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Georgia L Wiesner

Showing results (31-40 of 71) with videos related to

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Cancer Research|June 11, 2009
Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patientsKishore Guda, Leanna Natale, James Lutterbaugh, et al.
Cancer Prevention Research (Philadelphia, Pa.)|May 20, 2014
Inactivating mutation in the prostaglandin transporter gene, SLCO2A1, associated with familial digital clubbing, colon neoplasia, and NSAID resistanceKishore Guda, Stephen P Fink, Ginger L Milne, et al.
Hereditary Cancer in Clinical Practice|May 16, 2018
Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviewsJennifer L Schneider, Katrina A B Goddard, Kristin R Muessig, et al.
The Oncologist|August 14, 2021
Framework for Implementing and Tracking a Molecular Tumor Board at a National Cancer Institute-Designated Comprehensive Cancer CenterNeha M Jain, Lauren Schmalz, Christopher Cann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 17, 2015
Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitatorsJennifer L Schneider, James Davis, Tia L Kauffman, et al.
Cancer|June 4, 2015
Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriersJessica Ezzell Hunter, Jamilyn M Zepp, Mari J Gilmore, et al.
Journal of Personalized Medicine|November 24, 2022
Outcomes of Returning Medically Actionable Genomic Results in Pediatric ResearchAmy A Blumling, Cynthia A Prows, Margaret H Harr, et al.
Journal of Genetic Counseling|September 5, 2023
Conducting inclusive research in genetics for transgender, gender-diverse, and sex-diverse individuals: Case analyses and recommendations from a clinical genomics studyHarris T Bland, Marian J Gilmore, Justin Andujar, et al.
Contemporary Clinical Trials|October 12, 2024
Family history and cancer risk study (FOREST): A clinical trial assessing electronic patient-directed family history input for identifying patients at risk of hereditary cancerKathleen F Mittendorf, Harris T Bland, Justin Andujar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2021
Neptune: an environment for the delivery of genomic medicineVenner Eric, Victoria Yi, David Murdock, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Cancer Research|June 11, 2009
Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patientsKishore Guda, Leanna Natale, James Lutterbaugh, et al.
Cancer Prevention Research (Philadelphia, Pa.)|May 20, 2014
Inactivating mutation in the prostaglandin transporter gene, SLCO2A1, associated with familial digital clubbing, colon neoplasia, and NSAID resistanceKishore Guda, Stephen P Fink, Ginger L Milne, et al.
Hereditary Cancer in Clinical Practice|May 16, 2018
Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviewsJennifer L Schneider, Katrina A B Goddard, Kristin R Muessig, et al.
The Oncologist|August 14, 2021
Framework for Implementing and Tracking a Molecular Tumor Board at a National Cancer Institute-Designated Comprehensive Cancer CenterNeha M Jain, Lauren Schmalz, Christopher Cann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 17, 2015
Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitatorsJennifer L Schneider, James Davis, Tia L Kauffman, et al.
Cancer|June 4, 2015
Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriersJessica Ezzell Hunter, Jamilyn M Zepp, Mari J Gilmore, et al.
Journal of Personalized Medicine|November 24, 2022
Outcomes of Returning Medically Actionable Genomic Results in Pediatric ResearchAmy A Blumling, Cynthia A Prows, Margaret H Harr, et al.
Journal of Genetic Counseling|September 5, 2023
Conducting inclusive research in genetics for transgender, gender-diverse, and sex-diverse individuals: Case analyses and recommendations from a clinical genomics studyHarris T Bland, Marian J Gilmore, Justin Andujar, et al.
Contemporary Clinical Trials|October 12, 2024
Family history and cancer risk study (FOREST): A clinical trial assessing electronic patient-directed family history input for identifying patients at risk of hereditary cancerKathleen F Mittendorf, Harris T Bland, Justin Andujar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2021
Neptune: an environment for the delivery of genomic medicineVenner Eric, Victoria Yi, David Murdock, et al.
Pageof 8