Deborah A. Goldspink

1.5k total citations
20 papers, 652 citations indexed

About

Deborah A. Goldspink is a scholar working on Surgery, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Deborah A. Goldspink has authored 20 papers receiving a total of 652 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Surgery, 7 papers in Molecular Biology and 7 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Deborah A. Goldspink's work include Pancreatic function and diabetes (9 papers), Diabetes Treatment and Management (6 papers) and Microtubule and mitosis dynamics (5 papers). Deborah A. Goldspink is often cited by papers focused on Pancreatic function and diabetes (9 papers), Diabetes Treatment and Management (6 papers) and Microtubule and mitosis dynamics (5 papers). Deborah A. Goldspink collaborates with scholars based in United Kingdom, United States and Netherlands. Deborah A. Goldspink's co-authors include Frank Reimann, Fiona M. Gribble, Pierre Larraufie, Richard G. Kay, Lawrence Billing, Mette M. Mogensen, Van B. Lu, Emily L. Miedzybrodzka, Rachel E. Foreman and Jo E. Lewis and has published in prestigious journals such as The Journal of Physiology, Scientific Reports and Journal of Cell Science.

In The Last Decade

Deborah A. Goldspink

19 papers receiving 641 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deborah A. Goldspink United Kingdom 13 286 190 180 120 113 20 652
Kihachi Ohshima Japan 17 277 1.0× 154 0.8× 193 1.1× 131 1.1× 234 2.1× 52 769
Sinju Sundaresan United States 14 411 1.4× 146 0.8× 75 0.4× 33 0.3× 131 1.2× 24 945
Y. Tokuyama Japan 15 297 1.0× 216 1.1× 131 0.7× 42 0.3× 95 0.8× 18 729
Mohammed Jarrar United States 12 201 0.7× 104 0.5× 216 1.2× 98 0.8× 145 1.3× 21 919
Iskandar Yakubov United States 9 261 0.9× 273 1.4× 49 0.3× 41 0.3× 145 1.3× 13 759
Yoshiro Kitahara Japan 12 164 0.6× 102 0.5× 152 0.8× 39 0.3× 116 1.0× 19 537
A. Stefanutti France 13 240 0.8× 169 0.9× 211 1.2× 30 0.3× 232 2.1× 15 646
Thomas S. Heard United States 11 354 1.2× 197 1.0× 106 0.6× 41 0.3× 94 0.8× 15 646
K. Tsuda Japan 14 301 1.1× 227 1.2× 217 1.2× 24 0.2× 118 1.0× 32 788
J.A. Chayvialle France 15 237 0.8× 284 1.5× 380 2.1× 35 0.3× 122 1.1× 38 969

Countries citing papers authored by Deborah A. Goldspink

Since Specialization
Citations

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

Fields of papers citing papers by Deborah A. Goldspink

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah A. Goldspink. 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 Deborah A. Goldspink. The network helps show where Deborah A. Goldspink may publish in the future.

