Iuliana Ionita-Laza

According to our database, Iuliana Ionita-Laza authored at least 7 papers between 2008 and 2021.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of three.

2021

Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies.

Danqing Xu, Chen Wang, Atlas Khan, Ning Shang, Zihuai He, Adam S. Gordon, Iftikhar J. Kullo, Shawn N. Murphy, Yizhao Ni, Wei-Qi Wei, Ali Gharavi, Krzysztof Kiryluk, Chunhua Weng, Iuliana Ionita-Laza

npj Digit. Medicine, 2021

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, Richard A. Dart, Murray H. Brilliant, Eric B. Larson, David S. Carrell, Sarah A. Pendergrass, Shefali Setia Verma, Marylyn D. Ritchie, Barbara Benoit, Vivian S. Gainer, Elizabeth W. Karlson, Adam S. Gordon, Gail P. Jarvik, Ian B. Stanaway, David R. Crosslin, Sumit Mohan, Iuliana Ionita-Laza, Nicholas P. Tatonetti, Ali G. Gharavi, George Hripcsak, Chunhua Weng, Krzysztof Kiryluk

npj Digit. Medicine, 2021

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

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, David K. Vawdrey

Proceedings of the Summit on Clinical Research Informatics, 2017

2013

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

2011

Discovering Influential Variables: A General Computer Intensive Method for Common Genetic Disorders.

Tian Zheng, Herman Chernoff, Inchi Hu, Iuliana Ionita-Laza, Shaw-Hwa Lo

Proceedings of the Handbook of Statistical Bioinformatics., 2011

2008

On the frequency of copy number variants.

Iuliana Ionita-Laza, Nan M. Laird, Benjamin A. Raby, Scott T. Weiss, Christoph Lange

Bioinform., 2008