Associated Papers
Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non-syndromic sagittal and metopic craniosynostosis.
Walton IS et al.
Journal of Anatomy, 2024
38760592 (PubMed )
Supplement: JOA-245-874-s001.zip › joa14052-sup-0001-Supinfo › joa14052-sup-0002-Supinfo.xlsx › Sheet1
Evolutionary history of adenomas to colorectal cancer in FAP families.
Yang C et al.
Frontiers in Genetics, 2024
39021676 (PubMed )
Supplement: DataSheet1.ZIP › Somatic › 19R03641.xls › SNVIndel
Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape.
Goovaerts S et al.
Nature Communications, 2023
Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis.
Cuellar A et al.
Bone, 2020
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