Robin Z Hayeems
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Explore the profile of Robin Z Hayeems including associated specialties, affiliations and a list of published articles.
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87
Citations
1254
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Recent Articles
1.
Mackley M, Weisz E, Hayeems R, Gaff C, Dawson-McClaren B
Eur J Hum Genet
. 2025 Jan;
PMID: 39753755
No abstract available.
2.
Degeling K, Tagimacruz T, MacDonald K, Seeger T, Fooks K, Venkataramanan V, et al.
Appl Health Econ Health Policy
. 2024 Dec;
PMID: 39739296
Background: Patients with suspected rare diseases often experience lengthy and uncertain diagnostic pathways. This study aimed to estimate the cost-effectiveness of exome sequencing (ES) in different positions in the diagnostic...
3.
Hayeems R, Luca S, Xiao B, Boswell-Patterson C, Venegas C, Abi Semaan C, et al.
Genet Med
. 2024 Nov;
27(1):101306.
PMID: 39489893
Purpose: To develop and assess the face and construct validity of the Clinician-reported Genetic Testing Utility Index (C-GUIDE) for genetic testing in prenatal care. Methods: After a literature review and...
4.
DAmours G, Clausen M, Luca S, Reble E, Kodida R, Assamad D, et al.
BMJ Open
. 2024 Sep;
14(9):e090084.
PMID: 39231549
Introduction: Genetic testing is used across medical disciplines leading to unprecedented demand for genetic services. This has resulted in excessive waitlists and unsustainable pressure on the standard model of genetic...
5.
Lee W, Hirjikaka D, Grewal S, Shaw A, Luca S, Clausen M, et al.
Genet Med
. 2024 Mar;
26(6):101122.
PMID: 38493336
Purpose: Digital tools are increasingly incorporated into genetics practice to address challenges with the current model of care. Yet, genetics providers' perspectives on digital tool use are not well characterized....
6.
Xiao B, Yan J, Hayeems R
Public Health Genomics
. 2024 Feb;
27(1):45-56.
PMID: 38382480
Introduction: Noninvasive prenatal testing (NIPT) can be used to detect fetal chromosomal abnormalities early in pregnancy. As eligibility criteria broaden and screening targets expand, gauging public acceptability of NIPT becomes...
7.
Liang N, Watts-Dickens A, Chitayat D, Babul-Hirji R, Chakraborty P, Hayeems R
Children (Basel)
. 2023 Aug;
10(8).
PMID: 37628361
The use of next-generation sequencing technologies such as genomic sequencing in newborn screening (NBS) could enable the detection of a broader range of conditions. We explored parental preferences and attitudes...
8.
DGama A, Mulhern S, Sheidley B, Boodhoo F, Buts S, Chandler N, et al.
Lancet Neurol
. 2023 Aug;
22(9):812-825.
PMID: 37596007
Background: Most neonatal and infantile-onset epilepsies have presumed genetic aetiologies, and early genetic diagnoses have the potential to inform clinical management and improve outcomes. We therefore aimed to determine the...
9.
Hartley T, Gillespie M, Graham I, Hayeems R, Li S, Sampson M, et al.
Genet Med
. 2023 Aug;
25(11):100948.
PMID: 37551668
Purpose: Exome and genome sequencing have rapidly transitioned from research methods to widely used clinical tests for diagnosing rare genetic diseases. We sought to synthesize the topics covered and appraise...
10.
Hayeems R, Luca S, Chad L, Quercia N, Xiao B, Hossain A, et al.
Clin Ther
. 2023 Jul;
45(8):729-735.
PMID: 37516567
Purpose: Advanced genomic and genetic testing technologies are quickly diffusing into clinical practice, but standardized approaches to assessing their clinical utility are limited. Previous work developed and generated preliminary evidence...