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Laura M Amendola

Showing results (1-10 of 75) with videos related to

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Annual Review of Genomics and Human Genetics|March 16, 2021
Scaling Genetic Counseling in the Genomics EraLaura M Amendola, Katie Golden-Grant, Sarah Scollon
Journal of Community Genetics|July 14, 2022
Variation among DNA banking consent forms: points for clinicians to bank onSamuel J Huang, Laura M Amendola, Darci L Sternen
BMC Medical Genomics|May 10, 2018
Clinical providers' experiences with returning results from genomic sequencing: an interview studyJulia Wynn, Katie Lewis, Laura M Amendola, et al.
Journal of Genetic Counseling|July 17, 2016
Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational ToolLauren T Garrett, Nathan Hickman, Angela Jacobson, et al.
Journal of Genetic Counseling|July 19, 2019
Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer testsLaura M Amendola, M Ragan Hart, Robin L Bennett, et al.
BMC Medical Genomics|January 7, 2021
ShareDNA: a smartphone app to facilitate family communication of genetic resultsChethan Jujjavarapu, Jeevan Anandasakaran, Laura M Amendola, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|October 20, 2015
Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their DeathLaura M Amendola, Martha Horike-Pyne, Susan B Trinidad, et al.
Case Reports in Genetics|December 5, 2025
Long-Read Sequencing as a Diagnostic Tool for Primary Ciliary DyskinesiaLiora H Feshbach, Morgan Similuk, Laura M Amendola, et al.
Molecular Genetics & Genomic Medicine|April 1, 2017
Discordance in selected designee for return of genomic findings in the event of participant death and estate executorJessie L Goodman, Laura M Amendola, Martha Horike-Pyne, et al.
European Journal of Medical Genetics|April 15, 2026
STAT3 Dominant Negative Hyper-IgE Syndrome: A Patient Report with Actionable Genomic FindingsAislinn S Bloom, Laura M Amendola, Nadjalisse Reynolds-Lallement, et al.
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Annual Review of Genomics and Human Genetics|March 16, 2021
Scaling Genetic Counseling in the Genomics EraLaura M Amendola, Katie Golden-Grant, Sarah Scollon
Journal of Community Genetics|July 14, 2022
Variation among DNA banking consent forms: points for clinicians to bank onSamuel J Huang, Laura M Amendola, Darci L Sternen
BMC Medical Genomics|May 10, 2018
Clinical providers' experiences with returning results from genomic sequencing: an interview studyJulia Wynn, Katie Lewis, Laura M Amendola, et al.
Journal of Genetic Counseling|July 17, 2016
Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational ToolLauren T Garrett, Nathan Hickman, Angela Jacobson, et al.
Journal of Genetic Counseling|July 19, 2019
Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer testsLaura M Amendola, M Ragan Hart, Robin L Bennett, et al.
BMC Medical Genomics|January 7, 2021
ShareDNA: a smartphone app to facilitate family communication of genetic resultsChethan Jujjavarapu, Jeevan Anandasakaran, Laura M Amendola, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|October 20, 2015
Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their DeathLaura M Amendola, Martha Horike-Pyne, Susan B Trinidad, et al.
Case Reports in Genetics|December 5, 2025
Long-Read Sequencing as a Diagnostic Tool for Primary Ciliary DyskinesiaLiora H Feshbach, Morgan Similuk, Laura M Amendola, et al.
Molecular Genetics & Genomic Medicine|April 1, 2017
Discordance in selected designee for return of genomic findings in the event of participant death and estate executorJessie L Goodman, Laura M Amendola, Martha Horike-Pyne, et al.
European Journal of Medical Genetics|April 15, 2026
STAT3 Dominant Negative Hyper-IgE Syndrome: A Patient Report with Actionable Genomic FindingsAislinn S Bloom, Laura M Amendola, Nadjalisse Reynolds-Lallement, et al.
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