Nicola Bienz

688 total citations
15 papers, 456 citations indexed

About

Nicola Bienz is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Nicola Bienz has authored 15 papers receiving a total of 456 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Hematology and 4 papers in Molecular Biology. Recurrent topics in Nicola Bienz's work include Chronic Lymphocytic Leukemia Research (4 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Eosinophilic Disorders and Syndromes (3 papers). Nicola Bienz is often cited by papers focused on Chronic Lymphocytic Leukemia Research (4 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Eosinophilic Disorders and Syndromes (3 papers). Nicola Bienz collaborates with scholars based in United Kingdom, India and Ireland. Nicola Bienz's co-authors include John Willan, Katie Jeffery, Andrew J. King, Denise White, NH Russell, Sally A. Anderson, A. P. Haynes, Grant McQuaker, Gaurav Agarwal and Adam J. Mead and has published in prestigious journals such as Nature Medicine, Blood and BMJ.

In The Last Decade

Nicola Bienz

14 papers receiving 441 citations

Peers

Nicola Bienz
Medha Sasané United States
Stuart Seropian United States
Cheryl A. Brewer United States
A. A. M. Blaauw Netherlands
Lisa L. Wood United States
Janet Poole South Africa
María Eva Mingot‐Castellano Spain
Thomas Chatzikonstantinou Greece
Olive Tengera Spain
Lee McCaffrey United States
Medha Sasané United States
Nicola Bienz
Citations per year, relative to Nicola Bienz Nicola Bienz (= 1×) peers Medha Sasané

Countries citing papers authored by Nicola Bienz

Since Specialization
Citations

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

Fields of papers citing papers by Nicola Bienz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicola Bienz

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

All Works

15 of 15 papers shown
1.
Willan, John, Gaurav Agarwal, & Nicola Bienz. (2023). Mortality and burden of post‐COVID‐19 syndrome have reduced with time across SARS‐CoV‐2 variants in haematology patients. British Journal of Haematology. 201(4). 640–644. 11 indexed citations
2.
Sousos, Nikolaos, Máire Ní Leathlobhair, Christina Simoglou Karali, et al.. (2022). In utero origin of myelofibrosis presenting in adult monozygotic twins. Nature Medicine. 28(6). 1207–1211. 33 indexed citations
3.
Willan, John, Andrew J. King, Katie Jeffery, & Nicola Bienz. (2020). Challenges for NHS hospitals during covid-19 epidemic. BMJ. 368. m1117–m1117. 174 indexed citations
4.
Mead, Adam J., Onima Chowdhury, C. Pecquet, et al.. (2013). Impact of isolated germline JAK2V617I mutation on human hematopoiesis. Blood. 121(20). 4156–4165. 35 indexed citations
5.
Mead, Adam J., Petter Woll, Ruth Clifford, et al.. (2011). Germline Activating JAK2 V617I Mutation in a Family with Hereditary Thrombocytosis. Blood. 118(21). 1738–1738. 1 indexed citations
6.
7.
Bienz, Nicola, et al.. (1999). The sequential analysis of trisomy 12 in B‐cell chronic lymphocytic leukaemia. British Journal of Haematology. 104(4). 742–744. 11 indexed citations
8.
Byrne, Jenny, et al.. (1998). Adjuvant α-interferon improves complete remission rates following allogeneic transplantation for multiple myeloma. Bone Marrow Transplantation. 22(7). 639–643. 17 indexed citations
9.
White, Denise, et al.. (1997). Deletions at 11q identify a subset of patients with typical CLL who show consistent disease progression and reduced survival. Leukemia. 11(11). 1929–1932. 89 indexed citations
10.
Russell, NH, Gail Miflin, C Stainer, et al.. (1997). Allogeneic Bone Marrow Transplant for Multiple Myeloma. Blood. 89(7). 2610–2610. 24 indexed citations
11.
12.
Haynes, A. P., et al.. (1995). Engraftment characteristics of peripheral blood stem cells mobilised with cyclophosphamide and the delayed addition of G-CSF.. PubMed. 16(3). 359–63. 38 indexed citations
13.
Bienz, Nicola, D. L. N. Cardy, M. J. Leyland, & M.A. Hultén. (1993). Trisomy 12 in B‐cell chronic lymphocytic leultaemia: an evaluation of 33 patients by direct fluorescence in situ hybridization (FISH). British Journal of Haematology. 85(4). 819–822. 14 indexed citations
14.
Bienz, Nicola, et al.. (1991). CMV prophylaxis in allogeneic BMT with ganciclovir and CMV immune globulin.. PubMed. 7 Suppl 2. 44–44. 1 indexed citations
15.
Patton, W. N., Nicola Bienz, Ian M. Franklin, & J. G. M. Hastings. (1991). Enterococcal meningitis in an HIV positive haemophilic patient.. Journal of Clinical Pathology. 44(7). 608–609. 5 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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