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Lu Xia
Lu Xia
National Insitiute of Health, Central South University
在 sklmg.edu.cn 的电子邮件经过验证
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引用次数
引用次数
年份
De novo genic mutations among a Chinese autism spectrum disorder cohort
T Wang, H Guo, B Xiong, HAF Stessman, H Wu, BP Coe, TN Turner, Y Liu, ...
Nature communications 7 (1), 13316, 2016
3962016
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
T Wang, K Hoekzema, D Vecchio, H Wu, A Sulovari, BP Coe, ...
Nature communications 11 (1), 4932, 2020
1782020
Plasmodium Genomics and Genetics: New Insights into Malaria Pathogenesis, Drug Resistance, Epidemiology, and Evolution
X Su, KD Lane, L Xia, JM Sá, TE Wellems
Clinical microbiology reviews 32 (4), 10.1128/cmr. 00019-19, 2019
1522019
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model
H Guo, T Wang, H Wu, M Long, BP Coe, H Li, G Xun, J Ou, B Chen, ...
Molecular autism 9, 1-12, 2018
1522018
SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia
H Guo, X Jin, T Zhu, T Wang, P Tong, L Tian, Y Peng, L Sun, A Wan, ...
Journal of medical genetics 51 (8), 518-525, 2014
1272014
Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia
H Guo, P Tong, Y Liu, L Xia, T Wang, Q Tian, Y Li, Y Hu, Y Zheng, X Jin, ...
Genetics in Medicine 17 (4), 300-306, 2015
802015
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort
H Guo, Y Peng, Z Hu, Y Li, G Xun, J Ou, L Sun, Z Xiong, Y Liu, T Wang, ...
Scientific reports 7 (1), 44155, 2017
702017
Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans
G Zhao, K Li, B Li, Z Wang, Z Fang, X Wang, Y Zhang, T Luo, Q Zhou, ...
Nucleic acids research 48 (D1), D913-D926, 2020
692020
Mutation analysis of the NRXN1 gene in a Chinese autism cohort
Y Liu, Z Hu, G Xun, Y Peng, L Lu, X Xu, Z Xiong, L Xia, D Liu, W Li, J Zhao, ...
Journal of psychiatric research 46 (5), 630-634, 2012
522012
RTP4 inhibits IFN-I response and enhances experimental cerebral malaria and neuropathology
X He, AW Ashbrook, Y Du, J Wu, HH Hoffmann, C Zhang, L Xia, YC Peng, ...
Proceedings of the National Academy of Sciences 117 (32), 19465-19474, 2020
482020
Type I interferons and malaria: a double-edge sword against a complex parasitic disease
X He, L Xia, KC Tumas, J Wu, XZ Su
Frontiers in cellular and infection microbiology 10, 594621, 2020
462020
The E3 ubiquitin ligase MARCH1 regulates antimalaria immunity through interferon signaling and T cell activation
J Wu, L Xia, X Yao, X Yu, KC Tumas, W Sun, Y Cheng, X He, Y Peng, ...
Proceedings of the National Academy of Sciences 117 (28), 16567-16578, 2020
352020
Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss
XZ Cai, Y Li, L Xia, Y Peng, CF He, L Jiang, Y Feng, K Xia, XZ Liu, LY Mei, ...
Journal of human genetics 62 (2), 317-320, 2017
272017
New ZNF644 mutations identified in patients with high myopia
X Xiang, T Wang, P Tong, Y Li, H Guo, A Wan, L Xia, Y Liu, Y Li, Q Tian, ...
Molecular Vision 20, 939, 2014
232014
Detection of host pathways universally inhibited after Plasmodium yoelii infection for immune intervention
L Xia, J Wu, S Pattaradilokrat, K Tumas, X He, Y Peng, R Huang, ...
Scientific Reports 8 (1), 15280, 2018
222018
Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathy
A Ahmed, M Wang, G Bergant, R Maroofian, R Zhao, M Alfadhel, ...
Human Genetics 140, 579-592, 2021
202021
Genome‐wide association analysis of autism identified multiple loci that have been reported as strong signals for neuropsychiatric disorders
L Xia, J Ou, K Li, H Guo, Z Hu, T Bai, J Zhao, K Xia, F Zhang
Autism Research 13 (3), 382-396, 2020
192020
Performance comparison of computational methods for the prediction of the function and pathogenicity of non-coding variants
Z Wang, G Zhao, B Li, Z Fang, Q Chen, X Wang, T Luo, Y Wang, Q Zhou, ...
Genomics, Proteomics & Bioinformatics 21 (3), 649-661, 2023
172023
Plasmodium yoelii erythrocyte-binding-like protein modulates host cell membrane structure, immunity, and disease severity
Y Peng, Y Qi, C Zhang, X Yao, J Wu, S Pattaradilokrat, L Xia, KC Tumas, ...
MBio 11 (1), 10.1128/mbio. 02995-19, 2020
172020
GPCards: An integrated database of genotype–phenotype correlations in human genetic diseases
B Li, Z Wang, Q Chen, K Li, X Wang, Y Wang, Q Zeng, Y Han, B Lu, ...
Computational and Structural Biotechnology Journal 19, 1603-1611, 2021
152021
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