|
| 37953324 | The Human Phenotype Ontology in 2024: phenotypes around the world. | Nucleic Acids Res | 2024 |
| 36621676 | Association between mitochondria-related genes and cognitive performance in the PsyCourse Study. | J Affect Disord | 2023 |
| 37686257 | Genetic Architecture of Ischaemic Strokes after COVID-19 Shows Similarities with Large Vessel Strokes. | Int J Mol Sci | 2023 |
| 37375064 | T-Cell-Dominated Immune Response Resolves Protracted SARS-CoV-2 Infection in the Absence of Neutralizing Antibodies in an Immunocompromised Individual. | Microorganisms | 2023 |
| 37433967 | Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder. | Mol Psychiatry | 2023 |
| 36652833 | Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. | Schizophr Res | 2023 |
| 34656040 | Genetic risk for psychiatric illness is associated with the number of hospitalizations of bipolar disorder patients. | J Affect Disord | 2022 |
| 35708486 | Novel genes and sex differences in COVID-19 severity. | Hum Mol Genet | 2022 |
| 35567871 | A novel longitudinal clustering approach to psychopathology across diagnostic entities in the hospital-based PsyCourse study. | Schizophr Res | 2022 |
| 35935431 | Biobanking in everyday clinical practice in psychiatry-The Munich Mental Health Biobank. | Front Psychiatry | 2022 |
| 36327219 | Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. | PLoS Genet | 2022 |
| 36351892 | Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles. | Transl Psychiatry | 2022 |
| 34889978 | Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity. | Hum Genet | 2022 |
| 35221906 | Editorial: Cross-disorder Genetics in Neuropsychiatry. | Front Neurosci | 2022 |
| 35126191 | Medication Adherence in a Cross-Diagnostic Sample of Patients From the Affective-to-Psychotic Spectrum: Results From the PsyCourse Study. | Front Psychiatry | 2022 |
| 35232513 | Stability over time of scores on psychiatric rating scales, questionnaires and cognitive tests in healthy controls. | BJPsych Open | 2022 |
| 33426733 | Cerebral venous thrombosis and severe acute respiratory syndrome coronavirus-2 infection: A systematic review and meta-analysis. | Eur J Neurol | 2021 |
| 33758887 | Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. | medRxiv | 2021 |
| 35048876 | Characterisation of age and polarity at onset in bipolar disorder. | Br J Psychiatry | 2021 |
| 34789355 | Interplay between the Genetics of Personality Traits, severe Psychiatric Disorders, and COVID-19 Host Genetics in the Susceptibility to SARS-CoV-2 Infection - ADDENDUM. | BJPsych Open | 2021 |
| 34659794 | Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection. | BJPsych Open | 2021 |
| 34836939 | Polygenic risk scores across the extended psychosis spectrum. | Transl Psychiatry | 2021 |
| 34656879 | SARS-CoV-2 vaccination in multiple sclerosis: A clearer picture for the time point during CD20 depleting therapy. | EBioMedicine | 2021 |
| 34597274 | Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. | J Clin Invest | 2021 |
| 34247186 | A genome-wide association study of the longitudinal course of executive functions. | Transl Psychiatry | 2021 |
| 34060708 | Systematic review of cases of acute myelitis in individuals with COVID-19. | Eur J Neurol | 2021 |
| 34002096 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. | Nat Genet | 2021 |
| 32048126 | The role of environmental stress and DNA methylation in the longitudinal course of bipolar disorder. | Int J Bipolar Disord | 2020 |
| 32049274 | An Investigation of Psychosis Subgroups With Prognostic Validation and Exploration of Genetic Underpinnings: The PsyCourse Study. | JAMA Psychiatry | 2020 |
| 30696448 | Cerebrovascular manifestations of herpes simplex virus infection of the central nervous system: a systematic review. | J Neuroinflammation | 2019 |
| 30070057 | A longitudinal approach to biological psychiatric research: The PsyCourse study. | Am J Med Genet B Neuropsychiatr Genet | 2019 |
| 29956436 | Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study. | Bipolar Disord | 2019 |
| 31462630 | The genetic relationship between educational attainment and cognitive performance in major psychiatric disorders. | Transl Psychiatry | 2019 |
| 29700475 | Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. | Nat Genet | 2018 |
| 26808974 | Alterations in Lipid and Inositol Metabolisms in Two Dopaminergic Disorders. | PLoS One | 2016 |
| 25604855 | Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease. | Eur J Hum Genet | 2015 |
| 27081517 | Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer's disease. | Hum Genome Var | 2015 |
| 24241507 | Rare variants in LRRK1 and Parkinson's disease. | Neurogenetics | 2014 |
| 30363981 | Iron in Restless Legs Syndrome. | Mov Disord Clin Pract | 2014 |
| 24995868 | Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome. | Am J Hum Genet | 2014 |
| 24875634 | Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome. | PLoS One | 2014 |
| 24325808 | "Malignant restless legs syndrome"--a curse or a blessing? | Sleep Med | 2014 |
| 23408458 | The role of SCARB2 as susceptibility factor in Parkinson's disease. | Mov Disord | 2013 |
| 24386122 | Niemann-Pick C disease gene mutations and age-related neurodegenerative disorders. | PLoS One | 2013 |
| 24244438 | Rare variants in PLXNA4 and Parkinson's disease. | PLoS One | 2013 |
| 23643657 | When restless legs syndrome turns malignant. | Sleep Med | 2013 |
| 23436634 | Mitochondrial membrane protein associated neurodegenration: a novel variant of neurodegeneration with brain iron accumulation. | Mov Disord | 2013 |
| 22707335 | Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease. | Neurogenetics | 2012 |
| 21174071 | [Restless legs syndrome and cardiovascular risk]. | Nervenarzt | 2011 |
| 21779176 | Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. | PLoS Genet | 2011 |