Éric Pasmant

6.3k total citations · 1 hit paper
82 papers, 3.5k citations indexed

About

Éric Pasmant is a scholar working on Molecular Biology, Neurology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Éric Pasmant has authored 82 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 32 papers in Neurology and 22 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Éric Pasmant's work include Neurofibromatosis and Schwannoma Cases (28 papers), Sarcoma Diagnosis and Treatment (20 papers) and Neuroblastoma Research and Treatments (10 papers). Éric Pasmant is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (28 papers), Sarcoma Diagnosis and Treatment (20 papers) and Neuroblastoma Research and Treatments (10 papers). Éric Pasmant collaborates with scholars based in France, United States and United Kingdom. Éric Pasmant's co-authors include Michel Vidaud, Ivan Bièche, Dominique Vidaud, Audrey Sabbagh, Ingrid Laurendeau, Delphine Héron, P. Wolkenstein, Béatrice Parfait, Julien Masliah‐Planchon and Ingrid Laurendeau and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Éric Pasmant

74 papers receiving 3.5k 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.

Characterization of a Germ-Line Deletion, Including the Entire INK4/ARF Locus, in a Melanoma-Neural System Tumor Family: Identification of ANRIL , an Antisense Noncoding RNA Whose Expression Coclusters with ARF

2007 500 citations Éric Pasmant, Ingrid Laurendeau et al. Cancer Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Éric Pasmant France	29	1.9k	1.1k	998	587	370	82	3.5k
Luíz Gonzaga Tone Brazil	30	1.9k 1.0×	807 0.7×	287 0.3×	368 0.6×	639 1.7×	226	3.6k
Janice A. Royds United Kingdom	35	2.1k 1.1×	682 0.6×	306 0.3×	469 0.8×	1.4k 3.7×	100	3.7k
Karlheinz Holzmann Germany	32	1.6k 0.8×	723 0.6×	200 0.2×	231 0.4×	800 2.2×	83	3.4k
A D Pearson United Kingdom	29	1.1k 0.6×	525 0.5×	1.1k 1.1×	377 0.6×	686 1.9×	69	3.0k
Tamotsu Takeuchi Japan	31	1.6k 0.9×	356 0.3×	162 0.2×	458 0.8×	820 2.2×	159	3.3k
Karen Leroy France	38	1.3k 0.7×	760 0.7×	531 0.5×	766 1.3×	2.0k 5.3×	126	4.8k
Carlos Alberto Scrideli Brazil	28	1.6k 0.9×	784 0.7×	183 0.2×	226 0.4×	502 1.4×	172	2.8k
Koji Okudela Japan	30	1.3k 0.7×	487 0.4×	130 0.1×	1.4k 2.4×	858 2.3×	171	3.2k
A Hittmair Austria	34	1.8k 1.0×	728 0.7×	230 0.2×	2.3k 3.9×	818 2.2×	99	4.7k
Roland Kappler Germany	29	1.6k 0.8×	399 0.4×	130 0.1×	183 0.3×	431 1.2×	96	2.4k

Countries citing papers authored by Éric Pasmant

Since Specialization

Citations

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

Fields of papers citing papers by Éric Pasmant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Éric Pasmant

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

Jouinot, Anne, Nadim Hamzaoui, Olivier Huillard, et al.. (2025). Predisposition to prostate cancer and clinical implications in a real-life cohort. European Journal of Human Genetics. 33(9). 1163–1172.

Gross, John, David Suster, Ying Zou, et al.. (2025). Expanding the Clinicopathologic Spectrum of EWSR1::SSX-Rearranged Sarcomas: Series of 11 Cases Including Osteosarcomas and a Novel EWSR1::SSX4 Fusion. Modern Pathology. 39(1). 100922–100922.

Vidaud, Dominique, Ingrid Laurendeau, Benoît Funalot, et al.. (2024). Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaics. npj Genomic Medicine. 9(1). 2 indexed citations

Bottosso, Michele, Benjamin Verret, Olivier Caron, et al.. (2024). Efficacy and Safety of Immune Checkpoint Blockade in Patients With Li-Fraumeni Syndrome. JCO Precision Oncology. 8(8). e2400139–e2400139. 3 indexed citations

Jouinot, Anne, Lucas Bouys, Stéphanie Espiard, et al.. (2024). Carney complex predisposes to breast cancer: prospective study of 50 women. European Journal of Endocrinology. 190(2). 121–129.

