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Author Details

Angel Carracedo
1982
721
80
PMIDPaper TitleJournal TitlePublished Year
36917866Development and evaluations of the ancestry informative markers of the VISAGE Enhanced Tool for Appearance and Ancestry.2023
37736027Uncovering a population of gravitational lens galaxies with magnified standard candle SN Zwicky.2023
37637419Deletion of the gene as a likely explanation for the serious side effects of the antipsychotic drug pimozide: a case report.2023
38056433Expanding the clinical and molecular spectrum of FOXG1- and ZBTB18-associated neurodevelopmental disorders.2023
37690961HLA alleles: important pieces to the COVID-19 puzzle.2023
37094658The genomics of visuospatial neurocognition in obsessive-compulsive disorder: A preliminary GWAS.2023
36910046Is SARS-COV-2 associated with alpha-1 antitrypsin deficiency?J Thorac Dis2023
36907526BMPR2 as a Novel Predisposition Gene for Hereditary Colorectal Polyposis.2023
37023975The non-coding genome in Autism Spectrum Disorders.2023
36507580RSPO4 is a potential risk gene of stages III-IV, grade C periodontitis through effects on innate immune response and oral barrier integrity.2023
37015164Examining the association between exposome score for schizophrenia and cognition in schizophrenia, siblings, and healthy controls: Results from the EUGEI study.Psychiatry Res2023
36867994Childhood exposure to non-persistent endocrine disrupting chemicals and multi-omic profiles: A panel study.2023
36695417DNA polymorphisms associated with lactase persistence, self-perceived symptoms of lactose intolerance, milk and dairy consumption, and ancestry, in the Uruguayan population.2023
36864434NAD pool as an antitumor target against cancer stem cells in head and neck cancer.2023
37046291Prenatal environmental exposures associated with sex differences in childhood obesity and neurodevelopment.2023
36674414Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men.Int J Mol Sci2023
36535842In memoriam: Peter Schneider.2023
37100676Editorial considerations for publication in Forensic Science International: Genetics.2023
36454422Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel Sequencing.2023
37528566HLA-A*11:01 and HLA-C*04:01 are associated with severe COVID-19.HLA2023
37500326A Genome-Wide Association Study of Small Cell Lung Cancer.Arch Bronconeumol2023
35322241Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disability.Eur J Hum Genet2022
35708486Novel genes and sex differences in COVID-19 severity.Hum Mol Genet2022
35456396Utility of Circulating Cell-Free DNA in Assessing Microsatellite Instability and Loss of Heterozygosity in Breast Cancer Using Human Identification Approach.Genes2022
36029870Neuropsychological performance and predictors of pharmacological treatment response in obsessive compulsive disorder.Journal of Affective Disorders2022
35379992New insights into the genetic etiology of Alzheimer's disease and related dementias.Nat Genet2022
35690418Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation.Mutat Res Rev Mutat Res2022
36066633Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers.Acta Neuropathol2022
35615066A Machine Learning Approach in Autism Spectrum Disorders: From Sensory Processing to Behavior Problems.Frontiers in Molecular Neuroscience2022
35550596The early-life exposome modulates the effect of polymorphic inversions on DNA methylation.Communications Biology2022
36055075The association between cannabis use and facial emotion recognition in schizophrenia, siblings, and healthy controls: Results from the EUGEI study.Eur Neuropsychopharmacol2022
36428603Transcriptomic and Proteomic Profiles for Elucidating Cisplatin Resistance in Head-and-Neck Squamous Cell Carcinoma.Cancers2022
36411288Multi-omics signatures of the human early life exposome.Nat Commun2022
35777200Remission of obesity and insulin resistance is not sufficient to restore mitochondrial homeostasis in visceral adipose tissue.Redox Biology2022
35465610Identification of Sodium Transients Through Na1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons.Frontiers in Cellular Neuroscience2022
36657129Colorectal cancer. Genetic variants in BMP signaling pathway and ancestry in the Mexican population.2022
33046166A replication study of JTC bias, genetic liability for psychosis and delusional ideation.Psychol Med2022
33070791Evidence, and replication thereof, that molecular-genetic and environmental risks for psychosis impact through an affective pathway.Psychol Med2022
35302492Identification of autosomal cis expression quantitative trait methylation (cis eQTMs) in children's blood.Elife2022
34536513Examining facial emotion recognition as an intermediate phenotype for psychosis: Findings from the EUGEI study.Prog Neuropsychopharmacol Biol Psychiatry2022
35060122CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative.Clin Genet2022
35221957Viability Study of Machine Learning-Based Prediction of COVID-19 Pandemic Impact in Obsessive-Compulsive Disorder Patients.Frontiers in Neuroinformatics2022
34638436SDCBP Modulates Stemness and Chemoresistance in Head and Neck Squamous Cell Carcinoma through Src Activation.Cancers2021
32359158Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk.J Natl Cancer Inst2021
33592388Forensic Science International: Genetics Reviewer Hall of Fame 2020.2021
34289836Variability of multi-omics profiles in a population-based child cohort.BMC Med2021
33745150Genome-wide association study of stage III/IV grade C periodontitis (former aggressive periodontitis) in a Spanish population.Journal of Clinical Periodontology2021
33588347Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.2021
34068396Schuurs-Hoeijmakers Syndrome (<i>PACS1</i> Neurodevelopmental Disorder): Seven Novel Patients and a Review.Genes (Basel)2021
33471991Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.N Engl J Med2021
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Instituto de Investigacion Sanitaria de Santiago
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Instituto de Salud Carlos III
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Sidra Medical Center
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Center for Cancer Genetic Epidemiology, University of Cambridge
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Children's Hospital of Philadelphia
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German Cancer Research Center (DKFZ)
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Institute of Human Genetics, University Hospital Bonn
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University of Cambridge
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Instituto de Investigacion Sanitaria de Santiago (IDIS)
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Familial Cancer Clinical Unit, Spanish National Cancer Research Centre
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Otto-Friedrich-University Bamberg
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Centro de Investigacion Biomedica en Red en Epidemiologia y Salud Publica (CIBERESP)
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Institute of Cancer and Genomic Sciences, University of Birmingham
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National Cancer Institute, National Institutes of Health
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University of Oxford
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