| Common variants contribute to intrinsic human brain functional networks B Zhao, T Li, SM Smith, D Xiong, X Wang, Y Yang, T Luo, Z Zhu, Y Shan, ... Nature Genetics 54 (4), 508-517, 2022 | 53 | 2022 |
| SnapHiC: a computational pipeline to identify chromatin loops from single-cell Hi-C data M Yu, A Abnousi, Y Zhang, G Li, L Lee, Z Chen, R Fang, TM Lagler, ... Nature methods 18 (9), 1056-1059, 2021 | 52* | 2021 |
| Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program Y Hu, AM Stilp, CP McHugh, S Rao, D Jain, X Zheng, J Lane, ... The American Journal of Human Genetics 108 (5), 874-893, 2021 | 43* | 2021 |
| Leveraging base-pair mammalian constraint to understand genetic variation and human disease PF Sullivan, JRS Meadows, S Gazal, BDN Phan, X Li, DP Genereux, ... Science 380 (6643), eabn2937, 2023 | 34 | 2023 |
| Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies Q Sun, M Graff, B Rowland, J Wen, L Huang, TW Miller-Fleming, ... Journal of human genetics 67 (2), 87-93, 2022 | 30 | 2022 |
| TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data L Huang, JD Rosen, Q Sun, J Chen, MM Wheeler, Y Zhou, YI Min, ... The American Journal of Human Genetics 109 (6), 1175-1181, 2022 | 28 | 2022 |
| From GWAS variant to function: A study of∼ 148,000 variants for blood cell traits Q Sun, CA Crowley, L Huang, J Wen, J Chen, EL Bao, PL Auer, G Lettre, ... Human Genetics and Genomics Advances 3 (1), 2022 | 17 | 2022 |
| Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program AV Mikhaylova, CP McHugh, LM Polfus, LM Raffield, MP Boorgula, ... The American Journal of Human Genetics 108 (10), 1836-1851, 2021 | 15 | 2021 |
| Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients Q Sun, W Liu, JD Rosen, L Huang, RG Pace, H Dang, PJ Gallins, EE Blue, ... Human Genetics and Genomics Advances 3 (2), 2022 | 14 | 2022 |
| Transcriptome-Wide association study of blood cell traits in African ancestry and Hispanic/Latino populations J Wen, M Xie, B Rowland, JD Rosen, Q Sun, J Chen, AL Tapia, H Qian, ... Genes 12 (7), 1049, 2021 | 12 | 2021 |
| Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study Y Hu, SA Bien, KK Nishimura, J Haessler, CJ Hodonsky, AR Baldassari, ... BMC genomics 22 (1), 432, 2021 | 12 | 2021 |
| Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative A Little, Y Hu, Q Sun, D Jain, J Broome, MH Chen, F Thibord, C McHugh, ... Human molecular genetics 31 (3), 347-361, 2022 | 10 | 2022 |
| Genetic modifiers of cystic fibrosis lung disease severity: whole-genome analysis of 7,840 patients YH Zhou, PJ Gallins, RG Pace, H Dang, MA Aksit, EE Blue, ... American journal of respiratory and critical care medicine 207 (10), 1324-1333, 2023 | 9 | 2023 |
| Understanding the function of regulatory DNA interactions in the interpretation of non-coding GWAS variants W Zhong, W Liu, J Chen, Q Sun, M Hu, Y Li Frontiers in cell and developmental biology 10, 957292, 2022 | 9 | 2022 |
| Course and predictors of eating disorder symptoms, anxiety symptoms, and pandemic‐related eating disorder concerns among adults with eating disorders during the first year of … KA Thompson, EL Hedlund, Q Sun, CM Peat, RW Goode, ... International Journal of Eating Disorders 56 (1), 151-168, 2023 | 8 | 2023 |
| MagicalRsq: Machine-learning-based genotype imputation quality calibration Q Sun, Y Yang, JD Rosen, MZ Jiang, J Chen, W Liu, J Wen, LM Raffield, ... The American Journal of Human Genetics 109 (11), 1986-1997, 2022 | 8 | 2022 |
| Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI Q Sun, BT Rowland, J Chen, AV Mikhaylova, C Avery, U Peters, J Lundin, ... Nature Communications 15 (1), 1016, 2024 | 7* | 2024 |
| Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits B Rowland, S Venkatesh, M Tardaguila, J Wen, JD Rosen, AL Tapia, ... Human Molecular Genetics 31 (14), 2333-2347, 2022 | 7 | 2022 |
| The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes A Huerta-Chagoya, P Schroeder, R Mandla, AJ Deutsch, W Zhu, L Petty, ... Diabetologia 66 (7), 1273-1288, 2023 | 6 | 2023 |
| Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis MA Aksit, H Ling, RG Pace, KS Raraigh, F Onchiri, AV Faino, K Pagel, ... The American Journal of Human Genetics 109 (10), 1894-1908, 2022 | 6 | 2022 |
