Bianca G. Lisboa

Sao Paulo, SP 05403903, Brazil

Last Updated: 09/26/2026

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Found 14 publications

Environmental Influences Measured by Epigenetic Clock and Vulnerability Components at Birth Impact Clinical ASD Heterogeneity.

Environmental Influences Measured by Epigenetic Clock and Vulnerability Components at Birth Impact Clinical ASD Heterogeneity.

Journal: Genes
Published: July 21, 2021

Brain areas involved with obsessive-compulsive disorder present different DNA methylation modulation.

Brain areas involved with obsessive-compulsive disorder present different DNA methylation modulation.

Journal: BMC genomic data
Published: May 22, 2021

Are the 50's, the transition decade, in choroid plexus aging?

Are the 50's, the transition decade, in choroid plexus aging?

Journal: GeroScience
Published: November 05, 2020

Initial findings of striatum tripartite model in OCD brain samples based on transcriptome analysis.

Initial findings of striatum tripartite model in OCD brain samples based on transcriptome analysis.

Journal: Scientific reports
Published: May 01, 2018

Putative contributions of the sex chromosome proteins SOX3 and SRY to neurodevelopmental disorders.

Putative contributions of the sex chromosome proteins SOX3 and SRY to neurodevelopmental disorders.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: February 28, 2018

Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.

Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.

Journal: PloS one
Published: June 30, 2016

A novel mechanism of NPM1 cytoplasmic localization in acute myeloid leukemia: the recurrent gene fusion NPM1-HAUS1.

A novel mechanism of NPM1 cytoplasmic localization in acute myeloid leukemia: the recurrent gene fusion NPM1-HAUS1.

Journal: Haematologica
Published: April 03, 2016

Clinical features of JAK2V617F- or CALR-mutated essential thrombocythemia and primary myelofibrosis.

Clinical features of JAK2V617F- or CALR-mutated essential thrombocythemia and primary myelofibrosis.

Journal: Blood cells, molecules & diseases
Published: December 31, 2015

Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive-compulsive disorder.

Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive-compulsive disorder.

Journal: BMC neuroscience
Published: December 08, 2015

Identification of ANLN as ETV6 partner gene in recurrent t(7;12)(p15;p13): a possible role of deregulated ANLN expression in leukemogenesis.

Identification of ANLN as ETV6 partner gene in recurrent t(7;12)(p15;p13): a possible role of deregulated ANLN expression in leukemogenesis.

Journal: Molecular cancer
Published: August 04, 2015

KRAS gene mutation in a series of unselected colorectal carcinoma patients with prognostic morphological correlations: a pyrosequencing method improved by nested PCR.

KRAS gene mutation in a series of unselected colorectal carcinoma patients with prognostic morphological correlations: a pyrosequencing method improved by nested PCR.

Journal: Experimental and molecular pathology
Published: March 17, 2015

KRAS insertions in colorectal cancer: what do we know about unusual KRAS mutations?

KRAS insertions in colorectal cancer: what do we know about unusual KRAS mutations?

Journal: Experimental and molecular pathology
Published: February 21, 2014
Showing 1-12 of 14

Last Updated: 09/26/2026