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Journal of Genetic Counseling
|
December 28, 2022
Elective genetic testing: Genetics professionals' perspectives and practices
Madison S Miura, Sabrina A Suckiel, Hetanshi Naik, et al.
Pancreas
|
May 3, 2021
Genetic Variants in Patients With a Family History of Pancreatic Cancer: Impact of Multigene Panel Testing
Huili Zhu, Sara Welinsky, Emily R Soper, et al.
Cancer Genetics
|
March 19, 2026
Association of high and moderate penetrance monogenic variants, polygenic risk, and family history with breast cancer in an ancestrally diverse population
Emily R Soper, Nicole A Casasanta, Bethany Dubois, et al.
Journal of Registry Management
|
March 30, 2018
Co-Care: A Registry for Individuals at Increased Risk for Colorectal Cancer
Dylan Sperling, Lina Jandorf, Pathu Sriphanlop, et al.
Journal of Personalized Medicine
|
January 20, 2021
Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis
Emily R Soper, Sabrina A Suckiel, Giovanna T Braganza, et al.
Familial Cancer
|
April 22, 2021
CDH1 pathogenic variants and cancer risk in an unselected patient population
Ariel Bar-Mashiah, Emily R Soper, Sinead Cullina, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
January 7, 2023
Association of HSD17B13 and PNPLA3 With Liver Enzymes and Fibrosis in Hispanic/Latino Individuals of Diverse Genetic Ancestries
Stephanie M Rutledge, Emily R Soper, Ning Ma, et al.
Journal of Genetic Counseling
|
January 4, 2023
Elective genomic testing: Practice resource of the National Society of Genetic Counselors
Carrie L Blout Zawatsky, David Bick, Louise Bier, et al.
JCO Precision Oncology
|
December 7, 2020
Lynch Syndrome-Associated Variants and Cancer Rates in an Ancestrally Diverse Biobank
Rachel E Rosenblum, Celina Ang, Sabrina A Suckiel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 14, 2020
Loss-of-function variants in CTNNA1 detected on multigene panel testing in individuals with gastric or breast cancer
Dana Farengo Clark, Scott T Michalski, Rashmi Tondon, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Journal of Genetic Counseling
|
December 28, 2022
Elective genetic testing: Genetics professionals' perspectives and practices
Madison S Miura, Sabrina A Suckiel, Hetanshi Naik, et al.
Pancreas
|
May 3, 2021
Genetic Variants in Patients With a Family History of Pancreatic Cancer: Impact of Multigene Panel Testing
Huili Zhu, Sara Welinsky, Emily R Soper, et al.
Cancer Genetics
|
March 19, 2026
Association of high and moderate penetrance monogenic variants, polygenic risk, and family history with breast cancer in an ancestrally diverse population
Emily R Soper, Nicole A Casasanta, Bethany Dubois, et al.
Journal of Registry Management
|
March 30, 2018
Co-Care: A Registry for Individuals at Increased Risk for Colorectal Cancer
Dylan Sperling, Lina Jandorf, Pathu Sriphanlop, et al.
Journal of Personalized Medicine
|
January 20, 2021
Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis
Emily R Soper, Sabrina A Suckiel, Giovanna T Braganza, et al.
Familial Cancer
|
April 22, 2021
CDH1 pathogenic variants and cancer risk in an unselected patient population
Ariel Bar-Mashiah, Emily R Soper, Sinead Cullina, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
January 7, 2023
Association of HSD17B13 and PNPLA3 With Liver Enzymes and Fibrosis in Hispanic/Latino Individuals of Diverse Genetic Ancestries
Stephanie M Rutledge, Emily R Soper, Ning Ma, et al.
Journal of Genetic Counseling
|
January 4, 2023
Elective genomic testing: Practice resource of the National Society of Genetic Counselors
Carrie L Blout Zawatsky, David Bick, Louise Bier, et al.
JCO Precision Oncology
|
December 7, 2020
Lynch Syndrome-Associated Variants and Cancer Rates in an Ancestrally Diverse Biobank
Rachel E Rosenblum, Celina Ang, Sabrina A Suckiel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 14, 2020
Loss-of-function variants in CTNNA1 detected on multigene panel testing in individuals with gastric or breast cancer
Dana Farengo Clark, Scott T Michalski, Rashmi Tondon, et al.
Page
of 2