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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1996 | 1 |
1999 | 1 |
2002 | 2 |
2003 | 1 |
2006 | 1 |
2008 | 1 |
2024 | 0 |
PubMed (cited) for id: 300425
7 results
Results by year
Filters applied: . Clear all
Page 1
Hypothesis: dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders.
Am J Med Genet A. 2008 Sep 1;146A(17):2213-20. doi: 10.1002/ajmg.a.32396.
Am J Med Genet A. 2008.
PMID: 18698615
Review.
Evidence for multiple loci from a genome scan of autism kindreds.
Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM.
Schellenberg GD, et al.
Mol Psychiatry. 2006 Nov;11(11):1049-60, 979. doi: 10.1038/sj.mp.4001874. Epub 2006 Aug 1.
Mol Psychiatry. 2006.
PMID: 16880825
Free article.
Item in Clipboard
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Jamain S, Quach H, Betancur C, Råstam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T; Paris Autism Research International Sibpair Study.
Jamain S, et al.
Nat Genet. 2003 May;34(1):27-9. doi: 10.1038/ng1136.
Nat Genet. 2003.
PMID: 12669065
Free PMC article.
Item in Clipboard
A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27.
Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-Oja T, Sinsheimer JS, Peltonen L, Järvelä I.
Auranen M, et al.
Am J Hum Genet. 2002 Oct;71(4):777-90. doi: 10.1086/342720. Epub 2002 Aug 21.
Am J Hum Genet. 2002.
PMID: 12192642
Free PMC article.
Item in Clipboard
Genomic screen and follow-up analysis for autistic disorder.
Shao Y, Wolpert CM, Raiford KL, Menold MM, Donnelly SL, Ravan SA, Bass MP, McClain C, von Wendt L, Vance JM, Abramson RH, Wright HH, Ashley-Koch A, Gilbert JR, DeLong RG, Cuccaro ML, Pericak-Vance MA.
Shao Y, et al.
Am J Med Genet. 2002 Jan 8;114(1):99-105. doi: 10.1002/ajmg.10153.
Am J Med Genet. 2002.
PMID: 11840513
Item in Clipboard
A genomic screen of autism: evidence for a multilocus etiology.
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Petersen PB, Pingree C, McMahon W, Wong DL, Cavalli-Sforza LL, Kraemer HC, Myers RM.
Risch N, et al.
Am J Hum Genet. 1999 Aug;65(2):493-507. doi: 10.1086/302497.
Am J Hum Genet. 1999.
PMID: 10417292
Free PMC article.
Item in Clipboard
Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives.
Bailey A, Phillips W, Rutter M.
Bailey A, et al.
J Child Psychol Psychiatry. 1996 Jan;37(1):89-126. doi: 10.1111/j.1469-7610.1996.tb01381.x.
J Child Psychol Psychiatry. 1996.
PMID: 8655659
Review.
Item in Clipboard
Cite
Cite