Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nykole Sutherland"'
Autor:
Nykole Sutherland, Wendy Kohlmann, Karen Curtin, Debra Ma, Therese Berry, Kelly Stantuci, Alison Fraser, Lisa Pappas, Taylor Jump, Nephi Walton, Nicola Camp
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100059- (2023)
Externí odkaz:
https://doaj.org/article/5a7d3a10c1c0438eb6681f70cf31d247
Autor:
Wendy Kohlmann, Kristen Pauley, Anne Naumer, Samantha Greenberg, Nicole Stevenson, Kelsey Ellis, Aciana Franco Roberts, Joshua Kawasaki, Taylor Jump, Nykole Sutherland
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100102- (2023)
Externí odkaz:
https://doaj.org/article/cd0df1a57aca4b658f19e099880600ef
Autor:
Nephi A. Walton, Brent Hafen, Sara Graceffo, Nykole Sutherland, Melanie Emmerson, Rachel Palmquist, Christine M. Formea, Maricel Purcell, Bret Heale, Matthew A. Brown, Christopher J. Danford, Sumathi I. Rachamadugu, Thomas N. Person, Katherine A. Shortt, G. Bryce Christensen, Jared M. Evans, Sharanya Raghunath, Christopher P. Johnson, Stacey Knight, Viet T. Le, Jeffrey L. Anderson, Margaret Van Meter, Teresa Reading, Derrick S. Haslem, Ivy C. Hansen, Betsey Batcher, Tyler Barker, Travis J. Sheffield, Bhaskara Yandava, David P. Taylor, Pallavi Ranade-Kharkar, Christopher C. Giauque, Kenneth R. Eyring, Jesse W. Breinholt, Mickey R. Miller, Payton R. Carter, Jason L. Gillman, Andrew W. Gunn, Kirk U. Knowlton, Joshua L. Bonkowsky, Kari Stefansson, Lincoln D. Nadauld, Howard L. McLeod
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 11, p 1867 (2022)
The clinical use of genomic analysis has expanded rapidly resulting in an increased availability and utility of genomic information in clinical care. We have developed an infrastructure utilizing informatics tools and clinical processes to facilitate
Externí odkaz:
https://doaj.org/article/8b0660b1dc4e4da79aa63cdd53ff0344
Publikováno v:
Journal of genetic counselingREFERENCES. 29(4)
Transgender (TG) individuals have higher rates of mortality associated with cancer diagnoses, in part due to avoidance of gender-assigned cancer screenings resulting in later stages at diagnosis. Knowledge about the risks of breast or gynecological c
Autor:
Neetha Sama, Wendy Kohlmann, Lisa Pappas, Stevie Kinnear, Therese Berry, Debra Ma, Sarah Colonna, Alison Fraser, Nykole Sutherland, Joanne M. Jeter
Publikováno v:
Journal of Clinical Oncology. 39:e22529-e22529
e22529 Background: Genetic testing for hereditary breast/ovarian cancer (HBOC) continues to be underutilized, and options for population-based assessment of testing barriers and outcomes are lacking. This project uses linkages between statewide data