Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Giovanna T. Braganza"'
Autor:
Kathryn Dubowski, Giovanna T. Braganza, Anne Bozack, Elena Colicino, Nicholas DeFelice, Laura McGuinn, Duncan Maru, Alison G. Lee
Publikováno v:
Annals of Medicine, Vol 55, Iss 1, Pp 12-23 (2023)
AbstractBackground We have an incomplete understanding of COVID-19 characteristics at hospital presentation and whether underlying subphenotypes are associated with clinical outcomes and therapeutic responses.Methods For this cross-sectional study, w
Externí odkaz:
https://doaj.org/article/05d0f86fd4d146b38ea1cb4d68d3d30c
Autor:
Noura S. Abul-Husn, Emily R. Soper, Giovanna T. Braganza, Jessica E. Rodriguez, Natasha Zeid, Sinead Cullina, Dean Bobo, Arden Moscati, Amanda Merkelson, Ruth J. F. Loos, Judy H. Cho, Gillian M. Belbin, Sabrina A. Suckiel, Eimear E. Kenny
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-11 (2021)
Abstract Background Population-based genomic screening has the predicted ability to reduce morbidity and mortality associated with medically actionable conditions. However, much research is needed to develop standards for genomic screening and to und
Externí odkaz:
https://doaj.org/article/622c943747f5441b88bd76675c60c7ad
Autor:
Sabrina A. Suckiel, Giovanna T. Braganza, Karla López Aguiñiga, Jacqueline A. Odgis, Katherine E. Bonini, Eimear E. Kenny, Jada G. Hamilton, Noura S. Abul-Husn
Publikováno v:
Genetics in Medicine. 24:1217-1226
As polygenic risk scores (PRS) emerge as promising tools to inform clinical care, there is a pressing need for patient-centered evidence to guide their implementation, particularly in diverse populations. Here, we conducted in-depth interviews of div
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcc0b1477d4c9298b2ec88eefcfedbaf
https://doi.org/10.1016/j.gim.2022.03.006
https://doi.org/10.1016/j.gim.2022.03.006
Autor:
Giovanna T. Braganza, Emily R. Soper, Ruth J. F. Loos, Noura S. Abul-Husn, Sinead Cullina, Amanda Merkelson, Judy H. Cho, Arden Moscati, Jessica E. Rodriguez, Dean Bobo, Gillian M. Belbin, Sabrina A. Suckiel, Natasha Zeid, Eimear E. Kenny
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-11 (2021)
Genome Medicine
Genome Medicine
BackgroundPopulation-based genomic screening has the predicted ability to reduce morbidity and mortality associated with medically actionable conditions. However, much research is needed to develop standards for genomic screening and to understand th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e065aee1ec866a93892547e0a657cee
https://doaj.org/article/622c943747f5441b88bd76675c60c7ad
https://doaj.org/article/622c943747f5441b88bd76675c60c7ad
Autor:
Kathryn Dubowski, Giovanna T. Braganza, Anne Bozack, Elena Colicino, Nicholas DeFelice, Laura McGuinn, Duncan Maru, Alison G. Lee
We have an incomplete understanding of COVID-19 characteristics at hospital presentation and whether underlying subphenotypes are associated with clinical outcomes and therapeutic responses. For this cross-sectional study, we extracted electronic hea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b47eb2e80869a692472acb9bc8edd970
Autor:
Sabrina A. Suckiel, Amy R Kontorovich, Emily R. Soper, Noura S. Abul-Husn, Eimear E. Kenny, Giovanna T. Braganza
Publikováno v:
Journal of Personalized Medicine
Journal of Personalized Medicine, Vol 11, Iss 49, p 49 (2021)
Volume 11
Issue 1
Journal of Personalized Medicine, Vol 11, Iss 49, p 49 (2021)
Volume 11
Issue 1
The TTR V142I variant associated with hereditary transthyretin amyloidosis (hATTR) is present in up to 4% of African American (AA) and 1% of Hispanic/Latinx (HL) individuals and increases risk for heart failure. Delayed and missed diagnoses could pot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6ba7ad7c27782a7ba66135c3dd9f388
http://europepmc.org/articles/PMC7829706
http://europepmc.org/articles/PMC7829706
Autor:
Noura S. Abul-Husn, Sabrina A. Suckiel, Giovanna T. Braganza, Emily R. Soper, Eimear E. Kenny
Publikováno v:
Molecular Genetics and Metabolism. 132:S351-S352
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8033b400258790449098cb74cadfcfd
https://doi.org/10.1016/s1096-7192(21)00618-1
https://doi.org/10.1016/s1096-7192(21)00618-1