Caitlin A. Chang

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

Reham Alharatani, Athina Ververi, Ana Beleza‐Meireles et al. · Human Molecular Genetics · 2020 · 40 citations · Full text

Developmental Biology, Signaling Pathway, Genetic Disorder +14

Novel findings and expansion of phenotype in a mosaic <scp>RASopathy</scp> caused by somatic <scp><i>KRAS</i></scp> variants

Caitlin A. Chang, Renée Perrier, Kyle C. Kurek et al. · American Journal of Medical Genetics Part A · 2021 · 38 citations

Mechanisms of benzalkonium chloride toxicity in a human trabecular meshwork cell line and the protective role of preservative‐free tafluprost

Caitlin A. Chang, Angela Q. Zhang, Dov B. Kagan et al. · Clinical and Experimental Ophthalmology · 2014 · 32 citations

Isolated Horner Syndrome From an Elongated Styloid Process (Eagle Syndrome)

Caitlin A. Chang, Tony W. Lin, Kevin Fung et al. · Journal of Neuro-Ophthalmology · 2015 · 25 citations

Isolated Horner Syndrome, Elongated Styloid Process, Medicine +12

Transiently elevated plasma methionine, <i>S</i>‐adenosylmethionine and <i>S</i>‐adenosylhomocysteine: Unreported laboratory findings in a patient with NGLY1 deficiency, a congenital disorder of deglycosylation

Caitlin A. Chang, Xing‐Chang Wei, Steven R. Martin et al. · JIMD Reports · 2019 · 21 citations · Full text