User profiles for S. Walitza

Susanne Walitza

Psychiatrische Universitätsklinik Zürich
Verified email at pukzh.ch
Cited by 20072

[HTML][HTML] The world federation of ADHD international consensus statement: 208 evidence-based conclusions about the disorder

…, S Van der Oord, A Venter, B Vitiello, S Walitza… - Neuroscience & …, 2021 - Elsevier
Background Misconceptions about ADHD stigmatize affected people, reduce credibility of
providers, and prevent/delay treatment. To challenge misconceptions, we curated findings with …

[HTML][HTML] ADHD: Current concepts and treatments in children and adolescents

…, D Brandeis, E Grünblatt, G Berger, S Walitza - …, 2020 - thieme-connect.com
Attention deficit hyperactivity disorder (ADHD) is among the most frequent disorders within
child and adolescent psychiatry, with a prevalence of over 5%. Nosological systems, such as …

[HTML][HTML] Advances in problematic usage of the internet research–a narrative review by experts from the European network for problematic usage of the internet

…, J Burkauskas, E Grünblatt, S Walitza… - Comprehensive …, 2022 - Elsevier
Global concern about problematic usage of the internet (PUI), and its public health and
societal costs, continues to grow, sharpened in focus under the privations of the COVID-19 …

[HTML][HTML] Preventing problematic internet use during the COVID-19 pandemic: Consensus guidance

…, JM Menchon, J Zohar, L Pellegrini, S Walitza… - Comprehensive …, 2020 - Elsevier
As a response to the COVID-19 pandemic, many governments have introduced steps such
as spatial distancing and “staying at home” to curb its spread and impact. The fear resulting …

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

…, TJ Renner, M Romanos, J Romanos, S Walitza… - Journal of the American …, 2010 - Elsevier
OBJECTIVE: Although twin and family studies have shown attention-deficit/hyperactivity
disorder (ADHD) to be highly heritable, genetic variants influencing the trait at a genome-wide …

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

…, M Romanos, J Romanos, A Warnke, S Walitza… - Nature …, 2012 - nature.com
Attention deficit hyperactivity disorder (ADHD) is a common, heritable neuropsychiatric
disorder of unknown etiology. We performed a whole-genome copy number variation (CNV) …

Genome-wide association study of obsessive-compulsive disorder

…, HGM Westenberg, S Walitza… - Molecular …, 2013 - nature.com
Obsessive-compulsive disorder (OCD) is a common, debilitating neuropsychiatric illness
with complex genetic etiology. The International OCD Foundation Genetics Collaborative (…

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

…, H Palmason, J Meyer, M Romanos, S Walitza… - Molecular …, 2010 - nature.com
Attention-Deficit/Hyperactivity Disorder (ADHD) has a very high heritability (0.8), suggesting
that about 80% of phenotypic variance is due to genetic factors. We used the integration of …

Brain imaging of the cortex in ADHD: a coordinated analysis of large-scale clinical and population-based samples

…, K Rubia, L Lazaro, S Brem, S Walitza… - American Journal of …, 2019 - Am Psychiatric Assoc
Objective: Neuroimaging studies show structural alterations of various brain regions in children
and adults with attention deficit hyperactivity disorder (ADHD), although nonreplications …

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

…, C Seitz, TJ Renner, S Walitza… - American Journal of …, 2012 - Am Psychiatric Assoc
Objective: Attention deficit hyperactivity disorder (ADHD) is a common, highly heritable
psychiatric disorder. Because of its multifactorial etiology, however, identifying the genes involved …