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For: Snellings DA, Girard R, Lightle R, Srinath A, Romanos S, Li Y, Chen C, Ren AA, Kahn ML, Awad IA, Marchuk DA. Developmental venous anomalies are a genetic primer for cerebral cavernous malformations. Nat Cardiovasc Res 2022;1:246-252. [DOI: 10.1038/s44161-022-00035-7] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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1 Huo R, Yang Y, Sun Y, Zhou Q, Zhao S, Mo Z, Xu H, Wang J, Weng J, Jiao Y, Zhang J, He Q, Wang S, Zhao J, Wang J, Cao Y. Endothelial hyperactivation of mutant MAP3K3 induces cerebral cavernous malformation enhanced by PIK3CA GOF mutation. Angiogenesis 2023. [PMID: 36719480 DOI: 10.1007/s10456-023-09866-9] [Reference Citation Analysis]
2 Li Z, Ma L, Quan K, Liu P, Shi Y, Liu Y, Zhu W. Rehemorrhage of brainstem cavernous malformations: a benchmark approach to individualized risk and severity assessment. J Neurosurg 2022;:1-12. [PMID: 36585870 DOI: 10.3171/2022.11.JNS222277] [Reference Citation Analysis]
3 Ren J, Tu T, Hong T, Zhang H. Angioarchitecture and genetic variants of spinal cord cavernous malformations and associated DVAs — A case report.. [DOI: 10.21203/rs.3.rs-2201612/v1] [Reference Citation Analysis]
4 Aw WY, Cho C, Wang H, Cooper AH, Doherty EL, Rocco D, Huang SA, Kubik S, Whitworth CP, Armstrong R, Hickey AJ, Griffith B, Kutys ML, Blatt J, Polacheck WJ. Microphysiological vascular malformation model reveals a role of dysregulated Rac1 and mTORC1/2 in lesion formation.. [DOI: 10.1101/2022.09.03.506415] [Reference Citation Analysis]
5 Angulo-urarte A, Graupera M. When, where and which PIK3CA mutations are pathogenic in congenital disorders. Nat Cardiovasc Res 2022;1:700-714. [DOI: 10.1038/s44161-022-00107-8] [Reference Citation Analysis]