G. Stöber

发表

Hypofrontality in schizophrenic patients and its relevance for the choice of antipsychotic medication: An event-related potential study

M. Herrmann, A. Ehlis, A. Fallgatter, 2012, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders.

R. Murray, Tao Li, D. Collier, 1996, Molecular psychiatry.

Allelic Variation of Human Serotonin Transporter Gene Expression

P Riederer, K. Lesch, P. Riederer, 1996, Journal of neurochemistry.

P300 in schizophrenia: Interactions between amplitudes and topography

W. Strik, T. Dierks, K. Maurer, 1994, Biological Psychiatry.

P300 asymmetries in schizophrenia revisited with reference-independent methods

Thomas Dierks, Konrad Maurer, W. Strik, 1994, Psychiatry Research: Neuroimaging.

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

P. Riederer, K. Lesch, P. Riederer, 1998, Journal of Neural Transmission.

Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics

D. Rujescu, K. Hashimoto, P. Falkai, 2016, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

The role of Pannexin gene variants in schizophrenia: systematic analysis of phenotypes

B. Pfuhlmann, G. Stöber, M. Gawlik, 2016, European Archives of Psychiatry and Clinical Neuroscience.

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders

H. Stefánsson, D. Rujescu, A. Ingason, 2016, PLoS genetics.

Periodic catatonia: A schizophrenic subtype with major gene effect and anticipation

K. Lesch, G. Stöber, H. Beckmann, 2005, European Archives of Psychiatry and Clinical Neuroscience.

Cycloid psychoses: Leonhard's descriptions revisited

W. Verhoeven, F. V. D. Heijden, B. Pfuhlmann, 2012 .

The human dopamine transporter gene: the 5′-flanking region reveals five diallelic polymorphic sites in a Caucasian population sample

P. Riederer, M. Knapp, Jobst Meyer, 2001, Neuroscience Letters.

Norepinephrine transporter gene (NET) variants in patients with panic disorder

M. Nöthen, K. Lesch, W. Maier, 2002, Neuroscience Letters.

A Recombination Hotspot in a Schizophrenia-Associated Region of GABRB2

Qiang Yang, H. Xue, Weichuan Yu, 2010, PloS one.

Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening.

S. Cichon, M. Nöthen, F. Poustka, 1999, American journal of medical genetics.

Exclusion of the neuronal nicotinic acetylcholine receptor α7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13–22 locus

T. Wienker, K. Lesch, F. Rüschendorf, 2002, Molecular Psychiatry.

Obstetrie complications in distinct schizophrenie subgroups

G. Stöber, H. Beckmann, E. Franzek, 2013 .

Obstetric complications in distinct schizophrenic subgroups

G. Stöber, H. Beckmann, E. Franzek, 1993, European Psychiatry.

A promoter-associated polymorphic repeat modulates PAX-6 expression in human brain.

K. Lesch, P. Riederer, Y. Syagailo, 1998, Biochemical and biophysical research communications.

Pharmacological properties of naturally occurring variants of the human norepinephrine transporter.

H. Bönisch, P. Propping, M. Brüss, 2000, Pharmacogenetics.

First‐trimester maternal gestational infection and cycloid psychosis

G. Stöber, H. Beckmann, E. Franzek, 1997, Acta psychiatrica Scandinavica.

Maternal infectious diseases during pregnancy and obstetric complications in the etiology of distinct subtypes of schizophrenia: further evidence from maternal hospital records

G. Stöber, E. Franzek, 1995, European Psychiatry.

OBSTETRIC COMPLICATIONS AND AGE AT ONSET IN SCHIZOPHRENIA : AN INTERNATIONAL COLLABORATIVE META-ANALYSIS OF INDIVIDUAL PATIENT DATA

R. Murray, S. Lawrie, J. Eagles, 1998 .

Exposure to prenatal infections, genetics and the risk of systematic and periodic catatonia

A. Schmidtke, G. Stöber, H. Beckmann, 2002, Journal of Neural Transmission.

Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15

S. Küry, J. Moisan, C. Rubie, 2003, Journal of Neural Transmission.

Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia

T. Meitinger, T. Bettecken, C. Rubie, 2005, BMC psychiatry.

Genetic predisposition and environmental causes in periodic and systematic catatonia

G. Stöber, 2011, European Archives of Psychiatry and Clinical Neuroscience.

Cycloid psychoses – from clinical concepts to biological foundations

A. Bartsch, B. Pfuhlmann, G. Stöber, 2002, Journal of Neural Transmission.

Functional PAX-6 gene-linked polymorphic region: potential association with paranoid schizophrenia

Michael Knapp, Helmut Beckmann, Klaus-Peter Lesch, 1999, Biological Psychiatry.

