Nereida Gil-Bravo

Sevilla, AN, Spain

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 17 publications

A genomic strategy for precision medicine in rare diseases: integrating customized algorithms into clinical practice.

A genomic strategy for precision medicine in rare diseases: integrating customized algorithms into clinical practice.

Journal: Journal of translational medicine

Published: July 04, 2024

New genetic diagnoses for inherited retinal dystrophies by integrating splicing tools into NGS pipelines.

New genetic diagnoses for inherited retinal dystrophies by integrating splicing tools into NGS pipelines.

Journal: NPJ genomic medicine

Published: January 22, 2024

Delving into the Role of lncRNAs in Papillary Thyroid Cancer: Upregulation of LINC00887 Promotes Cell Proliferation, Growth and Invasion.

Delving into the Role of lncRNAs in Papillary Thyroid Cancer: Upregulation of LINC00887 Promotes Cell Proliferation, Growth and Invasion.

Journal: International journal of molecular sciences

Published: December 30, 2023

Bioinformatics Prediction for Network-Based Integrative Multi-Omics Expression Data Analysis in Hirschsprung Disease.

Bioinformatics Prediction for Network-Based Integrative Multi-Omics Expression Data Analysis in Hirschsprung Disease.

Journal: Biomolecules

Published: December 05, 2023

Identification of Novel Candidate Genes for Familial Thyroid Cancer by Whole Exome Sequencing.

Identification of Novel Candidate Genes for Familial Thyroid Cancer by Whole Exome Sequencing.

Journal: International journal of molecular sciences

Published: March 31, 2023

Genetic profile in patients with complicated acute aortic syndrome: the GEN-AOR study.

Genetic profile in patients with complicated acute aortic syndrome: the GEN-AOR study.

Journal: Revista espanola de cardiologia (English ed.)

Published: May 25, 2022

A comprehensive WGS-based pipeline for the identification of new candidate genes in inherited retinal dystrophies.

A comprehensive WGS-based pipeline for the identification of new candidate genes in inherited retinal dystrophies.

Journal: NPJ genomic medicine

Published: April 29, 2021

A Multi-Strategy Sequencing Workflow in Inherited Retinal Dystrophies: Routine Diagnosis, Addressing Unsolved Cases and Candidate Genes Identification.

A Multi-Strategy Sequencing Workflow in Inherited Retinal Dystrophies: Routine Diagnosis, Addressing Unsolved Cases and Candidate Genes Identification.

Journal: International journal of molecular sciences

Published: November 18, 2020

Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants.

Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants.

Journal: Journal of translational medicine

Published: September 27, 2019

Expanding the clinical and mutational spectrum of germline ABL1 mutations-associated syndrome: A case report.

Expanding the clinical and mutational spectrum of germline ABL1 mutations-associated syndrome: A case report.

Journal: Medicine

Published: March 12, 2019

Searching the second hit in patients with inherited retinal dystrophies and monoallelic variants in ABCA4, USH2A and CEP290 by whole-gene targeted sequencing.

Searching the second hit in patients with inherited retinal dystrophies and monoallelic variants in ABCA4, USH2A and CEP290 by whole-gene targeted sequencing.

Journal: Scientific reports

Published: April 11, 2018

Unravelling the genetic basis of simplex Retinitis Pigmentosa cases.

Unravelling the genetic basis of simplex Retinitis Pigmentosa cases.

Journal: Scientific reports

Published: June 27, 2016

Showing 1-12 of 17

Last Updated: 09/26/2026