Publicacións nas que colabora con Diana Valverde Pérez (33)

2022

  1. Limited genomic reconstruction of SARS-CoV-2 transmission history within local epidemiological clusters

    Virus Evolution, Vol. 8, Núm. 1

2021

  1. Alterations in respiratory function test three months after hospitalisation for covid-19 pneumonia: Value of determining nitric oxide diffusion

    Journal of Clinical Medicine, Vol. 10, Núm. 10

  2. Spread of a SARS-CoV-2 variant through Europe in the summer of 2020

    Nature, Vol. 595, Núm. 7869, pp. 707-712

  3. The first wave of the COVID-19 epidemic in Spain was associated with early introductions and fast spread of a dominating genetic variant

    Nature Genetics, Vol. 53, Núm. 10, pp. 1405-1414

2020

  1. Characterization of rare ABCC8 variants identified in Spanish pulmonary arterial hypertension patients

    Scientific Reports, Vol. 10, Núm. 1

  2. Comparison of bisulfite pyrosequencing and methylation-specific qPCR for methylation assessment

    International Journal of Molecular Sciences, Vol. 21, Núm. 23, pp. 1-13

2019

  1. Methylation assessment for the prediction of malignancy in mediastinal adenopathies obtained by endobronchial ultrasound-guided transbronchial needle aspiration in patients with lung cancer

    Cancers, Vol. 11, Núm. 10

2018

  1. Functional assessment of the BMPR2 gene in lymphoblastoid cell lines from Graves’ disease patients

    Journal of Cellular and Molecular Medicine, Vol. 22, Núm. 3, pp. 1538-1547

  2. Pulmonary arterial hypertension associated to systemic erythematosus lupus: molecular characterization of 3 cases

    Medicina Clinica, Vol. 151, Núm. 3, pp. 111-115

2017

  1. Cribado mutacional en genes relacionados con la hipertensión portopulmonar: análisis de 6 casos

    Medicina Clinica, Vol. 148, Núm. 7, pp. 310-313

  2. Estudio de la prevalencia de marcadores genéticos asociados a la lenta progresión del virus de la inmunodeficiencia humana tipo 1 en la población gallega

    Enfermedades Infecciosas y Microbiologia Clinica, Vol. 35, Núm. 2, pp. 104-107

  3. Functional analysis by minigene assay of putative splicing variants found in Bardet–Biedl syndrome patients

    Journal of Cellular and Molecular Medicine, Vol. 21, Núm. 10, pp. 2268-2275

  4. Molecular and functional characterization of the BMPR2 gene in Pulmonary Arterial Hypertension

    Scientific Reports, Vol. 7, Núm. 1

2016

  1. Complex inheritance in Pulmonary Arterial Hypertension patients with several mutations

    Scientific Reports, Vol. 6

  2. HLA-DQ B1*0201 and A1*0102 alleles are not responsible for antituberculosis drug-induced hepatotoxicity risk in Spanish population

    Frontiers in Medicine, Vol. 3, Núm. AUG

  3. Hipertensión arterial pulmonar asociada a infección por el virus de la inmunodeficiencia humana: análisis de 4 casos

    Medicina Clinica, Vol. 146, Núm. 8, pp. 350-353

  4. Methylation Analysis of the BMPR2 Gene Promoter Region in Patients With Pulmonary Arterial Hypertension

    Archivos de Bronconeumologia, Vol. 52, Núm. 6, pp. 293-298

  5. Mutational and clinical analysis of the ENG gene in patients with pulmonary arterial hypertension

    BMC Genetics, Vol. 17, Núm. 1

2015

  1. Estudio clínico y molecular de 4 casos de hipertensión pulmonar asociada a sarcoidosis

    Archivos de Bronconeumologia, Vol. 51, Núm. 4, pp. e19-e21

  2. K198N polymorphism in the EDN1 gene in patients with pulmonary arterial hypertension

    Medicina Clinica, Vol. 144, Núm. 8, pp. 348-352