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Berenice B. Mendonca

Berenice B. Mendonca

D-Index & Metrics

Medicine

D-Index
90
Citations
28749
World Ranking
12231
National Ranking
32

Overview

Berenice B. Mendonca is affiliated with the Universidade de São Paulo in Brazil. Their research publications span several areas within medicine and molecular biology, with a focus on endocrinology, genetics, and metabolism.

The scientist's recent papers include:

  • Genetics of ovarian insufficiency and defects of folliculogenesis, 2021, Best Practice & Research Clinical Endocrinology & Metabolism
  • The Congenital and Acquired Mechanisms Implicated in the Etiology of Central Precocious Puberty, 2022, Endocrine Reviews
  • Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency, 2020, PLoS ONE
  • High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency, 2021, The American Journal of Human Genetics
  • XAF1 as a modifier of p53 function and cancer susceptibility, 2020, Science Advances

The main fields of study associated with their work are:

  • Medicine
  • Biochemistry, Genetics and Molecular Biology

The subfields in which they have contributed include:

  • Endocrinology, Diabetes and Metabolism
  • Molecular Biology
  • Genetics
  • Surgery
  • Cancer Research

The topics extensively covered in their publications are:

  • Sexual Differentiation and Disorders
  • Adrenal and Paraganglionic Tumors
  • Hormonal Regulation and Hypertension
  • Cancer, Hypoxia, and Metabolism
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Adrenal Hormones and Disorders
  • Growth Hormone and Insulin-like Growth Factors

Berenice B. Mendonca collaborates frequently with several colleagues, including:

  • Ana Cláudia Latronico
  • Madson Q. Almeida
  • Sorahia Domenice
  • Mirian Yumie Nishi
  • Maria Candida Barisson Villares Fragoso

Their publications appear regularly in key scientific venues such as:

  • Journal of the Endocrine Society
  • The Journal of Clinical Endocrinology & Metabolism
  • Clinics
  • European Journal of Endocrinology
  • Sexual Development

Best Publications

  • Male pseudohermaphroditism caused by mutations of testicular 17β-hydroxysteroid dehydrogenase 3

    Wayne M. Geissler;Daphne L. Davis;Ling Wu;Karen D. Bradshaw

  • A GPR54-Activating Mutation in a Patient with Central Precocious Puberty

    Milena Gurgel Teles;Suzy D.C. Bianco;Vinicius Nahime Brito;Ericka B. Trarbach

  • Comprehensive Pan-Genomic Characterization of Adrenocortical Carcinoma

    Zheng S;Cherniack Ad;Cherniack Ad;Dewal N;Moffitt Ra

  • Central precocious puberty caused by mutations in the imprinted gene MKRN3

    Ana Paula Abreu;Andrew Dauber;Delanie B. Macedo;Sekoni D. Noel

  • Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome

    Christa Flück;Toshihro Tajima;Amit Vikram Pandey;Wiebke Arlt

  • Molecular genetics of steroid 5α-reductase 2 deficiency

    Anice E. Thigpen;Daphne L. Davis;Athena Milatovich;Berenice B. Mendonca

  • Testicular and Ovarian Resistance to Luteinizing Hormone Caused by Inactivating Mutations of the Luteinizing Hormone–Receptor Gene

    Ana C. Latronico;James Anasti;Ivo J.P. Arnhold;Robert Rapaport

  • Mutations of the KISS1 gene in disorders of puberty

    Leticia G. Silveira;S. D. Noel;A. P. Silveira-Neto;A. P. Abreu

  • Ectopic Adrenocorticotropic Hormone Syndrome

    Bernardo Leo Wajchenberg;Berenice B. Mendonca;Bernardo Liberman;Maria A. Albergaria Pereira

  • TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

    Elena Gianetti;Cintia Tusset;Sekoni D. Noel;Margaret G. Au

  • The genetic and functional basis of isolated 17,20–lyase deficiency

    David H. Geller;Richard J. Auchus;Berenice B. Mendonça;Walter L. Miller

  • THE ESSENTIAL ROLE OF ZINC IN GROWTH

    José Brandão-Neto;Vivian Stefan;Berenice B. Mendonça;Walter Bloise

  • The PROP1 2-Base Pair Deletion Is a Common Cause of Combined Pituitary Hormone Deficiency*

    Joy D. Cogan;Wei Wu;John A. Phillips;Ivo J. P. Arnhold

  • Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiency.

    S Andersson;W M Geissler;L Wu;D L Davis

  • BRIEF REPORT : TESTICULAR AND OVARIAN RESISTANCE TO LUTEINIZING HORMONE CAUSED BY INACTIVATING MUTATIONS OF THE LUTEINIZING HORMONE-RECEPTOR GENE

    Ana C. Latronico;James Anasti;Ivo J. P. Arnhold;Robert Rapaport

  • 46,XY disorders of sex development (DSD)

    Berenice Bilharinho Mendonca;Sorahia Domenice;Ivo J. P. Arnhold;Elaine M. F. Costa

  • Reproductive outcome of women with 21 -hydroxylase-deficient nonclassic adrenal hyperplasia

    C. Moran;R. Azziz;N. Weintrob;S. F. Witchel

  • An inherited mutation outside the highly conserved DNA-binding domain of the p53 tumor suppressor protein in children and adults with sporadic adrenocortical tumors.

    Ana Claudia Latronico;Emilia Modolo Pinto;Sorahia Domenice;Maria Candida Barisson Villares Fragoso

  • 17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations.

    Alm Boehmer;AO Brinkmann;LA Sandkuijl;Djj Halley

  • Erratum: Comprehensive Pan-Genomic Characterization of Adrenocortical Carcinoma (Cancer Cell (2016) 29(5) (723–736) (S153561081630160X) (10.1016/j.ccell.2016.04.002))

    Siyuan Zheng;Andrew D. Cherniack;Ninad Dewal;Richard A. Moffitt

Frequent Co-Authors

Ursula B. Kaiser
Ursula B. Kaiser Brigham and Women's Hospital
David W. Russell
David W. Russell University of Washington
Jean D. Wilson
Jean D. Wilson The University of Texas Southwestern Medical Center
Sally A. Camper
Sally A. Camper University of Michigan–Ann Arbor
Richard J. Ross
Richard J. Ross University of Sheffield
Carla Rosenberg
Carla Rosenberg Universidade de São Paulo
Márta Korbonits
Márta Korbonits Queen Mary University of London
Jun Li
Jun Li University of Oklahoma Health Sciences Center
Wiebke Arlt
Wiebke Arlt University of Birmingham
Mehul T. Dattani
Mehul T. Dattani University College London

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