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Rapamycin improves TIE2-mutated venous malformation in murine model and human subjectsElisa Boscolo, Nisha Limaye, Lan Huang et al.|Journal of Clinical Investigation|2015Cited by 240
Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromesM. H. Basha, Miikka Vikkula|Journal of Medical Genetics|2018Cited by 113
Loss-of-function mutations of the TIE1 receptor tyrosine kinase cause late-onset primary lymphedemaPascal Brouillard, Miikka Vikkula|Journal of Clinical Investigation|2024Cited by 15
Somatic Loss-of-Function PIK3R1 and Activating Non-hotspot PIK3CA Mutations Associated with Capillary Malformation with Dilated Veins (CMDV)Martina De Bortoli, Miikka Vikkula|Journal of Investigative Dermatology|2024Cited by 12