Ausgabe 3/2017
Inhalt (27 Artikel)
Standards for the Reporting of Genetic Counseling Interventions in Research and Other Studies (GCIRS): an NSGC Task Force Report
Gillian W. Hooker, D Babu, MF Myers, H Zierhut, M McAllister
A Rapid Systematic Review of Outcomes Studies in Genetic Counseling
Lisa Madlensky, Angela M. Trepanier, Deborah Cragun, Barbara Lerner, Kristen M. Shannon, Heather Zierhut
Clinical Cancer Genetics Disparities among Latinos
Marcia Cruz-Correa, Julyann Pérez-Mayoral, Julie Dutil, Miguel Echenique, Rafael Mosquera, Keila Rivera-Román, Sharee Umpierre, Segundo Rodriguez-Quilichini, Maria Gonzalez-Pons, Myrta I. Olivera, Sherly Pardo
A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes
Sarah Scollon, Amanda Knoth Anglin, Martha Thomas, Joyce T. Turner, Kami Wolfe Schneider
The Confluence of Psychiatric Symptoms and Neurodegenerative Disease: Impact on Genetic Counseling
Jill S. Goldman, Edward D. Huey, Deborah Z. Thorne
Genetic Counseling Dilemmas for a Patient with Sporadic Amyotrophic Lateral Sclerosis, Frontotemporal Degeneration & Parkinson’s Disease
Vittorio Mantero, Claudia Tarlarini, Angelo Aliprandi, Giuseppe Lauria, Andrea Rigamonti, Lucia Abate, Paola Origone, Paola Mandich, Silvana Penco, Andrea Salmaggi
Knowledge and Attitudes Regarding Non-Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in Sweden
Susanne Georgsson, Ellika Sahlin, Moa Iwarsson, Magnus Nordenskjöld, Peter Gustavsson, Erik Iwarsson
“I Don’t Want to Be an Ostrich”: Managing Mothers’ Uncertainty during BRCA1/2 Genetic Counseling
Carla L. Fisher, Thomas Roccotagliata, Camella J. Rising, David W. Kissane, Emily A. Glogowski, Carma L. Bylund
A Qualitative Study of Anticipated Decision Making around Type 2 Diabetes Genetic Testing: the Role of Scientifically Concordant and Discordant Expectations
Alicia G. Carmichael, Bailey B. Hulswit, Emily J. Moe, Toby Epstein Jayaratne, Beverly M. Yashar
Factors Associated with Interest in Gene-Panel Testing and Risk Communication Preferences in Women from BRCA1/2 Negative Families
Kristina G. Flores, Laurie E. Steffen, Christopher J. McLouth, Belinda E. Vicuña, Amanda Gammon, Wendy Kohlmann, Lucretia Vigil, Zoneddy R. Dayao, Melanie E. Royce, Anita Y. Kinney
Is Symptomatic Long QT Syndrome Associated with Depression in Women and Men?
Karolina Wesołowska, Marko Elovainio, Mikael Koponen, Annukka M. Tuiskula, Mirka Hintsanen, Liisa Keltikangas-Järvinen, Ilmari Määttänen, Heikki Swan, Taina Hintsa
A Pilot Study of Fragile X Syndrome Screening in Pregnant Women and Women Planning Pregnancy: Implementation, Acceptance, Awareness, and Geographic Factors
Ramona Alfaro Arenas, Jordi Rosell Andreo, Damián Heine Suñer, María Pía, Consuelo Fernández Yagüe, Catalina Cerdà, Jerónima Amengual, Margalida Lladó, Elena Pascual de Juan, Teresa Mariscal, Pilar López Redondo, Olga Román, Andrés Calvo Pérez, Sabine Rehkugler, Francisco Javier Agüera, Azucena Bande Seisdedos, Mª Jesús Fernández Castaño, Roser Gallardo Ferrer, Margalida Alomar Castell, Concha Manzanares Mir, Carmen Carrascosa Martín, Mª Teresa Sánchez-Puga Crusat, Joana Crespí Rullan, Catalina Serra Calafat, Catalina Artigues Mascaró, Antonia Cladera Riera, Joana Guardiola Martínez, Margalida Pujol Ferragut, Rocío Aguilar González, Miguel Juan Clar, Albert Tubau, Maria Antonia Ferragut, Elena Portells Miralles, Carmen Ribera Gómez, Jessica Holster, Elena Montes de Oca, Dolores García, Carmen Vallejo Burgada, Agustín Hernández, Juan Trias Rojas, Ines Pomar, Joana Boyeras, Eva Navarro, Yolanda Vives Fuster, María Maimó Vaquer, Mariana Garces Más, Matteu Taylor, Silvia Miralles Corrales, Marian García Baratas, María A. Blanco García, Catalina Torrens Grau, Francisca Llinàs Alzina, Regina Sastre Arbós, Verónica Molina Gilfillan, Mª Paz Nadal Casasnovas, Mª Carmen Vidal Llampurdanes, Carmen Santos Pons, Juan Carlos Hermoso García, Jorge Casal Moro, Miriam Ribes Redondo, Marcial Moreno Pons, Montserrat Pastor, Raquel Gastón, Rodolfo Moreno Mira, Marta Cortés
Information Topics of Greatest Interest for Return of Genome Sequencing Results among Women Diagnosed with Breast Cancer at a Young Age
Joann Seo, Jennifer Ivanovich, Melody S. Goodman, Barbara B. Biesecker, Kimberly A. Kaphingst
What Do Parents of Children with Down Syndrome Think about Non-Invasive Prenatal Testing (NIPT)?
