Serge Amselem

14.5k citations

191 papers · 7.8k indexed · h-index 52

Impact in

Endocrinology, Diabetes and Metabolism top 0.5%
- Growth Hormone and Insulin-like Growth Factors
Genetics top 0.5%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting

Papers in

Endocrinology, Diabetes and Metabolism 49
- Growth Hormone and Insulin-like Growth Factors 48
Immunology 39
- IL-33, ST2, and ILC Pathways 19

Co-authors: Philippe Duquesnoy Michel Goossens Marie‐Laure Sobrier Gilles Grateau Bénédicte Duriez Estelle Escudier Florence Dastot Isabelle Jéru
Journals: The Journal of Clinical Endocrinology & Metabolism (12 papers)The American Journal of Human Genetics (11 papers)PLoS ONE (7 papers)Human Mutation (6 papers)Proceedings of the National Academy of Sciences (5 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Serge Amselem

181 papers receiving 7.6k citations

Peers

Countries citing papers authored by Serge Amselem

Since Specialization

Citations

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

Fields of papers citing papers by Serge Amselem

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Serge Amselem, 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 Serge Amselem Line = papers co-authored together Serge Amselem links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Association between familial Mediterranean fever and multiple sclerosis: A case series from the JIR cohort and systematic literature review Multiple Sclerosis and Related Disorders ·A. Elhaddad, Anaël Dumont, 张雄伟, Samuel Ardois, M. Le Besnerais, H. Lévesque, Jean‐Christophe Ouallet, Léa Savey, Achille Aouba, Serge Amselem, Irina Giurgea, Jean Capron, Gilles Grateau, Sophie Georgin‐Lavialle	2021	9
2	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, Zuzanna Sycz, 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
3	Monoclonal Gammopathy, Arthralgias, and Recurrent Fever Syndrome: A New Autoinflammatory Syndrome? The Journal of Rheumatology ·Yik Ching Lee, Alexis Talbot, Camille Louvrier, 源吾中島, Matthieu Mahévas, David Boutboul, Serge Amselem, Irina Giurgea, Gilles Grateau, Sophie Georgin‐Lavialle	2019	4
4	Photoaging and skin cancer: Is the inflammasome the missing link? Mechanisms of Ageing and Development ·Fawaz Awad, Eman Assrawi, Camille Louvrier, Claire Jumeau, Irina Giurgea, Serge Amselem, Sonia‐Athina Karabina	2018	74
5	Clinical and Preliminary Molecular Description of a Cohort of Patients with Growth Retardation due to Severe Primary IGF1 Deficiency (GROWPATI Study) HAL (Le Centre pour la Communication Scientifique Directe) ·Athanasia Stoupa, Qiao Li, Isabelle Flechtner, Graziella Pinto, Dinane Samara‐Boustani, Caroline Thalassinos, Mariella Ramalheiro Loureiro, Jacques Beltrand, Irène Netchine, Frédéric Brioude, Marie Legendre, Serge Amselem, Michel Polak	2018	1
6	Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance - Identification of New Variants and Impact on the Inheritance Pattern Marie Legendre, Florence Dastot, Nathalie Collot, Philippe Duquesnoy, F. Etaee, Marie‐Laure Sobrier, S B Mirov, Cheree Causey, S. Baron, Sylvie Cabrol, Bert Callewaert, Maryse Cartigny, Margarita Craen, Patricia Crock, Lan Yu-ming, Cecilia Lazea, Michel Polak, Lars Sävendahl, 坂場聡, Serge Amselem	2016	1
7	Clinical and molecular findings in a Moroccan patient with popliteal pterygium syndrome: a case report Journal of Medical Case Reports ·Juo Lien Wang, Hirsto Djidjev, Marie Legendre, Nathalie Collot, Serge Amselem, Abdelaziz Sefiani	2014	3
8	A novel POU1F1 mutation (p.Thr168IlefsX7) associated with an early and severe form of combined pituitary hormone deficiency: functional analysis and follow-up from infancy to adulthood Clinical Endocrinology ·Yardena Tenenbaum‐Rakover, Marie‐Laure Sobrier, Serge Amselem	2011	11
9	Mutations in the autoinflammatory cryopyrin-associated periodic syndrome gene: epidemiological study and lessons from eight years of genetic analysis in France Annals of the Rheumatic Diseases ·Laurence Cuisset, Isabelle Jéru, Bruno Dumont, Aurélie Fabre, Emmanuelle Cochet, Thomas Raiser, Marc Delpech, Serge Amselem, Isabelle Touitou	2010	117
10	Functional consequences of a germline mutation in the leucine‐rich repeat domain of NLRP3 identified in an atypical autoinflammatory disorder Arthritis & Rheumatism ·Isabelle Jéru, Sandrine Marlin, أحمد خالد العبيد, Emmanuelle Cochet, Sylvain Normand, Philippe Duquesnoy, Florence Dastot‐Le Moal, Laurence Cuisset, Véronique Hentgen, F Bois, Jean‐Claude Lecron, Robin Dhôte, Gilles Grateau, Emad S. Alnemri, Serge Amselem	2010	25
