| Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome F Bu, T Maga, NC Meyer, K Wang, CP Thomas, CM Nester, RJH Smith Journal of the American Society of Nephrology 25 (1), 55-64, 2014 | 262 | 2014 |
| Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects FX Bu, L Armas, J Lappe, Y Zhou, G Gao, HW Wang, R Recker, LJ Zhao Human genetics 128, 549-556, 2010 | 193 | 2010 |
| Statistical validation of rare complement variants provides insights into the molecular basis of atypical hemolytic uremic syndrome and C3 glomerulopathy AJ Osborne, M Breno, NG Borsa, F Bu, V Frémeaux-Bacchi, DP Gale, ... The Journal of Immunology 200 (7), 2464-2478, 2018 | 156 | 2018 |
| TBC1D24 Mutation Causes Autosomal‐Dominant Nonsyndromic Hearing Loss H Azaiez, KT Booth, F Bu, P Huygen, SB Shibata, AE Shearer, D Kolbe, ... Human mutation 35 (7), 819-823, 2014 | 110 | 2014 |
| High-throughput genetic testing for thrombotic microangiopathies and C3 glomerulopathies F Bu, NG Borsa, MB Jones, E Takanami, C Nishimura, JJ Hauer, H Azaiez, ... Journal of the American Society of Nephrology 27 (4), 1245-1253, 2016 | 109 | 2016 |
| Genetic analysis of 400 patients refines understanding and implicates a new gene in atypical hemolytic uremic syndrome F Bu, Y Zhang, K Wang, NG Borsa, MB Jones, AO Taylor, E Takanami, ... Journal of the American Society of Nephrology 29 (12), 2809-2819, 2018 | 70 | 2018 |
| HOMER2, a stereociliary scaffolding protein, is essential for normal hearing in humans and mice H Azaiez, AR Decker, KT Booth, AC Simpson, AE Shearer, PLM Huygen, ... PLoS genetics 11 (3), e1005137, 2015 | 63 | 2015 |
| Factors predicting vitamin D response variation in non-Hispanic white postmenopausal women LJ Zhao, Y Zhou, F Bu, D Travers-Gustafson, A Ye, X Xu, L Hamm, ... The Journal of Clinical Endocrinology & Metabolism 97 (8), 2699-2705, 2012 | 62 | 2012 |
| Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population X Li, Z Hu, Y He, Z Xiong, Z Long, Y Peng, F Bu, J Ling, G Xun, X Mo, ... Psychiatric genetics 20 (3), 113-117, 2010 | 62 | 2010 |
| Soluble c5b-9 as a biomarker for complement activation in atypical hemolytic uremic syndrome F Bu, NC Meyer, Y Zhang, NG Borsa, C Thomas, C Nester, RJH Smith American journal of kidney diseases 65 (6), 968-969, 2015 | 52 | 2015 |
| Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspects F Bu, N Borsa, A Gianluigi, RJH Smith Journal of Immunology Research 2012, 2012 | 52 | 2012 |
| DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss F Bu, M Zhong, Q Chen, Y Wang, X Zhao, Q Zhang, X Li, KT Booth, ... Human genetics 141 (3), 401-411, 2022 | 9 | 2022 |
| CYP2R1 is a potential candidate for predicting serum 25 (OH) D variation as suggested by genetic and epigenetic studies Y Zhou, F Bu, J Lappe, L Armas, R Recker, L Zhao J Bone Miner Res 25, 2010 | 8 | 2010 |
| High performance of a GPU-accelerated variant calling tool in genome data analysis Q Zhang, H Liu, F Bu bioRxiv, 2021.12. 12.472266, 2021 | 3 | 2021 |
| Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women QH Zhou, LJ Zhao, P Wang, R Badr, XJ Xu, FX Bu, J Lappe, R Recker, ... PloS one 9 (11), e112358, 2014 | 3 | 2014 |
| Identifying genetic factors of polycystic ovary syndrome in women with epilepsy: a whole-genome sequencing study W Lai, Y Wu, L Sha, Q Lai, X Yang, F Ai, Q Zhang, F Bu, S He, X Zhu, ... Neuroendocrinology 114 (3), 223-233, 2024 | 2 | 2024 |
| NCAD v1. 0: a database for non-coding variant annotation and interpretation X Feng, S Liu, K Li, F Bu, H Yuan Journal of Genetics and Genomics 51 (2), 230-242, 2024 | 1 | 2024 |
| seGMM: A new tool for gender determination from massively parallel sequencing data S Liu, Y Zeng, C Wang, Q Zhang, M Chen, X Wang, L Wang, Y Lu, H Guo, ... Frontiers in Genetics 13, 850804, 2022 | 1 | 2022 |
| Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort X Yan, J Wang, W Yang, L Li, T Shen, J Geng, Q Zhang, M Zhong, ... Journal of Medical Genetics, 2024 | | 2024 |
| Exploring noncoding variants in genetic diseases: from detection to functional insights K Wu, F Bu, Y Wu, G Zhang, X Wang, S He, MF Liu, R Chen, H Yuan Journal of Genetics and Genomics, 2024 | | 2024 |
Richard J SmithUniversity of IowaVerified email at uiowa.edu