Rachèl V. van Schendel, Adriana Kater-Kuipers, Elsbeth H. van Vliet-Lachotzki, Wybo J. Dondorp, Martina C. Cornel, Lidewij Henneman
The Dynamics of a Genetic Counseling Peer Supervision Group
Katie L. Lewis, Lori A. H. Erby, Amanda L. Bergner, E. Kate Reed, Maria R. Johnson, Jessica Y. Adcock, Meredith A. Weaver
Parents’ Understanding of Genetics and Heritability
Brittany Harding, Rylan Egan, Peter Kannu, Jennifer J. MacKenzie
Prevalence and Characteristics of Patients with Suspected Inherited Renal Cell Cancer: Application of the ACMG/NSGC Genetic Referral Guidelines to Patient Cohorts
Hong Truong, Sarah E. Hegarty, Leonard G. Gomella, William K. Kelly, Edouard J. Trabulsi, Costas D. Lallas, Veda N. Giri
Decisions Regarding Pregnancy Termination Due to β-Thalassemia Major: a Mixed-Methods Study in Sistan and Baluchestan, Iran
Zahra Moudi, Ebrahim Miri-Moghaddam
Genetic Counselor Workforce Issues: a Survey of Genetic Counselors Licensed in the State of Indiana
Stephanie A. Cohen, Megan E. Tucker, Paula Delk
Feasibility and Preliminary Efficacy of an Internet Support Group for Parents of a Child with Neurofibromatosis Type 1: a Pilot Study
S. Martin, M. C. Roderick, R. Lockridge, M. A. Toledo-Tamula, A. Baldwin, P. Knight, P. Wolters
Genetic Counselor Practices Involving Pediatric Patients with FAP: an Investigation of their Self-Reported Strategies for Genetic Testing and Hepatoblastoma Screening
Caitlin E. Lawson, Thomas M. Attard, Hongying Dai, Seth Septer
Reproductive Decision-Making in Women with BRCA1/2 Mutations
Jessica L. Chan, Lauren N. C. Johnson, Mary D. Sammel, Laura DiGiovanni, Chan Voong, Susan M. Domchek, Clarisa R. Gracia
Patients with Amyotrophic Lateral Sclerosis Have High Interest in and Limited Access to Genetic Testing
Karin N. Wagner, Haikady Nagaraja, Dawn C. Allain, Adam Quick, Stephen Kolb, Jennifer Roggenbuck
The Subjective Experience of Patients Diagnosed with Hereditary Hemorrhagic Telangiectasia: a Qualitative Study
Laura Geerts, Carole Fantini-Hauwel, Elodie Brugallé, Odile Boute, Frédéric Frénois, Lydie Defrance, Sylvie Manouvrier-Hanu, Florence Petit, Pascal Antoine
Knowledge and Self-Esteem of Individuals with Neurofibromatosis Type 1 (NF1)
Kayla Rosnau, S. Shahrukh Hashmi, Hope Northrup, John Slopis, Sarah Noblin, Myla Ashfaq
Genetic Counseling for Couples Seeking Noninvasive Prenatal Testing in Japan: Experiences of Pregnant Women and their Partners
Motoko Watanabe, Mari Matsuo, Masaki Ogawa, Toshitaka Uchiyama, Satoru Shimizu, Naoko Iwasaki, Akemi Yamauchi, Mari Urano, Hironao Numabe, Kayoko Saito
Factors Influencing the Decision-Making Process and Long-Term Interpersonal Outcomes for Parents Who Undergo Preimplantation Genetic Diagnosis for Fanconi Anemia: a Qualitative Investigation
K. Haude, P. McCarthy Veach, B. LeRoy, H. Zierhut