Bruno Copin

2.6k citations

23 papers · 922 · h-index 14

Impact in

Ophthalmology top 1%
- Glaucoma and retinal disorders
- Retinal Diseases and Treatments
Cell Biology top 10%
- Proteoglycans and glycosaminoglycans research

Papers in

Molecular Biology 16
- Inflammasome and immune disorders 8
- Retinal Development and Disorders 4
Genetics 7
- Genetic and Kidney Cyst Diseases 5

Co-authors: J C Dascotte (4 shared papers)A Béchetoille (4 shared papers)Henri‐Jean Garchon (3 shared papers)Serge Amselem (16 shared papers)F Valtot (4 shared papers)Lucienne Gomez (4 shared papers)Ahmed Belmouden (3 shared papers)Philippe Duquesnoy (11 shared papers)
Journals: The American Journal of Human Genetics (3 papers)Journal of Allergy and Clinical Immunology (2 papers)Human Molecular Genetics (2 papers)Arthritis & Rheumatology (2 papers)Pediatric Rheumatology (1 paper)
Partner nations: France United States Switzerland

In The Last Decade

Bruno Copin

23 papers receiving 908 citations

Peers

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-authors

The 25 scholars most cited alongside Bruno Copin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bruno Copin Line = papers co-authored together Bruno Copin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Recurrent Mutations in a Single Exon Encoding the Evolutionarily Conserved Olfactomedin-Homology Domain of TIGR in Familial Open-Angle Glaucoma Human Molecular Genetics ·M F Adam, Ahmed Belmouden, P. Binisti, Antoine P. Brézin, F Valtot, A Béchetoille, J C Dascotte, Bruno Copin, Lucienne Gomez, A. Chaventre, Jean‐François Bach, Henri‐Jean Garchon	1997	251
2	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 ·Esther Kott, Philippe Duquesnoy, Bruno Copin, Marie Legendre, Florence Dastot‐Le Moal, Guy Montantin, Ludovic Jeanson, Aline Tamalet, Jean‐François Papon, Jean‐Pierre Siffroi, Nathalie Rives, Valérie Mitchell, (unknown), A. Coste, Annick Clément, Denise Escalier, Aminata Touré, Estelle Escudier, Serge Amselem	2012	124
3	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 ·Bruno Copin, Antoine P. Brézin, Françoise Valtot, J C Dascotte, A Béchetoille, Henri‐Jean Garchon	2002	92
4	RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes The American Journal of Human Genetics ·Ludovic Jeanson, Bruno Copin, Jean‐François Papon, Florence Dastot-Le Moal, Philippe Duquesnoy, Guy Montantin, Jacques Cadranel, Harriet Corvol, A. Coste, Julie Désir, Anissa Souayah, Esther Kott, Nathalie Collot, S. Tissier, Bruno Louis, Aline Tamalet, (unknown), Annick Clément, Estelle Escudier, Serge Amselem, Marie Legendre	2015	66
5	Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia SHILAP Revista de lepidopterología ·Marie Legendre, Sylvain Blanchon, Bruno Copin, Philippe Duquesnoy, Guy Montantin, Esther Kott, Florence Dastot, L. Jeanson, Marine Cachanado, Alexandra Rousseau, Jean‐François Papon, Aline Tamalet, AM Vojtek, Denise Escalier, A. Coste, J. de Blic, A. Clément, Estelle Escudier, Serge Amselem	2012	60
6	NLRP3-associated autoinflammatory diseases: Phenotypic and molecular characteristics of germline versus somatic mutations Journal of Allergy and Clinical Immunology ·Camille Louvrier, Eman Assrawi, Elma El Khouri, Isabelle Melki, Bruno Copin, E. Bourrat, Noémie Lachaume, B. Cador-Rousseau, Philippe Duquesnoy, William Piterboth, Fawaz Awad, Claire Jumeau, Marie Legendre, Gilles Grateau, Sophie Georgin‐Lavialle, Sonia Karabina, Serge Amselem, Irina Giurgea	2019	45
