Bianca Tesi

3.0k total citations · 1 hit paper
43 papers, 1.1k citations indexed

About

Bianca Tesi is a scholar working on Immunology, Hematology and Genetics. According to data from OpenAlex, Bianca Tesi has authored 43 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Immunology, 20 papers in Hematology and 10 papers in Genetics. Recurrent topics in Bianca Tesi's work include Immune Cell Function and Interaction (19 papers), Autoimmune and Inflammatory Disorders Research (14 papers) and Acute Myeloid Leukemia Research (6 papers). Bianca Tesi is often cited by papers focused on Immune Cell Function and Interaction (19 papers), Autoimmune and Inflammatory Disorders Research (14 papers) and Acute Myeloid Leukemia Research (6 papers). Bianca Tesi collaborates with scholars based in Sweden, Norway and United States. Bianca Tesi's co-authors include Yenan T. Bryceson, Heinrich Schlums, Samuel C. C. Chiang, Jeffrey S. Miller, Frank Cichocki, Jakob Theorell, Hans‐Gustaf Ljunggren, Hongya Han, Vivien Béziat and Bree Foley and has published in prestigious journals such as The Journal of Experimental Medicine, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Bianca Tesi

38 papers receiving 1.1k citations

Hit Papers

align trajectories

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.

Cytomegalovirus Infection Drives Adaptive Epigenetic Diversification of NK Cells with Altered Signaling and Effector Function

2015 551 citations Heinrich Schlums, Frank Cichocki et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bianca Tesi Sweden	14	843	229	203	164	119	43	1.1k
Colleen M. Lau United States	22	1.5k 1.8×	228 1.0×	271 1.3×	142 0.9×	381 3.2×	37	1.9k
Myew–Ling Toh France	18	541 0.6×	174 0.8×	185 0.9×	120 0.7×	213 1.8×	23	1.0k
Hélène Decaluwe Canada	17	553 0.7×	131 0.6×	134 0.7×	203 1.2×	162 1.4×	41	918
Fabian Hauck Germany	20	736 0.9×	105 0.5×	197 1.0×	215 1.3×	238 2.0×	64	1.2k
Takuya Sekine United States	12	507 0.6×	199 0.9×	233 1.1×	126 0.8×	147 1.2×	27	885
Martie C. M. Verschuren Netherlands	15	1.1k 1.3×	175 0.8×	238 1.2×	176 1.1×	204 1.7×	21	1.5k
Jean L. Scholz United States	16	1.2k 1.4×	68 0.3×	91 0.4×	185 1.1×	157 1.3×	23	1.5k
Emily Charrier France	13	1.1k 1.3×	162 0.7×	319 1.6×	142 0.9×	208 1.7×	29	1.4k
Richard Mitchell Australia	18	419 0.5×	199 0.9×	148 0.7×	93 0.6×	211 1.8×	38	982
К. И. Киргизов Russia	11	427 0.5×	185 0.8×	311 1.5×	74 0.5×	162 1.4×	83	982

Countries citing papers authored by Bianca Tesi

Since Specialization

Citations

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

Fields of papers citing papers by Bianca Tesi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bianca Tesi

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

All Works

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20 of 20 papers shown

Creignou, Maria, Bianca Tesi, Elsa Bernard, et al.. (2025). Comorbidities and mutations including single‐ and multihit TET2 mutations in relation to outcome in chronic myelomonocytic leukaemia—A population‐based study. British Journal of Haematology. 208(2). 514–523.

Kvist, Anders, Anders Kämpe, Therese Törngren, et al.. (2025). Polygenic scores in Familial breast cancer cases with and without pathogenic variants and the risk of contralateral breast cancer. Breast Cancer Research. 27(1). 160–160.

Delgado-Vega, A M, Fulya Taylan, Kristina Lagerstedt‐Robinson, et al.. (2024). Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature. American Journal of Medical Genetics Part A. 194(12). e63812–e63812.

Baliakas, Panagiotis, Bianca Tesi, Jörg Cammenga, et al.. (2024). How to manage patients with germline DDX41 variants: Recommendations from the Nordic working group on germline predisposition for myeloid neoplasms. HemaSphere. 8(8). e145–e145. 3 indexed citations

Tesi, Bianca, et al.. (2023). “Health is a serious game”: Gamification as a tool for primary prevention in Public Health. European Journal of Public Health. 33(Supplement_2).

