Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Julie Harris-Wai"'
Autor:
Amy A. Lemke, Edward D. Esplin, Aaron J. Goldenberg, Claudia Gonzaga-Jauregui, Neil A. Hanchard, Julie Harris-Wai, Justin E. Ideozu, Rosario Isasi, Andrew P. Landstrom, Anya E.R. Prince, Erin Turbitt, Maya Sabatello, Samantha A. Schrier Vergano, Matthew R.G. Taylor, Joon-Ho Yu, Kyle B. Brothers, Nanibaa’ A. Garrison
Publikováno v:
Am J Hum Genet
The vision of the American Society of Human Genetics (ASHG) is that people everywhere will realize the benefits of human genetics and genomics. Implicit in that vision is the importance of ensuring that the benefits of human genetics and genomics res
Autor:
Joni A. Mayer, Julie Harris-Wai, Deborah J. Bowen, Jennifer L. Hay, Hendrika Meischke, Wylie Burke
Publikováno v:
Cancer Causes & Control. 30:225-233
OBJECTIVES: Melanoma can be prevented through reducing sun exposure and detected early by increasing examination of skin for lesions. First-degree relatives of melanoma cases have higher risk than the general population and therefore could be targets
Publikováno v:
The patient. 13(5)
Hemophilia is an inherited disease for which current treatment is noncurative. While gene therapy and gene editing are being researched, we do not know how the hemophilia community perceives them. Herein, we explore the beliefs and values regarding t
Publikováno v:
Public Health Genomics. 21:207-216
Background: Beginning in 2005, researchers at Kaiser Permanente Northern California (KPNC) Division of Research developed the Research Program on Genes, Environment, and Health (RPGEH), a research resource of linked biospecimens, health surveys, and
Autor:
Deborah J. Bowen, Jingjing Yu, Kathleen M. West, Julie Harris-Wai, T Hyams, Melody S. Goodman
Publikováno v:
Clinical and Translational Science. 10:314-336
Stakeholder engagement in research has received increasing attention in recent years.1, 2 The term “stakeholder engagement” refers to the process of meaningful involvement of those who are engaged in making decisions about programs.3 Engaging mem
Autor:
Alexander Guminski, Rajneesh Kaur, Craig R. Lewis, Bettina Meiser, Melvin Chin, Robyn L. Ward, Sian K Smith, Nadine A. Kasparian, A.M. Menzies, Georgina V. Long, Julie Harris-Wai, Roger Liang
Publikováno v:
Asia-Pacific Journal of Clinical Oncology. 11:105-182
Families often bear the burden of communication about cancer risk, as well as support during and after treatment for cancer in family members. These activities are left up to survivors and their families, with little support or knowledge of useful me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd0eee7333a37f03339978068bdd9050
https://europepmc.org/articles/PMC5624814/
https://europepmc.org/articles/PMC5624814/
Autor:
Pui-Yan Kwok, Joshua E. Petrikin, Galen Joseph, Cynthia M. Powell, Barbara A. Koenig, Joseph T. Shieh, Anastasia L. Wise, Megan A. Lewis, Robert Currier, Flavia Chen, Julie Harris-Wai, Sean D. Mooney, Richard B. Parad, Timothy W. Yu, Michael S. Watson, Myra I. Roche, Tiina K. Urv, Neil Risch, Bradford C. Powell, Robert C. Green, Ozge Ceyhan-Birsoy, Laurel K. Willig, Ingrid A. Holm, Stephen F. Kingsmore, Amy L. McGuire, Heidi L. Rehm, Julie A. Cakici, Donald B. Bailey, Steven J. Leeder, Stacey Pereira, Alan H. Beggs, Narayanan Veeraraghavan, Dmitry Dukhovny, Steven E. Brenner, Amy Brower, Jennifer M. Puck, Pankaj B. Agrawal, John D. Lantos, Laura V. Milko, Jonathan S. Berg, Brenda Iglesias, Kee Chan
Publikováno v:
Pediatrics, vol 139, iss 2
Berg, JS; Agrawal, PB; Bailey, DB; Beggs, AH; Brenner, SE; Brower, AM; et al.(2017). Newborn sequencing in genomic medicine and public health. Pediatrics, 139(2). doi: 10.1542/peds.2016-2252. UCSF: Retrieved from: http://www.escholarship.org/uc/item/68b8k0r9
Berg, JS; Agrawal, PB; Bailey, DB; Beggs, AH; Brenner, SE; Brower, AM; et al.(2017). Newborn sequencing in genomic medicine and public health. Pediatrics, 139(2). doi: 10.1542/peds.2016-2252. UCSF: Retrieved from: http://www.escholarship.org/uc/item/68b8k0r9
© 2017 by the American Academy of Pediatrics. The rapid development of genomic sequencing technologies has decreased the cost of genetic analysis to the extent that it seems plausible that genomescale sequencing could have widespread availability in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd0f5cc7bcb558bee0675ccdbd1e7569
https://escholarship.org/uc/item/68b8k0r9
https://escholarship.org/uc/item/68b8k0r9
Autor:
Barbara A. Koenig, Jennifer M. Puck, Charlotte Young, Flavia Chen, Julie Harris-Wai, Galen Joseph
Publikováno v:
Joseph, G; Chen, F; Harris-Wai, J; Puck, JM; Young, C; & Koenig, BA. (2016). Parental views on expanded newborn screening using whole-genome sequencing. Pediatrics, 137, S36-S46. doi: 10.1542/peds.2015-3731H. UCSF: Retrieved from: http://www.escholarship.org/uc/item/49b3h8wj
Pediatrics, vol 137 Suppl 1, iss Suppl 1
Pediatrics, vol 137 Suppl 1, iss Supplement
Pediatrics, vol 137 Suppl 1, iss Suppl 1
Pediatrics, vol 137 Suppl 1, iss Supplement
Copyright © 2016 by the American Academy of Pediatrics. BACKGROUND AND OBJECTIVE: The potential application of whole-genome sequencing (WGS) to state-mandated standard newborn screening (NBS) challenges the traditional public health approach to NBS
Autor:
Amy A. Lemke, Julie Harris-Wai
Along with rapid advances in human genomics, policies governing genomic data and clinical technologies have proliferated. Stakeholder engagement is widely lauded as an important methodology for improving clinical, scientific, and public health policy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b97701fe96db73e12b91d98d3f9fb8aa
https://europepmc.org/articles/PMC4567945/
https://europepmc.org/articles/PMC4567945/