| Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders T Singh, MI Kurki, D Curtis, SM Purcell, L Crooks, J McRae, J Suvisaari, ... Nature neuroscience 19 (4), 571-577, 2016 | 431 | 2016 |
| A central role for astrocytes in the inflammatory response to β-amyloid; chemokines, cytokines and reactive oxygen species are produced M Johnstone, AJH Gearing, KM Miller Journal of neuroimmunology 93 (1-2), 182-193, 1999 | 415 | 1999 |
| Synaptic scaffold evolution generated components of vertebrate cognitive complexity J Nithianantharajah, NH Komiyama, A McKechanie, M Johnstone, ... Nature neuroscience 16 (1), 16-24, 2013 | 269 | 2013 |
| Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ... The American Journal of Human Genetics 105 (2), 267-282, 2019 | 230 | 2019 |
| The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability T Singh, JTR Walters, M Johnstone, D Curtis, J Suvisaari, M Torniainen, ... Nature genetics 49 (8), 1167-1173, 2017 | 230 | 2017 |
| Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene J Nithianantharajah, AG McKechanie, TJ Stewart, M Johnstone, ... Scientific reports 5 (1), 14613, 2015 | 122 | 2015 |
| DISC1 in schizophrenia: genetic mouse models and human genomic imaging M Johnstone, PA Thomson, J Hall, AM McIntosh, SM Lawrie, DJ Porteous Schizophrenia bulletin 37 (1), 14-20, 2011 | 120 | 2011 |
| Genetics of schizophrenia I Escudero, M Johnstone Current psychiatry reports 16, 1-6, 2014 | 81 | 2014 |
| A phosphorylation epitope on MAP 1B that is transiently expressed in growing axons in the developing rat nervous system PR Gordon‐Weeks, SG Mansfield, C Alberto, M Johnstone, F Moya European Journal of Neuroscience 5 (10), 1302-1311, 1993 | 61 | 1993 |
| Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not? MJ Van Den Bossche, M Johnstone, M Strazisar, BS Pickard, D Goossens, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159 …, 2012 | 44 | 2012 |
| An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis DW Morris, RD Pearson, P Cormican, EM Kenny, CT O'Dushlaine, ... Human molecular genetics 23 (12), 3316-3326, 2014 | 42 | 2014 |
| Reversal of proliferation deficits caused by chromosome 16p13. 11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor … M Johnstone, NA Vasistha, MC Barbu, O Dando, K Burr, E Christopher, ... Molecular psychiatry 24 (2), 294-311, 2019 | 40 | 2019 |
| Swedish Schizophrenia Study; INTERVAL Study; DDD Study; UK10 K Consortium. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders T Singh, MI Kurki, D Curtis, SM Purcell, L Crooks, J McRae, J Suvisaari, ... Nat Neurosci 19 (4), 571-577, 2016 | 36 | 2016 |
| Localisation of microtubule‐associated protein 1B phosphorylation sites recognised by monoclonal antibody SMI‐31 M Johnstone, RG Goold, D Bei, I Fischer, PR Gordon‐Weeks Journal of neurochemistry 69 (4), 1417-1424, 1997 | 36 | 1997 |
| Association of whole-genome and NETRIN1 signaling pathway–derived polygenic risk scores for major depressive disorder and white matter microstructure in the UK Biobank MC Barbu, Y Zeng, X Shen, SR Cox, TK Clarke, J Gibson, MJ Adams, ... Biological Psychiatry: Cognitive Neuroscience and Neuroimaging 4 (1), 91-100, 2019 | 27 | 2019 |
| Using mouse transgenic and human stem cell technologies to model genetic mutations associated with schizophrenia and autism D St. Clair, M Johnstone Philosophical Transactions of the Royal Society B: Biological Sciences 373 …, 2018 | 27 | 2018 |
| Copy number variations in DISC1 and DISC1-interacting partners in major mental illness M Johnstone, A Maclean, L Heyrman, AS Lenaerts, A Nordin, LG Nilsson, ... Complex Psychiatry 1 (3), 175-190, 2015 | 24 | 2015 |
| The neurofilament antibody RT97 recognises a developmentally regulated phosphorylation epitope on microtubule-associated protein 1B M JOHNSTONE, RG GOOLD, I FISCHER, PR GORDON-WEEKS The Journal of Anatomy 191 (2), 229-244, 1997 | 24 | 1997 |
| A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability EM Derks, M Ayub, K Chambert, J Del Favero, M Johnstone, S MacGregor, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 …, 2013 | 23 | 2013 |
| Understanding the clinical manifestations of 16p11. 2 deletion syndrome: a series of developmental case reports in children R Fetit, DJ Price, SM Lawrie, M Johnstone Psychiatric genetics 30 (5), 136-140, 2020 | 22 | 2020 |
