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Fengxiao Bu

Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome
2013 · Fengxiao Bu, Tara Maga, et al. · Journal of the American Society of Nephrology · 242
A pangenome reference of 36 Chinese populations
2023 · Yang Gao, Xiaofei Yang, et al. · Nature · 177
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Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy
2018 · Amy J Osborne, Matteo Breno, et al. · The Journal of Immunology · 172
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Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects
2010 · Feng-Xiao Bu, Laura Armas, et al. · Human Genetics · 147
High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies
2015 · Fengxiao Bu, Nicolo Ghiringhelli Borsa, et al. · Journal of the American Society of Nephrology · 114
TBC1D24Mutation Causes Autosomal-Dominant Nonsyndromic Hearing Loss
2014 · Hela Azaiez, Kevin T. Booth, et al. · Human Mutation · 86
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Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic Syndrome
2018 · Fengxiao Bu, Yuzhou Zhang, et al. · Journal of the American Society of Nephrology · 67
HOMER2, a Stereociliary Scaffolding Protein, Is Essential for Normal Hearing in Humans and Mice
2015 · Hela Azaiez, Amanda R. Decker, et al. · PLoS Genetics · 64
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Soluble C5b-9 as a Biomarker for Complement Activation in Atypical Hemolytic Uremic Syndrome
2015 · Fengxiao Bu, Nicole C. Meyer, et al. · American Journal of Kidney Diseases · 60
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Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population
2010 · Xiaoping Li, Zhengmao Hu, et al. · Psychiatric Genetics · 57
Factors Predicting Vitamin D Response Variation in Non-Hispanic White Postmenopausal Women
2012 · Lan-Juan Zhao, Yu Zhou, et al. · The Journal of Clinical Endocrinology & Metabolism · 52
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Familial Atypical Hemolytic Uremic Syndrome: A Review of Its Genetic and Clinical Aspects
2012 · Fengxiao Bu, Nicolo Borsa, et al. · Clinical and Developmental Immunology · 44
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Exploring noncoding variants in genetic diseases: from detection to functional insights
2024 · Ke Wu, Fengxiao Bu, et al. · Journal of genetics and genomics/Journal of Genetics and Genomics · 37
Population genomics of Central Asian peoples unveil ancient Trans-Eurasian genetic admixture and cultural exchanges
2024 · Guanglin He, Mengge Wang, et al. · hLife · 33
Sequencing and characterizing human mitochondrial genomes in the biobank-based genomic research paradigm
2025 · Lintao Luo, Mengge Wang, et al. · Science China Life Sciences · 32
Paleolithic divergence and multiple Neolithic expansions of ancestral nomadic emperor-related paternal lineages
2024 · Mengge Wang, Qiuxia Sun, et al. · Journal of genetics and genomics/Journal of Genetics and Genomics · 18
DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss
2022 · Fengxiao Bu, Mingjun Zhong, et al. · Human Genetics · 15
Largest-Scale Genomic Resource Reconstructing the Genetic Origin, Population Structure, and Biological Adaptations of the Hui People
2025 · Guanglin He, Jing Chen, et al. · Molecular Biology and Evolution · 13
High performance of a GPU-accelerated variant calling tool in genome data analysis
2021 · Qian Zhang, Hao Liu, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 13
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GDC: Integration of Multi‐Omic and Phenotypic Resources to Unravel the Genetic Pathogenesis of Hearing Loss
2025 · Hui Cheng, Xuegang Wang, et al. · Advanced Science · 10
Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss
2023 · Sihan Liu, Mingjun Zhong, et al. · Genome Medicine · 10
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Human Population Genetic History and Evolutionary Dynamics on the Eastern Tibetan Plateau
2025 · Guanglin He, Shuhan Duan, et al. · Molecular Biology and Evolution · 8
Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort
2024 · Xiaohong Yan, Jing Wang, et al. · Journal of Medical Genetics · 8
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Short tandem repeats in populations of the Qinghai-Tibet Plateau and adjacent regions provide insights into high-altitude adaptation
2025 · Yuguo Huang, Mengge Wang, et al. · Science Advances · 7
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seGMM: A New Tool for Gender Determination From Massively Parallel Sequencing Data
2022 · Sihan Liu, Yuanyuan Zeng, et al. · Frontiers in Genetics · 7
Works count: 61
Citation count: 1,542
H-index: 16
I10-index: 21
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