Departamento de Ciencias Forenses, Anatomía Patolóxica, Xinecoloxía e Obstetricia e Pediatría
Departamento
Universidad de Valladolid
Valladolid, EspañaPublicacións en colaboración con investigadores/as de Universidad de Valladolid (18)
2024
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Editorial: Bioethics in neonatology
Frontiers in Pediatrics
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Novel risk loci for COVID-19 hospitalization among admixed American populations
eLife, Vol. 13
2022
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A genome-wide association study of survival in patients with sepsis
Critical Care, Vol. 26, Núm. 1
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2021
2015
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Predicting proliferative vitreoretinopathy: Temporal and external validation of models based on genetic and clinical variables
British Journal of Ophthalmology, Vol. 99, Núm. 1, pp. 41-48
2014
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Holistic screening of collapsing honey bee colonies in Spain: A case study
BMC Research Notes, Vol. 7, Núm. 1
2013
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A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy
Investigative Ophthalmology and Visual Science, Vol. 54, Núm. 3, pp. 1665-1678
2012
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Prevalence of psychoactive substances, alcohol, illicit drugs, and medicines, in Spanish drivers: A roadside study
Forensic Science International, Vol. 223, Núm. 1-3, pp. 106-113
2010
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A strong genetic association between the tumor necrosis factor locus and proliferative vitreoretinopathy: The Retina 4 Project
Ophthalmology, Vol. 117, Núm. 12
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Erratum: Prevalence of CYP2C9 polymorphisms in the south of Europe (Pharmacogenomics Journal (2009) DOI: 10.1038/tpj.2009.16))
Pharmacogenomics Journal
2009
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Prevalence of CYP2C9 polymorphisms in the south of Europe
Pharmacogenomics Journal, Vol. 9, Núm. 5, pp. 306-310
2006
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Childhood obesity. Recommendations of the Nutrition Committee of the Spanish Association of Pediatrics. Part I. Prevention. Early detection. Role of the pediatrician
Anales de Pediatria, Vol. 65, Núm. 6, pp. 607-615
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Genomic rearrangements at the BRCA1 locus in Spanish families with breast/ovarian cancer
Clinical Chemistry, Vol. 52, Núm. 8, pp. 1480-1485
2004
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The variant E233G of the rad51d gene could be a low-penetrance allele in high-risk breast cancer families without BRCA1/2 mutations
International Journal of Cancer, Vol. 110, Núm. 6, pp. 845-849
2003
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Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: A high proportion of mutations unique to Spain and evidence of founder effects
Human Mutation, Vol. 22, Núm. 4, pp. 301-312
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Over-representation of two specific haplotypes among chromosomes harbouring BRCA1 mutations
European Journal of Human Genetics