Toon Rosseel
5PUBLICATIONS
146CO-AUTHORS
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Publications (5)
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|Mar 07, 2025
Uncovering the genetic architecture of inherited retinal disease in a consanguineous Iranian cohort.Lieselot Vincke, Kristof Van Schil, Hamid Ahmadieh
|Jul 14, 2023
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.Lenka Stolarova, Petra Kleiblova, Petra Zemankova
|Sep 10, 2021
Prevalence of Germline Pathogenic Variants in Cancer Predisposing Genes in Czech and Belgian Pancreatic Cancer Patients.Greet Wieme, Jan Kral, Toon Rosseel
|Jan 31, 2020
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility.Giulia Ascari, Frank Peelman, Pietro Farinelli
|Aug 05, 2016
NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development.Dorien Baetens, Hans Stoop, Frank Peelman
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Frequent Collaborators
2 joint publications
Robin De Putter
2 joint publications
Zdenek Kleibl
2 joint publications
Jana Soukupova
2 joint publications
Kathleen B M Claes
2 joint publications
Petra Kleiblova
2 joint publications
Elfride De Baere
1 joint publications
Reiner A Veitia
1 joint publications
Miriam Bauwens
1 joint publications
Giulia Ascari
1 joint publications
Frank Peelman
