Nicolas Cagnard
Overview
Explore the profile of Nicolas Cagnard including associated specialties, affiliations and a list of published articles.
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Articles
92
Citations
5038
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Recent Articles
1.
Zhu G, Didry-Barca B, Seabra L, Rice G, Uggenti C, Touimy M, et al.
Lancet Neurol
. 2025 Feb;
24(3):218-229.
PMID: 39986310
Background: Through the agnostic screening of patients with uncharacterised disease phenotypes for an upregulation of type I interferon (IFN) signalling, we identified a cohort of individuals heterozygous for mutations in...
2.
Bal E, Park H, Belaid-Choucair Z, Kayserili H, Naville M, Madrange M, et al.
Nat Med
. 2025 Feb;
PMID: 39915680
No abstract available.
3.
Riller Q, Sorin B, Courteille C, Ho-Nhat D, Le Voyer T, Debray J, et al.
J Exp Med
. 2025 Jan;
222(2.
PMID: 39812688
IKKα, encoded by CHUK, is crucial in the non-canonical NF-κB pathway and part of the IKK complex activating the canonical pathway alongside IKKβ. The absence of IKKα causes fetal encasement...
4.
Zerad L, Gacem N, Gayda F, Day L, Sinigaglia K, Richard L, et al.
Cells
. 2024 Dec;
13(23).
PMID: 39682701
Adenosine deaminase acting on RNA 1 (ADAR1) is the principal enzyme for the adenosine-to-inosine RNA editing that prevents the aberrant activation of cytosolic nucleic acid sensors by endogenous double stranded...
5.
Erjavec E, Angee C, Hadjadj D, Passet B, David P, Kostic C, et al.
Am J Hum Genet
. 2024 Sep;
111(10):2265-2282.
PMID: 39293448
Congenital microcoria (MCOR) is a rare hereditary developmental defect of the iris dilator muscle frequently associated with high axial myopia and high intraocular pressure (IOP) glaucoma. The condition is caused...
6.
Jeanpierre M, Cognard J, Tusseau M, Riller Q, Bui L, Berthelet J, et al.
J Exp Med
. 2024 Jul;
221(9.
PMID: 39028869
An exome sequencing strategy employed to identify pathogenic variants in patients with pediatric-onset systemic lupus or Evans syndrome resulted in the discovery of six novel monoallelic mutations in PTPN2. PTPN2...
7.
Dorval G, Le Gac G, Moriniere V, Ka C, Goursaud C, Knebelmann B, et al.
Kidney Int
. 2024 Jun;
106(3):532-535.
PMID: 38944240
No abstract available.
8.
Riller Q, Sorin B, Courteille C, Ho-Nhat D, Le Voyer T, Debray J, et al.
medRxiv
. 2024 May;
PMID: 38798321
IKKα, encoded by , is crucial in the non-canonical NF-κB pathway and part of the IKK complex activating the canonical pathway alongside IKKβ. Absence of IKKα cause fetal encasement syndrome...
9.
Regnier P, Vetillard M, Bansard A, Pierre E, Li X, Cagnard N, et al.
Cell Rep Med
. 2023 Dec;
4(12):101256.
PMID: 38118422
FLT3-L-dependent classical dendritic cells (cDCs) recruit anti-tumor and tumor-protecting lymphocytes. We evaluate cancer growth in mice with low, normal, or high levels of cDCs. Paradoxically, both low or high numbers...
10.
Didier-Mathon H, Stoupa A, Kariyawasam D, Yde S, Cochant-Priollet B, Groussin L, et al.
Front Endocrinol (Lausanne)
. 2023 Nov;
14:1286747.
PMID: 37964961
Background: / mutations are associated with congenital hypothyroidism and thyroid dysgenesis. Borealin is involved in mitosis as part of the Chromosomal Passenger Complex. Although mutations decrease thyrocyte adhesion and migration,...