Veronica A. Kinsler

4.4k total citations · 1 hit paper
53 papers, 1.7k citations indexed

About

Veronica A. Kinsler is a scholar working on Oncology, Genetics and Cell Biology. According to data from OpenAlex, Veronica A. Kinsler has authored 53 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Oncology, 23 papers in Genetics and 19 papers in Cell Biology. Recurrent topics in Veronica A. Kinsler's work include Cutaneous Melanoma Detection and Management (26 papers), Genetic and rare skin diseases. (20 papers) and melanin and skin pigmentation (16 papers). Veronica A. Kinsler is often cited by papers focused on Cutaneous Melanoma Detection and Management (26 papers), Genetic and rare skin diseases. (20 papers) and melanin and skin pigmentation (16 papers). Veronica A. Kinsler collaborates with scholars based in United Kingdom, United States and India. Veronica A. Kinsler's co-authors include David J. Atherton, W.K. Chong, Neil J. Sebire, Sarah Aylett, Neil Bulstrode, J. L. T. Birley, R. H. S. Carpenter, Regula Waelchli, Olga Slater and Claude Jourdan Le Saux and has published in prestigious journals such as The Lancet, Nature Communications and PLoS ONE.

In The Last Decade

Veronica A. Kinsler

52 papers receiving 1.7k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Senescent cells evade immune clearance via HLA-E-mediated NK and CD8+ T cell inhibition

2019 375 citations Neil J. Sebire, Veronica A. Kinsler et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Veronica A. Kinsler United Kingdom	21	791	492	411	315	306	53	1.7k
Soo‐Chan Kim South Korea	29	247 0.3×	411 0.8×	247 0.6×	382 1.2×	202 0.7×	194	2.7k
Anthonie J. van Essen Netherlands	27	419 0.5×	1.4k 2.8×	920 2.2×	277 0.9×	56 0.2×	49	2.3k
Emily S. Gillett United States	8	1.2k 1.6×	1.4k 2.8×	190 0.5×	266 0.8×	56 0.2×	15	2.0k
Éliane Chouery Lebanon	29	141 0.2×	1.7k 3.5×	621 1.5×	205 0.7×	526 1.7×	130	2.8k
Koichi Miyake Japan	26	149 0.2×	1.2k 2.5×	379 0.9×	93 0.3×	144 0.5×	73	2.1k
Susanne Lorenz Norway	26	268 0.3×	894 1.8×	248 0.6×	64 0.2×	172 0.6×	57	1.7k
Jay W. Shin Japan	25	818 1.0×	1.2k 2.5×	83 0.2×	94 0.3×	391 1.3×	49	2.2k
Yo Niida Japan	21	244 0.3×	453 0.9×	334 0.8×	68 0.2×	338 1.1×	93	1.6k
Fabrizio Fantini Italy	23	207 0.3×	369 0.8×	54 0.1×	119 0.4×	180 0.6×	59	1.5k
Alexandre N. Ermilov United States	18	433 0.5×	1.2k 2.5×	509 1.2×	169 0.5×	59 0.2×	24	1.7k

Countries citing papers authored by Veronica A. Kinsler

Since Specialization

Citations

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

Fields of papers citing papers by Veronica A. Kinsler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Veronica A. Kinsler

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Kinsler, Veronica A.. (2025). Mosaic disorders affecting pigmentation – part 2: how to make a genetic diagnosis. British Journal of Dermatology. 193(6). 1047–1055. 2 indexed citations

Kinsler, Veronica A., Nicole Knöpfel, & Satyamaanasa Polubothu. (2025). Segmental macular hyperpigmentation: new genes, new clinical implications. British Journal of Dermatology. 193(5). 987–995. 2 indexed citations

Kinsler, Veronica A.. (2025). Mosaic disorders affecting pigmentation – part 1: how to make a clinical diagnosis. British Journal of Dermatology. 193(5). 819–829. 2 indexed citations

Valle, Ignacio del, William Baird, Charalambos Demetriou, et al.. (2024). RNA Therapy for Oncogenic NRAS-Driven Nevi Induces Apoptosis. Journal of Investigative Dermatology. 145(1). 122–134.e11. 4 indexed citations

