Yoann Seeleuthner
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Explore the profile of Yoann Seeleuthner including associated specialties, affiliations and a list of published articles.
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49
Citations
4222
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Recent Articles
1.
Sbruzzi R, Prado M, Fam B, Prolla H, Hellwig A, Rodrigues G, et al.
Front Immunol
. 2024 Nov;
15:1472957.
PMID: 39611146
Inborn errors of immunity (IEI) encompass a broad range of disorders with heterogeneous clinical presentations, often leading to challenges in early diagnosis. This study presents a case of a Brazilian...
2.
Bellos E, Santillo D, Vantourout P, Jackson H, Duret A, Hearn H, et al.
J Exp Med
. 2024 Nov;
221(12).
PMID: 39576310
Multisystem inflammatory syndrome in children (MIS-C) is a rare condition following SARS-CoV-2 infection associated with intestinal manifestations. Genetic predisposition, including inborn errors of the OAS-RNAseL pathway, has been reported. We...
3.
Bohlen J, Bagaric I, Vatovec T, Ogishi M, Ahmed S, Cederholm A, et al.
J Clin Invest
. 2024 Oct;
134(20).
PMID: 39403923
Patients heterozygous for germline CBL loss-of-function (LOF) variants can develop myeloid malignancy, autoinflammation, or both, if some or all of their leukocytes become homozygous for these variants through somatic loss...
4.
Arango-Franco C, Ogishi M, Unger S, Delmonte O, Orrego J, Yatim A, et al.
J Clin Invest
. 2024 Oct;
134(19).
PMID: 39352394
Infants with biallelic IL7R loss-of-function variants have severe combined immune deficiency (SCID) characterized by the absence of autologous T lymphocytes, but normal counts of circulating B and NK cells (T-B+NK+...
5.
Arias A, Neehus A, Ogishi M, Meynier V, Krebs A, Lazarov T, et al.
Nature
. 2024 Aug;
633(8029):417-425.
PMID: 39198650
Severe defects in human IFNγ immunity predispose individuals to both Bacillus Calmette-Guérin disease and tuberculosis, whereas milder defects predispose only to tuberculosis. Here we report two adults with recurrent pulmonary...
6.
Chan Y, Liu Z, Bastard P, Khobrekar N, Hutchison K, Yamazaki Y, et al.
Nature
. 2024 Jul;
632(8024):390-400.
PMID: 39048830
Most cases of herpes simplex virus 1 (HSV-1) encephalitis (HSE) remain unexplained. Here, we report on two unrelated people who had HSE as children and are homozygous for rare deleterious...
7.
Chan Y, Lundberg V, Le Pen J, Yuan J, Lee D, Pinci F, et al.
J Exp Med
. 2024 Jul;
221(9).
PMID: 39023559
Inherited deficiency of the RNA lariat-debranching enzyme 1 (DBR1) is a rare etiology of brainstem viral encephalitis. The cellular basis of disease and the range of viral predisposition are unclear....
8.
Neehus A, Carey B, Landekic M, Panikulam P, Deutsch G, Ogishi M, et al.
Cell
. 2024 May;
187(13):3460.
PMID: 38776920
No abstract available.
9.
Momenilandi M, Levy R, Sobrino S, Li J, Lagresle-Peyrou C, Esmaeilzadeh H, et al.
Cell
. 2024 May;
187(11):2817-2837.e31.
PMID: 38701783
FMS-related tyrosine kinase 3 ligand (FLT3L), encoded by FLT3LG, is a hematopoietic factor essential for the development of natural killer (NK) cells, B cells, and dendritic cells (DCs) in mice....
10.
Johnson M, Ogishi M, Domingo-Vila C, De Franco E, Wakeling M, Imane Z, et al.
J Exp Med
. 2024 Apr;
221(6).
PMID: 38634869
We previously reported two siblings with inherited PD-1 deficiency who died from autoimmune pneumonitis at 3 and 11 years of age after developing other autoimmune manifestations, including type 1 diabetes...