Mariza De Andrade


Ontology type: schema:Person     


Person Info

NAME

Mariza

SURNAME

De Andrade

Publications in SciGraph latest 50 shown

  • 2018-09 The challenge of detecting genotype-by-methylation interaction: GAW20 in BMC GENETICS
  • 2018-09 GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics in BMC PROCEEDINGS
  • 2018-05 Correction to: Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study in HUMAN GENETICS
  • 2017-07 Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study in HUMAN GENETICS
  • 2017-02 Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease in NATURE GENETICS
  • 2016-08 eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants in BMC MEDICAL GENOMICS
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2015-12 The association of copy number variation and percent mammographic density in BMC RESEARCH NOTES
  • 2015-12 International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways in NATURE COMMUNICATIONS
  • 2015-12 Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network in GENOME MEDICINE
  • 2015-11 A Robust e-Epidemiology Tool in Phenotyping Heart Failure with Differentiation for Preserved and Reduced Ejection Fraction: the Electronic Medical Records and Genomics (eMERGE) Network in JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH
  • 2015-10 A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease in NATURE GENETICS
  • 2015-09 Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome in HUMAN GENETICS
  • 2015-05 Genome-wide association study of kidney function decline in individuals of European descent in KIDNEY INTERNATIONAL
  • 2015-04 Multi-ethnic analysis reveals soluble l-selectin may be post-transcriptionally regulated by 3′UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA) in HUMAN GENETICS
  • 2015-01 Genetic variation in the HLA region is associated with susceptibility to herpes zoster in GENES & IMMUNITY
  • 2014-10 Biochemical response to ursodeoxycholic acid predicts survival in a North American cohort of primary biliary cirrhosis patients in JOURNAL OF GASTROENTEROLOGY
  • 2014-01 A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects in HUMAN GENETICS
  • 2013-06 Nutrients from Fruit and Vegetable Consumption Reduce the Risk of Pancreatic Cancer in JOURNAL OF GASTROINTESTINAL CANCER
  • 2012-12 SNP interaction detection with Random Forests in high-dimensional genetic data in BMC BIOINFORMATICS
  • 2012-12 Genetic analyses of smoking initiation, persistence, quantity, and age-at-onset of regular cigarette use in Brazilian families: the Baependi Heart Study in BMC MEDICAL GENETICS
  • 2012-06 Detectable clonal mosaicism from birth to old age and its relationship to cancer in NATURE GENETICS
  • 2012-06 A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance in NATURE GENETICS
  • 2012-04 Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network in HUMAN GENETICS
  • 2012-01 Brazilian urban population genetic structure reveals a high degree of admixture in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-12 Heritability of physical activity traits in Brazilian families: the Baependi Heart Study in BMC MEDICAL GENETICS
  • 2011-12 Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform in BMC BIOINFORMATICS
  • 2011-12 Fruit and vegetable consumption is inversely associated with having pancreatic cancer in CANCER CAUSES & CONTROL
  • 2011-06 Genome partitioning of genetic variation for complex traits using common SNPs in NATURE GENETICS
  • 2010-12 Linkage analysis of obesity phenotypes in pre- and post-menopausal women from a United States mid-western population in BMC MEDICAL GENETICS
  • 2010-12 Evaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian families in BMC MEDICAL GENETICS
  • 2010-05 New loci associated with kidney function and chronic kidney disease in NATURE GENETICS
  • 2010-04 Familial Aggregation of Irritable Bowel Syndrome: A Family Case–Control Study in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2010-03 A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33 in NATURE GENETICS
  • 2009-12 Assessment of genotype imputation methods in BMC PROCEEDINGS
  • 2009-12 Identification of gene-gene interaction using principal components in BMC PROCEEDINGS
  • 2009-12 Adjusting for HLA-DRβ1 in a genome-wide association analysis of rheumatoid arthritis and related biomarkers in BMC PROCEEDINGS
  • 2009-12 Identification of genes and haplotypes that predict rheumatoid arthritis using random forests in BMC PROCEEDINGS
  • 2009-09 Temporal Association of Changes in Fasting Blood Glucose and Body Mass Index With Diagnosis of Pancreatic Cancer in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2009-09 Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer in NATURE GENETICS
  • 2008-12 Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart Study in BMC MEDICAL GENETICS
  • 2008-02 Genomic regions that influence plasma levels of inflammatory markers in hypertensive sibships in JOURNAL OF HUMAN HYPERTENSION
  • 2008-01 Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2007-12 Comparison of variable and model selection methods for genetic association studies using the GAW15 simulated data in BMC PROCEEDINGS
  • 2007-12 The genetics of gene expression: comparison of linkage scans using two phenotype normalization methods in BMC PROCEEDINGS
  • 2007-12 Comparison of tagging single-nucleotide polymorphism methods in association analyses in BMC PROCEEDINGS
  • 2007-12 Analysis of variation in NF-κB genes and expression levels of NF-κB-regulated molecules in BMC PROCEEDINGS
  • 2007-12 Linkage analysis using principal components of gene expression data in BMC PROCEEDINGS
  • 2007-12 Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci in BMC PROCEEDINGS
  • 2007-01 Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury in HUMAN GENETICS
  • 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": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
        "affiliation": [
          {
            "affiliation": {
              "id": "https://www.grid.ac/institutes/grid.66875.3a", 
              "type": "Organization"
            }, 
            "isCurrent": true, 
            "type": "OrganizationRole"
          }, 
          {
            "id": "https://www.grid.ac/institutes/grid.267308.8", 
            "type": "Organization"
          }, 
          {
            "id": "https://www.grid.ac/institutes/grid.4367.6", 
            "type": "Organization"
          }, 
          {
            "id": "https://www.grid.ac/institutes/grid.214572.7", 
            "type": "Organization"
          }, 
          {
            "id": "https://www.grid.ac/institutes/grid.240145.6", 
            "type": "Organization"
          }, 
          {
            "id": "https://www.grid.ac/institutes/grid.224260.0", 
            "type": "Organization"
          }
        ], 
        "familyName": "De Andrade", 
        "givenName": "Mariza", 
        "id": "sg:person.01350776501.81", 
        "identifier": {
          "name": "orcid_id", 
          "type": "PropertyValue", 
          "value": [
            "0000-0003-2329-2686"
          ]
        }, 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01350776501.81", 
          "https://orcid.org/0000-0003-2329-2686"
        ], 
        "sdDataset": "persons", 
        "sdDatePublished": "2019-03-07T15:20", 
        "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        }, 
        "sdSource": "s3://com-uberresearch-data-dimensions-researchers-20181010/20181011/dim_researchers/base/researchers_999.json", 
        "type": "Person"
      }
    ]
     

