Jessica N Hartley

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 7

Top Topics

Breast Cancer Risk

Intellectual Disability

Hepatitis C Virus

Top Venues

Journal of genetic counseling

American journal of medical genetics. Part A

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Jessica N Hartley, Maxine Holmqvist
"Learning with each other, about each other": Interdisciplinary learning among genetic counseling students and clinical health psychology residents. Journal of genetic counseling (2023)
Ashley Tohms, Angela Krutish, Jessica N Hartley
Refining the activities of genetic assistants: Development of task statements applicable across practice settings. American journal of medical genetics. Part A (2023)
Selina Casalino, Sharon Bruce, Kim Serfas, Alon D Altman, Sarah Kean, Pascal Lambert, Kirk James McManus, Jessica N Hartley, Mark William Nachtigal
Exploring the role of a multidisciplinary hereditary gynecologic oncology clinic in epithelial ovarian cancer risk-reducing surgical decision-making practices: A mixed-methods study. Journal of genetic counseling (2023)
Angela Krutish, Xiao-Qing Liu, Christine Kelly, Shannon R Chin, Jessica N Hartley
Insights into genetic assistant practice and the workforce in North America. Journal of genetic counseling (2023)
Angela Krutish, Robert F Balshaw, Xuejing Jiang, Jessica N Hartley
Integrating genetic assistants into the workforce: An 18-year productivity analysis and development of a staff mix planning tool. Journal of genetic counseling 31 (5) (2022)
Sandra Whalen, Marie Shaw, Cyril Mignot, Delphine Héron, Sandra Chantot Bastaraud, Cecile Cieuta Walti, Jan Liebelt, Frances Elmslie, Patrick Yap, Jane Hurst, Elisabeth Forsythe, Brian Kirmse, Jillian Ozmore, Alessandro Mauro Spinelli, Olga Calabrese, Thierry Billette de Villemeur, Anne Claude Tabet, Jonathan Levy, Agnes Guet, Manoëlle Kossorotoff, Benjamin Kamien, Jenny Morton, Anne McCabe, Elise Brischoux-Boucher, Annick Raas-Rothschild, Antonella Pini, Renée Carroll, Jessica N Hartley, null null, Patrick Frosk, Anne Slavotinek, Kristen Truxal, Jennifer Carroll, Annelies Dheedene, Hong Cui, Vishal Kumar, Glen Thomson, Florence Riccardi, Jozef Gecz, Laurent Villard
Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants. European journal of human genetics : EJHG 29 (9) (2021)
Jessica N Hartley, Louise R Simard, Valentina Ly, Marc R Del Bigio, Patrick Frosk
A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree families. American journal of medical genetics. Part A 179 (2) (2018)