The ciliopathies: an emerging class of human genetic disorders.
By José L. Badano, N. Mitsuma, P. Beales, N. Katsanis. Annual review of genomics and human genetics (Print), 2006
1,198 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/785386a3b94356a12687a829c233516c5c69f55a
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Genetics
In Molecular Biology
- Arturo Alvarez-Buylla
- Jose Manuel García-Verdugo
- Julie Dawn Thompson
- Alexis Allot
- Guo-li Ming
- Rebecca A. Ihrie
- Hongjun Song
- Erik S. Wright
Citations in the corpus
- Hedgehog signaling and primary cilia are required for the formation of adult neural stem cells (2008, background): “Defective primary cilia have been associated with diverse human diseases including Alstrom, Bardet-Biedl, Joubert, Meckel-Gruber and Oral-facial-digital type 1 syndrome”
- Insights into Ciliary Genes and Evolution from Multi-Level Phylogenetic Profiling (2017, background): “With such a diversity of ciliary functions, ciliary dysfunctions are linked to a wide range of human genetic diseases, known as ciliopathies, encompassing a large variety of symptoms (Badano et al. 2006).”