Cunningham, Michael L.

Intellectual and academic functioning of school-age children with single-suture craniosynostosis

Speltz, M. L., Collett, B. R., Wallace, E. R., Starr, J. R., Cradock, M. M., Buono, L., Cunningham, M., & Kapp-Simon, K. (2015) · PEDIATRICS

Craniofacial Disorders and TreatmentsPectus Deformity Diagnosis and Treatment

Cited by 150

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

Justice, C. M., Yagnik, G., Kim, Y., Peter, I., Jabs, E. W., Erazo, M., Ye, X., Ainehsazan, E., Shi, L., Cunningham, M. L., et al. (2012) · Nature Genetics

Craniofacial Disorders and TreatmentsGenomics and Rare Diseases

Cited by 140

Progressive Postnatal Craniosynostosis and Increased Intracranial Pressure

Connolly, J. P., Gruss, J., Seto, M. L., Whelan, M. F., Ellenbogen, R., Weiss, A., Buchman, S. R., & Cunningham, M. L. (2004) · Plastic and Reconstructive Surgery

Craniofacial Disorders and TreatmentsTraumatic Brain Injury and Neurovascular Disturbances

Cited by 115

Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations

Seto, M. L., Hing, A. V., Chang, J., Hu, M., Kapp‐Simon, K. A., Patel, P. K., Burton, B. K., Kane, A. A., Smyth, M. D., Hopper, R., et al. (2007) · American Journal of Medical Genetics Part A

Craniofacial Disorders and Treatmentsdental development and anomalies

Cited by 108

New scaphocephaly severity indices of sagittal craniosynostosis: A comparative study with cranial index quantifications

Ruiz-Correa, S., Sze, R. W., Starr, J. R., Lin, H.-T. J., Speltz, M. L., Cunningham, M. L., & Hing, A. V. (2006) · The Cleft Palate-Craniofacial Journal

Craniofacial Disorders and TreatmentsPectus Deformity Diagnosis and Treatment

Cited by 90

Copy number variation analysis in single‐suture craniosynostosis: Multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis

Mefford, H. C., Shafer, N., Antonacci, F., Tsai, J. M., Park, S. S., Hing, A. V., Rieder, M. J., Smyth, M. D., Speltz, M. L., Eichler, E. E., et al. (2010) · American Journal of Medical Genetics Part A

Craniofacial Disorders and TreatmentsGenomic variations and chromosomal abnormalities

Cited by 78

Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms

Clarke, C. M., Fok, V. T., Gustafson, J. A., Smyth, M. D., Timms, A. E., Frazar, C. D., Smith, J. D., Birgfeld, C. B., Lee, A., Ellenbogen, R. G., et al. (2018) · American Journal of Medical Genetics Part A

Craniofacial Disorders and TreatmentsGenomics and Rare Diseases

Cited by 44

Craniosynostosis and risk factors related to thyroid dysfunction

Carmichael, S. L., Ma, C., Rasmussen, S. A., Cunningham, M. L., Browne, M. L., Dosiou, C., Lammer, E. J., & Shaw, G. M. (2015) · American Journal of Medical Genetics Part A

Craniofacial Disorders and TreatmentsThyroid Disorders and Treatments

Cited by 32

Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosis

Park, S. S., Beyer, R. P., Smyth, M. D., Clarke, C. M., Timms, A. E., Bammler, T. K., Stamper, B. D., Mecham, B. H., Gustafson, J. A., & Cunningham, M. L. (2015) · Bone

Craniofacial Disorders and TreatmentsBone Metabolism and Diseases

Cited by 27

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

Kobren, S. N., Baldridge, D., Velinder, M., Krier, J. B., LeBlanc, K., Esteves, C., Pusey, B. N., Züchner, S., Blue, E., Lee, H., et al. (2021) · Genetics in Medicine

Genomics and Rare DiseasesGenomics and Phylogenetic Studies

Cited by 27

Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes

Lapehn, S., Gustafson, J. A., Timms, A. E., Cunningham, M. L., & Paquette, A. G. (2023) · International Journal of Molecular Sciences

Craniofacial Disorders and Treatmentsdental development and anomalies

Cited by 3