M. Cunningham

PC16. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia
20230 citationsauthor #3
Isolated frontosphenoidal craniosynostosis: An argument for genetic testing
20230 citationsauthor #5
Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes
20232 citationsauthor #4
Mechanism of Disease: Recessive ADAMTSL4 Mutations and Craniosynostosis with Ectopia Lentis
20227 citationsauthor #4
Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants
202212 citationsauthor #4
Damaging variants in FOXI3 cause microtia and craniofacial microsomia
202217 citationsauthor #4
Complex Airway Management in Patients with Tracheal Cartilaginous Sleeves
20215 citationsauthor #2
Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders
20217 citationsauthor #6
Accuracy and Reliability of 4D-CT and Flexible Laryngoscopy in Upper Airway Evaluation in Robin Sequence
20215 citationsauthor #7
Haploinsufficiency of SF3B2 causes craniofacial microsomia
202169 citationsauthor #5
42. Laboratory and clinician collaboration yields results: Development of a comprehensive craniosynostosis genetic testing panel with a high diagnostic rate
20210 citationsauthor #7
SMAD6 variants in craniosynostosis: genotype and phenotype evaluation
202046 citationsauthor #9
Genotype–Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice
202015 citationsauthor #8
Predicting calvarial morphology in sagittal craniosynostosis
202025 citationsauthor #5
A Comparative Study of Two Infant Feeding Tools: The Nifty Cup and The Paladai
20207 citationsauthor #5
The legacy of language: Disfigurement bias in the NICU
20201 citationsauthor #2
Motor Function in School-Aged Children With Positional Plagiocephaly or Brachycephaly
20206 citationsauthor #4
Do Infant Motor Skills Mediate the Association Between Positional Plagiocephaly/Brachycephaly and Cognition in School-Aged Children?
20206 citationsauthor #5
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis
202028 citationsauthor #5
Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluation
20201 citationsauthor #9
S7A-02 SESSION 7A
20190 citationsauthor #4
Heterozygous Mutations of FREM 1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice
20196 citationsauthor #15
Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model
20198 citationsauthor #3
Cognitive Outcomes and Positional Plagiocephaly
201966 citationsauthor #4
A randomized crossover trial comparing the Nifty cup to a medicine cup in preterm infants who have difficulty breastfeeding at Komfo Anokye Teaching Hospital (KATH) in Kumasi, Ghana
201911 citationsauthor #4
Associations between laterality of orofacial clefts and medical and academic outcomes
201820 citationsauthor #6
Genetic associations and phenotypic heterogeneity in the craniosynostotic rabbit
20182 citationsauthor #6
Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290‐300
20181 citationsauthor #13
A genotype-specific surgical approach for patients with Pfeiffer syndrome due to W290C pathogenic variant in FGFR2 is associated with improved developmental outcomes and reduced mortality
201812 citationsauthor #5
Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms
201840 citationsauthor #13
Associations between laterality of orofacial clefts and medical and academic outcomes
20182 citationsauthor #6
Cell Mechanics of Craniosynostosis.
201723 citationsauthor #2
Structural brain differences in school-age children with and without single-suture craniosynostosis.
201723 citationsauthor #10
A Standard Set of Outcome Measures for the Comprehensive Appraisal of Cleft Care
2017161 citationsauthor #7
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development
2017113 citationsauthor #46
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology
2016161 citationsauthor #7
The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community
2016102 citationsauthor #5
Activation of the IGF1 pathway mediates changes in cellular contractility and motility in single-suture craniosynostosis
201617 citationsauthor #11
Using the 3D Facial Norms Database to investigate craniofacial sexual dimorphism in healthy children, adolescents, and adults
201683 citationsauthor #4
Feeding Neonates by Cup: A Systematic Review of the Literature
201630 citationsauthor #6
Intracranial pressure changes during mouse development.
201633 citationsauthor #6
Craniosynostosis and risk factors related to thyroid dysfunction
201526 citationsauthor #4
Molecular Genetics and Biology of Craniofacial Craniosynostoses
20151 citationsauthor #4
Intellectual and Academic Functioning of School-Age Children With Single-Suture Craniosynostosis
2015122 citationsauthor #7
Craniosynostosis: The Potential Contribution of Thyroid-Related Mechanisms
20154 citationsauthor #3
Maternofetal Trauma in Craniosynostosis
201525 citationsauthor #6
Final report on exposure during pregnancy from a pregnancy registry for quadrivalent human papillomavirus vaccine.
201548 citationsauthor #5
Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders
201545 citationsauthor #3
Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosis.
201522 citationsauthor #10
Transcriptional analysis of human cranial compartments with different embryonic origins.
201515 citationsauthor #8
Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndrome
20147 citationsauthor #11
Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis.
