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

Billie R Lianoglou

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Prenatal Diagnosis|September 27, 2023
Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the USNuriye N Sahin-Hodoglugil, Billie R Lianoglou, Sara Ackerman, et al.
Prenatal Diagnosis|September 11, 2025
Diagnostic Yield After Postnatal Reanalysis of Prenatal Exome Sequencing ResultsKate Swanson, Ugur Hodoglugil, Teresa N Sparks, et al.
American Journal of Obstetrics and Gynecology|July 31, 2021
Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalisMary E Norton, Jessica Van Ziffle, Billie R Lianoglou, et al.
Prenatal Diagnosis|March 13, 2026
Gene Panel Versus Whole Exome Sequencing for Fetal AnomaliesKate Swanson, Matthew A Shear, Teresa N Sparks, et al.
Prenatal Diagnosis|December 29, 2023
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomaliesHarriet T Rothschild, Billie R Lianoglou, Nuriye N Sahin Hodoglugil, et al.
Prenatal Diagnosis|June 20, 2022
The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencingKate Swanson, Mary E Norton, Billie R Lianoglou, et al.
Prenatal Diagnosis|September 20, 2025
The Expanding Role of Gene Sequencing in Shaping Fetal Therapies: Clinical and Ethical ConsiderationsMatthew A Shear, Beltran Borges, Billie R Lianoglou, et al.
American Journal of Surgery|July 28, 2021
Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variantsMarisa E Schwab, Shan Dong, Billie R Lianoglou, et al.
American Journal of Obstetrics and Gynecology|May 10, 2025
Genetic diseases underlying a spectrum of fetal effusionsNatalie B Gulrajani, Billie R Lianoglou, Katie Tick, et al.
Frontiers in Genetics|June 7, 2022
"Let's Just Wait Until She's Born": Temporal Factors That Shape Decision-Making for Prenatal Genomic Sequencing Amongst Families Underrepresented in Genomic ResearchJulia E H Brown, Astrid N Zamora, Simon Outram, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Prenatal Diagnosis|September 27, 2023
Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the USNuriye N Sahin-Hodoglugil, Billie R Lianoglou, Sara Ackerman, et al.
Prenatal Diagnosis|September 11, 2025
Diagnostic Yield After Postnatal Reanalysis of Prenatal Exome Sequencing ResultsKate Swanson, Ugur Hodoglugil, Teresa N Sparks, et al.
American Journal of Obstetrics and Gynecology|July 31, 2021
Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalisMary E Norton, Jessica Van Ziffle, Billie R Lianoglou, et al.
Prenatal Diagnosis|March 13, 2026
Gene Panel Versus Whole Exome Sequencing for Fetal AnomaliesKate Swanson, Matthew A Shear, Teresa N Sparks, et al.
Prenatal Diagnosis|December 29, 2023
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomaliesHarriet T Rothschild, Billie R Lianoglou, Nuriye N Sahin Hodoglugil, et al.
Prenatal Diagnosis|June 20, 2022
The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencingKate Swanson, Mary E Norton, Billie R Lianoglou, et al.
Prenatal Diagnosis|September 20, 2025
The Expanding Role of Gene Sequencing in Shaping Fetal Therapies: Clinical and Ethical ConsiderationsMatthew A Shear, Beltran Borges, Billie R Lianoglou, et al.
American Journal of Surgery|July 28, 2021
Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variantsMarisa E Schwab, Shan Dong, Billie R Lianoglou, et al.
American Journal of Obstetrics and Gynecology|May 10, 2025
Genetic diseases underlying a spectrum of fetal effusionsNatalie B Gulrajani, Billie R Lianoglou, Katie Tick, et al.
Frontiers in Genetics|June 7, 2022
"Let's Just Wait Until She's Born": Temporal Factors That Shape Decision-Making for Prenatal Genomic Sequencing Amongst Families Underrepresented in Genomic ResearchJulia E H Brown, Astrid N Zamora, Simon Outram, et al.
Pageof 2