Bingbing Wu

2009-2015 Agency for Science, Technology and Research (A*STAR), Singapore 
"Bingbing Wu"
Mean distance: 16.04 (cluster 11)
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Xiao F, Lu Y, Wu B, et al. (2021) High-Frequency Exon Deletion of DNA Cross-Link Repair 1C Accounting for Severe Combined Immunodeficiency May Be Missed by Whole-Exome Sequencing. Frontiers in Genetics. 12: 677748
Zhang Y, Liu C, Wu B, et al. (2021) The missing linker between SUN5 and PMFBP1 in sperm head-tail coupling apparatus. Nature Communications. 12: 4926
Xiao T, Wu B, Cao Y, et al. (2021) Genetic identification of pathogenic variations of the gene: a retrospective study from 10,481 neonatal patients based on next-generation sequencing data. Annals of Translational Medicine. 9: 766
Ge M, Gan M, Yan K, et al. (2021) Combining Metagenomic Sequencing With Whole Exome Sequencing to Optimize Clinical Strategies in Neonates With a Suspected Central Nervous System Infection. Frontiers in Cellular and Infection Microbiology. 11: 671109
Dai D, Mei M, Hu L, et al. (2021) Prevalence of monogenic disease in paediatric patients with a predominant respiratory phenotype. Archives of Disease in Childhood
Wu B, Yu X, Liu C, et al. (2021) Essential Role of CFAP53 in Sperm Flagellum Biogenesis. Frontiers in Cell and Developmental Biology. 9: 676910
Li Y, Wu B, An C, et al. (2021) Mass cytometry and transcriptomic profiling reveal body-wide pathology induced by Loxl1 deficiency. Cell Proliferation. e13077
Chen J, Lin F, Zhai Y, et al. (2021) Diagnostic and clinical utility of genetic testing in children with kidney failure. Pediatric Nephrology (Berlin, Germany)
Qian Y, Wu B, Liu R, et al. (2021) Case Report: Complete Maternal Uniparental Isodisomy of Chromosome 5 (iUPD(5)mat) With Nonsense Variant in an Infant With Recurrent Diarrhea. Frontiers in Genetics. 12: 668326
Xiao F, Liu X, Lu Y, et al. (2021) Overdosage of Gene Associated With Annular Pancreas Detected in Neonate Patients With 17q12 Duplication. Frontiers in Genetics. 12: 615072
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