Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Linda S Robinson"'
Autor:
Linda S. Robinson, Ashley Hendrix, Xian-Jin Xie, Jingsheng Yan, Sara Pirzadeh-Miller, Mary Pritzlaff, Parker Read, Sarah Pass, David Euhus, Theodora S. Ross
Publikováno v:
EBioMedicine, Vol 2, Iss 11, Pp 1827-1833 (2015)
Background: The US Preventative Service Task Force recommends that physicians perform a genetic risk assessment to identify women at risk for BRCA1/2 mutations associated with hereditary breast and ovarian cancer (HBOC) syndrome. However, outcomes da
Externí odkaz:
https://doaj.org/article/a8538bdf7e24433eb2dcded4c125fc8e
Autor:
Samantha B. Foley, Jonathan J. Rios, Victoria E. Mgbemena, Linda S. Robinson, Heather L. Hampel, Amanda E. Toland, Leslie Durham, Theodora S. Ross
Publikováno v:
EBioMedicine, Vol 2, Iss 1, Pp 74-81 (2015)
Despite the potential of whole-genome sequencing (WGS) to improve patient diagnosis and care, the empirical value of WGS in the cancer genetics clinic is unknown. We performed WGS on members of two cohorts of cancer genetics patients: those with BRCA
Externí odkaz:
https://doaj.org/article/1f198127c83440ceb15c422f19f3476a
Publikováno v:
Journal of Genetic Counseling. 26:716-727
This study explores the potential impact of the genetic counseling assistant (GCA) position on the efficiency of the genetic counseling field, evaluates attitudes regarding expansion of the genetic counseling field to include the GCA, and presents da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a889225e72c8c6a635ad7286629a84a5
https://doi.org/10.1007/s10897-016-0039-6
https://doi.org/10.1007/s10897-016-0039-6
Autor:
Parker Read, Sarah Pass, Sara Pirzadeh-Miller, Jingsheng Yan, David M. Euhus, Ashley Hendrix, Xian Jin Xie, Theodora S. Ross, Linda S. Robinson, Mary Pritzlaff
Publikováno v:
EBioMedicine, Vol 2, Iss 11, Pp 1827-1833 (2015)
EBioMedicine
EBioMedicine
Background The US Preventative Service Task Force recommends that physicians perform a genetic risk assessment to identify women at risk for BRCA1/2 mutations associated with hereditary breast and ovarian cancer (HBOC) syndrome. However, outcomes dat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15c8abd85cc6be4f43bbc68cfc5116ba
http://www.sciencedirect.com/science/article/pii/S2352396415301845
http://www.sciencedirect.com/science/article/pii/S2352396415301845
Autor:
Will K Thompson, K Floros, Isabel S Moore, Pieter E Krüger, Judy M Simpson, M N Pemberton, Devon M. Middleton, M Galliford, B Mastroianni, R R Rai, P. A. Higgins, Scott C. Steffensen, K Malcolm, Linda S Robinson, M Tarollo, L O Ingram, H Wooding, P Shorter, Janet A. Seeley, D Starkey, Kelly M. Gatfield, S M McPhail, M-T Borland, Stuart A Sievers, G Denham, K Lipski, S. Thomas, Daniel A Lim, Charles A. Steward, Taylor L. Delaney, David J. McInerney, David M Ng, K Squibb, Luiz C. di Stasi, C. Leigh Allen, A A Moore, Jacqueline M. Shanahan, R. Lane, M M Lewis, B Subramanian, N. Lawrence Edwards, F Foroudi, A. A. Roger Thompson, R Hallinan, Laurie K Stewart, H Neser, N Latta, S. T Hettige, C Lombardi, K Barnett, W Starbuck, B Lunt, M Bressel, S Soteriou, k Hailey, J McAlpine, Truyen D. Pham, P Rowntree, Megan K. Donovan, M. J Neep, D Robb, Nicola J. Platt, Katie A. Mullen, Hana M Russo, Jennifer J. Summerfield, A. A Brown, B Chesson, M Job, E Ungureanu, R Louwe, Gregory B. Taylor, P Podias, S G Nicholls, M van Beekhuizen, F Siddiqi, Melinda S Merchant, Jordan D. Collier, G Fogarty, T Kron, D Dephoff, I Tohotoa, K Piper, Kirsten E. Beattie, N Woznitza, K. Robert Clarke, Vinu S. Siva, E. J. Baxter, H Gunn, Jesse T Steffens, Heather K. Neilson, Christopher T. Barry, S Keats, Ernesto S. Lang, R. Kumar, L. L. Richter, Mark A Ainsworth, T.-T Nguyen, Nick E. Phillips
Publikováno v:
Journal of Medical Radiation Sciences. 62:1-36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62505a8cc4237527dd42bcf494aa25da
https://doi.org/10.1002/jmrs.112
https://doi.org/10.1002/jmrs.112
Autor:
Theodora S. Ross, Sara Pirzadeh-Miller, David M. Euhus, Mary Pritzlaff, Linda S. Robinson, Arielle Yorczyk, Tirun Lin
Publikováno v:
Journal of Genetic Counseling. 23:1034-1044
CancerGene Connect (CGC) is a web-based program that combines the collection of family and medical history, cancer risk assessment, psychosocial assessment, report templates, a result tracking system, and a patient follow up system. The performance o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::408651dda2d9f2ebe55953322da9520f
https://doi.org/10.1007/s10897-014-9732-5
https://doi.org/10.1007/s10897-014-9732-5
Autor:
Linda S. Robinson, Richard Fagen
Publikováno v:
Foreign Affairs. 66:441
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e59e3f9ddc99a4deb54558d6a654ada
https://doi.org/10.2307/20043419
https://doi.org/10.2307/20043419