7	Founder effect in GLC1A-linked familial open-angle glaucoma in Northern France American Journal of Medical Genetics ·Antoine P. Br�zin, Marie F. Adam, Ahmed Belmouden, Marie‐Aude Lureau, A. Chaventr�, Bruno Copin, Lucienne Gomez, S. Dupont de Dinechin, M Berkani, F Valtot, Jean-Fran�ois Rouland, J C Dascotte, J F Bach, H J Garchon	1998	44
8	Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open‐angle glaucoma Clinical Genetics ·Evelyne Colomb, TD Nguyen, A Béchetoille, J‐C Dascotte, F Valtot, AP Brézin, M Berkani, Bruno Copin, Lucienne Gomez, JR Polansky, H‐J Garchon	2001	41
9	Mutations inGAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization Human Mutation ·Ludovic Jeanson, Lucie Thomas, Bruno Copin, A. Coste, Isabelle Sermet‐Gaudelus, Florence Dastot‐Le Moal, Philippe Duquesnoy, Guy Montantin, Nathalie Collot, S. Tissier, Jean‐François Papon, Annick Clément, Bruno Louis, Estelle Escudier, Serge Amselem, Marie Legendre	2016	41
10	Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD Human Molecular Genetics ·Marie‐Laure Sobrier, Yu‐Cheng Tsai, Christelle Pérez, Bruno Leheup, Tahar Bouceba, Philippe Duquesnoy, Bruno Copin, Daria Sizova, Alfredo Penzo, Ben Z. Stanger, Nancy E. Cooke, Stephen A. Liebhaber, Serge Amselem	2015	30
11	Brief Report: Involvement of TNFRSF11A Molecular Defects in Autoinflammatory Disorders Arthritis & Rheumatology ·Isabelle Jéru, Emmanuelle Cochet, Philippe Duquesnoy, Véronique Hentgen, Bruno Copin, Maria Teresa Mitjavila‐Garcia, Shayan Sheykholeslami, Gaëlle Le Borgne, Florence Dastot‐Le Moal, Valérie Malan, Sonia Karabina, Mathieu Mahévas, Sandra Chantot‐Bastaraud, Jean‐Claude Lecron, Laurence Faivre, Serge Amselem	2014	23
12	Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesia Journal of Medical Genetics ·Sylvain Blanchon, Marie Legendre, Mathieu Bottier, Aline Tamalet, Guy Montantin, Nathalie Collot, Catherine Faucon, Florence Dastot, Bruno Copin, Annick Clément, Marcel Filoche, A. Coste, Serge Amselem, Estelle Escudier, Jean‐François Papon, Bruno Louis	2019	22
13	Somatic Mosaic NLRP3 Mutations and Inflammasome Activation in Late-Onset Chronic Urticaria Journal of Investigative Dermatology ·Eman Assrawi, Camille Louvrier, C. Lepelletier, Sophie Georgin‐Lavialle, Jean‐David Bouaziz, Fawaz Awad, F. Moinet, Philippe Moguelet, Marie‐Dominique Vignon‐Pennamen, William Piterboth, Claire Jumeau, Laetitia Cobret, Elma El Khouri, Bruno Copin, Philippe Duquesnoy, Marie Legendre, Gilles Grateau, Sonia Karabina, Serge Amselem, Irina Giurgea	2019	21
14	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 ·Marie‐Laure Sobrier, Cécile Brachet, Marie-Pierre Vié-Luton, Christelle Pérez, Bruno Copin, Marie Legendre, Claudine Heinrichs, Serge Amselem	2012	19
15	De Novo Gain‐Of‐Function Variations in LYN Associated With an Early‐Onset Systemic Autoinflammatory Disorder Arthritis & Rheumatology ·Camille Louvrier, Elma El Khouri, Martine Grall Lerosey, Pierre Quartier, Anne‐Marie Guerrot, Brigitte Bader Meunier, Julie Chican, Malaïka Mohammad, Eman Assrawi, Aphrodite Daskalopoulou, Angela Arenas Garcia, Bruno Copin, William Piterboth, F. Moal, Sonia Karabina, Serge Amselem, Irina Giurgea	2022	10
