Alexander Gheldof

8PUBLICATIONS
37CO-AUTHORS
Obstetrics and gynaecologyPredictive and prognostic markersCancer geneticsAdolescent healthGene expression (incl. microarray and other genome-wide approaches)
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Publications (8)

|Oct 29, 2026
Exploring genetic variants in premature ovarian insufficiency: a cohort-based investigation of monogenic etiologies.

|May 09, 2025
Development and validation of a high-throughput screening pipeline of compound libraries to target EMT.

Sven Jonckheere, Joachim Taminau, Jamie Adams

|Jan 27, 2025
Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variants.

Annelore Van Der Kelen, Sophie Uyttebroeck, Stefanie Van de Voorde

|Oct 24, 2024
MCM9 compound heterozygosity in an adolescent with premature ovarian insufficiency.

Elise Nauwynck, Michel De Vos, Alexander Gheldof

|Dec 26, 2022
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

|Dec 01, 2022
EDIR: exome database of interspersed repeats.

Laura D T Vo Ngoc, Randy Osei, Katrin Dohr

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Frequent Collaborators

3 joint publications

Annelore Van Der Kelen

3 joint publications

Frederik J Hes

2 joint publications

Bart Johan H Dequeker

2 joint publications

Willem Verpoest