Rose E. Goodchild

2.9k total citations
25 papers, 2.2k citations indexed

About

Rose E. Goodchild is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Rose E. Goodchild has authored 25 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 12 papers in Molecular Biology and 9 papers in Neurology. Recurrent topics in Rose E. Goodchild's work include Genetic Neurodegenerative Diseases (10 papers), Neurological disorders and treatments (9 papers) and Nuclear Structure and Function (6 papers). Rose E. Goodchild is often cited by papers focused on Genetic Neurodegenerative Diseases (10 papers), Neurological disorders and treatments (9 papers) and Nuclear Structure and Function (6 papers). Rose E. Goodchild collaborates with scholars based in Belgium, United States and Germany. Rose E. Goodchild's co-authors include William T. Dauer, Ana Cascalho, Julie Jacquemyn, Patrik Verstreken, Elsa Lauwers, Robert E. Burke, René Hen, Nikolai Kholodilov, Kristin E. Larsen and Serge Przedborski and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and Journal of Neuroscience.

In The Last Decade

Rose E. Goodchild

25 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rose E. Goodchild Belgium 18 1.1k 1.1k 928 463 233 25 2.2k
Diana Zala France 22 1.7k 1.5× 497 0.5× 1.9k 2.1× 405 0.9× 205 0.9× 30 2.6k
Vikram G. Shakkottai United States 29 2.0k 1.8× 665 0.6× 2.2k 2.4× 245 0.5× 368 1.6× 68 3.1k
James K. Kubilus United States 13 1.5k 1.4× 604 0.6× 1.8k 1.9× 222 0.5× 199 0.9× 18 2.4k
Ben Woodman United Kingdom 26 2.0k 1.8× 644 0.6× 2.4k 2.6× 361 0.8× 259 1.1× 29 3.0k
Jacqueline C. Mitchell United Kingdom 21 369 0.3× 1.2k 1.1× 1.3k 1.4× 443 1.0× 430 1.8× 41 2.4k
Zachary P. Wills United States 18 838 0.8× 273 0.3× 1.3k 1.4× 502 1.1× 193 0.8× 28 2.1k
Jef Swerts Belgium 20 517 0.5× 395 0.4× 912 1.0× 487 1.1× 462 2.0× 27 1.8k
Amber L. Southwell Canada 31 2.0k 1.8× 687 0.6× 2.3k 2.4× 157 0.3× 310 1.3× 48 3.2k
Sarah Mizielinska United Kingdom 17 454 0.4× 1.3k 1.2× 971 1.0× 134 0.3× 398 1.7× 28 2.1k
Cindy V. Ly United States 13 757 0.7× 254 0.2× 1.1k 1.2× 374 0.8× 254 1.1× 22 1.6k

Countries citing papers authored by Rose E. Goodchild

Since Specialization
Citations

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

Fields of papers citing papers by Rose E. Goodchild

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rose E. Goodchild. 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 Rose E. Goodchild. The network helps show where Rose E. Goodchild may publish in the future.

