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Year
Focus on local: Detecting lane marker from bottom up via key point
Z Qu, H Jin, Y Zhou, Z Yang, W Zhang
Proceedings of the IEEE/CVF conference on computer vision and pattern …, 2021
1182021
Transformer-based multimodal information fusion for facial expression analysis
W Zhang, F Qiu, S Wang, H Zeng, Z Zhang, R An, B Ma, Y Ding
Proceedings of the IEEE/CVF Conference on Computer Vision and Pattern …, 2022
952022
Learning a facial expression embedding disentangled from identity
W Zhang, X Ji, K Chen, Y Ding, C Fan
Proceedings of the IEEE/CVF conference on computer vision and pattern …, 2021
712021
Ferv39k: A large-scale multi-scene dataset for facial expression recognition in videos
Y Wang, Y Sun, Y Huang, Z Liu, S Gao, W Zhang, W Ge, W Zhang
Proceedings of the IEEE/CVF conference on computer vision and pattern …, 2022
682022
A case of deficiency of plasma plasminogen activator inhibitor-1 related to Ala15Thr mutation in its signal peptide
ZY Zhang, ZY Wang, NZ Dong, X Bai, W Zhang, CG Ruan
Blood coagulation & fibrinolysis 16 (1), 79-84, 2005
422005
Prior aided streaming network for multi-task affective recognitionat the 2nd abaw2 competition
W Zhang, Z Guo, K Chen, L Li, Z Zhang, Y Ding
arXiv preprint arXiv:2107.03708, 2021
342021
Efficacy and safety of fenofibrate add-on therapy for patients with primary biliary cholangitis and a suboptimal response to UDCA
W Duan, X Ou, X Wang, Y Wang, X Zhao, Q Wang, X Wu, W Zhang, H Ma, ...
Revista Española de Enfermedades Digestivas 110 (9), 557-563, 2018
322018
Non-HFE mutations in haemochromatosis in China: combination of heterozygous mutations involving HJV signal peptide variants
T Lv, W Zhang, A Xu, Y Li, D Zhou, B Zhang, X Li, X Zhao, Y Wang, ...
Journal of medical genetics 55 (10), 650-660, 2018
312018
Effective viral suppression is necessary to reduce hepatocellular carcinoma development in cirrhotic patients with chronic hepatitis B: Results of a 10-year follow up
W Zhang, X Wang, Y Wang, X Zhao, W Duan, Q Wang, X Wu, Y Kong, ...
Medicine 96 (44), e8454, 2017
282017
Mutation analysis of the ABCC2 gene in Chinese patients with Dubin‑Johnson syndrome
L Wu, W Zhang, S Jia, X Zhao, D Zhou, A Xu, W Duan, Z Wu, H Li, ...
Experimental and Therapeutic Medicine 16 (5), 4201-4206, 2018
262018
A novel SLC40A1 p.Y333H mutation with gain of function of ferroportin: A recurrent cause of haemochromatosis in China
W Zhang, A Xu, Y Li, S Zhao, D Zhou, L Wu, B Zhang, X Zhao, Y Wang, ...
Liver international 39 (6), 1120-1127, 2019
252019
Recent advance in the molecular genetics of Wilson disease and hereditary hemochromatosis
T Lv, X Li, W Zhang, X Zhao, X Ou, J Huang
European journal of medical genetics 59 (10), 532-539, 2016
242016
Multi-modal facial affective analysis based on masked autoencoder
W Zhang, B Ma, F Qiu, Y Ding
Proceedings of the IEEE/CVF Conference on Computer Vision and Pattern …, 2023
212023
Type 4B hereditary hemochromatosis associated with a novel mutation in the SLC40A1 gene: a case report and a review of the literature
W Zhang, T Lv, J Huang, X Ou
Medicine 96 (38), e8064, 2017
202017
A new polyhydroxysteroidal glycoside from the starfish Anthenea chinensis
N Ma, HF Tang, F Qiu, HW Lin, XR Tian, W Zhang
Chinese Chemical Letters 20 (10), 1231-1234, 2009
192009
Prior aided streaming network for multi-task affective analysis
W Zhang, Z Guo, K Chen, L Li, Z Zhang, Y Ding, R Wu, T Lv, C Fan
Proceedings of the IEEE/CVF International Conference on Computer Vision …, 2021
182021
A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China
L Wu, Y Li, Y Song, D Zhou, S Jia, A Xu, W Zhang, H You, J Jia, J Huang, ...
Orphanet Journal of Rare Diseases 15, 1-8, 2020
182020
Molecular alterations of the NF2 gene in hepatocellular carcinoma and intrahepatic cholangiocarcinoma
N Zhang, Z Zhao, J Long, H Li, B Zhang, G Chen, X Li, T Lv, W Zhang, ...
Oncology Reports 38 (6), 3650-3658, 2017
182017
Facial affective analysis based on mae and multi-modal information for 5th abaw competition
W Zhang, B Ma, F Qiu, Y Ding
arXiv preprint arXiv:2303.10849 2 (5), 6, 2023
152023
Complex ATP7B mutation patterns in Wilson disease and evaluation of a yeast model for functional analysis of variants
X Li, W Zhang, D Zhou, T Lv, A Xu, H Wang, X Zhao, B Zhang, Y Li, S Jia, ...
Human Mutation 40 (5), 552-565, 2019
152019
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