• About Us
  • Contact Us
  • Sitemap
  • Permissions
  • Disclaimer
  • Connect

  • Point of Care Tools
    • Cancer genomics
      • BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Syndrome
      • General Hereditary Cancer Syndrome Triage Tool
      • Lynch Syndrome
      • Renal Cell Cancers
    • Cardiogenomics
      • Factor V Leiden
      • Familial hypercholesterolemia
      • Hypertrophic Cardiomyopathy
      • Long QT syndrome
    • General genomics
      • Family History
      • Family history red flags
      • Hereditary Hemochromatosis
    • Neurogenomics
      • Autism spectrum disorder
      • Epilepsy
    • Preconception and prenatal genomics
      • Carrier Screening in Canada
      • Expanded Carrier Screening
      • [A guide to understanding] Prenatal Screening
  • Educational Resources
    • Cancer Genomics
      • BRCA1/BRCA2 Hereditary Breast and Ovarian Cancer Syndrome
      • Lynch Syndrome (Hereditary colorectal cancer)
    • Cardiogenomics
      • Factor V Leiden
      • Familial hypercholesterolemia
      • Hypertrophic cardiomyopathy
      • Long QT syndrome 
    • General Genomics
      • Basic genomic resources
      • Hearing loss (the genetics of)
      • Hereditary Hemochromatosis
      • Schizophrenia
      • Type 2 Diabetes
    • Neurogenomics
      • Alzheimer disease
      • Autism spectrum disorder (ASD)
      • Epilepsy
      • Huntington disease
      • Multiple sclerosis
    • Pharmacogenomics
      • Codeine and breastfeeding
      • Additional resources
    • Prenatal and Preconception Genomics
      • Consanguinity
      • Carrier screening in Canada
      • Expanded carrier screening
      • Non-invasive prenatal testing (NIPT)
      • Prenatal Screening
    • Technologies
      • Chromosomal microarray
      • Chromosomal microarray – PRENATAL
      • Direct-to-consumer genetic testing
      • Expanded carrier screening
      • Non-invasive prenatal testing (NIPT)
      • Prenatal Screening
      • Whole Exome and Genome Sequencing
    • Basic Genomic Resources
    • Glossary
    • Additional Resources
  • PowerPoint Seminars
    • Cardiogenomics
    • Prenatal and Preconception Genetics
    • Pediatric Genetics
    • Adult Genetics
    • General Genetic Counselling
  • Genetics Centres
    • Canada
      • Clinics
      • Laboratories
    • Outside Canada
  • Public Resources
    • General Resources
    • Prenatal and Preconception Genetics
      • Guide to understanding prenatal screening tests
    • Newborn Genetics
    • Adult Genetics
  • News & Events

Not-for-profit genetics and genomics education for non-genetics health professionals

#UntanglingTheHelix

Family History App in Personalized Medicine (FHAMe): Diabetes

morrison    2 months ago  

FHAMe Diabetes

morrison

Posts

Subscribe

News

  • Direct-to-Consumer genetic testing in Canada
  • Access to genomic services
  • GEC-KO on the run

Events

  • 2014 Founders Award for Excellence in Medical Genetics
  • 52nd Ontario College of Family Physicians’ Annual Scientific Assembly
  • 2014 Family Medicine Forum – Nov 13-15 in Quebec City

Recent Posts

  • Family History App in Personalized Medicine (FHAMe): Diabetes
  • Family History App in Personalized Medicine (FHAMe): Cardiovascular disease
  • Genetic Non-Discrimination in Canada

Archives

  • April 2021
  • May 2017
  • October 2016
  • October 2015
  • January 2015
  • November 2014
  • October 2014
  • September 2014
  • August 2014
  • July 2014
  • About Us
  • Contact Us
  • Sitemap
  • Permissions
  • Disclaimer
  • Connect

Tweets

CDC Genomics & Precision Health
11 Jun
CDC Genomics & Precision Health
@CDC_Genomics

Our Genomics and Precision Health Hot Topics of the Day include #COVID19, polygenic risk scores, machine learning, gene therapy and more. Check it out! #PHGKB #MedGeneEd21 phgkb.cdc.gov/PHGKB/phgHome.… pic.twitter.com/Y2aRuXPGr7

Retweeted by GEC-KORetweeted by GEC-KO
Expand reply reply retweet retweet favorite favorite
Eric Green
11 Jun
Eric Green
@NHGRI_Director

@genome_gov is supporting research that is advancing how genomics is being used to advance understanding about more common diseases. I encourage you to look through our resource list for educators and healthcare providers: bit.ly/3cy4sCr #MedGeneEd21

Retweeted by GEC-KORetweeted by GEC-KO
Expand reply reply retweet retweet favorite favorite
New England Genetics
10 Jun
New England Genetics
@negenetics

Kim, mother of a child with a treatable rare disease, discusses her journey and the importance of #NewbornScreening in this short video. Find it here from @RareDiseases - ow.ly/CFTY50EQvJL pic.twitter.com/HvbhjiEpY8

Retweeted by GEC-KORetweeted by GEC-KO
Expand reply reply retweet retweet favorite favorite
autism speaks
10 Jun
autism speaks
@autismspeaks

Autistic people may: 👀 Not make eye contact 👋 Use gestures or notice your gestures 👧 Not make facial expressions or understand facial expressions but that does not mean that they are not listening!

Retweeted by GEC-KORetweeted by GEC-KO
Expand reply reply retweet retweet favorite favorite
JAX Clinical Education
10 Jun
JAX Clinical Education
@JAXClinicalEd

Learn about the benefits, risks and limitations of germline multigene panels for different patients in the 15-minute video - Breast Cancer Genetic Testing Strategy. #MedGeneEd21 jax.org/education-and-… pic.twitter.com/eWxQ2Zex1u

Retweeted by GEC-KORetweeted by GEC-KO
Expand reply reply retweet retweet favorite favorite
  • Twitter
© 2020. GEC-KO | Genetics Education Canada - Knowledge Organization
Scroll
×

Subscribe


Subscribe to our updates and be the first to know about new GEC-KO resources.