Étienne Mornet

5.9k total citations
107 papers, 4.3k citations indexed

About

Étienne Mornet is a scholar working on Endocrinology, Diabetes and Metabolism, Rheumatology and Molecular Biology. According to data from OpenAlex, Étienne Mornet has authored 107 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Endocrinology, Diabetes and Metabolism, 44 papers in Rheumatology and 40 papers in Molecular Biology. Recurrent topics in Étienne Mornet's work include Alkaline Phosphatase Research Studies (69 papers), Heterotopic Ossification and Related Conditions (38 papers) and Selenium in Biological Systems (27 papers). Étienne Mornet is often cited by papers focused on Alkaline Phosphatase Research Studies (69 papers), Heterotopic Ossification and Related Conditions (38 papers) and Selenium in Biological Systems (27 papers). Étienne Mornet collaborates with scholars based in France, United States and Germany. Étienne Mornet's co-authors include Perrin C. White, Jakob Dupont, A. Taillandier, Brigitte Simon‐Bouy, Anne-Sophie Lia-Baldini, Delphine Fauvert, Hermann Girschick, J.L. Serre, Isabelle Brun‐Heath and Isabel Tejada and has published in prestigious journals such as The Lancet, Journal of Biological Chemistry and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Étienne Mornet

105 papers receiving 4.2k citations

Peers

Countries citing papers authored by Étienne Mornet

Since Specialization

Citations

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

Fields of papers citing papers by Étienne Mornet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Étienne Mornet

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

#	Work	Indexed citations
1	Identification of a p.Arg708Gln variant in COL1A2 in atypical femoral fractures 2016 ·Joint Bone Spine ·Thomas Funck‐Brentano, Agnès Ostertag, Françoise Debiais, Patrice Fardellone, Corinne Collet, Étienne Mornet, Martine Cohen‐Solal	14
2	Pseudotumor Cerebri as a Rare Presentation of Infantile Hypophosphatasia: A Case Report 2015 ·AACE Clinical Case Reports ·Abeer Alassaf, Amira Masri, Étienne Mornet, Rasha Odeh, Abdelkarim A. Al-Qudah	0
3	Unexpected high intrafamilial phenotypic variability observed in hypophosphatasia 2014 ·European Journal of Human Genetics ·Christine Hofmann, Hermann Girschick, Étienne Mornet, Doris Schneider, Franz Jakob, Birgit Mentrup	64
4	Vestibular schwannoma and cell-phones. Results, limits and perspectives of clinical studies 2013 ·European Annals of Otorhinolaryngology Head and Neck Diseases ·Étienne Mornet, R. Kania, E. Sauvaget, Philippe Herman, Patrice Tran Ba Huy	6
5	Oro-Dental Features In Hypophosphatasia : A Valuable Phenotype For Disease Diagnosis And Evaluation Of Future Treatment Outcomes 2012 ·Revistes Científiques de la University of Barcelona (University of Barcelona) ·Agnès Bloch‐Zupan, Yves Alembik, B Doray, Agnès Linglart, Étienne Mornet, (unknown), D Droz, (unknown)	1
6	A sequence variation in the promoter of the placental alkaline phosphatase gene (ALPP) is associated with allele-specific expression in human term placenta 2010 ·Placenta ·(unknown), (unknown), (unknown), Isabelle Brun‐Heath, A. Taillandier, Philippe de Mazancourt, Marie‐Noëlle Dieudonné, Étienne Mornet	5
7	Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene. 2009 ·PubMed ·Danijela Petković Ramadža, Feodora Stipoljev, Vladimir Sarnavka, (unknown), Kristina Potočki, Ksenija Fumić, Étienne Mornet, Ivo Barić	4
8	Hypophosphatasia may lead to bone fragility: don’t miss it 2008 ·European Journal of Pediatrics ·Pierre Moulin, Frédéric Vaysse, Éric Bieth, Étienne Mornet, Isabelle Gennero, Sara Laurencin‐Dalicieux, C. Baunin, M. Tauber, Jérôme Sales de Gauzy, Jean‐Pierre Salles	30
9	Specific ultrasonographic features of perinatal lethal hypophosphatasia 2008 ·American Journal of Medical Genetics Part A ·Andreas Zankl, Étienne Mornet, Shell Fean Wong	16
10	A new mechanism of dominance in hypophosphatasia: the mutated protein can disturb the cell localization of the wild-type protein 2008 ·Human Genetics ·Anne-Sophie Lia-Baldini, Isabelle Brun‐Heath, Claire Carrion, Brigitte Simon‐Bouy, J.L. Serre, Mark E. Nuñes, Étienne Mornet	38
11	Hypophosphatasia 2008 ·Best Practice & Research Clinical Rheumatology ·Étienne Mornet	96
12	Characterization of Missense Mutations and Large Deletions in the ALPL Gene by Sequencing and Quantitative Multiplex PCR of Short Fragments 2006 ·Genetic Testing ·Marc Spentchian, Isabelle Brun‐Heath, A. Taillandier, Delphine Fauvert, Jean‐Louis Serre, Brigitte Simon‐Bouy, Filipa Carvalho, (unknown), Sarju Mehta, Grit Müller, Saskia A.J. Lesnik Oberstein, Gönül Oğur, Saba Sharif, Étienne Mornet	20
13	Hypophosphatasie de l'enfant : à propos d'un cas caractérisé par une nouvelle mutation 2004 ·Archives de Pédiatrie ·(unknown), Y. Gillerot, Étienne Mornet	5
14	Characterization of 11 novel mutations in the tissue non-specific alkaline phosphatase gene responsible for hypophosphatasia and genotype–phenotype correlations 2004 ·Molecular Genetics and Metabolism ·Isabelle Brun‐Heath, A. Taillandier, Jean‐Louis Serre, Étienne Mornet	27
15	Severe cleidocranial dysplasia can mimic hypophosphatasia 2002 ·European Journal of Pediatrics ·Sheila Unger, Étienne Mornet, Stefan Mundlos, Susan Blasér, David E.C. Cole	39
16	Characterization of a family with dominant hypophosphatasia 2000 ·European Journal Of Oral Sciences ·Jan C.‐C. Hu, R. Plaetke, Étienne Mornet, Chuhua Zhang, Xiaoling Sun, Huw F. Thomas, James P. Simmer	63
17	Screening of CYP21 gene mutations in 129 French patients affected by steroid 21-hydroxylase deficiency 1995 ·Human Mutation ·(unknown), (unknown), M C Raux-Demay, (unknown), Joëlle Boué, Brigitte Simon‐Bouy, (unknown), A Boué, Étienne Mornet	62
18	Molecular analysis of a ring chromosome X in a family with fragile X syndrome 1993 ·Human Genetics ·Étienne Mornet, (unknown), (unknown), Brigitte Simon‐Bouy, Michèle Mathieu, (unknown), (unknown), Éric Leguern, Joëlle Boué, A Boué	4
19	Affected sibs with fragde X syndrome exhibit an age‐dependent decrease in the size of the fragile X full mutation 1993 ·Clinical Genetics ·Étienne Mornet, (unknown), (unknown), Isabel Tejada, (unknown), Joëlle Boué, A Boué	9
20	Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patients 1991 ·Clinical Genetics ·Brigitte Simon‐Bouy, Étienne Mornet, J.L. Serre, A. Taillandier, J Boué, A Boué	7

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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