Concepedia

Author

Jeanne Oiticica

Universidade de São PauloORCID

Also Known As

J. Oiticica, Jeanne Oiticica, Oiticica, J., Oiticica, Jeanne

59

Publications

774

Citations

15

H-Index

41

Concepts

All Affiliations

Universidade de São PauloHospital das Clínicas da Faculdade de Medicina da Universidade de São PauloUniversidade Federal de São Paulo
JO

About

Jeanne Oiticica is an author at Universidade de São Paulo specializing in hearing loss, arts, and audiology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Arts

7

7

129

2

Medicine

5

5

106

3

Health Sciences

2

2

26

4

Biology

1

1

17

5

Hearing Sciences

1

1

12

Jeanne Oiticica

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20

Publications

470

Citations

14

H-Index

YearCitations

Tinnitus prevalence in the city of São Paulo

Jeanne Oiticica, Roseli Saraiva Moreira Bittar

Brazilian Journal of Otorhinolaryngology

2014

87

Population epidemiological study on the prevalence of dizziness in the city of São Paulo

Roseli Saraiva Moreira Bittar, Jeanne Oiticica, Fernando Freitas Ganança,

Brazilian Journal of Otorhinolaryngology

2013

62

Metabolic disorders prevalence in sudden deafness

Jeanne Oiticica, Roseli Saraiva Moreira Bittar

Clinics

2010

33

Genomic copy number alterations in non‐syndromic hearing loss

Carla Rosenberg, Érika L. Freitas, Daniela Tiaki Uehara,

Clinical Genetics

2015

33

Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea

Jeanne Oiticica, Luiz Carlos M Barboza-Junior, Ana Carla Batissoco,

Journal of Translational Medicine

2010

23

Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss

Érika L. Freitas, Jeanne Oiticica, Amanda G Silva,

European Journal of Medical Genetics

2014

22

<i>NCOA3</i> identified as a new candidate to explain autosomal dominant progressive hearing loss

Rodrigo Salazar‐Silva, Vitor Lima Goes Dantas, Leandro Ucela Alves,

Human Molecular Genetics

2020

21

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

Karina Lezirovitz, Gleiciele Alice Vieira-Silva, Ana Carla Batissoco,

Human Molecular Genetics

2020

19

Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominant deafness in a Brazilian family

Karina Lezirovitz, Ana Carla Batissoco, Fernanda Teresa de Lima,

Gene

2012

17

Effect of Fractal Tones on the Improvement of Tinnitus Handicap Inventory Functional Scores among Chronic Tinnitus Patients: An Open-label Pilot Study

Patricia Simonetti, Laura Garcia E. Vasconcelos, Jeanne Oiticica

International Archives of Otorhinolaryngology

2018

17

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