34. Iuliana Ionita-Laza, Bin Xu, V Makarov, Joseph Buxbaum, J. Louw Roos, Joseph Gogos, Maria Karayiorgou, "A Scan-Statistic Based Analysis of Exome Sequencing Data Identifies FAN1 at 15q13.3 as a Susceptibility Gene for Schizophrenia and Autism", Proceedings of the National Academy of Sciences USA, in press, 2013
33. Iuliana Ionita-Laza, Seunggeun Lee, Vlad Makarov, Joseph Buxbaum, Xihong Lin "Sequence kernel association tests for the combined effect of rare and common variants", American Journal of Human Genetics, accepted, 2013
32. Chu JH, Rogers A, Ionita-Laza I, Darvishi K, Mills RE, Lee C, Raby BA "Copy Number Variation Genotyping Using Family Information", BMC Bioinformatics, accepted, 2013
31. Buxbaum JD, Daly MJ, Devlin B, Lehner T, Roeder K, State MW; Autism Sequencing Consortium "The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders" Neuron, 2012
30. Bin Xu, Iuliana Ionita-Laza, J Louw Roos, Braden Boone, Scarlet Woodrick, Yan Sun, Shawn Levy, Joseph A Gogos, Maria Karayiorgou "De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia", Nature Genetics, 2012
29. Iuliana Ionita-Laza, Seunggeun Lee, Vlad Makarov, Joseph Buxbaum, Xihong Lin "General class of family-based association tests for sequence data, and comparisons with population-based association tests", European Journal of Human Genetics, 2013
28. Iuliana Ionita-Laza, Vlad Makarov, Joseph Buxbaum, the AASC "Scan-statistic approach identifies clusters of rare disease variants in three independent datasets in LRP2, a gene linked and associated with autism spectrum disorders", American Journal of Human Genetics, in press, 2012
27. Gourab De, Wai-Ki Yip, Iuliana Ionita-Laza, Nan Laird "Rare Variant Analysis for Family-based Designs", PloS One, 2012
26. Iuliana Ionita-Laza, Michael Cho, Nan Laird "Statistical challenges in sequence-based association studies with population- and family-based designs", Statistics in Biosciences, 2012 (invited article)
25. Louis ED, Hernandez N, Ionita-Laza I, Ottman R, Clark LN "Does rate of progression run in essential tremor families? Slower vs. faster progressors", Parkinsonism Relat Disord, 2012
24. Rogers AJ, Chu JH, Darvishi K, Ionita-Laza I, Lehmann H, Mills R, Lee C, Raby BA "Copy number variation prevalence in known asthma genes and their impact on asthma susceptibility", Clinical & Experimental Allergy 2012
23. Iuliana Ionita-Laza, Vlad Makarov, Seungtai Yoon, Benjamin Raby, Joseph Buxbaum, Dan Nicolae, Xihong Lin "Finding genes in Mendelian disorders using sequence data: methods and applications" American Journal of Human Genetics, 2011, Source Code
22. Yuan-Yuan Ho, Iuliana Ionita-Laza, Ruth Ottman "Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF" Neurology, 2011
21. Fan R, Huang CH, Lo SH, Zheng T, Ionita-Laza I "Identifying rare disease variants in the Genetic Analysis Workshop 17 simulated data: a comparison of several statistical approaches"
BMC Proc, 2011
20. Iuliana Ionita-Laza and Ruth Ottman "Design of association studies with rare variants" Genetics, 2011, Source Code (EPV), and Source Code (Power), and Documentation
19. Omer Gokcumen, Paul Babb, Rebecca Iskow, Xinghua Shi, Ryan Mills, Iuliana Ionita-Laza, Eric Vallender, Andrew Clark, Welkin Johnson, Charles Lee "Refinement of primate CNV hotspots identifies candidate genomic regions evolving under positive selection" Genome Biology, 2011
18. Tian Zheng, Herman Chernoff, Inchi Hu, Iuliana Ionita-Laza, Shaw-Hwa Lo: Discovering influential variables: a general computer intensive method for common genetic disorders. In: Handbook of Computational Statistics: Statistical Bioinformatics. Edited by Lu HHS, Scholkopf B, Zhao H. New York: Springer-Verlag; 2011.
17. Iuliana Ionita-Laza, Joseph Buxbaum, Nan Laird and Christoph Lange "A new testing strategy to identify rare variants with either risk or protective effect on disease" Plos Genetics, 2011 -- Source Code and Documentation
16. Iuliana Ionita-Laza, Nan Laird "On the optimal design of genetic variant discovery studies" Statistical Applications in Genetics and Molecular Biology, 2010
15. Iuliana Ionita-Laza, Christoph Lange, Nan Laird "On a method to count the number of unseen variants in the human genome" Proceedings of the National Academy of Sciences 2009
14. David Fardo, Iuliana Ionita-Laza, Christoph Lange "On quality control measures in genome-wide association studies: A test to assess the genotyping quality of individual probands in family-based association studies and an application to the HapMap data" Plos Genetics 2009
13. Jinbo Fan*, Iuliana Ionita-Laza*, et al., Nan Laird, Jordan Smoller "Linkage Disequilibrium Mapping of the Chromosome 6q21-22.31 Bipolar I Disorder Susceptibility Locus" Neuropsychiatric Genetics 2009
12. Rogers AJ, Brasch-Andersen C, Ionita-Laza I, Murphy A, Sharma S, Klanderman BJ, Raby BA "The interaction of glutathione S-transferase M1-null variants with tobacco smoke exposure and the development of childhood asthma" Clinical & Experimental Allergy, 2009
11. Lars Bertram, Christoph Lange et al., Iuliana Ionita-Laza, et al. R Tanzi "Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE" American Journal of Human Genetics 2008
10. Iuliana Ionita-Laza, Nan Laird, Benjamin Raby, Scott Weiss, Christoph Lange "On the frequency of copy number variants" Bioinformatics 2008
9. Iuliana Ionita-Laza, Angela Rogers, Christoph Lange, Benjamin Raby, Charles Lee "Genetic association analysis of copy number variation in human disease pathogenesis" Genomics 2009
8. Iuliana Ionita-Laza, George Perry, Benjamin Raby, Barbara Klanderman, Charles Lee, Nan Laird, Scott Weiss, Christoph Lange "On the analysis of copy-number variations in genome-wide association studies: A translation of the family-based association test" Genetic Epidemiology 2008
7. Ding Y, Cong L, Ionita-Laza I, Lo SH, Zheng T "Constructing gene association networks for rheumatoid arthritis using the backward genotype-trait association (BGTA) algorithm" BMC Proc, 2007
6. Zheng T, Wang S, Cong L, Ding Y, Ionita-Laza I, Lo SH "Joint study of genetic regulators for expression traits related to breast cancer" BMC Proc, 2007
5. 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 "Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4" Genetic Epidemiology, 2007
4. Iuliana Ionita-Laza, Matthew McQueen, Nan Laird, Christoph Lange "Genomewide Weighted Hypothesis Testing in Family-Based Association Studies, with an Application to a 100K Scan" American Journal of Human Genetics 2007
3. Iuliana Ionita, Raul-Sam Daruwala, Bud Mishra "Mapping Tumor Suppressor Genes using Multipoint Statistics from Copy-Number Variation Data" American Journal of Human Genetics 2006
2. Iuliana Ionita, Shaw-Hwa Lo "Multilocus Linkage Analysis of Affected Sib Pairs" Human Heredity 2005
1. Iuliana Ionita, Michael Man "Optimal two-stage strategy for detecting interacting genes in complex diseases" BMC Genetics 2006