Anthony J Brookes


Ontology type: schema:Person     


Person Info

NAME

Anthony J

SURNAME

Brookes

Publications in SciGraph latest 50 shown

  • 2018-12 Responsible sharing of biomedical data and biospecimens via the “Automatable Discovery and Access Matrix” (ADA-M) in NPJ GENOMIC MEDICINE
  • 2018-03-14 Simplifying research access to genomics and health data with Library Cards in SCIENTIFIC DATA
  • 2017-12 Characteristics and longitudinal progression of chronic obstructive pulmonary disease in GOLD B patients in BMC PULMONARY MEDICINE
  • 2017-12 Blood and sputum eosinophils in COPD; relationship with bacterial load in RESPIRATORY RESEARCH
  • 2016-03-15 The FAIR Guiding Principles for scientific data management and stewardship in SCIENTIFIC DATA
  • 2015-12 Human genotype-phenotype databases: aims, challenges and opportunities in NATURE REVIEWS GENETICS
  • 2014-07 GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-05 A P3G generic access agreement for population genomic studies in NATURE BIOTECHNOLOGY
  • 2012-12 VarioML framework for comprehensive variation data representation and exchange in BMC BIOINFORMATICS
  • 2012-12 A mechanistic basis for amplification differences between samples and between genome regions in BMC GENOMICS
  • 2012-12 Semantically enabling a genome-wide association study database in JOURNAL OF BIOMEDICAL SEMANTICS
  • 2012-11 Toward a roadmap in global biobanking for health in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-11-16 Identity in research infrastructure and scientific communication: Report from the 1st IRISC workshop, Helsinki Sep 12-13, 2011 in NATURE PRECEDINGS
  • 2011-11-16 Identity in research infrastructure and scientific communication: Report from the 1st IRISC workshop, Helsinki Sep 12-13, 2011 in NATURE PRECEDINGS
  • 2011-09 Clarity and claims in variation/mutation databasing in NATURE BIOTECHNOLOGY
  • 2010-12 The MOLGENIS toolkit: rapid prototyping of biosoftware at the push of a button in BMC BIOINFORMATICS
  • 2010-04 Locus Reference Genomic sequences: an improved basis for describing human DNA variants in GENOME MEDICINE
  • 2009-01 Genotype–phenotype databases: challenges and solutions for the post-genomic era in NATURE REVIEWS GENETICS
  • 2007-10 MegaPlex PCR: a strategy for multiplex amplification in NATURE METHODS
  • 2007-02 Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis in NATURE GENETICS
  • 2006-05 Seventh international meeting on single nucleotide polymorphism and complex genome analysis: ‘ever bigger scans and an increasingly variable genome’ in HUMAN GENETICS
  • 2006-03 Longitudinal Memory Performance During Normal Aging: Twin Association Models of APOE and Other Alzheimer Candidate Genes in BEHAVIOR GENETICS
  • 2006-03 Quantitative trait loci in ABCA1 modify cerebrospinal fluid amyloid-β1-42 and plasma apolipoprotein levels in JOURNAL OF HUMAN GENETICS
  • 2006-03 Towards compendia of negative genetic association studies: an example for Alzheimer disease in HUMAN GENETICS
  • 2005-12 Comprehensive genetic evaluation of common E-cadherin sequence variants and prostate cancer risk: strong confirmation of functional promoter SNP in HUMAN GENETICS
  • 2005-05 MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction in NATURE GENETICS
  • 2005-05 Linkage disequilibrium patterns vary substantially among populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2004-12 Lower rate of genomic variation identified in the trans-membrane domain of monoamine sub-class of Human G-Protein Coupled Receptors: The Human GPCR-DB Database in BMC GENOMICS
  • 2004-08 Complex SNP-related sequence variation in segmental genome duplications in NATURE GENETICS
  • 2004-08 40th EASD Annual Meeting of the European Association for the Study of Diabetes in DIABETOLOGIA
  • 2004-06 Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer disease in NEUROGENETICS
  • 2004-05 Variants of CYP46A1 may interact with age and APOE to influence CSF Aβ42 levels in Alzheimer’s disease in HUMAN GENETICS
  • 2004-04 Common variants of ACE contribute to variable age-at-onset of Alzheimer’s disease in HUMAN GENETICS
  • 2004-02 A novel screen for nuclear mitochondrial gene associations with Parkinson’s disease in JOURNAL OF NEURAL TRANSMISSION
  • 2003-06 Evidence for an important role of perilipin in the regulation of human adipocyte lipolysis in DIABETOLOGIA
  • 2002-12 A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans in NATURE GENETICS
  • 2002-02 4th International Meeting on Single Nucleotide Polymorphism and Complex Genome AnalysisVarious Uses for DNA Variations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2001-06 Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's disease in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2001-06 TheTNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease in HUMAN GENETICS
  • 2001-04 3rd International Meeting on Single Nucleotide Polymorphism and Complex Genome Analysis: SNPs: ‘Some Notable Progress’ in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2000-10 Apolipoprotein-E dependent role for the FAS receptor in early onset Alzheimer's disease: finding of a positive association for a polymorphism in the TNFRSF6 gene in HUMAN GENETICS
  • 2000-08 No association between the α2-macroglobulin (A2M) deletion and Alzheimer's disease, and no change in A2M mRNA, protein, or protein expression in JOURNAL OF NEURAL TRANSMISSION
  • 2000-02 Discovery, scoring and utilization of human single nucleotide polymorphisms: a multidisciplinary problem in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1999-01 First International SNP Meeting at Skokloster, Sweden, August 1998. Enthusiasm mixed with scepticism about single-nucleotide polymorphism markers for dissecting complex disorders in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1999-01 Dynamic allele-specific hybridization in NATURE BIOTECHNOLOGY
  • 1998-09 The NIK protein kinase and C17orf1 genes: chromosomal mapping, gene structures and mutational screening in frontotemporal dementia and parkinsonism linked to chromosome 17 in HUMAN GENETICS
  • 1996-06 Coincidence cloning in MOLECULAR BIOTECHNOLOGY
  • 1995-04 Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness in MAMMALIAN GENOME
  • 1994 Identifying and Directly Purifying Transcribed Elements by Coincident Sequence Cloning in IDENTIFICATION OF TRANSCRIBED SEQUENCES
  • 1993-07 A series of vectors that simplify mammalian gene targeting in TRANSGENIC RESEARCH
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