Raul J. Heredia

Vienna, Austria

Last Updated: 09/26/2026

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Found 13 publications

Author Correction: GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway.

Author Correction: GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway.

Journal: Nature immunology

Published: February 12, 2024

GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway.

GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway.

Journal: Nature immunology

Published: April 19, 2023

Polymerase-δ-deficiency as a novel cause of inborn cancer predisposition associated with human papillomavirus infection.

Polymerase-δ-deficiency as a novel cause of inborn cancer predisposition associated with human papillomavirus infection.

Journal: The British journal of dermatology

Published: July 29, 2022

Case Report of a Novel NFkB Mutation in a Lymphoproliferative Disorder Patient.

Case Report of a Novel NFkB Mutation in a Lymphoproliferative Disorder Patient.

Journal: Endocrine, metabolic & immune disorders drug targets

Published: December 06, 2021

Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency.

Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency.

Journal: Journal of clinical immunology

Published: April 05, 2021

Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency.

Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency.

Journal: Journal of clinical immunology

Published: February 07, 2021

BCGitis as the primary manifestation of chronic granulomatous disease.

BCGitis as the primary manifestation of chronic granulomatous disease.

Journal: IDCases

Published: November 22, 2020

Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity.

Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity.

Journal: The Journal of allergy and clinical immunology

Published: October 05, 2020

Germline IKAROS dimerization haploinsufficiency causes hematologic cytopenias and malignancies.

Germline IKAROS dimerization haploinsufficiency causes hematologic cytopenias and malignancies.

Journal: Blood

Published: May 28, 2020

Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis.

Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis.

Journal: Journal of clinical immunology

Published: May 23, 2020

Unreported Missense Mutation in the Dimerization Domain of ADA2 Leads to ADA2 Deficiency Associated with Severe Oral Ulcers and Neutropenia in a Female Somalian Patient-Addendum to the Genotype-Phenotype Puzzle.

Unreported Missense Mutation in the Dimerization Domain of ADA2 Leads to ADA2 Deficiency Associated with Severe Oral Ulcers and Neutropenia in a Female Somalian Patient-Addendum to the Genotype-Phenotype Puzzle.

Journal: Journal of clinical immunology

Published: May 03, 2019

F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects.

F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects.

Journal: The Journal of allergy and clinical immunology

Published: January 14, 2019

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Last Updated: 09/26/2026