M. Johnstone

发表

Synaptic scaffold evolution generated components of vertebrate cognitive complexity

Richard D Emes, D. Clair, L. Saksida, 2012, Nature Neuroscience.

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

S. Lawrie, M. Bastin, A. McIntosh, 2019, bioRxiv.

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

S. Lawrie, M. Bastin, A. McIntosh, 2019, bioRxiv.

Effects of a mis‐sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia

S. Lawrie, H. Whalley, E. Johnstone, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Schizophrenia

P. McKenna, M. Johnstone, S. Jauhar, 2002, The Lancet.

Association of whole-genome and NETRIN1 signaling pathway-derived polygenic risk scores for Major Depressive Disorder and thalamic radiation white matter microstructure in UK Biobank

I. Deary, S. Lawrie, H. Whalley, 2018, bioRxiv.

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

Minna Männikkö, David Curtis, Peter Holmans, 2016, Nature Neuroscience.

A Family With Multiple Cases of Schizophrenia and Mild Intellectual Impairment Also Associated With Retinitis Pigmentosa and / or Progressive Hearing Loss

P. Visscher, N. Wray, A. McRae, 2013 .

Localisation of Microtubule‐Associated Protein 1B Phosphorylation Sites Recognised by Monoclonal Antibody SMI‐31

I. Fischer, M. Johnstone, P. Gordon-Weeks, 1997, Journal of neurochemistry.

Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?

D. Blackwood, B. Pickard, J. Mendlewicz, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

DISC1 in schizophrenia: genetic mouse models and human genomic imaging.

S. Lawrie, A. McIntosh, D. Porteous, 2011, Schizophrenia bulletin.

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

D. St. Clair, M. Johnstone, 2018, Philosophical Transactions of the Royal Society B: Biological Sciences.

Stem Cells to Inform the Neurobiology of Mental Illness.

D. St. Clair, M. Johnstone, R. Hillary, 2018, Current topics in behavioral neurosciences.

The contribution of rare variants to risk of 1 schizophrenia in individuals with and without 2 intellectual disability

Elvira Bramon, David Curtis, Mandy Johnstone, 2017 .

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

Michael R. Johnson, S. Gabriel, M. Daly, 2019, bioRxiv.

Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

D. Geschwind, J. Suvisaari, E. Bramon, 2016, bioRxiv.

HippoCA3mpal Stem Cell Models Expose Dysfunctional Circuits in Schizophrenia.

M. Johnstone, Rana Fetit, 2018, Cell stem cell.

The neurofilament antibody RT97 recognises a developmentally regulated phosphorylation epitope on microtubule‐associated protein 1B

I. Fischer, M. Johnstone, P. Gordon-Weeks, 1997, Journal of anatomy.

Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness

D. Clair, S. Lawrie, A. McIntosh, 2015, Molecular Neuropsychiatry.

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

Bradley P. Coe, M. Pirinen, C. Spencer, 2014, Human molecular genetics.

Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children

S. Lawrie, D. Price, M. Johnstone, 2020, Psychiatric genetics.

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

John P. Rice, Warren W. Kretzschmar, Robert M. Maier, 2019, Biological psychiatry. Cognitive neuroscience and neuroimaging.

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

D. Clair, S. Lawrie, H. Whalley, 2018, Molecular Psychiatry.

Genetics of Schizophrenia

M. Johnstone, I. Escudero, 2014, Current Psychiatry Reports.

A central role for astrocytes in the inflammatory response to β-amyloid; chemokines, cytokines and reactive oxygen species are produced

M. Johnstone, A. Gearing, K. Miller, 1999, Journal of Neuroimmunology.

A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability

P. Visscher, N. Wray, A. McRae, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene

D. Clair, L. Saksida, T. Bussey, 2015, Scientific Reports.

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

S. Lawrie, A. McIntosh, D. Blackwood, 2018, bioRxiv.

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

S. Lawrie, A. McIntosh, D. Blackwood, 2018, bioRxiv.

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

J. Danesh, M. Daly, M. Hurles, 2016, bioRxiv.

Copy-number variations in DISC 1 and DISC 1-interacting partners in major mental illness

A. McIntosh, D. Blackwood, B. Pickard, 2016 .

Bridging the translational divide : identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene

D. Clair, L. Saksida, T. Bussey, 2016 .

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

D. Geschwind, J. Suvisaari, E. Bramon, 2017, Nature Genetics.

D. Clair, S. Lawrie, H. Whalley, 2018, Molecular Psychiatry.

Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness

S. Lawrie, A. McIntosh, D. Blackwood, 2015, Molecular Neuropsychiatry.

Contents Vol. 5, 2019

S. Hyman, K. Brennand, J. Kelsoe, 2019, Molecular Neuropsychiatry.