| Year |
Citation |
Score |
| 2020 |
Fetit R, Price DJ, Lawrie SM, Johnstone M. Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children. Psychiatric Genetics. PMID 32732550 DOI: 10.1097/Ypg.0000000000000259 |
0.353 |
|
| 2019 |
Vasistha NA, Johnstone M, Barton SK, Mayerl SE, Thangaraj Selvaraj B, Thomson PA, Dando O, Grünewald E, Alloza C, Bastin ME, Livesey MR, Economides K, Magnani D, Makedonopolou P, Burr K, et al. Transplanted t(1;11) patient-derived OPCs form shorter myelin internodes in the hypomyelinated shiverer mice. Molecular Psychiatry. 24: 1567. PMID 31645684 DOI: 10.1038/S41380-019-0543-9 |
0.652 |
|
| 2019 |
Vasistha NA, Johnstone M, Barton SK, Mayerl SE, Thangaraj Selvaraj B, Thomson PA, Dando O, Grünewald E, Alloza C, Bastin ME, Livesey MR, Economides K, Magnani D, Makedonopolou P, Burr K, et al. Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunction. Molecular Psychiatry. PMID 31481758 DOI: 10.1038/S41380-019-0505-2 |
0.686 |
|
| 2019 |
Barbu M, Zeng Y, Shen X, Cox S, Clarke T, Gibson J, Adams M, Johnstone M, Haley CS, Lawrie S, Deary IJ, McIntosh A, Whalley H. Sa81Association Of Whole-Genome And Netrin1 Signaling Pathway-Derived Polygenic Risk Scores For Major Depressive Disorder And White Matter Microstructure In Uk Biobank European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.303 |
0.325 |
|
| 2019 |
Johnstone M, Vasistha N, Barbu M, Dando O, Burr K, Christopher E, Glen S, Johnstone EC, Whalley H, McIntosh A, Lawrie S, Chandran S. 23MODELING A GENETIC RISK FOR SCHIZOPHRENIA: PHENOTYPIC DIFFERENCES IN HUMAN NEURAL PRECURSORS AND CEREBRAL ORGANOIDS FROM PATIENTS WITH CHR16P13.11 MICRODUPLICATIONS European Neuropsychopharmacology. 29: S1079. DOI: 10.1016/J.Euroneuro.2018.08.030 |
0.708 |
|
| 2018 |
Johnstone M, Vasistha NA, Barbu MC, Dando O, Burr K, Christopher E, Glen S, Robert C, Fetit R, Macleod KG, Livesey MR, Clair DS, Blackwood DHR, Millar K, Carragher NO, et al. 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. Molecular Psychiatry. PMID 30401811 DOI: 10.1038/S41380-018-0292-1 |
0.679 |
|
| 2018 |
Barbu MC, Zeng Y, Shen X, Cox SR, Clarke TK, Gibson J, Adams MJ, Johnstone M, Haley CS, Lawrie SM, Deary IJ, McIntosh AM, Whalley HC. Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank. Biological Psychiatry. Cognitive Neuroscience and Neuroimaging. PMID 30197049 DOI: 10.1016/J.Bpsc.2018.07.006 |
0.346 |
|
| 2018 |
Malavasi ELV, Economides KD, Grünewald E, Makedonopoulou P, Gautier P, Mackie S, Murphy LC, Murdoch H, Crummie D, Ogawa F, McCartney DL, O'Sullivan ST, Burr K, Torrance HS, Phillips J, ... ... Johnstone M, et al. DISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness. Translational Psychiatry. 8: 184. PMID 30190480 DOI: 10.1038/S41398-018-0228-1 |
0.426 |
|
| 2018 |
Johnstone M, Hillary RF, St Clair D. Stem Cells to Inform the Neurobiology of Mental Illness. Current Topics in Behavioral Neurosciences. PMID 30030769 DOI: 10.1007/7854_2018_57 |
0.423 |
|
| 2018 |
Johnstone M, Fetit R. HippoCA3mpal Stem Cell Models Expose Dysfunctional Circuits in Schizophrenia. Cell Stem Cell. 22: 609-611. PMID 29727672 DOI: 10.1016/J.Stem.2018.04.008 |
0.44 |
|
| 2018 |
St Clair D, Johnstone M. Using mouse transgenic and human stem cell technologies to model genetic mutations associated with schizophrenia and autism. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 373. PMID 29352035 DOI: 10.1098/Rstb.2017.0037 |
0.466 |
|
| 2017 |
Singh T, Walters JTR, Johnstone M, Curtis D, Suvisaari J, Torniainen M, Rees E, Iyegbe C, Blackwood D, McIntosh AM, Kirov G, Geschwind D, Murray RM, Di Forti M, Bramon E, et al. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nature Genetics. PMID 28650482 DOI: 10.1038/Ng.3903 |