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

K. Lesch, A. Heils, G. Stöber, 1998, Neurochemistry International.

Schizophrenia: From the brain to peripheral markers. A consensus paper of the WFSBP task force on biological markers

P. Falkai, J. Thome, J. Kornhuber, 2009, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Genetic heterogeneity in catatonic schizophrenia : A family study

G. Stöber, H. Beckmann, E. Franzek, 1996 .

Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13.

T. Wienker, K. Lesch, M. Schmid, 2000, American journal of medical genetics.

hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia

T. Wienker, K. Lesch, M. Schmid, 2000, European Archives of Psychiatry and Clinical Neuroscience.

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

K. Lesch, P. Riederer, A. Heils, 1998, European Archives of Psychiatry and Clinical Neuroscience.

Association analysis of the functional monoamine oxidase A gene promoter polymorphism in psychiatric disorders.

K. Lesch, M. Knapp, J. Meyer, 2001, American journal of medical genetics.

Novel 5'-regulatory region polymorphisms of the 5-HT2C receptor gene: association study with panic disorder.

M. Nöthen, K. Lesch, W. Maier, 2000, The international journal of neuropsychopharmacology.

Polymorphic MAO-A and 5-HT-Transporter Genes: Analysis of Interactions in Panic Disorder

M. Nöthen, K. Lesch, W. Maier, 2000, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Evidence against unusual sex concordance and pseudoautosomal inheritance in the catatonic subtype of schizophrenia

A. Schmidtke, G. Stöber, H. Beckmann, 1995, Psychiatry Research.

Towards the genetic basis of periodic catatonia: pedigree sample for genome scan I and II

T. Wienker, G. Nürnberg, A. Reis, 2011, European Archives of Psychiatry and Clinical Neuroscience.

[Cycloid psychoses as atypical manic-depressive disorders. Results of a family study].

A. Bartsch, A. Schmidtke, B. Pfuhlmann, 2006, Der Nervenarzt.

Cycloid psychoses are not part of a bipolar affective spectrum: results of a controlled family study.

A. Bartsch, A. Schmidtke, B. Pfuhlmann, 2004, Journal of affective disorders.

The different conceptions of catatonia: historical overview and critical discussion

B. Pfuhlmann, G. Stöber, 2011, European Archives of Psychiatry and Clinical Neuroscience.

Functional characterization of the human PAX3 gene regulatory region.

K. Lesch, P. Riederer, Y. Syagailo, 1999, Genomics.

Cloning and functional characterization of the human norepinephrine transporter gene promoter

K. Lesch, P. Riederer, H. Bönisch, 1998, Journal of Neural Transmission.

Cloning and functional characterization of the human norepinephrine transporter gene promoter Rapid Communication

K. Lesch, P. Riederer, H. Bönisch, 1998 .

Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders.

M Knapp, M. Nöthen, H. Bönisch, 1996, American journal of medical genetics.

Cycloid psychoses predominate in severe postpartum psychiatric disorders.

B. Pfuhlmann, G. Stöber, H. Beckmann, 1998, Journal of affective disorders.

Is computerized tomography ventricular abnormality related to cycloid psychosis?

G. Stöber, E. Hofmann, H. Beckmann, 1996, Biological Psychiatry.

Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.

T. Wienker, K. Lesch, F. Rüschendorf, 2000, American journal of human genetics.

Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity

D. Seelow, A. Ekici, F. Rüschendorf, 2002, Human Genetics.

Copy number variants in a sample of patients with psychotic disorders: is standard screening relevant for actual clinical practice?

