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Mandy Johnstone
Observed names:
Johnstone, M.,
Johnstone, Mandy,
M. Johnstone,
MANDY JOHNSTONE
Institution:
King's College London
Observed institutions:
King's College London,
South London and Maudsley NHS Foundation Trust,
Oulu University Hospital,
Western General Hospital,
Royal Edinburgh Hospital,
Institute of Genetics and Cancer,
University of Oulu,
University of Edinburgh
show all 8
ORCID:
0000-0002-8398-0862
Observed ORCID:
0000-0002-8398-0862
OpenAlex ID:
A5078812408
Schizophrenia
2022
·
Sameer Jauhar
, Mandy Johnstone
, et al.
·
The Lancet
·
1,031
PDF
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
2016
·
Swedish Schizophrenia Study
, Tarjinder Singh
, et al.
·
Nature Neuroscience
·
452
PDF
A central role for astrocytes in the inflammatory response to β-amyloid; chemokines, cytokines and reactive oxygen species are produced
1999
·
Mandy Johnstone
, Andrew J.H Gearing
, et al.
·
Journal of Neuroimmunology
·
314
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
2019
·
Yen-Chen Anne Feng
, Daniel P. Howrigan
, et al.
·
The American Journal of Human Genetics
·
297
PDF
Synaptic scaffold evolution generated components of vertebrate cognitive complexity
2012
·
Jess Nithianantharajah
, Noboru H Komiyama
, et al.
·
Nature Neuroscience
·
256
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability
2017
·
Tarjinder Singh
, James T R Walters
, et al.
·
Nature Genetics
·
231
Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene
2015
·
J. Nithianantharajah
, A. G. McKechanie
, et al.
·
Scientific Reports
·
116
PDF
DISC1 in Schizophrenia: Genetic Mouse Models and Human Genomic Imaging
2010
·
M. Johnstone
, P. A. Thomson
, et al.
·
Schizophrenia Bulletin
·
101
PDF
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
2024
·
Epi25 Collaborative
, Siwei Chen
, et al.
·
Nature Neuroscience
·
72
PDF
Genetics of Schizophrenia
2014
·
Irene Escudero
, Mandy Johnstone
·
Current Psychiatry Reports
·
61
A Phosphorylation Epitope on MAP 1B that is Transiently Expressed in Growing Axons in the Developing Rat Nervous System
1993
·
Phillip R. Gordon‐Weeks
, S. Gary Mansfield
, et al.
·
European Journal of Neuroscience
·
44
Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children
2020
·
Rana Fetit
, David J. Price
, et al.
·
Psychiatric Genetics
·
42
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
2018
·
Mandy Johnstone
, Navneet A. Vasistha
, et al.
·
Molecular Psychiatry
·
42
PDF
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis
2014
·
D. W. Morris
, R. D. Pearson
, et al.
·
Human Molecular Genetics
·
42
PDF
Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
2012
·
Maarten J. Van Den Bossche
, Mandy Johnstone
, et al.
·
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
39
Localisation of Microtubule‐Associated Protein 1B Phosphorylation Sites Recognised by Monoclonal Antibody SMI‐31
1997
·
Mandy Johnstone
, Robert G. Goold
, et al.
·
Journal of Neurochemistry
·
37
PDF
DISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness
2018
·
Elise L. V. Malavasi
, Kyriakos D. Economides
, et al.
·
Translational Psychiatry
·
26
PDF
Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte–myelin dysfunction
2019
·
Navneet A. Vasistha
, Mandy Johnstone
, et al.
·
Molecular Psychiatry
·
24
PDF
Using mouse transgenic and human stem cell technologies to model genetic mutations associated with schizophrenia and autism
2018
·
David St. Clair
, Mandy Johnstone
·
Philosophical Transactions of the Royal Society B Biological Sciences
·
24
PDF
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability
2013
·
Eske M. Derks
, Muhammad Ayub
, et al.
·
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
23
PDF
Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank
2018
·
Miruna C. Barbu
, Yanni Zeng
, et al.
·
Biological Psychiatry Cognitive Neuroscience and Neuroimaging
·
21
PDF
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness
2015
·
Mandy Johnstone
, Alan Maclean
, et al.
·
Complex Psychiatry
·
20
PDF
The neurofilament antibody RT97 recognises a developmentally regulated phosphorylation epitope on microtubule‐associated protein 1B
1997
·
MANDY JOHNSTONE
, ROBERT G. GOOLD
, et al.
·
Journal of Anatomy
·
20
Distinct gene-set burden patterns underlie common generalized and focal epilepsies
2021
·
Mahmoud Koko
, Roland Krause
, et al.
·
EBioMedicine
·
18
PDF
Effects of a mis‐sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia
2012
·
Heather C. Whalley
, Jessika E. Sussmann
, et al.
·
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
15
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Works count:
53
Citation count:
3,407
H-index:
21
I10-index:
26
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