Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kate, Shane"'
Autor:
Tasleem J. Padamsee, Christina Bijou, Paige Swinehart-Hord, Megan Hils, Anna Muraveva, Rachel J. Meadows, Kate Shane-Carson, Lisa D. Yee, Celia E. Wills, Electra D. Paskett
Publikováno v:
Breast Cancer Research, Vol 26, Iss 1, Pp 1-20 (2024)
Abstract Background To understand the dynamics that limit use of risk-management options by women at high risk of breast cancer, there is a critical need for research that focuses on patient perspectives. Prior research has left important gaps: exclu
Externí odkaz:
https://doaj.org/article/44ca7529ef874dbda6c9d1ed8c17f98b
Autor:
Rachel J Meadows, Anna Muraveva, Christina Bijou, Kate Shane-Carson, Coralia Balasca, Celia E Wills, Lisa D Yee, Electra D Paskett, Tasleem J Padamsee
Publikováno v:
Journal of the National Comprehensive Cancer Network. 20:EPR22-113
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66afa7e88132ce3535bd6549441e59eb
https://doi.org/10.6004/jnccn.2021.7263
https://doi.org/10.6004/jnccn.2021.7263
Autor:
Richard L. Haspel, Jonathan R. Genzen, Jay Wagner, Karen Fong, Rebecca Wilcox, Patricia V. Adem, Hana Anderson, James B. Atkinson, Leah W. Burke, Loren Joseph, Robin D. LeGallo, Madelyn Lew, Christina M. Lockwood, Rizwan Naeem, Hasan Rizvi, Julian Sanz Ortega, Kate Shane-Carson, Mark E. Sobel, Eric Suarez, Laura J. Tafe, Jason Wang, Rebecca L. Wilcox
Publikováno v:
Genetics in Medicine. 23:1151-1157
Purpose To assess, from the student perspective, medical school training in genetics and genomics. Methods In 2019, the Undergraduate Training in Genomics (UTRIG) Working Group developed genetics-related survey and knowledge questions for the RISE-FI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a957ed3bb096446b5548bd9f10550137
https://doi.org/10.1038/s41436-021-01100-5
https://doi.org/10.1038/s41436-021-01100-5
Autor:
Whitney, Espinel, Marjan, Champine, Heather, Hampel, Joanne, Jeter, Kevin, Sweet, Robert, Pilarski, Rachel, Pearlman, Kate, Shane, Pamela, Brock, Judith A, Westman, Lindsay, Kipnis, Jilliane, Sotelo, Anu, Chittenden, Samantha, Culver, Jill E, Stopfer, Katherine A, Schneider, Rosalba, Sacca, Diane R, Koeller, Shraddha, Gaonkar, Erica, Vaccari, Sarah, Kane, Scott T, Michalski, Shan, Yang, Sarah M, Nielsen, Sara L, Bristow, Stephen E, Lincoln, Robert L, Nussbaum, Edward D, Esplin
Publikováno v:
Cancers. 14(10)
Consensus guidelines for hereditary breast and ovarian cancer include management recommendations for pathogenic/likely pathogenic (P/LP) variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::24cf0bd64bd4582859098cbce772d872
https://pubmed.ncbi.nlm.nih.gov/35626031
https://pubmed.ncbi.nlm.nih.gov/35626031
Autor:
Kate Shane-Carson, Joanne M. Jeter
Publikováno v:
Fundamentals of Cancer Prevention ISBN: 9783030159344
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b66b657b3b229a9702d1bf6a47b90e78
https://doi.org/10.1007/978-3-030-15935-1_6
https://doi.org/10.1007/978-3-030-15935-1_6
Autor:
Alexander Asamoah, Elizabeth A. Geiger, Bassem A. Bejjani, Berkley R. Powell, David D. Weaver, William I. Cohen, Elaine H. Zackai, Karen R Schmidt, Donna M. McDonald-McGinn, Heidi M. Feldman, Chad R. Haldeman-Englert, Justine Coppinger, Judy Phalin, Sulagna C. Saitta, Lisa G. Shaffer, Susan Lansky-Shafer, Blake C. Ballif, Aaron Theisen, Kate Shane, Joan F. Atkin, Robert Leland, Tamim H. Shaikh
Publikováno v:
Human Molecular Genetics. 18:1377-1383
Deletions of the 22q11.2 region distal to the 22q11.21 microdeletion syndrome region have recently been described in individuals with mental retardation and congenital anomalies. Because these deletions are mediated by low-copy repeats (LCRs), locate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0afe86b3fbca61e5c323b70573caad8
https://doi.org/10.1093/hmg/ddp042
https://doi.org/10.1093/hmg/ddp042
Autor:
Kristi K. Fitzgerald, Paige Kaplan, Manuela Priolo, Patrick Edery, Maarit Peippo, Kate Shane, Holly H. Hobart, Esra Manguoğlu, Edwin J. Young, Carolyn B. Mervis, Yves Lacassie, Masafumi Morimoto, Cédric Howald, Lucy R. Osborne, Sibel Berker-Karauzum, Ariel M. Pani, Alexandre Reymond, Colleen A. Morris, Ronald G. Gregg, Christian R. Marshall, Orsetta Zuffardi, May Tassabehji, Ikuko Kondo, Stephen W. Scherer, Mary Louise Freckmann
Publikováno v:
The American Journal of Human Genetics. 83(1):106-111
Infantile spasms (IS) is the most severe and common form of epilepsy occurring in the first year of life. At least half of IS cases are idiopathic in origin, with others presumed to arise because of brain insult or malformation. Here, we identify a l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f5c8785609bc173c596be5c3a450ef8
Autor:
Kate, Shane
Publikováno v:
Securities Industry News. Summer2003 Supplement, Vol. 15 Issue 23, p4. 2p.