Michael L Cunningham
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Explore the profile of Michael L Cunningham including associated specialties, affiliations and a list of published articles.
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160
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3257
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Recent Articles
1.
Linkugel A, Cunningham M, Susarla S
Plast Reconstr Surg
. 2024 Nov;
154(6):1359-1360.
PMID: 39589294
No abstract available.
2.
Richardson C, Lam A, Nicholas G, Wang X, Sie K, Perkins J, et al.
Otolaryngol Head Neck Surg
. 2024 Sep;
172(1):307-312.
PMID: 39248218
Objective: The aim of this study was to assess the utility of ultrasound (US) imaging for diagnosis of abnormal tracheal morphology, such as tracheal cartilaginous sleeves (TCS), in patients with...
3.
Timberlake A, Hemal K, Gustafson J, Hao L, Valenzuela I, Slavotinek A, et al.
J Neurosurg Pediatr
. 2024 Jun;
34(3):246-251.
PMID: 38905707
Objective: Occurring once in every 2000 live births, craniosynostosis (CS) is the most frequent cranial birth defect. Although the genetic etiologies of syndromic CS cases are well defined, the genetic...
4.
Musolf A, Justice C, Erdogan-Yildirim Z, Goovaerts S, Cuellar A, Shaffer J, et al.
Sci Rep
. 2024 Apr;
14(1):8533.
PMID: 38609424
Craniosynostosis (CS) is a major birth defect resulting from premature fusion of cranial sutures. Nonsyndromic CS occurs more frequently than syndromic CS, with sagittal nonsyndromic craniosynostosis (sNCS) presenting as the...
5.
Hodapp M, Hing A, Gallagher E, Blessing M, Cunningham M
Am J Med Genet A
. 2023 Jul;
191(10):2651-2655.
PMID: 37421219
Isolated frontosphenoidal craniosynostosis (IFSC) is a rare congenital defect defined as premature fusion of the frontosphenoidal suture in the absence of other suture fusion. Until now, IFSC was regarded as...
6.
Aldawood Z, Mancinelli L, Geng X, Yeh S, Di Carlo R, C Leite T, et al.
Proc Natl Acad Sci U S A
. 2023 Apr;
120(16):e2120826120.
PMID: 37040407
In newborn humans, and up to approximately 2 y of age, calvarial bone defects can naturally regenerate. This remarkable regeneration potential is also found in newborn mice and is absent...
7.
Lapehn S, Gustafson J, Timms A, Cunningham M, Paquette A
Int J Mol Sci
. 2023 Mar;
24(6).
PMID: 36982425
Craniosynostosis is a birth defect where calvarial sutures close prematurely, as part of a genetic syndrome or independently, with unknown cause. This study aimed to identify differences in gene expression...
8.
Quiat D, Timberlake A, Curran J, Cunningham M, McDonough B, Artunduaga M, et al.
Genet Med
. 2022 Oct;
25(1):143-150.
PMID: 36260083
Purpose: Craniofacial microsomia (CFM) represents a spectrum of craniofacial malformations, ranging from isolated microtia with or without aural atresia to underdevelopment of the mandible, maxilla, orbit, facial soft tissue, and/or...
9.
Gustafson J, Bjork M, van Ravenswaaij-Arts C, Cunningham M
Case Rep Genet
. 2022 Apr;
2022:3239260.
PMID: 35378950
Craniosynostosis, the premature fusion of the calvarial bones, has numerous etiologies. Among them, several involve mutations in genes related to the TGFb signaling pathway, a critical molecular mediator of human...
10.
Kanai S, Heffner C, Cox T, Cunningham M, Perez F, Bauer A, et al.
Dis Model Mech
. 2022 Mar;
15(4).
PMID: 35284927
Auriculocondylar syndrome 2 (ARCND2) is a rare autosomal dominant craniofacial malformation syndrome linked to multiple genetic variants in the coding sequence of phospholipase C β4 (PLCB4). PLCB4 is a direct...