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Lauren Badalato

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European Journal of Human Genetics : EJHG|August 24, 2017
Third party interpretation of raw genetic data: an ethical explorationLauren Badalato, Louiza Kalokairinou, Pascal Borry
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2016
Ethical considerations for genetic testing in the context of mandated cardiac screening before athletic participationEmma F Magavern, Lauren Badalato, Gherardo Finocchiaro, et al.
American Journal of Medical Genetics. Part A|May 14, 2024
Adults with paternal UPD14 causing Kagami-Ogata syndrome: Case report and review of the literatureChristopher S Smith, Madison Riddell, Lauren Badalato, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2017
Fragile X testing as a second-tier testTaila Hartley, Ryan Potter, Lauren Badalato, et al.
American Journal of Medical Genetics. Part A|December 20, 2016
KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connectionLauren Badalato, Sali M K Farhan, Allison A Dilliott, et al.
Brain : a Journal of Neurology|February 9, 2022
Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphologySiddharth Banka, Abigail Bennington, Martin J Baker, et al.
Prenatal Diagnosis|November 14, 2024
Fetal Presentation of MYRF-Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal DiagnosisMaud Favier, Elise Brischoux-Boucher, Louise C Pyle, et al.
BMJ Open|March 27, 2026
Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational studyDaniel Assamad, Abigail Hansen, Katharine Fooks, et al.
Journal of Genetic Counseling|May 5, 2026
Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencingAbigail Hansen, Stephanie Luca, Olivia Moran, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2023
Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort studyTaila Hartley, Deborah Marshall, Meryl Acker, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
European Journal of Human Genetics : EJHG|August 24, 2017
Third party interpretation of raw genetic data: an ethical explorationLauren Badalato, Louiza Kalokairinou, Pascal Borry
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2016
Ethical considerations for genetic testing in the context of mandated cardiac screening before athletic participationEmma F Magavern, Lauren Badalato, Gherardo Finocchiaro, et al.
American Journal of Medical Genetics. Part A|May 14, 2024
Adults with paternal UPD14 causing Kagami-Ogata syndrome: Case report and review of the literatureChristopher S Smith, Madison Riddell, Lauren Badalato, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2017
Fragile X testing as a second-tier testTaila Hartley, Ryan Potter, Lauren Badalato, et al.
American Journal of Medical Genetics. Part A|December 20, 2016
KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connectionLauren Badalato, Sali M K Farhan, Allison A Dilliott, et al.
Brain : a Journal of Neurology|February 9, 2022
Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphologySiddharth Banka, Abigail Bennington, Martin J Baker, et al.
Prenatal Diagnosis|November 14, 2024
Fetal Presentation of MYRF-Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal DiagnosisMaud Favier, Elise Brischoux-Boucher, Louise C Pyle, et al.
BMJ Open|March 27, 2026
Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational studyDaniel Assamad, Abigail Hansen, Katharine Fooks, et al.
Journal of Genetic Counseling|May 5, 2026
Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencingAbigail Hansen, Stephanie Luca, Olivia Moran, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2023
Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort studyTaila Hartley, Deborah Marshall, Meryl Acker, et al.
Pageof 2