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Wendy Kohlmann

Showing results (51-60 of 122) with videos related to

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JMIR Medical Informatics|August 15, 2022
Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing ApproachJianlin Shi, Keaton L Morgan, Richard L Bradshaw, et al.
Annals of Behavioral Medicine : a Publication of the Society of Behavioral Medicine|May 17, 2020
Priority of Risk (But Not Perceived Magnitude of Risk) Predicts Improved Sun-Protection Behavior Following Genetic Counseling for Familial MelanomaJennifer M Taber, Lisa G Aspinwall, Danielle M Drummond, et al.
JMIR Medical Informatics|September 13, 2022
Correction: Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing ApproachJianlin Shi, Keaton L Morgan, Richard L Bradshaw, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|June 19, 2017
Colon Pathology Characteristics in Li-Fraumeni SyndromeWilliam Rengifo-Cam, Hailey M Shepherd, Kory W Jasperson, et al.
Journal of Community Genetics|January 20, 2020
Parent and child perspectives on family interactions related to melanoma risk and prevention after CDKN2A/p16 testing of minor childrenYelena P Wu, Lisa G Aspinwall, Bridget Parsons, et al.
Journal of Genetic Counseling|January 20, 2018
Genetic Test Reporting and Counseling for Melanoma Risk in Minors May Improve Sun Protection Without Inducing DistressTammy K Stump, Lisa G Aspinwall, Wendy Kohlmann, et al.
JCO Clinical Cancer Informatics|January 18, 2020
Standards-Based Clinical Decision Support Platform to Manage Patients Who Meet Guideline-Based Criteria for Genetic Evaluation of Familial CancerGuilherme Del Fiol, Wendy Kohlmann, Richard L Bradshaw, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|July 2, 2019
Determining Onset for Familial Breast and Colorectal Cancer from Family History Comments in the Electronic Health RecordDanielle L Mowery, Kensaku Kawamoto, Rick Bradshaw, et al.
American Journal of Medical Genetics. Part A|June 18, 2014
Congenital abnormalities and hepatoblastoma: a report from the Children's Oncology Group (COG) and the Utah Population Database (UPDB)Rajkumar Venkatramani, Logan G Spector, Michael Georgieff, et al.
Familial Cancer|May 26, 2009
Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individualsWendy McKinnon, Kimberly C Banks, Joan Skelly, et al.
Pageof 13

Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
JMIR Medical Informatics|August 15, 2022
Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing ApproachJianlin Shi, Keaton L Morgan, Richard L Bradshaw, et al.
Annals of Behavioral Medicine : a Publication of the Society of Behavioral Medicine|May 17, 2020
Priority of Risk (But Not Perceived Magnitude of Risk) Predicts Improved Sun-Protection Behavior Following Genetic Counseling for Familial MelanomaJennifer M Taber, Lisa G Aspinwall, Danielle M Drummond, et al.
JMIR Medical Informatics|September 13, 2022
Correction: Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing ApproachJianlin Shi, Keaton L Morgan, Richard L Bradshaw, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|June 19, 2017
Colon Pathology Characteristics in Li-Fraumeni SyndromeWilliam Rengifo-Cam, Hailey M Shepherd, Kory W Jasperson, et al.
Journal of Community Genetics|January 20, 2020
Parent and child perspectives on family interactions related to melanoma risk and prevention after CDKN2A/p16 testing of minor childrenYelena P Wu, Lisa G Aspinwall, Bridget Parsons, et al.
Journal of Genetic Counseling|January 20, 2018
Genetic Test Reporting and Counseling for Melanoma Risk in Minors May Improve Sun Protection Without Inducing DistressTammy K Stump, Lisa G Aspinwall, Wendy Kohlmann, et al.
JCO Clinical Cancer Informatics|January 18, 2020
Standards-Based Clinical Decision Support Platform to Manage Patients Who Meet Guideline-Based Criteria for Genetic Evaluation of Familial CancerGuilherme Del Fiol, Wendy Kohlmann, Richard L Bradshaw, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|July 2, 2019
Determining Onset for Familial Breast and Colorectal Cancer from Family History Comments in the Electronic Health RecordDanielle L Mowery, Kensaku Kawamoto, Rick Bradshaw, et al.
American Journal of Medical Genetics. Part A|June 18, 2014
Congenital abnormalities and hepatoblastoma: a report from the Children's Oncology Group (COG) and the Utah Population Database (UPDB)Rajkumar Venkatramani, Logan G Spector, Michael Georgieff, et al.
Familial Cancer|May 26, 2009
Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individualsWendy McKinnon, Kimberly C Banks, Joan Skelly, et al.
Pageof 13