Mark P. DeAndrade

848 total citations
18 papers, 595 citations indexed

About

Mark P. DeAndrade is a scholar working on Neurology, Epidemiology and Cognitive Neuroscience. According to data from OpenAlex, Mark P. DeAndrade has authored 18 papers receiving a total of 595 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 10 papers in Epidemiology and 6 papers in Cognitive Neuroscience. Recurrent topics in Mark P. DeAndrade's work include Parkinson's Disease Mechanisms and Treatments (15 papers), Restless Legs Syndrome Research (10 papers) and Neurological disorders and treatments (6 papers). Mark P. DeAndrade is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (15 papers), Restless Legs Syndrome Research (10 papers) and Neurological disorders and treatments (6 papers). Mark P. DeAndrade collaborates with scholars based in United States, United Kingdom and Germany. Mark P. DeAndrade's co-authors include Yuqing Li, Fumiaki Yokoi, Thomas van Groen, Matthew J. LaVoie, Jerry B. Lingrel, Erica L. Unger, John Sanderson, Jason Schapansky, Heather L. Melrose and Jonathan Nardozzi and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neuroscience.

In The Last Decade

Mark P. DeAndrade

18 papers receiving 591 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark P. DeAndrade United States 13 454 225 186 132 102 18 595
Michele L. Rajput Canada 13 716 1.6× 238 1.1× 142 0.8× 126 1.0× 86 0.8× 15 793
Thora Lohnau Germany 15 497 1.1× 295 1.3× 174 0.9× 98 0.7× 84 0.8× 16 709
K. Lohmann-Hedrich Germany 9 458 1.0× 229 1.0× 112 0.6× 114 0.9× 80 0.8× 9 576
Susen Winkler Germany 15 559 1.2× 342 1.5× 82 0.4× 90 0.7× 76 0.7× 19 750
Arlene R. Ng Philippines 12 406 0.9× 214 1.0× 38 0.2× 63 0.5× 80 0.8× 24 593
Mónica Díez-Fairén Spain 11 242 0.5× 112 0.5× 55 0.3× 35 0.3× 101 1.0× 19 385
Mahadevan Gajendiran United States 8 506 1.1× 440 2.0× 176 0.9× 35 0.3× 148 1.5× 11 790
Jaione Irigoyen Spain 10 436 1.0× 178 0.8× 32 0.2× 90 0.7× 82 0.8× 11 597
Emiko Miura Japan 7 347 0.8× 117 0.5× 92 0.5× 24 0.2× 178 1.7× 11 526
Nathan Levine United States 10 432 1.0× 292 1.3× 42 0.2× 36 0.3× 149 1.5× 15 700

Countries citing papers authored by Mark P. DeAndrade

Since Specialization
Citations

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

Fields of papers citing papers by Mark P. DeAndrade

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark P. DeAndrade. 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 Mark P. DeAndrade. The network helps show where Mark P. DeAndrade may publish in the future.

Co-authorship network of co-authors of Mark P. DeAndrade

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

All Works

18 of 18 papers shown
1.
Plasschaert, Robert N., Mark P. DeAndrade, Aimin Yan, et al.. (2022). High-throughput analysis of hematopoietic stem cell engraftment after intravenous and intracerebroventricular dosing. Molecular Therapy. 30(10). 3209–3225. 9 indexed citations
2.
Xing, Hong, Yi Sheng, Mark P. DeAndrade, et al.. (2020). BTBD9 and dopaminergic dysfunction in the pathogenesis of restless legs syndrome. Brain Structure and Function. 225(6). 1743–1760. 19 indexed citations
3.
DeAndrade, Mark P., Erica L. Unger, Stefan Müeller, et al.. (2020). Mu opioid receptor knockout mouse: Phenotypes with implications on restless legs syndrome. Journal of Neuroscience Research. 98(8). 1532–1548. 9 indexed citations
4.
Xing, Hong, Mark P. DeAndrade, Pablo D. Pérez, et al.. (2020). The Role of BTBD9 in the Cerebellum, Sleep-like Behaviors and the Restless Legs Syndrome. Neuroscience. 440. 85–96. 17 indexed citations
5.
Sheng, Yi, Mark P. DeAndrade, Youfeng Yang, et al.. (2020). Probing the relationship between BTBD9 and MEIS1 in C. elegans and mouse. SHILAP Revista de lepidopterología. 1. 1 indexed citations
6.
Sanyal, Anwesha, Mark P. DeAndrade, Steven C. Lin, et al.. (2020). Lysosome and Inflammatory Defects in GBA1‐Mutant Astrocytes Are Normalized by LRRK2 Inhibition. Movement Disorders. 35(5). 760–773. 72 indexed citations
7.
Xing, Hong, Mark P. DeAndrade, Pablo D. Pérez, et al.. (2019). The role of BTBD9 in the cerebral cortex and the pathogenesis of restless legs syndrome. Experimental Neurology. 323. 113111–113111. 14 indexed citations
8.
DeAndrade, Mark P., et al.. (2019). Hyperactivity, dopaminergic abnormalities, iron deficiency and anemia in an in vivo opioid receptors knockout mouse: Implications for the restless legs syndrome. Behavioural Brain Research. 374. 112123–112123. 16 indexed citations
9.
Xing, Hong, Mark P. DeAndrade, Yuning Liu, et al.. (2019). The Role of BTBD9 in Striatum and Restless Legs Syndrome. eNeuro. 6(5). ENEURO.0277–19.2019. 29 indexed citations
10.
Schapansky, Jason, Saurabh Khasnavis, Mark P. DeAndrade, et al.. (2017). Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons. Neurobiology of Disease. 111. 26–35. 101 indexed citations
11.
12.
Yokoi, Fumiaki, et al.. (2013). Engineering animal models of dystonia. Movement Disorders. 28(7). 990–1000. 42 indexed citations
13.
DeAndrade, Mark P., Russell L. Johnson, Erica L. Unger, et al.. (2012). Motor restlessness, sleep disturbances, thermal sensory alterations and elevated serum iron levels in Btbd9 mutant mice. Human Molecular Genetics. 21(18). 3984–3992. 67 indexed citations
14.
DeAndrade, Mark P., Fumiaki Yokoi, Huanxin Chen, et al.. (2012). Enhanced Hippocampal Long-Term Potentiation and Fear Memory in Btbd9 Mutant Mice. PLoS ONE. 7(4). e35518–e35518. 28 indexed citations
15.
Zhang, Lin, Fumiaki Yokoi, Mark P. DeAndrade, et al.. (2011). Altered Dendritic Morphology of Purkinje cells in Dyt1 ΔGAG Knock-In and Purkinje Cell-Specific Dyt1 Conditional Knockout Mice. PLoS ONE. 6(3). e18357–e18357. 65 indexed citations
16.
Li, Yuqing, et al.. (2011). W-L-087 CHARACTERIZATION OF BTBD9 HOMOLOG KNOCKOUT IN C.ELEGANS. Sleep Medicine. 12. S117–S117. 1 indexed citations
17.
DeAndrade, Mark P., Fumiaki Yokoi, Thomas van Groen, Jerry B. Lingrel, & Yuqing Li. (2010). Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism. Behavioural Brain Research. 216(2). 659–665. 68 indexed citations
18.
Yokoi, Fumiaki, et al.. (2010). Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce. The Journal of Biochemistry. 148(4). 459–466. 34 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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