<style face="normal" font="default" size="100%">A genomic strategy for precision medicine in rare diseases: integrating customized algorithms into clinical practice.</style>

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<style face="normal" font="default" size="100%">A genomic strategy for precision medicine in rare diseases: integrating customized algorithms into clinical practice.</style>

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<style face="normal" font="default" size="100%">Metatranscriptomic analysis reveals gut microbiome bacterial genes in pyruvate and amino acid metabolism associated with hyperuricemia and gout in humans.</style>

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<style face="normal" font="default" size="100%">Aripiprazole as protector against COVID-19 mortality.</style>

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<style face="normal" font="default" size="100%">Characterization of the Common Genetic Variation in the Spanish Population of Navarre.</style>

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<style face="normal" font="default" size="100%">Genotypic characterization and antimicrobial susceptibility of human isolates in Southern Spain.</style>

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<style face="normal" font="default" size="100%">HMGA1 regulates trabectedin sensitivity in advanced soft-tissue sarcoma (STS): A Spanish Group for Research on Sarcomas (GEIS) study.</style>

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<style face="normal" font="default" size="100%">Shared germline genomic variants in two patients with double primary gastrointestinal stromal tumours (GISTs).</style>

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<style face="normal" font="default" size="100%">Real world evidence of calcifediol or vitamin D prescription and mortality rate of COVID-19 in a retrospective cohort of hospitalized Andalusian patients.</style>

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<style face="normal" font="default" size="100%">Community Assessment of the Predictability of Cancer Protein and Phosphoprotein Levels from Genomics and Transcriptomics.</style>

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<style face="normal" font="default" size="100%">Mechanistic Models of Signaling Pathways Reveal the Drug Action Mechanisms behind Gender-Specific Gene Expression for Cancer Treatments.</style>

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<style face="normal" font="default" size="100%">Nivolumab and sunitinib combination in advanced soft tissue sarcomas: a multicenter, single-arm, phase Ib/II trial.</style>

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<style face="normal" font="default" size="100%">Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies.</style>

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<style face="normal" font="default" size="100%">Pazopanib for treatment of typical solitary fibrous tumours: a multicentre, single-arm, phase 2 trial.</style>

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<style face="normal" font="default" size="100%">Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses.</style>

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<style face="normal" font="default" size="100%">Pazopanib for treatment of advanced malignant and dedifferentiated solitary fibrous tumour: a multicentre, single-arm, phase 2 trial.</style>

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<style face="normal" font="default" size="100%">The effects of death and post-mortem cold ischemia on human tissue transcriptomes.</style>

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<style face="normal" font="default" size="100%">LRH-1 agonism favours an immune-islet dialogue which protects against diabetes mellitus.</style>

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<style face="normal" font="default" size="100%">The modular network structure of the mutational landscape of Acute Myeloid Leukemia.</style>

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<style face="normal" font="default" size="100%">GGPS1 Mutation and Atypical Femoral Fractures with Bisphosphonates.</style>

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<style face="normal" font="default" size="100%">Graph-theoretical comparison of normal and tumor networks in identifying BRCA genes.</style>

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<style face="normal" font="default" size="100%">Human DNA methylomes of neurodegenerative diseases show common epigenomic patterns.</style>

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<style face="normal" font="default" size="100%">Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa.</style>

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<style face="normal" font="default" size="100%">Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.</style>

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<style face="normal" font="default" size="100%">Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes.</style>

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<style face="normal" font="default" size="100%">Serum metabolomic profiling facilitates the non-invasive identification of metabolic biomarkers associated with the onset and progression of non-small cell lung cancer.</style>

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<style face="normal" font="default" size="100%">Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype.</style>

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<style face="normal" font="default" size="100%">Deregulation of key signaling pathways involved in oocyte maturation in FMR1 premutation carriers with Fragile X-associated primary ovarian insufficiency.</style>

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<style face="normal" font="default" size="100%">The EGR2 gene is involved in axonal Charcot-Marie-Tooth disease.</style>

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<style face="normal" font="default" size="100%">Exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies.</style>

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<style face="normal" font="default" size="100%">Permanent cardiac sarcomere changes in a rabbit model of intrauterine growth restriction.</style>

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<style face="normal" font="default" size="100%">Sequencing and functional analysis of the genome of a nematode egg-parasitic fungus, Pochonia chlamydosporia.</style>

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<style face="normal" font="default" size="100%">Differential gene-expression analysis defines a molecular pattern related to olive pollen allergy.</style>

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<style face="normal" font="default" size="100%">Exome sequencing identifies a new mutation in SERAC1 in a patient with 3-methylglutaconic aciduria.</style>

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<style face="normal" font="default" size="100%">Intrauterine growth restriction is associated with cardiac ultrastructural and gene expression changes related to the energetic metabolism in a rabbit model.</style>

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<style face="normal" font="default" size="100%">Mammosphere formation in breast carcinoma cell lines depends upon expression of E-cadherin.</style>

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<style face="normal" font="default" size="100%">Pathways systematically associated to Hirschsprung's disease.</style>

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<style face="normal" font="default" size="100%">Role of CPI-17 in restoring skin homoeostasis in cutaneous field of cancerization: effects of topical application of a film-forming medical device containing photolyase and UV filters.</style>

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<style face="normal" font="default" size="100%">Four new loci associations discovered by pathway-based and network analyses of the genome-wide variability profile of Hirschsprung's disease.</style>

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<style face="normal" font="default" size="100%">Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient.</style>

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<style face="normal" font="default" size="100%">Early peroxisome proliferator-activated receptor gamma regulated genes involved in expansion of pancreatic beta cell mass.</style>

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<style face="normal" font="default" size="100%">DNA methylation epigenotypes in breast cancer molecular subtypes.</style>

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<style face="normal" font="default" size="100%">Exploring the link between germline and somatic genetic alterations in breast carcinogenesis.</style>

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<style face="normal" font="default" size="100%">Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa.</style>

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<style face="normal" font="default" size="100%">Gene set internal coherence in the context of functional profiling.</style>

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<style face="normal" font="default" size="100%">Gene set-based analysis of polymorphisms: finding pathways or biological processes associated to traits in genome-wide association studies.</style>

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<style face="normal" font="default" size="100%">Direct functional assessment of the composite phenotype through multivariate projection strategies.</style>

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<style face="normal" font="default" size="100%">Molecular profiling related to poor prognosis in thyroid carcinoma. Combining gene expression data and biological information.</style>