Julia TCW

5.1k total citations
25 papers, 1.1k citations indexed

About

Julia TCW is a scholar working on Molecular Biology, Physiology and Neurology. According to data from OpenAlex, Julia TCW has authored 25 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 12 papers in Physiology and 6 papers in Neurology. Recurrent topics in Julia TCW's work include Alzheimer's disease research and treatments (12 papers), Pluripotent Stem Cells Research (7 papers) and Neuroinflammation and Neurodegeneration Mechanisms (6 papers). Julia TCW is often cited by papers focused on Alzheimer's disease research and treatments (12 papers), Pluripotent Stem Cells Research (7 papers) and Neuroinflammation and Neurodegeneration Mechanisms (6 papers). Julia TCW collaborates with scholars based in United States, Spain and Switzerland. Julia TCW's co-authors include Alison Goate, Kristen Brennand, Paul A. Slesinger, Brigham J. Hartley, Sarah M. Neuner, Kathryn R. Bowles, Bin Zhang, Anna A. Pimenova, Emre Lacin and Celeste M. Karch and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Journal of Neuroscience.

In The Last Decade

Julia TCW

22 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julia TCW United States 15 633 394 302 210 165 25 1.1k
Charles Arber United Kingdom 16 642 1.0× 351 0.9× 294 1.0× 331 1.6× 183 1.1× 32 1.1k
Matheus B. Victor United States 12 877 1.4× 324 0.8× 386 1.3× 359 1.7× 176 1.1× 16 1.4k
Heather C. Rice United States 14 484 0.8× 465 1.2× 164 0.5× 324 1.5× 119 0.7× 22 964
Anna A. Pimenova United States 8 370 0.6× 288 0.7× 447 1.5× 171 0.8× 152 0.9× 10 906
Yuan-Ta Lin United States 7 569 0.9× 314 0.8× 217 0.7× 218 1.0× 191 1.2× 8 965
Michael Sasner United States 14 429 0.7× 343 0.9× 273 0.9× 272 1.3× 60 0.4× 31 974
Jessica E. Young United States 20 1.2k 1.9× 586 1.5× 207 0.7× 772 3.7× 121 0.7× 52 1.9k
Desirée Loreth Germany 13 360 0.6× 311 0.8× 190 0.6× 210 1.0× 71 0.4× 23 850
Israel Hernández United States 8 617 1.0× 495 1.3× 194 0.6× 233 1.1× 66 0.4× 11 1.1k
Kenichi Nagata Japan 14 522 0.8× 601 1.5× 237 0.8× 263 1.3× 63 0.4× 30 1.2k

Countries citing papers authored by Julia TCW

Since Specialization
Citations

This map shows the geographic impact of Julia TCW'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 Julia TCW with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julia TCW more than expected).

Fields of papers citing papers by Julia TCW

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julia TCW. 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 Julia TCW. The network helps show where Julia TCW may publish in the future.

