Karen Low

18PUBLICATIONS
72CO-AUTHORS
Infant and child healthDevelopmental genetics (incl. sex determination)Organisational, interpersonal and intercultural communicationEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (18)

|Jan 19, 2026
How do clinician and parent-reported data differ? An analysis of similarity and difference in the datasets from a cross-syndrome genetics cohort study (GenROC).

Karen Jaqueline Low, Huw Day, Mevmi Lasanya Kodippuli Thanthilla

|Dec 08, 2025
Charting Brain Structure in 22q11.2 Deletion Syndrome with Clinical Neuroimaging.

Benjamin Jung, J Eric Schmitt, Jakob Seidlitz

|Nov 28, 2025
Social Media Use Among Parents and Caregivers of Children With Rare Genetic Diseases: Scoping Review.

Charlotte Davis, Laura Bogaert, John Powell

|Oct 14, 2025
Parental Use of Social Media and the Internet in the Context of Their Child's Genetic Neurodevelopmental Disorder: Mixed Methods Study Nested in the GenROC Cohort Study.

Karen Jaqueline Low, Georgia Treneman-Evans, Sarah L Wynn

|Oct 12, 2025
The LMSz method - an automatable scalable approach to constructing gene-specific growth charts in rare disorders.

Karen J Low, Julia Foreman, Rachel J Hobson

|Oct 03, 2025
The Head Circumference Height Index (HCH-I) to Quantify Relative Macrocephaly and Aid Identification of Hypochondroplasia in Children.

Moira S Cheung, Ruggero Lanzafame, Karen J Low

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Frequent Collaborators

4 joint publications

Tim J Cole

3 joint publications

Jenny Ingram

3 joint publications

Charlotte W Ockeloen

2 joint publications

Emily Woods