Lone Schejbel

847 total citations
43 papers, 604 citations indexed

About

Lone Schejbel is a scholar working on Immunology, Hematology and Pathology and Forensic Medicine. According to data from OpenAlex, Lone Schejbel has authored 43 papers receiving a total of 604 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Immunology, 14 papers in Hematology and 11 papers in Pathology and Forensic Medicine. Recurrent topics in Lone Schejbel's work include Complement system in diseases (12 papers), Lymphoma Diagnosis and Treatment (10 papers) and Chronic Lymphocytic Leukemia Research (7 papers). Lone Schejbel is often cited by papers focused on Complement system in diseases (12 papers), Lymphoma Diagnosis and Treatment (10 papers) and Chronic Lymphocytic Leukemia Research (7 papers). Lone Schejbel collaborates with scholars based in Denmark, Sweden and Türkiye. Lone Schejbel's co-authors include Peter Garred, Hanne Vibeke Marquart, Torben Barington, Henrik Permin, Arne Svejgaard, Vagn Andersen, Carsten Heilmann, Pernille Andersen, Lennart Truedsson and Tom Eirik Mollnes and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Lone Schejbel

40 papers receiving 596 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lone Schejbel Denmark	13	454	165	99	84	64	43	604
Jérémie Rosain France	13	494 1.1×	144 0.9×	156 1.6×	95 1.1×	88 1.4×	38	693
A.G. Sjöholm Sweden	17	489 1.1×	191 1.2×	129 1.3×	102 1.2×	66 1.0×	29	700
Jeanette Seyfarth Denmark	7	392 0.9×	240 1.5×	66 0.7×	45 0.5×	99 1.5×	8	716
Neubury M. Lardy Netherlands	18	566 1.2×	165 1.0×	68 0.7×	28 0.3×	114 1.8×	47	911
Mohammed Al-Adhami United States	14	470 1.0×	87 0.5×	158 1.6×	85 1.0×	157 2.5×	51	729
R. Steffensen Denmark	12	463 1.0×	129 0.8×	81 0.8×	57 0.7×	58 0.9×	15	576
Hirotsugu Kano Japan	8	261 0.6×	127 0.8×	97 1.0×	39 0.5×	286 4.5×	18	576
Anne Barra France	12	541 1.2×	86 0.5×	49 0.5×	21 0.3×	73 1.1×	16	710
Serena Bettoni Sweden	10	551 1.2×	231 1.4×	42 0.4×	425 5.1×	77 1.2×	17	679
Peter J. Norsworthy United Kingdom	12	510 1.1×	108 0.7×	110 1.1×	88 1.0×	123 1.9×	21	794

Countries citing papers authored by Lone Schejbel

Since Specialization

Citations

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

Fields of papers citing papers by Lone Schejbel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lone Schejbel

This figure shows the co-authorship network connecting the top 25 collaborators of Lone Schejbel. A scholar is included among the top collaborators of Lone Schejbel 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 Lone Schejbel. Lone Schejbel 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

Schejbel, Lone, Anne Ortved Gang, Ib Jarle Christensen, et al.. (2024). TP53 Mutation Is the Only Robust Mutational Biomarker for Outcome Found in a Consecutive Clinical Cohort of Real‐Word Patients With Primary Large B‐Cell Lymphoma. European Journal Of Haematology. 114(3). 573–579. 1 indexed citations

Schejbel, Lone, et al.. (2024). Evaluation of the Oncomine Comprehensive Assay Plus NGS Panel and the OncoScan CNV Assay for Homologous Recombination Deficiency Detection. Molecular Diagnosis & Therapy. 29(1). 117–127. 1 indexed citations

Gallon, Richard, Christine Hayes, Ove Andersen, et al.. (2023). Mismatch repair deficiency testing in Lynch syndrome-associated urothelial tumors. Frontiers in Oncology. 13. 1147591–1147591. 3 indexed citations

Østergaard, Simon, Lone Schejbel, Peter Nørgaard, et al.. (2022). Bone Involvement as a Primary Rare Manifestation of Waldenstrom Macroglobulinemia: A Case Report and Prevalence in a Nationwide Population-Based Cohort Study. Journal of Hematology. 11(6). 233–239. 2 indexed citations

Biskup, Edyta, Lone Schejbel, Douglas V.N.P. Oliveira, & Estrid Høgdall. (2022). Test of the FlashFREEZE unit in tissue samples freezing for biobanking purposes. Cell and Tissue Banking. 24(2). 435–447. 3 indexed citations

