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Author Details
Full Name
Scott M Weissman
Affiliation
Center for Medical Genetics, NorthShore University HealthSystem
ORCID
Career Start Year
2001
Papers
30
H Index
17
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36327324
Patient experiences with clinical confirmatory genetic testing after using direct-to-consumer raw DNA and third-party genetic interpretation services.
Transl Behav Med
2023
36327324
Patient experiences with clinical confirmatory genetic testing after using direct-to-consumer raw DNA and third-party genetic interpretation services.
Transl Behav Med
2023
35001450
Risk 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 Couns
2022
35001450
Risk 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 Couns
2022
34076301
Utilization of breast cancer risk prediction models by cancer genetic counselors in clinical practice predominantly in the United States.
J Genet Couns
2021
34076301
Utilization of breast cancer risk prediction models by cancer genetic counselors in clinical practice predominantly in the United States.
J Genet Couns
2021
34404389
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
BMC Med
2021
34732190
Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
BMC Med
2021
34732190
Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
BMC Med
2021
34404389
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
BMC Med
2021
32516092
Implementation of Germline Testing for Prostate Cancer: Philadelphia Prostate Cancer Consensus Conference 2019.
J Clin Oncol
2020
32516092
Implementation of Germline Testing for Prostate Cancer: Philadelphia Prostate Cancer Consensus Conference 2019.
J Clin Oncol
2020
31414022
Coordinating an Oncology Precision Medicine Clinic Within an Integrated Health System: Lessons Learned in Year One.
J Patient Cent Res Rev
2019
31693579
At-home genetic testing in pediatrics.
Curr Opin Pediatr
2019
31414022
Coordinating an Oncology Precision Medicine Clinic Within an Integrated Health System: Lessons Learned in Year One.
J Patient Cent Res Rev
2019
31693579
At-home genetic testing in pediatrics.
Curr Opin Pediatr
2019
28780754
FDA Approval of PARP Inhibitors and the Impact on Genetic Counseling and Genetic Testing Practices.
J Genet Couns
2018
28780754
FDA Approval of PARP Inhibitors and the Impact on Genetic Counseling and Genetic Testing Practices.
J Genet Couns
2018
29512889
The dawn of consumer-directed testing.
Am J Med Genet C Semin Med Genet
2018
29204808
Implementing a Virtual Health Telemedicine Program in a Community Setting.
J Genet Couns
2018
29512889
The dawn of consumer-directed testing.
Am J Med Genet C Semin Med Genet
2018
29204808
Implementing a Virtual Health Telemedicine Program in a Community Setting.
J Genet Couns
2018
29087641
Implementing an oncology precision medicine clinic in a large community health system.
Am J Manag Care
2017
29087641
Implementing an oncology precision medicine clinic in a large community health system.
Am J Manag Care
2017
26869169
Evaluation of laboratory perspectives on hereditary cancer panels.
Fam Cancer
2016
26869169
Evaluation of laboratory perspectives on hereditary cancer panels.
Fam Cancer
2016
27087319
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.
Am J Hum Genet
2016
26462740
Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease.
Hum Mutat
2016
26681312
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
Genet Med
2016
26462740
Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease.
Hum Mutat
2016
26681312
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
Genet Med
2016
27087319
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.
Am J Hum Genet
2016
25023546
Nipple-sparing mastectomy in BRCA1/2 mutation carriers: an interim analysis and review of the literature.
Ann Surg Oncol
2015
25023546
Nipple-sparing mastectomy in BRCA1/2 mutation carriers: an interim analysis and review of the literature.
Ann Surg Oncol
2015
25117502
Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.
Fam Cancer
2014
25117502
Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.
Fam Cancer
2014
23390885
Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Genet Test Mol Biomarkers
2013
23390885
Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Genet Test Mol Biomarkers
2013
22167527
Identification 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 Couns
2012
22846732
Genetic testing by cancer site: ovary.
Cancer J
2012
22723373
Lifetime cancer risks of PTEN mutation carriers--letter.
Clin Cancer Res
2012
22167527
Identification 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 Couns
2012
22723373
Lifetime cancer risks of PTEN mutation carriers--letter.
Clin Cancer Res
2012
22846732
Genetic testing by cancer site: ovary.
Cancer J
2012
20931355
Genetic counseling considerations in the evaluation of families for Lynch syndrome--a review.
J Genet Couns
2011
20931355
Genetic counseling considerations in the evaluation of families for Lynch syndrome--a review.
J Genet Couns
2011
19959799
Detection of BRCA1 and BRCA2 Ashkenazi Jewish founder mutations in formalin-fixed paraffin-embedded tissues using conventional PCR and heteroduplex/amplicon size differences.
J Mol Diagn
2010
19959799
Detection of BRCA1 and BRCA2 Ashkenazi Jewish founder mutations in formalin-fixed paraffin-embedded tissues using conventional PCR and heteroduplex/amplicon size differences.
J Mol Diagn
2010
18661230
Psychological impact of recall in high-risk breast MRI screening.
Breast Cancer Res Treat
2009
18661230
Psychological impact of recall in high-risk breast MRI screening.
Breast Cancer Res Treat
2009
1 - 50 of 60
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row(s) 1 - 30 of 30
Collaborators
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Neaman Center for Personalized Medicine, NorthShore University HealthSystem
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7
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CancerLinQ LLC, American Society of Clinical Oncology
Co-authored papers
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Co-authored papers
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Co-authored papers
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SA Pathology at the Women's and Children's Hospital
Co-authored papers
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QIMR Berghofer Medical Research Institute
Co-authored papers
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Jonathan Beesley
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