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The SVOM/ECLAIRs image trigger with wavelet-based background correction optimised with a one-year simulation of observations

Autor: N. Dagoneau, S. Schanne

Publikováno v: Astronomy and Astrophysics-A&A
Astronomy and Astrophysics-A&A, 2022, 665, pp.A40. ⟨10.1051/0004-6361/202141891⟩

The SVOM mission under development will carry four instruments, and in particular the coded-mask telescope named ECLAIRs, with a large field of view of about 2 sr, operating in the 4-150 keV energy band. The trigger software on board ECLAIRs will sea

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5e0ec57392181fa3b321e26e373f114
http://arxiv.org/abs/2208.12767

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Detection of short high-energy transients in the local universe with SVOM/ECLAIRs

Autor: B. Arcier, O. Godet, N. Dagoneau, Jean-Luc Atteia, Sujay Mate, J. Rodriguez, M. G. Bernardini, S. Schanne, Diego Götz, S. Guillot

Publikováno v: Astrophys.Space Sci.
Astrophys.Space Sci., 2020, 365 (12), pp.185. ⟨10.1007/s10509-020-03898-z⟩

International audience; The coincidental detection of the gravitational wave event GW 170817 and the gamma-ray burst GRB 170817A marked the advent of multi-messenger astronomy and represented a milestone in the study of GRBs. Significant progress in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a26ba5eaf4a1f03528ee36e9879d4fb0
https://hal.archives-ouvertes.fr/hal-03070594

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Akademický článek

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Onboard catalogue of known X-ray sources for SVOM/ECLAIRs

Autor: N. Dagoneau, J. Rodriguez, Jean-Luc Atteia, S. Schanne, B. Cordier

Publikováno v: Astronomy and Astrophysics-A&A
Astronomy and Astrophysics-A&A, 2021, 645, pp.A18. ⟨10.1051/0004-6361/202038995⟩
Astronomy and Astrophysics-A&A, EDP Sciences, 2021, 645, pp.A18. ⟨10.1051/0004-6361/202038995⟩

The SVOM mission under development will carry various instruments, and in particular the coded-mask telescope ECLAIRs, with a large field of view of about 2 sr, operating in the 4--150 keV energy band, whose goal is to detect high energy transients s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2511e2180f8870c98d50614137690ad
https://doi.org/10.1051/0004-6361/202038995

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Mutations in Cytokine Receptor-Like Factor 1 (CRLF1) Account for Both Crisponi and Cold-Induced Sweating Syndromes

Autor: Pierre Sarda, C. Le Goff, S. Bellais, Lihadh Al-Gazali, M. Di Rocco, Valérie Cormier-Daire, N. Dagoneau, A. Munnich, Patricia Blanchet, C. Huber, Fatima Djouadi

Publikováno v: The American Journal of Human Genetics. 80:966-970

Crisponi syndrome is a rare autosomal recessive disorder characterized by congenital muscular contractions of facial muscles, with trismus in response to stimuli, dysmorphic features, bilateral camptodactyly, major feeding and respiratory difficultie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbe672ec33939f1d5f6e26f3c34762d2
https://doi.org/10.1086/513608

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Akademický článek

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Stüve-Wiedemann syndrome: long-term follow-up and genetic heterogeneity

Autor: M. Le Merrer, Sheila Unger, Valérie Cormier-Daire, Albert David, Ben C.J. Hamel, Andrea Superti-Furga, N Dagoneau, C Jung, Geneviève Baujat, André Mégarbané, Arnold Munnich, M. Di Rocco

Publikováno v: Clinical Genetics, 77, 3, pp. 266-72
Clinical Genetics, 77, 266-72

Stuve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene. The main characteristic features are bowing of the long bones, neonatal respiratory distress, s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70430a6b2140676cc48e6bcb2988471b
https://doi.org/10.1111/j.1399-0004.2009.01314.x

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In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome

Autor: John R. Samples, M. Le Merrer, Gwenaëlle Collod-Béroud, N. Dagoneau, Maurice Godfrey, Catherine Boileau, Mary K. Wirtz, Valérie Cormier-Daire, Arnold Munnich, Robert J. Gorlin, Laurence Faivre

Publikováno v: Journal of Medical Genetics
Journal of Medical Genetics, BMJ Publishing Group, 2003, 40 (1), pp.34-6

Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterised by short stature, brachydactyly, joint stiffness, and characteristic eye anomalies including microspherophakia, ectopia of the lenses, severe myopia, and glaucoma. Both aut

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc03e6c8f7a795cc981ac20c49bb415a
http://www.hal.inserm.fr/inserm-00143439/document

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