| Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies C Dong, P Wei, X Jian, R Gibbs, E Boerwinkle, K Wang, X Liu Human Molecular Genetics, 2015 | 1167 | 2015 |
| Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD With Transfusions Changing to … RE Ware, BR Davis, WH Schultz, RC Brown, B Aygun, S Sarnaik, I Odame, ... The Lancet, 2016 | 507 | 2016 |
| A powerful and adaptive association test for rare variants W Pan, J Kim, Y Zhang, X Shen, P Wei Genetics, 2014 | 199 | 2014 |
| Current challenges and new opportunities for gene-environment interaction studies of complex diseases K McAllister, LE Mechanic, C Amos, H Aschard, IA Blair, N Chatterjee, ... American journal of epidemiology 186 (7), 753-761, 2017 | 197 | 2017 |
| Assessment of luminal and basal phenotypes in bladder cancer CB Guo CC, Bondaruk J, Yao H, Wang Z, Zhang L, Lee S, Lee JG, Cogdell D ... Scientific Reports 10, 2020 | 134 | 2020 |
| Activation of endothelial and coagulation systems in left ventricular assist device recipients R John, S Panch, J Hrabe, P Wei, A Solovey, L Joyce, R Hebbel The Annals of thoracic surgery 88 (4), 1171-1179, 2009 | 127 | 2009 |
| WGSA: an annotation pipeline for human genome sequencing studies X Liu, S White, B Peng, AD Johnson, JA Brody, AH Li, Z Huang, A Carroll, ... Journal of Medical Genetics, 2016 | 115 | 2016 |
| Dysregulation of EMT drives the progression to clinically aggressive sarcomatoid bladder cancer CC Guo, T Majewski, L Zhang, H Yao, J Bondaruk, Y Wang, S Zhang, ... Cell reports 27 (6), 1781-1793. e4, 2019 | 113 | 2019 |
| An adaptive two-sample test for high-dimensional means G Xu, L Lin, P Wei, W Pan Biometrika 103 (3), 609-624, 2016 | 110 | 2016 |
| Site disparities in apoptotic variants as predictors of risk for second primary malignancy in patients with squamous cell carcinoma of the head and neck Y Sun, W Yu, EM Sturgis, P Wei, D Lei, Q Wei, X Song, G Li BMC Cancer, 2016 | 107* | 2016 |
| Incorporating gene networks into statistical tests for genomic data via a spatially correlated mixture model P Wei, W Pan Bioinformatics 24 (3), 404-411, 2008 | 102 | 2008 |
| Dietary inflammatory potential in relation to the gut microbiome: results from a cross-sectional study J Zheng, KL Hoffman, JS Chen, N Shivappa, A Sood, GJ Browman, ... British Journal of Nutrition 124 (9), 931-942, 2020 | 93 | 2020 |
| Common and rare von Willebrand factor (VWF) coding variants, von Willebrand factor levels, and factor VIII levels in African Americans: the NHLBI exome sequencing project JM Johnsen, PL Auer, AC Morrison, S Jiao, P Wei, J Haessler, K Fox, ... Blood 122 (4), 590-597, 2013 | 90* | 2013 |
| Insights into Pancreatic Cancer Etiology from Pathway Analysis of Genome-Wide Association Study Data P Wei, H Tang, D Li PLoS ONE 7 (10), e46887, 2012 | 90 | 2012 |
| A Powerful Framework for Integrating eQTL and GWAS Summary Data Z Xu, C Wu, P Wei, W Pan Genetics, 2017 | 79 | 2017 |
| TP53 copy number and protein expression inform mutation status across risk categories in acute myeloid leukemia M Tashakori, T Kadia, S Loghavi, N Daver, R Kanagal-Shamanna, ... Blood, The Journal of the American Society of Hematology 140 (1), 58-72, 2022 | 69 | 2022 |
| Persistent IDH1/2 mutations in remission can predict relapse in patients with acute myeloid leukemia CY Ok, S Loghavi, D Sui, P Wei, R Kanagal-Shamanna, CC Yin, Z Zuo, ... Haematologica 104 (2), 305, 2018 | 69 | 2018 |
| Genetic endothelial systems biology of sickle stroke risk L Chang Milbauer, P Wei, J Enenstein, A Jiang, CA Hillery, JP Scott, ... Blood, The Journal of the American Society of Hematology 111 (7), 3872-3879, 2008 | 67 | 2008 |
| A powerful pathway-based adaptive test for genetic association with common or rare variants W Pan, IY Kwak, P Wei American Journal of Human Genetics, 2015 | 65 | 2015 |
| A versatile omnibus test for detecting mean and variance heterogeneity Y Cao, P Wei, M Bailey, JSK Kauwe, TJ Maxwell, ... Genetic epidemiology 38 (1), 51-59, 2014 | 64 | 2014 |
