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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 4 |
2012 | 2 |
2013 | 1 |
2014 | 2 |
2024 | 0 |
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7 results
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Page 1
Prevalence of autism spectrum disorders in a total population sample.
Am J Psychiatry. 2011 Sep;168(9):904-12. doi: 10.1176/appi.ajp.2011.10101532. Epub 2011 May 9.
Am J Psychiatry. 2011.
PMID: 21558103
Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.
Henkhaus RS, Kim SJ, Kimonis VE, Gold JA, Dykens EM, Driscoll DJ, Butler MG.
Henkhaus RS, et al.
Genet Test Mol Biomarkers. 2012 Mar;16(3):178-86. doi: 10.1089/gtmb.2011.0115. Epub 2011 Oct 6.
Genet Test Mol Biomarkers. 2012.
PMID: 21977908
Free PMC article.
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A comparison of DSM-IV pervasive developmental disorder and DSM-5 autism spectrum disorder prevalence in an epidemiologic sample.
Kim YS, Fombonne E, Koh YJ, Kim SJ, Cheon KA, Leventhal BL.
Kim YS, et al.
J Am Acad Child Adolesc Psychiatry. 2014 May;53(5):500-8. doi: 10.1016/j.jaac.2013.12.021. Epub 2014 Jan 21.
J Am Acad Child Adolesc Psychiatry. 2014.
PMID: 24745950
Free PMC article.
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Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.
Kim SJ, Miller JL, Kuipers PJ, German JR, Beaudet AL, Sahoo T, Driscoll DJ.
Kim SJ, et al.
Eur J Hum Genet. 2012 Mar;20(3):283-90. doi: 10.1038/ejhg.2011.187. Epub 2011 Nov 2.
Eur J Hum Genet. 2012.
PMID: 22045295
Free PMC article.
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Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait.
Chaste P, Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Lese Martin C, Martin DM, Morrow EM, Walsh CA, Sutcliffe JS, State MW, Devlin B, Cook EH Jr, Kim SJ.
Chaste P, et al.
Biol Psychiatry. 2013 Oct 15;74(8):576-84. doi: 10.1016/j.biopsych.2013.04.018. Epub 2013 Jun 6.
Biol Psychiatry. 2013.
PMID: 23746936
Free PMC article.
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Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
Chaste P, Sanders SJ, Mohan KN, Klei L, Song Y, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Martin DM, Morrow EM, Walsh CA, Sutcliffe JS, State MW, Martin CL, Devlin B, Beaudet AL, Cook EH Jr, Kim SJ.
Chaste P, et al.
Autism Res. 2014 Jun;7(3):355-62. doi: 10.1002/aur.1378. Epub 2014 May 12.
Autism Res. 2014.
PMID: 24821083
Free PMC article.
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Family-based association testing of glutamate transporter genes in autism.
Jacob S, Brune CW, Badner JA, Ernstrom K, Courchesne E, Lord C, Leventhal BL, Cook EH, Kim SJ.
Jacob S, et al.
Psychiatr Genet. 2011 Aug;21(4):212-3. doi: 10.1097/YPG.0b013e328341a323.
Psychiatr Genet. 2011.
PMID: 21085054
Free PMC article.
No abstract available.
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