Susanne Walitza

[Validation of the German version of the Australian Scale of Asperger's Syndrome (ASAS)].

Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessive-compulsive disorder.

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder.

Effects of methylphenidate on multiple components of attention in children with attention deficit hyperactivity disorder.

The extent of social anxiety in combination with mental disorders.

Brain dopamine and kinematics of graphomotor functions.

[Severe early-childhood obsessive-compulsive disorder--case report on a 4-year-old girl].

The effect of caffeine on handwriting movements in skilled writers.

Attention and movement execution during handwriting.

Transmission disequilibrium analysis of the functional 5-HT3A receptor variant C178T in early-onset obsessive compulsive-disorder.

Co-morbidity of adult attention-deficit/hyperactivity disorder with focus on personality traits and related disorders in a tertiary referral center.

Novel mutations of the extraneuronal monoamine transporter gene in children and adolescents with obsessive-compulsive disorder.

Does methylphenidate cause a cytogenetic effect in children with attention deficit hyperactivity disorder?

Tetrahydroisoquinoline derivatives: a new perspective on monoaminergic dysfunction in children with ADHD?

Vigilance and sustained attention in children and adults with ADHD.

Transmission disequilibrium studies in early onset of obsessive-compulsive disorder for polymorphisms in genes of the dopaminergic system.

[Genetics of child and adolescent psychiatric disorders].

[Genetic findings in obsessive-compulsive disorder in childhood and adolescence and in adulthood].

[Obsessive-compulsive disorder in children and adolescents].

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder.

No elevated genomic damage in children and adolescents with attention deficit/hyperactivity disorder after methylphenidate therapy.

Genotoxicity of the neurotransmitter dopamine in vitro.

[Children and adolescents with obsessive-compulsive disorders].

Familiality and molecular genetics of attention networks in ADHD.

[Graphomotor functions in children with attention deficit hyperactivity disorder (ADHD)].

Prospective follow-up studies found no chromosomal mutagenicity of methylphenidate therapy in ADHD affected children.

Reduced NoGo-anteriorisation during continuous performance test in deletion syndrome 22q11.2.

Genetics of early-onset obsessive-compulsive disorder.

No increased chromosomal damage in L-DOPA-treated patients with Parkinson's disease: a pilot study.

Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.

Case-control genome-wide association study of attention-deficit/hyperactivity disorder.

Detection of malingered attention deficit hyperactivity disorder.

Animal models of attention deficit/hyperactivity disorder (ADHD): a critical review.

To Andreas Warnke, Professor of Child and Adolescent Psychiatry, Head of the Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy at the University of Wuerzburg, Germany, to celebrate his professional life and work at the occasion of his 65th anniversary.

Effects of methylphenidate: the cellular point of view.

Obsessive-compulsive disorder in children and adolescents.

DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders.

Pilot study on HTR2A promoter polymorphism, -1438G/A (rs6311) and a nearby copy number variation showed association with onset and severity in early onset obsessive-compulsive disorder.

Altered mRNA expression of monoaminergic candidate genes in the blood of children with attention deficit hyperactivity disorder and autism spectrum disorder.

[Psychometric properties and clinical norms for the German version (SPAIK) of the Social Phobia and Anxiety Inventory for Children (SPAI-C)].

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.

Candidate system analysis in ADHD: evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1.

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

Pilot study: potential transcription markers for adult attention-deficit hyperactivity disorder in whole blood.

First clinical trial of tomographic neurofeedback in attention-deficit/hyperactivity disorder: evaluation of voluntary cortical control.

Neuroimaging of cognitive brain function in paediatric obsessive compulsive disorder: a review of literature and preliminary meta-analysis.

In vitro study methodologies to investigate genetic aspects and effects of drugs used in attention-deficit hyperactivity disorder.

KCNIP4 as a candidate gene for personality disorders and adult ADHD.

5-HT2A serotonin receptor agonist DOI alleviates cytotoxicity in neuroblastoma cells: role of the ERK pathway.

[In Process Citation].

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.

The feedback-related negativity (FRN) revisited: new insights into the localization, meaning and network organization.

Attitudes towards help-seeking and stigma among young people at risk for psychosis.

Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated German multi-generation families.

Partitioning the heritability of tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.

Comparing tomographic EEG neurofeedback and EMG biofeedback in children with attention-deficit/hyperactivity disorder.

[School refusal and dropping out of school: positioning regarding a Swiss perspective].

Aberrant Coupling Within and Across the Default Mode, Task-Positive, and Salience Network in Subjects at Risk for Psychosis.

Well-being among persons at risk of psychosis: the role of self-labeling, shame, and stigma stress.

Extraordinarily fast response to low-dose sertraline in a child with severe obsessive-compulsive disorder and high functioning serotonin transporter genotype.

Altered peripheral BDNF mRNA expression and BDNF protein concentrations in blood of children and adolescents with autism spectrum disorder.

[Obsessive-compulsive disorders in DSM-5 – what is new?].

The neurobiological link between OCD and ADHD.

Region-specific regulation of the serotonin 2A receptor expression in development and aging in postmortem human brain.

Imaging genetics in obsessive-compulsive disorder: Linking genetic variations to alterations in neuroimaging.

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.

Longitudinal course of self-labeling, stigma stress and well-being among young people at risk of psychosis.

Trio study and meta-analysis support the association of genetic variation at the serotonin transporter with early-onset obsessive-compulsive disorder.