| Defining the effect of the 16p11. 2 duplication on cognition, behavior, and medical comorbidities D D’Angelo, S Lebon, Q Chen, S Martin-Brevet, LAG Snyder, L Hippolyte, ... JAMA psychiatry 73 (1), 20-30, 2016 | 224 | 2016 |
| Psychiatric disorders in children with 16p11. 2 deletion and duplication M Niarchou, SJRA Chawner, JL Doherty, AM Maillard, S Jacquemont, ... Translational psychiatry 9 (1), 8, 2019 | 138 | 2019 |
| Using common genetic variation to examine phenotypic expression and risk prediction in 22q11. 2 deletion syndrome RW Davies, AM Fiksinski, EJ Breetvelt, NM Williams, SR Hooper, ... Nature Medicine 26 (12), 1912-1918, 2020 | 101 | 2020 |
| Genotype–phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study SJRA Chawner, MJ Owen, P Holmans, FL Raymond, D Skuse, J Hall, ... The Lancet Psychiatry 6 (6), 493-505, 2019 | 99 | 2019 |
| A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants SJRA Chawner, JL Doherty, RJL Anney, KM Antshel, CE Bearden, ... American Journal of Psychiatry 178 (1), 77-86, 2021 | 68 | 2021 |
| Childhood cognitive development in 22q11. 2 deletion syndrome: case–control study SJRA Chawner, JL Doherty, H Moss, M Niarchou, JTR Walters, MJ Owen, ... The British Journal of Psychiatry 211 (4), 223-230, 2017 | 46 | 2017 |
| Variance of IQ is partially dependent on deletion type among 1,427 22q11. 2 deletion syndrome subjects Y Zhao, T Guo, A Fiksinski, E Breetvelt, DM McDonald‐McGinn, ... American Journal of Medical Genetics Part A 176 (10), 2172-2181, 2018 | 41 | 2018 |
| Cognitive deficits in childhood, adolescence and adulthood in 22q11. 2 deletion syndrome and association with psychopathology S Morrison, SJRA Chawner, TAMJ van Amelsvoort, A Swillen, ... Translational psychiatry 10 (1), 53, 2020 | 36 | 2020 |
| Genes to Mental Health (G2MH): a framework to map the combined effects of rare and common variants on dimensions of cognition and psychopathology S Jacquemont, G Huguet, M Klein, SJRA Chawner, KA Donald, ... American Journal of Psychiatry 179 (3), 189-203, 2022 | 35 | 2022 |
| 16p11. 2 locus modulates response to satiety before the onset of obesity AM Maillard, L Hippolyte, B Rodriguez-Herreros, S Chawner, D Dremmel, ... International Journal of Obesity 40 (5), 870-876, 2016 | 34 | 2016 |
| Deletion size analysis of 1680 22q11. 2DS subjects identifies a new recombination hotspot on chromosome 22q11. 2 T Guo, A Diacou, H Nomaru, DM McDonald-McGinn, M Hestand, ... Human molecular genetics 27 (7), 1150-1163, 2018 | 30 | 2018 |
| The emergence of psychotic experiences in the early adolescence of 22q11. 2 Deletion Syndrome SJRA Chawner, M Niarchou, JL Doherty, H Moss, MJ Owen, ... Journal of psychiatric research 109, 10-17, 2019 | 26 | 2019 |
| Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11. 2 deletion syndrome M Niarchou, SJRA Chawner, A Fiksinski, JAS Vorstman, J Maeder, ... Schizophrenia research 204, 320-325, 2019 | 24 | 2019 |
| Neurodevelopmental trajectories and psychiatric morbidity: lessons learned from the 22q11. 2 deletion syndrome AM Fiksinski, M Schneider, J Zinkstok, D Baribeau, SJRA Chawner, ... Current Psychiatry Reports 23, 1-11, 2021 | 23 | 2021 |
| Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study J Wolstencroft, F Wicks, R Srinivasan, S Wynn, T Ford, K Baker, ... The Lancet Psychiatry 9 (9), 715-724, 2022 | 18 | 2022 |
| ‘We have been in lockdown since he was born’: a mixed methods exploration of the experiences of families caring for children with intellectual disability during the COVID-19 … J Wolstencroft, L Hull, L Warner, TN Akhtar, W Mandy, D Skuse BMJ open 11 (9), e049386, 2021 | 17 | 2021 |
| Clinical evaluation of patients with a neuropsychiatric risk copy number variant SJRA Chawner, CJ Watson, MJ Owen Current Opinion in Genetics & Development 68, 26-34, 2021 | 15 | 2021 |
| Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD D Drakulic, S Djurovic, YA Syed, S Trattaro, N Caporale, A Falk, R Ofir, ... Molecular autism 11, 1-18, 2020 | 15 | 2020 |
| A normative chart for cognitive development in a genetically selected population AM Fiksinski, CE Bearden, AS Bassett, RS Kahn, JR Zinkstok, SR Hooper, ... Neuropsychopharmacology 47 (7), 1379-1386, 2022 | 14 | 2022 |
| The psychiatric phenotypes of 1q21 distal deletion and duplication SC Linden, CJ Watson, J Smith, SJRA Chawner, TM Lancaster, F Evans, ... Translational psychiatry 11 (1), 105, 2021 | 10 | 2021 |
