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Lauren Westerfield

Showing results (1-10 of 8) with videos related to

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Journal of Clinical Medicine|August 4, 2015
Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and DiagnosisLauren Westerfield, Sandra Darilek, Ignatia B van den Veyver
Clinical Obstetrics and Gynecology|June 4, 2025
Prenatal Genetic Consultation and TestingSarah Araji, Lauren Westerfield, Roni Zemet, et al.
American Journal of Medical Genetics. Part A|December 20, 2019
A family affair-Severe fetal and neonatal hemolytic anemia due to novel alpha-spectrin mutations in two siblingsRoopali Donepudi, Lauren Westerfield, Ashley Stonecipher, et al.
Journal of Genetic Counseling|February 9, 2023
Expanded carrier screening for reproductive risk assessment: An evidence-based practice guideline from the National Society of Genetic CounselorsKatelynn G Sagaser, Jennifer Malinowski, Lauren Westerfield, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Improving Automated Deep Phenotyping Through Large Language Models Using Retrieval Augmented GenerationBrandon T Garcia, Lauren Westerfield, Priya Yelemali, et al.
Genome Medicine|August 18, 2025
Improving automated deep phenotyping through large language models using retrieval-augmented generationBrandon T Garcia, Lauren Westerfield, Priya Yelemali, et al.
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.
American Journal of Human Genetics|December 30, 2019
Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency DisordersJustin O Szot, Carla Campagnolo, Ye Cao, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Clinical Medicine|August 4, 2015
Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and DiagnosisLauren Westerfield, Sandra Darilek, Ignatia B van den Veyver
Clinical Obstetrics and Gynecology|June 4, 2025
Prenatal Genetic Consultation and TestingSarah Araji, Lauren Westerfield, Roni Zemet, et al.
American Journal of Medical Genetics. Part A|December 20, 2019
A family affair-Severe fetal and neonatal hemolytic anemia due to novel alpha-spectrin mutations in two siblingsRoopali Donepudi, Lauren Westerfield, Ashley Stonecipher, et al.
Journal of Genetic Counseling|February 9, 2023
Expanded carrier screening for reproductive risk assessment: An evidence-based practice guideline from the National Society of Genetic CounselorsKatelynn G Sagaser, Jennifer Malinowski, Lauren Westerfield, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Improving Automated Deep Phenotyping Through Large Language Models Using Retrieval Augmented GenerationBrandon T Garcia, Lauren Westerfield, Priya Yelemali, et al.
Genome Medicine|August 18, 2025
Improving automated deep phenotyping through large language models using retrieval-augmented generationBrandon T Garcia, Lauren Westerfield, Priya Yelemali, et al.
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.
American Journal of Human Genetics|December 30, 2019
Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency DisordersJustin O Szot, Carla Campagnolo, Ye Cao, et al.
Pageof 1