FRANCISCO DAVID
CARMONA LÓPEZ
PROFESOR TITULAR DE UNIVERSIDAD
Hospital Universitario Virgen de las Nieves
Granada, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario Virgen de las Nieves (13)
2022
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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
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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
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Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia
Frontiers in Cell and Developmental Biology, Vol. 10
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Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility
Communications Biology, Vol. 5, Núm. 1
2021
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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
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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
2020
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Genetic landscape of nonobstructive azoospermia and new perspectives for the clinic
Journal of Clinical Medicine, Vol. 9, Núm. 2
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Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment
Fertility and Sterility, Vol. 114, Núm. 2, pp. 398-406
2019
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Association between Genetic Polymorphisms of Inflammatory Response Genes and Acute Pancreatitis
Immunological Investigations, Vol. 48, Núm. 6, pp. 585-596
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GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
Nature Communications, Vol. 10, Núm. 1
2012
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Evaluation of a shared autoimmune disease-associated polymorphism of TRAF6 in systemic sclerosis and giant cell arteritis
Journal of Rheumatology, Vol. 39, Núm. 6, pp. 1275-1279
2011
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Association of a non-synonymous functional variant of the ITGAM gene with systemic sclerosis
Annals of the Rheumatic Diseases
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No evidence for association between the CCR5/Delta32CCR5 polymorphism and systemic sclerosis
Clinical and Experimental Rheumatology