Maricilda Palandi de Mello

About Maricilda Palandi de Mello

Maricilda Palandi de Mello, With an exceptional h-index of 30 and a recent h-index of 14 (since 2020), a distinguished researcher at Universidade Estadual de Campinas, specializes in the field of Genética Molecular Humana.

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

X‐linked congenital adrenal hypoplasia: Report of long clinical follow‐up and description of a new complex variant in the NR0B1 gene

Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil

SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism

Diferenciação sexual diferente

DHX37 and the implications in Disorders of Sex Development: an update review.

DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis

Are NR5A1 Variations a Frequent Cause of 46,XX Ovotesticular Disorders of Sex Development? Analysis from a Single Center and Systematic Review

A Novel Look at Dosage-Sensitive Sex Locus Xp21.2 in a Case of 46,XY Partial Gonadal Dysgenesis without NR0B1 Duplication

Maricilda Palandi de Mello Information

University

Position

___

Citations(all)

2924

Citations(since 2020)

1008

Cited By

2349

hIndex(all)

30

hIndex(since 2020)

14

i10Index(all)

101

i10Index(since 2020)

37

Email

University Profile Page

Google Scholar

Maricilda Palandi de Mello Skills & Research Interests

Genética Molecular Humana

Top articles of Maricilda Palandi de Mello

X‐linked congenital adrenal hypoplasia: Report of long clinical follow‐up and description of a new complex variant in the NR0B1 gene

American Journal of Medical Genetics Part A

2024/1/19

Maricilda Palandi De Mello
Maricilda Palandi De Mello

H-Index: 17

Mara Sanches Guaragna
Mara Sanches Guaragna

H-Index: 8

Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil

Fetal Diagnosis and Therapy

2024/1/4

SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism

American Journal of Medical Genetics Part A

2023/2

Mara Sanches Guaragna
Mara Sanches Guaragna

H-Index: 8

Maricilda Palandi De Mello
Maricilda Palandi De Mello

H-Index: 17

Diferenciação sexual diferente

2023

Maricilda Palandi De Mello
Maricilda Palandi De Mello

H-Index: 17

DHX37 and the implications in Disorders of Sex Development: an update review.

2023/12/23

DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis

Life

2023/4/27

Are NR5A1 Variations a Frequent Cause of 46,XX Ovotesticular Disorders of Sex Development? Analysis from a Single Center and Systematic Review

2023/2/14

A Novel Look at Dosage-Sensitive Sex Locus Xp21.2 in a Case of 46,XY Partial Gonadal Dysgenesis without NR0B1 Duplication

International Journal of Molecular Sciences

2022/12/28

Can non-coding NR5A1 gene variants explain phenotypes of disorders of sex development?

Sexual Development

2022/12/28

Trends in Time Regarding Sex Assignment of Patients with Disorders of Sex Development: Experience of an Interdisciplinary Service

Sexual Development

2022/12/28

Suggested cutoff point for testosterone by liquid chromatography with tandem mass spectrometry (LC-MS/MS) after stimulation with recombinant human chorionic gonadotropin

Sexual Development

2022/12/28

Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study

Sao Paulo Medical Journal

2022/11/28

Sex dimorphism of weight and length at birth: evidence based on disorders of sex development

Annals of human biology

2022/11/17

Bilateral Wilms’ tumor in a child with Denys-Drash syndrome: novel frameshift variant disrupts the WT1 nuclear location signaling region

Journal of Pediatric Endocrinology and Metabolism

2022/6/27

Mara Sanches Guaragna
Mara Sanches Guaragna

H-Index: 8

Maricilda Palandi De Mello
Maricilda Palandi De Mello

H-Index: 17

So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity

Italian Journal of Pediatrics

2022/6/10

Leydig and Sertoli cell function in individuals with genital ambiguity, 46, XY karyotype, palpable gonads and normal testosterone secretion: a case-control study

Sao Paulo Medical Journal

2022/2/7

APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses

Pediatric Nephrology

2021/8

Association between Down Syndrome and Disorders of Sex Development: Report of Three Cases and Review of 188 Cases in the Literature

Sexual Development

2021/7/30

Sex Dimorphism of Birth Weight and Length: Evidence Based on Disorders of Sex Development

2021/5/17

P0267/# 595: ASSOCIATION BETWEEN APPARENT STRONG ION DIFFERENCE (SIDAPP) AND OUTCOMES IN TERTIARY PEDIATRIC INTENSIVE CARE UNIT (PICU) FROM BRAZILIAN AMAZON: AN OBSERVATIONAL STUDY

Pediatric Critical Care Medicine

2021/3/1

See List of Professors in Maricilda Palandi de Mello University(Universidade Estadual de Campinas)

Co-Authors

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