Sophie J Adams

7PUBLICATIONS
10CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Gene mappingObstetrics and gynaecologyNeonatologyNeurogenetics
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Publications (7)

|Oct 05, 2026
Universal Prenatal cfDNA-Single Gene Disorder Screening for Autosomal Dominant Conditions in a Low-Risk Cohort: A Cost-Effectiveness Analysis.

|May 19, 2026
Severe Early-Onset Fetal Growth Restriction: The Yield of Antenatal and Postnatal Genetic Testing.

|Feb 01, 2026
Theoretical Performance of Comprehensive Non-Invasive Prenatal Screening in Congenital Heart Defects.

Emily Yang, Megan E Bunnell, Sophie Adams

|Jan 03, 2025
Routine Prenatal cfDNA Screening for Autosomal Dominant Single-Gene Conditions.

Sophie Adams, Olivia Maher Trocki, Christina Miller

|Nov 16, 2023
Risk factors for delayed termination of pregnancy following increased nuchal translucency.

Megan E Bunnell, Sophie Adams, Andrea Pelletier

|Apr 10, 2023
Postnatal genetic testing on cord blood for prenatally identified high-probability cases.

Sophie Adams, Hannah Llorin, Lori J Dobson

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Frequent Collaborators

3 joint publications

Louise Wilkins-Haug

3 joint publications

Stephanie H Guseh

3 joint publications

Megan E Bunnell

2 joint publications

Hannah Llorin