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Author Details

Georgia L Wiesner
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
1986
91
31
PMIDPaper TitleJournal TitlePublished Year
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
37579253Germline <i>EGFR</i> Mutations and Familial Lung Cancer.J Clin Oncol2023
37015332Esophageal and Esophagogastric Junction Cancers, Version 2.2023, NCCN Clinical Practice Guidelines in Oncology.J Natl Compr Canc Netw2023
34665896Do research participants share genomic screening results with family members?J Genet Couns2022
35446370Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.JAMA Oncol2022
36422086Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research.J Pers Med2022
36048450Hereditary Cancer Syndromes-A Broader Clinical Spectrum Than Previously Understood?-Reply.JAMA Oncol2022
35943490Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results.Genet Med2022
35130500Gastric Cancer, Version 2.2022, NCCN Clinical Practice Guidelines in Oncology.J Natl Compr Canc Netw2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
35341654Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network.Genet Med2022
33389527Increased ease of access to genetic counseling for low-income women with breast cancer using a point of care screening tool.J Community Genet2021
34377931Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.JNCI Cancer Spectr2021
34666312NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 1.2021.J Natl Compr Canc Netw2021
34390291Framework for Implementing and Tracking a Molecular Tumor Board at a National Cancer Institute-Designated Comprehensive Cancer Center.Oncologist2021
34347061Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry.JAMA Netw Open2021
34257418Neptune: an environment for the delivery of genomic medicine.Genet Med2021
33420026Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics.Nat Commun2021
31553110Patients' willingness to reconsider cancer genetic testing after initially declining: Mention it again.J Genet Couns2020
31967672Breast cancer screening implications of risk modeling among female relatives of ATM and CHEK2 carriers.Cancer2020
32634774A Web-Based Tool to Automate Portions of Pretest Genetic Counseling for Inherited Cancer.J Natl Compr Canc Netw2020
32413979Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.J Pers Med2020
32329193Patient perspectives on variant reclassification after cancer susceptibility testing.Mol Genet Genomic Med2020
32349224Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.J Pers Med2020
30729418Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting.Fam Cancer2019
31890059Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study.Hered Cancer Clin Pract2019
31737042Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network.Front Genet2019
29904163Physicians' perspectives on receiving unsolicited genomic results.Genet Med2019
29875428The impact of variant classification on the clinical management of hereditary cancer syndromes.Genet Med2019
29301385Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.J Pers Med2018
30055521Subsequent breast and high grade serous carcinomas after risk-reducing salpingo-oophorectomy in BRCA mutation carriers and patients with history of breast cancer.Ann Diagn Pathol2018
29760830Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews.Hered Cancer Clin Pract2018
28040716NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.J Natl Compr Canc Netw2017
28176204Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives.Fam Cancer2017
28973705Identification and Management of <i>TP53</i> Gene Carriers Detected Through Multigene Panel Testing.South Med J2017
25880440Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitators.Genet Med2016
27767224Ethical, Legal, and Social Implications of Personalized Genomic Medicine Research: Current Literature and Suggestions for the Future.Bioethics2016
26850485Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.J Natl Compr Canc Netw2016
25394175A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.Genet Med2015
26036338Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers.Cancer2015
24838973Inactivating mutation in the prostaglandin transporter gene, SLCO2A1, associated with familial digital clubbing, colon neoplasia, and NSAID resistance.Cancer Prev Res (Phila)2014
25190699Gene panel testing for inherited cancer risk.J Natl Compr Canc Netw2014
25190698Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.J Natl Compr Canc Netw2014
22241094IRB perspectives on the return of individual results from genomic research.Genet Med2012
22241102Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis.Genet Med2012
21487211Attitudes toward genetic research review: results from a survey of human genetics researchers.Public Health Genomics2011
19797908Program update and novel use of the DESPAIR program to design a genome-wide linkage study using relative pairs.Hum Hered2010
20551049Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22.Cancer Res2010
20235866Attitudes toward genetic research review: results from a national survey of professionals involved in human subjects protection.J Empir Res Hum Res Ethics2010
19509225Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients.Cancer Res2009
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