Katsanis, Nicholas

Context-Dependent Regulation of Wnt Signaling through the Primary Cilium

Oh, E. C., & Katsanis, N. (2013) · Journal of the American Society of Nephrology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 73

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Strunz, T., Lauwen, S., Kiel, C., International AMD Genomics Consortium (IAMDGC), Fritsche, L. G., Igl, W., Bailey, J. N. C., Grassmann, F., Sengupta, S., Bragg-Gresham, J. L., et al. (2020) · Scientific Reports

Genetic Associations and EpidemiologyRetinal Diseases and Treatments

Cited by 60

Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions

Arbogast, T., Razaz, P., Ellegood, J., McKinstry, S. U., Erdin, S., Currall, B., Aneichyk, T., Lerch, J. P., Qiu, L. R., Rodriguiz, R. M., et al. (2019) · Human Molecular Genetics

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 52

Microtubule transport defects in neurological and ciliary disease

Gerdes, J. M., & Katsanis, N. (2005) · Cellular and Molecular Life Sciences

Genetic and Kidney Cyst DiseasesMicrotubule and mitosis dynamics

Cited by 51

The complexity of the cilium: spatiotemporal diversity of an ancient organelle

Heydeck, W., Fievet, L., Davis, E. E., & Katsanis, N. (2018) · Current Opinion in Cell Biology

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 25

Life without Centrioles: Cilia in the Spotlight

Badano, J. L., & Katsanis, N. (2006) · Cell

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 19

De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder

Küry, S., Besnard, T., Ebstein, F., Khan, T. N., Gambin, T., Douglas, J., Bacino, C. A., Craigen, W. J., Sanders, S. J., Lehmann, A., et al. (2017) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersUbiquitin and proteasome pathways

Cited by 19