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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 |
2024 | 0 |
Search Results
5 results
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Page 1
A copy number variation morbidity map of developmental delay.
Nat Genet. 2011 Aug 14;43(9):838-46. doi: 10.1038/ng.909.
Nat Genet. 2011.
PMID: 21841781
Free PMC article.
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, Turner EH, Stanaway IB, Vernot B, Malig M, Baker C, Reilly B, Akey JM, Borenstein E, Rieder MJ, Nickerson DA, Bernier R, Shendure J, Eichler EE.
O'Roak BJ, et al.
Nature. 2012 Apr 4;485(7397):246-50. doi: 10.1038/nature10989.
Nature. 2012.
PMID: 22495309
Free PMC article.
Item in Clipboard
Evidence for involvement of GNB1L in autism.
Chen YZ, Matsushita M, Girirajan S, Lisowski M, Sun E, Sul Y, Bernier R, Estes A, Dawson G, Minshew N, Shellenberg GD, Eichler EE, Rieder MJ, Nickerson DA, Tsuang DW, Tsuang MT, Wijsman EM, Raskind WH, Brkanac Z.
Chen YZ, et al.
Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):61-71. doi: 10.1002/ajmg.b.32002. Epub 2011 Nov 16.
Am J Med Genet B Neuropsychiatr Genet. 2012.
PMID: 22095694
Free PMC article.
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Detection of structural variants and indels within exome data.
Karakoc E, Alkan C, O'Roak BJ, Dennis MY, Vives L, Mark K, Rieder MJ, Nickerson DA, Eichler EE.
Karakoc E, et al.
Nat Methods. 2011 Dec 18;9(2):176-8. doi: 10.1038/nmeth.1810.
Nat Methods. 2011.
PMID: 22179552
Free PMC article.
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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, Mackenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, Eichler EE.
O'Roak BJ, et al.
Nat Genet. 2011 Jun;43(6):585-9. doi: 10.1038/ng.835. Epub 2011 May 15.
Nat Genet. 2011.
PMID: 21572417
Free PMC article.
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