Ionita-Laza I - Search Results

1

Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.

Liu L, Khan A, Sanchez-Rodriguez E, Zanoni F, Li Y, Steers N, Balderes O, Zhang J, Krithivasan P, LeDesma RA, Fischman C, Hebbring SJ, Harley JB, Moncrieffe H, Kottyan LC, Namjou-Khales B, Walunas TL, Knevel R, Raychaudhuri S, Karlson EW, Denny JC, Stanaway IB, Crosslin D, Rauen T, Floege J, Eitner F, Moldoveanu Z, Reily C, Knoppova B, Hall S, Sheff JT, Julian BA, Wyatt RJ, Suzuki H, Xie J, Chen N, Zhou X, Zhang H, Hammarström L, Viktorin A, Magnusson PKE, Shang N, Hripcsak G, Weng C, Rundek T, Elkind MSV, Oelsner EC, Barr RG, Ionita-Laza I, Novak J, Gharavi AG, Kiryluk K. Liu L, et al. Nat Commun. 2023 Feb 6;14(1):655. doi: 10.1038/s41467-023-36340-3. Nat Commun. 2023. PMID: 36746961 Free PMC article. No abstract available.

2

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.

3

Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locus.

Fan J, Ionita-Laza I, McQueen MB, Devlin B, Purcell S, Faraone SV, Allen MH, Bowden CL, Calabrese JR, Fossey MD, Friedman ES, Gyulai L, Hauser P, Ketter TB, Marangell LB, Miklowitz DJ, Nierenberg AA, Patel JK, Sachs GS, Thase ME, Molay FB, Escamilla MA, Nimgaonkar VL, Sklar P, Laird NM, Smoller JW. Fan J, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):29-37. doi: 10.1002/ajmg.b.30942. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19308960 Free PMC article.

4

Rare-variant association tests in longitudinal studies, with an application to the Multi-Ethnic Study of Atherosclerosis (MESA).

He Z, Lee S, Zhang M, Smith JA, Guo X, Palmas W, Kardia SLR, Ionita-Laza I, Mukherjee B. He Z, et al. Genet Epidemiol. 2017 Dec;41(8):801-810. doi: 10.1002/gepi.22081. Epub 2017 Oct 27. Genet Epidemiol. 2017. PMID: 29076270 Free PMC article.

5

Constructing gene association networks for rheumatoid arthritis using the backward genotype-trait association (BGTA) algorithm.

Ding Y, Cong L, Ionita-Laza I, Lo SH, Zheng T. Ding Y, et al. BMC Proc. 2007;1 Suppl 1(Suppl 1):S13. doi: 10.1186/1753-6561-1-s1-s13. Epub 2007 Dec 18. BMC Proc. 2007. PMID: 18466472 Free PMC article.

6

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.

7

On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test.

Ionita-Laza I, Perry GH, Raby BA, Klanderman B, Lee C, Laird NM, Weiss ST, Lange C. Ionita-Laza I, et al. Genet Epidemiol. 2008 Apr;32(3):273-84. doi: 10.1002/gepi.20302. Genet Epidemiol. 2008. PMID: 18228561

8

Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4.

Yang Q, Biernacka JM, Chen MH, Houwing-Duistermaat JJ, Bergemann TL, Basu S, Fan R, Liu L, Bourgey M, Clerget-Darpoux F, Lin WY, Elston RC, Cupples LA, Apprey V, Cui J, Dupuis J, Ionita-Laza I, Li R, Lou X, Perdry H, Sherva R, Shugart YY, Suarez B, Wang H, Wormald H, Xing G, Xing C. Yang Q, et al. Genet Epidemiol. 2007;31 Suppl 1:S34-42. doi: 10.1002/gepi.20278. Genet Epidemiol. 2007. PMID: 18046758

9

A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies.

Liu Y, Liang Y, Cicek AE, Li Z, Li J, Muhle RA, Krenzer M, Mei Y, Wang Y, Knoblauch N, Morrison J, Zhao S, Jiang Y, Geller E, Ionita-Laza I, Wu J, Xia K, Noonan JP, Sun ZS, He X. Liu Y, et al. Am J Hum Genet. 2018 Jun 7;102(6):1031-1047. doi: 10.1016/j.ajhg.2018.03.023. Epub 2018 May 10. Am J Hum Genet. 2018. PMID: 29754769 Free PMC article.

10

Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene.

Takata A, Xu B, Ionita-Laza I, Roos JL, Gogos JA, Karayiorgou M. Takata A, et al. Neuron. 2014 May 21;82(4):773-80. doi: 10.1016/j.neuron.2014.04.043. Neuron. 2014. PMID: 24853937 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

91 results

Search Page

Filters