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

    HOW TO GET THIS DATA PROGRAMMATICALLY:

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

    curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/person.01350776501.81'

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

    curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/person.01350776501.81'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/person.01350776501.81'

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

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/person.01350776501.81'


     

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

    31 TRIPLES      11 PREDICATES      18 URIs      8 LITERALS      3 BLANK NODES

    Subject Predicate Object
    1 sg:person.01350776501.81 schema:affiliation N35d965192d4f41088d6a9d9f411cac9e
    2 https://www.grid.ac/institutes/grid.214572.7
    3 https://www.grid.ac/institutes/grid.224260.0
    4 https://www.grid.ac/institutes/grid.240145.6
    5 https://www.grid.ac/institutes/grid.267308.8
    6 https://www.grid.ac/institutes/grid.4367.6
    7 schema:familyName De Andrade
    8 schema:givenName Mariza
    9 schema:identifier N213825bdb70449369cce39c8feb11c9c
    10 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01350776501.81
    11 https://orcid.org/0000-0003-2329-2686
    12 schema:sdDatePublished 2019-03-07T15:20
    13 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    14 schema:sdPublisher N1b8f93482d1643be9d4fb63ef779e795
    15 sgo:license sg:explorer/license/
    16 sgo:sdDataset persons
    17 rdf:type schema:Person
    18 N1b8f93482d1643be9d4fb63ef779e795 schema:name Springer Nature - SN SciGraph project
    19 rdf:type schema:Organization
    20 N213825bdb70449369cce39c8feb11c9c schema:name orcid_id
    21 schema:value 0000-0003-2329-2686
    22 rdf:type schema:PropertyValue
    23 N35d965192d4f41088d6a9d9f411cac9e schema:affiliation https://www.grid.ac/institutes/grid.66875.3a
    24 sgo:isCurrent true
    25 rdf:type schema:OrganizationRole
    26 https://www.grid.ac/institutes/grid.214572.7 schema:Organization
    27 https://www.grid.ac/institutes/grid.224260.0 schema:Organization
    28 https://www.grid.ac/institutes/grid.240145.6 schema:Organization
    29 https://www.grid.ac/institutes/grid.267308.8 schema:Organization
    30 https://www.grid.ac/institutes/grid.4367.6 schema:Organization
    31 https://www.grid.ac/institutes/grid.66875.3a schema:Organization
     




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


    ...