Maoxu Lu - Search Results

Year	Number of Results
2006	2
2007	4
2008	8
2009	5
2010	9
2011	3
2012	6
2013	5
2014	4
2015	1
2016	2
2017	5
2018	4
2019	7
2020	6
2021	8
2022	5
2023	7
2024	1

1

Clinical and Molecular Features of a Chinese Cohort With Syndromic and Nonsyndromic Retinal Dystrophies Related to the CEP290 Gene.

Zhu T, Shen Y, Sun Z, Han X, Wei X, Li W, Lu C, Cheng T, Zou X, Li H, Cao Z, Gao H, Ma X, Luo M, Sui R. Zhu T, et al. Among authors: ma x. Am J Ophthalmol. 2023 Apr;248:96-106. doi: 10.1016/j.ajo.2022.11.023. Epub 2022 Dec 7. Am J Ophthalmol. 2023. PMID: 36493848

2

Machine Learning Approaches for Rice Seedling Growth Stages Detection.

Tan S, Liu J, Lu H, Lan M, Yu J, Liao G, Wang Y, Li Z, Qi L, Ma X. Tan S, et al. Among authors: ma x. Front Plant Sci. 2022 Jun 9;13:914771. doi: 10.3389/fpls.2022.914771. eCollection 2022. Front Plant Sci. 2022. PMID: 35755682 Free PMC article.

3

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: ma x. 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.

4

An Effective Dual Self-Attention Residual Network for Seizure Prediction.

Yang X, Zhao J, Sun Q, Lu J, Ma X. Yang X, et al. Among authors: ma x. IEEE Trans Neural Syst Rehabil Eng. 2021;29:1604-1613. doi: 10.1109/TNSRE.2021.3103210. Epub 2021 Aug 20. IEEE Trans Neural Syst Rehabil Eng. 2021. PMID: 34370668

5

Machine Learning-Based Prediction Model of Preterm Birth Using Electronic Health Record.

Sun Q, Zou X, Yan Y, Zhang H, Wang S, Gao Y, Liu H, Liu S, Lu J, Yang Y, Ma X. Sun Q, et al. Among authors: ma x. J Healthc Eng. 2022 Apr 13;2022:9635526. doi: 10.1155/2022/9635526. eCollection 2022. J Healthc Eng. 2022. PMID: 35463669 Free PMC article.

6

Increased Risk of Stillbirth among Women whose Partner Has Tuberculosis.

Sun Q, Zhang H, Zhang Y, Peng Z, Lu J, Ma X. Sun Q, et al. Among authors: ma x. Biomed Res Int. 2021 Sep 14;2021:1837881. doi: 10.1155/2021/1837881. eCollection 2021. Biomed Res Int. 2021. PMID: 34568487 Free PMC article.

7

Association Between Carbon Emission and Low Birth Weight in Mainland China.

Sun Q, Zhang Y, Wang Y, Lu J, Ma X. Sun Q, et al. Among authors: ma x. J Occup Environ Med. 2023 Mar 1;65(3):e147-e154. doi: 10.1097/JOM.0000000000002775. Epub 2022 Dec 23. J Occup Environ Med. 2023. PMID: 36728925

8

Novel compound heterozygous variants in ARL13B lead to Joubert syndrome.

Lin Z, Shen Y, Li Y, Lu C, Zhu Y, He R, Cao Z, Yin Z, Gao H, Guo B, Ma X, Cao M, Luo M. Lin Z, et al. Among authors: ma x. J Cell Physiol. 2024 Apr;239(4):e31189. doi: 10.1002/jcp.31189. Epub 2024 Jan 14. J Cell Physiol. 2024. PMID: 38219074

9

Novel Compound Heterozygous Variants in MKS1 Leading to Joubert Syndrome.

Luo M, He R, Lin Z, Shen Y, Zhang G, Cao Z, Lu C, Meng D, Zhang J, Ma X, Cao M. Luo M, et al. Among authors: ma x. Front Genet. 2020 Oct 14;11:576235. doi: 10.3389/fgene.2020.576235. eCollection 2020. Front Genet. 2020. PMID: 33193692 Free PMC article.

10

Novel mutations in HSF4 cause congenital cataracts in Chinese families.

Cao Z, Zhu Y, Liu L, Wu S, Liu B, Zhuang J, Tong Y, Chen X, Xie Y, Nie K, Lu C, Ma X, Yang J. Cao Z, et al. Among authors: ma x. BMC Med Genet. 2018 Aug 24;19(1):150. doi: 10.1186/s12881-018-0636-3. BMC Med Genet. 2018. PMID: 30143024 Free PMC article.

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