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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

75,795 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
A large pedigree study confirmed the CGG repeat expansion of RILPL1 Is associated with oculopharyngodistal myopathy.
Yang X, Zhang D, Shen S, Li P, Li M, Niu J, Ma D, Xu D, Li S, Guo X, Wang Z, Zhao Y, Ren H, Ling C, Wang Y, Fan Y, Shen J, Zhu Y, Wang D, Cui L, Chen L, Shi C, Dai Y. Yang X, et al. Among authors: li s, li m, li p. BMC Med Genomics. 2023 Oct 20;16(1):253. doi: 10.1186/s12920-023-01586-9. BMC Med Genomics. 2023. PMID: 37864208 Free PMC article.
ARSA gene variants and Parkinson's disease.
Fan Y, Mao CY, Dong YL, Shen S, Zhang QM, Yao DB, Liu F, Li MJ, Hu XC, Wang T, Liu YT, Liu H, Wang YL, Yuan YP, Zhang C, Yang J, Shi CH, Xu YM. Fan Y, et al. Brain. 2020 Jun 1;143(6):e47. doi: 10.1093/brain/awaa134. Brain. 2020. PMID: 32437521 No abstract available.
GIPC1 CGG Repeat Expansion Is Associated with Movement Disorders.
Fan Y, Shen S, Yang J, Yao D, Li M, Mao C, Wang Y, Hao X, Ma D, Li J, Shi J, Guo M, Li S, Yuan Y, Liu F, Yang Z, Zhang S, Hu Z, Fan L, Liu H, Zhang C, Wang Y, Wang Q, Zheng H, He Y, Song B, Xu Y, Shi C. Fan Y, et al. Among authors: li s, li j, li m. Ann Neurol. 2022 May;91(5):704-715. doi: 10.1002/ana.26325. Epub 2022 Mar 8. Ann Neurol. 2022. PMID: 35152460
Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22.
Li M, Liu F, Hao X, Fan Y, Li J, Hu Z, Shi J, Fan L, Zhang S, Ma D, Guo M, Xu Y, Shi C. Li M, et al. Among authors: li j. Front Mol Neurosci. 2022 Jun 23;15:919199. doi: 10.3389/fnmol.2022.919199. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35813061 Free PMC article.
75,795 results
You have reached the last available page of results. Please see the User Guide for more information.