander; Herbert Schulz; A M Vieira-Saeker; A Bianchi; U Sailer; Gerhard Bauer; A Scaramelli; Thomas F Wienker; Kathrin Saar; André Reis; Dieter Janz; JT Epplen; Olaf Riess
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14.
American journal of medical genetics 1999;88(2):182-7.
1999: Jerzy Samochowiec; Michael N Smolka; Georg Winterer; Hans Rommelspacher; Lutz G Schmidt; Thomas Sander
Association analysis between a Cys23Ser substitution polymorphism of the human 5-HT2c receptor gene and neuronal hyperexcitability.
American journal of medical genetics 1999;88(2):126-30.
1999: Thomas Sander; M Ladehoff; Jerzy Samochowiec; Ulrich Finckh; Hans Rommelspacher; Lutz G Schmidt
Lack of an allelic association between polymorphisms of the dopamine D2 receptor gene and alcohol dependence in the German population.
Alcoholism, clinical and experimental research 1999;23(4):578-81.
1999: Thomas Sander; D Ball; R Murray; J Patel; Jerzy Samochowiec; Georg Winterer; Hans Rommelspacher; Lutz G Schmidt; E W Loh
Association analysis of sequence variants of GABA(A) alpha6, beta2, and gamma2 gene cluster and alcohol dependence.
Alcoholism, clinical and experimental research 1999;23(3):427-31.
1999: Thomas Sander; L Schölz; Dieter Janz; J T Epplen; Olaf Riess
Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsy.
Epilepsy research 1999;33(2-3):227-33.
1998: Thomas Sander; N Gscheidel; Birgit Wendel; Jerzy Samochowiec; Michael N Smolka; Hans Rommelspacher; Lutz G Schmidt; Margret R Hoehe
Human mu-opioid receptor variation and alcohol dependence.
Alcoholism, clinical and experimental research 1998;22(9):2108-10.
1998: Thomas Sander; R Kretz; Herbert Schulz; U Sailer; Gerhard Bauer; A Scaramelli; JT Epplen; Olaf Riess; Dieter Janz
Replication analysis of a putative susceptibility locus (EGI) for idiopathic generalized epilepsy on chromosome 8q24.
Epilepsia 1998;39(7):715-20.
1998: Thomas Sander; H Harms; P Dufeu; S Kuhn; Margret R Hoehe; Klaus-Peter Lesch; Hans Rommelspacher; Lutz G Schmidt
Serotonin transporter gene variants in alcohol-dependent subjects with dissocial personality disorder.
Biological psychiatry 1998;43(12):908-12.
1998: Lutz G Schmidt; H Harms; S Kuhn; Hans Rommelspacher; Thomas Sander
Modification of alcohol withdrawal by the A9 allele of the dopamine transporter gene.
The American journal of psychiatry 1998;155(4):474-8.
1998: Margret R Hoehe; Birgit Wendel; Ingrid Grunewald; P Chiaroni; N Levy; Deborah J Morris-Rosendahl; Jean-Paul Macher; Thomas Sander; Marc-Antoine Crocq
Serotonin transporter (5-HTT) gene polymorphisms are not associated with susceptibility to mood disorders.
American journal of medical genetics 1998;81(1):1-3.
1998: Thomas Sander; H Harms; Hans Rommelspacher; Margret R Hoehe; Lutz G Schmidt
Possible allelic association of a tyrosine hydroxylase polymorphism with vulnerability to alcohol-withdrawal delirium.
Psychiatric genetics 1998;8(1):13-7.
1998: Thomas Sander; C Peters; Dieter Janz; A Bianchi; Gerhard Bauer; Thomas F Wienker; T Hildmann; JT Epplen; Olaf Riess
The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy.
Epilepsy research 1998;29(2):115-22.
1997: Thomas Sander; H Harms; Klaus-Peter Lesch; P Dufeu; S Kuhn; Margret R Hoehe; Hans Rommelspacher; Lutz G Schmidt
Association analysis of a regulatory variation of the serotonin transporter gene with severe alcohol dependence.
Alcoholism, clinical and experimental research 1997;21(8):1356-9.
1997: Thomas Sander; H Harms; P Dufeu; S Kuhn; Hans Rommelspacher; Lutz G Schmidt
Dopamine D4 receptor exon III alleles and variation of novelty seeking in alcoholics.
American journal of medical genetics 1997;74(5):483-7.
1997: Thomas Sander; B Bockenkamp; T Hildmann; R Blasczyk; R Kretz; Thomas F Wienker; Armin Volz; Bettina Schmitz; G Beck-Mannagetta; Olaf Riess; JT Epplen; Dieter Janz; Andreas Ziegler
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
Neurology 1997;49(3):842-7.
1997: Ulrich Finckh; Hans Rommelspacher; S Kuhn; P Dufeu; G Otto; A Heinz; Michael Dettling; M Giraldo-Velasquez; J Pelz; KJ Gräf; H Harms; Thomas Sander; Lutz G Schmidt; A Rolfs
Influence of the dopamine D2 receptor (DRD2) genotype on neuroadaptive effects of alcohol and the clinical outcome of alcoholism.
Pharmacogenetics 1997;7(4):271-81.
1997: Ortrud K Steinlein; Thomas Sander; J Stoodt; R Kretz; Dieter Janz; Peter Propping
Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies.
American journal of medical genetics 1997;74(4):445-9.
1997: Thomas Sander; T Hildmann; R Kretz; R Fürst; U Sailer; Gerhard Bauer; Bettina Schmitz; G Beck-Mannagetta; Thomas F Wienker; Dieter Janz
Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism.
American journal of medical genetics 1997;74(4):416-21.
