Ángel Carracedo Catedrático de Medicina Legal, investigador, experto internacional en Xenética e divulgador científico
Carracedo, Ángel, 1955-
Carracedo Álvarez, Ángel, 1955-
Carracedo, Angel
VIAF ID: 41545976 (Personal)
Permalink: http://viaf.org/viaf/41545976
Preferred Forms
- 100 1 0 ‡a Carracedo Álvarez, Ángel ‡d 1955-
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- 100 1 _ ‡a Carracedo, Angel
- 100 1 _ ‡a Carracedo, Angel
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- 100 1 _ ‡a Carracedo, Ángel, ‡d 1955-
- 100 0 _ ‡a Ángel Carracedo ‡c Catedrático de Medicina Legal, investigador, experto internacional en Xenética e divulgador científico
4xx's: Alternate Name Forms (19)
Works
Title | Sources |
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Document on genetic tests of filiation | |
Documento sobre pruebas genéticas de filiación | |
Erratum: Corrigendum: Reconstructing Native American population history | |
Estimating Exposome Score for Schizophrenia Using Predictive Modeling Approach in Two Independent Samples: The Results From the EUGEI Study | |
Estudio sobre los polimorfismos enzimáticos eritrocitarios en la población gallega, su aplicación a la investigación biológica de la paternidad | |
Ethical-legal problems of DNA databases in criminal investigation | |
Eurasiaplex: a forensic SNP assay for differentiating European and South Asian ancestries. | |
A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics | |
Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes | |
Evaluating new candidate SNPs as low penetrance risk factors in sporadic breast cancer: a two-stage Spanish case-control study | |
Evaluation of DXS9902, DXS7132, DXS6809, DXS7133, and DXS7423 in humans and chimpanzees: sequence variation, repeat structure, and nomenclature. | |
Evidence, and replication thereof, that molecular-genetic and environmental risks for psychosis impact through an affective pathway | |
Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome | |
Examining the independent and joint effects of molecular genetic liability and environmental exposures in schizophrenia: results from the EUGEI study | |
Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer | |
Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia | |
Exploration of SNP variants affecting hair colour prediction in Europeans. | |
Exploring iris colour prediction and ancestry inference in admixed populations of South America | |
Exploring mitochondrial DNA variation in the Italian Peninsula | |
Exploring the biological role of postzygotic and germinal de novo mutations in ASD | |
Extending STR markers in Y chromosome haplotypes. | |
Failed PCR amplifications of MBP-STR alleles due to polymorphism in the primer annealing region | |
Family history and breast cancer hormone receptor status in a Spanish cohort | |
FAS system deregulation in T-cell lymphoblastic lymphoma | |
Fast isoelectric focusing of some polymorphic proteins and enzymes in miniaturized gels using an automated system | |
Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion | |
Finding genes that underlie physical traits of forensic interest using genetic tools | |
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk | |
Fine mapping of the myosin light chain kinase (MYLK) gene replicates the association with asthma in populations of Spanish descent | |
Focus issue—Analysis and biostatistical interpretation of complex and low template DNA samples | |
Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels: Results of a collaborative EDNAP exercise. | |
Forensic considerations on STR databases in Argentina | |
Forensic DNA analysis in Europe: current situation and standardization efforts | |
Forensic DNA typing protocols | |
Forensic genetics and genomics: Much more than just a human affair | |
Forensic performance of two insertion-deletion marker assays | |
Forensic sci. int., Genet. (Online) | |
Forensic science international, an international journal dedicated to the application of genetics in the administration of justice | |
Forensic validation and implementation of Y-chromosome SNP multiplexes | |
Forensic validation of the Genplex SNP typing system—Results of an inter-laboratory study | |
Further development of forensic eye color predictive tests. | |
GATA C4 allele 17 as a marker for sub-Saharan origin of Y-chromosome lineages | |
Gender bias in the multiethnic genetic composition of central Argentina | |
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome | |
Genetic analysis of autosomal and Y-specific STRs in the Karimojong population from Uganda | |
Genetic analysis of the SNPforID 34-plex ancestry informative SNP panel in Tunisian and Libyan populations | |
Genetic analysis of three US population groups using an X-chromosomal STR decaplex | |
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization | |
Genetic associations in the vitamin D receptor and colorectal cancer in African Americans and Caucasians | |
A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy. | |
Genetic characterization of 52 autosomal SNPs in two sub-Saharan African populations | |
Genetic data of 10 X-chromosomal loci in Vitória population (Espírito Santo State, Brazil) | |
Genetic data on eight STRs (D5S818, D7S820, F13B, LPL, TH01, TPOX, VWA31, CSF1PO) from a Colombian population | |
Genetic data on three complex STRs (ACTBP2, D21S11 and HUMFIBRA/FGA) in the Galician population (NW Spain). | |
Genetic diversity of nine STRs in two northwest Iberian populations: Galicia and northern Portugal. | |
Genetic diversity of Y-specific STRs in chimpanzees (Pan troglodytes). | |
Genetic epistasis in female suicide attempters. | |
Genetic markers in alcoholic liver cirrhosis | |
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing | |
Genetic patterns of 10 X chromosome short tandem repeats in an Asian population from Macau | |
Genetic profile characterization of 10 X-STRs in four populations of the southeastern region of Brazil. | |
Genetic structure of the Kuwaiti population revealed by paternal lineages | |
Genetic susceptibility variants associated with colorectal cancer prognosis | |
Genetic variability at nine STR loci in the Chueta (Majorcan Jews) and the Balearic populations investigated by a single multiplex reaction | |
Genetic variability of 17 Y chromosome STRs in two Native American populations from Argentina | |
Genetic variability of the SNPforID 52-plex identification-SNP panel in Central West Colombia. | |
Genetic variants associated with addictive behavior in Colombian addicted and non-addicted to heroin or cocaine | |
Genetic variants in genes related to lipid metabolism and atherosclerosis, dyslipidemia and atorvastatin response | |
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration | |
A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk | |
A multiplex PCR design for simultaneous genotyping of X chromosome short tandem repeat markers | |
A new multiplex for human identification using insertion/deletion polymorphisms | |
A new SNP assay for identification of highly degraded human DNA. | |
New technologies in the genetic approach to sudden cardiac death in the young. | |
A novel mutation in the OFD1 (Cxorf5) gene may contribute to oral phenotype in patients with oral-facial-digital syndrome type 1. | |
A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy | |
A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease | |
A pathway-based association study reveals variants from Wnt signalling genes contributing to asthma susceptibility | |
Problemas bioestadísticos en genética forense | |
Progress in forensic genetics 9, 2003: | |
A silver staining method for the detection of polymorphic proteins in minute bloodstains after isoelectric focusing | |
Xenética e historia no noroeste peninsular : unha perspectiva interdisciplinaria : actas das xornadas celebradas os dias 11, 12 e 13 de abril de 2002 en Santiago de Compostela |