Fundación Pública Galega de Medicina Xenómica
Centro de investigación
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Universidad Complutense de Madrid
Madrid, EspañaPublicacións en colaboración con investigadores/as de Universidad Complutense de Madrid (21)
2024
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Worldwide distribution of genetic factors related to severity of COVID-19 infection
Annals of Human Biology, Vol. 51, Núm. 1
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Differences in Patterns of Stimulant Use and Their Impact on First-Episode Psychosis Incidence: An Analysis of the EUGEI Study
Schizophrenia Bulletin, Vol. 49, Núm. 5, pp. 1269-1280
2022
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How Executive Functions Correlate with Intelligence in Children and Adolescents in Autism Spectrum Disorders
Journal of Cognition and Development, Vol. 23, Núm. 5, pp. 776-790
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Nature Genetics, Vol. 54, Núm. 9, pp. 1320-1331
2021
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Genome-wide association study of stage III/IV grade C periodontitis (former aggressive periodontitis) in a Spanish population
Journal of Clinical Periodontology, Vol. 48, Núm. 7, pp. 896-906
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The search process: Integrating the investigation and identification of missing and unidentified persons
Forensic Science International: Synergy
2020
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Psychiatric comorbidities in Asperger syndrome are related with polygenic overlap and differ from other Autism subtypes
Translational Psychiatry, Vol. 10, Núm. 1
2017
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Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain
Scientific Reports, Vol. 7, Núm. 1
2016
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Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing
Nature, Vol. 535, Núm. 7613, pp. 561-565
2015
2014
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Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia
Clinical Genetics, Vol. 85, Núm. 2, pp. 154-158
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Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers
Breast Cancer Research and Treatment, Vol. 148, Núm. 2, pp. 415-421
2013
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The genetic landscape of Equatorial Guinea and the origin and migration routes of the y chromosome haplogroup R-V88
European Journal of Human Genetics, Vol. 21, Núm. 3, pp. 324-331
2011
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The natural tissue plasminogen activator inhibitor neuroserpin and acute ischaemic stroke outcome
Thrombosis and Haemostasis, Vol. 105, Núm. 3, pp. 421-429
2010
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The exon 3-deleted growth hormone receptor is associated with better response to pegvisomant therapy in acromegaly
Journal of Clinical Endocrinology and Metabolism, Vol. 95, Núm. 1, pp. 222-229
2008
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Results of the GEP-ISFG collaborative study on an X-STR Decaplex
Forensic Science International: Genetics Supplement Series, Vol. 1, Núm. 1, pp. 677-679
2007
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In vivo functional analysis of the counterbalance of hyperactive phosphatidylinositol 3-kinase p110 catalytic oncoproteins by the tumor suppressor PTEN
Cancer Research, Vol. 67, Núm. 20, pp. 9731-9739
2000
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Distribution of choline acetyltransferase immunoreactivity in the brain of an elasmobranch, the lesser spotted dogfish (Scyliorhinus canicula)
Journal of Comparative Neurology, Vol. 420, Núm. 2, pp. 139-170