Megan E. Grout

Long-distance communication by specialized cellular projections during pigment pattern development and evolution

Dae Seok Eom, Emily J. Bain, Larissa B. Patterson et al. · eLife · 2015 · 127 citations · Full text

Cytoskeleton, Gene Activity, Optogenetics +26

Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish

Julie C. Van De Weghe, Tamara D. S. Rusterholz, Brooke Latour et al. · The American Journal of Human Genetics · 2017 · 88 citations · Full text

Basal Body Protein, Developmental Biology, Mendelian Disorder +8

MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance

William B. Dobyns, Kimberly A. Aldinger, Gisele E. Ishak et al. · The American Journal of Human Genetics · 2018 · 84 citations · Full text

Axon Guidance, Molecular Neuroscience, Cellular Neurobiology +9

Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome

Brooke Latour, Julie C. Van De Weghe, Tamara D. S. Rusterholz et al. · Journal of Clinical Investigation · 2020 · 82 citations · Full text

Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction

Miroslav P. Milev, Megan E. Grout, Djenann Saint‐Dic et al. · The American Journal of Human Genetics · 2017 · 55 citations · Full text

Neurodegenerative Diseases, Genetic Disorder, Genetics +9