Tracy L. Young‐Pearse

7.7k total citations
82 papers, 4.4k citations indexed

About

Tracy L. Young‐Pearse is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Tracy L. Young‐Pearse has authored 82 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 39 papers in Physiology and 24 papers in Cellular and Molecular Neuroscience. Recurrent topics in Tracy L. Young‐Pearse's work include Alzheimer's disease research and treatments (39 papers), Neuroinflammation and Neurodegeneration Mechanisms (16 papers) and Neuroscience and Neuropharmacology Research (10 papers). Tracy L. Young‐Pearse is often cited by papers focused on Alzheimer's disease research and treatments (39 papers), Neuroinflammation and Neurodegeneration Mechanisms (16 papers) and Neuroscience and Neuropharmacology Research (10 papers). Tracy L. Young‐Pearse collaborates with scholars based in United States, United Kingdom and Canada. Tracy L. Young‐Pearse's co-authors include Constance L. Cepko, Dennis J. Selkoe, Tomoki Matsuda, Priya Srikanth, Christina Muratore, Rui B. Chang, Dominic M. Walsh, Dana G. Callahan, Heather C. Rice and Jilin Bai and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Tracy L. Young‐Pearse

73 papers receiving 4.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tracy L. Young‐Pearse United States	35	2.8k	1.5k	1.0k	588	550	82	4.4k
Yuji Owada Japan	40	2.8k 1.0×	620 0.4×	1.0k 1.0×	600 1.0×	367 0.7×	178	5.1k
Michal Hetman United States	39	2.8k 1.0×	617 0.4×	1.7k 1.6×	412 0.7×	430 0.8×	82	4.9k
Ronit Pinkas‐Kramarski Israel	38	2.9k 1.0×	856 0.6×	907 0.9×	300 0.5×	470 0.9×	69	5.5k
Santosh R. D’Mello United States	38	3.3k 1.2×	592 0.4×	1.6k 1.5×	397 0.7×	367 0.7×	92	4.9k
Raymond J. Kelleher United States	34	3.6k 1.3×	1.4k 0.9×	1.7k 1.6×	452 0.8×	406 0.7×	56	6.4k
Sonja Forss‐Petter Austria	30	2.8k 1.0×	924 0.6×	775 0.7×	262 0.4×	334 0.6×	59	4.1k
Taro Saito Japan	36	2.2k 0.8×	993 0.7×	1.1k 1.0×	211 0.4×	306 0.6×	122	4.2k
Judith A. Steen United States	29	2.8k 1.0×	659 0.4×	738 0.7×	273 0.5×	233 0.4×	67	4.1k
Raya Eilam Israel	40	1.7k 0.6×	547 0.4×	718 0.7×	506 0.9×	549 1.0×	70	4.3k
Santiago Rivera France	36	1.3k 0.5×	1.0k 0.7×	907 0.9×	929 1.6×	573 1.0×	73	3.3k

Countries citing papers authored by Tracy L. Young‐Pearse

Since Specialization

Citations

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

Fields of papers citing papers by Tracy L. Young‐Pearse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tracy L. Young‐Pearse. 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 Tracy L. Young‐Pearse. The network helps show where Tracy L. Young‐Pearse may publish in the future.

Co-authorship network of co-authors of Tracy L. Young‐Pearse

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

All Works

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20 of 20 papers shown

Pasławski, Wojciech, Sheng-Bin Peng, Tracy L. Young‐Pearse, et al.. (2025). Parkinson disease–associated toxic exposures selectively up-regulate vesicular glutamate transporter vGlut2 in a model of human cortical neurons. Molecular Biology of the Cell. 36(2). br4–br4.

Lee, Hyo, Richard V. Pearse, Zachary M. Augur, et al.. (2025). Contributions of Genetic Variation in Astrocytes to Cell and Molecular Mechanisms of Risk and Resilience to Late‐Onset Alzheimer's Disease. Glia. 73(6). 1166–1187. 9 indexed citations

Galle, Peter R., et al.. (2025). Protocol for generating a human iPSC-derived tri-culture model to study interactions between neurons, astrocytes, and microglia. STAR Protocols. 6(4). 104152–104152.

