Lista de obras - Branko Aleksic - Dominio Público Uruguay

A case control association study and cognitive function analysis of neuropilin and tolloid-like 1 gene and schizophrenia in the Japanese population

artículo científico publicado en 2011

A genetic association study of the FXYD domain containing ion transport regulator 6 (FXYD6) gene, encoding phosphohippolin, in susceptibility to schizophrenia in a Japanese population

artículo científico publicado en 2008

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility

artículo científico publicado en 2017

A two-stage case-control association study of the dihydropyrimidinase-like 2 gene (DPYSL2) with schizophrenia in Japanese subjects

artículo científico publicado en 2010

ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk

artículo científico publicado en 2020

An association study of tachykinin receptor 3 gene with schizophrenia in the Japanese population.

artículo científico publicado en 2008

An evaluation of polymorphisms in casein kinase 1 delta and epsilon genes in major psychiatric disorders

artículo científico publicado en 2012

Analysis of the VAV3 as candidate gene for schizophrenia: evidences from voxel-based morphometry and mutation screening

artículo científico publicado en 2012

Assessment of a glyoxalase I frameshift variant, p.P122fs, in Japanese patients with schizophrenia

artículo científico publicado en 2018

Association analysis of the GDNF gene with methamphetamine use disorder in a Japanese population

artículo científico publicado en 2011

Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia

artículo científico publicado en 2016

Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population

artículo científico publicado en 2015

Association study of bromodomain-containing 1 gene with schizophrenia in Japanese population

artículo científico publicado en 2010

Association study of ubiquitin-specific peptidase 46 (USP46) with bipolar disorder and schizophrenia in a Japanese population

artículo científico publicado en 2010

Author Correction: Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

artículo científico publicado en 2019

BDNF is not associated with schizophrenia: data from a Japanese population study and meta-analysis

artículo científico publicado en 2009

Characterization of a schizophrenia patient with a rare RELN deletion by combining genomic and patient-derived cell analyses

scientific article published on 14 December 2019

Common Variants in BCL9 Gene and Schizophrenia in a Japanese Population: Association Study, Meta-Analysis and Cognitive Function Analysis / UOBIČAJENE VARIJANTE BCL9 GENA I ŠIZOFRENIJA U JAPANSKOJ POPULACIJI: ŠTUDIJA POVEZANOSTI, METAANALIZA I ANA

article

Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients

artículo científico publicado en 2012

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights

artículo científico publicado en 2018

Copy number variant in the region of adenosine kinase (ADK) and its possible contribution to schizophrenia susceptibility

artículo científico publicado en 2017

Copy number variation in schizophrenia in the Japanese population

artículo científico publicado en 2009

Copy-number variation in the pathogenesis of autism spectrum disorder

artículo científico

Definition and refinement of the 7q36.3 duplication region associated with schizophrenia.

artículo científico publicado en 2013

Depression associated with alcohol intake and younger age in Japanese office workers: a case-control and a cohort study

artículo científico publicado en 2011

Drug-induced Extrapyramidal Symptoms Scale (DIEPSS) Serbian Language version: Inter-rater and Test-retest Reliability.

artículo científico publicado en 2017

Effects of Snoezelen-Multisensory environment on CARS scale in adolescents and adults with autism spectrum disorder

scientific article published on 29 March 2019

Effects of maternal depressive symptomatology during pregnancy and the postpartum period on infant-mother attachment

artículo científico publicado en 2014

Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia

artículo científico publicado en 2013

Factor structure of the Japanese version of the Edinburgh Postnatal Depression Scale in the postpartum period

artículo científico publicado en 2014

Failure to replicate the association between NRG1 and schizophrenia using Japanese large sample

scientific article published on 20 February 2008

Gap junction coding genes and schizophrenia: a genetic association study

artículo científico publicado en 2007

Gene-wide association study between the methylenetetrahydrofolate reductase gene (MTHFR) and schizophrenia in the Japanese population, with an updated meta-analysis on currently available data

artículo científico publicado en 2010

Genetic analysis of the gene coding for DARPP-32 (PPP1R1B) in Japanese patients with schizophrenia or bipolar disorder

artículo científico publicado en 2007

Genetic and animal model analyses reveal the pathogenic role of a novel deletion of RELN in schizophrenia

artículo científico publicado en 2018

Genetic association study between the detected risk variants based upon type II diabetes GWAS and psychotic disorders in the Japanese population

artículo científico publicado en 2013

Genetic association study of KREMEN1 and DKK1 and schizophrenia in a Japanese population

artículo científico publicado en 2010

Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.

artículo científico publicado en 2013

Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect

article

Genome-wide association study of cognitive decline in schizophrenia

artículo científico publicado en 2013

Genome-wide association study of schizophrenia in a Japanese population

artículo científico publicado en 2010

Glia-related genes and their contribution to schizophrenia

artículo científico publicado en 2015

High-resolution copy number variation analysis of schizophrenia in Japan.