0.481 |
|
| 2017 |
Johnstone M, Vasistha N, Livesey M, Burr K, Whalley H, Clair DS, Blackwood D, Wyllie D, Lawrie S, Johnstone EC, McIntosh AM, Chandran S. Modelling a Genetic Risk for Schizophrenia in Human Induced Pluripotent Stem Cells (Ipscs): Phenotypic Differences in Patients with Mutations in Nde1 European Neuropsychopharmacology. 27: S509-S510. DOI: 10.1016/J.Euroneuro.2016.09.618 |
0.722 |
|
| 2017 |
Reiner O, Johnstone M, Sapir T. Novel Insights, Modeling and Translational Approaches in Autism-Schizophrenia Spectrum Diseases European Neuropsychopharmacology. 27: S509. DOI: 10.1016/J.Euroneuro.2016.09.616 |
0.404 |
|
| 2017 |
Johnstone M, Vasistha N, Whalley H, Burr K, St. Clair D, Blackwood D, Johnstone E, Lawrie S, McIntosh A, Chandran S. 437. Modeling Schizophrenia in Human Induced Pluripotent Stem Cells (hiPSCs): Phenotypic Differences in Patients with Mutations in NDE1 Biological Psychiatry. 81: S178-S179. DOI: 10.1016/J.Biopsych.2017.02.921 |
0.698 |
|
| 2016 |
Singh T, Kurki MI, Curtis D, Purcell SM, Crooks L, McRae J, Suvisaari J, Chheda H, Blackwood D, Breen G, Pietiläinen O, Gerety SS, Ayub M, Blyth M, Cole T, ... ... Johnstone M, et al. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. Nature Neuroscience. PMID 26974950 DOI: 10.1038/Nn.4267 |
0.464 |
|
| 2015 |
Johnstone M, Maclean A, Heyrman L, Lenaerts AS, Nordin A, Nilsson LG, De Rijk P, Goossens D, Adolfsson R, St Clair DM, Hall J, Lawrie SM, McIntosh AM, Del-Favero J, Blackwood DH, et al. Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness. Molecular Neuropsychiatry. 1: 175-190. PMID 27239468 DOI: 10.1159/000438788 |
0.326 |
|
| 2015 |
Nithianantharajah J, McKechanie AG, Stewart TJ, Johnstone M, Blackwood DH, St Clair D, Grant SG, Bussey TJ, Saksida LM. Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene. Scientific Reports. 5: 14613. PMID 26423861 DOI: 10.1038/Srep14613 |
0.314 |
|
| 2014 |
Escudero I, Johnstone M. Genetics of schizophrenia. Current Psychiatry Reports. 16: 502. PMID 25200985 DOI: 10.1007/S11920-014-0502-8 |
0.442 |
|
| 2014 |
Morris DW, Pearson RD, Cormican P, Kenny EM, O'Dushlaine CT, Perreault LP, Giannoulatou E, Tropea D, Maher BS, Wormley B, Kelleher E, Fahey C, Molinos I, Bellini S, Pirinen M, ... ... Johnstone M, et al. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics. 23: 3316-26. PMID 24474471 DOI: 10.1093/Hmg/Ddu025 |
0.417 |
|
| 2013 |
Derks EM, Ayub M, Chambert K, Del Favero J, Johnstone M, Macgregor S, Maclean A, Mckechanie AG, Mcrae AF, Moran JL, Pickard BS, Purcell S, Sklar P, Stclair DM, Wray NR, et al. A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 162: 847-854. PMID 24115684 DOI: 10.1002/Ajmg.B.32189 |
0.455 |
|
| 2012 |
Pickard BS, Van Den Bossche MJ, Malloy MP, Johnstone M, Lenaerts AS, Nordin A, Goossens D, St Clair D, Muir WJ, Nilsson LG, Sabbe B, Adolfsson R, Blackwood DH, Del-Favero J. Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder. Psychiatric Genetics. 22: 269-70. PMID 22392056 DOI: 10.1097/Ypg.0B013E32835185B3 |
0.388 |
|
| 2012 |
Whalley HC, Sussmann JE, Johnstone M, Romaniuk L, Redpath H, Chakirova G, Mukherjee P, Hall J, Johnstone EC, Lawrie SM, McIntosh AM. Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 343-53. PMID 22337479 DOI: 10.1002/Ajmg.B.32035 |
0.394 |
|
| 2011 |
Johnstone M, Thomson PA, Hall J, McIntosh AM, Lawrie SM, Porteous DJ. DISC1 in schizophrenia: genetic mouse models and human genomic imaging. Schizophrenia Bulletin. 37: 14-20. PMID 21149852 DOI: 10.1093/Schbul/Sbq135 |
0.485 |
|
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