Stephanie K Allen

4PUBLICATIONS
27CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Cell and nuclear division
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Publications (4)

|Sep 25, 2026
Diagnostic Yield of Sequencing in Prenatal Agenesis of the Corpus Callosum in a Well-Phenotyped International Cohort.

|Dec 08, 2023
Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies.

Stephanie K Allen, Natalie J Chandler, Esther Kinning

|Dec 06, 2023
Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.

Gillian V Blayney, Eoghan Laffan, Preethi A Jacob

|Sep 02, 2020
Cytogenomic results following high-chance non-invasive prenatal testing: a UK national audit.

Fiona S Togneri, Stephanie K Allen, Kathy Mann

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Frequent Collaborators

3 joint publications

Natalie J Chandler

2 joint publications

Lyn S Chitty

1 joint publications

Caitlin D Baptiste

1 joint publications

Teresa N Sparks