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Year
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ...
Molecular psychiatry 25 (8), 1859-1875, 2020
2342020
Potent paracrine effects of human induced pluripotent stem cell-derived mesenchymal stem cells attenuate doxorubicin-induced cardiomyopathy
Y Zhang, X Liang, S Liao, W Wang, J Wang, X Li, Y Ding, Y Liang, F Gao, ...
Scientific reports 5 (1), 11235, 2015
1172015
Next generation sequencing has lower sequence coverage and poorer SNP-detection capability in the regulatory regions
W Wang, Z Wei, TW Lam, J Wang
Scientific reports 1 (1), 1-7, 2011
1002011
A fast and accurate SNP detection algorithm for next-generation sequencing data
F Xu, W Wang, P Wang, M Jun Li, P Chung Sham, J Wang
Nature communications 3 (1), 1258, 2012
572012
Whole genome sequencing of Caribbean Hispanic families with late‐onset Alzheimer's disease
BN Vardarajan, S Barral, J Jaworski, GW Beecham, E Blue, G Tosto, ...
Annals of clinical and translational neurology 5 (4), 406-417, 2018
412018
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease
X Zhang, C Zhu, G Beecham, BN Vardarajan, Y Ma, D Lancour, JJ Farrell, ...
Alzheimer's & Dementia 15 (3), 441-452, 2019
382019
FaSD-somatic: a fast and accurate somatic SNV detection algorithm for cancer genome sequencing data
W Wang, P Wang, F Xu, R Luo, MP Wong, TW Lam, J Wang
Bioinformatics 30 (17), 2498-2500, 2014
252014
Abnormal global alternative RNA splicing in COVID-19 patients
C Wang, L Chen, Y Chen, W Jia, X Cai, Y Liu, F Ji, P Xiong, A Liang, R Liu, ...
PLoS genetics 18 (4), e1010137, 2022
222022
Integrative DNA copy number detection and genotyping from sequencing and array-based platforms
Z Zhou, W Wang, LS Wang, NR Zhang
Bioinformatics 34 (14), 2349-2355, 2018
122018
Human ocular epithelial cells endogenously expressing SOX2 and OCT4 yield high efficiency of pluripotency reprogramming
MW Poon, J He, X Fang, Z Zhang, W Wang, J Wang, F Qiu, HF Tse, W Li, ...
PloS one 10 (7), e0131288, 2015
122015
Correction: whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ...
Molecular psychiatry 25 (8), 1901-1903, 2020
52020
Assessment of mapping and SNP-detection algorithms for next-generation sequencing data in Cancer Genomics
W Wang, F Xu, J Wang
Next Generation Sequencing in Cancer Research: Volume 1: Decoding the Cancer …, 2013
32013
Profiling the m6A-regulated RNA expression patterns and alternative splicing features in esophageal carcinoma
L Kong, F Gao, F Zhao, R Xia, C Cai, W Wang, D Huang, Z Li, Q Yi, ...
Genes & Diseases 10 (5), 1812, 2023
22023
TransFlow: a Snakemake workflow for transmission analysis of Mycobacterium tuberculosis whole-genome sequencing data
J Pan, X Li, M Zhang, Y Lu, Y Zhu, K Wu, Y Wu, W Wang, B Chen, Z Liu, ...
Bioinformatics 39 (1), btac785, 2023
2023
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation (vol 25, pg …
JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ...
2020
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (Molecular …
J Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ...
Molecular Psychiatry, 2019
2019
P1‐129: Structural Variation (SV) in Heterogenous Whole‐Genome Sequencing Data from 111 Families at Risk For Alzheimer's Disease: Alzheimer's Disease Sequencing Project SV Study
LC Xia, J Farrell, N Zhang, W Salerno, J Malamon, SC Murali, W Wang, ...
Alzheimer's & Dementia 12, P453-P453, 2016
2016
P1‐001: Prediction of late‐onset Alzheimer's disease‐associated enhancer elements
M Tang, C Kramer, G Xu, M Hawk, YC Hwang, CF Lin, P Kuksa, W Wang, ...
Alzheimer's & Dementia 11 (7S_Part_7), P336-P336, 2015
2015
O3‐05‐03: Multiple deletion copy number variants (CNVs) are associated with late‐onset Alzheimer's disease: The Alzheimer's disease genetics consortium
W Wang, CF Lin, AB Partch, O Valladares, L Cantwell, AC Naj, LS Wang, ...
Alzheimer's & Dementia 11 (7S_Part_5), P228-P229, 2015
2015
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
AS Feolo, F Rajabli, M Schmidt, YYL Kuzma, HJ Lin, J Malamon, ...
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