1997: Thomas Sander; R Kretz; Magali P Williamson; Frances V Elmslie; Michele Rees; T Hildmann; A Bianchi; Gerhard Bauer; U Sailer; A Scaramelli; Bettina Schmitz; R Mark Gardiner; Dieter Janz; G Beck-Mannagetta
Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15.
Acta neurologica Scandinavica 1997;96(1):1-7.
1997: Thomas Sander; H Harms; J Podschus; Ulrich Finckh; B Nickel; A Rolfs; Hans Rommelspacher; Lutz G Schmidt
Allelic association of a dopamine transporter gene polymorphism in alcohol dependence with withdrawal seizures or delirium.
Biological psychiatry 1997;41(3):299-304.
1997: SJ Delbrück; Birgit Wendel; Ingrid Grunewald; Thomas Sander; Deborah J Morris-Rosendahl; Marc-Antoine Crocq; W H Berrettini; Margret R Hoehe
A novel allelic variant of the human serotonin transporter gene regulatory polymorphism.
Cytogenetics and cell genetics 1997;79(3-4):214-20.
1996: Ulrich Finckh; M Giraldo-Velasquez; J Pelz; G Otto; Thomas Sander; Lutz G Schmidt; Hans Rommelspacher; A Rolfs
Dopamine D2 receptor gene (DRD2) haplotypes in Caucasians.
Gene 1996;179(2):251-5.
1996: Thomas Sander; T Hildmann; Dieter Janz; A Bianchi; Gerhard Bauer; A Scaramelli; G Beck-Mannagetta
Lack of linkage between idiopathic generalized epilepsies and the gene encoding the neural cell adhesion molecule.
Epilepsy research 1996;25(2):139-45.
1996: A Heinz; Thomas Sander; H Harms; Ulrich Finckh; S Kuhn; P Dufeu; Michael Dettling; KJ Gräf; A Rolfs; Hans Rommelspacher; Lutz G Schmidt
Lack of allelic association of dopamine D1 and D2 (TaqIA) receptor gene polymorphisms with reduced dopaminergic sensitivity to alcoholism.
Alcoholism, clinical and experimental research 1996;20(6):1109-13.
1996: Ulrich Finckh; O von Widdern; M Giraldo-Velasquez; J Podschus; P Dufeu; Thomas Sander; H Harms; Lutz G Schmidt; Hans Rommelspacher; A Rolfs
No association of the structural dopamine D2 receptor (DRD2) variant 311Cys with alcoholism.
Alcoholism, clinical and experimental research 1996;20(3):528-32.
1996: D Shimron-Abarbanell; H Harms; Jeanette Erdmann; Margot Albus; W Maier; Marcella Rietschel; J Körner; B Weigelt; E Franzek; Thomas Sander; Michael Knapp; Peter Propping; Markus M Nöthen
Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia.
American journal of medical genetics 1996;67(2):225-8.
1996: Thomas Sander
The genetics of idiopathic generalized epilepsy: implications for the understanding of its aetiology.
Molecular medicine today 1996;2(4):173-80.
1996: Thomas Sander; T Hildmann; Dieter Janz; Thomas F Wienker; A Bianchi; Gerhard Bauer; U Sailer; A Scaramelli; Heidemarie Neitzel; Bettina Schmitz; M E Bailey; G Beck-Mannagetta; keith jack johnson; M G Darlison
Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.
Epilepsy research 1996;23(3):235-44.
1996: Thomas Sander; T Hildmann; Thomas F Wienker; C Ramel; G Beck-Mannagetta; A Bianchi; U Sailer; K Berek; Gerhard Bauer; Heidemarie Neitzel; Bettina Schmitz; Martina Durner; keith jack johnson; Dieter Janz
Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.
American journal of medical genetics 1996;67(1):31-9.
1995: Thomas Sander; Dieter Janz; C Ramel; Christopher A Ross; W Paschen; T Hildmann; Thomas F Wienker; A Bianchi; Gerhard Bauer; U Sailer
Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies.
Neurology 1995;45(9):1713-20.
1995: Thomas Sander; T Hildmann; Dieter Janz; Thomas F Wienker; Heidemarie Neitzel; A Bianchi; Gerhard Bauer; U Sailer; K Berek; Bettina Schmitz
The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1".
Annals of neurology 1995;38(2):210-7.
1995: Thomas Sander; H Harms; J Podschus; Ulrich Finckh; B Nickel; A Rolfs; Hans Rommelspacher; Lutz G Schmidt
Dopamine D1, D2 and D3 receptor genes in alcohol dependence.
Psychiatric genetics 1995;5(4):171-6.
1992: keith jack johnson; Thomas Sander; A A Hicks; A van Marle; Dieter Janz; Michael Mullan; B P Riley; MG Darlison
Confirmation of the localization of the human GABAA receptor alpha 1-subunit gene (GABRA1) to distal 5q by linkage analysis.
Genomics 1992;14(3):745-8.
1992: Dieter Janz; G Beck-Mannagetta; Thomas Sander
Do idiopathic generalized epilepsies share a common susceptibility gene?
Neurology 1992;42(4 Suppl 5):48-55.
1992: H R Schwabe; R Herrmann; M Mathew; KJ Gräf; Thomas Sander; M Cordes; R Nagel; L Weissbach; Dieter Huhn
[The long-term toxicity of polychemotherapy in successfully treated testicular carcinoma].
Deutsche medizinische Wochenschrift (1946) 1992;117(4):121-6.
1991: Martina Durner; Thomas Sander; David A Greenberg; K Johnson; G Beck-Mannagetta; Dieter Janz
Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients.
Neurology 1991;41(10):1651-5.