Ana C. Batissoco

Sao Paulo, SP, Brazil

Last Updated: 09/26/2026

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Found 16 publications

Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population-Specific Variants and Clinical Correlations.

Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population-Specific Variants and Clinical Correlations.

Journal: Clinical genetics
Published: March 18, 2026

A Structural Variant in the 5' Regulatory Region of DIAPH3 Segregates with Postlingual Hearing Loss and Auditory Neuropathy in a Multigenerational Brazilian Family.

A Structural Variant in the 5' Regulatory Region of DIAPH3 Segregates with Postlingual Hearing Loss and Auditory Neuropathy in a Multigenerational Brazilian Family.

Journal: International archives of otorhinolaryngology
Published: February 26, 2026

Direct connexin-26 interactions with membrane proteins functionally relevant to the cochlea.

Direct connexin-26 interactions with membrane proteins functionally relevant to the cochlea.

Journal: Human genetics
Published: February 24, 2025

GJB2 c.35del variant up-regulates GJA1 gene expression and affects differentiation of human stem cells.

GJB2 c.35del variant up-regulates GJA1 gene expression and affects differentiation of human stem cells.

Journal: Genetics and molecular biology
Published: June 02, 2023

Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A).

Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A).

Journal: Stem cell research
Published: April 25, 2023

New Insights into the Identity of the DFNA58 Gene.

New Insights into the Identity of the DFNA58 Gene.

Journal: Genes
Published: October 18, 2022

Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss.

Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss.

Journal: Human genetics
Published: May 17, 2021

Cochlea cell-specific marker expression upon in vitro Hes1 knockdown.

Cochlea cell-specific marker expression upon in vitro Hes1 knockdown.

Journal: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica
Published: August 25, 2020

NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.

NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.

Journal: Human molecular genetics
Published: May 31, 2020

Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.

Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.

Journal: Human molecular genetics
Published: May 31, 2020

A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58.

A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58.

Journal: Human molecular genetics
Published: April 02, 2020

Stem-cell therapy for hearing loss: are we there yet?

Stem-cell therapy for hearing loss: are we there yet?

Journal: Brazilian journal of otorhinolaryngology
Published: March 01, 2019
Showing 1-12 of 16

Last Updated: 09/26/2026