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Sapna Syngal

Showing results (171-180 of 216) with videos related to

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Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|December 8, 2014
KRAS and guanine nucleotide-binding protein mutations in pancreatic juice collected from the duodenum of patients at high risk for neoplasia undergoing endoscopic ultrasoundJames R Eshleman, Alexis L Norris, Yoshihiko Sadakari, et al.
Genetics in Medicine Open|December 13, 2024
Feasibility of an electronic patient-facing cancer family history tool in medically underserved populationsHeather Spencer Feigelson, Kathleen F Mittendorf, Sonia Okuyama, et al.
Journal of the National Cancer Institute|November 20, 2015
Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal CancerFay Kastrinos, Rohit P Ojha, Celine Leenen, et al.
Hereditary Cancer in Clinical Practice|January 1, 2020
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods studyKathleen F Mittendorf, Jessica Ezzell Hunter, Jennifer L Schneider, et al.
Hereditary Cancer in Clinical Practice|June 10, 2022
Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviewsKathleen F Mittendorf, Hannah S Lewis, Devan M Duenas, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 31, 2017
Cancer Susceptibility Gene Mutations in Individuals With Colorectal CancerMatthew B Yurgelun, Matthew H Kulke, Charles S Fuchs, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE studyDavid B Zhen, Kari G Rabe, Steven Gallinger, et al.
Familial Cancer|March 23, 2021
Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>™) for lynch syndrome risk assessment in a diverse populationKathleen F Mittendorf, Chinedu Ukaegbu, Marian J Gilmore, et al.
JAMA Oncology|July 3, 2024
Pancreatic Cancer Surveillance and Survival of High-Risk IndividualsAmanda L Blackford, Marcia Irene Canto, Mohamad Dbouk, et al.
Genetics in Medicine Open|June 15, 2026
RecQ DNA helicases germline variants in Lynch-like syndromeMar Giner-Calabuig, Seila De Leon, Gemma Vidal-Pedrola, et al.
Pageof 22

Showing results (171-180 of 216) with videos related to

Sort By:
Pageof 22
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|December 8, 2014
KRAS and guanine nucleotide-binding protein mutations in pancreatic juice collected from the duodenum of patients at high risk for neoplasia undergoing endoscopic ultrasoundJames R Eshleman, Alexis L Norris, Yoshihiko Sadakari, et al.
Genetics in Medicine Open|December 13, 2024
Feasibility of an electronic patient-facing cancer family history tool in medically underserved populationsHeather Spencer Feigelson, Kathleen F Mittendorf, Sonia Okuyama, et al.
Journal of the National Cancer Institute|November 20, 2015
Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal CancerFay Kastrinos, Rohit P Ojha, Celine Leenen, et al.
Hereditary Cancer in Clinical Practice|January 1, 2020
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods studyKathleen F Mittendorf, Jessica Ezzell Hunter, Jennifer L Schneider, et al.
Hereditary Cancer in Clinical Practice|June 10, 2022
Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviewsKathleen F Mittendorf, Hannah S Lewis, Devan M Duenas, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 31, 2017
Cancer Susceptibility Gene Mutations in Individuals With Colorectal CancerMatthew B Yurgelun, Matthew H Kulke, Charles S Fuchs, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE studyDavid B Zhen, Kari G Rabe, Steven Gallinger, et al.
Familial Cancer|March 23, 2021
Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>™) for lynch syndrome risk assessment in a diverse populationKathleen F Mittendorf, Chinedu Ukaegbu, Marian J Gilmore, et al.
JAMA Oncology|July 3, 2024
Pancreatic Cancer Surveillance and Survival of High-Risk IndividualsAmanda L Blackford, Marcia Irene Canto, Mohamad Dbouk, et al.
Genetics in Medicine Open|June 15, 2026
RecQ DNA helicases germline variants in Lynch-like syndromeMar Giner-Calabuig, Seila De Leon, Gemma Vidal-Pedrola, et al.
Pageof 22