Publicacións (82) Publicacións de FRANCISCO DAVID CARMONA LÓPEZ

2023

  1. Celiac Disease Is a Risk Factor for Mature T and NK Cell Lymphoma: A Mendelian Randomization Study

    International Journal of Molecular Sciences, Vol. 24, Núm. 8

  2. Identification of new risk loci shared across systemic vasculitides points towards potential target genes for drug repurposing

    Annals of the Rheumatic Diseases, Vol. 82, Núm. 6, pp. 837-847

  3. Mucosal Immune Defence Gene Polymorphisms as Relevant Players in the Pathogenesis of IgA Vasculitis?

    International Journal of Molecular Sciences, Vol. 24, Núm. 17

  4. Sex-specific association of SELL gene polymorphisms with pattern hair loss in the Thai population: A candidate gene association study and in silico functional characterization

    Journal of Dermatological Science

2022

  1. A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels

    The Journal of clinical endocrinology and metabolism, Vol. 107, Núm. 8, pp. 2350-2361

  2. Antioxidation, Anti-Inflammation, and Regulation of SRD5A Gene Expression of Oryza sativa cv. Bue Bang 3 CMU Husk and Bran Extracts as Androgenetic Alopecia Molecular Treatment Substances

    Plants, Vol. 11, Núm. 3

  3. Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome

    Journal of Personalized Medicine, Vol. 12, Núm. 6

  4. Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility

    Andrology, Vol. 10, Núm. 7, pp. 1339-1350

  5. Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia

    Frontiers in Cell and Developmental Biology, Vol. 10

  6. Genes en cromosomas sexuales: La excepción que confirma la regla

    La herencia del mendelismo: La genética 200 años después del nacimiento de Gregor Mendel (Editorial Universidad de Granada), pp. 125-144

  7. Genome-wide compound heterozygote analysis highlights DPY19L2 alleles in a non-consanguineous Spanish family with total globozoospermia

    Reproductive BioMedicine Online, Vol. 45, Núm. 2, pp. 332-340

  8. Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility

    Communications Biology, Vol. 5, Núm. 1

2021

  1. Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort

    Andrology, Vol. 9, Núm. 4, pp. 1151-1165

  2. Effects on steroid 5-alpha reductase gene expression of thai rice bran extracts and molecular dynamics study on SRD5A2

    Biology, Vol. 10, Núm. 4

  3. Evaluation of male fertility-associated loci in a european population of patients with severe spermatogenic impairment

    Journal of Personalized Medicine, Vol. 11, Núm. 1, pp. 1-19

  4. Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet’s Disease

    Arthritis and Rheumatology, Vol. 73, Núm. 7, pp. 1244-1252

  5. Methylenetetrahydrofolate reductase (MTHFR) gene polymorphism and infant’s anthropometry at birth

    Nutrients, Vol. 13, Núm. 3, pp. 1-14

2020

  1. Deficiency of the onco-miRNA cluster, miR-106b∼25, causes oligozoospermia and the cooperative action of miR-106b∼25 and miR-17∼92 is required to maintain male fertility

    Molecular Human Reproduction, Vol. 26, Núm. 6, pp. 389-401

  2. GNAI2 variants predict nonsteroidal anti-inflammatory drug hypersensitivity in a genome-wide study

    Allergy: European Journal of Allergy and Clinical Immunology

  3. Genetic landscape of nonobstructive azoospermia and new perspectives for the clinic

    Journal of Clinical Medicine, Vol. 9, Núm. 2