| Mapping the human genetic architecture of COVID-19 Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ... Nature 600 (7889), 472-477, 2021 | 741 | 2021 |
| A harmonized data quality assessment terminology and framework for the secondary use of electronic health record data MG Kahn, TJ Callahan, J Barnard, AE Bauck, J Brown, BN Davidson, ... Egems 4 (1), 2016 | 400 | 2016 |
| Criteria2Query: a natural language interface to clinical databases for cohort definition C Yuan, PB Ryan, C Ta, Y Guo, Z Li, J Hardin, R Makadia, P Jin, N Shang, ... Journal of the American Medical Informatics Association 26 (4), 294-305, 2019 | 138 | 2019 |
| LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins WQ Wei, X Li, Q Feng, M Kubo, IJ Kullo, PL Peissig, EW Karlson, ... Circulation 138 (17), 1839-1849, 2018 | 96 | 2018 |
| Harmonizing clinical sequencing and interpretation for the eMERGE III network H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ... The American Journal of Human Genetics 105 (3), 588-605, 2019 | 93 | 2019 |
| Identifying plausible adverse drug reactions using knowledge extracted from the literature N Shang, H Xu, TC Rindflesch, T Cohen Journal of biomedical informatics 52, 293-310, 2014 | 79 | 2014 |
| Genome-wide polygenic score to predict chronic kidney disease across ancestries A Khan, MC Turchin, A Patki, V Srinivasasainagendra, N Shang, ... Nature medicine 28 (7), 1412-1420, 2022 | 65 | 2022 |
| Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19 G Povysil, G Butler-Laporte, N Shang, C Wang, A Khan, M Alaamery, ... The Journal of clinical investigation 131 (14), 2021 | 65 | 2021 |
| Facilitating phenotype transfer using a common data model G Hripcsak, N Shang, PL Peissig, LV Rasmussen, C Liu, B Benoit, ... Journal of Biomedical Informatics, 103253, 2019 | 64 | 2019 |
| Multisite evaluation of a data quality tool for patient-level clinical data sets V Huser, FJ DeFalco, M Schuemie, PB Ryan, N Shang, M Velez, RW Park, ... EGEMs 4 (1), 2016 | 64 | 2016 |
| Effect of vocabulary mapping for conditions on phenotype cohorts G Hripcsak, ME Levine, N Shang, PB Ryan Journal of the American Medical Informatics Association 25 (12), 1618-1625, 2018 | 48 | 2018 |
| Development and validation of a pragmatic electronic phenotype for CKD JM Norton, K Ali, CT Jurkovitz, K Kiryluk, M Park, K Kawamoto, N Shang, ... Clinical Journal of the American Society of Nephrology 14 (9), 1306-1314, 2019 | 45 | 2019 |
| Returning integrated genomic risk and clinical recommendations: The eMERGE study JE Linder, A Allworth, HT Bland, PJ Caraballo, RL Chisholm, EW Clayton, ... Genetics in Medicine 25 (4), 100006, 2023 | 43 | 2023 |
| Medical records-based chronic kidney disease phenotype for clinical care and “big data” observational and genetic studies N Shang, A Khan, F Polubriaginof, F Zanoni, K Mehl, D Fasel, PE Drawz, ... Npj Digital Medicine 4 (1), 70, 2021 | 42 | 2021 |
| Generalizability of polygenic risk scores for breast cancer among women with European, African, and Latinx ancestry C Liu, N Zeinomar, WK Chung, K Kiryluk, AG Gharavi, G Hripcsak, ... JAMA network open 4 (8), e2119084-e2119084, 2021 | 41 | 2021 |
| Making work visible for electronic phenotype implementation: lessons learned from the eMERGE network N Shang, C Liu, LV Rasmussen, CN Ta, RJ Caroll, B Benoit, T Lingren, ... Journal of biomedical informatics 99, 103293, 2019 | 37 | 2019 |
| What made a successful hepatitis B program for reducing liver cancer disparities: an examination of baseline characteristics and educational intervention, infection status, and … CE Hsu, G Zhang, FA Yan, N Shang, T Le Journal of Community Health 35, 325-335, 2010 | 36 | 2010 |
| Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative G Butler-Laporte, G Povysil, JA Kosmicki, ET Cirulli, T Drivas, S Furini, ... PLoS genetics 18 (11), e1010367, 2022 | 34 | 2022 |
| A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments JA Pacheco, LV Rasmussen, RC Kiefer, TR Campion, P Speltz, RJ Carroll, ... Journal of the American Medical Informatics Association 25 (11), 1540-1546, 2018 | 32 | 2018 |
| Ensembles of natural language processing systems for portable phenotyping solutions C Liu, CN Ta, JR Rogers, Z Li, J Lee, AM Butler, N Shang, FSP Kury, ... Journal of biomedical informatics 100, 103318, 2019 | 29 | 2019 |
