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  • Caroline Graham
 

Caroline Graham

RD-Connect

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Caroline Graham

Position: Manager – Service Planning, Office of Population Health Genomics
Organisation: Office of Population Health Genomics (OPHG)
Area of work: Bioinformatics, Registries

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Contact information:

Email

Address: Department of Health Western Australia, Level 3, C Block 189 Royal Street, , East Perth, WA 6004, Australia

Role in RD-Connect:

Caroline Graham is the Australian Secretariat, coordinator and manager of project activities.

Background:

Dr Caroline Graham establishes state-wide policies and programs in relation to genomic health services for WA. She provides advice and recommendations in relation to genetic services, policies and procedures to improve outcomes for people with rare or genetic disease. She identifies and promulgates best practice guidelines and represents the state’s interests in relation to the translation of new genomics knowledge, informatics and technology that improve the treatment, management, evidence, efficiency and cost-effectiveness of healthcare delivery

Dr Graham is the National coordinator of the Australian Neuromuscular Disorders Registries that includes Duchenne Muscular Dystrophy, Myotonic Dystrophy, and Spinal Muscular Atrophy. She coordinates the establishment and partnering of Australia-wide and international registries and biobanks. Dr Graham has been instrumental in driving efficiencies in the operational capacity of Genetic Services of WA to deliver health benefit. She has achieved this by undertaking stakeholder consultations, evaluation of existing infrastructure and clinical service delivery, and development of recommendations for a quality framework.

Underpinning her policy and planning activities is 10+ years experience in biomedical research and 5 years as a Forensic Scientist.

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Go to Genome-Phenome Analysis Platform

Go to Registry & Biobank Finder

Go to Sample Catalogue

See the Bioinformatic tools

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Recent news

62,000 samples available via RD-Connect sample catalogue

Published: February 5, 2019

RD-Connect – six years on and outlooks to the future

Published: October 31, 2018

New FAQ section for Sample Catalogue is out!

Published: October 19, 2018

Today is the World MCT8-AHDS Day!

Published: October 8, 2018

Recommendations to create Rare Disease Registries

Published: September 28, 2018

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An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. Visit the platform:

Genome-Phenome Analysis Platform

Analyse and share genomic data

Registry & Biobank Finder

Directory of rare disease biobanks and patient registries

Sample Catalogue

Browse rare disease biosamples stored in biobanks

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  • NEWS
  • EVENTS
  • CONTACT
    • Contact
    • Project partners
    • Partner organisations
  • About
    • Introduction to rare diseases
    • RD-Connect Community
      • About the RD-Connect Community
      • Register as member
      • Structure
    • Funding and collaborations
    • RD-Connect (2012 – 2018)
      • The original EU-funded project
      • Project partners
      • Partner organisations
      • Executive Management Committee (EMC)
      • Scientific Advisory Board (SAB)
      • Patient Advisory Council (PAC)
      • Rare Disease Patient and Ethics Council (RD-PEC)
      • Periodic activity reports
  • What we do
    • Omics data
      • Genome-Phenome Analysis Platform
      • FAQ
      • Data Submission Guide
      • PhenoTips Guide
    • Data linkage
      • FAIRification of rare disease registries
      • Linked data and ontology task force
      • Ontologies in rare disease registries
    • Patient registry data
      • Registry & Biobank Finder for patient registries
      • Registry common data elements
      • Core Implementation Group
    • Biosamples data
      • Registry & Biobank Finder for biobanks
      • Sample Catalogue
      • Biobank assessment process
      • Biobank Assessment Panel
    • Bioinformatic tools
    • Ethical, Legal and Social Issues (ELSI)
      • Sharing of biosamples and data
      • Standards for informed consent
    • Patient engagement
  • Resources
    • Forms and user guides
      • See all forms and guides
      • PhenoTips Guide
      • Data Submission Guide
    • FAQs
      • FAQ: Genome-Phenome Analysis Platform
      • FAQ: Sample Catalogue
    • Newsletters
    • Presentations and flyers
    • Videos
    • Scientific publications
    • Glossary
    • Privacy policy
  • For Patients and Families
  • News
  • Events
  • Contact

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  • Genome-Phenome Analysis Platform
  • Registry & Biobank Finder
  • Sample Catalogue

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RD-Connect

RD-Connect coordination team

Centro Nacional de Análisis Genómico (CNAG-CRG)
Baldiri Reixac, 4,
Barcelona, 08028
Spain

Email: Sergi Beltran Agulló (Project Lead) or info@rd-connect.eu.

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