Shane McKee

9PUBLICATIONS
104CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeonatologyAnthropological geneticsMolecular targetsNeurogenetics
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Publications (9)

|Jun 19, 2026
Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?

|Apr 09, 2026
Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome.

Amber S E van Oirsouw, Tzung-Chien Hsieh, Martijn Koetsier

|Apr 03, 2026
Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research Library.

Jenny Lord, Alistair T Pagnamenta, Letizia Vestito

|Feb 25, 2026
Familial pneumothorax in twins with Tatton-Brown-Rahman DNMT3A overgrowth syndrome.

Sarju G Mehta, Simon Holden, Judith Babar

|May 01, 2023
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.

Victoria Patterson, Farid Ullah, Laura Bryant

|Nov 10, 2018
Quantifying the contribution of recessive coding variation to developmental disorders.

Hilary C Martin, Wendy D Jones, Rebecca McIntyre

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Frequent Collaborators

1 joint publications

A Gibbs

1 joint publications

R Braham

1 joint publications

V Ramachandran

1 joint publications

T Ashraf