دنبال کردن
Lu Xia
Lu Xia
National Insitiute of Health, Central South University
ایمیل تأیید شده در sklmg.edu.cn
عنوان
نقل شده توسط
نقل شده توسط
سال
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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مقاله‌ها 1–20