Manuel Moruno-Solis

Barcelona, CT, Spain

Last Updated: 09/26/2026

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Found 11 publications

Case report: Novel compound heterozygous IL1RN mutations as the likely cause of a lethal form of deficiency of interleukin-1 receptor antagonist.

Case report: Novel compound heterozygous IL1RN mutations as the likely cause of a lethal form of deficiency of interleukin-1 receptor antagonist.

Journal: Frontiers in immunology

Published: February 03, 2024

Spanish cohort of VEXAS syndrome: clinical manifestations, outcome of treatments and novel evidences about UBA1 mosaicism.

Spanish cohort of VEXAS syndrome: clinical manifestations, outcome of treatments and novel evidences about UBA1 mosaicism.

Journal: Annals of the rheumatic diseases

Published: June 07, 2023

Somatic Mutations Detected in Parkinson Disease Could Affect Genes With a Role in Synaptic and Neuronal Processes.

Somatic Mutations Detected in Parkinson Disease Could Affect Genes With a Role in Synaptic and Neuronal Processes.

Journal: Frontiers in aging

Published: January 08, 2022

Somatic genetic variation in healthy tissue and non-cancer diseases.

Somatic genetic variation in healthy tissue and non-cancer diseases.

Journal: European journal of human genetics : EJHG

Published: November 04, 2021

Publisher Correction: Assessment of the gene mosaicism burden in blood and its implications for immune disorders.

Publisher Correction: Assessment of the gene mosaicism burden in blood and its implications for immune disorders.

Journal: Scientific reports

Published: August 18, 2021

Assessment of the gene mosaicism burden in blood and its implications for immune disorders.

Assessment of the gene mosaicism burden in blood and its implications for immune disorders.

Journal: Scientific reports

Published: May 14, 2020

Genetic diagnosis of autoinflammatory disease patients using clinical exome sequencing.

Genetic diagnosis of autoinflammatory disease patients using clinical exome sequencing.

Journal: European journal of medical genetics

Published: December 04, 2019

Flow Sorting Enrichment and Nanopore Sequencing of Chromosome 1 From a Chinese Individual.

Flow Sorting Enrichment and Nanopore Sequencing of Chromosome 1 From a Chinese Individual.

Journal: Frontiers in genetics

Published: September 18, 2019

Author Correction: Potential damaging mutation in LRP5 from genome sequencing of the first reported chimpanzee with the Chiari malformation.

Author Correction: Potential damaging mutation in LRP5 from genome sequencing of the first reported chimpanzee with the Chiari malformation.

Journal: Scientific reports

Published: May 06, 2018

Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.

Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.

Journal: Frontiers in immunology

Published: December 12, 2017

Potential damaging mutation in LRP5 from genome sequencing of the first reported chimpanzee with the Chiari malformation.

Potential damaging mutation in LRP5 from genome sequencing of the first reported chimpanzee with the Chiari malformation.

Journal: Scientific reports

Published: July 13, 2017

Showing 1-11 of 11

Last Updated: 09/26/2026