201456 citationsauthor #11
MAPK/ERK Signaling Pathway Analysis in Primary Osteoblasts from Patients with Nonsyndromic Sagittal Craniosynostosis
20148 citationsauthor #3
Quantification of skull deformity for craniofacial research
20143 citationsauthor #2
Using Induced Pluripotent Stem Cells as a Tool to Understand Neurocristopathies
20143 citationsauthor #3
Classifying Craniosynostosis with a 3D Projection-Based Feature Extraction System
20148 citationsauthor #2
Oculoauriculofrontonasal syndrome: Case series revealing new bony nasal anomalies in an old syndrome
201317 citationsauthor #4
“Mandibulofacial dysostosis with microcephaly” caused by EFTUD2 mutations: Expanding the phenotype
201372 citationsauthor #8
Directed differentiation of human pluripotent cells to neural crest stem cells
2013197 citationsauthor #6
Development at Age 36 Months in Children With Deformational Plagiocephaly
2013111 citationsauthor #5
Preferential Associated Anomalies in 818 Cases of Microtia in South America
201328 citationsauthor #5
Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome
201351 citationsauthor #46
Bathrocephaly: A Head Shape Associated with a Persistent Mendosal Suture
201318 citationsauthor #4
Laypersons’ Ratings of Appearance in Children With and Without Single-Suture Craniosynostosis
201313 citationsauthor #5
Evaluating fontanels in the newborn skull
20134 citationsauthor #3
Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations
201326 citationsauthor #9
Perspectives and challenges in advancing research into craniofacial anomalies
201319 citationsauthor #3
Skull Retrieval for Craniosynostosis Using Sparse Logistic Regression Models
201214 citationsauthor #3
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.
201293 citationsauthor #19
Brain volume and shape in infants with deformational plagiocephaly
201247 citationsauthor #6
Erratum: A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome ((The American Journal of Human Genetics (2012) 90 (907-914))
20120 citationsauthor #19
Unique Sex-Based Approach Identifies Transcriptomic Biomarkers Associated with Non-Syndromic Craniosynostosis
20125 citationsauthor #5
Multicenter study of neurodevelopment in 3-year-old children with and without single-suture craniosynostosis.
201294 citationsauthor #6
Longitudinal, three-dimensional analysis of head shape in children with and without deformational plagiocephaly or brachycephaly.
201230 citationsauthor #5
Table 1. [Summary of Molecular Genetic Testing Used in Saethre-Chotzen Syndrome].
20120 citationsauthor #3
New developments in genetic diagnosis: implications for the craniofacial surgeon.
20121 citationsauthor #3
A genome wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP 2 and within BBS 9
201223 citationsauthor #10
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
2012119 citationsauthor #10
Parameters of Care for Craniosynostosis
2012126 citationsauthor #5
Microtia: Epidemiology and genetics
2012388 citationsauthor #4
ALX4 gain‐of‐function mutations in nonsyndromic craniosynostosis
201229 citationsauthor #11
IGF1R variants associated with isolated single suture craniosynostosis
201132 citationsauthor #1
Craniosynostosis: Developing Parameters for Diagnosis, Treatment, and Management
20110 citationsauthor #3
Robin Sequence: From Diagnosis to Development of an Effective Management Plan
2011270 citationsauthor #6
Nasopharyngeal Airway for Management of Airway Obstruction in Infants with Micrognathia
201146 citationsauthor #5
Development in toddlers with and without deformational plagiocephaly.
2011113 citationsauthor #6
Differential Expression of Extracellular Matrix-Mediated Pathways in Single-Suture Craniosynostosis
201144 citationsauthor #7
The FaceBase Consortium: a comprehensive program to facilitate craniofacial research.
201177 citationsauthor #8
Mutation discovery in mice by whole exome sequencing
2011110 citationsauthor #25
Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes.
201137 citationsauthor #4
Genotype–phenotype analysis of the branchio‐oculo‐facial syndrome
201172 citationsauthor #12
Classification and feature selection for craniosynostosis
201117 citationsauthor #3
Disease risk of missense mutations using structural inference from predicted function.
20103 citationsauthor #4
Copy Number Variation Analysis in Single-Suture Craniosynostosis: Multiple Rare Variants Including RUNX2 Duplication in Two Cousins With Metopic Craniosynostosis
201081 citationsauthor #11
Reading in children with orofacial clefts versus controls.
201068 citationsauthor #4
Case-Control Study of Neurodevelopment in Deformational Plagiocephaly
2010125 citationsauthor #8
Pediatric sleep apnea and craniofacial anomalies: A population‐based case–control study
201087 citationsauthor #5
Shape-Based Classification of 3D Head Data
200912 citationsauthor #7
Picture Perfect? Reliability of Craniofacial Anthropometry Using Three-Dimensional Digital Stereophotogrammetry
2009109 citationsauthor #2
3 D Head Shape Quantification for Infants with and without
20091 citationsauthor #7

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