Julianne M O'Daniel (Julianne O'Daniel)

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 10

Top Topics

Urinary Tract Infection

Gestational Age

Top Venues

Genetics in medicine : official journal of the American College of Medical Genetics

Journal of personalized medicine

Journal of genetic counseling

Personalized medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Kimberly S Foss, Julianne M O'Daniel, Jonathan S Berg, Sabrina N Powell, Rosemary Jean Cadigan, Kristine J Kuczynski, Laura V Milko, Katherine W Saylor, Megan Roberts, Karen Weck, Gail E Henderson
Correction: Foss et al. The Rise of Population Genomic Screening: Characteristics of Current Programs and the Need for Evidence Regarding Optimal Implementation. J. Pers. Med. 2022, 12 , 692. Journal of personalized medicine 14 (3) (2024)
Kimberly S Foss, Julianne M O'Daniel, Jonathan S Berg, Sabrina N Powell, Rosemary Jean Cadigan, Kristine J Kuczynski, Laura V Milko, Katherine W Saylor, Megan Roberts, Karen Weck, Gail E Henderson
Correction: Foss et al. The Rise of Population Genomic Screening: Characteristics of Current Programs and the Need for Evidence Regarding Optimal Implementation. J. Pers. Med. 2022, 12 , 692. Journal of personalized medicine 14 (3) (2024)
Kimberly S Foss, Julianne M O'Daniel, Jonathan S Berg, Sabrina N Powell, Rosemary Jean Cadigan, Kristine J Kuczynski, Laura V Milko, Katherine W Saylor, Megan Roberts, Karen Weck, Gail E Henderson
The Rise of Population Genomic Screening: Characteristics of Current Programs and the Need for Evidence Regarding Optimal Implementation. Journal of personalized medicine 12 (5) (2022)
Sabrina A Suckiel, Julianne M O'Daniel, Katherine E Donohue, Katie M Gallagher, Marian J Gilmore, Laura Godfrey Hendon, Galen Joseph, Billie R Lianoglou, Jennifer M Mathews, Mary E Norton, Jacqueline A Odgis, Alexis F Poss, Shannon Rego, Sarah R Scollon, Tiffany Yip, Laura M Amendola
Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium. Journal of personalized medicine 11 (3) (2021)
Ida Griesemer, Brooke S Staley, Alexandra F Lightfoot, Lizzy Bain, Derrick Byrd, Carol Conway, Tracey L Grant, Barbara Leach, Laura V Milko, Lonna Mollison, Nadiah Porter, Sharron Reid, Gerri Smith, Margaret Waltz, Jonathan S Berg, Christine Rini, Julianne M O'Daniel
Engaging community stakeholders in research on best practices for clinical genomic sequencing. Personalized medicine 17 (6) (2020)
Christine M Rini, Gail E Henderson, James P Evans, Jonathan S Berg, Ann Katherine M Foreman, Ida Griesemer, Margaret Waltz, Julianne M O'Daniel, Myra I Roche
Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes. Genetics in medicine : official journal of the American College of Medical Genetics 22 (1) (2019)
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia
Secondary findings: How did we get here, and where are we going? Journal of genetic counseling 28 (2) (2019)
Nina Tan, Laura M Amendola, Julianne M O'Daniel, Amber A Burt, Martha J Horike-Pyne, Lacey Boshe, Gail E Henderson, Christine M Rini, Myra I Roche, Bert B A de Vries, Wylie Burke, Benjamin S Wilfond, David L Veenstra
Is "incidental finding" the best term?: a study of patients' preferences. Genetics in medicine : official journal of the American College of Medical Genetics 19 (2) (2016)
Jessica Ezzell Hunter, Stephanie A Irving, Leslie G Biesecker, Adam H Buchanan, Brian Jensen, Kristy Lee, Christa Lese Martin, Laura Milko, Kristin R Muessig, Annie D Niehaus, Julianne M O'Daniel, Margaret A Piper, Erin M Ramos, Sheri D Schully, Alan F Scott, Anne Slavotinek, Nara Sobreira, Natasha Strande, Meredith Weaver, Elizabeth M Webber, Marc S Williams, Jonathan S Berg, James P Evans, Katrina A B Goddard
A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation. Genetics in medicine : official journal of the American College of Medical Genetics 18 (12) (2016)
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin, Gregory M Cooper, Soma Das, Joshua L Deignan, Michael O Dorschner, James P Evans, Arezou A Ghazani, Katrina A B Goddard, Michele C Gornick, Kelly D F Hagman, Tina Hambuch, Madhuri Hegde, Lucia A Hindorff, Ingrid A Holm, Gail P Jarvik, Amy Knight Johnson, Lindsey Mighion, Massimo Morra, Sharon E Plon, Sumit Punj, Carolyn Sue Richards, Avni Santani, Brian H Shirts, Nancy B Spinner, Sha Tang, Karen E Weck, Susan M Wolf, Yaping Yang, Michael J Bamshad
A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories. Genetics in medicine : official journal of the American College of Medical Genetics 19 (5) (2016)
Jonathan S Berg, Ann Katherine M Foreman, Julianne M O'Daniel, Jessica K Booker, Lacey Boshe, Timothy Carey, Kristy R Crooks, Brian C Jensen, Eric T Juengst, Kristy Lee, Daniel K Nelson, Bradford C Powell, Cynthia M Powell, Myra I Roche, Cecile Skrzynia, Natasha T Strande, Karen E Weck, Kirk C Wilhelmsen, James P Evans
A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing. Genetics in medicine : official journal of the American College of Medical Genetics 18 (5) (2015)