Publications by authors named "Alexander Gheldof"

Claim this Profile
D
Development and validation of a high-throughput screening pipeline of compound libraries to target EMT.
Sven Jonckheere, Joachim Taminau, Jamie Adams, Jef Haerinck, Jordy De Coninck, Alexander Gheldof

Cell Death Differ· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variants.
Annelore Van Der Kelen, Sophie Uyttebroeck, Stefanie Van de Voorde, Ludovica Picchetta, Ingrid Segers, Alexander Gheldof

J Assist Reprod Genet· March 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
MCM9 compound heterozygosity in an adolescent with premature ovarian insufficiency.
Elise Nauwynck, Michel De Vos, Alexander Gheldof, Bart Jh Dequeker, Annelore Van Der Kelen

Endocrinol Diabetes Metab Case Rep· October 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult Patients.
Nathalie Smeets, Alexander Gheldof, Bart Dequeker, Margaux Poleur, Sofia Maldonado Slootjes

Pediatr Neurol· September 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of RAD17 as a candidate cancer predisposition gene in families with histories of pancreatic and breast cancers.
Sofie Joris, Philippe Giron, Catharina Olsen, Sara Seneca, Alexander Gheldof

BMC Cancer· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development.
Annelore Van Der Kelen, Özlem Okutman, Elodie Javey, Münevver Serdarogullari, Charlotte Janssens, Alexander Gheldof

Hum Reprod Update· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
EDIR: exome database of interspersed repeats.
Laura D T Vo Ngoc, Randy Osei, Katrin Dohr, Catharina Olsen, Sara Seneca, Alexander Gheldof

Bioinformatics· January 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres.
Luca Persani, Martine Cools, Stamatina Ioakim, S Faisal Ahmed, Silvia Andonova, Alexander Gheldof

Endocr Connect· December 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Case report: Coexistence of myotonia congenita and Brugada syndrome in one family.
Ann Cordenier, Anja Flamez, Thomy de Ravel, Alexander Gheldof, Luigi Pannone

Front Neurol· September 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Ascites in infantile onset type II Sialidosis.
Kaoutar Tazi, Vanessa Guy-Viterbo, Alexander Gheldof, Aurélie Empain, Anne Paternoster

JIMD Rep· July 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorder.
Nuno Maia, Sven Potelle, Hamide Yildirim, Sandrine Duvet, Shyam K Akula, Alexander Gheldof

Am J Hum Genet· February 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicing.
Silvie Franck, Edouard Couvreu De Deckersberg, Jodi L Bubenik, Christina Markouli, Lise Barbé, Alexander Gheldof

Biol Open· January 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Intra-amniotic levothyroxine infusions in a case of fetal goiter due to novel gene variants.
Olivier G Pollé, Alexander Gheldof, Philippe A Lysy, Pierre Bernard

Clin Case Rep· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells.
Silvie Franck, Lise Barbé, Simon Ardui, Yannick De Vlaeminck, Joke Allemeersch, Alexander Gheldof

Hum Mol Genet· January 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis.
Asma Sassi, Julie Désir, Véronique Janssens, Martina Marangoni, Dorien Daneels, Alexander Gheldof

F S Rep· December 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic diagnosis of subfertility: the impact of meiosis and maternal effects.
Alexander Gheldof, Deborah J G Mackay, Ying Cheong, Willem Verpoest

J Med Genet· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics.
Laura V Vandervore, Rachel Schot, Esmee Kasteleijn, Renske Oegema, Katrien Stouffs, Alexander Gheldof

Brain· April 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rare genetic variants potentially involved in ovarian hyperstimulation syndrome.
Katrien Stouffs, Sari Daelemans, Samuel Santos-Ribeiro, Sara Seneca, Alexander Gheldof

J Assist Reprod Genet· March 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical implementation of gene panel testing for lysosomal storage diseases.
Alexander Gheldof, Sara Seneca, Katrien Stouffs, Willy Lissens, Anna Jansen

Mol Genet Genomic Med· February 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations.
Katrien Stouffs, Stéphanie Moortgat, Tim Vanderhasselt, Laura Vandervore, Alice Dica, Alexander Gheldof

Eur J Med Genet· December 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Bi-allelic variants in encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts.
Laura Vandervore, Katrien Stouffs, Ibrahim Tanyalçin, Tim Vanderhasselt, Filip Roelens, Alexander Gheldof

J Med Genet· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Sertoli Cell-Only Syndrome: Behind the Genetic Scenes.
Katrien Stouffs, Alexander Gheldof, Herman Tournaye, Deborah Vandermaelen, Maryse Bonduelle

Biomed Res Int· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Convert your favorite protein modeling program into a mutation predictor: "MODICT".
Ibrahim Tanyalcin, Katrien Stouffs, Dorien Daneels, Carla Al Assaf, Willy Lissens, Alexander Gheldof

BMC Bioinformatics· October 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
I-PV: a CIRCOS module for interactive protein sequence visualization.
Ibrahim Tanyalcin, Carla Al Assaf, Alexander Gheldof, Katrien Stouffs, Willy Lissens

Bioinformatics· February 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 gene.
Jeroen de Filette, Danielle Hasaerts, Sara Seneca, Alexander Gheldof, Katrien Stouffs

Neurol Genet· February 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis