Ausgabe 3/2018
Inhalt (25 Artikel)
A Commentary on Commercial Genetic Testing and the Future of the Genetic Counseling Profession
Nicholas D. Wolff, Jon A. Wolff
Commentary on “Commercial Genetic Testing and the Future of the Genetic Counseling Profession”
Jennifer Hoskovec
Response to Commercial Genetic Testing and the Future of the Genetic Counseling Profession
McKinsey L. Goodenberger, Brittany C. Thomas, Teresa Kruisselbrink
Talking with Children About Adult-Onset Hereditary Cancer Risk: A Developmental Approach for Parents
Allison Werner-Lin, Shana L. Merrill, Amanda C. Brandt
Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood
Ebony Richardson, Catherine Spinks, Andrew Davis, Christian Turner, John Atherton, Julie McGaughran, Christopher Semsarian, Jodie Ingles
The Genetic Counselor in the Pediatric Arrhythmia Clinic: Review and Assessment of Services
Benjamin M. Helm, Samantha L. Freeze, Katherine G. Spoonamore, Stephanie M. Ware, Mark D. Ayers, Adam C. Kean
Working with the Hmong Population in a Genetics Setting: an Interpreter Perspective
Meghan Krieger, Aime Agather, Kathryn Douglass, Catherine A. Reiser, Elizabeth M. Petty
“Where Does it Come from?” Experiences Among Survivors and Parents of Children with Retinoblastoma in Kenya
Amal Gedleh, Siwon Lee, Jessica A. Hill, Yvonne Umukunda, Seemi Qaiser, Joy Kabiru, Kahaki Kimani, Lucy Njambi, Grace Kitonyi, Helen Dimaras
Psychosocial Distress and Knowledge Deficiencies in Parents of Children in Ireland Who Carry an Altered Cystic Fibrosis Gene
S. J Quigley, B. Linnane, S. Connellan, A. Ward, P. Ryan
“My Plate is Full”: Reasons for Declining a Genetic Evaluation of Hearing Loss
Marci M. Lesperance, Erin Winkler, Tori L. Melendez, Beverly M. Yashar
Evaluation of the Informational Content, Readability and Comprehensibility of Online Health Information on Monogenic Diabetes
Yue Guan, Kristin A. Maloney, Debra L. Roter, Toni I. Pollin
Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples
Caroline E. Ghiossi, James D. Goldberg, Imran S. Haque, Gabriel A. Lazarin, Kenny K. Wong
The Experience of Genetic Counselors Working with Patients Facing the Decision of Pregnancy Termination after 24 Weeks Gestation
Rachel N. A. Graziani, Laurie Nemzer, Jennifer Kerns
Experiences of a High-Risk Population with Prenatal Hemoglobinopathy Carrier Screening in a Primary Care Setting: a Qualitative Study
Kim C. A. Holtkamp, Phillis Lakeman, Hind Hader, Suze M. J. P. Jans, Maria Hoenderdos, Henna A. M. Playfair, Martina C. Cornel, Marjolein Peters, Lidewij Henneman
Women’s Understanding and Attitudes towards Down Syndrome and Other Genetic Conditions in the Context of Prenatal Screening
Sarah Long, Peter O’Leary, Roanna Lobo, Jan E. Dickinson
Parent Perspectives of Support Received from Physicians and/or Genetic Counselors Following a Decision to Continue a Pregnancy with a Prenatal Diagnosis of Trisomy 13/18
Stephanie E. Wallace, Sara Gilvary, Michael J. Smith, Siobhan M. Dolan
“Yeah that Made a Big Difference!”: The Importance of the Relationship between Health Professionals and Fathers Who Have a Child with Down Syndrome
Freyja Docherty, Rebecca Dimond
Patients’ Opinions on Genetic Counseling on the Increased Risk of Parkinson Disease among Gaucher Disease Carriers
Maureen Mulhern, Louise Bier, Roy N. Alcalay, Manisha Balwani
Assessment of Current Genetic Counselor Practices in Post-Visit Written Communications to Patients
Emily VandenBoom, Angela M. Trepanier, Erin P. Carmany
Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals
Sandi Dheensa, Anneke Lucassen, Angela Fenwick
Making Sense of SNPs: Women’s Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks
Mary-Anne Young, Laura Elenor Forrest, Victoria-Mae Rasmussen, Paul James, Gillian Mitchell, Sarah Dilys Sawyer, Katrina Reeve, Nina Hallowell
Impact of Receiving Secondary Results from Genomic Research: A 12-Month Longitudinal Study
Julia Wynn, Josue Martinez, Jessica Bulafka, Jimmy Duong, Yuan Zhang, Codruta Chiuzan, Jain Preti, Maria L. Cremona, Vaidehi Jobanputra, Abby J. Fyer, Robert L. Klitzman, Paul S. Appelbaum, Wendy K. Chung
Caregiver Quality of Life with Tyrosinemia Type 1
Hailey Campbell, Rani H. Singh, Eric Hall, Nadia Ali
Translation and Cross-Cultural Adaptation with Preliminary Validation of GCOS-24 for Use in Spain
Patricia Muñoz-Cabello, Sixto García-Miñaúr, Manuel Eliecer Espinel-Vallejo, Lorenzo Fernández-Franco, Alexandra Stephens, Fernando Santos-Simarro, Pablo Lapunzina-Badía, Marion McAllister