Jessica L Giordano

13PUBLICATIONS
189CO-AUTHORS
Women's studies (incl. girls' studies)Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)NeonatologyEducational counselling
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Journal

Publications (13)

|Dec 03, 2025
The Perspectives and Experiences of Prospective Parents Declining Diagnostic Prenatal Genome Sequencing in Continuing Pregnancies With Fetal Structural Anomalies.

Lisa S Weingarten, Allison Rosenbaum, Jessica de Voest

|Sep 06, 2025
Genome Sequencing for All Pregnant Persons: Navigating the Next Frontier in Prenatal Diagnosis Through Patient Reflections.

Kristen E Kelly, Stephanie Galloway, Alexandra Demers

|Jun 13, 2025
Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell-Silver Syndrome in Infancy.

Amanda Thomas-Wilson, Mythily Ganapathi, Nina Harkavy

|Sep 23, 2024
Prenatal Ultrasonographic Features Associated With ARSL and X-Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series.

Eleanor Broeren, Samantha Stover, Katya Bennett

|Feb 20, 2024
Processing the process: Reflections on genetic counselor-led student supervision groups and practical tips for future facilitators.

Michelle E Florido, Jessica L Giordano

|Jan 29, 2024
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease.

Emily Zhao, Miles Bomback, Atlas Khan

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Frequent Collaborators

4 joint publications

Neeta L Vora

3 joint publications

Ignatia Van den Veyver

3 joint publications

Ronald J Wapner

2 joint publications

Damian Smedley