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 (61-70 of 97) with videos related to

Pageof 10
Sort By:
BMC Genomics|July 1, 2021
Validation of reference genes for whole blood gene expression analysis in cord blood of preterm and full-term neonates and peripheral blood of healthy adultsKristin Hieronymus, Benjamin Dorschner, Felix Schulze, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|July 7, 2018
Targeted Multiplex Gene Expression Profiling to Measure High-Fat Diet and Metformin Effects on Fetal Gene Expression in a Mouse ModelNeeta L Vora, Matthew R Grace, Lisa Smeester, et al.
Prenatal Diagnosis|April 20, 2023
Position statement from the International Society for Prenatal Diagnosis on the use of non-invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnanciesLisa Hui, Katie Ellis, Dora Mayen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Use of a novel computerized decision aid for aneuploidy screening: a randomized controlled trialLaura M Carlson, Sarah Harris, Emily E Hardisty, et al.
Obstetrics and Gynecology|March 10, 2023
Maternal Malignancy After Atypical Findings on Single-Nucleotide Polymorphism-Based Prenatal Cell-Free DNA ScreeningGeorgina Goldring, Cindy Trotter, Jeffrey T Meltzer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2022
Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditionsJennifer Hoskovec, Emily E Hardisty, Asha N Talati, et al.
Prenatal Diagnosis|December 7, 2021
Prenatal phenotype of 47, XXY (Klinefelter syndrome)Kate Swanson, Juliet C Bishop, Huda B Al-Kouatly, et al.
Prenatal Diagnosis|July 15, 2021
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fractionDayne L Filer, Piotr A Mieczkowski, Alicia Brandt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 16, 2023
Association of deep phenotyping with diagnostic yield of prenatal exome sequencing for fetal brain abnormalitiesKathleen A Drexler, Asha N Talati, Kelly L Gilmore, et al.
Biorxiv : the Preprint Server for Biology|April 24, 2023
A Shared Pathogenic Mechanism for Valproic Acid and SHROOM3 Knockout in a Brain Organoid Model of Neural Tube DefectsTaylor N Takla, Jinghui Luo, Roksolana Sudyk, et al.
Pageof 10

Showing results (61-70 of 97) with videos related to

Sort By:
Pageof 10
BMC Genomics|July 1, 2021
Validation of reference genes for whole blood gene expression analysis in cord blood of preterm and full-term neonates and peripheral blood of healthy adultsKristin Hieronymus, Benjamin Dorschner, Felix Schulze, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|July 7, 2018
Targeted Multiplex Gene Expression Profiling to Measure High-Fat Diet and Metformin Effects on Fetal Gene Expression in a Mouse ModelNeeta L Vora, Matthew R Grace, Lisa Smeester, et al.
Prenatal Diagnosis|April 20, 2023
Position statement from the International Society for Prenatal Diagnosis on the use of non-invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnanciesLisa Hui, Katie Ellis, Dora Mayen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Use of a novel computerized decision aid for aneuploidy screening: a randomized controlled trialLaura M Carlson, Sarah Harris, Emily E Hardisty, et al.
Obstetrics and Gynecology|March 10, 2023
Maternal Malignancy After Atypical Findings on Single-Nucleotide Polymorphism-Based Prenatal Cell-Free DNA ScreeningGeorgina Goldring, Cindy Trotter, Jeffrey T Meltzer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2022
Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditionsJennifer Hoskovec, Emily E Hardisty, Asha N Talati, et al.
Prenatal Diagnosis|December 7, 2021
Prenatal phenotype of 47, XXY (Klinefelter syndrome)Kate Swanson, Juliet C Bishop, Huda B Al-Kouatly, et al.
Prenatal Diagnosis|July 15, 2021
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fractionDayne L Filer, Piotr A Mieczkowski, Alicia Brandt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 16, 2023
Association of deep phenotyping with diagnostic yield of prenatal exome sequencing for fetal brain abnormalitiesKathleen A Drexler, Asha N Talati, Kelly L Gilmore, et al.
Biorxiv : the Preprint Server for Biology|April 24, 2023
A Shared Pathogenic Mechanism for Valproic Acid and SHROOM3 Knockout in a Brain Organoid Model of Neural Tube DefectsTaylor N Takla, Jinghui Luo, Roksolana Sudyk, et al.
Pageof 10