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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 1 |
2009 | 1 |
2010 | 1 |
2011 | 1 |
2013 | 1 |
2014 | 2 |
2015 | 1 |
2016 | 1 |
2024 | 0 |
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7 results
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Page 1
Genome-wide analysis of copy number variants in age-related macular degeneration.
Hum Genet. 2011 Jan;129(1):91-100. doi: 10.1007/s00439-010-0904-6. Epub 2010 Oct 28.
Hum Genet. 2011.
PMID: 20981449
Free PMC article.
PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders.
Paemka L, Mahajan VB, Skeie JM, Sowers LP, Ehaideb SN, Gonzalez-Alegre P, Sasaoka T, Tao H, Miyagi A, Ueno N, Takao K, Miyakawa T, Wu S, Darbro BW, Ferguson PJ, Pieper AA, Britt JK, Wemmie JA, Rudd DS, Wassink T, El-Shanti H, Mefford HC, Carvill GL, Manak JR, Bassuk AG.
Paemka L, et al. Among authors: rudd ds.
PLoS One. 2013 Dec 3;8(12):e80737. doi: 10.1371/journal.pone.0080737. eCollection 2013.
PLoS One. 2013.
PMID: 24312498
Free PMC article.
Item in Clipboard
Pax6 3' deletion results in aniridia, autism and mental retardation.
Davis LK, Meyer KJ, Rudd DS, Librant AL, Epping EA, Sheffield VC, Wassink TH.
Davis LK, et al. Among authors: rudd ds.
Hum Genet. 2008 May;123(4):371-8. doi: 10.1007/s00439-008-0484-x. Epub 2008 Mar 6.
Hum Genet. 2008.
PMID: 18322702
Free PMC article.
Review.
Item in Clipboard
A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.
Rudd DS, Axelsen M, Epping EA, Andreasen NC, Wassink TH.
Rudd DS, et al.
Am J Med Genet B Neuropsychiatr Genet. 2014 Dec;165B(8):619-26. doi: 10.1002/ajmg.b.32266. Epub 2014 Sep 16.
Am J Med Genet B Neuropsychiatr Genet. 2014.
PMID: 25228354
Item in Clipboard
Early detection of subclinical visual damage after blast-mediated TBI enables prevention of chronic visual deficit by treatment with P7C3-S243.
Dutca LM, Stasheff SF, Hedberg-Buenz A, Rudd DS, Batra N, Blodi FR, Yorek MS, Yin T, Shankar M, Herlein JA, Naidoo J, Morlock L, Williams N, Kardon RH, Anderson MG, Pieper AA, Harper MM.
Dutca LM, et al. Among authors: rudd ds.
Invest Ophthalmol Vis Sci. 2014 Dec 2;55(12):8330-41. doi: 10.1167/iovs.14-15468.
Invest Ophthalmol Vis Sci. 2014.
PMID: 25468886
Free PMC article.
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RetFM-J, an ImageJ-based module for automated counting and quantifying features of nuclei in retinal whole-mounts.
Hedberg-Buenz A, Christopher MA, Lewis CJ, Meyer KJ, Rudd DS, Dutca LM, Wang K, Garvin MK, Scheetz TE, Abràmoff MD, Harper MM, Anderson MG.
Hedberg-Buenz A, et al. Among authors: rudd ds.
Exp Eye Res. 2016 May;146:386-392. doi: 10.1016/j.exer.2015.07.020. Epub 2015 Aug 14.
Exp Eye Res. 2016.
PMID: 26283021
Free PMC article.
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Novel copy number variants in children with autism and additional developmental anomalies.
Davis LK, Meyer KJ, Rudd DS, Librant AL, Epping EA, Sheffield VC, Wassink TH.
Davis LK, et al. Among authors: rudd ds.
J Neurodev Disord. 2009 Dec;1(4):292-301. doi: 10.1007/s11689-009-9013-z. Epub 2009 May 27.
J Neurodev Disord. 2009.
PMID: 21547721
Free PMC article.
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