Oveisgharan, Shahram, Lei Yu, Jingyun Yang, et al.. (2025). Cortical Gray Matter Proteins Associated With Cerebral Amyloid Angiopathy in Community-Dwelling Older Adults. Neurology. 105(6). e214024–e214024. 1 indexed citations

Pearse, Richard V., Sarah E. Heuer, Peter R. Galle, et al.. (2025). CLU alleviates Alzheimer’s disease-relevant processes by modulating astrocyte reactivity and microglia-dependent synaptic density. Neuron. 113(12). 1925–1946.e11. 8 indexed citations

Wang, Zemin, Ming Jin, Wei Hong, et al.. (2023). Learnings about Aβ from human brain recommend the use of a live-neuron bioassay for the discovery of next generation Alzheimer’s disease immunotherapeutics. Acta Neuropathologica Communications. 11(1). 39–39. 8 indexed citations

Zhu, Kuixi, Marc Henrion, Melissa Alamprese, et al.. (2023). Predictive network analysis identifies JMJD6 and other potential key drivers in Alzheimer’s disease. Communications Biology. 6(1). 503–503. 7 indexed citations

Nguyen, Lien D., Zhiyun Wei, M. Catarina Silva, et al.. (2023). Small molecule regulators of microRNAs identified by high-throughput screen coupled with high-throughput sequencing. Nature Communications. 14(1). 7575–7575. 31 indexed citations

Tran, Khanh V., Nathaniel Barton, Qi Wang, et al.. (2023). Transcriptomics‐based investigation of herpes simplex virus 1 infections and acyclovir treatment in human cerebral organoids. Alzheimer s & Dementia. 19(S24). 1 indexed citations

10.

Chou, Vicky, Richard V. Pearse, Mariko Taga, et al.. (2023). INPP5D regulates inflammasome activation in human microglia. Nature Communications. 14(1). 7552–7552. 38 indexed citations

11.

Lomoio, Selene, Ravi S. Pandey, Nicolas Rouleau, et al.. (2023). 3D bioengineered neural tissue generated from patient-derived iPSCs mimics time-dependent phenotypes and transcriptional features of Alzheimer’s disease. Molecular Psychiatry. 28(12). 5390–5401. 7 indexed citations

12.

Pearse, Richard V., Yi‐Chen Hsieh, Duc M. Duong, et al.. (2022). APP and DYRK1A regulate axonal and synaptic vesicle protein networks and mediate Alzheimer’s pathology in trisomy 21 neurons. Molecular Psychiatry. 27(4). 1970–1989. 23 indexed citations

13.

Yu, Lei, Yi‐Chen Hsieh, Richard V. Pearse, et al.. (2022). Association of AK4 Protein From Stem Cell–Derived Neurons With Cognitive Reserve. Neurology. 99(20). e2264–e2274. 6 indexed citations

14.

Clark, Lars E., Sarah A. Clark, Jianying Liu, et al.. (2021). VLDLR and ApoER2 are receptors for multiple alphaviruses. Nature. 602(7897). 475–480. 73 indexed citations

15.

Raj, Towfique, Yang Li, Garrett Wong, et al.. (2018). Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer’s disease susceptibility. Nature Genetics. 50(11). 1584–1592. 261 indexed citations

16.

Srikanth, Priya, et al.. (2018). Shared effects of DISC1 disruption and elevated WNT signaling in human cerebral organoids. Translational Psychiatry. 8(1). 77–77. 57 indexed citations

17.

Klein, Hans‐Ulrich, Cristin McCabe, Elizabeta Gjoneska, et al.. (2018). Epigenome-wide study uncovers large-scale changes in histone acetylation driven by tau pathology in aging and Alzheimer’s human brains. Nature Neuroscience. 22(1). 37–46. 173 indexed citations

18.

Jin, Ming, Brian O’Nuallain, Wei Hong, et al.. (2018). An in vitro paradigm to assess potential anti-Aβ antibodies for Alzheimer’s disease. Nature Communications. 9(1). 2676–2676. 48 indexed citations

19.

Sullivan, Sarah E. & Tracy L. Young‐Pearse. (2015). Induced pluripotent stem cells as a discovery tool for Alzheimer׳s disease. Brain Research. 1656. 98–106. 32 indexed citations

20.

Rowan, Sheldon, et al.. (2004). Transdifferentiation of the retina into pigmented cells in ocular retardation mice defines a new function of the homeodomain geneChx10. Development. 131(20). 5139–5152. 132 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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