artículo científico publicado en 2016

Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.

artículo científico publicado en 2014

Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility

artículo científico publicado en 2016

Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder

artículo científico publicado en 2022

Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.

artículo científico publicado en 2016

Issues on the diagnosis and etiopathogenesis of mood disorders: reconsidering DSM-5.

artículo científico publicado en 2017

Joint Degree Program for Graduate Students at the Nagoya University Graduate School of Medicine.

artículo científico publicado en 2019

Loss of function studies in mice and genetic association link receptor protein tyrosine phosphatase α to schizophrenia

artículo científico publicado en 2011

Methylation analysis for postpartum depression: a case control study.

artículo científico publicado en 2019

Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population

artículo científico publicado en 2016

Necessity for ethical consideration of research in the aftermath of disaster

artículo científico publicado en 2011

No association between the oligodendrocyte-related gene PLP1 and schizophrenia in the Japanese population

artículo científico publicado en 2008

No associations found between the genes situated at 6p22.1, HIST1H2BJ, PRSS16, and PGBD1 in Japanese patients diagnosed with schizophrenia

scientific article published on 09 April 2012

Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia.

artículo científico publicado en 2014

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.

artículo científico publicado en 2016

Postpartum depression among women in Nagoya indirectly exposed to the Great East Japan Earthquake

artículo científico publicado en 2018

Preoperative level of depression is a predictor of postoperative levels of depression in patients with head and neck cancer

artículo científico publicado en 2014

Prospective study of maternal depressive symptomatology among Japanese women

article by Naoko Ishikawa et al published 15 March 2011 in Journal of Psychosomatic Research

Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

artículo científico publicado en 2019

Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.

artículo científico publicado en 2017

Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder

artículo científico publicado en 2020

Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.

artículo científico publicado en 2018

Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis.

artículo científico publicado en 2014

Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders

artículo científico publicado en 2016

Resequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders.

artículo científico publicado en 2014

Resequencing and association analysis of the KALRN and EPHB1 genes and their contribution to schizophrenia susceptibility

artículo científico publicado en 2010

Schizophrenia polygenic risk score and prepubertal developmental impairments

artículo científico publicado en 2016

Serbian Language version of the Modified Checklist for Autism in Toddlers, Revised, with Follow-Up: Cross-Cultural Adaptation and Assessment of Reliability

artículo científico publicado en 2016

Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant

scientific article published on 19 July 2018

Social insecurity in relation to orbitofrontal activity in patients with eating disorders: a near-infrared spectroscopy study

artículo científico publicado en 2014

Social support helps protect against perinatal bonding failure and depression among mothers: a prospective cohort study

artículo científico publicado en 2017

Stable factor structure of the Edinburgh Postnatal Depression Scale during the whole peripartum period: Results from a Japanese prospective cohort study

artículo científico publicado en 2018

Summaries of oral sessions at the XXI World Congress of Psychiatric Genetics, Boston, Massachusetts, 17-21 October 2013: state of the field

artículo científico publicado en 2014

The polymorphism of YWHAE, a gene encoding 14-3-3epsilon, and brain morphology in schizophrenia: a voxel-based morphometric study

artículo científico publicado en 2014

The polymorphism of YWHAE, a gene encoding 14-3-3epsilon, and orbitofrontal sulcogyral pattern in patients with schizophrenia and healthy subjects.

artículo científico publicado en 2014

Validation and factor analysis of mother-infant bonding questionnaire in pregnant and postpartum women in Japan

artículo científico publicado en 2016

White matter microstructure between the pre-SMA and the cingulum bundle is related to response conflict in healthy subjects

artículo científico publicado en 2015

Lista de obras de Branko Aleksic

A case control association study and cognitive function analysis of neuropilin and tolloid-like 1 gene and schizophrenia in the Japanese population

A genetic association study of the FXYD domain containing ion transport regulator 6 (FXYD6) gene, encoding phosphohippolin, in susceptibility to schizophrenia in a Japanese population

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility

A two-stage case-control association study of the dihydropyrimidinase-like 2 gene (DPYSL2) with schizophrenia in Japanese subjects

ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk

An association study of tachykinin receptor 3 gene with schizophrenia in the Japanese population.

