[Prenatal diagnosis of hemophilia A by DNA analysis. First experience in Spain]

Final SeaQuest Results on the Flavor Asymmetry of the Proton Light-Quark Sea with Proton-Induced Drell-Yan Process.

Physical review letters·2026

Disentangling Centrality Bias and Final-State Effects in the Production of High-p_{T} Neutral Pions Using Direct Photon in d+Au Collisions at sqrt[s_{NN}]=200 GeV.

Physical review letters·2025

Five years' experience of the clinical exome sequencing in a Spanish single center.

Scientific reports·2022

Prevalence, multimodal imaging and genotype-phenotype assessment of trauma related subretinal fibrosis in stargardt disease.

European journal of ophthalmology·2022

Genetics and epidemiology of aniridia: Updated guidelines for genetic study.

Archivos de la Sociedad Espanola de Oftalmologia·2021

NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases.

Human genetics·2021

Overview of breast cancer screening in Spain and its impact on mortality: An ecological study examining temporal trends (2000-2023).

Medicina clinica·2026

One-year outcomes in patients with heart failure and chronic kidney disease: differences according to the type of heart failure and kidney disease stages.

Medicina clinica·2026

Agent-based simulation and digital twins in heart failure care: Current evidence, validation and implementation barriers.

Medicina clinica·2026

Analysis of clinical characteristics and risk factors of progressive pulmonary fibrosis associated with systemic sclerosis.

Medicina clinica·2026

Advanced neuroimaging in rare diseases: The paradigm of quantification in the era of personalized medicine.

Medicina clinica·2026

Parkinson's disease: Clinical update and new diagnostic and therapeutic approaches.

Medicina clinica·2026

A massively parallel reporter assay of MECP2cis-regulatory elements reveals genetic candidates for male-biased autism.

American journal of human genetics·2026

Multiple classification of childhood and juvenile autism spectrum disorder from ABIDE-II sMRI using BN-GO-CNN.

Biomedizinische Technik. Biomedical engineering·2026

Protocol to define Sox9 target programs during mouse limb chondrogenesis using scRNA-seq and CUT&RUN integration.

STAR protocols·2026

Genetic characterization of inherited retinal dystrophy in a Northwestern Chinese cohort: A single-center study over a 5-year period in Shaanxi, China.

Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie·2026

The genome sequence of a douglasiid moth, Tinagma dryadis Staudinger, 1872 (Lepidoptera: Douglasiidae).

Wellcome open research·2026

[Clinicopathological and molecular genetic characteristics of embryonal rhabdomyosarcoma with divergent neuroectodermal differentiation: an analysis of 17 cases].

Zhonghua bing li xue za zhi = Chinese journal of pathology·2026

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[Prenatal diagnosis of hemophilia A by DNA analysis. First experience in Spain]

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Final SeaQuest Results on the Flavor Asymmetry of the Proton Light-Quark Sea with Proton-Induced Drell-Yan Process.

Disentangling Centrality Bias and Final-State Effects in the Production of High-p_{T} Neutral Pions Using Direct Photon in d+Au Collisions at sqrt[s_{NN}]=200 GeV.

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Protocol to define Sox9 target programs during mouse limb chondrogenesis using scRNA-seq and CUT&RUN integration.

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