Melanie J. Percy

5.0k total citations
81 papers, 2.8k citations indexed

About

Melanie J. Percy is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Melanie J. Percy has authored 81 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 32 papers in Genetics and 27 papers in Cancer Research. Recurrent topics in Melanie J. Percy's work include Myeloproliferative Neoplasms: Diagnosis and Treatment (28 papers), Cancer, Hypoxia, and Metabolism (27 papers) and Erythrocyte Function and Pathophysiology (18 papers). Melanie J. Percy is often cited by papers focused on Myeloproliferative Neoplasms: Diagnosis and Treatment (28 papers), Cancer, Hypoxia, and Metabolism (27 papers) and Erythrocyte Function and Pathophysiology (18 papers). Melanie J. Percy collaborates with scholars based in United Kingdom, United States and Australia. Melanie J. Percy's co-authors include Terence R.J. Lappin, Mary Frances McMullin, Frank S. Lee, Paul W. Furlow, Patrick H. Maxwell, Claire Harrison, Adrian Flores, Guy Lucas, Philip Beer and Neil V. McFerran and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Melanie J. Percy

78 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Melanie J. Percy United Kingdom 31 1.1k 1.1k 876 787 677 81 2.8k
Shigehiko Imagawa Japan 24 411 0.4× 682 0.6× 324 0.4× 866 1.1× 162 0.2× 60 1.9k
Qingdu Liu United States 14 799 0.7× 695 0.6× 289 0.3× 563 0.7× 314 0.5× 14 1.7k
Johannes Schödel Germany 28 1.9k 1.7× 2.0k 1.8× 160 0.2× 252 0.3× 413 0.6× 52 3.4k
Huasheng Lu United States 10 1.2k 1.1× 1.2k 1.1× 151 0.2× 397 0.5× 207 0.3× 11 2.3k
Samir S. El‐Dahr United States 33 185 0.2× 1.7k 1.6× 543 0.6× 175 0.2× 272 0.4× 127 3.2k
Carol Moreno Spain 41 120 0.1× 1.0k 0.9× 3.3k 3.8× 934 1.2× 423 0.6× 155 5.5k
Ingrid Øra Sweden 28 801 0.7× 1.5k 1.4× 175 0.2× 107 0.1× 211 0.3× 81 2.6k
Mukesh K. Jain United States 23 490 0.4× 1.9k 1.8× 180 0.2× 210 0.3× 284 0.4× 33 2.8k
Gunther Zahner Germany 34 178 0.2× 1.0k 1.0× 300 0.3× 321 0.4× 194 0.3× 63 3.9k
Lynn G. Nicholls United Kingdom 11 1.0k 0.9× 849 0.8× 125 0.1× 326 0.4× 261 0.4× 15 1.7k

Countries citing papers authored by Melanie J. Percy

Since Specialization
Citations

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

Fields of papers citing papers by Melanie J. Percy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Melanie J. Percy. 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 Melanie J. Percy. The network helps show where Melanie J. Percy may publish in the future.

