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Public Health Genomics and Precision Health Knowledge Base (v10.0)
PHGKB
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CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
CDC-Authored Genomics and Precision Health Publications Database
Last data update: Sep 03, 2024
. (Total: 6282 publications)
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Year
Journal
Records 1-22 (of 22 Records)
Query Trace:
Lynch syndrome[original query]
Information needs persist after genetic counseling and testing for BRCA1/2 and Lynch Syndrome
Peipins LA
,
Dasari S , Viox MH ,
Rodriguez JL
.
Breast Cancer Res Treat 2024
Health equity in the implementation of genomics and precision medicine: A public health imperative.
Khoury MJ
,
Bowen S
,
Dotson WD
,
Drzymalla E
,
Green RF
,
Goldstein R
,
Kolor K
,
Liburd LC
,
Sperling LS
,
Bunnell R
.
Genet Med 2022 24 (8) 1630-1639
Implementing Cancer Genomics in State Health Agencies: Mapping Activities to an Implementation Science Outcome Framework.
Green RF
,
Kumerow MT
,
Rodriguez JL
,
Addie S , Beachy SH , Senier L .
Public Health Genomics 2020 23 1-12
Communication About Hereditary Cancers on Social Media: A Content Analysis of Tweets About Hereditary Breast and Ovarian Cancer and Lynch Syndrome.
Allen CG , Roberts M , Andersen B ,
Khoury MJ
.
J Cancer Educ 2018 35 (1) 131-137
Evaluating the role of public health in implementation of genomics-related recommendations: a case study of hereditary cancers using the CDC Science Impact Framework.
Green RF
,
Ari M
,
Kolor K
,
Dotson WD
,
Bowen S
,
Habarta N
,
Rodriguez JL
,
Richardson LC
,
Khoury MJ
.
Genet Med 2018 21 (1) 28-37
Is universal tumor testing for Lynch syndrome cost-effective? It depends!
Grosse SD
.
Genet Med 2018 21 (1) 252-253
Proposed outcomes measures for state public health genomic programs.
Doyle DL , Clyne M ,
Rodriguez JL
,
Cragun DL , Senier L , Hurst G , Chan K , Chambers DA .
Genet Med 2018 20 (9) 995-1003
CDC Grand Rounds: Family History and Genomics as Tools for Cancer Prevention and Control.
Rodriguez JL
,
Thomas CC
,
Massetti GM
,
Duquette D , Avner L ,
Iskander J
,
Khoury MJ
,
Richardson LC
.
MMWR Morb Mortal Wkly Rep 2016 65 (46) 1291-1294
Convergence of Implementation Science, Precision Medicine, and the Learning Health Care System: A New Model for Biomedical Research.
Chambers DA , Feero WG ,
Khoury MJ
.
JAMA 2016 315 (18) 1941-2
When is Genomic Testing Cost-Effective? Testing for Lynch Syndrome in Patients with Newly-Diagnosed Colorectal Cancer and Their Relatives.
Grosse SD
.
Healthcare (Basel) 2015 3 (4) 860-878
The cost-effectiveness of routine testing for Lynch syndrome in newly diagnosed patients with colorectal cancer in the United States: corrected estimates.
Grosse SD
,
Palomaki GE , Mvundura M , Hampel H .
Genet Med 2015 17 (6) 510-1
Genetic Testing Strategies in Newly Diagnosed Endometrial Cancer Patients Aimed at Reducing Morbidity or Mortality from Lynch Syndrome in the Index Case or Her Relatives.
Stewart A
.
PLoS Curr 2013 5
Modeling uncertain outcomes of genetic testing: factor V Leiden mutation and pregnant women.
Grosse SD
,
Caughey AB .
Genet Med 2013 15 (5) 335-7
Stakeholder assessment of the evidence for cancer genomic tests: insights from three case studies.
Deverka PA , Schully SD , Ishibe N , Carlson JJ , Freedman A , Goddard KA ,
Khoury MJ
,
Ramsey SD .
Genet Med 2012 14 (7) 656-62
Public health action in genomics is now needed beyond newborn screening.
Bowen MS
,
Kolor K
,
Dotson WD
,
Ned RM
,
Khoury MJ
.
Public Health Genomics 2012 15 (6) 327-34
Multilevel research and the challenges of implementing genomic medicine.
Khoury MJ
,
Coates RJ
,
Fennell ML , Glasgow RE , Scheuner MT , Schully SD , Williams MS , Clauser SB .
J Natl Cancer Inst Monogr 2012 2012 (44) 112-20
Relevance, pathogenesis, and testing algorithm for mismatch repair-defective colorectal carcinomas: a report of the association for molecular pathology.
Funkhouser WK Jr ,
Lubin IM
,
Monzon FA ,
Zehnbauer BA
,
Evans JP , Ogino S , Nowak JA .
J Mol Diagn 2012 14 (2) 91-103
Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting.
Bellcross CA
,
Bedrosian SR
,
Daniels E , Duquette D , Hampel H , Jasperson K ,
Joseph DA
,
Kaye C ,
Lubin I
,
Meyer LJ ,
Reyes M
,
Scheuner MT , Schully SD , Senter L ,
Stewart SL
,
St Pierre J
,
Westman J , Wise P , Yang VW ,
Khoury MJ
.
Genet Med 2011 14 (1) 152-62
Genetic testing for lynch syndrome in individuals newly diagnosed with colorectal cancer to reduce morbidity and mortality from colorectal cancer in their relatives.
Coates R
,
Williams M ,
Melillo S
,
Gudgeon J .
PLoS Curr 2011 3 RRN1246
The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer.
Mvundura M
,
Grosse SD
,
Hampel H , Palomaki GE .
Genet Med 2010 12 (2) 93-104
EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.
Palomaki GE , McClain MR ,
Melillo S
,
Hampel HL , Thibodeau SN .
Genet Med 2009 11 (1) 42-65
Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives.
. Genetics in medicine : official journal of the American College of Medical Genetics 2009 11(1) 35-41 .
Genetics in medicine : official journal of the American College of Medical Genetics 2009 11(1) 35-41
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Page last reviewed:
Feb 1, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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