| Making sense of cilia in disease: the human ciliopathies K Baker, PL Beales American journal of medical genetics part C: seminars in medical genetics …, 2009 | 418 | 2009 |
| Adolescents and young adults with 22qll deletion syndrome: psychopathology in an at-risk group KD Baker, DH Skuse The British Journal of Psychiatry 186 (2), 115-120, 2005 | 232 | 2005 |
| COMT Val108/158Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome K Baker, T Baldeweg, S Sivagnanasundaram, P Scambler, D Skuse Biological Psychiatry 58 (1), 23-31, 2005 | 179 | 2005 |
| Cognitive training enhances intrinsic brain connectivity in childhood DE Astle, JJ Barnes, K Baker, GL Colclough, MW Woolrich Journal of Neuroscience 35 (16), 6277-6283, 2015 | 161 | 2015 |
| Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling K Baker, SL Gordon, D Grozeva, M Van Kogelenberg, NY Roberts, M Pike, ... The Journal of clinical investigation 125 (4), 1670-1678, 2015 | 108 | 2015 |
| SYT1-associated neurodevelopmental disorder: a case series K Baker, SL Gordon, H Melland, F Bumbak, DJ Scott, TJ Jiang, D Owen, ... Brain 141 (9), 2576-2591, 2018 | 104 | 2018 |
| Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder A Chaudhry, A Noor, B Degagne, K Baker, LA Bok, AF Brady, D Chitayat, ... Clinical genetics 88 (3), 224-233, 2015 | 90 | 2015 |
| Expression of serotonin 5‐HT2A receptors in the human cerebellum and alterations in schizophrenia SL Eastwood, PWJ Burnet, R Gittins, K Baker, PJ Harrison Synapse 42 (2), 104-114, 2001 | 86 | 2001 |
| Towards a safety net for management of 22q11. 2 deletion syndrome: guidelines for our times A Habel, R Herriot, D Kumararatne, J Allgrove, K Baker, H Baxendale, ... European journal of pediatrics 173, 757-765, 2014 | 85 | 2014 |
| Is there a core neuropsychiatric phenotype in 22q11. 2 deletion syndrome? K Baker, JAS Vorstman Current opinion in neurology 25 (2), 131-137, 2012 | 76 | 2012 |
| Neocortical and hippocampal volume loss in a human ciliopathy: a quantitative MRI study in Bardet–Biedl syndrome K Baker, GB Northam, WK Chong, T Banks, P Beales, T Baldeweg American journal of medical genetics Part A 155 (1), 1-8, 2011 | 71 | 2011 |
| Assessing the landscape of STXBP1-related disorders in 534 individuals J Xian, S Parthasarathy, SM Ruggiero, G Balagura, E Fitch, K Helbig, ... Brain 145 (5), 1668-1683, 2022 | 61 | 2022 |
| The strengths and difficulties questionnaire predicts concurrent mental health difficulties in a transdiagnostic sample of struggling learners A Bryant, J Guy, CALM Team, J Holmes Frontiers in psychology 11, 587821, 2020 | 50 | 2020 |
| Training working memory in childhood enhances coupling between frontoparietal control network and task-related regions JJ Barnes, AC Nobre, MW Woolrich, K Baker, DE Astle Journal of Neuroscience 36 (34), 9001-9011, 2016 | 50 | 2016 |
| Childhood intellectual disability and parents' mental health: integrating social, psychological and genetic influences K Baker, RT Devine, E Ng-Cordell, FL Raymond, C Hughes The British Journal of Psychiatry 218 (6), 315-322, 2021 | 47 | 2021 |
| Speech and oromotor outcome in adolescents born preterm: relationship to motor tract integrity GB Northam, F Liégeois, WK Chong, K Baker, JD Tournier, JS Wyatt, ... The Journal of pediatrics 160 (3), 402-408. e1, 2012 | 44 | 2012 |
| The neurodevelopmental spectrum of synaptic vesicle cycling disorders A John, E Ng‐Cordell, N Hanna, D Brkic, K Baker Journal of neurochemistry 157 (2), 208-228, 2021 | 41 | 2021 |
| Protein structure and phenotypic analysis of pathogenic and population missense variants in STXBP1 M Suri, JMG Evers, RA Laskowski, S O'Brien, K Baker, J Clayton‐Smith, ... Molecular genetics & genomic medicine 5 (5), 495-507, 2017 | 39 | 2017 |
| Epilepsy, cognitive deficits and neuroanatomy in males with ZDHHC9 mutations K Baker, DE Astle, G Scerif, J Barnes, J Smith, G Moffat, J Gillard, ... Annals of clinical and translational neurology 2 (5), 559-569, 2015 | 36 | 2015 |
| Structural brain abnormalities in a single gene disorder associated with epilepsy, language impairment and intellectual disability J Bathelt, D Astle, J Barnes, FL Raymond, K Baker NeuroImage: Clinical 12, 655-665, 2016 | 35 | 2016 |
