Branko Aleksic
Affiliations: | Nagoya University, Graduate School of Medicine, Department of Psychiatry |
Area:
Genetics, Schizophrenia, AutismGoogle:
"Branko Aleksic"Mean distance: 106866
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Lo T, Kushima I, Kimura H, et al. (2023) Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case-control study. Neuropsychopharmacology Reports |
Furuta S, Aleksic B, Nawa Y, et al. (2022) Investigation of as a candidate gene for schizophrenia and autism spectrum disorder. Nagoya Journal of Medical Science. 84: 260-268 |
Kato H, Kimura H, Kushima I, et al. (2022) The genetic architecture of schizophrenia: review of large-scale genetic studies. Journal of Human Genetics |
Chen CH, Cheng MC, Hu TM, et al. (2022) Identification of rare mutations of the vasoactive intestinal peptide receptor 2 gene in schizophrenia. Psychiatric Genetics. 32: 125-130 |
Nawa Y, Kimura H, Mori D, et al. (2020) Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility. Human Genome Variation. 7: 37 |
Kato H, Kushima I, Mori D, et al. (2020) Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder. Translational Psychiatry. 10: 421 |
Sekiguchi M, Sobue A, Kushima I, et al. (2020) ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk. Translational Psychiatry. 10: 247 |
Suzuki T, Suzuki T, Raveau M, et al. (2020) A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders. Annals of Clinical and Translational Neurology |
Sawahata M, Mori D, Arioka Y, et al. (2020) Generation and analysis of novel Reln-deleted mouse model corresponding to exonic Reln deletion in schizophrenia. Psychiatry and Clinical Neurosciences |
Arioka Y, Hirata A, Kushima I, et al. (2020) Characterization of a schizophrenia patient with a rare RELN deletion by combining genomic and patient-derived cell analyses. Schizophrenia Research. 216: 511-515 |