Publications by authors named "Jessica Hartley"

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Success in changing stuttering attitudes: A retrospective analysis of 29 intervention studies.
Kenneth O St Louis, Katarzyna Węsierska, Aneta Przepiórka, Agata Błachnio, Chelsea Beucher, Jessica Hartley

J Commun Disord· September 2025

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Neurosurgery activity levels in the United Kingdom and republic of Ireland during the first wave of the covid-19 pandemic - a retrospective cross-sectional cohort study.
George E Richardson, Abdurrahman I Islim, Erminia Albanese, Ahmed Ahmed, Ahmed Aly, Jessica Hartley

Br J Neurosurg· August 2024

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Insights into genetic assistant practice and the workforce in North America.
Angela Krutish, Xiao-Qing Liu, Christine Kelly, Shannon R Chin, Jessica N Hartley

J Genet Couns· April 2024

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Refining the activities of genetic assistants: Development of task statements applicable across practice settings.
Ashley Tohms, Angela Krutish, Jessica N Hartley

Am J Med Genet A· April 2024

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

J Genet Couns· February 2024

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Exploring the role of a multidisciplinary hereditary gynecologic oncology clinic in epithelial ovarian cancer risk-reducing surgical decision-making practices: A mixed-methods study.
Selina Casalino, Sharon Bruce, Kim Serfas, Alon D Altman, Sarah Kean, Jessica N Hartley

J Genet Couns· June 2023

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Integrating genetic assistants into the workforce: An 18-year productivity analysis and development of a staff mix planning tool.
Angela Krutish, Robert F Balshaw, Xuejing Jiang, Jessica N Hartley

J Genet Couns· October 2022

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Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants.
Sandra Whalen, Marie Shaw, Cyril Mignot, Delphine Héron, Sandra Chantot Bastaraud, Jessica N Hartley

Eur J Hum Genet· September 2021

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Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38.
Kelsey Uminski, Donald S Houston, Jessica N Hartley, Jing Liu, Geoffrey D E Cuvelier

Pediatr Blood Cancer· October 2020

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Reflex Seizures in a Patient with CDKL5 Deficiency Disorder.
Tyler Peikes, Jessica N Hartley, Aizeddin A Mhanni, Cheryl R Greenberg, Juan Pablo Appendino

Can J Neurol Sci· July 2019

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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.
Jessica N Hartley, Louise R Simard, Valentina Ly, Marc R Del Bigio, Patrick Frosk

Am J Med Genet A· February 2019

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Compliance of camps in the United States with guidelines for health and safety practices.
Robert P Olympia, Kaylee Hollern, Caitlin Armstrong, Pelumi Adedayo, Jennifer Dunnick, Jessica Hartley

Pediatr Emerg Care· March 2015

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Chromosome microarray and undiagnosed seizures in a pediatric patient.
Angelika J Dawson, Aizeddin A Mhanni, Frances A Booth, Lorne Seargeant, Daniele Bernier, Jessica N Hartley

Can J Neurol Sci· March 2014

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Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia.
Jessica N Hartley, Frances A Booth, Marc R Del Bigio, Aizeddin A Mhanni

Case Rep Pediatr· August 2012

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Genetic counseling in a busy pediatric metabolic practice.
Jessica N Hartley, Cheryl R Greenberg, Aizeddin A Mhanni

J Genet Couns· February 2011

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Childhood-onset CADASIL: clinical, imaging, and neurocognitive features.
Jessica Hartley, Robyn Westmacott, Jochen Decker, Manohar Shroff, Grace Yoon

J Child Neurol· May 2010

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Intermediate-dose idebenone and quality of life in Friedreich ataxia.
John F Brandsema, Derek Stephens, Jessica Hartley, Grace Yoon

Pediatr Neurol· May 2010

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