Wenxian Yu - Search Results

Year	Number of Results
2015	2
2017	1
2018	1
2019	3
2021	4
2022	2
2023	3
2024	2

1

Singularity-Exponent-Domain Image Feature Transform.

Xiong G, Wang F, Yu W, Truong TK. Xiong G, et al. Among authors: yu w. IEEE Trans Image Process. 2021;30:8510-8525. doi: 10.1109/TIP.2021.3117055. Epub 2021 Oct 13. IEEE Trans Image Process. 2021. PMID: 34618671

2

A Pose-Only Solution to Visual Reconstruction and Navigation.

Cai Q, Zhang L, Wu Y, Yu W, Hu D. Cai Q, et al. Among authors: yu w. IEEE Trans Pattern Anal Mach Intell. 2023 Jan;45(1):73-86. doi: 10.1109/TPAMI.2021.3139681. Epub 2022 Dec 5. IEEE Trans Pattern Anal Mach Intell. 2023. PMID: 34971528

3

TextSLAM: Visual SLAM With Semantic Planar Text Features.

Li B, Zou D, Huang Y, Niu X, Pei L, Yu W. Li B, et al. Among authors: yu w. IEEE Trans Pattern Anal Mach Intell. 2024 Jan;46(1):593-610. doi: 10.1109/TPAMI.2023.3324320. Epub 2023 Dec 5. IEEE Trans Pattern Anal Mach Intell. 2024. PMID: 37831565

4

Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.

Liu J, Liu Q, Yang S, Ma N, Pang J, Peng Y, Xi H, Jia Z, Luo Y, Jiang M, Teng Y, Yu W, Li Z, Wang H. Liu J, et al. Among authors: yu w. Mol Genet Genomic Med. 2021 Aug;9(8):e1750. doi: 10.1002/mgg3.1750. Epub 2021 Jul 22. Mol Genet Genomic Med. 2021. PMID: 34293831 Free PMC article. Review.

5

Functional identification of two novel variants and a hypomorphic variant in ASS1 from patients with Citrullinemia type I.

Liu J, Wang Z, Yan H, Teng Y, Shi Q, Chen J, Tang W, Yu W, Peng Y, Xi H, Ma N, Liang D, Li Z, Wu L. Liu J, et al. Among authors: yu w. Front Genet. 2023 Jul 7;14:1172947. doi: 10.3389/fgene.2023.1172947. eCollection 2023. Front Genet. 2023. PMID: 37485339 Free PMC article.

6

The first case of a non-infertile female patient with Pitt-Hopkins syndrome.

Li H, Zhang Y, Yu W, Shu L, Mao X, Jia Z, Xi H, Wang H. Li H, et al. Among authors: yu w. Am J Med Genet A. 2019 Nov;179(11):2311-2314. doi: 10.1002/ajmg.a.61325. Epub 2019 Aug 28. Am J Med Genet A. 2019. PMID: 31464085 No abstract available.

7

Whole exome sequencing reveals two novel mutations in GREB1L in two chinese families with renal agenesis.

Xie F, Zhou L, Luo P, Xi H, Yu W, Ma N, Wang D, Peng Y. Xie F, et al. Among authors: yu w. QJM. 2024 Feb 26:hcae036. doi: 10.1093/qjmed/hcae036. Online ahead of print. QJM. 2024. PMID: 38410081 No abstract available.

8

Learning the Conformal Transformation Kernel for Image Recognition.

Xiong H, Yu W, Yang X, Swamy MN, Yu Q. Xiong H, et al. Among authors: yu w. IEEE Trans Neural Netw Learn Syst. 2017 Jan;28(1):149-163. doi: 10.1109/TNNLS.2015.2504538. Epub 2015 Dec 17. IEEE Trans Neural Netw Learn Syst. 2017. PMID: 26685272

9

Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family.

Peng Y, Yang S, Xi H, Hu J, Jia Z, Pang J, Liu J, Yu W, Tang C, Wang H. Peng Y, et al. Among authors: yu w. Mol Genet Genomic Med. 2021 Mar;9(3):e1604. doi: 10.1002/mgg3.1604. Epub 2021 Jan 20. Mol Genet Genomic Med. 2021. PMID: 33471964 Free PMC article.

10

MiR-21 in extracellular vesicles contributes to the growth of fertilized eggs and embryo development in mice.

Lv C, Yu WX, Wang Y, Yi DJ, Zeng MH, Xiao HM. Lv C, et al. Biosci Rep. 2018 Aug 31;38(4):BSR20180036. doi: 10.1042/BSR20180036. Print 2018 Aug 31. Biosci Rep. 2018. PMID: 29884767 Free PMC article.

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