Refining the activities of genetic assistants: Development of task statements applicable across practice settings.

Authors: Tohms, Ashley^1,2, Krutish, Angela^2,3, Hartley, Jessica N.^2,3, jessica.hartley@umanitoba.ca

Source: American Journal of Medical Genetics. Part A; Apr2024, Vol. 194 Issue 4, p1-7, 7p

Insights into genetic assistant practice and the workforce in North America.

Authors: Krutish, Angela, Liu, Xiao‐Qing, Kelly, Christine, Chin, Shannon R., Hartley, Jessica N.

Source: Journal of Genetic Counseling; Apr2024, Vol. 33 Issue 2, p281-290, 10p

"Learning with each other, about each other": Interdisciplinary learning among genetic counseling students and clinical health psychology residents.

Authors: Hartley, Jessica N., Holmqvist, Maxine

Source: Journal of Genetic Counseling; Feb2024, Vol. 33 Issue 1, p238-243, 6p

Exploring the role of a multidisciplinary hereditary gynecologic oncology clinic in epithelial ovarian cancer risk‐reducing surgical decision‐making practices: A mixed‐methods study.

Authors: Casalino, Selina, Bruce, Sharon, Serfas, Kim, Altman, Alon D., Kean, Sarah, Lambert, Pascal, McManus, Kirk J., Hartley, Jessica N., Nachtigal, Mark W.

Source: Journal of Genetic Counseling; Jun2023, Vol. 32 Issue 3, p728-743, 16p

Integrating genetic assistants into the workforce: An 18‐year productivity analysis and development of a staff mix planning tool.

Authors: Krutish, Angela, Balshaw, Robert F., Jiang, Xuejing, Hartley, Jessica N.

Source: Journal of Genetic Counseling; Oct2022, Vol. 31 Issue 5, p1183-1192, 10p

Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38.

Authors: Uminski, Kelsey, Houston, Donald S., Hartley, Jessica N., Liu, Jing, Cuvelier, Geoffrey D.E., Israels, Sara J.

Source: Pediatric Blood & Cancer; Oct2020, Vol. 67 Issue 10, p1-7, 7p

Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia.

Authors: Hartley, Jessica N.^1,2, Booth, Frances A.³, Bigio, Marc R. Del⁴, Mhanni, Aizeddin A.^1,2,3 amhanni@hsc.mb.ca

Source: Case Reports in Pediatrics. 2012, p1-4. 4p.

Subject Terms: *GENETIC mutation, *SPINOCEREBELLAR ataxia, *ETIOLOGY of diseases, *GENETIC code, *MITOCHONDRIAL DNA, *DNA replication, *PHENOTYPES, *DNA helicases

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A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree families.

Authors: Hartley, Jessica N.¹, Simard, Louise R.¹, Ly, Valentina¹, Del Bigio, Marc R.², Frosk, Patrick^1,3, pfrosk@exchange.hsc.mb.ca

Source: American Journal of Medical Genetics. Part A; Feb2019, Vol. 179 Issue 2, p206-218, 13p

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Cover Image, Volume 179A, Number 2, February 2019.

Authors: Hartley, Jessica N.¹, Simard, Louise R.¹, Ly, Valentina¹, Del Bigio, Marc R.², Frosk, Patrick^1,3, pfrosk@exchange.hsc.mb.ca

Source: American Journal of Medical Genetics. Part A; Feb2019, Vol. 179 Issue 2, pi-i, 1p