On the frequency of copy number variants. - Iuliana Ionita-Laza; Nan M. Laird; Benjamin A. Raby; Scott T. Weiss; Christoph Lange 003 (Bioinform., 2008)

Discovering Influential Variables: A General Computer Intensive Method for Common Genetic Disorders. - Tian Zheng; Herman Chernoff; Inchi Hu; Iuliana Ionita-Laza; Shaw-Hwa Lo (Handbook of Statistical Bioinformatics, 2011)

Copy number variation genotyping using family information. - Jen-hwa Chu; Angela J. Rogers; Iuliana Ionita-Laza; Katayoon Darvishi; Ryan Mills; Charles Lee; Benjamin A. Raby (BMC Bioinform., 2013)

Automated Identification of Families in Electronic Health Records to Support Clinical Research. - Fernanda Polubriaginof; Kayla Quinnies; Rami Vanguri; Alexandre Yahi; Mary Simmerling; Iuliana Ionita-Laza; Hojjat Salmasian; Suzanne Bakken; George Hripcsak; Krzysztof Kiryluk; David Goldstein; Nicholas P. Tatonetti; et al. (CRI, 2017)

QRank: a novel quantile regression tool for eQTL discovery. - Xiaoyu Song; Gen Li; Zhenwei Zhou; Xianling Wang; Iuliana Ionita-Laza; Ying Wei (Bioinform., 2017)

Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies. - Ning Shang; Atlas Khan; Fernanda Polubriaginof; Francesca Zanoni; Karla Mehl; David Fasel; Paul E. Drawz; Robert J. Carroll; Joshua C. Denny; Matthew A. Hathcock; Adelaide M. Arruda-Olson; Peggy L. Peissig; et al. (npj Digit. Medicine, 2021)

Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies. - Danqing Xu; Chen Wang 146; Atlas Khan; Ning Shang; Zihuai He; Adam S. Gordon; Iftikhar J. Kullo; Shawn N. Murphy; Yizhao Ni; Wei-Qi Wei; Ali Gharavi; Krzysztof Kiryluk; et al. (npj Digit. Medicine, 2021)