11. Genomic Testing: a Genetic Counselor's Personal Reflection on Three Years of Consenting and Testing. Issue 4 (5th August 2015) Authors: Wynn, Julia Journal: Journal of genetic counseling Issue: Volume 25:Issue 4(2016) Page Start: 691 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Illustrative case studies in the return of exome and genome sequencing results. (June 2015) Authors: Amendola, Laura M; Lautenbach, Denise; Scollon, Sarah; Bernhardt, Barbara; Biswas, Sawona; East, Kelly; Everett, Jessica; Gilmore, Marian J; Himes, Patricia; Raymond, Victoria M; Wynn, Julia; Hart, Ragan; Jarvik, Gail P Journal: Personalized medicine Issue: Volume 12:Number 3(Year 2015) Page Start: 283 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents. (13th July 2021) Authors: Ahimaz, Priyanka; Sabatello, Maya; Qian, Min; Wang, Aijin; Miller, Erin M.; Parrott, Ashley; Lal, Ashwin K.; Chatfield, Kathryn C.; Rossano, Joseph W.; Ware, Stephanie M.; Parent, John J.; Kantor, Paul; Yue, Lisa; Wynn, Julia; Lee, Teresa M.; Addonizio, Linda J.; Appelbaum, Paul S.; Chung, Wendy K. Journal: Circulation Issue: Volume 14:Number 4(2021) Page Start: e003189 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients. Issue 5 (29th March 2017) Authors: Lumish, Heidi S.; Steinfeld, Hallie; Koval, Carrie; Russo, Donna; Levinson, Elana; Wynn, Julia; Duong, James; Chung, Wendy K. Journal: Journal of genetic counseling Issue: Volume 26:Issue 5(2017) Page Start: 1116 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Impact of patient education videos on genetic counseling outcomes after exome sequencing. Issue 1 (January 2020) Authors: Hernan, Rebecca; Cho, Megan T.; Wilson, Ashley L.; Ahimaz, Priyanka; Au, Catherine; Berger, Sara M.; Guzman, Edwin; Primiano, Michelle; Shaw, Jessica E.; Ross, Meredith; Tabanfar, Leyla; Chilton, Ilana; Griffin, Emily; Ratner, Chana; Anyane-Yeboa, Kwame; Iglesias, Alejandro; Pisani, Laura; Roohi,... Journal: Patient education and counseling Issue: Volume 103:Issue 1(2020) Page Start: 127 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Impact of Receiving Secondary Results from Genomic Research: A 12‐Month Longitudinal Study. Issue 3 (22nd November 2017) Authors: Wynn, Julia; Martinez, Josue; Bulafka, Jessica; Duong, Jimmy; Zhang, Yuan; Chiuzan, Codruta; Preti, Jain; Cremona, Maria L.; Jobanputra, Vaidehi; Fyer, Abby J.; Klitzman, Robert L.; Appelbaum, Paul S.; Chung, Wendy K. Journal: Journal of genetic counseling Issue: Volume 27:Issue 3(2018) Page Start: 709 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies. (4th May 2022) Authors: Kernie, Catherine G.; Wynn, Julia; Rosenbaum, Allison; de Voest, Jessica; Galloway, Stephanie; Giordano, Jessica; Stover, Samantha; Westerfield, Lauren; Gilmore, Kelly; Wapner, Ronald J.; Van den Veyver, Ignatia B.; Vora, Neeta L.; Clifton, Rebecca G.; Caughey, Aaron B.; Chung, Wendy K. Other Names: Van den Veyver Igna guestEditor. Journal: Prenatal diagnosis Issue: Volume 42:Number 7(2022) Page Start: 947 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects. Issue 12 (7th June 2017) Authors: Kruszka, Paul; Tanpaiboon, Pranoot; Neas, Katherine; Crosby, Kathleen; Berger, Seth I; Martinez, Ariel F; Addissie, Yonit A; Pongprot, Yupada; Sittiwangkul, Rekwan; Silvilairat, Suchaya; Makonkawkeyoon, Krit; Yu, Lan; Wynn, Julia; Bennett, James T; Mefford, Heather C; Reynolds, William T; Liu, Xi... Journal: Journal of medical genetics Issue: Volume 54:Issue 12(2017) Page Start: 825 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Measuring quality and value in genetic counseling: The current landscape and future directions. Issue 2 (17th November 2022) Authors: Higgs, Emily; Wain, Karen E.; Wynn, Julia; Cho, Megan T.; Higgins, Sonja; Blaisdell, David; Dugan, Donna; Valek, Sara; Cohen, Stephanie Journal: Journal of genetic counseling Issue: Volume 32:Issue 2(2023) Page Start: 315 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Nonspecific phenotype of Noonan syndrome diagnosed by whole exome sequencing. Issue 4 (2nd February 2015) Authors: Coromilas, Alexandra; Wynn, Julia; Haverfield, Eden; Chung, Wendy K. Journal: Clinical case reports Issue: Volume 3:Issue 4(2015:Aug.) Page Start: 237 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