Co-authorship network of co-authors of Melanie J. Percy

This figure shows the co-authorship network connecting the top 25 collaborators of Melanie J. Percy. A scholar is included among the top collaborators of Melanie J. Percy 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 Melanie J. Percy. Melanie J. Percy 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.
Song, Daisheng, Wei Guan, Tao Wang, et al.. (2020). Tibetan PHD2 , an allele with loss-of-function properties. Proceedings of the National Academy of Sciences. 117(22). 12230–12238. 30 indexed citations
2.
Frawley, Thomas F., Cathal Ó’Brien, Eibhlin Conneally, et al.. (2018). Development of a Targeted Next-Generation Sequencing Assay to Detect Diagnostically Relevant Mutations of JAK2 , CALR , and MPL in Myeloproliferative Neoplasms. Genetic Testing and Molecular Biomarkers. 22(2). 98–103. 6 indexed citations
3.
Bento, Celeste, Mary Frances McMullin, Melanie J. Percy, & Holger Cario. (2016). Primary Familial and Congenital Polycythemia. 4 indexed citations
4.
Tan, Qiulin, Melanie J. Percy, Ralph A. Pietrofesa, et al.. (2013). Erythrocytosis and Pulmonary Hypertension in a Mouse Model of Human HIF2A Gain of Function Mutation. Journal of Biological Chemistry. 288(24). 17134–17144. 89 indexed citations
5.
Lee, Frank S. & Melanie J. Percy. (2011). The HIF Pathway and Erythrocytosis. Annual Review of Pathology Mechanisms of Disease. 6(1). 165–192. 138 indexed citations
6.
Formenti, Federico, Philip Beer, Quentin P. P. Croft, et al.. (2011). Cardiopulmonary function in two human disorders of the hypoxia‐inducible factor (HIF) pathway: von Hippel‐Lindau disease and HIF‐2α gain‐of‐function mutation. The FASEB Journal. 25(6). 2001–2011. 80 indexed citations
7.
Shi, Zhimin, et al.. (2010). Erythropoietin-induced activation of Rho/ROCK/MLC2 in a model of tumourigenesis. British Journal of Haematology. 149. 26–26. 1 indexed citations
8.
Huizinga, Eric G., et al.. (2009). Erythrocytosis associated with a novel missense mutation in the HIF2A gene. Haematologica. 95(5). 829–832. 30 indexed citations
9.
Furlow, Paul W., Melanie J. Percy, Charlene Bierl, et al.. (2009). Erythrocytosis-associated HIF-2α Mutations Demonstrate a Critical Role for Residues C-terminal to the Hydroxylacceptor Proline. Journal of Biological Chemistry. 284(14). 9050–9058. 42 indexed citations
10.
Percy, Melanie J., Paul W. Furlow, Philip Beer, et al.. (2009). Erythropoietin synthesis is primarily regulated by the PHD2-HIF-2alpha-VHL axis as documented by HIF-2alpha associated familial erythrocytosis. British Journal of Haematology. 145. 44–45.
11.
Percy, Melanie J., Philip Beer, Gavin Campbell, et al.. (2008). Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis. Blood. 111(11). 5400–5402. 97 indexed citations
12.
Percy, Melanie J.. (2008). Familial erythrocytosis arising from a gain-of-function mutation in the HIF2A gene of the oxygen sensing pathway.. PubMed. 77(2). 86–8. 8 indexed citations
13.
Percy, Melanie J. & Terence R.J. Lappin. (2008). Recessive congenital methaemoglobinaemia: cytochrome b5 reductase deficiency. British Journal of Haematology. 141(3). 298–308. 98 indexed citations
14.
Percy, Melanie J., Mayka Sánchez, Sabina Świerczek, et al.. (2007). Is congenital secondary erythrocytosis/polycythemia caused by activating mutations within the HIF-2α iron-responsive element?. Blood. 110(7). 2776–2777. 3 indexed citations
15.
Smith, Thomas G., George M. Balanos, D. Mark Layton, et al.. (2007). Mutation of the von Hippel-Lindau Gene Alters Human Cardiopulmonary Physiology. Advances in experimental medicine and biology. 605. 51–56. 14 indexed citations
16.
Percy, Melanie J., Linda M. Scott, Wendy N. Erber, et al.. (2007). The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels. Haematologica. 92(12). 1607–1614. 60 indexed citations
17.
Percy, Melanie J., Quan Zhao, Adrian Flores, et al.. (2006). A family with erythrocytosis establishes a role for prolyl hydroxylase domain protein 2 in oxygen homeostasis. Proceedings of the National Academy of Sciences. 103(3). 654–659. 252 indexed citations
18.
Percy, Melanie J. & Mary Frances McMullin. (2005). The V617F JAK2 mutation and the myeloproliferative disorders. Hematological Oncology. 23(3-4). 91–93. 28 indexed citations
19.
Percy, Melanie J., Mary Frances McMullin, Marilyn Treacy, et al.. (2002). Identification of the Chuvash-type congenital polycythemia in patients of Asian and western European ancestry.. Blood. 100. 1 indexed citations
20.
Percy, Melanie J., et al.. (1996). Erythrocytosis caused by the Finnish-type erythropoietin receptor mutation.. Blood. 88. 2781–2781. 1 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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