Ana Carla Batissoco - Concepedia

Author

Ana Carla Batissoco

Also Known As

A C Batissoco, A.C. BATISSOCO, A.C. Batissoco, Ana Batissoco, Ana C Batissoco, Ana C. Batissoco, Ana Carla Batissoco, Batissoco, A.C., Batissoco, Ana Carla

Publications

488

Citations

H-Index

Concepts

All Affiliations

Universidade de São Paulo Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo Pontifícia Universidade Católica de São Paulo Instituto Biológico

About

Ana Carla Batissoco is an author at Universidade de São Paulo specializing in hearing loss, genetics, and audiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Arts	5	5	181
2	Medicine	4	4	109
3	Molecular Genetics	3	3	47
4	Biology	1	1	17
5	Molecular Biology	1	1	11

Ana Carla Batissoco

Publications

425

Citations

H-Index

Page 1

	Year	Citations
Prevalence of GJB2 (Connexin-26) and GJB6 (Connexin-30) Mutations in a Cohort of 300 Brazilian Hearing-Impaired Individuals: Implications for Diagnosis and Genetic Counseling Ana Carla Batissoco, Ronaldo Serafim Abreu-Silva, Maria Cristina C. Braga, Ear and Hearing	2008	88
Novel OTOF mutations in Brazilian patients with auditory neuropathy Jihane Romanos, Lilian Kimura, Mariana Lopes Fávero, Journal of Human Genetics Genetic DisorderAuditory Neuropathy Spectrum DisorderAudiologyNovel Otof MutationsAuditory Physiology	2009	63
Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness Karina Lezirovitz, Eliete Pardono, Maria Teresa Balester De Mello Auricchio, European Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsAudiologyGenetic Heterogeneity	2007	62
The search of a genetic basis for noise-induced hearing loss (NIHL) Ronaldo Serafim Abreu-Silva, Daniel Rincon, Andréa Roseli Vançan Russo Horimoto, Annals of Human Biology	2010	38
Is autosomal recessive deafness associated with oculocutaneous albinism a “coincidence syndrome”? Karina Lezirovitz, Fernanda Stávale Nicastro, Eliete Pardono, Journal of Human Genetics Oculocutaneous AlbinismMendelian DisorderGenetic DisorderAudiologyArts	2006	23
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
<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 GeneticsGene CharacterizationMolecular GeneticsDisease Gene IdentificationQuantitative Analysis	2020	19
Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects Renata Watanabe Nonose, Karina Lezirovitz, Maria Teresa Balester De Mello Auricchio, BMC Medical Genetics	2018	18
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 BiologyBrazilian FamilyAberrant TranscriptMendelian DisorderTecta Gene	2012	17

Page 1