Dorota Rowczenio

9.3k total citations · 1 hit paper
86 papers, 3.8k citations indexed

About

Dorota Rowczenio is a scholar working on Molecular Biology, Nephrology and Rheumatology. According to data from OpenAlex, Dorota Rowczenio has authored 86 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Molecular Biology, 29 papers in Nephrology and 18 papers in Rheumatology. Recurrent topics in Dorota Rowczenio's work include Amyloidosis: Diagnosis, Treatment, Outcomes (59 papers), Inflammasome and immune disorders (24 papers) and Parathyroid Disorders and Treatments (21 papers). Dorota Rowczenio is often cited by papers focused on Amyloidosis: Diagnosis, Treatment, Outcomes (59 papers), Inflammasome and immune disorders (24 papers) and Parathyroid Disorders and Treatments (21 papers). Dorota Rowczenio collaborates with scholars based in United Kingdom, United States and Italy. Dorota Rowczenio's co-authors include Philip N. Hawkins, Helen J. Lachmann, Julian D. Gillmore, Janet A. Gilbertson, Ashutosh Wechalekar, Carol Whelan, Marianna Fontana, Simon Gibbs, Jennifer H. Pinney and Thirusha Lane and has published in prestigious journals such as Journal of Clinical Oncology, Blood and Gastroenterology.

In The Last Decade

Dorota Rowczenio

81 papers receiving 3.8k citations

Hit Papers

A new staging system for ... 2017 2026 2020 2023 2017 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dorota Rowczenio United Kingdom 33 3.3k 1.3k 687 670 538 86 3.8k
Thirusha Lane United Kingdom 25 2.5k 0.7× 839 0.6× 528 0.8× 427 0.6× 311 0.6× 66 2.8k
Janet A. Gilbertson United Kingdom 31 3.9k 1.2× 1.6k 1.2× 1.1k 1.6× 661 1.0× 647 1.2× 96 4.7k
Vaishali Sanchorawala United States 45 7.7k 2.3× 2.1k 1.6× 1.7k 2.5× 1.2k 1.8× 395 0.7× 281 8.3k
Simon Gibbs United Kingdom 18 1.8k 0.5× 689 0.5× 499 0.7× 285 0.4× 383 0.7× 76 2.2k
Candida Cristina Quarta Italy 29 3.8k 1.1× 1.9k 1.4× 1.0k 1.5× 722 1.1× 1.3k 2.4× 61 4.4k
Bruno Royer France 27 1.3k 0.4× 249 0.2× 623 0.9× 209 0.3× 52 0.1× 84 2.5k
Taxiarchis Kourelis United States 28 1.7k 0.5× 199 0.1× 813 1.2× 245 0.4× 71 0.1× 215 2.7k
Maria Lucia Angelotti Italy 21 1.4k 0.4× 1.1k 0.8× 270 0.4× 153 0.2× 44 0.1× 40 2.9k
MA Gertz United States 19 1.4k 0.4× 322 0.2× 450 0.7× 184 0.3× 101 0.2× 32 1.7k
Costanza Sagrinati Italy 16 1.6k 0.5× 884 0.7× 678 1.0× 118 0.2× 35 0.1× 19 3.0k

Countries citing papers authored by Dorota Rowczenio

Since Specialization
Citations

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

Fields of papers citing papers by Dorota Rowczenio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorota Rowczenio

