These resources are concise summaries for clinicians on genomic disorders, technologies or topics. They all feature a bottom line with key takeaway messages and relevant resources.

A GECKO on the run is about 2-3 pages in length and is meant to highlight practical clinical information for non-genomics clinicians, such as:

• What is the condition/topic/technology?
• What are the Red Flags to consider a genetic assessment?
• What does the genetic test result mean?
• How will genetic testing help you and your patient?
• Are there benefits, harms or limitations to genetic testing?
• What are the recommended surveillance and management guidelines?

Cancer genomics

• Hereditary Breast and Ovarian Cancer Syndrome
  • view
• Lynch Syndrome
  • view

Cardiogenomics

• Factor V Leiden
  • view
• Familial hypercholesterolemia
  • view
• Heritable thoracic aortic disease
  • view
• Hypertrophic cardiomyopathy
  • view
• Long QT syndrome
  • view

General genomics

• Hereditary Hemochromatosis
  • view
• Genomic test results
  • view

• Schizophrenia
  • view
• Type 2 diabetes
  • view

Neurogenomics

• Alzheimer disease
  • view
• Autism spectrum disorder (replaced by neurodevelopmental disorders)
• Epilepsy
  • view
• Huntington disease
  • view
• Multiple sclerosis
  • view
• Neurodevelopmental disorders (NDDs) and genomics
  • view

Pharmacogenomics

• Codeine and breast-feeding
  • view

Prenatal and preconception genomics

• Chromosomal microarray (prenatal)
  • view
• Consanguinity
  • view
• Non-invasive prenatal testing
  • view

Technologies

• Chromosomal microarray
  • view
• Chromosomal microarray (prenatal)
  • view
• Direct-to-consumer genetic testing
  • view
• Genomic test results
  • view
• Non-invasive prenatal testing
  • view