Katsanis N - Search Results

1

The continuum of causality in human genetic disorders.

Katsanis N. Katsanis N. Genome Biol. 2016 Nov 17;17(1):233. doi: 10.1186/s13059-016-1107-9. Genome Biol. 2016. PMID: 27855690 Free PMC article.

2

Point: Treating Human Genetic Disease One Base Pair at a Time: The Benefits of Gene Editing.

Katsanis N. Katsanis N. Clin Chem. 2018 Mar;64(3):486-488. doi: 10.1373/clinchem.2017.278309. Clin Chem. 2018. PMID: 29490998 No abstract available.

3

Molecular genetic testing and the future of clinical genomics.

Katsanis SH, Katsanis N. Katsanis SH, et al. Among authors: katsanis n. Nat Rev Genet. 2013 Jun;14(6):415-26. doi: 10.1038/nrg3493. Nat Rev Genet. 2013. PMID: 23681062 Free PMC article. Review.

4

From association to causality: the new frontier for complex traits.

Katsanis N. Katsanis N. Genome Med. 2009 Feb 25;1(2):23. doi: 10.1186/gm23. Genome Med. 2009. PMID: 19341494 Free PMC article.

5

Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.

Khan TN, Khan K, Sadeghpour A, Reynolds H, Perilla Y, McDonald MT, Gallentine WB, Baig SM; Task Force for Neonatal Genomics; Davis EE, Katsanis N. Khan TN, et al. Among authors: katsanis n. Am J Hum Genet. 2019 Jan 3;104(1):94-111. doi: 10.1016/j.ajhg.2018.11.017. Am J Hum Genet. 2019. PMID: 30609410 Free PMC article.

6

The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling.

Goetz SC, Bangs F, Barrington CL, Katsanis N, Anderson KV. Goetz SC, et al. Among authors: katsanis n. PLoS One. 2017 Mar 14;12(3):e0173399. doi: 10.1371/journal.pone.0173399. eCollection 2017. PLoS One. 2017. PMID: 28291807 Free PMC article.

7

Managing incidental genomic findings in clinical trials: fulfillment of the principle of justice.

Dal-Ré R, Katsanis N, Katsanis S, Parker LS, Ayuso C. Dal-Ré R, et al. Among authors: katsanis n, katsanis s. PLoS Med. 2014 Jan;11(1):e1001584. doi: 10.1371/journal.pmed.1001584. Epub 2014 Jan 14. PLoS Med. 2014. PMID: 24453945 Free PMC article.

8

Microtubule transport defects in neurological and ciliary disease.

Gerdes JM, Katsanis N. Gerdes JM, et al. Among authors: katsanis n. Cell Mol Life Sci. 2005 Jul;62(14):1556-70. doi: 10.1007/s00018-005-5007-5. Cell Mol Life Sci. 2005. PMID: 15924265 Review.

9

Ciliary proteins and exencephaly.

Katsanis N. Katsanis N. Nat Genet. 2006 Feb;38(2):135-6. doi: 10.1038/ng0206-135. Nat Genet. 2006. PMID: 16444248 No abstract available.

10

An age-old problem.

Katsanis N, Rosenberg SM. Katsanis N, et al. PLoS Genet. 2007 Feb 23;3(2):e37. doi: 10.1371/journal.pgen.0030037. PLoS Genet. 2007. PMID: 17319751 Free PMC article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

308 results

Search Page