Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Matthew Norstad"'
Publikováno v:
New Genetics and Society, Vol 41, Iss 3, Pp 216-226 (2022)
Addressing health disparities has become a central remit for conducting health research. In the following paper, we explore the conceptual and methodological challenges posed by the call to recruit medically underserved populations. This exploration
Externí odkaz:
https://doaj.org/article/ca9528a7c2254d85a22416a07958e406
Autor:
Julia E. H. Brown, Astrid N. Zamora, Simon Outram, Teresa N. Sparks, Billie R. Lianoglou, Matthew Norstad, Nuriye N. Sahin Hodoglugil, Mary E. Norton, Sara L. Ackerman
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Genomic sequencing has been increasingly utilized for prenatal diagnosis in recent years and this trend is likely to continue. However, decision-making for parents in the prenatal period is particularly fraught, and prenatal sequencing would signific
Externí odkaz:
https://doaj.org/article/780481f2793545d8a7c1a36291de325c
Autor:
Shannon Rego, Hannah Hoban, Simon Outram, Astrid N. Zamora, Flavia Chen, Nuriye Sahin-Hodoglugil, Beatriz Anguiano, Matthew Norstad, Tiffany Yip, Billie Lianoglou, Teresa N. Sparks, Mary E. Norton, Barbara A. Koenig, Anne M. Slavotinek, Sara L. Ackerman
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics, vol 24, iss 6
Genet Med
Genet Med
PURPOSE: Patients undergoing clinical exome sequencing (ES) are routinely offered the option to receive secondary findings (SF). However, little is known about the views of individuals from underrepresented minority pediatric or prenatal populations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd18a97d08f550f13061727b66733f0
https://doi.org/10.1016/j.gim.2022.02.004
https://doi.org/10.1016/j.gim.2022.02.004
Autor:
Barbara A. Koenig, Anne Slavotinek, Julia E.H. Brown, Mary E. Norton, Neil Risch, Matthew Norstad, Astrid N. Zamora, Simon Outram, Sara L. Ackerman
Publikováno v:
Genetics in Medicine. 24:410-418
This study aimed to understand broad data sharing decisions among predominantly underserved families participating in genomic research.Drawing on clinic observations, semistructured interviews, and survey data from prenatal and pediatric families enr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0ae57c0d6729e3b25fb35715e4b9374
https://doi.org/10.1016/j.gim.2021.09.021
https://doi.org/10.1016/j.gim.2021.09.021
Positive autoregulation has been repeatedly proposed as a mechanism for cells to adopt binary fates during embryonic development through bistability. However, without quantitatively determining their parameters, it is unclear whether the plethora of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b4c6339aac5d666d1207cd7dd6d7f06
https://doi.org/10.1101/2022.10.31.514335
https://doi.org/10.1101/2022.10.31.514335
Autor:
Barbara A. Koenig, Steven E. Brenner, Russ B. Altman, Gregory McInnes, Jodi Halpern, David Magnus, Sheng Wang, Aashish N. Adhikari, Megan L. Koleske, Renata C. Gallagher, Andrew G. Sharo, Kathleen M. Giacomini, Julia E.H. Brown, Matthew Norstad
Publikováno v:
American journal of human genetics, vol 108, iss 4
American Journal of Human Genetics
American Journal of Human Genetics
Summary Genome sequencing is enabling precision medicine—tailoring treatment to the unique constellation of variants in an individual’s genome. The impact of recurrent pathogenic variants is often understood, however there is a long tail of rare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a433117908dee100cd8bb1b9a46a185
https://escholarship.org/uc/item/0498z4kt
https://escholarship.org/uc/item/0498z4kt
Autor:
Renata C. Gallagher, Megan L. Koleske, Barbara A. Koenig, Jodi Halpern, Brown Jeh, Andrew G. Sharo, Steven E. Brenner, Aashish N. Adhikari, Russ B. Altman, Gregory McInnes, Kathleen M. Giacomini, David Magnus, Wang S, Matthew Norstad
Genome sequencing is enabling precision medicine—tailoring treatment to the unique constellation of variants in an individual’s genome. The impact of recurrent pathogenic variants is often understood, leaving a long tail of rare genetic variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4038116f0bd48764870274ada4e74e78
https://doi.org/10.20944/preprints202011.0599.v1
https://doi.org/10.20944/preprints202011.0599.v1