R. Pfundt, N. de Leeuw, W. Verhoeven, 2012, Neuropsychiatric disease and treatment.

No missense mutation of WKL1 in a subgroup of probands with schizophrenia

D. Stephan, G. Nestadt, J. Meyer, 2002, Molecular Psychiatry.

Obstetric complications and age at onset in schizophrenia: an international collaborative meta-analysis of individual patient data.

R. Murray, S. Lawrie, J. Eagles, 1997, The American journal of psychiatry.

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

K. Lesch, P. Riederer, D. Bengel, 1998, European Archives of Psychiatry and Clinical Neuroscience.

The role of maternal infectious diseases during pregnancy in the etiology of schizophrenia in offspring

G. Stöber, H. Beckmann, E. Franzek, 1992, European Psychiatry.

Exposure to prenatal infections and psychiatric nosology: A focus on schizophrenia phenotypes

G. Stöber, 2005 .

Family-based study of markers at the 5′-flanking region of the human dopamine transporter gene reveals potential association with schizophrenic psychoses

M. Knapp, B. Pfuhlmann, G. Stöber, 2006, European Archives of Psychiatry and Clinical Neuroscience.

Evaluation of conserved and ultra‐conserved non‐genic sequences in chromosome 15q15‐linked periodic catatonia

A. Ekici, A. Reis, B. Pfuhlmann, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

On interrater reliability for Leonhard's classification of endogenous psychoses.

B. Pfuhlmann, G. Stöber, M. Cetkovich-Bakmas, 1997, Psychopathology.

Long-Term Course and Outcome of Severe Postpartum Psychiatric Disorders

B. Pfuhlmann, G. Stöber, H. Beckmann, 1999, Psychopathology.

Triplet repeats in clinical subtypes of schizophrenia: variation at the DRPLA (B37 CAG repeat) locus is not associated with periodic catatonia

P. Riederer, G. Stöber, H. Beckmann, 2005, Journal of Neural Transmission / General Section JNT.

Short CAG repeats within the hSKCa3 gene associated with schizophrenia: results of a family‐based study

K. Lesch, M. Knapp, J. Meyer, 1998, Neuroreport.

GABRB2 in schizophrenia and bipolar disorder: disease association, gene expression and clinical correlations.

H. Xue, S. Fang, S. Tsang, 2009, Biochemical Society transactions.

GABRB 2 in schizophrenia and bipolar disorder : disease association , gene expression and clinical correlations

H. Xue, S. Fang, S. Tsang, 2009 .

Disturbed neural circuits in a subtype of chronic catatonic schizophrenia demonstrated by F-18-FDG-PET and F-18-DOPA-PET

H. Schirrmeister, S. Reske, A. Gerhard, 2001, Journal of Neural Transmission.

Sequence diversity of KIAA0027/MLC1: are megalencephalic leukoencephalopathy and schizophrenia allelic disorders?

T. Meitinger, P. Lichtner, G. Uziel, 2003, Human mutation.

Evaluation of risk loci for schizophrenia derived from genome‐wide association studies in a German population

A. Reis, B. Pfuhlmann, G. Stöber, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree

K. Lesch, T. Strom, J. Meyer, 2001, Molecular Psychiatry.

Differences in Quality of Life and Course of Illness between Cycloid and Schizophrenic Psychoses‐a Comparative Study

A. Bartsch, B. Pfuhlmann, G. Stöber, 2004, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Reduced amplification efficiency of KIAA0027/MLC1 alleles: implications for the molecular diagnosis of megalencephalic leukoencephalopathy with subcortical cysts.

T. Meitinger, P. Lichtner, T. Bettecken, 2002, Molecular and cellular probes.

The importance of a differentiated psychopathology of catatonia

B. Pfuhlmann, G. Stöber, 1997, Acta psychiatrica Scandinavica.

Gender Differences and Age of Onset in the Catatonic Subtypes of Schizophrenia

B. Pfuhlmann, G. Stöber, H. Beckmann, 1998, Psychopathology.

Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder.

S. Cichon, M. Rietschel, M. Nöthen, 1996, American journal of medical genetics.

Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene

S. Cichon, M. Rietschel, M. Nöthen, 1995, Psychiatric genetics.

High ethanol tolerance in young adults is associated with the low-activity variant of the promoter of the human serotonin transporter gene

K. Lesch, M. Knapp, G. Stöber, 1998, Neuroscience Letters.