Remko Hersmus - Publications

Ovarian-Specific FOXL2 Protein Expression in Testes from Patients with Complete Androgen Insensitivity Syndrome and Undescended Testes.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: September 23, 2025

Gonadal function and pathology in 17beta-HSD 3 and 5alpha-reductase deficiency.

Journal: European journal of endocrinology

Published: June 14, 2024

Response to letter to the editor: 'Gonadal tumour screening in XY gonadal dysgenesis'.

Journal: Clinical endocrinology

Published: January 29, 2024

Undetectable anti-Mullerian hormone and inhibin B do not preclude the presence of germ cell tumours in 45,X/46,XY or 46,XY gonadal dysgenesis.

Journal: Clinical endocrinology

Published: February 11, 2023

Under-reported aspects of diagnosis and treatment addressed in the Dutch-Flemish guideline for comprehensive diagnostics in disorders/differences of sex development.

Journal: Journal of medical genetics

Published: June 06, 2019

NR5A1 gene variants repress the ovarian-specific WNT signaling pathway in 46,XX disorders of sex development patients.

Journal: Human mutation

Published: June 28, 2018

Histological Assessment of Gonads in DSD: Relevance for Clinical Management.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: November 14, 2017

Multiparameter Investigation of a 46,XX/46,XY Tetragametic Chimeric Phenotypical Male Patient with Bilateral Scrotal Ovotestes and Ovulatory Activity.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: September 20, 2017

Functional characterization of novel NR5A1 variants reveals multiple complex roles in disorders of sex development.

Journal: Human mutation

Published: July 26, 2017

A Rare Case of Embryonal Carcinoma in a Patient with Turner Syndrome without Y Chromosomal Material but Mutations in KIT, AKT1, and ZNF358 Demonstrated Using Exome Sequencing.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: June 11, 2017

Malignant testicular germ cell tumors in postpubertal individuals with androgen insensitivity: prevalence, pathology and relevance of single nucleotide polymorphism-based susceptibility profiling.

Journal: Human reproduction (Oxford, England)

Published: April 25, 2017

The biology of germ cell tumors in disorders of sex development.

Journal: Clinical genetics

Published: August 22, 2016