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Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population.
Vanneste M, Hoskens H, Goovaerts S, Matthews H, Devine J, Aponte JD, Cole J, Shriver M, Marazita ML, Weinberg SM, Walsh S, Richmond S, Klein OD, Spritz RA, Peeters H, Hallgrímsson B, Claes P. Vanneste M, et al. Among authors: peeters h. Nat Commun. 2024 Dec 2;15(1):10458. doi: 10.1038/s41467-024-54839-1. Nat Commun. 2024. PMID: 39622794 Free PMC article.
Mapping genes for human face shape: Exploration of univariate phenotyping strategies.
Yuan M, Goovaerts S, Vanneste M, Matthews H, Hoskens H, Richmond S, Klein OD, Spritz RA, Hallgrimsson B, Walsh S, Shriver MD, Shaffer JR, Weinberg SM, Peeters H, Claes P. Yuan M, et al. Among authors: peeters h. PLoS Comput Biol. 2024 Dec 2;20(12):e1012617. doi: 10.1371/journal.pcbi.1012617. eCollection 2024 Dec. PLoS Comput Biol. 2024. PMID: 39621772 Free PMC article.
Multiple paralogues and recombination mechanisms contribute to the high incidence of 22q11.2 Deletion Syndrome.
Vervoort L, Dierckxsens N, Sousa Santos M, Meynants S, Souche E, Cools R, Heung T, Devriendt K, Peeters H, McDonald-McGinn D, Swillen A, Breckpot J, Emanuel BS, Van Esch H, Bassett AS, Vermeesch JR. Vervoort L, et al. Among authors: peeters h. Genome Res. 2024 Nov 13:gr.279331.124. doi: 10.1101/gr.279331.124. Online ahead of print. Genome Res. 2024. PMID: 39537358
Mapping genes for human face shape: exploration of univariate phenotyping strategies.
Yuan M, Goovaerts S, Vanneste M, Matthews H, Hoskens H, Richmond S, Klein OD, Spritz RA, Hallgrimsson B, Walsh S, Shriver MD, Shaffer JR, Weinberg SM, Peeters H, Claes P. Yuan M, et al. Among authors: peeters h. bioRxiv [Preprint]. 2024 Jun 7:2024.06.06.597731. doi: 10.1101/2024.06.06.597731. bioRxiv. 2024. Update in: PLoS Comput Biol. 2024 Dec 2;20(12):e1012617. doi: 10.1371/journal.pcbi.1012617 PMID: 38895298 Free PMC article. Updated. Preprint.
327 results