Adèle Telenius

5.1k total citations
31 papers, 1.6k citations indexed

About

Adèle Telenius is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Oncology. According to data from OpenAlex, Adèle Telenius has authored 31 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Pathology and Forensic Medicine, 10 papers in Molecular Biology and 8 papers in Oncology. Recurrent topics in Adèle Telenius's work include Lymphoma Diagnosis and Treatment (21 papers), Genetic factors in colorectal cancer (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Adèle Telenius is often cited by papers focused on Lymphoma Diagnosis and Treatment (21 papers), Genetic factors in colorectal cancer (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Adèle Telenius collaborates with scholars based in Canada, United States and Germany. Adèle Telenius's co-authors include Christian Steidl, Randy D. Gascoyne, Joseph M. Connors, Sohrab P. Shah, Susana Ben‐Neriah, Merrill Boyle, King Tan, Bruce W. Woolcock, Pedro Farinha and Fong Chun Chan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Journal of Cell Science.

In The Last Decade

Adèle Telenius

28 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adèle Telenius Canada 18 837 636 465 353 343 31 1.6k
Inga Vater Germany 21 701 0.8× 377 0.6× 594 1.3× 315 0.9× 139 0.4× 35 1.6k
Diane L. Pickering United States 16 490 0.6× 455 0.7× 271 0.6× 235 0.7× 134 0.4× 29 1.3k
Margaret E. Macy United States 19 192 0.2× 385 0.6× 521 1.1× 219 0.6× 126 0.4× 57 1.3k
K Offit United States 8 974 1.2× 765 1.2× 558 1.2× 362 1.0× 240 0.7× 10 1.8k
Monica Messina Italy 20 1.1k 1.3× 581 0.9× 803 1.7× 845 2.4× 45 0.1× 49 2.2k
K Weber-Matthiesen Germany 19 552 0.7× 323 0.5× 258 0.6× 341 1.0× 125 0.4× 33 1.1k
EJ Dreef Netherlands 13 261 0.3× 290 0.5× 320 0.7× 182 0.5× 135 0.4× 19 992
Lionel Coignet France 21 262 0.3× 280 0.4× 530 1.1× 253 0.7× 208 0.6× 42 1.1k
Carol Berger United States 22 304 0.4× 296 0.5× 831 1.8× 141 0.4× 530 1.5× 43 1.6k
Chrystelle Colas France 23 1.1k 1.3× 573 0.9× 577 1.2× 99 0.3× 358 1.0× 72 1.7k

