N. Katsanis
Molecular Biology · 2001–2016
A researcher in the Science corpus: 12 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 132 citations into it
- Genetics — 120 citations into it
Whom N. Katsanis trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- K. Anderson (in Genetics)
Papers from N. Katsanis's perspective
Ordered by how strongly the researchers N. Katsanis trusts endorse each paper. Same corpus, a different order for every researcher.
- Chlamydomonas IFT88 and Its Mouse Homologue, Polycystic Kidney Disease Gene Tg737, Are Required for Assembly of Cilia and Flagella (Journal of Cell Biology)
- Vertebrate Smoothened functions at the primary cilium (Nature)
- The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia. (Journal of the American Society of Nephrology)
- The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein (Nature Genetics)
- Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates (Nature Genetics)
- Pilus retraction powers bacterial twitching motility (Nature)
- Cell Cycle via Direct Activation of the JAK-STAT Signaling Pathway in a Process Requiring PKD2
- Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse. (Current Biology)
- The conserved Bardet-Biedl Syndrome proteins assemble a coat that traffics membrane proteins to cilia (Cell)
- Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents (Nature)
Their papers
- Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia (2016) — 1,080 citations
- Seven New Loci Associated with Age-Related Macular Degeneration (2013) — 796 citations
- Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder (2001) — 675 citations
- The ciliopathies: an emerging class of human genetic disorders. (2006) — 1,198 citations
- Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene. (2004) — 798 citations
- Disruptive CHD8 mutations define a subtype of autism early in development (2014) — 750 citations
- A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 (2005) — 1,760 citations
- A Transition Zone Complex Regulates Mammalian Ciliogenesis and Ciliary Membrane Composition (2011) — 654 citations
- Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates (2005) — 623 citations
- Identification of cis-suppression of human disease mutations by comparative genomics (2015) — 120 citations
- The Vertebrate Primary Cilium in Development, Homeostasis, and Disease (2009) — 751 citations
- Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome (2003) — 714 citations