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Weiliang Lu

MicroRNA-26a regulates glucose metabolism by direct targeting PDHX in colorectal cancer cells
2014 · Bing Chen, Yuling Liu, et al. · BMC Cancer · 116
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PGK1 contributes to tumorigenesis and sorafenib resistance of renal clear cell carcinoma via activating CXCR4/ERK signaling pathway and accelerating glycolysis
2022 · Yu He, Xixi Wang, et al. · Cell Death and Disease · 88
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Loss of hnRNPA2B1 inhibits malignant capability and promotes apoptosis via down-regulating Lin28B expression in ovarian cancer
2020 · Yu Yang, Qinglv Wei, et al. · Cancer Letters · 79
Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologies
2024 · Jinglan Zhang, Yanting Wu, et al. · Nature Medicine · 65
Genetic deconvolution of fetal and maternal cell-free DNA in maternal plasma enables next-generation non-invasive prenatal screening
2022 · Chenming Xu, Jianli Li, et al. · Cell Discovery · 39
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The Overexpression of IQGAP1 and β-Catenin Is Associated with Tumor Progression in Hepatocellular Carcinoma In Vitro and In Vivo
2015 · Xuewen Jin, Yuling Liu, et al. · PLoS ONE · 39
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Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort
2021 · J. Su, Z. Qin, et al. · Ultrasound in Obstetrics and Gynecology · 38
CNV profiles of Chinese pediatric patients with developmental disorders
2021 · Haiming Yuan, Shaofang Shangguan, et al. · Genetics in Medicine · 31
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PGRMC1 Is a Novel Potential Tumor Biomarker of Human Renal Cell Carcinoma Based on Quantitative Proteomic and Integrative Biological Assessments
2017 · Dan Zhang, Xiangying Xia, et al. · PLoS ONE · 28
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Downregulation of ARHGDIA contributes to human glioma progression through activation of Rho GTPase signaling pathway
2016 · Weiliang Lu, Xixi Wang, et al. · Tumor Biology · 17
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Clinical and Genetic Analysis of CHD7 Expands the Genotype and Phenotype of CHARGE Syndrome
2020 · Zailong Qin, Jiasun Su, et al. · Frontiers in Genetics · 16
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Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature
2019 · Jiasun Su, Huayu Fu, et al. · Molecular Cytogenetics · 13
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Novel compound heterozygous pathogenic variants in ASCC1 in a Chinese patient with spinal muscular atrophy with congenital bone fractures 2 : Evidence supporting a "Definitive" gene‐disease relationship
2020 · Weiliang Lu, Mingxing Liang, et al. · Molecular Genetics & Genomic Medicine · 11
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Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement
2021 · Jiasun Su, Weiliang Lu, et al. · Molecular Genetics & Genomic Medicine · 9
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Assessing the clinical application value of SNP-array in fetal central nervous system malformations
2025 · Wei Li, Jiasun Su, et al. · Human Genomics · 3
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RBM42 couples alternative splicing to cytoskeletal organization to direct cortical development
2026 · Bingxin Yang, Qingxin Xu, et al. · iScience
NSF gene variants cause developmental and epileptic encephalopathy 96: expanding genotype and phenotypic spectrum with prenatal-onset features
2026 · Qi Yang, Zailong Qin, et al. · Frontiers in Genetics
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Clinical and genetic analysis of Chinese patients with Leigh syndrome caused by biallelic loss-of-function variants of the NDUFAF6 gene
2026 · Qi Yang, Qiang Zhang, et al. · Frontiers in Neurology
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16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations
2025 · Xianglian Tang, Jiasun Su, et al. · BMC Pregnancy and Childbirth
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Loss of function variants in TMPRSS7 linked to a neurodevelopmental disorder disrupt synaptic function
2025 · Weiliang Lu, Shuyuan Li, et al. · Human Molecular Genetics
16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations
2025 · Tang, Xianglian, Su, Jiasun, et al. · Figshare
Additional file 1 of 16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations
2025 · Tang, Xianglian, Su, Jiasun, et al. · Figshare
P129: Trio-based whole exome sequencing reveals novel pathogenic variants in TMPRSS7 associated with neurodevelopmental disorders*
2024 · Weiliang Lu, Shuyuan Li, et al. · Genetics in Medicine Open
Advances in GTPases
2017 · Claire Morgan, Romain Derelle, et al.
Works count: 26
Citation count: 592
H-index: 12
I10-index: 13
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