| Twins early development study: A genetically sensitive investigation into behavioral and cognitive development from infancy to emerging adulthood K Rimfeld, M Malanchini, T Spargo, G Spickernell, S Selzam, A McMillan, ... Twin Research and Human Genetics 22 (6), 508-513, 2019 | 135 | 2019 |
| GEOexplorer: a webserver for gene expression analysis and visualisation GP Hunt, L Grassi, R Henkin, F Smeraldi, TP Spargo, R Kabiljo, S Koks, ... Nucleic Acids Research 50 (W1), W367-W374, 2022 | 27 | 2022 |
| The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration S Opie-Martin, A Iacoangeli, SD Topp, O Abel, K Mayl, PR Mehta, ... Nature communications 13 (1), 6901, 2022 | 20 | 2022 |
| An empirical investigation of parent-child shared reading of digital personalized books N Kucirkova, M Gattis, TP Spargo, BS de Vega, R Flewitt International Journal of Educational Research 105, 101710, 2021 | 13 | 2021 |
| Calculating variant penetrance from family history of disease and average family size in population-scale data TP Spargo, S Opie-Martin, H Bowles, CM Lewis, A Iacoangeli, ... Genome Medicine 14 (1), 141, 2022 | 8* | 2022 |
| Molecular dynamics analysis of superoxide dismutase 1 mutations suggests decoupling between mechanisms underlying ALS onset and progression M Kalia, M Miotto, D Ness, S Opie-Martin, TP Spargo, L Di Rienzo, ... Computational and Structural Biotechnology Journal 21, 5296-5308, 2023 | 5 | 2023 |
| Statistical examination of shared loci in neuropsychiatric diseases using genome-wide association study summary statistics TP Spargo, L Gilchrist, GP Hunt, RJB Dobson, P Proitsi, A Al-Chalabi, ... MedRxiv, 2023.03. 30.23287950, 2023 | 1 | 2023 |
| Mutations in the tail domain of the neurofilament heavy chain gene increase the risk of amyotrophic lateral sclerosis H Marriott, TP Spargo, AA Khleifat, I Fogh, ... medRxiv, 2022.11. 03.22281905, 2022 | 1 | 2022 |
| A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression JNG Marshall, A Fröhlich, L Li, AL Pfaff, B Middlehurst, TP Spargo, ... Frontiers in molecular neuroscience 15, 954928, 2022 | 1 | 2022 |
| SOD1-ALS-Browser: a web-utility for investigating the clinical phenotype in SOD1 amyotrophic lateral sclerosis TP Spargo, S Opie-Martin, GP Hunt, M Kalia, A Al Khleifat, SD Topp, ... Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24 (7-8), 736-745, 2023 | | 2023 |
| A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP correlates with differential isoform expression JNG Marshall, A Fröhlich, L Li, AL Pfa, B Middlehurst, TP Spargo, ... RNA at a breaking point? cytoplasmic cleavage and other post-transcriptional …, 2023 | | 2023 |
| Investigating the genetic relationship between depression symptoms and Alzheimer’s Disease in clinically diagnosed and proxy cases L Gilchrist, TP Spargo, RE Green, JRI Coleman, DM Howard, JG Thorp, ... medRxiv, 2023.06. 05.23290588, 2023 | | 2023 |
| Genetic and phenotype analyses of primary lateral sclerosis datasets from international cohorts M Kalia, TP Spargo, A Al Khleifat, S Opie Martin, R Kabiljo, R Dobson, ... medRxiv, 2023.07. 19.23292817, 2023 | | 2023 |
| Modelling population genetic screening in rare neurodegenerative diseases TP Spargo, alfredo iacoangeli, M Ryten, F Forzano, N Pearce, ... medRxiv, 2023.07. 03.23292187, 2023 | | 2023 |
| Unsupervised machine-learning identifies clinically distinct subtypes of ALS that reflect different genetic architectures and biological mechanisms TP Spargo, H Marriott, G Hunt, O Pain, R Kabiljo, H Bowles, W Sproviero, ... medRxiv, 2023.06. 12.23291304, 2023 | | 2023 |
| The relationship between genotype and phenotype in amyotrophic lateral sclerosis TP Spargo | | 2014 |