This figure shows the co-authorship network connecting the top 25 collaborators of Dorota Rowczenio. A scholar is included among the top collaborators of Dorota Rowczenio 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 Dorota Rowczenio. Dorota Rowczenio 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.
Rodríguez, A., Dorota Rowczenio, Alexandra Smith, et al.. (2025). Mapping VEXAS ‐associated and rare UBA1 variants in the United Kingdom : Insights from patient cohorts and the general population. British Journal of Haematology. 208(1). 116–128. 2 indexed citations
2.
Gomes, Sónia, Juan I. Aróstegui, Anna Mensa‐Vilaró, et al.. (2025). Somatic NLRP3 mosaicism in patients with “mutation-negative” CAPS: insights from a single centre UK cohort. Frontiers in Pediatrics. 13. 1598748–1598748. 1 indexed citations
3.
Lachmann, Helen J., Oliver Cohen, Marianna Fontana, et al.. (2024). OP0323 CAUSES OF AA AMYLOIDOSIS: ANALYSIS OF 952 PATIENTS SEEN AT A REFERENCE CENTRE OVER 34 YEARS. Annals of the Rheumatic Diseases. 83. 8–9. 1 indexed citations
4.
Rowczenio, Dorota & Ivona Aksentijevich. (2024). Genetic Approaches to Study Rheumatic Diseases and Its Implications in Clinical Practice. Arthritis & Rheumatology. 76(8). 1169–1181. 4 indexed citations
5.
Canetti, Diana, Nigel B. Rendell, Janet A. Gilbertson, et al.. (2021). Clinical ApoA‐IV amyloid is associated with fibrillogenic signal sequence. The Journal of Pathology. 255(3). 311–318. 8 indexed citations
6.
Law, Steven, Aviva Petrie, Liza Chacko, et al.. (2021). Change in N-terminal pro-B-type natriuretic peptide at 1 year predicts mortality in wild-type transthyretin amyloid cardiomyopathy. Heart. 108(6). 474–478. 20 indexed citations
7.
Petrushkin, Harry, Andrew R. Webster, Elena Moraitis, et al.. (2021). A Novel Pathogenic NOD2 Variant in a Mother and Daughter with Blau Syndrome. Ophthalmic Genetics. 42(6). 753–764. 3 indexed citations
8.
Peet, Claire J., Dorota Rowczenio, Ebun Omoyinmi, Francesca Capon, & Helen J. Lachmann. (2021). Genetic analysis of NLRP3 in recurrent pericarditis. European Heart Journal. 42(Supplement_1). 1 indexed citations
9.
Fontana, Marianna, Ana Martinez–Naharro, Liza Chacko, et al.. (2020). Reduction in CMR Derived Extracellular Volume With Patisiran Indicates Cardiac Amyloid Regression. JACC. Cardiovascular imaging. 14(1). 189–199. 128 indexed citations
10.
Rowczenio, Dorota, Taryn Youngstein, Hadija Trojer, et al.. (2019). British kindred with dominant FMF associated with high incidence of AA amyloidosis caused by novel MEFV variant, and a review of the literature. Lara D. Veeken. 59(3). 554–558. 14 indexed citations
11.
Youngstein, Taryn, Patrycja Hoffmann, Ahmet Gül, et al.. (2017). International multi-centre study of pregnancy outcomes with interleukin-1 inhibitors. Lara D. Veeken. 56(12). 2102–2108. 88 indexed citations
12.
Canetti, Diana, Nigel B. Rendell, Janet A. Gilbertson, et al.. (2017). Misidentification of transthyretin and immunoglobulin variants by proteomics due to methyl lysine formation in formalin-fixed paraffin-embedded amyloid tissue. Amyloid. 24(4). 229–237. 9 indexed citations
13.
Rowczenio, Dorota, Maria Stensland, Gustavo A. de Souza, et al.. (2016). Renal Amyloidosis Associated With 5 Novel Variants in the Fibrinogen A Alpha Chain Protein. Kidney International Reports. 2(3). 461–469. 23 indexed citations
14.
Mahmood, Shameem, Frank Bridoux, Christopher P. Venner, et al.. (2015). Natural history and outcomes in localised immunoglobulin light-chain amyloidosis: a long-term observational study. The Lancet Haematology. 2(6). e241–e250. 95 indexed citations
15.
Dungu, Jason, Oswaldo Valencia, Jennifer H. Pinney, et al.. (2014). CMR-Based Differentiation of AL and ATTR Cardiac Amyloidosis. JACC. Cardiovascular imaging. 7(2). 133–142. 235 indexed citations
16.
Rowczenio, Dorota, Julian D. Gillmore, Helen J. Lachmann, et al.. (2014). Online Registry for Mutations in Hereditary Amyloidosis Including Nomenclature Recommendations. Human Mutation. 35(9). E2403–E2412. 220 indexed citations
17.
Jiménez‐Zepeda, Víctor H., Nizar J. Bahlis, Janet A. Gilbertson, et al.. (2014). A novel transthyretin variant p.H110D (H90D) as a cause of familial amyloid polyneuropathy in a large Irish kindred. Amyloid. 22(1). 26–30. 2 indexed citations
18.
Pinney, Jennifer H., Helen J. Lachmann, Prayman Sattianayagam, et al.. (2012). Renal Transplantation in Systemic Amyloidosis—Importance of Amyloid Fibril Type and Precursor Protein Abundance. American Journal of Transplantation. 13(2). 433–441. 60 indexed citations
19.
Sattianayagam, Prayman, Simon Gibbs, Dorota Rowczenio, et al.. (2011). Hereditary lysozyme amyloidosis – phenotypic heterogeneity and the role of solid organ transplantation. Journal of Internal Medicine. 272(1). 36–44. 60 indexed citations
20.
Dinç, Ayhan, Hakan Erdem, Dorota Rowczenio, et al.. (2005). Autosomal dominant periodic fever with AA amyloidosis: Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Turkish family. Journal of Nephrology. 18(5). 626–629. 9 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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