16	RNF213-associated urticarial lesions with hypercytokinemia Journal of Allergy and Clinical Immunology ·Camille Louvrier, Fawaz Awad, A. Cosnes, Elma El Khouri, Eman Assrawi, Aphrodite Daskalopoulou, Bruno Copin, Hélène Bocquet, Sandra Chantot‐Bastaraud, Angela Arenas Garcia, F. Moal, Pierre de la Grange, Philippe Duquesnoy, Ida Chiara Guerrera, William Piterboth, Nicolás Ortonne, O. Chosidow, Sonia Karabina, Serge Amselem, Irina Giurgea	2022	8
17	Mosaic variants in TNFRSF1A: an emerging cause of tumour necrosis factor receptor-associated periodic syndrome Lara D. Veeken ·Eman Assrawi, Camille Louvrier, Elma El Khouri, J. Delaleu, Bruno Copin, Florence Dastot‐Le Moal, William Piterboth, Marie Legendre, Sonia Karabina, Gilles Grateau, Serge Amselem, Irina Giurgea	2022	7
18	A critical region of A20 unveiled by missense TNFAIP3 variations that lead to autoinflammation eLife ·Elma El Khouri, Farah Diab, Camille Louvrier, Eman Assrawi, Aphrodite Daskalopoulou, Alexandre Nguyen, William Piterboth, Samuel Deshayes, A. Desdoits, Bruno Copin, F. Moal, Sonia Karabina, Serge Amselem, Achille Aouba, Irina Giurgea	2023	5
19	Involvement of the Same TNFR1 Residue in Mendelian and Multifactorial Inflammatory Disorders PLoS ONE ·Isabelle Jéru, S. Charmion, Emmanuelle Cochet, Bruno Copin, Philippe Duquesnoy, Maria Teresa Mitjavila Garcia, Gaëlle Le Borgne, P. Cathébras, J. Gaillat, Sonia Karabina, Catherine Dodé, Peter Lohse, Véronique Hentgen, Serge Amselem	2013	4
20	Founder effect in GLC1A‐linked familial open‐angle glaucoma in Northern France American Journal of Medical Genetics ·Antoine P. Brézin, Marie F. Adam, Ahmed Belmouden, Marie‐Aude Lureau, André Chaventré, Bruno Copin, Lucienne Gomez, Stéphane Dupont de Dinechin, M Berkani, Françoise Valtot, Jean‐François Rouland, J C Dascotte, Jean‐François Bach, Henri‐Jean Garchon	1998	4

About Bruno Copin

Bruno Copin is a scholar working on Molecular Biology, Genetics, Immunology, Pulmonary and Respiratory Medicine and Ophthalmology, having authored 23 papers that have together received 922 indexed citations. Recurring topics across this work include Inflammasome and immune disorders (8 papers), Glaucoma and retinal disorders (6 papers), Retinal Diseases and Treatments (6 papers), Cystic Fibrosis Research Advances (5 papers), Genetic and Kidney Cyst Diseases (5 papers), Retinal Development and Disorders (4 papers), Immune Response and Inflammation (3 papers) and Urticaria and Related Conditions (2 papers). The work is most often cited by research in Ophthalmology (376 citations), Cell Biology (162 citations), Genetics (260 citations), Reproductive Medicine (56 citations) and Molecular Biology (452 citations). Bruno Copin has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include J C Dascotte, A Béchetoille, Henri‐Jean Garchon, Serge Amselem, F Valtot, Lucienne Gomez, Ahmed Belmouden, Philippe Duquesnoy, Marie Legendre and Jean‐François Bach. Their work appears in journals such as The American Journal of Human Genetics, Journal of Allergy and Clinical Immunology, Human Molecular Genetics, Arthritis & Rheumatology and Pediatric Rheumatology.

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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