LUIS IGNACIO
GONZÁLEZ GRANADO
Profesor asociado
Publicaciones (162) Publicaciones de LUIS IGNACIO GONZÁLEZ GRANADO
2024
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A Validated Highly Sensitive Microsatellite Instability Assay Accurately Identifies Individuals Harboring Biallelic Germline PMS2 Pathogenic Variants in Constitutional Mismatch Repair Deficiency
Clinical chemistry, Vol. 70, Núm. 5, pp. 737-746
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Enrichment of Immune Dysregulation Disorders in Adult Patients with Human Inborn Errors of Immunity
Journal of Clinical Immunology, Vol. 44, Núm. 3
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Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children
The Journal of experimental medicine, Vol. 221, Núm. 2
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JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study
Journal of Allergy and Clinical Immunology, Vol. 153, Núm. 1, pp. 275-286.e18
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Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection
Human Genetics and Genomics Advances, Vol. 5, Núm. 3
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Non-apoptotic FAS signaling controls mTOR activation and extrafollicular maturation in human B cells
Science Immunology, Vol. 9, Núm. 91
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Pseudo-catatonia and Acral Degos-like Lesions: An Atypical Form of the Aicardi–Goutières Syndrome
Actas Dermo-Sifiliograficas
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The complex nature of CXCR4 mutations in WHIM syndrome
Frontiers in Immunology, Vol. 15
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The lack of either IRF9, or STAT2, has surprisingly little effect on human natural killer cell development and function
Immunology, Vol. 172, Núm. 3, pp. 440-450
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Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival
Blood, Vol. 143, Núm. 24, pp. 2504-2516
2023
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Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity
Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 4, pp. 984-996.e10
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Clinical Non-penetrance Associated with Biallelic Mutations in the RNase H2 Complex
Journal of Clinical Immunology
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Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes
iScience, Vol. 26, Núm. 6
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Editorial: Primary immune regulatory disorders: Coming of age
Frontiers in Pediatrics
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Inborn Error of STAT2-Dependent IFN-I Immunity in a Patient Presented with Hemophagocytic Lymphohistiocytosis and Multisystem Inflammatory Syndrome in Children
Journal of Clinical Immunology, Vol. 43, Núm. 6, pp. 1278-1288
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Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome
Journal of Allergy and Clinical Immunology, Vol. 151, Núm. 4, pp. 1081-1095
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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Genome Medicine, Vol. 15, Núm. 1
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Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations
Journal of Allergy and Clinical Immunology, Vol. 151, Núm. 5, pp. 1391-1401.e7
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Scalable GMP-compliant gene correction of CD4+ T cells with IDLV template functionally validated in vitro and in vivo
Molecular Therapy - Methods and Clinical Development, Vol. 30, pp. 546-557
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TCF3 haploinsufficiency defined by immune, clinical, gene-dosage, and murine studies
Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 3, pp. 736-747