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

Neeta L Vora

Showing results (81-90 of 97) with videos related to

Pageof 10
Sort By:
Prenatal Diagnosis|April 27, 2022
Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomaliesCatherine G Kernie, Julia Wynn, Allison Rosenbaum, et al.
Journal of Clinical and Translational Science|April 10, 2026
Expanding access to genomic analysis and reporting in research studies: The GENYSIS research coreKimberly S Foss, Tam P Sneddon, Eleanor P Fensterle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2017
Prenatal exome sequencing in anomalous fetuses: new opportunities and challengesNeeta L Vora, Bradford Powell, Alicia Brandt, et al.
Prenatal Diagnosis|December 8, 2025
Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid CollectionsNatalie B Gulrajani, John Boscardin, Billie R Lianoglou, et al.
Prenatal Diagnosis|November 20, 2022
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case seriesBobby K Brar, Marisa Gilstrop Thompson, Neeta L Vora, et al.
The Journal of Pediatrics|March 11, 2019
An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn ScreeningLaura V Milko, Julianne M O'Daniel, Daniela M DeCristo, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 19, 2026
Ultrasound and SNP-based cell-free DNA zygosity testing in twin pregnanciesRuben Quintero, K Joseph Hurt, Neeta L Vora, et al.
Prenatal Diagnosis|December 3, 2025
The Perspectives and Experiences of Prospective Parents Declining Diagnostic Prenatal Genome Sequencing in Continuing Pregnancies With Fetal Structural AnomaliesLisa S Weingarten, Allison Rosenbaum, Jessica de Voest, et al.
American Journal of Obstetrics and Gynecology|June 24, 2024
Amniocentesis in pregnancies at or beyond 24 weeks: an international multicenter studyRoni Zemet, Mohamad Ali Maktabi, Alexandra Tinfow, et al.
American Journal of Human Genetics|September 10, 2025
Bi-allelic deleterious variants in SNAPIN, which encodes a retrograde dynein adaptor, cause a prenatal-onset neurodevelopmental disorderHammad Yousaf, Maayke A de Koning, Kamal Khan, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
Prenatal Diagnosis|April 27, 2022
Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomaliesCatherine G Kernie, Julia Wynn, Allison Rosenbaum, et al.
Journal of Clinical and Translational Science|April 10, 2026
Expanding access to genomic analysis and reporting in research studies: The GENYSIS research coreKimberly S Foss, Tam P Sneddon, Eleanor P Fensterle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2017
Prenatal exome sequencing in anomalous fetuses: new opportunities and challengesNeeta L Vora, Bradford Powell, Alicia Brandt, et al.
Prenatal Diagnosis|December 8, 2025
Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid CollectionsNatalie B Gulrajani, John Boscardin, Billie R Lianoglou, et al.
Prenatal Diagnosis|November 20, 2022
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case seriesBobby K Brar, Marisa Gilstrop Thompson, Neeta L Vora, et al.
The Journal of Pediatrics|March 11, 2019
An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn ScreeningLaura V Milko, Julianne M O'Daniel, Daniela M DeCristo, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 19, 2026
Ultrasound and SNP-based cell-free DNA zygosity testing in twin pregnanciesRuben Quintero, K Joseph Hurt, Neeta L Vora, et al.
Prenatal Diagnosis|December 3, 2025
The Perspectives and Experiences of Prospective Parents Declining Diagnostic Prenatal Genome Sequencing in Continuing Pregnancies With Fetal Structural AnomaliesLisa S Weingarten, Allison Rosenbaum, Jessica de Voest, et al.
American Journal of Obstetrics and Gynecology|June 24, 2024
Amniocentesis in pregnancies at or beyond 24 weeks: an international multicenter studyRoni Zemet, Mohamad Ali Maktabi, Alexandra Tinfow, et al.
American Journal of Human Genetics|September 10, 2025
Bi-allelic deleterious variants in SNAPIN, which encodes a retrograde dynein adaptor, cause a prenatal-onset neurodevelopmental disorderHammad Yousaf, Maayke A de Koning, Kamal Khan, et al.
Pageof 10