Michael Fahey

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 589 citations · Full text

Comparative analysis of transforming growth factor-β isoforms 1–3 in human and rabbit dentine matrices

N. Cassidy, Michael Fahey, Stephen S. Prime et al. · Archives of Oral Biology · 1997 · 198 citations

Developmental Biology, Growth Hormone, Bone Morphogenic Protein +9

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

Sheng Chih Jin, Sara A. Lewis, Somayeh Bakhtiari et al. · Nature Genetics · 2020 · 170 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +5

Mutations in <i>TPM3</i> are a common cause of congenital fiber type disproportion

Nigel F. Clarke, Hanna Kolski, Danielle E. Dye et al. · Annals of Neurology · 2008 · 168 citations

Development of a Suspicion Index to aid diagnosis of Niemann-Pick disease type C

Frits A. Wijburg, F. Sedel, M. Pineda et al. · Neurology · 2012 · 150 citations