Sarah S. Park

发表

A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.

Jason M. Johnson, M. Rieder, D. Nickerson, 2012, American journal of human genetics.

Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis.

D. Nickerson, Joshua D. Smith, B. Mecham, 2014, American journal of human genetics.

Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome

A. Munnich, M. Bitner-Glindzicz, E. Tobias, 2013, Journal of Medical Genetics.

Directed differentiation of human pluripotent cells to neural crest stem cells

S. Dalton, M. Kulik, M. Cunningham, 2013, Nature Protocols.

Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosis.

M. Smyth, B. Mecham, R. Beyer, 2015, Bone.

Copy Number Variation Analysis in Single-Suture Craniosynostosis: Multiple Rare Variants Including RUNX2 Duplication in Two Cousins With Metopic Craniosynostosis

Francesca Antonacci, Heather C Mefford, Evan E Eichler, 2010, American journal of medical genetics. Part A.

Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome.

M. Waldenberger, T. Wieland, T. Meitinger, 2014, American journal of human genetics.

IGF1R variants associated with isolated single suture craniosynostosis

M. Rieder, R. Samudrala, M. Cunningham, 2011, American journal of medical genetics. Part A.

“Mandibulofacial dysostosis with microcephaly” caused by EFTUD2 mutations: Expanding the phenotype

M. Rieder, D. Nickerson, Joshua D. Smith, 2013, American journal of medical genetics. Part A.

Differential Expression of Extracellular Matrix-Mediated Pathways in Single-Suture Craniosynostosis

B. Mecham, R. Beyer, M. Cunningham, 2011, PloS one.

Transcriptional analysis of human cranial compartments with different embryonic origins.

James W. MacDonald, B. Mecham, M. Cunningham, 2015, Archives of oral biology.

Activation of the IGF1 pathway mediates changes in cellular contractility and motility in single-suture craniosynostosis

Joshua D. Smith, M. Cunningham, N. Sniadecki, 2016, Journal of Cell Science.

Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model

M. Cunningham, Sarah S. Park, Jonas A. Gustafson, 2019, PloS one.

Unique Sex-Based Approach Identifies Transcriptomic Biomarkers Associated with Non-Syndromic Craniosynostosis

R. Beyer, M. Cunningham, T. Bammler, 2012, Gene regulation and systems biology.

Pfeiffer Syndrome Type 3 and Prune Belly Anomaly in a Female: Case Report and Review

Sarah S. Park, L. Bobadilla-Morales, J. Corona-Rivera, 2019, Fetal and pediatric pathology.

Transcriptional analysis of human cranial compartments with different embryonic origins.

James W. MacDonald, B. Mecham, M. Cunningham, 2015, Archives of oral biology.