Concepedia

Author

Eliete Pardono

Universidade de São PauloORCID

Also Known As

Eliete Pardono

16

Publications

345

Citations

8

H-Index

23

Concepts

All Affiliations

Universidade de São PauloHospital das Clínicas da Faculdade de Medicina da Universidade de São PauloPontifícia Universidade Católica de São Paulo
EP

About

Eliete Pardono is an author at Universidade de São Paulo specializing in genetics, medicine, and hearing loss.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Arts

3

3

99

2

Medicine

3

3

140

3

Public Health

1

1

64

4

Epidemiology

1

1

64

5

Molecular Genetics

1

1

14

Eliete Pardono

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8

Publications

326

Citations

8

H-Index

YearCitations

Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome

Juliana F. Mazzeu, Eliete Pardono, Angela Maria Vianna‐Morgante,

American Journal of Medical Genetics Part A

2007

100

Waardenburg syndrome: Clinical differentiation between types I and II

Eliete Pardono, Yolande van Bever, Jenneke van den Ende,

American Journal of Medical Genetics Part A

2003

64

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

2007

62

Waardenburg syndrome: Novel mutations in a large Brazilian sample

Magnolia Astrid Pretell Bocángel, Uirá Souto Melo, Leandro Ucela Alves,

European Journal of Medical Genetics

2018

38

Is autosomal recessive deafness associated with oculocutaneous albinism a “coincidence syndrome”?

Karina Lezirovitz, Fernanda Stávale Nicastro, Eliete Pardono,

Journal of Human Genetics

2006

23

A novel c.1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome

Leandro Ucela Alves, Eliete Pardono, Paulo Alberto Otto,

Genetics and Molecular Biology

2015

14

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

Ana Carla Batissoco, Vinicius Pedroso-Campos, Eliete Pardono,

Human Genetics

2021

14

A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects

Silvana Santos, Eliete Pardono, Maria Ione Ferreira da Costa,

American Journal of Medical Genetics Part A

2008

11

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