Andy Willaert
Overview
Explore the profile of Andy Willaert including associated specialties, affiliations and a list of published articles.
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Articles
54
Citations
1475
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Recent Articles
1.
Huybrechts Y, De Ridder R, Bergen D, De Samber B, Boudin E, Tonelli F, et al.
Calcif Tissue Int
. 2025 Mar;
116(1):52.
PMID: 40085271
The ubiquitin-binding protein p62, encoded by Sequestosome 1 (SQSTM1), is an essential molecular adaptor for selective autophagy. Heterozygous mutations deleting or disrupting the ubiquitin-associated (UBA) domain of p62 have been...
2.
Debaenst S, Jarayseh T, De Saffel H, Bek J, Boone M, Josipovic I, et al.
Elife
. 2025 Jan;
13.
PMID: 39817421
Heritable fragile bone disorders (FBDs), ranging from multifactorial to rare monogenic conditions, are characterized by an elevated fracture risk. Validating causative genes and understanding their mechanisms remain challenging. We assessed...
3.
Jarayseh T, Debaenst S, De Saffel H, Rosseel T, Milazzo M, Bek J, et al.
J Bone Miner Res
. 2024 Nov;
40(1):154-166.
PMID: 39566080
Rare monogenic disorders often exhibit significant phenotypic variability among individuals sharing identical genetic mutations. Bruck syndrome (BS), a prime example, is characterized by bone fragility and congenital contractures, although with...
4.
Lopez Soriano V, Duenas Rey A, Mukherjee R, Coppieters F, Bauwens M, Willaert A, et al.
Nat Commun
. 2024 May;
15(1):3935.
PMID: 38729949
No abstract available.
5.
Lopez Soriano V, Duenas Rey A, Mukherjee R, Coppieters F, Bauwens M, Willaert A, et al.
Nat Commun
. 2024 Feb;
15(1):1600.
PMID: 38383453
Cross-species genome comparisons have revealed a substantial number of ultraconserved non-coding elements (UCNEs). Several of these elements have proved to be essential tissue- and cell type-specific cis-regulators of developmental gene...
6.
Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development
Guillemyn B, De Saffel H, Bek J, Tapaneeyaphan P, De Clercq A, Jarayseh T, et al.
J Bone Miner Res
. 2023 Sep;
38(11):1718-1730.
PMID: 37718532
SNARE proteins comprise a conserved protein family responsible for catalyzing membrane fusion during vesicle traffic. Syntaxin18 (STX18) is a poorly characterized endoplasmic reticulum (ER)-resident t-SNARE. Recently, together with TANGO1 and...
7.
Daponte V, Tonelli F, Masiero C, Syx D, Exbrayat-Heritier C, Biggiogera M, et al.
Matrix Biol
. 2023 Jun;
121:105-126.
PMID: 37336269
Osteogenesis imperfecta (OI) is a family of rare heritable skeletal disorders associated with dominant mutations in the collagen type I encoding genes and recessive defects in proteins involved in collagen...
8.
Vierstraete J, Fieuws C, Creytens D, Van Dorpe J, Willaert A, Vral A, et al.
Genes Dis
. 2023 May;
10(2):381-384.
PMID: 37223540
No abstract available.
9.
Tonelli F, Leoni L, Daponte V, Gioia R, Cotti S, Fiedler I, et al.
Front Endocrinol (Lausanne)
. 2023 Feb;
14:1002914.
PMID: 36755921
Introduction: Trimeric intracellular potassium channels TRIC-A and -B are endoplasmic reticulum (ER) integral membrane proteins, involved in the regulation of calcium release mediated by ryanodine (RyRs) and inositol 1,4,5-trisphosphate (IPRs)...
10.
Jarayseh T, Guillemyn B, De Saffel H, Bek J, Syx D, Symoens S, et al.
Hum Genet
. 2023 Jan;
142(3):457-476.
PMID: 36697720
Bi-allelic mutations in the gene coding for human trans-membrane anterior-posterior transformation protein 1 (TAPT1) result in a broad phenotypic spectrum, ranging from syndromic disease with severe skeletal and congenital abnormalities...