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Maria Niarchou
Maria Niarchou
Research Assistant Professor, Vanderbilt University Medical Center
Verified email at vumc.org
Title
Cited by
Cited by
Year
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
7662014
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
1532019
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
1262021
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
1242020
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
1222021
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
1162014
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
1142014
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
1002017
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
932021
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
882017
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
872013
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
762015
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
692022
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
692015
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
672016
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
612013
Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction
RL Kember, R Vickers-Smith, H Xu, S Toikumo, M Niarchou, H Zhou, ...
Nature Neuroscience 25 (10), 1279-1287, 2022
542022
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
482017
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
462015
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
442018
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