Corica, Domenico, Jérôme Bertherat, Éric Pasmant, et al.. (2024). Adrenal Cushing Syndrome: Diagnosis and Management in a 10-Year-Old Boy with Carney Complex. Hormone Research in Paediatrics. 98(6). 612–621. 1 indexed citations

Bouys, Lucas, Franck Letourneur, Brigitte Izac, et al.. (2024). Somatic Molecular Heterogeneity in Bilateral Macronodular Adrenocortical Disease (BMAD) Differs Among the Pathological Subgroups. Endocrine Pathology. 35(3). 194–206. 2 indexed citations

Guerrini‐Rousseau, Léa, Éric Pasmant, Martine Muleris, et al.. (2023). Neurofibromatosis type 1 mosaicism in patients with constitutional mismatch repair deficiency. Journal of Medical Genetics. 61(2). 158–162. 4 indexed citations

Tlemsani, Camille, Fréderique Larousserie, Vincent Audard, et al.. (2023). Biology and Management of High-Grade Chondrosarcoma: An Update on Targets and Treatment Options. International Journal of Molecular Sciences. 24(2). 1361–1361. 19 indexed citations

10.

Groussin, Lionel, Fidéline Bonnet-Serrano, Béatrix Cochand‐Priollet, et al.. (2022). Redifferentiating Effect of Larotrectinib in NTRK -Rearranged Advanced Radioactive-Iodine Refractory Thyroid Cancer. Thyroid. 32(5). 594–598. 35 indexed citations

11.

Asselah, Tarik, David Durantel, Éric Pasmant, George Lau, & Raymond F. Schinazi. (2020). COVID-19: Discovery, diagnostics and drug development. 4.

12.

Asselah, Tarik, David Durantel, Éric Pasmant, George Lau, & Raymond F. Schinazi. (2020). COVID-19: Discovery, diagnostics and drug development. Journal of Hepatology. 74(1). 168–184. 279 indexed citations

13.

Colombo, Marina, Meriem Messaoudene, Sylvie Rusakiewicz, et al.. (2017). Shifting the Balance of Activating and Inhibitory Natural Killer Receptor Ligands on BRAF V600E Melanoma Lines with Vemurafenib. Cancer Immunology Research. 5(7). 582–593. 18 indexed citations

14.

Meseure, Didier, Sophie Vacher, Kinan Drak Alsibai, et al.. (2016). Expression of ANRIL –Polycomb Complexes– CDKN2A/B/ARF Genes in Breast Tumors: Identification of a Two-Gene ( EZH2/CBX7 ) Signature with Independent Prognostic Value. Molecular Cancer Research. 14(7). 623–633. 82 indexed citations

15.

Pasmant, Éric, Béatrice Parfait, Armelle Luscan, et al.. (2014). Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations?. European Journal of Human Genetics. 23(5). 596–601. 75 indexed citations

16.

Brems, Hilde, Éric Pasmant, Rick van Minkelen, et al.. (2012). Review and update ofSPRED1mutations causing legius syndrome. Human Mutation. 33(11). 1538–1546. 69 indexed citations

17.

Pasmant, Éric, Dominique Vidaud, Marcus Harrison, & Meena Upadhyaya. (2010). Different sized somatic NF1 locus rearrangements in neurofibromatosis 1-associated malignant peripheral nerve sheath tumors. Journal of Neuro-Oncology. 102(3). 341–346. 3 indexed citations

18.

Sabbagh, Audrey, Éric Pasmant, Ingrid Laurendeau, et al.. (2009). Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1. Human Molecular Genetics. 18(15). 2768–2778. 97 indexed citations

19.

Pasmant, Éric, Audrey Sabbagh, Julien Masliah‐Planchon, et al.. (2009). Detection and Characterization of NF1 Microdeletions by Custom High Resolution Array CGH. Journal of Molecular Diagnostics. 11(6). 524–529. 24 indexed citations

20.

Pasmant, Éric, Ingrid Laurendeau, Delphine Héron, et al.. (2007). Characterization of a Germ-Line Deletion, Including the Entire INK4/ARF Locus, in a Melanoma-Neural System Tumor Family: Identification of ANRIL , an Antisense Noncoding RNA Whose Expression Coclusters with ARF. Cancer Research. 67(8). 3963–3969. 500 indexed citations breakdown →

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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