Co-authorship network of co-authors of Rose E. Goodchild

This figure shows the co-authorship network connecting the top 25 collaborators of Rose E. Goodchild. A scholar is included among the top collaborators of Rose E. Goodchild 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 Rose E. Goodchild. Rose E. Goodchild 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.
Baatsen, Pieter, et al.. (2021). Preservation of Fluorescence Signal and Imaging Optimization for Integrated Light and Electron Microscopy. Frontiers in Cell and Developmental Biology. 9. 737621–737621. 8 indexed citations
2.
Cascalho, Ana, Jef Swerts, Christine Klein, et al.. (2020). Excess Lipin enzyme activity contributes to TOR1A recessive disease and DYT-TOR1A dystonia. Brain. 143(6). 1746–1765. 16 indexed citations
3.
Yu-Taeger, Libo, Thomas Ott, Paola Bonsi, et al.. (2019). Impaired dopamine- and adenosine-mediated signaling and plasticity in a novel rodent model for DYT25 dystonia. Neurobiology of Disease. 134. 104634–104634. 21 indexed citations
4.
Nieuwenhuijze, Annemarie van, Oliver T. Burton, Pierre Lemaître, et al.. (2018). Mice Deficient in Nucleoporin Nup210 Develop Peripheral T Cell Alterations. Frontiers in Immunology. 9. 2234–2234. 6 indexed citations
5.
Maltese, Marta, Giuseppina Martella, Paola Imbriani, et al.. (2017). Abnormal striatal plasticity in a DYT11/SGCE myoclonus dystonia mouse model is reversed by adenosine A2A receptor inhibition. Neurobiology of Disease. 108. 128–139. 32 indexed citations
6.
Jacquemyn, Julie, Ana Cascalho, & Rose E. Goodchild. (2017). The ins and outs of endoplasmic reticulum‐controlled lipid biosynthesis. EMBO Reports. 18(11). 1905–1921. 193 indexed citations
7.
Grillet, Micheline, Ana Cascalho, Sergio Hernández-Díaz, et al.. (2016). Torsins Are Essential Regulators of Cellular Lipid Metabolism. Developmental Cell. 38(3). 235–247. 69 indexed citations
8.
Lauwers, Elsa, Rose E. Goodchild, & Patrik Verstreken. (2016). Membrane Lipids in Presynaptic Function and Disease. Neuron. 90(1). 11–25. 166 indexed citations
9.
Goodchild, Rose E., Abigail Buchwalter, Teresa V. Naismith, et al.. (2015). Access of torsinA to the inner nuclear membrane is activity dependent and regulated in the endoplasmic reticulum. Journal of Cell Science. 128(15). 2854–65. 33 indexed citations
10.
Goodchild, Rose E., Kathrin Grundmann, & Antonio Pisani. (2013). New genetic insights highlight ‘old’ ideas on motor dysfunction in dystonia. Trends in Neurosciences. 36(12). 717–725. 42 indexed citations
11.
Kumar, Dhivya, et al.. (2011). The nuclear envelope localization of DYT1 dystonia torsinA-ΔE requires the SUN1 LINC complex component. BMC Cell Biology. 12(1). 24–24. 34 indexed citations
12.
Dear, Mary Lynn, et al.. (2009). Relative tissue expression of homologous torsinB correlates with the neuronal specific importance of DYT1 dystonia-associated torsinA. Human Molecular Genetics. 19(5). 888–900. 60 indexed citations
13.
Johnson, Matthew A., Michael D. Lieberman, Rose E. Goodchild, et al.. (2008). Type III Neuregulin-1 Is Required for Normal Sensorimotor Gating, Memory-Related Behaviors, and Corticostriatal Circuit Components. Journal of Neuroscience. 28(27). 6872–6883. 149 indexed citations
14.
Goodchild, Rose E. & William T. Dauer. (2005). The AAA+ protein torsinA interacts with a conserved domain present in LAP1 and a novel ER protein. The Journal of Cell Biology. 168(6). 855–862. 177 indexed citations
15.
Goodchild, Rose E., et al.. (2005). Loss of the Dystonia-Associated Protein TorsinA Selectively Disrupts the Neuronal Nuclear Envelope. Neuron. 48(6). 923–932. 304 indexed citations
16.
Goodchild, Rose E. & William T. Dauer. (2004). Mislocalization to the nuclear envelope: An effect of the dystonia-causing torsinA mutation. Proceedings of the National Academy of Sciences. 101(3). 847–852. 208 indexed citations
17.
Hamilton, William, A Round, Rose E. Goodchild, & Caroline Baker. (2003). Do community based self-reading sphygmomanometers improve detection of hypertension? A feasibility study. Journal of Public Health. 25(2). 125–130. 12 indexed citations
18.
Dauer, William T., Nikolai Kholodilov, Miquel Vila, et al.. (2002). Resistance of α-synuclein null mice to the parkinsonian neurotoxin MPTP. Proceedings of the National Academy of Sciences. 99(22). 14524–14529. 457 indexed citations
19.
Goodchild, Rose E., J.A. Court, Margaret A. Piggott, et al.. (1999). Distribution of histamine H3‐receptor binding in the normal human basal ganglia: comparison with Huntington's and Parkinson's disease cases. European Journal of Neuroscience. 11(2). 449–456. 57 indexed citations
20.
Perry, Elaine, J.A. Court, Rose E. Goodchild, et al.. (1998). Clinical neurochemistry: developments in dementia research based on brain bank material. Journal of Neural Transmission. 105(8-9). 915–933. 60 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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