Genetic testing for the epilepsies: A systematic review von Sheidley, Beth R., Malinowski, Jennifer, Bergner, Amanda L., Bier, Louise, Gloss, David S., Mu, Weiyi, Mulhern, Maureen M., Partack, Emily J., Poduri, Annapurna

Volltext

Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis von Steigerwald, Connolly G, Bertolini, Carina, McElhiney, Martin, Bergner, Amanda L, Harms, Matthew B, Harrington, Elizabeth A

Volltext

Efficacy and Biomarker Study of Bevacizumab for Hearing Loss Resulting From Neurofibromatosis Type 2-Associated Vestibular Schwannomas von Blakeley, Jaishri O, Ye, Xiaobu, Duda, Dan G, Halpin, Chris F, Bergner, Amanda L, Muzikansky, Alona, Merker, Vanessa L, Gerstner, Elizabeth R, Fayad, Laura M, Ahlawat, Shivani, Jacobs, Michael A, Jain, Rakesh K, Zalewski, Christopher, Dombi, Eva, Widemann, Brigitte C, Plotkin, Scott R

Volltext

Genetic counselors' utilization of ChatGPT in professional practice: A cross‐sectional study von Ahimaz, Priyanka, Bergner, Amanda L., Florido, Michelle E., Harkavy, Nina, Bhattacharyya, Sriya

Volltext

Exploring the evolving roles of clinical geneticists and genetic counselors in the era of genomic medicine von Freiman, Andrew, Rekab, Aisha, Bergner, Amanda L., Pereira, Elaine M., Lin, Yuhuan, Ahimaz, Priyanka

Volltext

Clinical utility of exome sequencing in a pediatric epilepsy cohort von Graifman, Jordana L., Lippa, Natalie C., Mulhern, Maureen S., Bergner, Amanda L., Sands, Tristan T.

Volltext

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas von Piotrowski, Arkadiusz, Xie, Jing, Liu, Ying F, Poplawski, Andrzej B, Gomes, Alicia R, Madanecki, Piotr, Fu, Chuanhua, Crowley, Michael R, Crossman, David K, Armstrong, Linlea, Babovic-Vuksanovic, Dusica, Bergner, Amanda, Blakeley, Jaishri O, Blumenthal, Andrea L, Daniels, Molly S, Feit, Howard, Gardner, Kathy, Hurst, Stephanie, Kobelka, Christine, Lee, Chung, Nagy, Rebecca, Rauen, Katherine A, Slopis, John M, Suwannarat, Pim, Westman, Judith A, Zanko, Andrea, Korf, Bruce R, Messiaen, Ludwine M

Volltext

Genetic Counseling for Neurofibromatosis 1, Neurofibromatosis 2, and Schwannomatosis—Practice Resource of the National Society of Genetic Counselors von Radtke, Heather B., Bergner, Amanda L., Goetsch, Allison L., McGowan, Caroline, Panzer, Karin, Cannon, Ashley

Volltext

Choices for return of primary and secondary genomic research results of 790 members of families with Mendelian disease von Fiallos, Katie, Applegate, Carolyn, Mathews, Debra Jh, Bollinger, Juli, Bergner, Amanda L, James, Cynthia A

Volltext

Patient-reported outcomes of pain and physical functioning in neurofibromatosis clinical trials von Wolters, Pamela L, Martin, Staci, Merker, Vanessa L, Tonsgard, James H, Solomon, Sondra E, Baldwin, Andrea, Bergner, Amanda L, Walsh, Karin, Thompson, Heather L, Gardner, Kathy L, Hingtgen, Cynthia M, Schorry, Elizabeth, Dudley, William N, Franklin, Barbara

Volltext

Knowledge and beliefs about epilepsy genetics among Hispanic and non-Hispanic patients von Trujillo, Shannon, Wetmore, John B, Camarillo, Itzel A, Misiewicz, Sylwia, May, Halie, Choi, Hyunmi, Siegel, Karolynn, Chung, Wendy K, Phelan, Jo C, Yang, Lawrence H, Leu, Cheng-Shiun, Bergner, Amanda L, Ottman, Ruth

Volltext

Dystrophic spinal deformities in a neurofibromatosis type 1 murine model von Rhodes, Steven D, Zhang, Wei, Yang, Dalong, Yang, Hao, Chen, Shi, Wu, Xiaohua, Li, Xiaohong, Yang, Xianlin, Mohammad, Khalid S, Guise, Theresa A, Bergner, Amanda L, Stevenson, David A, Yang, Feng-Chun

Volltext

The utility of limited Spanish proficiency in interpreted genetic counseling sessions von Waggoner, Rebecca M., Harkavy, Nina, Way, Lorraine, Florido, Michelle E., Sánchez, Adriana, Bergner, Amanda L.

Volltext

Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Resul... von Berrios, Courtney, James, Cynthia A., Raraigh, Karen, Bollinger, Juli, Murray, Brittney, Tichnell, Crystal, Applegate, Carolyn D., Bergner, Amanda L.

Volltext

Clinical response to bevacizumab in schwannomatosis von Blakeley, Jaishri, Schreck, Karisa C, Evans, D Gareth, Korf, Bruce R, Zagzag, David, Karajannis, Matthias A, Bergner, Amanda L, Belzberg, Allan J

Volltext

Patient experiences in receiving telegenetics care for inherited cardiovascular diseases von Temares, Dani S., Liang, Lusha W., Bergner, Amanda L., Reilly, Muredach P., Kalia, Isha

Volltext

Reflections on diversity, equity, and inclusion in genetic counseling education von Bao, Annie K., Bergner, Amanda L., Chan‐Smutko, Gayun, Villiers, Janelle

Volltext

The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm von Bergner, Amanda L., Ecker, Lindsey Alico, Ernst, Michelle E., Goelz, Monika Zak, Habermann, Kristina, Karger, Lisa, Zinberg, Randi E.

Volltext

Spectrum and Prevalence of Vasculopathy in Pediatric Neurofibromatosis Type 1 von Kaas, Bonnie, Huisman, Thierry A. G. M., Tekes, Aylin, Bergner, Amanda, Blakeley, Jaishri O., Jordan, Lori C.

Volltext

Improvement in Patient-reported Hearing After Treatment With Bevacizumab in People With Neurofibromatosis Type 2 von Huang, Victoria, Bergner, Amanda L, Halpin, Chris, Merker, Vanessa L, Sheridan, Monica R, Widemann, Brigitte C, Blakeley, Jaishri O, Plotkin, Scott R

Volltext