Countries citing papers authored by Adèle Telenius

Since Specialization
Citations

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

Fields of papers citing papers by Adèle Telenius

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adèle Telenius

This figure shows the co-authorship network connecting the top 25 collaborators of Adèle Telenius. A scholar is included among the top collaborators of Adèle Telenius 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 Adèle Telenius. Adèle Telenius 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.
Rai, Shinya, Aixiang Jiang, Alexander M. Xu, et al.. (2025). Tumor microenvironment differences between diagnostic and relapsed classic Hodgkin lymphoma revealed by scRNA-seq. Blood Advances. 10(1). 29–38.
2.
Li, Michael Y., Lauren C. Chong, Gerben Duns, et al.. (2024). TRAF3 loss-of-function reveals the noncanonical NF-κB pathway as a therapeutic target in diffuse large B cell lymphoma. Proceedings of the National Academy of Sciences. 121(18). e2320421121–e2320421121. 7 indexed citations
3.
Li, Michael Y., Lauren C. Chong, Bruce W. Woolcock, et al.. (2022). TRAF3 Loss-of-Function Reveals the Non-Canonical NF-Κb Pathway As a Therapeutic Target in Diffuse Large B-Cell Lymphoma. Blood. 140(Supplement 1). 2042–2043.
4.
Johnston, Rebecca L., Anja Mottok, Fong Chun Chan, et al.. (2021). A gene expression–based model predicts outcome in children with intermediate-risk classical Hodgkin lymphoma. Blood. 139(6). 889–893. 11 indexed citations
5.
Aoki, Tomohiro, Lauren C. Chong, Katsuyoshi Takata, et al.. (2021). Single-cell profiling reveals the importance of CXCL13/CXCR5 axis biology in lymphocyte-rich classic Hodgkin lymphoma. Proceedings of the National Academy of Sciences. 118(41). 36 indexed citations
6.
Aoki, Tomohiro, Lauren C. Chong, Katsuyoshi Takata, et al.. (2020). Single Cell Profiling Reveals Unique CXCL13 Positive T Cell Subsets in the Tumor Microenvironment of Lymphocyte Rich Classic Hodgkin Lymphoma. Blood. 136(Supplement 1). 32–33.
7.
Mottok, Anja, Stacy Hung, Elizabeth A. Chavez, et al.. (2019). Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma. Blood. 134(10). 802–813. 72 indexed citations
8.
Mottok, Anja, Bruce W. Woolcock, Fong Chun Chan, et al.. (2015). Genomic Alterations in CIITA Are Frequent in Primary Mediastinal Large B Cell Lymphoma and Are Associated with Diminished MHC Class II Expression. Cell Reports. 13(7). 1418–1431. 88 indexed citations
9.
Mottok, Anja, Bruce W. Woolcock, Fong Chun Chan, et al.. (2014). Genetic Alterations of the MHC Class II Transactivator CIITA Are Frequent in Primary Mediastinal Large B-Cell Lymphoma and Associated with Diminished MHC Class II Expression. Blood. 124(21). 3040–3040. 1 indexed citations
10.
Twa, David D. W., Fong Chun Chan, Susana Ben‐Neriah, et al.. (2014). Genomic rearrangements involving programmed death ligands are recurrent in primary mediastinal large B-cell lymphoma. Blood. 123(13). 2062–2065. 231 indexed citations
11.
Kridel, Robert, Barbara Meissner, Sanja Rogić, et al.. (2011). Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma. Blood. 119(9). 1963–1971. 241 indexed citations
12.
Steidl, Christian, Arjan Diepstra, Tang Lee, et al.. (2011). CSF1R Expression of Hodgkin Reed Sternberg Cells Is Associated with the Number of Macrophages in the Tumor Microenvironment and Is Correlated with Treatment Outcome. Blood. 118(21). 427–427. 1 indexed citations
13.
Cheung, K-John, Allen Delaney, Susana Ben‐Neriah, et al.. (2010). High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy‐neutral loss of heterozygosity and copy number alterations that target single genes. Genes Chromosomes and Cancer. 49(8). 669–681. 31 indexed citations
14.
Steidl, Christian, Adèle Telenius, Sohrab P. Shah, et al.. (2010). Genome-wide copy number analysis of Hodgkin Reed-Sternberg cells identifies recurrent imbalances with correlations to treatment outcome. Blood. 116(3). 418–427. 115 indexed citations
15.
Cheung, Katherine, Sohrab P. Shah, Christian Steidl, et al.. (2008). Genome-wide profiling of follicular lymphoma by array comparative genomic hybridization reveals prognostically significant DNA copy number imbalances. Blood. 113(1). 137–148. 77 indexed citations
16.
Jong, Gary de, et al.. (2001). Efficient in-vitro transfer of a 60-Mb mammalian artificial chromosome into murine and hamster cells using cationic lipids and dendrimers. Chromosome Research. 9(6). 475–485. 52 indexed citations
17.
18.
Robinson, Wendy P., Irene Barrett, L.E. Bernard, et al.. (1997). Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.. PubMed. 60(4). 917–27. 164 indexed citations
19.
Kalousek, Dagmar K., Sylvie Langlois, Wendy P. Robinson, et al.. (1996). Trisomy 7 CVS mosaicism: Pregnancy outcome, placental and DNA analysis in 14 cases. American Journal of Medical Genetics. 65(4). 348–352. 46 indexed citations
20.
Barrett, Irene, et al.. (1996). Distribution of mosaicism in human placentae. Human Genetics. 97(5). 650–654. 56 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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