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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 3 |
2012 | 1 |
2013 | 2 |
2019 | 1 |
2024 | 0 |
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7 results
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Page 1
A genome-wide scan statistic framework for whole-genome sequence data analysis.
Nat Commun. 2019 Jul 9;10(1):3018. doi: 10.1038/s41467-019-11023-0.
Nat Commun. 2019.
PMID: 31289270
Free PMC article.
Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets.
Ionita-Laza I, Makarov V; ARRA Autism Sequencing Consortium; Buxbaum JD.
Ionita-Laza I, et al.
Am J Hum Genet. 2012 Jun 8;90(6):1002-13. doi: 10.1016/j.ajhg.2012.04.010. Epub 2012 May 10.
Am J Hum Genet. 2012.
PMID: 22578327
Free PMC article.
Item in Clipboard
Finding disease variants in Mendelian disorders by using sequence data: methods and applications.
Ionita-Laza I, Makarov V, Yoon S, Raby B, Buxbaum J, Nicolae DL, Lin X.
Ionita-Laza I, et al.
Am J Hum Genet. 2011 Dec 9;89(6):701-12. doi: 10.1016/j.ajhg.2011.11.003. Epub 2011 Dec 1.
Am J Hum Genet. 2011.
PMID: 22137099
Free PMC article.
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Sequence kernel association tests for the combined effect of rare and common variants.
Ionita-Laza I, Lee S, Makarov V, Buxbaum JD, Lin X.
Ionita-Laza I, et al.
Am J Hum Genet. 2013 Jun 6;92(6):841-53. doi: 10.1016/j.ajhg.2013.04.015. Epub 2013 May 16.
Am J Hum Genet. 2013.
PMID: 23684009
Free PMC article.
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A new testing strategy to identify rare variants with either risk or protective effect on disease.
Ionita-Laza I, Buxbaum JD, Laird NM, Lange C.
Ionita-Laza I, et al.
PLoS Genet. 2011 Feb 3;7(2):e1001289. doi: 10.1371/journal.pgen.1001289.
PLoS Genet. 2011.
PMID: 21304886
Free PMC article.
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Family-based association tests for sequence data, and comparisons with population-based association tests.
Ionita-Laza I, Lee S, Makarov V, Buxbaum JD, Lin X.
Ionita-Laza I, et al.
Eur J Hum Genet. 2013 Oct;21(10):1158-62. doi: 10.1038/ejhg.2012.308. Epub 2013 Feb 6.
Eur J Hum Genet. 2013.
PMID: 23386037
Free PMC article.
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Study designs for identification of rare disease variants in complex diseases: the utility of family-based designs.
Ionita-Laza I, Ottman R.
Ionita-Laza I, et al.
Genetics. 2011 Nov;189(3):1061-8. doi: 10.1534/genetics.111.131813. Epub 2011 Aug 11.
Genetics. 2011.
PMID: 21840850
Free PMC article.
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