Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2015 1
2017 6
2018 5
2019 3
2020 12
2021 14
2022 13
2023 12
2024 5

Text availability

Article attribute

Article type

Publication date

Search Results

56 results

Results by year

Filters applied: . Clear all
Page 1
Did you mean shiqing wu (18 results)?
Intestinal Barrier Function and Neurodegenerative Disease.
Wu S, Yang L, Fu Y, Liao Z, Cai D, Liu Z. Wu S, et al. CNS Neurol Disord Drug Targets. 2023 Nov 24. doi: 10.2174/0118715273264097231116103948. Online ahead of print. CNS Neurol Disord Drug Targets. 2023. PMID: 38008941
Structural variants involved in high-altitude adaptation detected using single-molecule long-read sequencing.
Shi J, Jia Z, Sun J, Wang X, Zhao X, Zhao C, Liang F, Song X, Guan J, Jia X, Yang J, Chen Q, Yu K, Jia Q, Wu J, Wang D, Xiao Y, Xu X, Liu Y, Wu S, Zhong Q, Wu J, Cui S, Bo X, Wu Z, Park M, Kellis M, He K. Shi J, et al. Among authors: wu s. Nat Commun. 2023 Dec 13;14(1):8282. doi: 10.1038/s41467-023-44034-z. Nat Commun. 2023. PMID: 38092772 Free PMC article.
TNFRSF21 mutations cause high myopia.
Pan H, Wu S, Wang J, Zhu T, Li T, Wan B, Liu B, Luo Y, Ma X, Sui R, Wang B. Pan H, et al. Among authors: wu s. J Med Genet. 2019 Oct;56(10):671-677. doi: 10.1136/jmedgenet-2018-105684. Epub 2019 Jun 12. J Med Genet. 2019. PMID: 31189563
The phenotypic variability of HK1-associated retinal dystrophy.
Yuan Z, Li B, Xu M, Chang EY, Li H, Yang L, Wu S, Soens ZT, Li Y, Wong LC, Lewis RA, Sui R, Chen R. Yuan Z, et al. Among authors: wu s. Sci Rep. 2017 Aug 1;7(1):7051. doi: 10.1038/s41598-017-07629-3. Sci Rep. 2017. PMID: 28765615 Free PMC article.
Novel variants in PNPLA6 causing syndromic retinal dystrophy.
Wu S, Sun Z, Zhu T, Weleber RG, Yang P, Wei X, Pennesi ME, Sui R. Wu S, et al. Exp Eye Res. 2021 Jan;202:108327. doi: 10.1016/j.exer.2020.108327. Epub 2020 Oct 22. Exp Eye Res. 2021. PMID: 33141049 Free PMC article.
Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.
Luo M, Lin Z, Zhu T, Jin M, Meng D, He R, Cao Z, Shen Y, Lu C, Cai R, Zhao Y, Wang X, Li H, Wu S, Zou X, Luo G, Cao L, Huang M, Jiao H, Gao H, Sui R, Zhao C, Ma X, Cao M. Luo M, et al. Among authors: wu s. Genet Med. 2021 Jun;23(6):1041-1049. doi: 10.1038/s41436-021-01106-z. Epub 2021 Feb 2. Genet Med. 2021. PMID: 33531668 Free article.
56 results