Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alison D Archibald

Showing results (31-40 of 59) with videos related to

Pageof 6
Sort By:
Prenatal Diagnosis|January 9, 2023
Performance of a cell-free DNA prenatal screening test, choice of prenatal procedure, and chromosome conditions identified during pregnancy after low-risk cell-free DNA screeningKatrina L Scarff, Nicola Flowers, Clare J Love, et al.
NPJ Genomic Medicine|July 31, 2023
Scaling-up and future sustainability of a national reproductive genetic carrier screening programZoe Fehlberg, Stephanie Best, Janet C Long, et al.
American Journal of Medical Genetics. Part A|February 20, 2016
Clinical audit of genetic testing and referral patterns for fragile X and associated conditionsMegan Cotter, Alison D Archibald, Belinda J McClaren, et al.
European Journal of Human Genetics : EJHG|February 24, 2026
Parental experiences of receiving genomic newborn screening results: findings from the BabyScreen+ studyErin Tutty, Anaita Kanga-Parabia, Nathasha Kugenthiran, et al.
NPJ Genomic Medicine|February 14, 2026
Supporting decisions about genomic newborn screening at scale in the digital age: the BabyScreen+ studyLilian Downie, Jade Caruana, Nathasha Kugenthiran, et al.
European Journal of Medical Genetics|October 2, 2020
Which types of conditions should be included in reproductive genetic carrier screening? Views of parents of children with a genetic conditionLauren A Thomas, Sharon Lewis, John Massie, et al.
Human Genomics|May 9, 2024
Australian public perspectives on genomic newborn screening: which conditions should be included?Fiona Lynch, Stephanie Best, Clara Gaff, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
How parents decide whether to have genomic newborn screening: experiences from BabyScreenAnaita Kanga-Parabia, Erin Tutty, Nathasha Kugenthiran, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2022
Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et alSarah Righetti, Lisa Dive, Alison D Archibald, et al.
International Journal of Neonatal Screening|January 22, 2024
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for ImplementationFiona Lynch, Stephanie Best, Clara Gaff, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Prenatal Diagnosis|January 9, 2023
Performance of a cell-free DNA prenatal screening test, choice of prenatal procedure, and chromosome conditions identified during pregnancy after low-risk cell-free DNA screeningKatrina L Scarff, Nicola Flowers, Clare J Love, et al.
NPJ Genomic Medicine|July 31, 2023
Scaling-up and future sustainability of a national reproductive genetic carrier screening programZoe Fehlberg, Stephanie Best, Janet C Long, et al.
American Journal of Medical Genetics. Part A|February 20, 2016
Clinical audit of genetic testing and referral patterns for fragile X and associated conditionsMegan Cotter, Alison D Archibald, Belinda J McClaren, et al.
European Journal of Human Genetics : EJHG|February 24, 2026
Parental experiences of receiving genomic newborn screening results: findings from the BabyScreen+ studyErin Tutty, Anaita Kanga-Parabia, Nathasha Kugenthiran, et al.
NPJ Genomic Medicine|February 14, 2026
Supporting decisions about genomic newborn screening at scale in the digital age: the BabyScreen+ studyLilian Downie, Jade Caruana, Nathasha Kugenthiran, et al.
European Journal of Medical Genetics|October 2, 2020
Which types of conditions should be included in reproductive genetic carrier screening? Views of parents of children with a genetic conditionLauren A Thomas, Sharon Lewis, John Massie, et al.
Human Genomics|May 9, 2024
Australian public perspectives on genomic newborn screening: which conditions should be included?Fiona Lynch, Stephanie Best, Clara Gaff, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
How parents decide whether to have genomic newborn screening: experiences from BabyScreenAnaita Kanga-Parabia, Erin Tutty, Nathasha Kugenthiran, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2022
Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et alSarah Righetti, Lisa Dive, Alison D Archibald, et al.
International Journal of Neonatal Screening|January 22, 2024
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for ImplementationFiona Lynch, Stephanie Best, Clara Gaff, et al.
Pageof 6