Capanu M - Search Results

1

Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism.

Ionita-Laza I, Capanu M, De Rubeis S, McCallum K, Buxbaum JD. Ionita-Laza I, et al. Among authors: capanu m. PLoS Genet. 2014 Dec 11;10(12):e1004729. doi: 10.1371/journal.pgen.1004729. eCollection 2014 Dec. PLoS Genet. 2014. PMID: 25502226 Free PMC article.

2

False discovery rates for rare variants from sequenced data.

Capanu M, Seshan VE. Capanu M, et al. Genet Epidemiol. 2015 Feb;39(2):65-76. doi: 10.1002/gepi.21880. Epub 2014 Dec 30. Genet Epidemiol. 2015. PMID: 25556339 Free PMC article.

3

Integrative analysis of functional genomic annotations and sequencing data to identify rare causal variants via hierarchical modeling.

Capanu M, Ionita-Laza I. Capanu M, et al. Front Genet. 2015 May 8;6:17. doi: 10.3389/fgene.2015.00176. eCollection 2015. Front Genet. 2015. PMID: 26005447 Free PMC article.

4

Hierarchical modeling for estimating relative risks of rare genetic variants: properties of the pseudo-likelihood method.

Capanu M, Begg CB. Capanu M, et al. Biometrics. 2011 Jun;67(2):371-80. doi: 10.1111/j.1541-0420.2010.01469.x. Epub 2010 Aug 5. Biometrics. 2011. PMID: 20707869 Free PMC article.

5

Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling.

Capanu M, Concannon P, Haile RW, Bernstein L, Malone KE, Lynch CF, Liang X, Teraoka SN, Diep AT, Thomas DC, Bernstein JL; WECARE Study Collaborative Group; Begg CB. Capanu M, et al. Genet Epidemiol. 2011 Jul;35(5):389-97. doi: 10.1002/gepi.20587. Epub 2011 Apr 25. Genet Epidemiol. 2011. PMID: 21520273 Free PMC article.

6

Optimized variable selection via repeated data splitting.

Capanu M, Giurcanu M, Begg CB, Gönen M. Capanu M, et al. Stat Med. 2020 Jul 20;39(16):2167-2184. doi: 10.1002/sim.8538. Epub 2020 Apr 13. Stat Med. 2020. PMID: 32282097 Free PMC article.

7

Variation in genes related to obesity, weight, and weight change and risk of contralateral breast cancer in the WECARE Study population.

Brooks JD, Bernstein L, Teraoka SN, Knight JA, Mellemkjær L, John EM, Malone KE, Reiner AS, Lynch CF, Concannon P, Haile RW, Bernstein JL; WECARE Study Collaborative Group. Brooks JD, et al. Cancer Epidemiol Biomarkers Prev. 2012 Dec;21(12):2261-7. doi: 10.1158/1055-9965.EPI-12-1036. Epub 2012 Oct 2. Cancer Epidemiol Biomarkers Prev. 2012. PMID: 23033454 Free PMC article.

8

The use of hierarchical models for estimating relative risks of individual genetic variants: an application to a study of melanoma.

Capanu M, Orlow I, Berwick M, Hummer AJ, Thomas DC, Begg CB. Capanu M, et al. Stat Med. 2008 May 20;27(11):1973-92. doi: 10.1002/sim.3196. Stat Med. 2008. PMID: 18335566 Free PMC article.

9

Reproductive history and risk of second primary breast cancer: the WECARE study.

Largent JA, Capanu M, Bernstein L, Langholz B, Mellemkaer L, Malone KE, Begg CB, Haile RW, Lynch CF, Anton-Culver H, Wolitzer A, Bernstein JL. Largent JA, et al. Among authors: capanu m. Cancer Epidemiol Biomarkers Prev. 2007 May;16(5):906-11. doi: 10.1158/1055-9965.EPI-06-1003. Cancer Epidemiol Biomarkers Prev. 2007. PMID: 17507614

10

Misspecification tests for binomial and beta-binomial models.

Capanu M, Presnell B. Capanu M, et al. Stat Med. 2008 Jun 30;27(14):2536-54. doi: 10.1002/sim.3049. Stat Med. 2008. PMID: 17914713

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