Lucia Cavelier

2.7k total citations
63 papers, 1.7k citations indexed

About

Lucia Cavelier is a scholar working on Molecular Biology, Hematology and Cancer Research. According to data from OpenAlex, Lucia Cavelier has authored 63 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 25 papers in Hematology and 13 papers in Cancer Research. Recurrent topics in Lucia Cavelier's work include Acute Myeloid Leukemia Research (22 papers), Chronic Myeloid Leukemia Treatments (11 papers) and Acute Lymphoblastic Leukemia research (11 papers). Lucia Cavelier is often cited by papers focused on Acute Myeloid Leukemia Research (22 papers), Chronic Myeloid Leukemia Treatments (11 papers) and Acute Lymphoblastic Leukemia research (11 papers). Lucia Cavelier collaborates with scholars based in Sweden, United States and Denmark. Lucia Cavelier's co-authors include Ulf Gyllensten, Elena Jazin, Adam Ameur, Anna Wetterbom, Lars Feuk, Inger Eriksson, Lars Oreland, Ammar Zaghlool, Jonatan Halvardson and Lioudmila Elfineh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Lucia Cavelier

60 papers receiving 1.6k citations

Peers

Lucia Cavelier

PHEOH

HEMAT

GENET

I‐Shing Yu Taiwan

Lee Carpenter United Kingdom

Jianbiao Zheng United States

H.-J. Gröne Germany

Marta Sampaio de Freitas Brazil

Antonio Parrado Spain

Valérie Serre France

Mila Ljujić Serbia

Minoru Asada Japan

Zoë Webster United Kingdom

I‐Shing Yu Taiwan

Lucia Cavelier

1.2k ×1.1

137 ×0.5

PHEOH

292 ×1.2

103 ×0.4

HEMAT

240 ×1.2

GENET

Citations per year, relative to Lucia Cavelier Lucia Cavelier (= 1×) peers I‐Shing Yu

Countries citing papers authored by Lucia Cavelier

Since Specialization

Citations

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

Fields of papers citing papers by Lucia Cavelier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Cavelier

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

Wirta, Valtteri, Christina Orsmark‐Pietras, Lucia Cavelier, et al.. (2024). Micro-costing of genetic diagnostics in acute leukemia in Sweden: from standard-of-care to whole-genome sequencing. Journal of Medical Economics. 27(1). 1053–1060. 3 indexed citations

Eriksson, Anna, Lucy Mathot, Martin Rippin, et al.. (2023). Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia. Clinical Cancer Research. 29(15). 2826–2834. 3 indexed citations

Eriksson, Anna, et al.. (2023). Managing leukemia patients via liquid biopsy and super rolling circle amplification (superRCA). Journal of Internal Medicine. 294(2). 228–237. 2 indexed citations

Rezayee, Fatemah, Jesper Eisfeldt, Aron Skaftason, et al.. (2023). Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia. Frontiers in Oncology. 13. 1217712–1217712. 11 indexed citations

Berglund, Eva, Gisela Barbany, Christina Orsmark‐Pietras, et al.. (2022). A Study Protocol for Validation and Implementation of Whole-Genome and -Transcriptome Sequencing as a Comprehensive Precision Diagnostic Test in Acute Leukemias. Frontiers in Medicine. 9. 842507–842507. 13 indexed citations

Vesterlund, Mattias, Husen M. Umer, Saeed Eshtad, et al.. (2022). Proteogenomic analysis of acute myeloid leukemia associates relapsed disease with reprogrammed energy metabolism both in adults and children. Leukemia. 37(3). 550–559. 14 indexed citations

Eriksson, Anna, Simone Weström, Tatjana Pandzic, et al.. (2022). Ultra-sensitive monitoring of leukemia patients using superRCA mutation detection assays. Nature Communications. 13(1). 4033–4033. 19 indexed citations

Alexsson, Andrei, Christer Sundström, Claes Ladenvall, et al.. (2021). PD-L1 and IDO1 are potential targets for treatment in patients with primary diffuse large B-cell lymphoma of the CNS. Acta Oncologica. 60(4). 531–538. 13 indexed citations

Sun, Jitong, Aron Skaftason, Markus Mayrhofer, et al.. (2021). Transcriptomic analysis reveals proinflammatory signatures associated with acute myeloid leukemia progression. Blood Advances. 6(1). 152–164. 19 indexed citations

10.

Marincevic-Zuniga, Yanara, Johan Dahlberg, S. Nilsson, et al.. (2017). Transcriptome sequencing in pediatric acute lymphoblastic leukemia identifies fusion genes associated with distinct DNA methylation profiles. Journal of Hematology & Oncology. 10(1). 148–148. 35 indexed citations

11.

Ljungström, Viktor, Jakob Werner Hansen, Astrid Olsnes Kittang, et al.. (2016). Molecular Profiling In A Population Based Cohort Of Nordic Myelodysplastic Syndrome Patients. Haematologica. 101. 72–72. 1 indexed citations

12.

Sobol, Maria, et al.. (2015). Methods of Reprogramming to Induced Pluripotent Stem Cell Associated with Chromosomal Integrity and Delineation of a Chromosome 5q Candidate Region for Growth Advantage. Stem Cells and Development. 24(17). 2032–2040. 20 indexed citations

13.

Zaghlool, Ammar, Adam Ameur, Lucia Cavelier, & Lars Feuk. (2014). Splicing in the Human Brain. International review of neurobiology. 116. 95–125. 15 indexed citations

14.

Ameur, Adam, Ammar Zaghlool, Jonatan Halvardson, et al.. (2011). Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain. Nature Structural & Molecular Biology. 18(12). 1435–1440. 228 indexed citations

15.

Andersen, Mette Klarskov, K. Autio, Gisela Barbany, et al.. (2011). Paediatric B‐cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols. British Journal of Haematology. 155(2). 235–243. 24 indexed citations

16.

Wetterbom, Anna, Ulf Gyllensten, Lucia Cavelier, & Tomas F. Bergström. (2009). Genome-wide analysis of chimpanzee genes with premature termination codons. BMC Genomics. 10(1). 56–56. 7 indexed citations

17.

Wetterbom, Anna, et al.. (2006). Comparative Genomic Analysis of Human and Chimpanzee Indicates a Key Role for Indels in Primate Evolution. Journal of Molecular Evolution. 63(5). 682–690. 48 indexed citations

18.

Cavelier, Lucia, Martti T. Tammi, Paula Jalonen, et al.. (2004). MtDNA Mutations in Maternally Inherited Diabetes: Presence of the 3397 ND1 Mutation Previously Associated with Alzheimer's and Parkinson's Disease. Hereditas. 135(1). 65–70. 20 indexed citations

19.

Cavelier, Lucia, Elena Jazin, Paula Jalonen, & Ulf Gyllensten. (2000). MtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions. Human Genetics. 107(1). 45–50. 43 indexed citations

20.

Cavelier, Lucia, Ulf Gyllensten, & Niklas Dahl. (1993). Intrafamilial variation in Leber hereditary optic neuropathy revealed by direct mutation analysis. Clinical Genetics. 43(2). 69–72. 2 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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