Medicina Xenómica
GMX - USC
Universidad Autónoma de Madrid
Madrid, EspañaPublicacións en colaboración con investigadores/as de Universidad Autónoma de Madrid (22)
2024
-
A genome-wide association meta-analysis of all-cause and vascular dementia
Alzheimer's and Dementia, Vol. 20, Núm. 9, pp. 5973-5995
-
Novel risk loci for COVID-19 hospitalization among admixed American populations
eLife, Vol. 13
2023
-
A crowdsourcing database for the copy-number variation of the Spanish population
Human Genomics, Vol. 17, Núm. 1
-
A second update on mapping the human genetic architecture of COVID-19
Nature
2022
-
Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2021
-
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
-
Long runs of homozygosity are associated with Alzheimer’s disease
Translational Psychiatry, Vol. 11, Núm. 1
2019
-
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
-
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
-
FAS system deregulation in T-cell lymphoblastic lymphoma
Cell Death and Disease, Vol. 5, Núm. 3
-
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
-
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
-
Cognitive functioning in children and adults with Smith-Magenis syndrome
European Journal of Medical Genetics, Vol. 55, Núm. 6-7, pp. 394-399
-
Genetic epistasis in female suicide attempters
Progress in Neuro-Psychopharmacology and Biological Psychiatry, Vol. 38, Núm. 2, pp. 294-301
-
How executive functions are related to intelligence in Williams syndrome
Research in Developmental Disabilities, Vol. 33, Núm. 4, pp. 1169-1175
2011
-
Electrochemical DNA base pairs quantification and endonuclease cleavage detection
Biosensors and Bioelectronics, Vol. 27, Núm. 1, pp. 40-45
2010
-
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
-
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
-
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
-
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