Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Sarah Ratzel"'
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100683- (2023)
Externí odkaz:
https://doaj.org/article/c47594997f5242099017f93a43b532f5
Autor:
Adam Brufsky, Lauren Lenz, Anita Pudusseri, David Wright, Kashyap B. Patel, Brad T. Clifford, Tracey L. O'Connor, Sasha Strain, Fadi Kayali, Sarah Ratzel, Shelly Cummings, Ralf Kronenwett, Thomas Paul Slavin
Publikováno v:
Journal of Clinical Oncology. 40:537-537
537 Background: Current guidelines advise that individuals with estrogen receptor-positive (ER+) breast cancer (BC) undergo 5 years of endocrine therapy with consideration of up to 10 years of extended endocrine therapy (EET). The relative benefit of
Autor:
Sarah Ratzel, Sara B. Cullinan
Publikováno v:
The American Journal of Human Genetics. 108:1811-1812
Autor:
David Neil Cooper, Katsushi Tokunaga, Teri E. Klein, Karen E. Weck, Adya Misra, Johan T. den Dunnen, Kay E. Davies, Greg Barsh, Raymond Dalgleish, Sarah Ratzel, Huw Dorkins, Sara B. Cullinan, Jan Higgins, Heidi L. Rehm, Garry R. Cutting, Juergen K. V. Reichardt, Issei Imoto, Peter Freeman, Bruce R. Korf, Li Gong, Mark H. Paalman
Publikováno v:
Human Mutation: Variation, Informatics and Disease, 42(1), 3-7. WILEY
Higgins, J, Dalgleish, R, den Dunnen, J T, Barsh, G, Freeman, P J, Cooper, D N, Cullinan, S, Davies, K E, Dorkins, H, Gong, L, Imoto, I, Klein, T E, Korf, B, Misra, A, Paalman, M H, Ratzel, S, Reichardt, J K V, Rehm, H L, Tokunaga, K, Weck, K E & Cutting, G R 2020, ' Verifying Nomenclature of DNA Variants in Submitted Manuscripts : Guidance for Journals ', Human Mutation, vol. 42, no. 1, pp. 3-7 . https://doi.org/10.1002/humu.24144
Hum Mutat
Higgins, J, Dalgleish, R, den Dunnen, J T, Barsh, G, Freeman, P J, Cooper, D N, Cullinan, S, Davies, K E, Dorkins, H, Gong, L, Imoto, I, Klein, T E, Korf, B, Misra, A, Paalman, M H, Ratzel, S, Reichardt, J K V, Rehm, H L, Tokunaga, K, Weck, K E & Cutting, G R 2020, ' Verifying Nomenclature of DNA Variants in Submitted Manuscripts : Guidance for Journals ', Human Mutation, vol. 42, no. 1, pp. 3-7 . https://doi.org/10.1002/humu.24144
Hum Mutat
Documenting variation in our genomes is important for research and clinical care. Accuracy in the description of DNA variants is therefore essential. To address this issue, the Human Variome Project convened a committee to evaluate the feasibility of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a90f3a67def515123e59ab0ee9df5169
http://hdl.handle.net/1887/3195913
http://hdl.handle.net/1887/3195913
Autor:
Laura Brzeskiewicz, Breanna Roscow, April Beeks, Barb Kunz, Sarah Ratzel, Thomas Slavin, Shelly Cummings, Karen Tedesco, Robert Reid
Publikováno v:
Genetics in Medicine. 24:S34
Autor:
Sarah Ratzel, Sara B. Cullinan
Publikováno v:
The American Journal of Human Genetics. 107:1-2
Autor:
Sarah Ratzel, Sara B. Cullinan
Publikováno v:
The American Journal of Human Genetics. 105:443-444
Autor:
Sarah Ratzel, Sara Cullinan
Publikováno v:
The American Journal of Human Genetics. 103:633-634
Autor:
Sarah Ratzel, Sara B. Cullinan
Publikováno v:
The American Journal of Human Genetics. 100:839-840
Autor:
Sarah Ratzel, Sara B. Cullinan
Publikováno v:
The American Journal of Human Genetics. 99:1225-1226