Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sarina Madhavan"'
Autor:
Jessica I. Gold, Sarina Madhavan, Joseph Park, Hana Zouk, Emma Perez, Alanna Strong, Theodore G. Drivas, Amel Karaa, Marc Yudkoff, Daniel Rader, Robert C. Green, Nina B. Gold
Publikováno v:
HGG Advances, Vol 4, Iss 4, Pp 100226- (2023)
Summary: Inherited metabolic disorders (IMDs) are variably expressive, complicating identification of affected individuals. A genotype-first approach can identify individuals at risk for morbidity and mortality from undiagnosed IMDs and can lead to p
Externí odkaz:
https://doaj.org/article/d1d3645f62dc4a9d9cf9303eb1234dc1
Autor:
Sarina Madhavan, Emily Bullis, Rachel Myers, Chris J Zhou, Elise M Cai, Anu Sharma, Shreya Bhatia, Lori A Orlando, Susanne B Haga
Publikováno v:
PLoS ONE, Vol 14, Iss 10, p e0224283 (2019)
Family health history (FHH) is a key predictor of health risk and is universally important in preventive care. However, patients may not be aware of the importance of FHH, and thus, may fail to accurately or completely share FHH with health providers
Externí odkaz:
https://doaj.org/article/cd5b043b91c145999258517bd7145f15
Autor:
Eric A. Klein, Sarina Madhavan, Tomasz M. Beer, Chetan Bettegowda, Minetta C. Liu, Anne-Renee Hartman, Allan Hackshaw
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. :OF1-OF8
Cancer is a significant burden worldwide that adversely impacts life expectancy, quality of life, health care costs, and workforce productivity. Although currently recommended screening tests for individual cancers reduce mortality, they detect only
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbb4a6e17e45e7e38b968ea73dc8f4e3
https://doi.org/10.1158/1055-9965.epi-22-1275
https://doi.org/10.1158/1055-9965.epi-22-1275
Autor:
Allan Hackshaw, Anne-Renee Hartman, Minetta C. Liu, Chetan Bettegowda, Tomasz M. Beer, Sarina Madhavan, Eric A. Klein
Cancer types detected incidentally by NIPT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e31c4d59e0a8edc38382f9a123380fd
https://doi.org/10.1158/1055-9965.23268706
https://doi.org/10.1158/1055-9965.23268706
Autor:
Allan Hackshaw, Anne-Renee Hartman, Minetta C. Liu, Chetan Bettegowda, Tomasz M. Beer, Sarina Madhavan, Eric A. Klein
Cancer is a significant burden worldwide that adversely impacts life expectancy, quality of life, health care costs, and workforce productivity. Although currently recommended screening tests for individual cancers reduce mortality, they detect only
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bd140aadf5893f21f4f6f13767d7526
https://doi.org/10.1158/1055-9965.c.6672850
https://doi.org/10.1158/1055-9965.c.6672850
Autor:
Jade Connor, Natasha R. Johnson, Hanna Amanuel, Sarina Madhavan, Lydia E. Pace, Mugdha Mokashi, Deborah Bartz
Publikováno v:
Social Science & Medicine
Social Science & Medicine (1982)
Social Science & Medicine (1982)
Background The Covid-19 pandemic is straining healthcare systems in the US and globally, which has wide-reaching implications for health. Women experience unique health risks and outcomes influenced by their gender, and this narrative review aims to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65fa5651bed24651719adb5840b9039f
https://pubmed.ncbi.nlm.nih.gov/32950924
https://pubmed.ncbi.nlm.nih.gov/32950924
Autor:
Lori A. Orlando, Shreya Bhatia, Sarina Madhavan, Susanne B. Haga, Elise M. Cai, Rachel A. Myers, Emily Bullis, Chris J. Zhou, Anu Sharma
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 10, p e0224283 (2019)
PLoS ONE, Vol 14, Iss 10, p e0224283 (2019)
Family health history (FHH) is a key predictor of health risk and is universally important in preventive care. However, patients may not be aware of the importance of FHH, and thus, may fail to accurately or completely share FHH with health providers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6835c08bebfffcff4f5ac066419e8bbc
http://europepmc.org/articles/PMC6814221
http://europepmc.org/articles/PMC6814221
Autor:
David G. Ousterout, Eirik A. Moreb, Christopher E. Nelson, Sarina Madhavan, Xiufang Pan, Dongsheng Duan, Ruth M. Castellanos Rivera, Charles A. Gersbach, Feng Zhang, F. Ann Ran, Aravind Asokan, Pratiksha I. Thakore, Chady H. Hakim, Winston X. Yan
Publikováno v:
PMC
Duchenne muscular dystrophy (DMD) is a devastating disease affecting about 1 out of 5000 male births and caused by mutations in the dystrophin gene. Genome editing has the potential to restore expression of a modified dystrophin gene from the native
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4345882d294280cf1fd93584e113218
Autor:
Winston X. Yan, Ruth M. Castellanos, Charles A. Gersbach, Matthew Gemberling, Pratiksha I. Thakore, David G. Ousterout, Christopher E. Nelson, Dongsheng Duan, Chady H. Hakim, Xiufang Pan, Sarina Madhavan, Feng Zhang, F. Ann Ran, Aravind Asokan
Publikováno v:
Molecular Therapy. 24:S191
Duchenne muscular dystrophy (DMD) is a highly prevalent genetic disorder leading to muscle wasting, loss of ambulation, and premature death by the third decade of life. DMD is caused by gene deletions, duplications, or nonsense mutations leading to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b8246732c1e2f971d629bebe2bc8e4a
https://doi.org/10.1016/s1525-0016(16)33291-9
https://doi.org/10.1016/s1525-0016(16)33291-9