Zecchin, Davide, Nicole Knöpfel, Mark Stevenson, et al.. (2023). GNAQ/GNA11 Mosaicism Causes Aberrant Calcium Signaling Susceptible to Targeted Therapeutics. Journal of Investigative Dermatology. 144(4). 811–819.e4. 7 indexed citations

Polubothu, Satyamaanasa, Alicia L. Bruzos, Gavin Kelly, et al.. (2023). Mosaic BRAF Fusions Are a Recurrent Cause of Congenital Melanocytic Nevi Targetable by MAPK Pathway Inhibition. Journal of Investigative Dermatology. 144(3). 593–600.e7. 8 indexed citations

Stasi, Martina Di, Kshitij Mankad, Olivia Carney, et al.. (2023). Congenital melanocytic naevus syndrome and Dandy-Walker malformation — a mistaken association: case report and literature review. Neuroradiology. 65(6). 1077–1086. 1 indexed citations

Tummala, Hemanth, Amanda J. Walne, Roberto Buccafusca, et al.. (2022). Germline thymidylate synthase deficiency impacts nucleotide metabolism and causes dyskeratosis congenita. The American Journal of Human Genetics. 109(8). 1472–1483. 13 indexed citations

Kinsler, Veronica A., et al.. (2020). Misaligned foveal morphology and sector retinal dysfunction in AKT1-mosaic Proteus syndrome. Documenta Ophthalmologica. 142(1). 119–126. 2 indexed citations

10.

Polubothu, Satyamaanasa, et al.. (2020). Posters. British Journal of Dermatology. 183(S1). 26–77. 1 indexed citations

11.

Polubothu, Satyamaanasa & Veronica A. Kinsler. (2019). Final congenital melanocytic naevi colour is determined by normal skin colour and unaltered by superficial removal techniques: a longitudinal study. British Journal of Dermatology. 182(3). 721–728. 15 indexed citations

12.

Mathes, Erin F., et al.. (2019). The biker‐glove pattern of congenital melanocytic nevi. Pediatric Dermatology. 36(6). 918–921. 8 indexed citations

13.

Lee, Ming-Yang, Hong-Zhan Wang, Thomas W. White, et al.. (2019). Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome Keratinocytes. Journal of Investigative Dermatology. 140(5). 1035–1044.e7. 20 indexed citations

14.

Polubothu, Satyamaanasa, Nancy McGuire, Lara Al-Olabi, et al.. (2019). Does the gene matter? Genotype–phenotype and genotype–outcome associations in congenital melanocytic naevi. British Journal of Dermatology. 182(2). 434–443. 38 indexed citations

15.

Kinsler, Veronica A., O. Boccara, Sylvie Fraïtag, et al.. (2019). Mosaic abnormalities of the skin: review and guidelines from the European Reference Network for rare skin diseases. British Journal of Dermatology. 182(3). 552–563. 32 indexed citations

16.

Kinsler, Veronica A., et al.. (2019). Striking contiguous depigmentation across the lower limbs in piebaldism and its implications for understanding melanocytic migration and development. Pediatric Dermatology. 36(4). 511–513. 3 indexed citations

17.

Bizargity, Peyman, Haley Streff, Yi-Shan Lee, et al.. (2019). GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis. Neurology Genetics. 5(6). e366–e366. 2 indexed citations

18.

Kinsler, Veronica A. & Lionel Larue. (2017). The patterns of birthmarks suggest a novel population of melanocyte precursors arising around the time of gastrulation. Pigment Cell & Melanoma Research. 31(1). 95–109. 27 indexed citations

19.

Pawlikowski, Jeff S., Claire Brock, Sheau‐Chiann Chen, et al.. (2015). Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt Signaling. Journal of Investigative Dermatology. 135(11). 2902–2902. 4 indexed citations

20.

Kinsler, Veronica A., Glenn Anderson, B. Latimer, et al.. (2013). Immunohistochemical and ultrastructural features of congenital melanocytic naevus cells support a stem‐cell phenotype. British Journal of Dermatology. 169(2). 374–383. 17 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.

Explore authors with similar magnitude of impact