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Neurodevelopmental disorders (NDDs) and genomics

(these resources replace previous content on autism spectrum disorder)

GECKO on the run: A 4-page, evidence-based summary for clinicians. Features a bottom line, causes of NDDs including autism spectrum disorder and fragile X syndrome, benefits and considerations of genetic assessment and testing, when and how to offer first-tier genetic testing. (May 2024)

GECKO deep dive: A 21-page, comprehensive evidence-based resource for clinicians. Features a bottom line, causes of NDDs including autism spectrum disorder and fragile X syndrome, benefits and considerations of genetic assessment and testing, types of genetic investigations and results, when and how to offer first-tier genetic testing. (Sept 2025)

Point of care tool: To facilitate ordering first-tier genetic testing in your province. (Sept 2025)

Resource for individuals and families: A 2-page resource related to genetic testing, benefits and considerations and possible results, in addition to other resources. (Sept 2025)

GECKO aims to aid the practicing non-genetics clinician by providing informed opinions regarding genomic conditions, services and technologies that have been developed in a rigorous and evidence-based manner with periodic updating. The content on the GECKO site is for educational purposes only. No resource should be used as a substitute for clinical judgement. GECKO assumes no responsibility or liability resulting from the use of information contained herein. 

Highlight: What are others reading about on GECKO

A Guide to understanding prenatal screening

A Guide to understanding prenatal screening

A resource developed for pregnant persons and their providers. Everything you wanted to know about screening from deciding whether or not have it, to results…

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Latest News

The GEC-KO team will be presenting at the 2021 University of Ottawa’s Annual Refresher Course

Family history is the first genetic test.

Check out this latest study trialing an innovative strategy for collecting family history in primary care. 

Carroll et al Ann Fam Med 2025;23:399-406.

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