Matthew Wherlock

481 total citations
7 papers, 374 citations indexed

About

Matthew Wherlock is a scholar working on Molecular Biology, Nephrology and Cell Biology. According to data from OpenAlex, Matthew Wherlock has authored 7 papers receiving a total of 374 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Nephrology and 3 papers in Cell Biology. Recurrent topics in Matthew Wherlock's work include Renal Diseases and Glomerulopathies (3 papers), Protein Kinase Regulation and GTPase Signaling (2 papers) and Cellular transport and secretion (2 papers). Matthew Wherlock is often cited by papers focused on Renal Diseases and Glomerulopathies (3 papers), Protein Kinase Regulation and GTPase Signaling (2 papers) and Cellular transport and secretion (2 papers). Matthew Wherlock collaborates with scholars based in United Kingdom, Netherlands and Ireland. Matthew Wherlock's co-authors include Alexandra Gampel, Clare E. Futter, Gavin I. Welsh, Moin A. Saleem, Lan Ni, Jeremy M. Tavaré, Jack F.M. Wetzels, Hugh J. McCarthy, Bethan Lloyd‐Lewis and Rachel Lennon and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Cell Science and The Journal of Pathology.

In The Last Decade

Matthew Wherlock

7 papers receiving 371 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matthew Wherlock United Kingdom	7	255	126	69	34	30	7	374
Laiji Li Canada	13	332 1.3×	86 0.7×	23 0.3×	87 2.6×	27 0.9×	17	482
Kyla D. Baron Canada	7	217 0.9×	59 0.5×	15 0.2×	23 0.7×	25 0.8×	7	324
Simona Wagner Canada	9	192 0.8×	119 0.9×	12 0.2×	69 2.0×	17 0.6×	10	352
Debbie K.W. Hsu United States	9	263 1.0×	48 0.4×	12 0.2×	36 1.1×	70 2.3×	12	359
Christopher Hoover United States	11	131 0.5×	76 0.6×	13 0.2×	22 0.6×	91 3.0×	13	344
Pasquale Cervero Germany	8	152 0.6×	146 1.2×	10 0.1×	54 1.6×	51 1.7×	11	359
Rena Zheng United States	5	95 0.4×	59 0.5×	86 1.2×	14 0.4×	68 2.3×	9	262
Monica Piccini Italy	8	240 0.9×	17 0.1×	18 0.3×	35 1.0×	22 0.7×	8	378
Bettina Maier Germany	9	302 1.2×	276 2.2×	20 0.3×	94 2.8×	16 0.5×	11	438
David Casagolda Spain	6	321 1.3×	102 0.8×	5 0.1×	65 1.9×	29 1.0×	7	380

Countries citing papers authored by Matthew Wherlock

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Wherlock

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Wherlock

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

All Works

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7 of 7 papers shown

1.

Rollason, Ruth, et al.. (2016). Disease causing mutations in inverted formin 2 regulate its binding to G-actin, F-actin capping protein (CapZ α-1) and profilin 2. Bioscience Reports. 36(1). e00302–e00302. 17 indexed citations

2.

McCarthy, Hugh J., Lan Ni, Matthew Wherlock, et al.. (2012). Active proteases in nephrotic plasma lead to a podocin‐dependent phosphorylation of VASP in podocytes via protease activated receptor‐1. The Journal of Pathology. 229(5). 660–671. 53 indexed citations

3.

Lennon, Rachel, et al.. (2011). Establishment of conditionally immortalized human glomerular mesangial cells in culture, with unique migratory properties. American Journal of Physiology-Renal Physiology. 301(5). F1131–F1138. 29 indexed citations

4.

Welsh, Gavin I., Bethan Lloyd‐Lewis, Matthew Wherlock, et al.. (2007). Rip11 is a Rab11- and AS160-RabGAP-binding protein required for insulin-stimulated glucose uptake in adipocytes. Journal of Cell Science. 120(23). 4197–4208. 33 indexed citations

5.

Hers, Ingeborg, Matthew Wherlock, Yoshimi Homma, Hitoshi Yagisawa, & Jeremy M. Tavaré. (2005). Identification of p122RhoGAP (Deleted in Liver Cancer-1) Serine 322 as a Substrate for Protein Kinase B and Ribosomal S6 Kinase in Insulin-stimulated Cells. Journal of Biological Chemistry. 281(8). 4762–4770. 27 indexed citations

6.

Wherlock, Matthew, et al.. (2004). Farnesyltransferase inhibitors disrupt EGF receptor traffic through modulation of the RhoB GTPase. Journal of Cell Science. 117(15). 3221–3231. 100 indexed citations

7.

Wherlock, Matthew, et al.. (2002). The Rho GTPase family: a Racs to Wrchs story. Journal of Cell Science. 115(2). 239–240. 115 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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