BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Queisser A, Seront E, Boon LM, Vikkula M. Genetic Basis and Therapies for Vascular Anomalies. Circ Res 2021;129:155-73. [PMID: 34166070 DOI: 10.1161/CIRCRESAHA.121.318145] [Cited by in Crossref: 22] [Cited by in F6Publishing: 25] [Article Influence: 11.0] [Reference Citation Analysis]
Number Citing Articles
1 Popler J, Vece TJ, Liptzin DR, Gower WA. Pediatric pulmonology 2021 year in review: Rare and diffuse lung disease. Pediatr Pulmonol 2023;58:374-81. [PMID: 36426677 DOI: 10.1002/ppul.26227] [Reference Citation Analysis]
2 Petkova M, Kraft M, Stritt S, Martinez-Corral I, Ortsäter H, Vanlandewijck M, Jakic B, Baselga E, Castillo SD, Graupera M, Betsholtz C, Mäkinen T. Immune-interacting lymphatic endothelial subtype at capillary terminals drives lymphatic malformation. J Exp Med 2023;220:e20220741. [PMID: 36688917 DOI: 10.1084/jem.20220741] [Reference Citation Analysis]
3 Pang C, Nisbet R, Gibson M, Evans N, Khalifa M, Papadopoulou A, Tsui J, Hamilton G, Brookes J, Lim CS. Early follow-up quality of life and mental health of patients with congenital vascular malformations cared for in a multi-disciplinary specialist centre. Phlebology 2022. [DOI: 10.1177/02683555221147469] [Reference Citation Analysis]
4 Liu H, Yang X, Jia H, Hu L, Xu Z, Chen H, Lin X. Recurrence and restart of sirolimus in vascular anomalies after withdrawal. The Journal of Dermatology 2022. [DOI: 10.1111/1346-8138.16649] [Reference Citation Analysis]
5 Butnariu LI, Gorduza EV, Florea L, Țarcă E, Moisă ȘM, Trandafir LM, Stoleriu S, Bădescu MC, Luca A, Popa S, Radu I, Cojocaru E. The Genetic Architecture of Vascular Anomalies: Current Data and Future Therapeutic Perspectives Correlated with Molecular Mechanisms. IJMS 2022;23:12199. [DOI: 10.3390/ijms232012199] [Reference Citation Analysis]
6 Rose AL, Cathey SS. Genetic Causes of Vascular Malformations and Common Signaling Pathways Involved in Their Formation. Dermatologic Clinics 2022;40:449-459. [DOI: 10.1016/j.det.2022.07.002] [Reference Citation Analysis]
7 Nozawa A, Fujino A, Yuzuriha S, Suenobu S, Kato A, Shimizu F, Aramaki-Hattori N, Kuniyeda K, Sakaguchi K, Ohnishi H, Aoki Y, Ozeki M. Comprehensive targeted next-generation sequencing in patients with slow-flow vascular malformations. J Hum Genet 2022. [PMID: 36171295 DOI: 10.1038/s10038-022-01081-6] [Reference Citation Analysis]
8 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]
9 Huo R, Wang J, Sun Y, Weng J, Li H, Jiao Y, Xu H, Zhang J, Zhao S, He Q, Wang S, Zhao J, Cao Y. Simplex cerebral cavernous malformations with MAP3K3 mutation have distinct clinical characteristics. Front Neurol 2022;13:946324. [DOI: 10.3389/fneur.2022.946324] [Reference Citation Analysis]
10 Kemp SS, Lin PK, Sun Z, Castaño MA, Yrigoin K, Penn MR, Davis GE. Molecular basis for pericyte-induced capillary tube network assembly and maturation. Front Cell Dev Biol 2022;10:943533. [DOI: 10.3389/fcell.2022.943533] [Reference Citation Analysis]
11 Hongo H, Miyawaki S, Teranishi Y, Mitsui J, Katoh H, Komura D, Tsubota K, Matsukawa T, Watanabe M, Kurita M, Yoshimura J, Dofuku S, Ohara K, Ishigami D, Okano A, Kato M, Hakuno F, Takahashi A, Kunita A, Ishiura H, Shin M, Nakatomi H, Nagao T, Goto H, Takahashi SI, Ushiku T, Ishikawa S, Okazaki M, Morishita S, Tsuji S, Saito N. Somatic GJA4 gain-of-function mutation in orbital cavernous venous malformations. Angiogenesis 2022. [PMID: 35902510 DOI: 10.1007/s10456-022-09846-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
