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Journal of Genetic Counseling|February 20, 2024
Processing the process: Reflections on genetic counselor-led student supervision groups and practical tips for future facilitatorsMichelle E Florido, Jessica L GiordanoPrenatal Diagnosis|September 6, 2025
Genome Sequencing for All Pregnant Persons: Navigating the Next Frontier in Prenatal Diagnosis Through Patient ReflectionsKristen E Kelly, Stephanie Galloway, Alexandra Demers, et al.Journal of Genetic Counseling|November 10, 2021
Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID-19 pandemicDaria Ma, Priyanka R Ahimaz, James M Mirocha, et al.Clinical Case Reports|January 30, 2018
Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiencyAvinash Abhyankar, Michelle Lamendola-Essel, Kelly Brennan, et al.Prenatal Diagnosis|January 29, 2024
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart diseaseEmily Zhao, Miles Bomback, Atlas Khan, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2022
Diagnostic sequencing to support genetically stratified medicine in a tertiary care settingNatalie Lippa, Louise Bier, Anya Revah-Politi, et al.Lancet (London, England)|February 5, 2019
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort studySlavé Petrovski, Vimla Aggarwal, Jessica L Giordano, et al.HGG Advances|April 1, 2021
TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromesJulie C Van De Weghe, Jessica L Giordano, Inge B Mathijssen, 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.Pageof 2