Anthony J Brookes

Ontology type: schema:Person     

Person Info


Anthony J



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
  • JSON-LD is the canonical representation for SciGraph data.

    TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

        "@context": "", 
        "affiliation": [
            "affiliation": {
              "id": "", 
              "type": "Organization"
            "isCurrent": true, 
            "type": "OrganizationRole"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
        "familyName": "Brookes", 
        "givenName": "Anthony J", 
        "id": "sg:person.01310234412.29", 
        "sameAs": [
        "sdDataset": "persons", 
        "sdDatePublished": "2019-03-07T15:15", 
        "sdLicense": "", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        "sdSource": "s3://com-uberresearch-data-dimensions-researchers-20181010/20181011/dim_researchers/base/researchers_922.json", 
        "type": "Person"

    Download the RDF metadata as:  json-ld nt turtle xml License info


    JSON-LD is a popular format for linked data which is fully compatible with JSON.

    curl -H 'Accept: application/ld+json' ''

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' ''

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' ''

    RDF/XML is a standard XML format for linked data.

    curl -H 'Accept: application/rdf+xml' ''


    This table displays all metadata directly associated to this object as RDF triples.

    30 TRIPLES      10 PREDICATES      18 URIs      7 LITERALS      2 BLANK NODES

    Subject Predicate Object
    1 sg:person.01310234412.29 schema:affiliation Nb6471be42e184a11aa68c4144850b42f
    9 schema:familyName Brookes
    10 schema:givenName Anthony J
    11 schema:sameAs
    12 schema:sdDatePublished 2019-03-07T15:15
    13 schema:sdLicense
    14 schema:sdPublisher N3ac74cf50026413a9a2933a83f64b506
    15 sgo:license sg:explorer/license/
    16 sgo:sdDataset persons
    17 rdf:type schema:Person
    18 N3ac74cf50026413a9a2933a83f64b506 schema:name Springer Nature - SN SciGraph project
    19 rdf:type schema:Organization
    20 Nb6471be42e184a11aa68c4144850b42f schema:affiliation
    21 sgo:isCurrent true
    22 rdf:type schema:OrganizationRole
    23 schema:Organization
    24 schema:Organization
    25 schema:Organization
    26 schema:Organization
    27 schema:Organization
    28 schema:Organization
    29 schema:Organization
    30 schema:Organization

    Preview window. Press ESC to close (or click here)