Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Whitney, Espinel"'
Autor:
Samantha Greenberg, Saundra S. Buys, Sandra L. Edwards, Whitney Espinel, Alison Fraser, Amanda Gammon, Brent Hafen, Kimberly A. Herget, Wendy Kohlmann, Camille Roundy, Carol Sweeney
Publikováno v:
Cancer Medicine, Vol 8, Iss 15, Pp 6789-6798 (2019)
Abstract Background Personal cancer diagnosis and family cancer history factor into which individuals should undergo genetic testing for hereditary breast and ovarian cancer (HBOC) syndrome. Family history is often determined in the research setting
Externí odkaz:
https://doaj.org/article/3f74e0ad364245f5a1cd9bb163cbe299
Autor:
Bonnie Poteet, Nadia Ali, Cecelia Bellcross, Stephanie L. Sherman, Whitney Espinel, Heather Hipp, Emily G. Allen
Publikováno v:
Journal of Assisted Reproduction and Genetics. 40:179-190
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb9bdb6b7f153eb827e4c70b3ef7b71b
https://doi.org/10.1007/s10815-022-02671-1
https://doi.org/10.1007/s10815-022-02671-1
Publikováno v:
JCO Precis Oncol
PURPOSE National Comprehensive Cancer Network guidelines for germline genetic testing have included pancreatic cancer in the context of additional family cancer history for many years but this was not recommended for patients with pancreatic ductal a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8852c18020fbbc4c43aef3d881aaa147
https://doi.org/10.1200/po.20.00199
https://doi.org/10.1200/po.20.00199
Autor:
Carolyn Winskill, Melody S. Goodman, Brianne M. Daly, Ashley Elrick, Ryan Mooney, Whitney Espinel, Wendy Kohlmann, Kimberly A. Kaphingst
Publikováno v:
Public Health Genomics.
Introduction: Many individuals who previously received negative genetic test results are eligible for updated testing. This study examined intention to communicate updated genetic test results to relatives in participants who previously received nega
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea350549fb4f6d4f0faa9854d73101ad
https://doi.org/10.1159/000528522
https://doi.org/10.1159/000528522
Autor:
Wendy Kohlmann, Ryan Mooney, Whitney Espinel, Kelsey Kehoe, Kimberly A. Kaphingst, Ashley Elrick
Publikováno v:
J Genet Couns
Women with a personal history of breast or ovarian cancer who previously had BRCA1/2 testing now have the opportunity for additional genetic risk information through multi-gene panel testing. However, little is known about women's receptivity to furt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84f315a6215d83e5af8738053274c123
https://doi.org/10.1002/jgc4.1513
https://doi.org/10.1002/jgc4.1513
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:
David E. Goldgar, Whitney Espinel, Jennie Vagher, Amanda Gammon, Kelsi J Hagerty, Emily W. Moody
Publikováno v:
JCO precision oncology. 3
PURPOSE To compare the classification of genetic variants reported on tumor genomic profiling (TGP) reports with germline classifications on clinical test results and ClinVar. Results will help to inform germline testing discussions and decisions in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4d484f632332c67faa7a1052a14b844
https://pubmed.ncbi.nlm.nih.gov/35100725
https://pubmed.ncbi.nlm.nih.gov/35100725
Autor:
Saundra S. Buys, Brent Hafen, Samantha Greenberg, Alison Fraser, Sandra L. Edwards, Kimberly Herget, Wendy Kohlmann, Whitney Espinel, Amanda Gammon, Carol Sweeney, Camille Roundy
Publikováno v:
Cancer Medicine
Cancer Medicine, Vol 8, Iss 15, Pp 6789-6798 (2019)
Cancer Medicine, Vol 8, Iss 15, Pp 6789-6798 (2019)
Background Personal cancer diagnosis and family cancer history factor into which individuals should undergo genetic testing for hereditary breast and ovarian cancer (HBOC) syndrome. Family history is often determined in the research setting through k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93e03ca4d45ce9bef94fb3c2de2961b5
http://europepmc.org/articles/PMC6825998
http://europepmc.org/articles/PMC6825998
Autor:
Devin M. Mann, Kadyn E Kimball, Shane Loomis, Amanda Gammon, Kelsi J Hagerty, Guilherme Del Fiol, Wendy Kohlmann, Priscilla A Chan, Whitney Espinel, Javier Gonzalez, Rachelle Lorenz Chambers, Saundra S. Buys, Kensaku Kawamoto, Dani Temares, Eric Goldberg, Melody S. Goodman, Tiffany R Martinez, Kimberly A. Kaphingst, Cecilia Kessler, Daniel Chavez-Yenter, Jessica Everett, Joshua D. Schiffman, Kelsey Kehoe, Rachel Hess, David W. Wetter, Ophira Ginsburg, Sarah Colonna, Rachel Monahan, Richard L. Bradshaw, Katie Tobik
Publikováno v:
BMC Health Services Research
BMC Health Services Research, Vol 21, Iss 1, Pp 1-14 (2021)
BMC Health Services Research, Vol 21, Iss 1, Pp 1-14 (2021)
Background Advances in genetics and sequencing technologies are enabling the identification of more individuals with inherited cancer susceptibility who could benefit from tailored screening and prevention recommendations. While cancer family history
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6aa2455ce9063bc03b8d21cb7e4c2ff
http://europepmc.org/articles/PMC8170651
http://europepmc.org/articles/PMC8170651
Autor:
Rachelle Lorenz Chambers, Devin M. Mann, Danielle Temares, Rachel Hess, Guilherme Del Fiol, Ophira Ginsburg, Eric Goldberg, Kensaku Kawamoto, Katie Tobik, Kadyn E Kimball, Richard L. Bradshaw, Rachel Monahan, Amanda Gammon, Daniel Chavez-Yenter, Saundra S. Buys, Kelsi J Hagerty, Kimberly A. Kaphingst, Cecilia Kessler, Wendy Kohlmann, Whitney Espinel, Michael Flynn
Publikováno v:
Journal of Medical Internet Research
Background Cancer genetic testing to assess an individual’s cancer risk and to enable genomics-informed cancer treatment has grown exponentially in the past decade. Because of this continued growth and a shortage of health care workers, there is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98edebea56b9d029254b264fd3c1e89b
https://doi.org/10.2196/29447
https://doi.org/10.2196/29447