Hannes Syryn

7PUBLICATIONS
22CO-AUTHORS
Genetic immunologyMedical biotechnology diagnostics (incl. biosensors)Infant and child healthHaematological tumoursNeurogenetics
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Publications (7)

|May 08, 2026
Variant Curation of the Largest Compendium of FOXL2 Coding and Noncoding Sequence and Structural Variants in BPES.

|Jul 02, 2025
Approach to the Patient With a Difference of Sexual Development.

Hannes Syryn, Elfride De Baere, Martine Cools

|Apr 22, 2025
Role of the pediatrician in the initial management of a newborn with Differences of Sex Development or hypospadias.

Saskia van der Straaten, Hannes Syryn, Arianne Dessens

|Sep 02, 2024
Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesis.

Hannes Syryn, Julie Van de Velde, Griet De Clercq

|Mar 10, 2023
HRAS-related epidermal nevus syndromes: Expansion of the spectrum with first branchial arch defects.

Aude Beyens, Charlotte Lietaer, Kathleen Claes

|Apr 12, 2022
Identification of Codon 146 KRAS Variants in Isolated Epidermal Nevus and Multiple Lesions in Oculoectodermal Syndrome: Confirmation of the Phenotypic Continuum of Mosaic RASopathies.

Aude Beyens, Laure Dequeker, Hilde Brems

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Frequent Collaborators

3 joint publications

Elfride De Baere

3 joint publications

Martine Cools

1 joint publications

Aude Beyens

1 joint publications

Hilde Brems