Angel Carracedo

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Publications in SciGraph latest 50 shown

  • 2018-12 In situ characterization of stem cells-like biomarkers in meningiomas in CANCER CELL INTERNATIONAL
  • 2018-09 Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples in EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
  • 2017-12 Patterns of Default Mode Network Deactivation in Obsessive Compulsive Disorder in SCIENTIFIC REPORTS
  • 2017-12 Pleomorphism and drug resistant cancer stem cells are characteristic of aggressive primary meningioma cell lines in CANCER CELL INTERNATIONAL
  • 2017-12 Analysis of the R1b-DF27 haplogroup shows that a large fraction of Iberian Y-chromosome lineages originated recently in situ in SCIENTIFIC REPORTS
  • 2017-12 A new panel of SNPs to assess thyroid carcinoma risk: a pilot study in a Brazilian admixture population in BMC MEDICAL GENETICS
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-11 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2017-09 Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2017-09 Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder in NATURE NEUROSCIENCE
  • 2017-08 Touch Processing and Social Behavior in ASD in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2017-06 Evaluating the Calling Performance of a Rare Disease NGS Panel for Single Nucleotide and Copy Number Variants in MOLECULAR DIAGNOSIS & THERAPY
  • 2017-05 Candidate predisposing germline copy number variants in early onset colorectal cancer patients in CLINICAL AND TRANSLATIONAL ONCOLOGY
  • 2017-03 FAS system deregulation in T-cell lymphoblastic lymphoma in CELL DEATH & DISEASE
  • 2017-03 Medico-legal perspectives on sudden cardiac death in young athletes in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2017-02-06 Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia in NATURE COMMUNICATIONS
  • 2017-02 Corrigendum: Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing in NATURE
  • 2017 From Hemogenetics to Forensic Genomics in P5 MEDICINE AND JUSTICE
  • 2016-12 Alcohol and breast cancer tumor subtypes in a Spanish Cohort in SPRINGERPLUS
  • 2016-12 Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies in SCIENTIFIC REPORTS
  • 2016-07-06 Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing in NATURE
  • 2016-07 Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) in BMC GENOMICS
  • 2016-03 Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia in TRANSLATIONAL PSYCHIATRY
  • 2016-01 High-resolution copy number analysis of paired normal-tumor samples from diffuse large B cell lymphoma in ANNALS OF HEMATOLOGY
  • 2016-01 Inference of biogeographical ancestry across central regions of Eurasia in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2016 Inference of Ancestry in Forensic Analysis I: Autosomal Ancestry-Informative Marker Sets in FORENSIC DNA TYPING PROTOCOLS
  • 2016-01 The relationship between surname frequency and Y chromosome variation in Spain in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016 Inference of Ancestry in Forensic Analysis II: Analysis of Genetic Data in FORENSIC DNA TYPING PROTOCOLS
  • 2015-12 affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling in BMC BIOINFORMATICS
  • 2015-12 Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 in SCIENTIFIC REPORTS
  • 2015-12 Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer in SCIENTIFIC REPORTS
  • 2015-09 Exploration of SNP variants affecting hair colour prediction in Europeans in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2015-09 Mosaic maternal ancestry in the Great Lakes region of East Africa in HUMAN GENETICS
  • 2015-06 Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export in NATURE GENETICS
  • 2015-06 Brain activation of the defensive and appetitive survival systems in obsessive compulsive disorder in BRAIN IMAGING AND BEHAVIOR
  • 2015-06 High frequency and founder effect of the CYP3A4*20 loss-of-function allele in the Spanish population classifies CYP3A4 as a polymorphic enzyme in THE PHARMACOGENOMICS JOURNAL
  • 2015-02 Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer in GENETICS IN MEDICINE
  • 2015-01 Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2014-11 Synaptic, transcriptional and chromatin genes disrupted in autism in NATURE
  • 2014-08 A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1 in NATURE GENETICS
  • 2014-08 Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization in NATURE GENETICS
  • 2014-08 RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-05 A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer in HUMAN GENETICS
  • 2014-04 Pharmacogenomics of CRC treatments: putting bricks on the path to personalized medicine in BMC GENOMICS
  • 2014-03 Characterization of CYP1A2, CYP2C19, CYP3A4 and CYP3A5 polymorphisms in South Brazilians in MOLECULAR BIOLOGY REPORTS
  • 2014-01 Comparison of the genetic background of different Colombian populations using the SNPforID 52plex identification panel in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2014-01 Common variant at 16p11.2 conferring risk of psychosis in MOLECULAR PSYCHIATRY
  • 2013-12 A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12 in BMC GENOMICS
  • 2013-11 Reproducibility of high-throughput mRNA and small RNA sequencing across laboratories in NATURE BIOTECHNOLOGY
  • 2013-09 Global population variability in Promega PowerPlex CS7, D6S1043, and Penta B STRs in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
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