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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Recent Articles
11.
Timberlake A, Griffin C, Heike C, Hing A, Cunningham M, Chitayat D, et al.
Nat Commun
. 2021 Aug;
12(1):4680.
PMID: 34344887
Craniofacial microsomia (CFM) is the second most common congenital facial anomaly, yet its genetic etiology remains unknown. We perform whole-exome or genome sequencing of 146 kindreds with sporadic (n = ...
12.
Lam A, Bindschadler M, Evans K, Friedman S, Blessing M, Bly R, et al.
Otolaryngol Head Neck Surg
. 2021 Jul;
166(4):760-767.
PMID: 34253111
Objectives: To evaluate the performance of 4-dimensional computed tomography (4D-CT) in assessing upper airway obstruction (UAO) in patients with Robin sequence (RS) and compare the accuracy and reliability of 4D-CT...
13.
Noble A, Cunningham M, Lam A, Wenger T, Sie K, Perkins J, et al.
Laryngoscope
. 2021 Jun;
132(1):215-221.
PMID: 34133757
Objectives/hypothesis: A tracheal cartilaginous sleeve (TCS) is a rare anomaly characterized by anterior fusion of tracheal cartilages. TCS is associated with syndromic craniosynostoses including Apert, Crouzon and Pfeiffer syndromes and...
14.
Calpena E, Wurmser M, McGowan S, Atique R, Bertola D, Cunningham M, et al.
J Med Genet
. 2021 Jan;
59(2):165-169.
PMID: 33436522
Background: Pathogenic heterozygous variants (predominantly missense) occur in branchio-otic syndrome (BOS), but an association with craniosynostosis has not been reported. Methods: We investigated probands with craniosynostosis of unknown cause using...
15.
Collett B, Wallace E, Ola C, Kartin D, Cunningham M, Speltz M
Phys Ther
. 2020 Dec;
101(2).
PMID: 33340327
Objective: Positional plagiocephaly/brachycephaly (PPB) is associated with lower cognitive scores in school-aged children. This study tested the hypothesis that infant motor skills mediate this association. Methods: Children with a history...
16.
Lam A, Liu C, Deutsch G, Rivera J, Perkins J, Holmes G, et al.
Laryngoscope
. 2020 Sep;
131(4):E1349-E1356.
PMID: 32886384
Objectives: To characterize tracheal cartilage morphology in mouse models of fibroblast growth factor receptor (Fgfr2)-related craniosynostosis syndromes. To establish relationships between specific Fgfr2 mutations and tracheal cartilaginous sleeve (TCS) phenotypes...
17.
Calpena E, Cuellar A, Bala K, Swagemakers S, Koelling N, McGowan S, et al.
Genet Med
. 2020 Jul;
22(9):1567.
PMID: 32636483
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
18.
Calpena E, Cuellar A, Bala K, Swagemakers S, Koelling N, McGowan S, et al.
Genet Med
. 2020 Jun;
22(9):1498-1506.
PMID: 32499606
Purpose: Enrichment of heterozygous missense and truncating SMAD6 variants was previously reported in nonsyndromic sagittal and metopic synostosis, and interaction of SMAD6 variants with a common polymorphism nearBMP2 (rs1884302) was...
19.
Justice C, Cuellar A, Bala K, Sabourin J, Cunningham M, Crawford K, et al.
Hum Genet
. 2020 Apr;
139(8):1077-1090.
PMID: 32266521
Our previous genome-wide association study (GWAS) for sagittal nonsyndromic craniosynostosis (sNCS) provided important insights into the genetics of midline CS. In this study, we performed a GWAS for a second...
20.
Collett B, Kartin D, Wallace E, Cunningham M, Speltz M
Pediatr Phys Ther
. 2020 Mar;
32(2):107-112.
PMID: 32218071
Objective: To determine whether children with a history of positional plagiocephaly/brachycephaly (PPB) show persistent deficits in motor development. Methods: In a longitudinal cohort study, we completed follow-up assessments with 187...