C. Michael

Mutations disrupting neuritogenesis genes represent a major independent risk factor for cerebral palsy

Daniela C. Zarnescu, J. Gécz, S. Mane, 2020 .

Duffy-null genotype in clozapine-associated neutropenia

Karel, D. Rujescu, D. Collier, 2019 .

Analyses of de novo and common alleles implicate rare missense variants in SLC6A1 in schizophrenia

G. Kirov, M. Owen, P. Holmans, 2019 .

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture ofmajor depressive disorder

Li, Katharina, Warren W. Kretzschmar, 2018 .

Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder

M. Owen, Jinchuan Xing, M. State, 2022, medRxiv.

Analysis of Liver Microenvironment during Early Progression of Non-Alcoholic Fatty Liver Disease-Associated Hepatocellular Carcinoma in Zebrafish.

S. de Oliveira, F. J. Martínez-Navarro, C. Michael, 2021, Journal of Visualized Experiments.

risk variants and refine the genetic architecture ofmajor depressive disorder

Li, Katharina, Warren W. Kretzschmar, 2022 .

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia

M C O'Donovan, P M Visscher, P. Visscher, 2011, Molecular Psychiatry.