Bruno Copin

2.6k total citations
23 papers, 922 citations indexed

About

Bruno Copin is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Bruno Copin has authored 23 papers receiving a total of 922 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Genetics and 7 papers in Immunology. Recurrent topics in Bruno Copin's work include Inflammasome and immune disorders (8 papers), Retinal Diseases and Treatments (6 papers) and Glaucoma and retinal disorders (6 papers). Bruno Copin is often cited by papers focused on Inflammasome and immune disorders (8 papers), Retinal Diseases and Treatments (6 papers) and Glaucoma and retinal disorders (6 papers). Bruno Copin collaborates with scholars based in France, United States and Switzerland. Bruno Copin's co-authors include A Béchetoille, J C Dascotte, Henri‐Jean Garchon, Serge Amselem, Lucienne Gomez, F Valtot, Ahmed Belmouden, Philippe Duquesnoy, Marie Legendre and Jean‐François Bach and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Bruno Copin

23 papers receiving 908 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bruno Copin France	14	452	376	260	162	147	23	922
Louise Ocaka United Kingdom	19	729 1.6×	357 0.9×	420 1.6×	107 0.7×	30 0.2×	30	1.2k
María José Trujillo-Tiebas Spain	19	595 1.3×	213 0.6×	306 1.2×	75 0.5×	23 0.2×	59	964
Richard A Axton United Kingdom	14	611 1.4×	176 0.5×	198 0.8×	131 0.8×	118 0.8×	23	827
Olga Dratviman‐Storobinsky Israel	15	214 0.5×	126 0.3×	82 0.3×	39 0.2×	28 0.2×	31	509
Vincent Marion France	22	853 1.9×	59 0.2×	876 3.4×	140 0.9×	107 0.7×	42	1.5k
Yves Sznajer Belgium	19	623 1.4×	39 0.1×	373 1.4×	134 0.8×	136 0.9×	50	1.1k
Tanya Bardakjian United States	18	463 1.0×	123 0.3×	621 2.4×	65 0.4×	25 0.2×	51	993
Tadashi Yokoi Japan	16	374 0.8×	280 0.7×	90 0.3×	39 0.2×	89 0.6×	69	720
Astrid S. Plomp Netherlands	23	1.1k 2.5×	191 0.5×	1.2k 4.5×	573 3.5×	101 0.7×	51	2.1k

Countries citing papers authored by Bruno Copin

Since Specialization

Citations

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

Fields of papers citing papers by Bruno Copin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruno Copin

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

Khouri, Elma El, Camille Louvrier, Eman Assrawi, et al.. (2023). A critical region of A20 unveiled by missense TNFAIP3 variations that lead to autoinflammation. eLife. 12. 5 indexed citations

Louvrier, Camille, Elma El Khouri, Pierre Quartier, et al.. (2022). De Novo Gain‐Of‐Function Variations in LYN Associated With an Early‐Onset Systemic Autoinflammatory Disorder. Arthritis & Rheumatology. 75(3). 468–474. 10 indexed citations

Assrawi, Eman, Camille Louvrier, Elma El Khouri, et al.. (2022). Mosaic variants in TNFRSF1A: an emerging cause of tumour necrosis factor receptor-associated periodic syndrome. Lara D. Veeken. 62(1). 473–479. 7 indexed citations

Louvrier, Camille, Fawaz Awad, A. Cosnes, et al.. (2022). RNF213-associated urticarial lesions with hypercytokinemia. Journal of Allergy and Clinical Immunology. 150(6). 1545–1555. 8 indexed citations

Ballerini, Paola, Zoïa Mincheva, Bruno Copin, et al.. (2022). Germline RUNX1 variants in paediatric patients in a French specialised centre. SHILAP Revista de lepidopterología. 4(1). 145–152. 2 indexed citations

Assrawi, Eman, Camille Louvrier, C. Lepelletier, et al.. (2019). Somatic Mosaic NLRP3 Mutations and Inflammasome Activation in Late-Onset Chronic Urticaria. Journal of Investigative Dermatology. 140(4). 791–798.e2. 21 indexed citations

Louvrier, Camille, Eman Assrawi, Elma El Khouri, et al.. (2019). NLRP3-associated autoinflammatory diseases: Phenotypic and molecular characteristics of germline versus somatic mutations. Journal of Allergy and Clinical Immunology. 145(4). 1254–1261. 45 indexed citations

Blanchon, Sylvain, Marie Legendre, Mathieu Bottier, et al.. (2019). Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesia. Journal of Medical Genetics. 57(4). 237–244. 22 indexed citations

Jeanson, Ludovic, Lucie Thomas, Bruno Copin, et al.. (2016). Mutations inGAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization. Human Mutation. 37(8). 776–785. 41 indexed citations

10.

Sobrier, Marie‐Laure, Yu‐Cheng Tsai, Christelle Pérez, et al.. (2015). Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD. Human Molecular Genetics. 25(3). 472–483. 30 indexed citations

11.

Jeanson, Ludovic, Bruno Copin, Jean‐François Papon, et al.. (2015). RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes. The American Journal of Human Genetics. 97(1). 153–162. 66 indexed citations

12.

Jéru, Isabelle, Emmanuelle Cochet, Bruno Copin, et al.. (2013). Involvement of the Same TNFR1 Residue in Mendelian and Multifactorial Inflammatory Disorders. PLoS ONE. 8(7). e69757–e69757. 4 indexed citations

13.

Kott, Esther, Philippe Duquesnoy, Bruno Copin, et al.. (2012). Loss-of-Function Mutations in LRRC6 , a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms, Cause Primary Ciliary Dyskinesia. The American Journal of Human Genetics. 91(5). 958–964. 124 indexed citations

14.

Legendre, Marie, Sylvain Blanchon, Bruno Copin, et al.. (2012). Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia. SHILAP Revista de lepidopterología. 1(S1). 410–6. 60 indexed citations

15.

Sobrier, Marie‐Laure, Cécile Brachet, Christelle Pérez, et al.. (2012). Symptomatic Heterozygotes and Prenatal Diagnoses in a Nonconsanguineous Family with Syndromic Combined Pituitary Hormone Deficiency Resulting from Two NovelLHX3Mutations. The Journal of Clinical Endocrinology & Metabolism. 97(3). E503–E509. 19 indexed citations

16.

Copin, Bruno, et al.. (2002). Apolipoprotein E–Promoter Single-Nucleotide Polymorphisms Affect the Phenotype of Primary Open-Angle Glaucoma and Demonstrate Interaction with the Myocilin Gene. The American Journal of Human Genetics. 70(6). 1575–1581. 92 indexed citations

17.

Copin, Bruno, et al.. (2002). Apolipoprotein E (APOE) Promoter SNPs Affect the Phenotype of Primary Open-angle Glaucoma and Demonstrate Interaction With the MYOCILIN Gene. 43(13). 3014–3014. 2 indexed citations

18.

Colomb, Evelyne, et al.. (2001). Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open‐angle glaucoma. Clinical Genetics. 60(3). 220–225. 41 indexed citations

19.

Brézin, Antoine P., Ahmed Belmouden, André Chaventré, et al.. (1998). Founder effect in GLC1A‐linked familial open‐angle glaucoma in Northern France. American Journal of Medical Genetics. 76(5). 438–445. 4 indexed citations

20.

Belmouden, Ahmed, F Valtot, A Béchetoille, et al.. (1997). Recurrent Mutations in a Single Exon Encoding the Evolutionarily Conserved Olfactomedin-Homology Domain of TIGR in Familial Open-Angle Glaucoma. Human Molecular Genetics. 6(12). 2091–2097. 251 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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