Miho Ishida
5PUBLICATIONS
11CO-AUTHORS
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Publications (5)
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|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
|Nov 01, 2025
Pathogenesis of Noonan Syndrome is Modulated by NOC2L, a Novel Interactor of LZTR1 Leading to Impaired P53 Signalling.Sumana Chatterjee, Miho Ishida, Débora R Bertola
|Feb 25, 2025
A Tiered Approach to Exome Sequencing Analysis in Early-Onset Primary Ovarian Insufficiency.Sinéad M McGlacken-Byrne, Jenifer P Suntharalingham, Miho Ishida
|Jun 18, 2024
Approach to the Patient With Suspected Silver-Russell Syndrome.Uttara Kurup, David B N Lim, Helena Palau
|Dec 06, 2017
A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly.M Ishida, T Cullup, C Boustred
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Frequent Collaborators
3 joint publications
Avinaash V Maharaj
3 joint publications
Helen L Storr
2 joint publications
Uttara Kurup
2 joint publications
David B N Lim
2 joint publications
Justin H Davies
1 joint publications
Helena Palau
1 joint publications
Sinéad M McGlacken-Byrne
1 joint publications
Federica Buonocore
1 joint publications
John C Achermann
1 joint publications
Gerard S Conway
