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Regina Celia Mingroni Netto

About Regina Celia Mingroni Netto

Regina Celia Mingroni Netto, With an exceptional h-index of 26 and a recent h-index of 18 (since 2020), a distinguished researcher at Universidade de São Paulo,

His recent articles reflect a diverse array of research interests and contributions to the field:

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

Ca2+ binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing

Avanço na terapia gênica traz esperanças para o tratamento da surdez [Depoimento]

Ca2+ binding to the C

Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants

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 …

Correction to: Genetic etiology of non-syndromic hearing loss in Latin America

Genetic etiology of non-syndromic hearing loss in Latin America

Regina Celia Mingroni Netto Information

University

Position

Professor Associado Instituto de Biociências da

Citations(all)

2722

Citations(since 2020)

933

Cited By

2124

hIndex(all)

26

hIndex(since 2020)

18

i10Index(all)

64

i10Index(since 2020)

32

Email

University Profile Page

Google Scholar

Top articles of Regina Celia Mingroni Netto

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

Genetics and Molecular Biology

2024/4/15

Ana Carla Batissoco
Ana Carla Batissoco

H-Index: 7

Gerson Kobayashi
Gerson Kobayashi

H-Index: 12

Jeanne Oiticica
Jeanne Oiticica

H-Index: 12

Maria Rita Passos-Bueno
Maria Rita Passos-Bueno

H-Index: 34

Luciana Amaral Haddad
Luciana Amaral Haddad

H-Index: 8

Ca2+ binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing

Protein & Cell

2024/4/1

Han Chen
Han Chen

H-Index: 3

Qinghua Fang
Qinghua Fang

H-Index: 15

Jakob Neef
Jakob Neef

H-Index: 16

Nicola Strenzke
Nicola Strenzke

H-Index: 25

Barbara Vona
Barbara Vona

H-Index: 11

Tobias Moser
Tobias Moser

H-Index: 45

Avanço na terapia gênica traz esperanças para o tratamento da surdez [Depoimento]

Jornal da USP

2024

Miguel Angelo Hyppolito
Miguel Angelo Hyppolito

H-Index: 14

Regina Celia Mingroni Netto
Regina Celia Mingroni Netto

H-Index: 15

Ca2+ binding to the C

2023

Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants

Audiology Research

2023/12/21

Silvia Souza Da Costa
Silvia Souza Da Costa

H-Index: 15

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 …

Stem Cell Research

2023/9/1

Jeanne Oiticica
Jeanne Oiticica

H-Index: 12

Correction to: Genetic etiology of non-syndromic hearing loss in Latin America

Human Genetics

2022/4/1

Genetic etiology of non-syndromic hearing loss in Latin America

2022/4

Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (vol 13, 1004, 2022)

Nature communications

2022/3/4

Michel S Naslavsky
Michel S Naslavsky

H-Index: 14

Kelly Nunes
Kelly Nunes

H-Index: 9

Heloísa De Souza Andrade
Heloísa De Souza Andrade

H-Index: 3

Victor Borda
Victor Borda

H-Index: 7

Diogo Meyer
Diogo Meyer

H-Index: 20

Maria Rita Passos-Bueno
Maria Rita Passos-Bueno

H-Index: 34

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

Human Molecular Genetics

2022

Ana Carla Batissoco
Ana Carla Batissoco

H-Index: 7

Jeanne Oiticica
Jeanne Oiticica

H-Index: 12

Chrissy Hammond
Chrissy Hammond

H-Index: 20

Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss

European Journal of Human Genetics

2022/1

Kelly Nunes
Kelly Nunes

H-Index: 9

Jeroen Smits
Jeroen Smits

H-Index: 29

Diogo Meyer
Diogo Meyer

H-Index: 20

The human mitochondrial DNA

2021/6/8

Cochlea cell-specific marker expression upon in vitro Hes1 knockdown

Brazilian Journal of Medical and Biological Research

2021/5/17

O gene GJB2: da audição ao silêncio

Genética na Escola

2021/1/8

Ana Carla Batissoco
Ana Carla Batissoco

H-Index: 7

Estudos de dinâmica populacional, ancestralidade genética e saúde em comunidades quilombolas: relato de uma experiência

Tessituras: Revista de Antropologia e Arqueologia

2020/12/31

Kelly Nunes
Kelly Nunes

H-Index: 9

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

Human Molecular Genetics

2020/11/15

Ana Carla Batissoco
Ana Carla Batissoco

H-Index: 7

Jeanne Oiticica
Jeanne Oiticica

H-Index: 12

Yushi Yang
Yushi Yang

H-Index: 21

Chrissy Hammond
Chrissy Hammond

H-Index: 20

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

Human molecular genetics

2020/5/1

Nicolas Grillet
Nicolas Grillet

H-Index: 15

Jeanne Oiticica
Jeanne Oiticica

H-Index: 12

Estudos moleculares na perda auditiva de herança autossômica recessiva

2020

Renato de Mello-Silva: Botânico brilhante, cujo exemplo viverá para sempre

Jornal da USP

2020

Gregório Cardoso Tápias Ceccantini
Gregório Cardoso Tápias Ceccantini

H-Index: 16

Miguel Trefaut Rodrigues
Miguel Trefaut Rodrigues

H-Index: 40

See List of Professors in Regina Celia Mingroni Netto University(Universidade de São Paulo)