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Mandy Johnstone

5PUBLICATIONS

16CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Gene and molecular therapyGene expression (incl. microarray and other genome-wide approaches)

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Publications (5)

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|Sep 05, 2019

Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunction.

Navneet A Vasistha, Mandy Johnstone, Samantha K Barton

|Nov 08, 2018

Reversal of proliferation deficits caused by chromosome 16p13.11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor cells, cerebral organoids and in vivo brain imaging.

Mandy Johnstone, Navneet A Vasistha, Miruna C Barbu

|Sep 08, 2018

DISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness.

Elise L V Malavasi, Kyriakos D Economides, Ellen Grünewald

|Jan 21, 2018

Using mouse transgenic and human stem cell technologies to model genetic mutations associated with schizophrenia and autism.

David St Clair, Mandy Johnstone

|Jun 27, 2017

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.

Tarjinder Singh, James T R Walters, Mandy Johnstone

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Frequent Collaborators

4 joint publications

Andrew M McIntosh

3 joint publications

Douglas H R Blackwood

2 joint publications

Stephen M Lawrie

2 joint publications

Navneet A Vasistha

1 joint publications

Jaana Suvisaari

1 joint publications

Elvira Bramon

1 joint publications

Michael Gandal

1 joint publications

Michael C O'Donovan

1 joint publications

Michael J Owen

1 joint publications

Jeffrey C Barrett

Frequent Collaborators

4 joint publications

Andrew M McIntosh

3 joint publications

Douglas H R Blackwood

2 joint publications

Stephen M Lawrie

2 joint publications

Navneet A Vasistha

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