Shenzhao Lu

582 total citations
16 papers, 255 citations indexed

About

Shenzhao Lu is a scholar working on Molecular Biology, Cell Biology and Neurology. According to data from OpenAlex, Shenzhao Lu has authored 16 papers receiving a total of 255 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Cell Biology and 4 papers in Neurology. Recurrent topics in Shenzhao Lu's work include Cellular transport and secretion (4 papers), RNA regulation and disease (3 papers) and Lysosomal Storage Disorders Research (3 papers). Shenzhao Lu is often cited by papers focused on Cellular transport and secretion (4 papers), RNA regulation and disease (3 papers) and Lysosomal Storage Disorders Research (3 papers). Shenzhao Lu collaborates with scholars based in United States, China and Netherlands. Shenzhao Lu's co-authors include Hugo J. Bellen, Jiawei Zhou, Peizhou Liang, Yanqing Yin, Xueyang Pan, Debdeep Dutta, Mengqi Ma, Matthew J. Moulton, Rong Chen and Oguz Kanca and has published in prestigious journals such as The Journal of Experimental Medicine, Nature Neuroscience and Cell Metabolism.

In The Last Decade

Shenzhao Lu

16 papers receiving 253 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Shenzhao Lu United States	10	157	50	43	38	36	16	255
Gonzalo Ureta Chile	6	138 0.9×	34 0.7×	59 1.4×	44 1.2×	86 2.4×	8	281
M. Reza Jabalameli United Kingdom	10	147 0.9×	30 0.6×	46 1.1×	65 1.7×	30 0.8×	18	312
Phillippa J. Carling United Kingdom	8	232 1.5×	52 1.0×	62 1.4×	78 2.1×	24 0.7×	10	344
John Wizeman United States	7	134 0.9×	48 1.0×	58 1.3×	28 0.7×	24 0.7×	8	319
Christy Hung United Kingdom	8	130 0.8×	34 0.7×	149 3.5×	42 1.1×	55 1.5×	13	268
Natsuki Kawana Japan	7	172 1.1×	47 0.9×	83 1.9×	31 0.8×	29 0.8×	9	300
Babak Emamalizadeh Iran	11	144 0.9×	21 0.4×	30 0.7×	40 1.1×	27 0.8×	43	294
Zhi-hua Yang China	8	179 1.1×	45 0.9×	50 1.2×	60 1.6×	26 0.7×	15	324
Yoshika Hayakawa‐Yano Japan	10	283 1.8×	29 0.6×	50 1.2×	77 2.0×	49 1.4×	14	418
Tine Holemans Belgium	7	152 1.0×	21 0.4×	68 1.6×	28 0.7×	78 2.2×	8	265

Countries citing papers authored by Shenzhao Lu

Since Specialization

Citations

This map shows the geographic impact of Shenzhao Lu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Shenzhao Lu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shenzhao Lu more than expected).

Fields of papers citing papers by Shenzhao Lu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shenzhao Lu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Shenzhao Lu. The network helps show where Shenzhao Lu may publish in the future.

Co-authorship network of co-authors of Shenzhao Lu

This figure shows the co-authorship network connecting the top 25 collaborators of Shenzhao Lu. A scholar is included among the top collaborators of Shenzhao Lu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Shenzhao Lu. Shenzhao Lu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Goodman, Lindsey D., Isha Ralhan, Shenzhao Lu, et al.. (2024). Tau is required for glial lipid droplet formation and resistance to neuronal oxidative stress. Nature Neuroscience. 27(10). 1918–1933. 23 indexed citations

Pan, Xueyang, Mengqi Ma, Shenzhao Lu, et al.. (2023). Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays. eLife. 12. 2 indexed citations

Chung, Hyung-Lok, Qi Ye, Ye-Jin Park, et al.. (2023). Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation. Cell Metabolism. 35(5). 855–874.e5. 33 indexed citations

Pan, Xueyang, Debdeep Dutta, Shenzhao Lu, & Hugo J. Bellen. (2023). Sphingolipids in neurodegenerative diseases. Frontiers in Neuroscience. 17. 1137893–1137893. 27 indexed citations

Pan, Xueyang, Mengqi Ma, Shenzhao Lu, et al.. (2023). Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays. eLife. 12. 1 indexed citations

Ma, Mengqi, Xi Zhang, Yiming Zheng, et al.. (2022). The fly homolog ofSUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival. Human Molecular Genetics. 32(6). 984–997. 6 indexed citations

Lu, Shenzhao, Mengqi Ma, Xiao Mao, et al.. (2022). De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement. The American Journal of Human Genetics. 109(10). 1932–1943. 9 indexed citations

Huang, Yan, Gabrielle Lemire, Lauren C. Briere, et al.. (2022). The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability. The American Journal of Human Genetics. 109(10). 1923–1931. 10 indexed citations

Ma, Mengqi, Matthew J. Moulton, Shenzhao Lu, & Hugo J. Bellen. (2022). 'Fly-ing' from rare to common neurodegenerative disease mechanisms. Trends in Genetics. 38(9). 972–984. 19 indexed citations

10.

Lu, Shenzhao, Rebecca Hernan, Paul C. Marcogliese, et al.. (2022). Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures. The American Journal of Human Genetics. 109(4). 571–586. 17 indexed citations

11.

Lu, Shenzhao, Yue Wu, Peizhou Liang, et al.. (2022). Inhibition of astrocytic DRD2 suppresses CNS inflammation in an animal model of multiple sclerosis. The Journal of Experimental Medicine. 219(9). 14 indexed citations

12.

Huang, Yan, Mengqi Ma, Xiao Mao, et al.. (2022). Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanisms. Human Molecular Genetics. 31(16). 2751–2765. 5 indexed citations

13.

Chung, Hyung-Lok, Qi Ye, Ye-Jin Park, et al.. (2022). Very Long-Chain Fatty Acids Induce Glial-Derived Sphingosine-1-Phosphate Synthesis, Secretion, and Neuroinflammation. SSRN Electronic Journal. 2 indexed citations

14.

Lu, Shenzhao, Peizhou Liang, Shuzhen Zhang, et al.. (2019). Suppression of astrocytic autophagy by αB-crystallin contributes to α-synuclein inclusion formation. Translational Neurodegeneration. 8(1). 3–3. 45 indexed citations

15.

Liang, Peizhou, et al.. (2018). Extracellular αB-crystallin modulates the inflammatory responses. Biochemical and Biophysical Research Communications. 508(1). 282–288. 38 indexed citations

16.

Lu, Shenzhao & Jiawei Zhou. (2016). Finding the ‘Guilty’ Gene Variant of Sporadic Parkinson’s Disease Via CRISPR/Cas9. Neuroscience Bulletin. 33(1). 115–117. 4 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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