Schejbel, Lone, Anne Ortved Gang, Torsten Holm Nielsen, et al.. (2022). Inactivating BTK mutations in large B‐cell lymphoma in a real‐world cohort: Strong correlation with BCL2 translocation. SHILAP Revista de lepidopterología. 3(3). 936–939. 4 indexed citations

Dufva, Inge Høgh, Anne Ortved Gang, Lone Schejbel, et al.. (2021). Epigenetic therapy in combination with a multi-epitope cancer vaccine targeting shared tumor antigens for high-risk myelodysplastic syndrome - a phase I clinical trial. Cancer Immunology Immunotherapy. 71(2). 433–444. 10 indexed citations

Schejbel, Lone, Guy Wayne Novotny, Daniel El Fassi, et al.. (2021). Improved Variant Detection in Clinical Myeloid NGS Testing by Supplementing a Commercial Myeloid NGS Assay with Custom or Extended Data Filtering and Accessory Fragment Analysis. Molecular Diagnosis & Therapy. 25(2). 251–266. 6 indexed citations

Oliveira, Douglas V.N.P., Tobias Wirenfeldt Klausen, Anne Ortved Gang, et al.. (2021). High‐grade B‐cell lymphomas with MYC and BCL2 translocations lack tumor‐associated macrophages and PD‐L1 expression: A possible noninflamed subgroup. Hematological Oncology. 39(3). 284–292. 5 indexed citations

10.

Schejbel, Lone, et al.. (2015). Recurrent severe invasive pneumococcal disease in an adult with previously unknown hyposplenia. BMC Infectious Diseases. 15(1). 171–171. 5 indexed citations

11.

Schejbel, Lone, Ann-Charlotte Lundstedt, Lise Heilmann Jensen, et al.. (2015). Immunodeficiency Among Children with Recurrent Invasive Pneumococcal Disease. The Pediatric Infectious Disease Journal. 34(6). 644–651. 21 indexed citations

12.

Bay, Jakob Thaning, Terese L. Katzenstein, Klaus F. Kofoed, et al.. (2015). Novel CFI mutation in a patient with leukocytoclastic vasculitis may redefine the clinical spectrum of Complement Factor I deficiency. Clinical Immunology. 160(2). 315–318. 9 indexed citations

13.

Wilson, Valerie, Rebecca Darlay, William Wong, et al.. (2013). Genotype/Phenotype Correlations in Complement Factor H Deficiency Arising From Uniparental Isodisomy. American Journal of Kidney Diseases. 62(5). 978–983. 8 indexed citations

14.

Permin, H., et al.. (2013). Long-Term Follow-Up on Affinity Maturation and Memory B-Cell Generation in Patients with Common Variable Immunodeficiency. Journal of Clinical Immunology. 33(6). 1067–1077. 5 indexed citations

15.

Bay, Jakob Thaning, Lone Schejbel, Hans O. Madsen, et al.. (2013). Low C4 gene copy numbers are associated with superior graft survival in patients transplanted with a deceased donor kidney. Kidney International. 84(3). 562–569. 16 indexed citations

16.

Schejbel, Lone, Ida Maria Schmidt, Maria Kirchhoff, et al.. (2011). Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation. Genes and Immunity. 12(2). 90–99. 22 indexed citations

17.

Schejbel, Lone, Erik Michael Rasmussen, H. B. S. Kemp, et al.. (2011). Combined IL‐12 Receptor and IgA Deficiency in an Adult Man Intestinally Infested by an Unknown, Non‐Cultivable Mycobacterium. Scandinavian Journal of Immunology. 74(6). 548–553. 10 indexed citations

18.

Schejbel, Lone, Lillemor Skattum, Stefan Hagelberg, et al.. (2011). Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations. Genes and Immunity. 12(8). 626–634. 74 indexed citations

19.

Schejbel, Lone, Vibeke Rosenfeldt, Hanne Vibeke Marquart, Niels Henrik Valerius, & Peter Garred. (2009). Properdin deficiency associated with recurrent otitis media and pneumonia, and identification of male carrier with Klinefelter syndrome. Clinical Immunology. 131(3). 456–462. 21 indexed citations

20.

Schejbel, Lone, Hanne Vibeke Marquart, Vagn Andersen, et al.. (2005). Deficiency of Somatic Hypermutation of Immunoglobulin G Transcripts Is a Better Predictor of Severe Respiratory Tract Infections than Lack of Memory B Cells in Common Variable Immunodeficiency. Journal of Clinical Immunology. 25(4). 392–403. 15 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