Justin Huw Davies

29PUBLICATIONS
119CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Adolescent healthMedical genetics (excl. cancer genetics)
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Publications (29)

|Aug 11, 2026
Temple syndrome - an under-recognised multi-system growth disorder: large cohort analysis and proposed scoring system.

|Feb 13, 2026
Peri-kidney transplant management in autosomal dominant hypocalcaemia type 1.

Alice Glaysher, Matthew J Harmer, Ji Soo Kim

|Jan 16, 2026
International guideline on genetic testing of children with short stature.

Andrew Dauber, Alexander A L Jorge, Ola Nilsson

|Dec 23, 2025
Silver-Russell syndrome secondary to rare (epi)genotypes exhibits phenotypic heterogeneity challenging clinical diagnosis.

Uttara Kurup, David B N Lim, Avinaash V Maharaj

|Oct 14, 2025
Real-world utility of diagnostic gene panels for childhood short stature and pituitary hormone deficiency in the UK.

David B N Lim, Louise McClelland, Suzanne Page

|Apr 24, 2025
The use of bisphosphonate and testosterone in young people with Duchenne muscular dystrophy: an international clinician survey.

Sarah McCarrison, Shima Abdelrahman, Justin H Davies

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Frequent Collaborators

8 joint publications

Rebecca Jane Moon

6 joint publications

Helen L Storr

4 joint publications

David B. N. Lim

3 joint publications

Nicholas C Harvey