Research Explorer

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Researcher

Hannes Syryn

Awards & Distinctions

12 Results

2025

Cracking rare disorders : a new minimally invasive RNA-seq protocol

Laurenz De CockErika D'haenensLies VantommeLynn BackersAude BeyensKathleen ClaesGriet De ClercqRobin de PutterCandy KumpsNika Schuermans et al.

A1 Journal Article in NPJ GENOMIC MEDICINE

Role of the pediatrician in the initial management of a newborn with differences of sex development or hypospadias

Saskia van der StraatenHannes SyrynArianne DessensMartine CoolsLloyd Tack

A1 Journal Article in EUROPEAN JOURNAL OF PEDIATRICS

2024

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

Hannes SyrynJulie Van De VeldeGriet De ClercqHannah VerdinAnnelies DheedeneFrank PeelmanAndrew SinclairKatie L AyersRoss A D BathgateMartine Cools et al.

A1 Journal Article in HUMAN REPRODUCTION

2023

Benefits of whole exome sequencing to advance the genetic diagnosis in patients with differences (disorders) of sex development

Hannes SyrynHannah VerdinJulie Van De VeldeMarianne BeckerCécile BrachetMarieke Den BrinkerSylvia DepoorterJulie FudvoyeDaniel KlinkPhilippe Lysy et al.

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

Lloyd TackCecile BrachetVeronique BeauloyeClaudine HeinrichsE BorosKathleen De WaeleSaskia van der StraatenSara Van AkenAnnelies LemayAnne Rochtus et al.

A1 Journal Article in HUMAN REPRODUCTION OPEN

HRAS-related epidermal nevus syndromes : expansion of the spectrum with first branchial arch defects

Aude BeyensCharlotte LietaerKathleen ClaesElfride De BaereMarleen GoeteynBob LerutHannes SyrynOlivier VanakkerJoni Van der MeulenLieve Vanwalleghem et al.

A1 Journal Article in CLINICAL GENETICS

Ovotesticular difference of sex development : genetic background, histological features and clinical management

Hannes SyrynKoen Van de VijverMartine Cools

A1 Journal Article in HORMONE RESEARCH IN PAEDIATRICS

RXFP2 : validating its role in autosomal recessive bilateral cryptorchidism and a novel association with male infertility

Hannes SyrynHannah VerdinJulie Van De VeldeFrank PeelmanMarianne BeckerCecile BrachetMarieke den BrinkerSylvia DepoorterJulie FudvoyeDaniel Klink et al.

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 BeyensLaure DequekerHilde BremsSandra JanssensHannes SyrynAnne D’HooghePascale De PaepeLieve VanwalleghemAnnelies StockmanElena Vankwikelberge et al.

A1 Journal Article in INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

2021

Two cases of DCDC2‐related neonatal sclerosing cholangitis with developmental delay and literature review

Hannes SyrynAnne HoorensTassos GrammatikopoulosMaesha DeheragodaSofie SymoensSaskia Vande VeldeStephanie Van BiervlietMyriam Van WinckelPATRICK VERLOOBert Callewaert et al.

A1 Journal Article in CLINICAL GENETICS

2020

Mild clinical features aid in the interpretation of syndromic gene variants in apparent non-syndromic intellectual disability patients

Hannes SyrynOlivier Vanakker

2018

Ultrastructural elastic fiber morphology in cutis laxa reflects the underlying pathogenesis and supports a novel clinical classification

Aude BeyensRiet De RyckeHannes SyrynBjörn Fischer-ZirnsakTim Van DammeIngrid HausserMichiel De BruyneManrico MorroniS NampoothiriK. Mahesh et al.