| New insights into the genetic etiology of Alzheimer’s disease and related dementias C Bellenguez, F Küçükali, IE Jansen, L Kleineidam, S Moreno-Grau, ... Nature genetics 54 (4), 412-436, 2022 | 918 | 2022 |
| Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ... Nature genetics 49 (9), 1373-1384, 2017 | 912 | 2017 |
| The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes K Brookes, X Xu, W Chen, K Zhou, B Neale, N Lowe, R Aneey, B Franke, ... Molecular psychiatry 11 (10), 934-953, 2006 | 706 | 2006 |
| A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy KJ Brookes, J Mill, C Guindalini, S Curran, X Xu, J Knight, CK Chen, ... Archives of general psychiatry 63 (1), 74-81, 2006 | 399 | 2006 |
| Confirmation that a specific haplotype of the dopamine transporter gene is associated with combined-type ADHD P Asherson, K Brookes, B Franke, W Chen, M Gill, RP Ebstein, J Buitelaar, ... American Journal of Psychiatry 164 (4), 674-677, 2007 | 177 | 2007 |
| Association of fatty acid desaturase genes with attention-deficit/hyperactivity disorder KJ Brookes, W Chen, X Xu, E Taylor, P Asherson Biological psychiatry 60 (10), 1053-1061, 2006 | 167 | 2006 |
| Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies KE Tansey, KJ Brookes, MJ Hill, LE Cochrane, M Gill, D Skuse, C Correia, ... Neuroscience letters 474 (3), 163-167, 2010 | 131 | 2010 |
| 5HTT genotype moderates the influence of early institutional deprivation on emotional problems in adolescence: evidence from the English and Romanian Adoptee (ERA) study R Kumsta, S Stevens, K Brookes, W Schlotz, J Castle, C Beckett, ... Journal of Child Psychology and Psychiatry 51 (7), 755-762, 2010 | 124 | 2010 |
| Dopamine transporter gene polymorphism moderates the effects of severe deprivation on ADHD symptoms: Developmental continuities in gene–environment interplay SE Stevens, R Kumsta, JM Kreppner, KJ Brookes, M Rutter, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150 …, 2009 | 117 | 2009 |
| Recalibrating the epigenetic clock: implications for assessing biological age in the human cortex GL Shireby, JP Davies, PT Francis, J Burrage, EM Walker, GWA Neilson, ... Brain 143 (12), 3763-3775, 2020 | 116 | 2020 |
| Relationship between VNTR polymorphisms of the human dopamine transporter gene and expression in post‐mortem midbrain tissue KJ Brookes, BM Neale, K Sugden, N Khan, P Asherson, UM D'Souza American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007 | 113 | 2007 |
| Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD J Park, M Willmott, G Vetuz, C Toye, A Kirley, Z Hawi, KJ Brookes, M Gill, ... Progress in Neuro-Psychopharmacology and Biological Psychiatry 34 (4), 697-702, 2010 | 109 | 2010 |
| Alzheimer’s disease polygenic risk score as a predictor of conversion from mild-cognitive impairment S Chaudhury, KJ Brookes, T Patel, A Fallows, T Guetta-Baranes, ... Translational psychiatry 9 (1), 154, 2019 | 95 | 2019 |
| A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16 P Asherson, K Zhou, RJL Anney, B Franke, J Buitelaar, R Ebstein, M Gill, ... Molecular psychiatry 13 (5), 514-521, 2008 | 95 | 2008 |
| Genetic variability in response to amyloid beta deposition influences Alzheimer’s disease risk DA Salih, S Bayram, S Guelfi, RH Reynolds, M Shoai, M Ryten, ... Brain communications 1 (1), fcz022, 2019 | 84 | 2019 |
| A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene N Magusali, AC Graham, TM Piers, P Panichnantakul, U Yaman, M Shoai, ... Brain 144 (12), 3727-3741, 2021 | 81 | 2021 |
| Family‐based association study between brain‐derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples X Xu, J Mill, K Zhou, K Brookes, CK Chen, P Asherson American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007 | 77 | 2007 |
| Increased cerebral perfusion in adult attention deficit hyperactivity disorder is normalised by stimulant treatment: a non-invasive MRI pilot study RL O'Gorman, MA Mehta, P Asherson, FO Zelaya, KJ Brookes, BK Toone, ... Neuroimage 42 (1), 36-41, 2008 | 74 | 2008 |
| DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: no evidence for association X Xu, J Knight, K Brookes, J Mill, P Sham, I Craig, E Taylor, P Asherson American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 134 …, 2005 | 74 | 2005 |
| New insights on the genetic etiology of Alzheimer’s and related dementia C Bellenguez, F Küçükali, I Jansen, V Andrade, S Moreno-Grau, N Amin, ... MedRxiv, 2020.10. 01.20200659, 2020 | 71 | 2020 |
