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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 2
2008 4
2009 5
2010 4
2011 7
2012 3
2013 1
2014 3
2015 1
2016 1
2017 2
2020 0
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28 results
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Page 1
Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility.
Bacchelli E, Battaglia A, Cameli C, Lomartire S, Tancredi R, Thomson S, Sutcliffe JS, Maestrini E. Bacchelli E, et al. Am J Med Genet A. 2015 Apr;167A(4):715-23. doi: 10.1002/ajmg.a.36847. Epub 2015 Feb 5. Am J Med Genet A. 2015. PMID: 25655306
The Gain-of-Function Integrin β3 Pro33 Variant Alters the Serotonin System in the Mouse Brain.
Dohn MR, Kooker CG, Bastarache L, Jessen T, Rinaldi C, Varney S, Mazalouskas MD, Pan H, Oliver KH, Velez Edwards DR, Sutcliffe JS, Denny JC, Carneiro AMD. Dohn MR, et al. J Neurosci. 2017 Nov 15;37(46):11271-11284. doi: 10.1523/JNEUROSCI.1482-17.2017. Epub 2017 Oct 16. J Neurosci. 2017. PMID: 29038237 Free PMC article.
Most genetic risk for autism resides with common variation.
Gaugler T, Klei L, Sanders SJ, Bodea CA, Goldberg AP, Lee AB, Mahajan M, Manaa D, Pawitan Y, Reichert J, Ripke S, Sandin S, Sklar P, Svantesson O, Reichenberg A, Hultman CM, Devlin B, Roeder K, Buxbaum JD. Gaugler T, et al. Nat Genet. 2014 Aug;46(8):881-5. doi: 10.1038/ng.3039. Epub 2014 Jul 20. Nat Genet. 2014. PMID: 25038753 Free PMC article.
Genetic analysis of biological pathway data through genomic randomization.
Yaspan BL, Bush WS, Torstenson ES, Ma D, Pericak-Vance MA, Ritchie MD, Sutcliffe JS, Haines JL. Yaspan BL, et al. Hum Genet. 2011 May;129(5):563-71. doi: 10.1007/s00439-011-0956-2. Epub 2011 Jan 30. Hum Genet. 2011. PMID: 21279722 Free PMC article.
Parent-of-origin effects of the serotonin transporter gene associated with autism.
Kistner-Griffin E, Brune CW, Davis LK, Sutcliffe JS, Cox NJ, Cook EH Jr. Kistner-Griffin E, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):139-44. doi: 10.1002/ajmg.b.31146. Epub 2010 Dec 8. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302342 Free PMC article.
De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder.
Hamilton PJ, Campbell NG, Sharma S, Erreger K, Herborg Hansen F, Saunders C, Belovich AN; NIH ARRA Autism Sequencing Consortium, Sahai MA, Cook EH, Gether U, McHaourab HS, Matthies HJ, Sutcliffe JS, Galli A. Hamilton PJ, et al. Mol Psychiatry. 2013 Dec;18(12):1315-23. doi: 10.1038/mp.2013.102. Epub 2013 Aug 27. Mol Psychiatry. 2013. PMID: 23979605 Free PMC article.
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