Hannes Syryn

Years Active: 2021-2024
Publications (10 Years): 4

This page only lists publications with an associated author ORCID identifier.

Publications

Hannes Syryn, Julie Van de Velde, Griet De Clercq, Hannah Verdin, Annelies Dheedene, Frank Peelman, Andrew Sinclair, Katie L Ayers, Ross A D Bathgate, Martine Cools, Elfriede De Baere
Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesis. Human reproduction (Oxford, England) (2024)
Aude Beyens, Charlotte Lietaer, Kathleen Claes, Elfride De Baere, Marleen Goeteyn, Bob Lerut, Hannes Syryn, Olivier Vanakker, Joni Van der Meulen, Lieve Vanwalleghem, Bert Callewaert
HRAS-related epidermal nevus syndromes: Expansion of the spectrum with first branchial arch defects. Clinical genetics (2023)
Aude Beyens, Laure Dequeker, Hilde Brems, Sandra Janssens, Hannes Syryn, Anne D'Hooghe, Pascale De Paepe, Lieve Vanwalleghem, Annelies Stockman, Elena Vankwikelberge, Sofie De Schepper, Marleen Goeteyn, Patricia Delbeke, Bert Callewaert
Identification of Codon 146 KRAS Variants in Isolated Epidermal Nevus and Multiple Lesions in Oculoectodermal Syndrome: Confirmation of the Phenotypic Continuum of Mosaic RASopathies. International journal of molecular sciences 23 (7) (2022)
Hannes Syryn, Anne Hoorens, Tassos Grammatikopoulos, Maesha Deheragoda, Sofie Symoens, Saskia Vande Velde, Stephanie Van Biervliet, Myriam Van Winckel, Patrick Verloo, Bert Callewaert, Ruth De Bruyne
Two cases of DCDC2-related neonatal sclerosing cholangitis with developmental delay and literature review. Clinical genetics 100 (4) (2021)

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