11	A 20-year experience of electron microscopy in the diagnosis of primary ciliary dyskinesia European Respiratory Journal ·Jean‐François Papon, A. Coste, Françoise Roudot‐Thoraval, M. Boucherat, G. Roger, Aline Tamalet, Anne-Marie Vojtek, Serge Amselem, Estelle Escudier	2009	96
12	Mutations in NALP12 cause hereditary periodic fever syndromes Proceedings of the National Academy of Sciences ·Isabelle Jéru, Philippe Duquesnoy, Teresa Fernandes‐Alnemri, Emmanuelle Cochet, Je‐Wook Yu, Yuan Lan-xi, E. Grimprel, Judith Landman‐Parker, Véronique Hentgen, Sandrine Marlin, Ken McElreavey, Tamara Sarkisian, Gilles Grateau, Emad S. Alnemri, Serge Amselem	2008	288
13	Matrix Metalloproteinase Gene Polymorphisms and Bronchopulmonary Dysplasia: Identification of MMP16 as a New Player in Lung Development PLoS ONE ·Alice Hadchouel, Fabrice Decobert, Marie‐Laure Franco‐Montoya, 康邦山根, Pierre‐Henri Jarreau, Olivier Boucherat, Emmanuel Martin, Alexandra Benachi, Serge Amselem, Jacques R. Bourbon, Claude Danan, Christophe Delacourt	2008	54
14	Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations Arthritis & Rheumatism ·Cécile Cazeneuve, Lilian Jaramillo Naranjo, David Geneviève, Hasmik Hayrapetyan, Stéphanie Papin, 繁宮本, Brigitte Boissier, Josué Feingold, G. S.P. Gunarathne, Tamara Sarkisian, Serge Amselem	2003	36
15	Causes génétiques de déficit en hormone de croissance Sophie Vallette-Kasic, Irène Netchine, Rachel Reynaud, Serge Amselem, A Enjalbert, Thierry Brue	2002	1
16	Identification of MEFV-Independent Modifying Genetic Factors for Familial Mediterranean Fever The American Journal of Human Genetics ·Cécile Cazeneuve, Yi-Shiou Lin, Stéphanie Papin, Françoise Roudot‐Thoraval, David Geneviève, Erfan Abolfazli, Gianka Salustiano Bezerril de Bastos Gomes, Mustafa Afifi Ab Halim, Ara Babloyan, Brigitte Boissier, Philippe Duquesnoy, Jean‐Claude Kouyoumdjian, 繁宮本, Gilles Grateau, Tamara Sarkisian, Serge Amselem	2000	155
17	MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications The American Journal of Human Genetics ·Cécile Cazeneuve, Tamara Sarkisian, Christophe Pécheux, M Dervichian, Brigitte Nédelec, Philippe Reinert, Mihál, Jean‐Claude Kouyoumdjian, Yi-Shiou Lin, Marc Delpech, Michel Goossens, Catherine Dodé, Gilles Grateau, Serge Amselem	1999	203
18	Extensive Phenotypic Analysis of a Family with Growth Hormone (GH) Deficiency Caused by a Mutation in the GH-Releasing Hormone Receptor Gene¹ The Journal of Clinical Endocrinology & Metabolism ·Irène Netchine, Philippe Talon, Florence Dastot, 上村良一, Michel Goossens, Serge Amselem	1998	91
19	Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene. Journal of Clinical Investigation ·Alain Hovnanian, Philippe Duquesnoy, C Blanchet‐Bardon, Robert G. Knowlton, Serge Amselem, Mark Lathrop, 正文教学, Jouni Uitto, Michel Goossens	1992	122
20	Recurrent nonsense mutations in the growth hormone receptor from patients with Laron dwarfism. Journal of Clinical Investigation ·Serge Amselem, Marie‐Laure Sobrier, Philippe Duquesnoy, R Rappaport, M C Postel-Vinay, M Gourmelen, Bruno Dallapiccola, Michel Goossens	1991	72

About Serge Amselem

Serge Amselem is a scholar working on Endocrinology, Diabetes and Metabolism, Immunology, Genetics, Molecular Biology and Nephrology, having authored 191 papers that have together received 7.8k indexed citations. Recurring topics across this work include Inflammasome and immune disorders (50 papers), Growth Hormone and Insulin-like Growth Factors (48 papers), IL-33, ST2, and ILC Pathways (19 papers), Cystic Fibrosis Research Advances (16 papers), Genetic Syndromes and Imprinting (15 papers), Neonatal Respiratory Health Research (14 papers), Genetic and Kidney Cyst Diseases (13 papers) and RNA modifications and cancer (12 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (2.0k citations), Genetics (2.3k citations), Immunology (1.5k citations), Molecular Biology (4.3k citations) and Nephrology (444 citations). Serge Amselem has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Philippe Duquesnoy, Michel Goossens, Marie‐Laure Sobrier, Gilles Grateau, Bénédicte Duriez, Estelle Escudier, Florence Dastot, Isabelle Jéru, Annick Clément and Marie Legendre. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics, PLoS ONE, Human Mutation and Proceedings of the National Academy of Sciences.

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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