Cecilia D. Conde

Vienna, Austria

Last Updated: 09/26/2026

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Found 12 publications

Narrowing Down Key Players in Autoimmunity via Single-Cell Multiomics.

Narrowing Down Key Players in Autoimmunity via Single-Cell Multiomics.

Journal: European journal of immunology

Published: December 16, 2024

Multimodal profiling reveals tissue-directed signatures of human immune cells altered with age.

Multimodal profiling reveals tissue-directed signatures of human immune cells altered with age.

Journal: Nature immunology

Published: December 16, 2024

Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.

Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.

Journal: Journal of clinical immunology

Published: October 06, 2023

MultiMAP: dimensionality reduction and integration of multimodal data.

MultiMAP: dimensionality reduction and integration of multimodal data.

Journal: Genome biology

Published: August 26, 2021

SARS-CoV-2 infection of the oral cavity and saliva.

SARS-CoV-2 infection of the oral cavity and saliva.

Journal: Nature medicine

Published: October 20, 2020

Polymerase δ deficiency causes syndromic immunodeficiency with replicative stress.

Polymerase δ deficiency causes syndromic immunodeficiency with replicative stress.

Journal: The Journal of clinical investigation

Published: March 25, 2019

Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function.

Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function.

Journal: Haematologica

Published: March 26, 2018

Hypomorphic mutation in TTC7A causes combined immunodeficiency with mild structural intestinal defects.

Hypomorphic mutation in TTC7A causes combined immunodeficiency with mild structural intestinal defects.

Journal: Blood

Published: March 07, 2015

Clinical features of interleukin 10 receptor gene mutations in children with very early-onset inflammatory bowel disease.

Clinical features of interleukin 10 receptor gene mutations in children with very early-onset inflammatory bowel disease.

Journal: Journal of pediatric gastroenterology and nutrition

Published: November 07, 2014

Inflammatory Bowel Disease With Lethal Disease Course Caused by a Nonsense Mutation in BIRC4 Encoding X-Linked Inhibitor of Apoptosis Protein (XIAP).

Inflammatory Bowel Disease With Lethal Disease Course Caused by a Nonsense Mutation in BIRC4 Encoding X-Linked Inhibitor of Apoptosis Protein (XIAP).

Journal: Journal of pediatric gastroenterology and nutrition

Published: July 16, 2014

Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity.

Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity.

Journal: Nature communications

Published: April 10, 2014

JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia.

JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia.

Journal: Nature genetics

Published: January 26, 2014

Showing 1-12 of 12

Last Updated: 09/26/2026