| Genomic variation in 3,010 diverse accessions of Asian cultivated rice W Wang, R Mauleon, Z Hu, D Chebotarov, S Tai, Z Wu, M Li, T Zheng, ... Nature 557 (7703), 43-49, 2018 | 1174 | 2018 |
| A saturated map of common genetic variants associated with human height L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ... Nature 610 (7933), 704-712, 2022 | 296 | 2022 |
| Genomics-first evaluation of heart disease associated with titin-truncating variants CM Haggerty, SM Damrauer, MG Levin, D Birtwell, DJ Carey, AM Golden, ... Circulation 140 (1), 42-54, 2019 | 119 | 2019 |
| Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations J Park, AM Lucas, X Zhang, K Chaudhary, JH Cho, G Nadkarni, A Dobbyn, ... Nature medicine 27 (1), 66-72, 2021 | 41 | 2021 |
| Collective feature selection to identify crucial epistatic variants SS Verma, A Lucas, X Zhang, Y Veturi, S Dudek, B Li, R Li, R Urbanowicz, ... BioData mining 11, 1-22, 2018 | 29 | 2018 |
| Real world scenarios in rare variant association analysis: the impact of imbalance and sample size on the power in silico X Zhang, AO Basile, SA Pendergrass, MD Ritchie BMC bioinformatics 20, 1-10, 2019 | 28 | 2019 |
| Rare variants in drug target genes contributing to complex diseases, phenome-wide SS Verma, N Josyula, A Verma, X Zhang, Y Veturi, FE Dewey, DN Hartzel, ... Scientific reports 8 (1), 4624, 2018 | 16 | 2018 |
| Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network X Zhang, Y Veturi, S Verma, W Bone, A Verma, A Lucas, S Hebbring, ... BIOCOMPUTING 2019: Proceedings of the Pacific Symposium, 272-283, 2018 | 15* | 2018 |
| H. L (2018) Genomic variation in 3010 diverse accessions of Asian cultivated rice W Wang, R Mauleon, Z Hu, D Chebotarov, S Tai, Z Wu, M Li, T Zheng, ... Nature 557, 43-49, 0 | 11 | |
| Mendelian pathway analysis of laboratory traits reveals distinct roles for ciliary subcompartments in common disease pathogenesis TG Drivas, A Lucas, X Zhang, MDR Ritchie The American Journal of Human Genetics 108 (3), 482-501, 2021 | 8 | 2021 |
| Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders X Zhang, AM Lucas, Y Veturi, TG Drivas, WP Bone, A Verma, WK Chung, ... Nature communications 13 (1), 3428, 2022 | 7 | 2022 |
| Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics R Li, R Duan, X Zhang, T Lumley, S Pendergrass, C Bauer, ... Nature communications 12 (1), 168, 2021 | 4 | 2021 |
| Polygenic risk vectors (PRV) improve genetic risk stratification for cardio-metabolic diseases R Li, X Zhang, B Li, Q Feng, L Kottyan, Y Luo, KT Sawicki, A Khan, ... medRxiv, 2022.03. 02.22271425, 2022 | 2 | 2022 |
| Exome-by-phenome-wide rare variant gene burden association with electronic health record phenotypes J Park, N Katz, X Zhang, AM Lucas, A Verma, RL Judy, RL Kember, ... bioRxiv, 798330, 2019 | 2 | 2019 |
| Statistical Impact of Sample Size and Imbalance on Multivariate Analysis in silico and A Case Study in the UK Biobank X Zhang, R Li, MD Ritchie AMIA Annual Symposium Proceedings 2020, 1383, 2020 | 1 | 2020 |
| A saturated map of common genetic variants associated with human height from 5.4 million individuals of diverse ancestries Y Loic, V Sailaja, M Eirini, S Julia, B Eric, S Saori, G Marielisa BioRxiv 1, 07.475305, 2022 | | 2022 |
