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2020 – today
- 2021
[j5]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:
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies. npj Digit. Medicine 4 (2021)- [j4]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:
Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies. npj Digit. Medicine 4 (2021)
2010 – 2019
- 2017
- [j3]Xiaoyu Song, Gen Li, Zhenwei Zhou, Xianling Wang, Iuliana Ionita-Laza, Ying Wei:
QRank: a novel quantile regression tool for eQTL discovery. Bioinform. 33(14): 2123-2130 (2017) - [c1]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:
Automated Identification of Families in Electronic Health Records to Support Clinical Research. CRI 2017 - 2013
- [j2]Jen-hwa Chu, Angela J. Rogers, Iuliana Ionita-Laza, Katayoon Darvishi, Ryan Mills, Charles Lee, Benjamin A. Raby:
Copy number variation genotyping using family information. BMC Bioinform. 14: 157 (2013) - 2011
- [p1]Tian Zheng, Herman Chernoff, Inchi Hu, Iuliana Ionita-Laza, Shaw-Hwa Lo:
Discovering Influential Variables: A General Computer Intensive Method for Common Genetic Disorders. Handbook of Statistical Bioinformatics 2011: 87-107
2000 – 2009
- 2008
- [j1]Iuliana Ionita-Laza, Nan M. Laird, Benjamin A. Raby, Scott T. Weiss, Christoph Lange:
On the frequency of copy number variants. Bioinform. 24(20): 2350-2355 (2008)
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