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Tier-Classified Guidelines Database


Genomics & Health Impact Scan Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)

Last data update: Apr 10, 2024. (Total: 533 Documents since 2012)
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Records 1-5 (of 5 Record(s))
Reminder!

The tier level is assigned to the guideline, NOT to the specific search terms. For example, a Tier 1 guideline has at least one recommendation that meets criteria for Tier 1, but also could include tier 2 or 3 recommendations.
DO read the guidelines to find out about specific search terms.
DON’T rely on the overall tier classification of the guideline for the specified search terms.
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Query Trace: Autism[original query]
Publication Tier
Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG).
Melissa T Carter et al. Journal of medical genetics 2023
Tier 2
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.
Srivastava Siddharth et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Jun
Tier 2
Consensus Statement of the Indian Academy of Pediatrics on Diagnosis and Management of Fragile X Syndrome in India.
Sachdeva Anupam et al. Indian pediatrics 2019 Mar 56(3) 221-228
 Tier 2
Guideline recommendations for diagnosis and clinical management of Ring14 syndrome-first report of an ad hoc task force.
Rinaldi Berardo et al. Orphanet journal of rare diseases 2017 12(1) 69
 Tier 2
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
Schaefer GB, et al Genet Med. 2013 May;15(5):399-407. doi: 10.1038/gim.2013.32. Epub 2013 Mar 21.
 Tier 2
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