Damien Faury

11.1k total citations
25 papers, 845 citations indexed

About

Damien Faury is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Damien Faury has authored 25 papers receiving a total of 845 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 7 papers in Neurology. Recurrent topics in Damien Faury's work include Glioma Diagnosis and Treatment (13 papers), Neuroblastoma Research and Treatments (4 papers) and Chromatin Remodeling and Cancer (3 papers). Damien Faury is often cited by papers focused on Glioma Diagnosis and Treatment (13 papers), Neuroblastoma Research and Treatments (4 papers) and Chromatin Remodeling and Cancer (3 papers). Damien Faury collaborates with scholars based in Canada, United States and United Kingdom. Damien Faury's co-authors include Nada Jabado, Miklós Garami, Péter Hauser, László Bognár, Rolando F. Del Maestro, Steffen Albrecht, Torsten Pietsch, Sandra E. Dunn, Haiming Li and Zoltán Hanzély and has published in prestigious journals such as Journal of Clinical Oncology, The Journal of Clinical Endocrinology & Metabolism and Cancer Research.

In The Last Decade

Damien Faury

23 papers receiving 836 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Damien Faury Canada 15 504 431 222 138 87 25 845
Jonathan Serrano United States 15 369 0.7× 373 0.9× 169 0.8× 172 1.2× 146 1.7× 35 907
Daniele Peroni Italy 13 456 0.9× 215 0.5× 119 0.5× 179 1.3× 92 1.1× 25 784
Paula Ravin United States 10 284 0.6× 196 0.5× 187 0.8× 121 0.9× 98 1.1× 15 697
Caterina Marchetti Italy 7 748 1.5× 173 0.4× 228 1.0× 118 0.9× 179 2.1× 8 1.1k
Michal Yalon Israel 18 451 0.9× 302 0.7× 228 1.0× 254 1.8× 157 1.8× 43 945
Chunxing Yang United States 18 930 1.8× 254 0.6× 382 1.7× 269 1.9× 60 0.7× 22 1.2k
Robert C. Castellino United States 21 901 1.8× 306 0.7× 128 0.6× 163 1.2× 253 2.9× 49 1.2k
Morag Stewart Canada 12 1.1k 2.1× 202 0.5× 165 0.7× 80 0.6× 135 1.6× 15 1.4k
Bong Gu Kang South Korea 13 564 1.1× 361 0.8× 81 0.4× 218 1.6× 364 4.2× 22 1.1k
Violaine Harris United States 20 953 1.9× 289 0.7× 89 0.4× 149 1.1× 189 2.2× 31 1.5k

