Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Rachel Reingold"'
Autor:
Alexander Fedotov, Karen Marder, Anya Revah-Politi, Robert L. Klitzman, M. Verbitsky, Xueru Mu, Julia Wynn, Ian Halim, Hila Milo Rasouly, Karolynn Siegel, Sheena Kapoor, Stacy Piva, Manuela Orjuela, Elizabeth Cohn, Louise Bier, Jordan G. Nestor, Nicole Cuneo, Wendy K. Chung, Paul S. Appelbaum, Maria C. Alvarez, David Fasel, Anoushka Sinha, Yat S. So, Ali G. Gharavi, Karla Mehl, Natalie Lippa, Maddalena Marasa, Aileen Espinal, Krzysztof Kiryluk, Bianca Haser, Chunhua Weng, Rachel Reingold, Jill Goldman, Debanjana Chatterjee, Byum Hee Kil, Michelle E. Ernst, Jacqueline Jamir Thompson, Katherine D. Crew
Publikováno v:
Genet Med
Purpose: Recruitment of participants from diverse backgrounds is crucial to the generalizability of genetic research, but has proven challenging. We retrospectively evaluated recruitment methods used for a study on return of genetic results. Methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::061d146d4285fa1d4cea3f50ee45a67f
https://doi.org/10.1038/s41436-019-0497-y
https://doi.org/10.1038/s41436-019-0497-y
Autor:
Hila Milo-Rasouly, Sophia R. Cameron-Christie, Vimla Aggarwal, Carolina Haefliger, Byum Hee Kil, Adam Platt, Brett Copeland, Andrew S. Bomback, Wan Yee Lam, Natalie S Uy, Simone Sanna-Cherchi, Junying Zhang, Rachel Reingold, Zhong Ren, Stacy Piva, Adele Mitrotti, David J. Cohen, Debanjana Chatterjee, Ruth March, Emily E. Groopman, Maddalena Marasa, Drew Bradbury, Sumit Mohan, Michael DiVecchia, David Goldstein, Shumyle Alam, Colin D. Malone, Jordan G. Nestor, Jan Fleckner, Chunhua Weng, Gerald B. Appel, Yifu Li, Priya Krithivasan, Russell J. Crew, Neha Dagaonkar, Olivia Balderes, Karla Mehl, David Fasel, Holly J. Snyder, Maya K. Rao, Joshua Bridgers, Geoffrey K. Dube, Krzysztof Kiryluk, Pietro A. Canetta, Bengt Fellström, Ali G. Gharavi, Jai Radhakrishnan, Wooin Ahn, Caroline Mebane, Slavé Petrovski, Xueru Mu, Sitharthan Kamalakaran
Publikováno v:
New England Journal of Medicine. 380:142-151
BACKGROUND: Exome sequencing is emerging as a first-line diagnostic method in some clinical disciplines, but its usefulness has yet to be examined for most constitutional disorders in adults, including chronic kidney disease, which affects more than
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1e8c8b3cbd348e504a27d334077dccd
https://doi.org/10.1056/nejmoa1806891
https://doi.org/10.1056/nejmoa1806891
Publikováno v:
Pediatric dermatology. 34(5)
Alopecia areata (AA) is a common autoimmune disease and it is challenging to predict which patients will have severe disease. The purpose of this retrospective study was to identify comorbidities in children enrolled in the National Alopecia Areata R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf09228b5e3686836f82e4f96c7cd8dc
https://pubmed.ncbi.nlm.nih.gov/28884897
https://pubmed.ncbi.nlm.nih.gov/28884897
Autor:
BALDWIN, KARIN KRAMER, LEVIN, FRAYDA, MANDEL, RACHEL REINGOLD, CHECCHIO, ROBERT, CURTIUS, MARY, UDALL, JAY, VIRMANI, RON A., DODDS, LYNDON
Publikováno v:
New York Times. 6/7/2022, Vol. 171 Issue 59447, pA20-A20. 1/3p.
Publikováno v:
Affiliate; Jan/Feb2008, Vol. 33 Issue 3, p7-7, 1/2p