12 Banerjee K, Lin Y, Gahn J, Gupta P, Graupera M, Dobreva G, Schwartz M, Ola R. Excessive fluid shear stress-mediated Klf4 leads to arteriovenous pathogenesis.. [DOI: 10.1101/2022.07.04.498236] [Reference Citation Analysis]
13 Diociaiuti A, Rotunno R, Pisaneschi E, Cesario C, Carnevale C, Condorelli AG, Rollo M, Di Cecca S, Quintarelli C, Novelli A, Zambruno G, El Hachem M. Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study. Biomedicines 2022;10:1460. [PMID: 35740480 DOI: 10.3390/biomedicines10061460] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
14 Petkova M, Kraft M, Stritt S, Martinez-corral I, Ortsäter H, Sun Y, Vanlandewijck M, Jakic B, Baselga E, Castillo SD, Graupera M, Betsholtz C, Mäkinen T. Immunoregulatory subtype of dermal lymphatic endothelial cells at capillary terminals drives lymphatic malformations.. [DOI: 10.1101/2022.05.22.492950] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 van der Vleuten CJM. Genetic understanding of vascular anomalies: better classification and risk-stratification with targeted therapeutic options - a new horizon for vascular anomaly patients. J Eur Acad Dermatol Venereol 2022;36:765-6. [PMID: 35536170 DOI: 10.1111/jdv.18155] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Zhang J, Abou-Fadel J, Renteria M, Belkin O, Chen B, Zhu Y, Dammann P, Rigamonti D. Cerebral cavernous malformations do not fall in the spectrum of PIK3CA-related overgrowth. J Neurol Neurosurg Psychiatry 2022:jnnp-2022-328901. [PMID: 35477890 DOI: 10.1136/jnnp-2022-328901] [Reference Citation Analysis]
17 Byrne AB, Brouillard P, Sutton DL, Kazenwadel J, Montazaribarforoushi S, Secker GA, Oszmiana A, Babic M, Betterman KL, Brautigan PJ, White M, Piltz SG, Thomas PQ, Hahn CN, Rath M, Felbor U, Korenke GC, Smith CL, Wood KH, Sheppard SE, Adams DM, Kariminejad A, Helaers R, Boon LM, Revencu N, Moore L, Barnett C, Haan E, Arts P, Vikkula M, Scott HS, Harvey NL. Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema. Sci Transl Med 2022;14:eabm4869. [PMID: 35235341 DOI: 10.1126/scitranslmed.abm4869] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Sun Z, Kemp SS, Lin PK, Aguera KN, Davis GE. Endothelial k-RasV12 Expression Induces Capillary Deficiency Attributable to Marked Tube Network Expansion Coupled to Reduced Pericytes and Basement Membranes. Arterioscler Thromb Vasc Biol 2022;42:205-22. [PMID: 34879709 DOI: 10.1161/ATVBAHA.121.316798] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
19 Snyder E, Sarma A, Borst AJ, Tekes A. Lymphatic Anomalies in Children: Update on Imaging Diagnosis, Genetics and Treatment. AJR Am J Roentgenol 2022. [PMID: 35043669 DOI: 10.2214/AJR.21.27200] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
20 Schmidt VF, Masthoff M, Czihal M, Cucuruz B, Häberle B, Brill R, Wohlgemuth WA, Wildgruber M. Imaging of peripheral vascular malformations - current concepts and future perspectives. Mol Cell Pediatr 2021;8:19. [PMID: 34874510 DOI: 10.1186/s40348-021-00132-w] [Cited by in Crossref: 3] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
21 Blei F. Update August 2021. Lymphatic Research and Biology 2021;19:391-405. [DOI: 10.1089/lrb.2021.29108.fb] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
22 Janardhan HP, Saheera S, Jung R, Trivedi CM. Vascular and Lymphatic Malformations: Perspectives From Human and Vertebrate Studies. Circ Res 2021;129:131-5. [PMID: 34166069 DOI: 10.1161/CIRCRESAHA.121.319587] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]