Alexander Gheldof

Vrije Universiteit Brussel

Belgium

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Articles (17)

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2026

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2025

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2025

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2021

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2021

Collaborators (25)

Nuno Maia

Invited associated professor

Instituto Politécnico de Leiria

PORTUGAL

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Yannick De Vlaeminck

Vrije Universiteit Brussel

BELGIUM

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Thomy de Ravel

Vrije Universiteit Brussel

BELGIUM

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Erik Teugels

Vrije Universiteit Brussel

BELGIUM

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Katrien Stouffs

Vrije Universiteit Brussel

BELGIUM

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Gudrun Pappaert

Vrije Universiteit Brussel

BELGIUM

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Inge Gies

Vrije Universiteit Brussel

BELGIUM

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Jodi Bubenik

Research Assistant Professor

University of Florida

UNITED STATES

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Frederik Hes

Vrije Universiteit Brussel

BELGIUM

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Martine Cools

Ghent University

BELGIUM

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Véronique Bissay

Vrije Universiteit Brussel

BELGIUM

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Antonio Capalbo

Adjunct Professor

University of Chieti-Pescara

ITALY

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Jean De Schepper

Head of Division Pediatric Endocrinology

Vrije Universiteit Brussel

BELGIUM

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Ingrid Segers

Vrije Universiteit Brussel

BELGIUM

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Philippe Giron

Vrije Universiteit Brussel

BELGIUM

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Karen Sermon

Vrije Universiteit Brussel

BELGIUM

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S. Faisal Ahmed

University of Glasgow

UNITED KINGDOM

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Michel De Vos

Vrije Universiteit Brussel

BELGIUM

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Marius Regin

Vrije Universiteit Brussel

BELGIUM

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Randy Osei

Vrije Universiteit Brussel

BELGIUM

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Maurice Swanson

Professor

University of Florida

UNITED STATES

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Pieter Verdyck

Vrije Universiteit Brussel

BELGIUM

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willem verpoest

Professor

Vrije Universiteit Brussel

BELGIUM

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Sara Seneca

Vrije Universiteit Brussel

BELGIUM

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Claudia Spits

Vrije Universiteit Brussel

BELGIUM

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Alexander Gheldof

Research Interests

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Articles (17)

Transcriptional profiling reveals glucose-dependent regulation of COL13A1 mRNA in Pompe patients: Prospect for a novel disease mechanism

Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variants

Development and validation of a high-throughput screening pipeline of compound libraries to target EMT

Identification of RAD17 as a candidate cancer predisposition gene in families with histories of pancreatic and breast cancers

Congenital Myasthenic Syndromes in Belgium

MCM9 compound heterozygosity in an adolescent with premature ovarian insufficiency

A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development

EDIR: exome database of interspersed repeats

The Diagnostic and Therapeutic Challenges of Fabry Nephropathy—A Review of the Literature, Illustrated by a Clinical Case

Case report

The genetic diagnosis of rare endocrine disorders of sex development and maturation

Ascites in infantile onset type II Sialidosis

Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorder

Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicing

Intra-amniotic levothyroxine infusions in a case of fetal goiter due to novel Thyroglobulin gene variants

Sustained intrinsic WNT and BMP4 activation impairs hESC differentiation to definitive endoderm and drives the cells towards extra-embryonic mesoderm

MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells

Collaborators (25)

Nuno Maia

Yannick De Vlaeminck

Thomy de Ravel

Erik Teugels

Katrien Stouffs

Gudrun Pappaert

Inge Gies

Jodi Bubenik

Frederik Hes

Martine Cools

Véronique Bissay

Antonio Capalbo

Jean De Schepper

Ingrid Segers

Philippe Giron

Karen Sermon

S. Faisal Ahmed

Michel De Vos

Marius Regin

Randy Osei

Maurice Swanson

Pieter Verdyck

willem verpoest

Sara Seneca

Claudia Spits

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