An evaluation of polymorphisms in casein kinase 1 delta and epsilon genes in major psychiatric disorders

Analysis of the VAV3 as candidate gene for schizophrenia: evidences from voxel-based morphometry and mutation screening

Assessment of a glyoxalase I frameshift variant, p.P122fs, in Japanese patients with schizophrenia

Association analysis of the GDNF gene with methamphetamine use disorder in a Japanese population

Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia

Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population

Association study of bromodomain-containing 1 gene with schizophrenia in Japanese population

Association study of ubiquitin-specific peptidase 46 (USP46) with bipolar disorder and schizophrenia in a Japanese population

Author Correction: Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

BDNF is not associated with schizophrenia: data from a Japanese population study and meta-analysis

Characterization of a schizophrenia patient with a rare RELN deletion by combining genomic and patient-derived cell analyses

Common Variants in BCL9 Gene and Schizophrenia in a Japanese Population: Association Study, Meta-Analysis and Cognitive Function Analysis / UOBIČAJENE VARIJANTE BCL9 GENA I ŠIZOFRENIJA U JAPANSKOJ POPULACIJI: ŠTUDIJA POVEZANOSTI, METAANALIZA I ANA

Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights

Copy number variant in the region of adenosine kinase (ADK) and its possible contribution to schizophrenia susceptibility

Copy number variation in schizophrenia in the Japanese population

Copy-number variation in the pathogenesis of autism spectrum disorder

Definition and refinement of the 7q36.3 duplication region associated with schizophrenia.

Depression associated with alcohol intake and younger age in Japanese office workers: a case-control and a cohort study

Drug-induced Extrapyramidal Symptoms Scale (DIEPSS) Serbian Language version: Inter-rater and Test-retest Reliability.

Effects of Snoezelen-Multisensory environment on CARS scale in adolescents and adults with autism spectrum disorder

Effects of maternal depressive symptomatology during pregnancy and the postpartum period on infant-mother attachment

Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia

Factor structure of the Japanese version of the Edinburgh Postnatal Depression Scale in the postpartum period

Failure to replicate the association between NRG1 and schizophrenia using Japanese large sample

Gap junction coding genes and schizophrenia: a genetic association study

Gene-wide association study between the methylenetetrahydrofolate reductase gene (MTHFR) and schizophrenia in the Japanese population, with an updated meta-analysis on currently available data

Genetic analysis of the gene coding for DARPP-32 (PPP1R1B) in Japanese patients with schizophrenia or bipolar disorder

Genetic and animal model analyses reveal the pathogenic role of a novel deletion of RELN in schizophrenia

Genetic association study between the detected risk variants based upon type II diabetes GWAS and psychotic disorders in the Japanese population

Genetic association study of KREMEN1 and DKK1 and schizophrenia in a Japanese population

Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.

Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect

Genome-wide association study of cognitive decline in schizophrenia

Genome-wide association study of schizophrenia in a Japanese population

Glia-related genes and their contribution to schizophrenia

High-resolution copy number variation analysis of schizophrenia in Japan.

Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.

Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility

Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder

Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.

Issues on the diagnosis and etiopathogenesis of mood disorders: reconsidering DSM-5.

Joint Degree Program for Graduate Students at the Nagoya University Graduate School of Medicine.

Loss of function studies in mice and genetic association link receptor protein tyrosine phosphatase α to schizophrenia

Methylation analysis for postpartum depression: a case control study.

Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population

Necessity for ethical consideration of research in the aftermath of disaster

No association between the oligodendrocyte-related gene PLP1 and schizophrenia in the Japanese population

No associations found between the genes situated at 6p22.1, HIST1H2BJ, PRSS16, and PGBD1 in Japanese patients diagnosed with schizophrenia

Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia.

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.

Postpartum depression among women in Nagoya indirectly exposed to the Great East Japan Earthquake

Preoperative level of depression is a predictor of postoperative levels of depression in patients with head and neck cancer

Prospective study of maternal depressive symptomatology among Japanese women

Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients

Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.

Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder

Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.

Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis.

Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders

Resequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders.

Resequencing and association analysis of the KALRN and EPHB1 genes and their contribution to schizophrenia susceptibility

Schizophrenia polygenic risk score and prepubertal developmental impairments

Serbian Language version of the Modified Checklist for Autism in Toddlers, Revised, with Follow-Up: Cross-Cultural Adaptation and Assessment of Reliability

Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant

Social insecurity in relation to orbitofrontal activity in patients with eating disorders: a near-infrared spectroscopy study

Social support helps protect against perinatal bonding failure and depression among mothers: a prospective cohort study

Stable factor structure of the Edinburgh Postnatal Depression Scale during the whole peripartum period: Results from a Japanese prospective cohort study

Summaries of oral sessions at the XXI World Congress of Psychiatric Genetics, Boston, Massachusetts, 17-21 October 2013: state of the field

The polymorphism of YWHAE, a gene encoding 14-3-3epsilon, and brain morphology in schizophrenia: a voxel-based morphometric study

The polymorphism of YWHAE, a gene encoding 14-3-3epsilon, and orbitofrontal sulcogyral pattern in patients with schizophrenia and healthy subjects.

Validation and factor analysis of mother-infant bonding questionnaire in pregnant and postpartum women in Japan

White matter microstructure between the pre-SMA and the cingulum bundle is related to response conflict in healthy subjects