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/vufind/Search/Results?lookfor=%22Aleksic%2C+Branko%22&type=Person&sort=year
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PubPharm (237)
1
Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder : A case-control study
enthalten in:
Neuropsychopharmacology reports
| 2024
von
Lo, T.
|
Kushima, I.
|
Kimura, H.
| +31
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2
Phenotypes for general behavior, activity, and body temperature in 3q29 deletion model mice
enthalten in:
Translational psychiatry
| 2024
von
Mori, D.
|
Ikeda, R.
|
Sawahata, M.
| +22
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3
Association between copy number variations in parkin ( PRKN) and schizophrenia and autism spectrum disorder : A case–control study
enthalten in:
Neuropsychopharmacology Reports
| 2024
von
Lo, T.
|
Kushima, I.
|
Kimura, H.
| +31
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4
Internationalization of higher medical education in the post-COVID-19 era
enthalten in:
Medical education online
| 2023
von
Skokauskas, N.
|
Aleksic, B.
|
Moe, M.
| +2
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5
Case reports of two siblings with autism spectrum disorder and 15q13.3 deletions
enthalten in:
Neuropsychopharmacology reports
| 2023
von
Furukawa, S.
|
Kushima, I.
|
Aleksic, B.
| +1
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6
De novo MCM6 variants in neurodevelopmental disorders : a recognizable phenotype related to zinc binding residues
enthalten in:
Human genetics
| 2023
von
Smits, D.
|
Schot, R.
|
Popescu, C.
| +16
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7
Slovenian Version of the Drug-Induced Extrapyramidal Symptoms Scale : Evaluation of Interrater and Test-Retest Reliability
enthalten in:
Journal of clinical psychopharmacology
| 2023
von
Senica, N.
|
Aleksic, B.
|
Inada, T.
| +3
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8
Clinical characterization of patients with schizophrenia and 16p13.11 duplication : A case series
enthalten in:
Neuropsychopharmacology reports
| 2023
von
Kimura, H.
|
Kushima, I.
|
Banno, M.
| +4
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9
De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues
enthalten in:
Human genetics
| 2023
von
Smits, D.
|
Schot, R.
|
Popescu, C.
| +16
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10
De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues
enthalten in:
Human genetics
| 2023
von
Smits, D.
|
Schot, R.
|
Popescu, C.
| +16
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