Hannah Verdin

Gent, VLG, Belgium

Last Updated: 09/26/2026

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Found 36 publications

Variant Curation of the Largest Compendium of FOXL2 Coding and Noncoding Sequence and Structural Variants in BPES.

Variant Curation of the Largest Compendium of FOXL2 Coding and Noncoding Sequence and Structural Variants in BPES.

Journal: Human mutation
Published: October 26, 2025

Insight into the role of TXNRD2 in steroidogenesis through a novel homozygous TXNRD2 splice variant.

Insight into the role of TXNRD2 in steroidogenesis through a novel homozygous TXNRD2 splice variant.

Journal: European journal of endocrinology
Published: March 29, 2024

Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesis.

Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesis.

Journal: Human reproduction (Oxford, England)
Published: March 12, 2024

Spleen function is reduced in individuals with NR5A1 variants with or without a difference of sex development: a cross-sectional study.

Spleen function is reduced in individuals with NR5A1 variants with or without a difference of sex development: a cross-sectional study.

Journal: European journal of endocrinology
Published: September 19, 2023

Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP).

Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP).

Journal: Journal of neurology
Published: July 19, 2023

Etiology, histology, and long-term outcome of bilateral testicular regression: a large Belgian series.

Etiology, histology, and long-term outcome of bilateral testicular regression: a large Belgian series.

Journal: Human reproduction open
Published: June 19, 2023

Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital Experience.

Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital Experience.

Journal: Frontiers in medicine
Published: March 31, 2023

The Role of MCM9 in the Etiology of Sertoli Cell-Only Syndrome and Premature Ovarian Insufficiency.

The Role of MCM9 in the Etiology of Sertoli Cell-Only Syndrome and Premature Ovarian Insufficiency.

Journal: Journal of clinical medicine
Published: December 03, 2022

Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders.

Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders.

Journal: Neurology. Genetics
Published: October 19, 2022

Marked hypotonia: An additional feature of ANO3-related movement disorder.

Marked hypotonia: An additional feature of ANO3-related movement disorder.

Journal: European journal of medical genetics
Published: May 30, 2022

Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA).

Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA).

Journal: Orphanet journal of rare diseases
Published: December 17, 2021

Endocrine outcome and seminal parameters in young adult men born with hypospadias: A cross-sectional cohort study.

Endocrine outcome and seminal parameters in young adult men born with hypospadias: A cross-sectional cohort study.

Journal: EBioMedicine
Published: November 07, 2021
Showing 1-12 of 36

Last Updated: 09/26/2026