Tesi, Bianca, Cathérine Boileau, Kym M. Boycott, et al.. (2023). Precision medicine in rare diseases: What is next?. Journal of Internal Medicine. 294(4). 397–412. 13 indexed citations

Lagerstedt‐Robinson, Kristina, Fulya Taylan, Bianca Tesi, et al.. (2023). Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation. Frontiers in Medicine. 10. 1172565–1172565.

Laurell, Tobias, Anna Lindstrand, Helena Malmgren, et al.. (2022). Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants. Molecular Genetics & Genomic Medicine. 10(4). e1880–e1880. 10 indexed citations

Vulliamy, Tom, Inderjeet Dokal, Jean Soulier, et al.. (2021). Multinational Study on the Clinical and Genetic Features of the ERCC6L2-Disease. Blood. 138(Supplement 1). 864–864. 1 indexed citations

10.

Popko, Katarzyna, Yenan T. Bryceson, Bianca Tesi, et al.. (2021). Molecular Genetics Diversity of Primary Hemophagocytic Lymphohistiocytosis among Polish Pediatric Patients. Archivum Immunologiae et Therapiae Experimentalis. 69(1). 31–31. 8 indexed citations

11.

Kvedaraite, Egle, Magda Lourda, Hongya Han, et al.. (2020). Patients with both Langerhans cell histiocytosis and Crohn’s disease highlight a common role of interleukin‐23. Acta Paediatrica. 110(4). 1315–1321. 4 indexed citations

12.

Greenwood, Tatiana von Bahr, Bernhard Holzgraefe, Samuel C. C. Chiang, et al.. (2020). Clinical and laboratory signs of haemophagocytic lymphohistiocytosis associated with pandemic influenza A (H1N1) infection in patients needing extracorporeal membrane oxygenation. European Journal of Anaesthesiology. 38(7). 692–701. 4 indexed citations

13.

Galgano, Donatella, Matthias Voß, Bianca Tesi, et al.. (2020). Alternative UNC13D Promoter Encodes a Functional Munc13-4 Isoform Predominantly Expressed in Lymphocytes and Platelets. Frontiers in Immunology. 11. 1154–1154. 6 indexed citations

14.

Thams, Sebastian, Mominul Islam, Marie Lindefeldt, et al.. (2020). Heterozygous variants in DCC. Neurology Genetics. 6(6). e526–e526. 6 indexed citations

15.

Baliakas, Panagiotis, Bianca Tesi, Ulla Wartiovaara‐Kautto, et al.. (2019). Nordic Guidelines for Germline Predisposition to Myeloid Neoplasms in Adults: Recommendations for Genetic Diagnosis, Clinical Management and Follow-up. HemaSphere. 3(6). e321–e321. 53 indexed citations

16.

Taylan, Fulya, Inger Nennesmo, Göran Annerén, et al.. (2019). Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth. Clinical Genetics. 96(2). 118–125. 9 indexed citations

17.

Barbany, Gisela, Agne Liedén, Magnus Nordenskjöld, et al.. (2019). Cell‐free tumour DNA testing for early detection of cancer – a potential future tool. Journal of Internal Medicine. 286(2). 118–136. 53 indexed citations

18.

Tesi, Bianca, Heinrich Schlums, Frank Cichocki, & Yenan T. Bryceson. (2016). Epigenetic Regulation of Adaptive NK Cell Diversification. Trends in Immunology. 37(7). 451–461. 40 indexed citations

19.

Balcı, Yasemin Işık, et al.. (2015). A Hemophagocytic Lymphohistiocytosis Case with Newly Defined UNC13D (c.175G>C; p.Ala59Pro) Mutation and a Rare Complication. SHILAP Revista de lepidopterología. 32(4). 355–358. 3 indexed citations

20.

Theorell, Jakob, Anna‐Lena Gustavsson, Bianca Tesi, et al.. (2014). Immunomodulatory activity of commonly used drugs on Fc-receptor-mediated human natural killer cell activation. Cancer Immunology Immunotherapy. 63(6). 627–641. 25 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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