Emma Clement
6PUBLICATIONS
29CO-AUTHORS
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Publications (6)
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|Dec 19, 2025
Loss of CTLH component MAEA impairs DNA repair and replication and leads to developmental delay.Søren H Hough, Satpal S Jhujh, Samah W Awwad
|Dec 18, 2025
Analysis of familial exudative vitreoretinopathy (FEVR) cases in the UK 100 000 genomes project increases diagnostic rate and implicates heterozygous CTNND1 mutations in FEVR.Dong Sun, Robert H Henderson, Emma Clement
|Jul 29, 2025
A New GlyT2 Variant Associated with Hyperekplexia.Jorge Sarmiento-Jiménez, Raquel Felipe, Enrique Núñez
|Dec 22, 2022
Subtle Malformation of the Cochlear Apex and Genetic Abnormalities: Beyond the "Thorny" Cochlea.F D'Arco, A Biswas, E Clement
|Sep 29, 2022
The Cochlea in Branchio-Oto-Renal Syndrome: An Objective Method for the Diagnosis of Offset Cochlear Turns.A F Juliano, F D'Arco, J Pao
|Jan 21, 2022
Re-Examining the Cochlea in Branchio-Oto-Renal Syndrome: Genotype-Phenotype Correlation.J Pao, F D'Arco, E Clement
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Frequent Collaborators
3 joint publications
F D'Arco
3 joint publications
A F Juliano
2 joint publications
J Pao
2 joint publications
S Picariello
2 joint publications
G Moonis
2 joint publications
C D Robson
1 joint publications
A Biswas
1 joint publications
K Rajput
1 joint publications
Jorge Sarmiento-Jiménez
1 joint publications
Cristina Benito-Muñoz