Co-authorship network of co-authors of Deborah A. Goldspink

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah A. Goldspink. A scholar is included among the top collaborators of Deborah A. Goldspink 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 Deborah A. Goldspink. Deborah A. Goldspink 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.
Macphee, Colin H., Xinzhong Dong, Peng Qi, et al.. (2024). Pharmacological blockade of the mast cell MRGPRX2 receptor supports investigation of its relevance in skin disorders. Frontiers in Immunology. 15. 1433982–1433982. 8 indexed citations
2.
Smith, Christopher A., Van B. Lu, Rula Bany Bakar, et al.. (2024). Single‐cell transcriptomics of human organoid‐derived enteroendocrine cell populations from the small intestine. The Journal of Physiology. 603(24). 7751–7763. 3 indexed citations
3.
Yang, Ming, Tamana Darwish, Pierre Larraufie, et al.. (2021). Inhibition of mitochondrial function by metformin increases glucose uptake, glycolysis and GDF-15 release from intestinal cells. Scientific Reports. 11(1). 2529–2529. 72 indexed citations
4.
Miedzybrodzka, Emily L., Rachel E. Foreman, Van B. Lu, et al.. (2021). Stimulation of motilin secretion by bile, free fatty acids, and acidification in human duodenal organoids. Molecular Metabolism. 54. 101356–101356. 19 indexed citations
5.
Miedzybrodzka, Emily L., Rachel E. Foreman, Van B. Lu, et al.. (2021). Stimulation of motilin secretion by bile, free fatty acids and acidification in human duodenal organoids. Endocrine Abstracts.
6.
Miedzybrodzka, Emily L., Rachel E. Foreman, Pierre Larraufie, et al.. (2020). Organoid Sample Preparation and Extraction for LC-MS Peptidomics. STAR Protocols. 1(3). 100164–100164. 10 indexed citations
7.
Goldspink, Deborah A., Van B. Lu, Emily L. Miedzybrodzka, et al.. (2020). Labeling and Characterization of Human GLP-1-Secreting L-cells in Primary Ileal Organoid Culture. Cell Reports. 31(13). 107833–107833. 54 indexed citations
8.
Lewis, Jo E., Emily L. Miedzybrodzka, Rachel E. Foreman, et al.. (2020). Selective stimulation of colonic L cells improves metabolic outcomes in mice. Diabetologia. 63(7). 1396–1407. 46 indexed citations
9.
Larraufie, Pierre, Richard G. Kay, Tamana Darwish, et al.. (2019). Characterisation of proguanylin expressing cells in the intestine – evidence for constitutive luminal secretion. Scientific Reports. 9(1). 15574–15574. 11 indexed citations
11.
Billing, Lawrence, Christopher A. Smith, Pierre Larraufie, et al.. (2018). Co-storage and release of insulin-like peptide-5, glucagon-like peptide-1 and peptideYY from murine and human colonic enteroendocrine cells. Molecular Metabolism. 16. 65–75. 52 indexed citations
12.
Goldspink, Deborah A., Frank Reimann, & Fiona M. Gribble. (2018). Models and Tools for Studying Enteroendocrine Cells. Endocrinology. 159(12). 3874–3884. 26 indexed citations
14.
Psichas, Arianna, Pierre Larraufie, Deborah A. Goldspink, Fiona M. Gribble, & Frank Reimann. (2017). Chylomicrons stimulate incretin secretion in mouse and human cells. Diabetologia. 60(12). 2475–2485. 48 indexed citations
15.
Goldspink, Deborah A., James D. Perkins, Elizabeth K. Lund, et al.. (2017). Ninein is essential for apico-basal microtubule formation and CLIP-170 facilitates its redeployment to non-centrosomal microtubule organizing centres. Open Biology. 7(2). 160274–160274. 44 indexed citations
16.
Goldspink, Deborah A., Van B. Lu, Lawrence Billing, et al.. (2017). Mechanistic insights into the detection of free fatty and bile acids by ileal glucagon-like peptide-1 secreting cells. Molecular Metabolism. 7. 90–101. 50 indexed citations
18.
Goldspink, Deborah A., et al.. (2013). The microtubule end-binding protein EB2 is a central regulator of microtubule reorganisation in apico-basal epithelial differentiation. Journal of Cell Science. 126(Pt 17). 4000–14. 38 indexed citations
19.
Goldspink, Deborah A., et al.. (2009). Microtubule plus‐end and minus‐end capture at adherens junctions is involved in the assembly of apico‐basal arrays in polarised epithelial cells. Cell Motility and the Cytoskeleton. 66(10). 893–908. 58 indexed citations
20.
Sampieri, Clara Luz, Robert K. Nuttall, David A. Young, et al.. (2007). Activation of p38 and JNK MAPK pathways abrogates requirement for new protein synthesis for phorbol ester mediated induction of select MMP and TIMP genes. Matrix Biology. 27(2). 128–138. 29 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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