Countries citing papers authored by Damien Faury

Since Specialization
Citations

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

Fields of papers citing papers by Damien Faury

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Damien Faury

This figure shows the co-authorship network connecting the top 25 collaborators of Damien Faury. A scholar is included among the top collaborators of Damien Faury 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 Damien Faury. Damien Faury 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.
Huang, Sidong, Éric Bouffet, Adriana Fonseca, et al.. (2024). Recurrent primary intracranial sarcoma, DICER1-mutant in a pediatric patient with DICER1 syndrome: the importance of molecular testing. Child s Nervous System. 40(6). 1965–1969. 1 indexed citations
2.
Jessa, Selin, Antonella De Cola, Michael McNicholas, et al.. (2024). FOXR2 Targets LHX6+/DLX+ Neural Lineages to Drive Central Nervous System Neuroblastoma. Cancer Research. 85(2). 231–250.
3.
McNicholas, Michael, Antonella De Cola, Steven Hébert, et al.. (2023). A Compendium of Syngeneic, Transplantable Pediatric High-Grade Glioma Models Reveals Subtype-Specific Therapeutic Vulnerabilities. Cancer Discovery. 13(7). 1592–1615. 16 indexed citations
4.
Monje, Michelle, Tabitha Cooney, John Glod, et al.. (2023). Phase I trial of panobinostat in children with diffuse intrinsic pontine glioma: A report from the Pediatric Brain Tumor Consortium (PBTC-047). Neuro-Oncology. 25(12). 2262–2272. 31 indexed citations
5.
Gomez, Ricardo Santiago, Thaís dos Santos Fontes Pereira, Tenzin Gayden, et al.. (2023). Comprehensive Genomic Analysis of Cemento-Ossifying Fibroma. Modern Pathology. 37(2). 100388–100388. 3 indexed citations
6.
Cola, Antonella De, Michael McNicholas, Steven Hébert, et al.. (2023). DIPG-35. IDENTIFYING DRIVER-SPECIFIC VULNERABILITIES IN PAEDIATRIC HIGH GRADE GLIOMA SUBTYPES. Neuro-Oncology. 25(Supplement_1). i20–i21.
7.
Hu, Bo, Michael J. Johnston, Emily M. Nakada, et al.. (2022). Detection and genomic analysis of BRAF fusions in Juvenile Pilocytic Astrocytoma through the combination and integration of multi-omic data. BMC Cancer. 22(1). 1297–1297. 3 indexed citations
8.
Serletis, Demitre, Colin Kazina, Mubeen F. Rafay, et al.. (2021). Management of Inoperable Supra-Sellar Low-Grade Glioma With BRAF Mutation in Young Children. Cureus. 13(11). e19400–e19400. 1 indexed citations
9.
Béchet, Denise, Andrey Korshunov, Stefan M. Pfister, et al.. (2014). Specific detection of methionine 27 mutation in histone 3 variants (H3K27M) in fixed tissue from high-grade astrocytomas. Acta Neuropathologica. 128(5). 733–741. 94 indexed citations
10.
Gerges, Noha, et al.. (2013). Pediatric high-grade astrocytomas: a distinct neuro-oncological paradigm. Genome Medicine. 5(7). 66–66. 22 indexed citations
11.
Vinh, Donald C., Khalid Bin Dhuban, Helen Mason, et al.. (2011). Acquired Omenn-Like Syndrome, a Novel Posttransplant Autoaggression Syndrome Reversed by Rapamycin. Clinical and Vaccine Immunology. 19(1). 109–112. 1 indexed citations
12.
Qu, Hui‐Qi, Karine Jacob, Bing Ge, et al.. (2010). Genome-wide profiling using single-nucleotide polymorphism arrays identifies novel chromosomal imbalances in pediatric glioblastomas. Neuro-Oncology. 12(2). 153–163. 48 indexed citations
13.
Gao, Yuanyuan, Abbas Fotovati, Cathy Lee, et al.. (2009). Inhibition of Y-box binding protein-1 slows the growth of glioblastoma multiforme and sensitizes to temozolomide independent O 6-methylguanine-DNA methyltransferase. Molecular Cancer Therapeutics. 8(12). 3276–3284. 45 indexed citations
14.
Jacob, Karine, Steffen Albrecht, Damien Faury, et al.. (2009). Duplication of 7q34 is specific to juvenile pilocytic astrocytomas and a hallmark of cerebellar and optic pathway tumours. British Journal of Cancer. 101(4). 722–733. 132 indexed citations
15.
Valera, Elvis Terci, María Angélica Cortez, Rosane Gomes de Paula Queiróz, et al.. (2008). Pediatric glioblastoma cell line shows different patterns of expression of transmembrane ABC transporters after in vitro exposure to vinblastine. Child s Nervous System. 25(1). 39–45. 15 indexed citations
16.
Haque, Takrima, Damien Faury, Steffen Albrecht, et al.. (2007). Gene Expression Profiling from Formalin-Fixed Paraffin-Embedded Tumors of Pediatric Glioblastoma. Clinical Cancer Research. 13(21). 6284–6292. 47 indexed citations
17.
Li, Haiming, Damien Faury, & Rolf Morosoli. (2006). Impact of amino acid changes in the signal peptide on the secretion of the Tat-dependent xylanase C fromStreptomyces lividans. FEMS Microbiology Letters. 255(2). 268–274. 19 indexed citations
18.
Werbowetski‐Ogilvie, Tamra E., Mohamad Seyed Sadr, Nada Jabado, et al.. (2006). Inhibition of medulloblastoma cell invasion by Slit. Oncogene. 25(37). 5103–5112. 58 indexed citations
19.
Faury, Damien, et al.. (2004). Secretion of active xylanase C from Streptomyces lividans is exclusively mediated by the Tat protein export system. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1699(1-2). 155–162. 22 indexed citations
20.
Naville, Danielle, Laure Barjhoux, Céline Jaillard, et al.. (1996). Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiency.. The Journal of Clinical Endocrinology & Metabolism. 81(4). 1442–1448. 69 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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