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Author Details

Scott M Weissman
Center for Medical Genetics, NorthShore University HealthSystem
2001
30
17
PMIDPaper TitleJournal TitlePublished Year
36327324Patient experiences with clinical confirmatory genetic testing after using direct-to-consumer raw DNA and third-party genetic interpretation services.Transl Behav Med2023
36327324Patient experiences with clinical confirmatory genetic testing after using direct-to-consumer raw DNA and third-party genetic interpretation services.Transl Behav Med2023
35001450Risk assessment and genetic counseling for Lynch syndrome - Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.J Genet Couns2022
35001450Risk assessment and genetic counseling for Lynch syndrome - Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.J Genet Couns2022
34076301Utilization of breast cancer risk prediction models by cancer genetic counselors in clinical practice predominantly in the United States.J Genet Couns2021
34076301Utilization of breast cancer risk prediction models by cancer genetic counselors in clinical practice predominantly in the United States.J Genet Couns2021
34404389Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.BMC Med2021
34732190Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.BMC Med2021
34732190Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.BMC Med2021
34404389Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.BMC Med2021
32516092Implementation of Germline Testing for Prostate Cancer: Philadelphia Prostate Cancer Consensus Conference 2019.J Clin Oncol2020
32516092Implementation of Germline Testing for Prostate Cancer: Philadelphia Prostate Cancer Consensus Conference 2019.J Clin Oncol2020
31414022Coordinating an Oncology Precision Medicine Clinic Within an Integrated Health System: Lessons Learned in Year One.J Patient Cent Res Rev2019
31693579At-home genetic testing in pediatrics.Curr Opin Pediatr2019
31414022Coordinating an Oncology Precision Medicine Clinic Within an Integrated Health System: Lessons Learned in Year One.J Patient Cent Res Rev2019
31693579At-home genetic testing in pediatrics.Curr Opin Pediatr2019
28780754FDA Approval of PARP Inhibitors and the Impact on Genetic Counseling and Genetic Testing Practices.J Genet Couns2018
28780754FDA Approval of PARP Inhibitors and the Impact on Genetic Counseling and Genetic Testing Practices.J Genet Couns2018
29512889The dawn of consumer-directed testing.Am J Med Genet C Semin Med Genet2018
29204808Implementing a Virtual Health Telemedicine Program in a Community Setting.J Genet Couns2018
29512889The dawn of consumer-directed testing.Am J Med Genet C Semin Med Genet2018
29204808Implementing a Virtual Health Telemedicine Program in a Community Setting.J Genet Couns2018
29087641Implementing an oncology precision medicine clinic in a large community health system.Am J Manag Care2017
29087641Implementing an oncology precision medicine clinic in a large community health system.Am J Manag Care2017
26869169Evaluation of laboratory perspectives on hereditary cancer panels.Fam Cancer2016
26869169Evaluation of laboratory perspectives on hereditary cancer panels.Fam Cancer2016
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
26462740Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease.Hum Mutat2016
26681312Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.Genet Med2016
26462740Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease.Hum Mutat2016
26681312Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.Genet Med2016
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
25023546Nipple-sparing mastectomy in BRCA1/2 mutation carriers: an interim analysis and review of the literature.Ann Surg Oncol2015
25023546Nipple-sparing mastectomy in BRCA1/2 mutation carriers: an interim analysis and review of the literature.Ann Surg Oncol2015
25117502Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.Fam Cancer2014
25117502Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.Fam Cancer2014
23390885Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.Genet Test Mol Biomarkers2013
23390885Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.Genet Test Mol Biomarkers2013
22167527Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline.J Genet Couns2012
22846732Genetic testing by cancer site: ovary.Cancer J2012
22723373Lifetime cancer risks of PTEN mutation carriers--letter.Clin Cancer Res2012
22167527Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline.J Genet Couns2012
22723373Lifetime cancer risks of PTEN mutation carriers--letter.Clin Cancer Res2012
22846732Genetic testing by cancer site: ovary.Cancer J2012
20931355Genetic counseling considerations in the evaluation of families for Lynch syndrome--a review.J Genet Couns2011
20931355Genetic counseling considerations in the evaluation of families for Lynch syndrome--a review.J Genet Couns2011
19959799Detection of BRCA1 and BRCA2 Ashkenazi Jewish founder mutations in formalin-fixed paraffin-embedded tissues using conventional PCR and heteroduplex/amplicon size differences.J Mol Diagn2010
19959799Detection of BRCA1 and BRCA2 Ashkenazi Jewish founder mutations in formalin-fixed paraffin-embedded tissues using conventional PCR and heteroduplex/amplicon size differences.J Mol Diagn2010
18661230Psychological impact of recall in high-risk breast MRI screening.Breast Cancer Res Treat2009
18661230Psychological impact of recall in high-risk breast MRI screening.Breast Cancer Res Treat2009
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Collaborators

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University of Utah
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SA Pathology at the Women's and Children's Hospital
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University of Queensland
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