Co-authorship network of co-authors of Julia TCW

This figure shows the co-authorship network connecting the top 25 collaborators of Julia TCW. A scholar is included among the top collaborators of Julia TCW 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 Julia TCW. Julia TCW is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Inoue, Yasuteru, Hu Wang, Michael G. Heckman, et al.. (2025). Impact of APOE on cerebrovascular lipid profile in Alzheimer’s disease. Acta Neuropathologica. 150(1). 39–39.
2.
Yassine, Hussein N., Bernadette O’Donovan, Lance A. Johnson, et al.. (2025). APOE-Targeted Therapeutics for Alzheimer's Disease. Journal of Neuroscience. 45(46). e1388252025–e1388252025. 1 indexed citations
3.
Wang, Shaowei, Boyang Li, Jie Li, et al.. (2025). Cellular senescence induced by cholesterol accumulation is mediated by lysosomal ABCA1 in APOE4 and AD. Molecular Neurodegeneration. 20(1). 15–15. 9 indexed citations
4.
Saha, Orthis, Karine Guyot, Yun Shen, et al.. (2024). The Alzheimer’s disease risk gene BIN1 regulates activity-dependent gene expression in human-induced glutamatergic neurons. Molecular Psychiatry. 29(9). 2634–2646. 12 indexed citations
5.
Vance, Jeffery M., Lindsay A. Farrer, Yadong Huang, et al.. (2024). Report of the APOE4 National Institute on Aging/Alzheimer Disease Sequencing Project Consortium Working Group: Reducing APOE4 in Carriers is a Therapeutic Goal for Alzheimer's Disease. Annals of Neurology. 95(4). 625–634. 21 indexed citations
6.
TCW, Julia & Amaia M. Arranz. (2023). hiPSC-based models to decipher the contribution of human astrocytes to Alzheimer’s disease and potential therapeutics. Molecular Neurodegeneration. 18(1). 19–19.
7.
Lü, Qian, et al.. (2023). Clearance of intracellular lipids by lipophagy impaired in APOE ε4 human astrocytes. Alzheimer s & Dementia. 19(S13). 1 indexed citations
8.
Kerman, Bilal E., Joon Lee, Shaowei Wang, et al.. (2023). Mechanisms of reduced Apolipoprotein E4 lipidation in iPSC‐derived astrocytes. Alzheimer s & Dementia. 19(S13).
9.
Preman, Pranav, Julia TCW, Sara Calafate, et al.. (2021). Human iPSC-derived astrocytes transplanted into the mouse brain undergo morphological changes in response to amyloid-β plaques. Molecular Neurodegeneration. 16(1). 44 indexed citations
10.
Cao, Jiqing, Min Huang, Lei Guo, et al.. (2020). MicroRNA-195 rescues ApoE4-induced cognitive deficits and lysosomal defects in Alzheimer’s disease pathogenesis. Molecular Psychiatry. 26(9). 4687–4701. 56 indexed citations
11.
Neuner, Sarah M., Julia TCW, & Alison Goate. (2020). Genetic architecture of Alzheimer's disease. Neurobiology of Disease. 143. 104976–104976. 74 indexed citations
12.
Novikova, Gloriia, Edoardo Marcora, Manav Kapoor, et al.. (2020). Integration of Alzheimer’s disease genetics and myeloid genomics reveals novel disease risk mechanisms. Alzheimer s & Dementia. 16(S3). 4 indexed citations
13.
Bowles, Kathryn R., et al.. (2019). Reduced variability of neural progenitor cells and improved purity of neuronal cultures using magnetic activated cell sorting. PLoS ONE. 14(3). e0213374–e0213374. 29 indexed citations
14.
TCW, Julia. (2019). Human iPSC application in Alzheimer’s disease and Tau-related neurodegenerative diseases. Neuroscience Letters. 699. 31–40. 29 indexed citations
15.
Grochowski, Christopher M., Shen Gu, Bo Yuan, et al.. (2018). Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes. Human Mutation. 39(7). 939–946. 19 indexed citations
16.
TCW, Julia, Minghui Wang, Anna A. Pimenova, et al.. (2017). An Efficient Platform for Astrocyte Differentiation from Human Induced Pluripotent Stem Cells. Stem Cell Reports. 9(2). 600–614. 245 indexed citations
17.
TCW, Julia, Claudia M.B. Carvalho, Bo Yuan, et al.. (2017). Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis. Stem Cell Reports. 8(3). 519–528. 6 indexed citations
18.
TCW, Julia & Alison Goate. (2016). Genetics of β-Amyloid Precursor Protein in Alzheimer's Disease. Cold Spring Harbor Perspectives in Medicine. 7(6). a024539–a024539. 149 indexed citations
19.
Ho, Seok‐Man, Brigham J. Hartley, Julia TCW, et al.. (2015). Rapid Ngn2-induction of excitatory neurons from hiPSC-derived neural progenitor cells. Methods. 101. 113–124. 94 indexed citations
20.
Ichida, Justin K., Julia TCW, Luis A. Williams, et al.. (2014). Notch inhibition allows oncogene-independent generation of iPS cells. Nature Chemical Biology. 10(8). 632–639. 54 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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