| Psychiatric disorders from childhood to adulthood in 22q11. 2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11. 2 Deletion Syndrome M Schneider, M Debbané, AS Bassett, EWC Chow, WLA Fung, ... American Journal of Psychiatry 171 (6), 627-639, 2014 | 670 | 2014 |
| 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 | 114 | 2019 |
| Psychopathology and cognition in children with 22q11. 2 deletion syndrome M Niarchou, S Zammit, SHM van Goozen, A Thapar, HM Tierling, ... The British Journal of Psychiatry 204 (1), 46-54, 2014 | 106 | 2014 |
| Further evidence for high rates of schizophrenia in 22q11. 2 deletion syndrome S Monks, M Niarchou, AR Davies, JTR Walters, N Williams, MJ Owen, ... Schizophrenia research 153 (1-3), 231-236, 2014 | 98 | 2014 |
| Rare genome-wide copy number variation and expression of schizophrenia in 22q11. 2 deletion syndrome AS Bassett, C Lowther, D Merico, G Costain, EWC Chow, ... American Journal of Psychiatry 174 (11), 1054-1063, 2017 | 91 | 2017 |
| Genetic contributors to risk of schizophrenia in the presence of a 22q11. 2 deletion I Cleynen, W Engchuan, MS Hestand, T Heung, AM Holleman, ... Molecular psychiatry 26 (8), 4496-4510, 2021 | 90 | 2021 |
| 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 | 84 | 2020 |
| Enhanced maternal origin of the 22q11. 2 deletion in velocardiofacial and DiGeorge syndromes M Delio, T Guo, DM McDonald-McGinn, E Zackai, S Herman, ... The American Journal of Human Genetics 92 (3), 439-447, 2013 | 73 | 2013 |
| A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11. 2 Deletion Syndrome Brain Behavior Consortium RE Gur, AS Bassett, DM McDonald-McGinn, CE Bearden, E Chow, ... Molecular psychiatry 22 (12), 1664-1672, 2017 | 70 | 2017 |
| Copy-number variation of the glucose transporter gene SLC2A3 and congenital heart defects in the 22q11. 2 deletion syndrome EE Mlynarski, MB Sheridan, M Xie, T Guo, SE Racedo, ... The American Journal of Human Genetics 96 (5), 753-764, 2015 | 66 | 2015 |
| Rare copy number variants and congenital heart defects in the 22q11. 2 deletion syndrome EE Mlynarski, M Xie, D Taylor, MB Sheridan, T Guo, SE Racedo, ... Human genetics 135, 273-285, 2016 | 60 | 2016 |
| The Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort as a resource for studying psychopathology in childhood and adolescence: a summary of findings for … M Niarchou, S Zammit, G Lewis Social psychiatry and psychiatric epidemiology 50, 1017-1027, 2015 | 58 | 2015 |
| Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohort M Niarchou, S Zammit, J Walters, G Lewis, MJ Owen, MB van den Bree American Journal of Psychiatry 170 (5), 550-557, 2013 | 55 | 2013 |
| Genetic contributions to autism spectrum disorder A Havdahl, M Niarchou, A Starnawska, M Uddin, C van der Merwe, ... Psychological medicine 51 (13), 2260-2273, 2021 | 51 | 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 | 45 | 2017 |
| The clinical presentation of attention deficit‐hyperactivity disorder (ADHD) in children with 22q11. 2 deletion syndrome M Niarchou, J Martin, A Thapar, MJ Owen, MBM van den Bree American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 …, 2015 | 37 | 2015 |
| Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease JK Dennis, JM Sealock, P Straub, YH Lee, D Hucks, KE Actkins, A Faucon, ... Genome medicine 13, 1-16, 2021 | 33 | 2021 |
| 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 | 32 | 2018 |
| Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits M Niarchou, EM Byrne, M Trzaskowski, J Sidorenko, KE Kemper, ... Translational Psychiatry 10 (1), 51, 2020 | 26 | 2020 |
| Genome-wide association study of musical beat synchronization demonstrates high polygenicity M Niarchou, DE Gustavson, JF Sathirapongsasuti, M Anglada-Tort, ... Nature Human Behaviour 6 (9), 1292-1309, 2022 | 25 | 2022 |
Dr Samuel ChawnerMedical Research Foundation Fellow, Cardiff University在 cardiff.ac.uk 的电子邮件经过验证
