Hartley JN - Search Results

1

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

Casalino S, Bruce S, Serfas K, Altman AD, Kean S, Lambert P, McManus KJ, Hartley JN, Nachtigal MW. Casalino S, et al. Among authors: hartley jn. J Genet Couns. 2023 Jun;32(3):728-743. doi: 10.1002/jgc4.1684. Epub 2023 Feb 20. J Genet Couns. 2023. PMID: 36808790

2

Genetic counseling in a busy pediatric metabolic practice.

Hartley JN, Greenberg CR, Mhanni AA. Hartley JN, et al. J Genet Couns. 2011 Feb;20(1):20-2. doi: 10.1007/s10897-010-9324-y. Epub 2010 Sep 14. J Genet Couns. 2011. PMID: 20839038

3

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

Krutish A, Balshaw RF, Jiang X, Hartley JN. Krutish A, et al. Among authors: hartley jn. J Genet Couns. 2022 Oct;31(5):1183-1192. doi: 10.1002/jgc4.1589. Epub 2022 May 22. J Genet Couns. 2022. PMID: 35598107

4

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

Krutish A, Liu XQ, Kelly C, Chin SR, Hartley JN. Krutish A, et al. Among authors: hartley jn. J Genet Couns. 2024 Apr;33(2):281-290. doi: 10.1002/jgc4.1720. Epub 2023 Apr 27. J Genet Couns. 2024. PMID: 37106568

5

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

Hartley JN, Holmqvist M. Hartley JN, et al. J Genet Couns. 2024 Feb;33(1):238-243. doi: 10.1002/jgc4.1836. Epub 2023 Nov 15. J Genet Couns. 2024. PMID: 37965972

6

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

Tohms A, Krutish A, Hartley JN. Tohms A, et al. Among authors: hartley jn. Am J Med Genet A. 2024 Apr;194(4):e63487. doi: 10.1002/ajmg.a.63487. Epub 2023 Dec 1. Am J Med Genet A. 2024. PMID: 38041235

7

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

Uminski K, Houston DS, Hartley JN, Liu J, Cuvelier GDE, Israels SJ. Uminski K, et al. Among authors: hartley jn. Pediatr Blood Cancer. 2020 Oct;67(10):e28623. doi: 10.1002/pbc.28623. Epub 2020 Aug 13. Pediatr Blood Cancer. 2020. PMID: 32790119

8

Reflex Seizures in a Patient with CDKL5 Deficiency Disorder.

Peikes T, Hartley JN, Mhanni AA, Greenberg CR, Appendino JP. Peikes T, et al. Among authors: hartley jn. Can J Neurol Sci. 2019 Jul;46(4):482-485. doi: 10.1017/cjn.2019.29. Epub 2019 Apr 29. Can J Neurol Sci. 2019. PMID: 31030687 No abstract available.

9

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

Hartley JN, Simard LR, Ly V, Del Bigio MR, Frosk P. Hartley JN, et al. Am J Med Genet A. 2019 Feb;179(2):206-218. doi: 10.1002/ajmg.a.60690. Epub 2018 Dec 17. Am J Med Genet A. 2019. PMID: 30556349

10

Successful therapy for protein-losing enteropathy caused by chronic neuronopathic Gaucher disease.

Mhanni AA, Kozenko M, Hartley JN, Deneau M, El-Matary W, Rockman-Greenberg C. Mhanni AA, et al. Among authors: hartley jn. Mol Genet Metab Rep. 2015 Dec 29;6:13-5. doi: 10.1016/j.ymgmr.2015.12.001. eCollection 2016 Mar. Mol Genet Metab Rep. 2015. PMID: 27014572 Free PMC article.

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