Ionita-Laza I - Search Results

1

KnockoffTrio: A knockoff framework for the identification of putative causal variants in genome-wide association studies with trio design.

Yang Y, Wang C, Liu L, Buxbaum J, He Z, Ionita-Laza I. Yang Y, et al. Am J Hum Genet. 2022 Oct 6;109(10):1761-1776. doi: 10.1016/j.ajhg.2022.08.013. Epub 2022 Sep 22. Am J Hum Genet. 2022. PMID: 36150388 Free PMC article.

2

Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan.

Ionita-Laza I, McQueen MB, Laird NM, Lange C. Ionita-Laza I, et al. Am J Hum Genet. 2007 Sep;81(3):607-14. doi: 10.1086/519748. Epub 2007 Jul 17. Am J Hum Genet. 2007. PMID: 17701906 Free PMC article.

3

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.

4

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.

5

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.

6

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.

7

The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders.

Buxbaum JD, Daly MJ, Devlin B, Lehner T, Roeder K, State MW; Autism Sequencing Consortium. Buxbaum JD, et al. Neuron. 2012 Dec 20;76(6):1052-6. doi: 10.1016/j.neuron.2012.12.008. Neuron. 2012. PMID: 23259942 Free PMC article.

8

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.

9

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.

10

Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism.

Ionita-Laza I, Xu B, Makarov V, Buxbaum JD, Roos JL, Gogos JA, Karayiorgou M. Ionita-Laza I, et al. Proc Natl Acad Sci U S A. 2014 Jan 7;111(1):343-8. doi: 10.1073/pnas.1309475110. Epub 2013 Dec 16. Proc Natl Acad Sci U S A. 2014. PMID: 24344280 Free PMC article.

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