Graham SA - Search Results

1

Estruch SB, Graham SA, Deriziotis P, Fisher SE. Estruch SB, et al. Among authors: graham sa. Sci Rep. 2016 Feb 12;6:20911. doi: 10.1038/srep20911. Sci Rep. 2016. PMID: 26867680 Free PMC article.

2

Decoding the genetics of speech and language.

Graham SA, Fisher SE. Graham SA, et al. Curr Opin Neurobiol. 2013 Feb;23(1):43-51. doi: 10.1016/j.conb.2012.11.006. Epub 2012 Dec 7. Curr Opin Neurobiol. 2013. PMID: 23228431 Review.

3

De novo TBR1 mutations in sporadic autism disrupt protein functions.

Deriziotis P, O'Roak BJ, Graham SA, Estruch SB, Dimitropoulou D, Bernier RA, Gerdts J, Shendure J, Eichler EE, Fisher SE. Deriziotis P, et al. Among authors: graham sa. Nat Commun. 2014 Sep 18;5:4954. doi: 10.1038/ncomms5954. Nat Commun. 2014. PMID: 25232744 Free PMC article.

4

Understanding Language from a Genomic Perspective.

Graham SA, Fisher SE. Graham SA, et al. Annu Rev Genet. 2015;49:131-60. doi: 10.1146/annurev-genet-120213-092236. Epub 2015 Oct 5. Annu Rev Genet. 2015. PMID: 26442845 Review.

5

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.

Estruch SB, Graham SA, Chinnappa SM, Deriziotis P, Fisher SE. Estruch SB, et al. Among authors: graham sa. J Neurodev Disord. 2016 Nov 28;8:44. doi: 10.1186/s11689-016-9177-2. eCollection 2016. J Neurodev Disord. 2016. PMID: 27933109 Free PMC article.

6

Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.

Estruch SB, Graham SA, Quevedo M, Vino A, Dekkers DHW, Deriziotis P, Sollis E, Demmers J, Poot RA, Fisher SE. Estruch SB, et al. Among authors: graham sa. Hum Mol Genet. 2018 Apr 1;27(7):1212-1227. doi: 10.1093/hmg/ddy035. Hum Mol Genet. 2018. PMID: 29365100

7

Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer.

Deriziotis P, Graham SA, Estruch SB, Fisher SE. Deriziotis P, et al. Among authors: graham sa. J Vis Exp. 2014 May 26;(87):51438. doi: 10.3791/51438. J Vis Exp. 2014. PMID: 24893771 Free PMC article.

8

Insights into the genetic foundations of human communication.

Graham SA, Deriziotis P, Fisher SE. Graham SA, et al. Neuropsychol Rev. 2015 Mar;25(1):3-26. doi: 10.1007/s11065-014-9277-2. Epub 2015 Jan 18. Neuropsychol Rev. 2015. PMID: 25597031 Review.

9

Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.

Sollis E, Graham SA, Vino A, Froehlich H, Vreeburg M, Dimitropoulou D, Gilissen C, Pfundt R, Rappold GA, Brunner HG, Deriziotis P, Fisher SE. Sollis E, et al. Among authors: graham sa. Hum Mol Genet. 2016 Feb 1;25(3):546-57. doi: 10.1093/hmg/ddv495. Epub 2015 Dec 8. Hum Mol Genet. 2016. PMID: 26647308

10

BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.

Dias C, Estruch SB, Graham SA, McRae J, Sawiak SJ, Hurst JA, Joss SK, Holder SE, Morton JE, Turner C, Thevenon J, Mellul K, Sánchez-Andrade G, Ibarra-Soria X, Deriziotis P, Santos RF, Lee SC, Faivre L, Kleefstra T, Liu P, Hurles ME; DDD Study; Fisher SE, Logan DW. Dias C, et al. Among authors: graham sa. Am J Hum Genet. 2016 Aug 4;99(2):253-74. doi: 10.1016/j.ajhg.2016.05.030. Epub 2016 Jul 21. Am J Hum Genet. 2016. PMID: 27453576 Free PMC article.

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