Department of Forensic Science, Pathological Anatomy, Gynaecology and Obstetrics and Paediatrics
Department
Queen Mary University of London
Londres, Reino UnidoPublications in collaboration with researchers from Queen Mary University of London (43)
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Erratum: Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19 (Nature (2023) 617 7962 (764-768))
Nature
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GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Nature, Vol. 617, Núm. 7962, pp. 764-768
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Genomic investigations of unexplained acute hepatitis in children
Nature, Vol. 617, Núm. 7961, pp. 564-573
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Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study
The Lancet Rheumatology, Vol. 5, Núm. 4, pp. e184-e199
2019
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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
Nature Communications, Vol. 10, Núm. 1
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Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1)
Nature Communications
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Genome-wide association study of germline variants and breast cancer-specific mortality
British Journal of Cancer, Vol. 120, Núm. 6, pp. 647-657
2018
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Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants
Nature Communications, Vol. 9, Núm. 1
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Germline variation at 8q24 and prostate cancer risk in men of European ancestry
Nature Communications, Vol. 9, Núm. 1
2016
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Comprehensive Analysis of Pan-African Mitochondrial DNA Variation Provides New Insights into Continental Variation and Demography
Journal of Genetics and Genomics, Vol. 43, Núm. 3, pp. 133-143
2014
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Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Nature Genetics, Vol. 46, Núm. 8, pp. 826-836
2013
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RNA/DNA co-analysis from human saliva and semen stains-Results of a third collaborative EDNAP exercise
Forensic Science International: Genetics, Vol. 7, Núm. 2, pp. 230-239
2012
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The recombination landscape around forensic STRs: Accurate measurement of genetic distances between syntenic STR pairs using HapMap high density SNP data
Forensic Science International: Genetics, Vol. 6, Núm. 3, pp. 354-365
2008
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Forensic typing of autosomal SNPs with a 29 SNP-multiplex-Results of a collaborative EDNAP exercise
Forensic Science International: Genetics, Vol. 2, Núm. 3, pp. 176-183
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Forensic validation of the Genplex SNP typing system-Results of an inter-laboratory study
Forensic Science International: Genetics Supplement Series, Vol. 1, Núm. 1, pp. 389-393
2007
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Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel
Forensic Science International: Genetics, Vol. 1, Núm. 2, pp. 180-185
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Forensic validation of the SNPforID 52-plex assay
Forensic Science International: Genetics, Vol. 1, Núm. 2, pp. 186-190
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Inferring ancestral origin using a single multiplex assay of ancestry-informative marker SNPs
Forensic Science International: Genetics, Vol. 1, Núm. 3-4, pp. 273-280
2006
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A compact population analysis test using 32 SNPs with highly diverse allele frequency distributions
International Congress Series, Vol. 1288, pp. 58-60