Publicaciones en colaboración con investigadores/as de Universidad Autónoma de Madrid (21)

2024

  1. A genome-wide association meta-analysis of all-cause and vascular dementia

    Alzheimer's and Dementia, Vol. 20, Núm. 9, pp. 5973-5995

  2. Novel risk loci for COVID-19 hospitalization among admixed American populations

    eLife, Vol. 13

2023

  1. A crowdsourcing database for the copy-number variation of the Spanish population

    Human Genomics, Vol. 17, Núm. 1

  2. A second update on mapping the human genetic architecture of COVID-19

    Nature

2022

  1. Novel genes and sex differences in COVID-19 severity

    Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806

2021

  1. Genomic characterization of host factors related to SARS-CoV-2 infection in people with dementia and control populations: The GR@ACE/DEGESCO study

    Journal of Personalized Medicine, Vol. 11, Núm. 12

  2. Long runs of homozygosity are associated with Alzheimer’s disease

    Translational Psychiatry, Vol. 11, Núm. 1

2019

  1. Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project

    Alzheimer's and Dementia, Vol. 15, Núm. 10, pp. 1333-1347

2015

  1. Autism spectrum symptoms in Smith-Magenis syndrome and Williams syndrome: Comparisons and contrasts

    International Journal of Developmental Disabilities, Vol. 61, Núm. 1, pp. 49-55

2014

  1. FAS system deregulation in T-cell lymphoblastic lymphoma

    Cell Death and Disease, Vol. 5, Núm. 3

  2. Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain

    Schizophrenia Research, Vol. 159, Núm. 1, pp. 107-113

2013

  1. Association of thromboxane A1 synthase (TBXAS1) gene polymorphism with acute urticaria induced by nonsteroidal anti-inflammatory drugs

    Journal of Allergy and Clinical Immunology, Vol. 132, Núm. 4, pp. 989-991

2012

  1. Cognitive functioning in children and adults with Smith-Magenis syndrome

    European Journal of Medical Genetics, Vol. 55, Núm. 6-7, pp. 394-399

  2. Genetic epistasis in female suicide attempters

    Progress in Neuro-Psychopharmacology and Biological Psychiatry, Vol. 38, Núm. 2, pp. 294-301

  3. How executive functions are related to intelligence in Williams syndrome

    Research in Developmental Disabilities, Vol. 33, Núm. 4, pp. 1169-1175

2011

  1. Electrochemical DNA base pairs quantification and endonuclease cleavage detection

    Biosensors and Bioelectronics, Vol. 27, Núm. 1, pp. 40-45

2010

  1. Nucleotide variation in central nervous system genes among male suicide attempters

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 1, pp. 208-213

2009

  1. Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 150, Núm. 6, pp. 808-816

2008

  1. 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

  2. The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula

    American Journal of Human Genetics, Vol. 83, Núm. 6, pp. 725-736