| A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies Z Li, X Li, H Zhou, SM Gaynor, MS Selvaraj, T Arapoglou, C Quick, Y Liu, ... Nature methods 19 (12), 1599-1611, 2022 | 48 | 2022 |
| Label‐free electrochemical aptasensor for carcino‐embryonic antigen based on ternary nanocomposite of gold nanoparticles, hemin and graphene Z Liu, Y Wang, Y Guo, C Dong Electroanalysis 28 (5), 1023-1028, 2016 | 35 | 2016 |
| Whole genome sequence analysis of blood lipid levels in> 66,000 individuals MS Selvaraj, X Li, Z Li, A Pampana, DY Zhang, J Park, S Aslibekyan, ... Nature communications 13 (1), 5995, 2022 | 34 | 2022 |
| Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis S Kanoni, SE Graham, Y Wang, I Surakka, S Ramdas, X Zhu, SL Clarke, ... Genome biology 23 (1), 268, 2022 | 29 | 2022 |
| A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids S Ramdas, J Judd, SE Graham, S Kanoni, Y Wang, I Surakka, B Wenz, ... The American Journal of Human Genetics 109 (8), 1366-1387, 2022 | 27 | 2022 |
| Genetic modification of inflammation-and clonal hematopoiesis–associated cardiovascular risk Z Yu, TP Fidler, Y Ruan, C Vlasschaert, T Nakao, MM Uddin, T Mack, ... The Journal of clinical investigation 133 (18), 2023 | 17 | 2023 |
| A comparison of analytical strategies for cluster randomized trials with survival outcomes in the presence of competing risks F Li, W Lu, Y Wang, Z Pan, EJ Greene, G Meng, C Meng, O Blaha, Y Zhao, ... Statistical methods in medical research 31 (7), 1224-1241, 2022 | 9 | 2022 |
| Whole genome DNA and RNA sequencing of whole blood elucidates the genetic architecture of gene expression underlying a wide range of diseases C Liu, R Joehanes, J Ma, Y Wang, X Sun, A Keshawarz, M Sooda, T Huan, ... Scientific reports 12 (1), 20167, 2022 | 8 | 2022 |
| Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: the Framingham Heart Study A Keshawarz, H Bui, R Joehanes, J Ma, C Liu, T Huan, SJ Hwang, ... Scientific reports 13 (1), 12952, 2023 | 7 | 2023 |
| Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study Y Wang, MS Selvaraj, X Li, Z Li, JA Holdcraft, DK Arnett, JC Bis, ... The American Journal of Human Genetics 110 (10), 1704-1717, 2023 | 5 | 2023 |
| Simulating time-to-event data subject to competing risks and clustering: A review and synthesis C Meng, D Esserman, F Li, Y Zhao, O Blaha, W Lu, Y Wang, P Peduzzi, ... Statistical Methods in Medical Research 32 (2), 305-333, 2023 | 2 | 2023 |
| A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies X Li, H Chen, MS Selvaraj, E Van Buren, H Zhou, Y Wang, R Sun, ... bioRxiv, 2023 | 1 | 2023 |
| Shared genetic architecture of blood eosinophil counts and asthma in UK Biobank B Li, Y Wang, Z Wang, X Li, S Kay, GL Chupp, H Zhao, JL Gomez ERJ Open Research 9 (4), 2023 | 1 | 2023 |
| Lipid levels and risk of acute pancreatitis using bidirectional Mendelian randomization B Wang, JS Dron, Y Wang, SH Choi, JE Huffman, K Cho, PWF Wilson, ... Scientific Reports 14 (1), 6267, 2024 | | 2024 |
| Prioritizing genes from genome-wide meta-analyses of blood lipid levels Y Wang, S Graham, S Kanoni, S Ramdas, K Bhatti, I Surakka, P Natarajan, ... ASHG 2021, 2021 | | 2021 |
Fan LiDepartment of Biostatistics, Yale University在 yale.edu 的电子邮件经过验证
