| SOAP3-dp: fast, accurate and sensitive GPU-based short read aligner R Luo, T Wong, J Zhu, CM Liu, X Zhu, E Wu, LK Lee, H Lin, W Zhu, ... PloS one 8 (5), e65632, 2013 | 168 | 2013 |
| Hypertrophic cardiomyopathy: an overview of genetics and management P Teekakirikul, W Zhu, HC Huang, E Fung Biomolecules 9 (12), 878, 2019 | 156 | 2019 |
| Genetic architecture and selection of Chinese cattle revealed by whole genome resequencing C Mei, H Wang, Q Liao, L Wang, G Cheng, H Wang, C Zhao, S Zhao, ... Molecular biology and evolution 35 (3), 688-699, 2018 | 100 | 2018 |
| Amphibian cathelicidin fills the evolutionary gap of cathelicidin in vertebrate X Hao, H Yang, L Wei, S Yang, W Zhu, D Ma, H Yu, R Lai Amino acids 43, 677-685, 2012 | 73 | 2012 |
| Deep whole-genome sequencing of 90 Han Chinese genomes T Lan, H Lin, W Zhu, TCAM Laurent, M Yang, X Liu, J Wang, J Wang, ... Gigascience 6 (9), gix067, 2017 | 50 | 2017 |
| Uncompensated mitochondrial oxidative stress underlies heart failure in an iPSC-derived model of congenital heart disease X Xu, K Jin, AS Bais, W Zhu, H Yagi, TN Feinstein, PK Nguyen, ... Cell Stem Cell 29 (5), 840-855. e7, 2022 | 46 | 2022 |
| Gene cloning, expression and characterization of avian cathelicidin orthologs, Cc‐CATHs, from Coturnix coturnix F Feng, C Chen, W Zhu, W He, H Guang, Z Li, D Wang, J Liu, M Chen, ... The FEBS journal 278 (9), 1573-1584, 2011 | 46 | 2011 |
| Whole-genome sequencing of the endangered bovine species Gayal (Bos frontalis) provides new insights into its genetic features C Mei, H Wang, W Zhu, H Wang, G Cheng, K Qu, X Guang, A Li, C Zhao, ... Scientific reports 6 (1), 19787, 2016 | 43 | 2016 |
| Copy number variation detection in Chinese indigenous cattle by whole genome sequencing C Mei, Z Junjvlieke, SHA Raza, H Wang, G Cheng, C Zhao, W Zhu, L Zan Genomics 112 (1), 831-836, 2020 | 41 | 2020 |
| Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by … Y Wang, P Su, B Hu, W Zhu, Q Li, P Yuan, J Li, X Guan, F Li, X Jing, R Li, ... Human genetics 134, 589-603, 2015 | 27 | 2015 |
| Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease P Teekakirikul, W Zhu, GC Gabriel, CB Young, K Williams, LJ Martin, ... Human Genetics and Genomics Advances 2 (3), 2021 | 17 | 2021 |
| Whole-genome sequencing of Finnish type 1 diabetic siblings discordant for kidney disease reveals DNA variants associated with diabetic nephropathy J Guo, OJL Rackham, N Sandholm, B He, AM Österholm, E Valo, ... Journal of the American Society of Nephrology 31 (2), 309-323, 2020 | 17 | 2020 |
| Concurrent nucleotide substitution mutations in the human genome are characterized by a significantly decreased transition/transversion ratio W Zhu, DN Cooper, Q Zhao, Y Wang, R Liu, Q Li, C Férec, Y Wang, ... Human Mutation 36 (3), 333-341, 2015 | 12 | 2015 |
| Hy-pertrophic Cardiomyopathy: An Overview of Genetics and Management. Biomolecules, 9, 878 P Teekakirikul, W Zhu, HC Huang, E Fung | 10 | 2019 |
| Genetic Resiliency Associated With Dominant Lethal TPM1 Mutation Causing Atrial Septal Defect With High Heritability P Teekakirikul, W Zhu, X Xu, C Young, T Tan, AM Smith, C Wang, ... Cell Reports Medicine, 2022 | 8 | 2022 |
| KCTD1/KCTD15 complexes control ectodermal and neural crest cell functions, and their impairment causes aplasia cutis JR Raymundo, H Zhang, G Smaldone, W Zhu, KE Daly, BJ Glennon, ... The Journal of Clinical Investigation 134 (4), 2024 | 6 | 2024 |
| A robust pipeline for ranking carrier frequencies of autosomal recessive and X-linked Mendelian disorders W Zhu, C Wang, N Mullapudi, Y Cao, L Li, IFM Lo, SKW Tsui, X Chen, ... NPJ Genomic Medicine 7 (1), 72, 2022 | 6 | 2022 |
| Rare and common variants uncover the role of the atria in coarctation of the aorta W Zhu, K Williams, C Young, JH Lin, P Teekakirikul, CW Lo Genes 13 (4), 636, 2022 | 6 | 2022 |
| Disclosing the hidden structure and underlying mutational mechanism of a novel type of duplication CNV responsible for hereditary multiple osteochondromas P Su, Y Wang, DN Cooper, W Zhu, D Huang, C Férec, Y Wang, JM Chen Human Mutation 36 (8), 758-763, 2015 | 5 | 2015 |
| Insights into the genetic architecture of congenital heart disease from animal modeling W Zhu, CW Lo Zoological Research 44 (3), 577, 2023 | 4 | 2023 |
