Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Kelsey Moyes"'
Autor:
Serenedy Smith, Kelsey Moyes, Christopher Arnell, Susan Manley, Jeanie Schaller, Ingrid Marino
Publikováno v:
Personalized Medicine. 14:213-220
Aim: To evaluate one laboratory's hereditary cancer testing clinical quality assurance (QA) process to minimize test-ordering errors. Methods: The proportion of tests canceled/revised due to pre-analytic QA processes or provider consultation prior to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b53467543be59f11203ecd6110649f89
https://doi.org/10.2217/pme-2016-0091
https://doi.org/10.2217/pme-2016-0091
Autor:
Ann G. Schwartz, David B. Zhen, Donghui Li, Lisa A. Cannon-Albright, Steven Gallinger, Gloria M. Petersen, Daniela Seminara, Michele L. Cote, Richard J. Wenstrup, Michael Goggins, Sapna Syngal, Kelsey Moyes, Nicholas J. Roberts, Kari G. Rabe, Robert R. McWilliams, Alison P. Klein, Anne Renee Hartman, Ralph H. Hruban
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
Familial pancreatic cancer kindreds contain at least two affected first-degree relatives. Comprehensive data are needed to assist clinical risk assessment and genetic testing.Germ-line DNA samples from 727 unrelated probands with positive family hist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a907d8ef712bde7c43eaa30ede54c70
https://doi.org/10.1038/gim.2014.153
https://doi.org/10.1038/gim.2014.153
Autor:
Richard J. Wenstrup, Jennifer Saam, John Abernethy, Heidi McCoy, Kelsey Moyes, Lavania Sharma, Michelle Landon
Publikováno v:
Cancer Research. 75:P4-12
Introduction: With the advancements of next generation sequencing, patients with a personal and/or family history of cancer that may not be suggestive of one cancer syndrome may be offered testing for mutations in multiple cancer-predisposing genes s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf53ca5bf6cfe78d1e05f546a84297cb
https://doi.org/10.1158/1538-7445.sabcs14-p4-12-02
https://doi.org/10.1158/1538-7445.sabcs14-p4-12-02
Autor:
Brent Evans, Richard J. Wenstrup, Kelsey Moyes, Krystal Brown, Michelle Landon, Jennifer Saam
Publikováno v:
Oncology. 89:221-226
Objective: Patients diagnosed with colorectal cancer before the age of 50 years are recommended for Lynch syndrome (LS) testing according to current clinical guidelines. However, many patients are not identified because of the stringent guidelines on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a35d69a5ee176fb3aa2b888fc910d441
https://doi.org/10.1159/000430097
https://doi.org/10.1159/000430097
Autor:
Aaron Theisen, Brian Morris, Richard J. Wenstrup, Iain D. Kerr, Paris Vail, Julie M. Eggington, Kelsey Moyes, Brianna C. Burdett, Aric van Kan
Publikováno v:
Journal of Community Genetics
Genetic variants of uncertain clinical significance (VUSs) are a common outcome of clinical genetic testing. Locus-specific variant databases (LSDBs) have been established for numerous disease-associated genes as a research tool for the interpretatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4fcc6dea9af2cc1332a17d4b1c2b42f
https://pubmed.ncbi.nlm.nih.gov/25782689
https://pubmed.ncbi.nlm.nih.gov/25782689
Publikováno v:
Breast cancer research and treatment. 149(1)
An estimated 1:40 individuals of Ashkenazi Jewish (AJ) ancestry carry one of three common founder mutations in BRCA1 or BRCA2, resulting in the inherited cancer condition, Hereditary Breast and Ovarian Cancer (HBOC) syndrome. Targeted testing for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::483bbca21af11a37eef1f3e1575a59c9
https://pubmed.ncbi.nlm.nih.gov/25850536
https://pubmed.ncbi.nlm.nih.gov/25850536
Autor:
Jennifer Saam, Michelle Landon, Kelsey Moyes, Richard J. Wenstrup, Christopher Arnell, Rajesh R. Kaldate, Kayon Williams
Publikováno v:
Oncology. 88(4)
Objectives: Patients with hereditary cancer syndromes are at high risk for a second primary cancer. Early identification of these patients after an initial cancer diagnosis is the key to implementing cancer risk-reducing strategies. Methods: A commer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81e50f972299a4a05ba893eac137e65f
https://pubmed.ncbi.nlm.nih.gov/25503195
https://pubmed.ncbi.nlm.nih.gov/25503195
Autor:
Debora Mancini-DiNardo, Adam Murray, Matthew Ryder, Jeremy Schoenberger, Collin Burton, Nick Woolstenhulme, Christopher Arnell, Jayson Holladay, Natalia Gutin, Kelsey Moyes, Jonathan Craft, Thaddeus Judkins, Benjamin B. Roa, Aaron Theisen
Publikováno v:
Journal of Experimental & Clinical Cancer Research : CR
Background Conventional Sanger sequencing reliably detects the majority of genetic mutations associated with hereditary cancers, such as single-base changes and small insertions or deletions. However, detection of genomic rearrangements, such as larg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af92b170a04328953ae9790da7f2b7e4
https://pubmed.ncbi.nlm.nih.gov/25204323
https://pubmed.ncbi.nlm.nih.gov/25204323
Publikováno v:
Breast Cancer Research and Treatment. 151:233-233
In Table 2 of the original publication, the HGVS and legacy nomenclature were mismatched and the HGVS nomenclature did not correlate with data listed in the table. The corrected table is listed below.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5eaa7e1ff6e9fc02b218862d5303497
https://doi.org/10.1007/s10549-015-3361-z
https://doi.org/10.1007/s10549-015-3361-z
Autor:
Brian L. Abbott, Kelsey Moyes, Rajesh R. Kaldate, Michelle Landon, Kayon Williams, Jennifer Saam, Christopher Arnell, Brian Strike, Lynn Anne Burbidge
Publikováno v:
Journal of Clinical Oncology. 32:1542-1542
1542 Background: Patients with Hereditary Breast and Ovarian cancer (HBOC) or Lynch syndrome (LS) hereditary cancer syndromes are at a greater risk for developing second cancers after an initial ca...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e62e199fc782863a4c229874aceff9d0
https://doi.org/10.1200/jco.2014.32.15_suppl.1542
https://doi.org/10.1200/jco.2014.32.15_suppl.1542