Katsanis N - Search Results

1

Regulation of autism-relevant behaviors by cerebellar-prefrontal cortical circuits.

Kelly E, Meng F, Fujita H, Morgado F, Kazemi Y, Rice LC, Ren C, Escamilla CO, Gibson JM, Sajadi S, Pendry RJ, Tan T, Ellegood J, Basson MA, Blakely RD, Dindot SV, Golzio C, Hahn MK, Katsanis N, Robins DM, Silverman JL, Singh KK, Wevrick R, Taylor MJ, Hammill C, Anagnostou E, Pfeiffer BE, Stoodley CJ, Lerch JP, du Lac S, Tsai PT. Kelly E, et al. Among authors: katsanis n. Nat Neurosci. 2020 Sep;23(9):1102-1110. doi: 10.1038/s41593-020-0665-z. Epub 2020 Jul 13. Nat Neurosci. 2020. PMID: 32661395 Free PMC article.

2

Mitochondrial Copy Number as a Biomarker for Autism?

Golzio C, Katsanis N. Golzio C, et al. Among authors: katsanis n. Pediatrics. 2016 Apr;137(4):e20160049. doi: 10.1542/peds.2016-0049. Epub 2016 Mar 31. Pediatrics. 2016. PMID: 27033113 Free PMC article. No abstract available.

3

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

Arbogast T, Razaz P, Ellegood J, McKinstry SU, Erdin S, Currall B, Aneichyk T, Lerch JP, Qiu LR, Rodriguiz RM, Henkelman RM, Talkowski ME, Wetsel WC, Golzio C, Katsanis N. Arbogast T, et al. Among authors: katsanis n. Hum Mol Genet. 2019 May 1;28(9):1474-1486. doi: 10.1093/hmg/ddy436. Hum Mol Genet. 2019. PMID: 30590535 Free PMC article.

4

Genetic architecture of reciprocal CNVs.

Golzio C, Katsanis N. Golzio C, et al. Among authors: katsanis n. Curr Opin Genet Dev. 2013 Jun;23(3):240-8. doi: 10.1016/j.gde.2013.04.013. Epub 2013 Jun 5. Curr Opin Genet Dev. 2013. PMID: 23747035 Free PMC article. Review.

5

Rbm8a haploinsufficiency disrupts embryonic cortical development resulting in microcephaly.

Mao H, Pilaz LJ, McMahon JJ, Golzio C, Wu D, Shi L, Katsanis N, Silver DL. Mao H, et al. Among authors: katsanis n. J Neurosci. 2015 May 6;35(18):7003-18. doi: 10.1523/JNEUROSCI.0018-15.2015. J Neurosci. 2015. PMID: 25948253 Free PMC article.

6

Identification of cis-suppression of human disease mutations by comparative genomics.

Jordan DM, Frangakis SG, Golzio C, Cassa CA, Kurtzberg J; Task Force for Neonatal Genomics; Davis EE, Sunyaev SR, Katsanis N. Jordan DM, et al. Among authors: katsanis n. Nature. 2015 Aug 13;524(7564):225-9. doi: 10.1038/nature14497. Epub 2015 Jun 29. Nature. 2015. PMID: 26123021 Free PMC article.

7

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.

Golzio C, Willer J, Talkowski ME, Oh EC, Taniguchi Y, Jacquemont S, Reymond A, Sun M, Sawa A, Gusella JF, Kamiya A, Beckmann JS, Katsanis N. Golzio C, et al. Among authors: katsanis n. Nature. 2012 May 16;485(7398):363-7. doi: 10.1038/nature11091. Nature. 2012. PMID: 22596160 Free PMC article.

8

Phosphorylation of Threonine 794 on Tie1 by Rac1/PAK1 Reveals a Novel Angiogenesis Regulatory Pathway.

Reinardy JL, Corey DM, Golzio C, Mueller SB, Katsanis N, Kontos CD. Reinardy JL, et al. Among authors: katsanis n. PLoS One. 2015 Oct 5;10(10):e0139614. doi: 10.1371/journal.pone.0139614. eCollection 2015. PLoS One. 2015. PMID: 26436659 Free PMC article.

9

In vivo modeling of the morbid human genome using Danio rerio.

Niederriter AR, Davis EE, Golzio C, Oh EC, Tsai IC, Katsanis N. Niederriter AR, et al. Among authors: katsanis n. J Vis Exp. 2013 Aug 24;(78):e50338. doi: 10.3791/50338. J Vis Exp. 2013. PMID: 23995499 Free PMC article.

10

Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome.

Helm BM, Willer JR, Sadeghpour A, Golzio C, Crouch E, Vergano SS, Katsanis N, Davis EE. Helm BM, et al. Among authors: katsanis n. Hum Genomics. 2017 Jul 19;11(1):16. doi: 10.1186/s40246-017-0111-9. Hum Genomics. 2017. PMID: 28724397 Free PMC article.

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