Genomic sequencing research in pediatric cancer care: Decision making, attitudes, and perceived utility among adolescents and young adults and their parents

Authors: Gutierrez, Amanda M., Robinson, Jill O., Smith, Hadley S., Desrosiers-Battu, Lauren R., Scollon, Sarah R., Canfield, Isabel, Hsu, Rebecca L., Schneider, Nicole M., Parsons, D. Williams, Plon, Sharon E., Allen-Rhoades, Wendy, Majumder, Mary A., Malek, Janet, McGuire, Amy L.

Source: In Genetics in Medicine August 2024 26(8)

Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications

Authors: Murdock, David R., Venner, Eric, Muzny, Donna M., Metcalf, Ginger A., Murugan, Mullai, Hadley, Trevor D., Chander, Varuna, de Vries, Paul S., Jia, Xiaoming, Hussain, Aliza, Agha, Ali M., Sabo, Aniko, Li, Shoudong, Meng, Qingchang, Hu, Jianhong, Tian, Xia, Cohen, Michelle, Yi, Victoria, Kovar, Christie L., Gingras, Marie-Claude, Korchina, Viktoriya, Howard, Chad, Riconda, Daniel L., Pereira, Stacey, Smith, Hadley S., Huda, Zohra A., Buentello, Alexandria, Marino, Patricia R., Leiber, Lee, Balasubramanyam, Ashok, Amos, Christopher I., Civitello, Andrew B., Chelu, Mihail G., Maag, Ronald, McGuire, Amy L., Boerwinkle, Eric, Wehrens, Xander H.T., Ballantyne, Christie M., Gibbs, Richard A.

Source: In Genetics in Medicine December 2021 23(12):2404-2414

Where the Genetic Code Meets the Zip Code: Advancing Equity in Rare Disease Genomics.

Authors: Wojcik, Monica H., Smith, Hadley S., Fraiman, Yarden S.

Source: Hastings Center Report. Dec2024 Supplement 2, Vol. 54, pS49-S55. 7p.

Subject Terms: *HEALTH services accessibility, *GENOMICS, *MEDICAL technology, *DIVERSITY & inclusion policies, *SOCIAL determinants of health, *RARE diseases, *EQUALITY, *EVALUATION of medical care, *RACE, *QUALITY of life, *HEALTH equity, *MEDICAL screening, *SEQUENCE analysis

The motivation and process for developing a consortium‐wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient care.

Authors: Hoban, Hannah G., Yip, Tiffany A., Chau, Joanna C., Bensen, Jeannette T., Desrosiers, Lauren R., Finnila, Candice R., Hindorff, Lucia A., Kelly, Nicole R., Lynch, Frances L., Rolf, Bradley A., Smith, Hadley S., Wasserstein, Melissa P., Hassmiller Lich, Kristen

Source: CTS: Clinical & Translational Science; Jan2024, Vol. 17 Issue 1, p1-11, 11p

Subject Terms: PATIENT care, GENETIC testing, CONSORTIA, ACQUISITION of data, FLOW charts, NUCLEOTIDE sequencing

Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication.

Authors: Makhnoon, Sukh, Smith, Hadley S., Bednar, Erica M., Bhatt, Arjun, Turner, Llaran, Arun, Banu, Volk, Robert J., Peterson, Susan K.

Source: Journal of Community Genetics; Jul2021, Vol. 12 Issue 3, p439-447, 9p

Cost-effectiveness of Population-Wide Genomic Screening for Hereditary Breast and Ovarian Cancer in the United States.

Authors: Guzauskas, Gregory F., Garbett, Shawn, Zhou, Zilu, Spencer, Scott J., Smith, Hadley S., Hao, Jing, Hassen, Dina, Snyder, Susan R., Graves, John A., Peterson, Josh F., Williams, Marc S., Veenstra, David L.

Source: JAMA Network Open; 10/29/2020, Vol. 3 Issue 10, pe2022874-e2022874, 1p