1. A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data. Issue 6 (15th July 2022) Authors: Niarchou, Maria; Sealock, Julia M.; Straub, Peter; Sanchez‐Roige, Sandra; Sutcliffe, James S.; Davis, Lea K. Journal: American journal of medical genetics Issue: Volume 189:Issue 6(2022) Page Start: 185 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Attention Deficit Hyperactivity Disorder Symptoms and Psychosis in 22q11.2 Deletion Syndrome. (10th October 2017) Authors: Niarchou, Maria; Calkins, Monica E; Moore, Tyler M; Tang, Sunny X; McDonald-McGinn, Donna M; Zackai, Elaine H; Emanuel, Beverly S; Gur, Ruben C; Gur, Raquel E Journal: Schizophrenia bulletin Issue: Volume 44:Number 4(2018:Jul.) Page Start: 824 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Childhood cognitive development in 22q11.2 deletion syndrome: Case–control study. (October 2017) Authors: Chawner, Samuel J. R. A.; Doherty, Joanne L.; Moss, Hayley; Niarchou, Maria; Walters, James T. R.; Owen, Michael J.; van den Bree, Marianne B. M. Journal: British journal of psychiatry Issue: Volume 211:Number 4(2017) Page Start: 223 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Corrigendum to "The dimensional structure of psychopathology in 22q11.2 Deletion Syndrome" [J. Psychiatr. Res. 92 (2017) 124–131]. (November 2019) Authors: Niarchou, Maria; Moore, Tyler M.; Tang, Sunny X.; Calkins, Monica E.; McDonald-McGuinn, Donna M.; Zackai, Elaine H.; Emanuel, Beverly S.; Gur, Ruben C.; Gur, Raquel E. Journal: Journal of psychiatric research Issue: Volume 118(2019) Page Start: 8 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Exploring the indirect effects of catechol‐O‐methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children. Issue 5 (27th May 2014) Authors: Niarchou, Maria; Zammit, Stanley; Escott‐Price, Valentina; Owen, Michael J.; van den Bree, Marianne B. M. Journal: American journal of medical genetics Issue: Volume 165:Issue 5(2014) Page Start: 410 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Investigating the genetic pathways of insomnia in Autism Spectrum Disorder. (September 2022) Authors: Niarchou, Maria; Singer, Emily V.; Straub, Peter; Malow, Beth A.; Davis, Lea K. Journal: Research in developmental disabilities Issue: Volume 128(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Linking the genomic signatures of human beat synchronization and learned song in birds. (11th October 2021) Authors: Gordon, Reyna L.; Ravignani, Andrea; Hyland Bruno, Julia; Robinson, Cristina M.; Scartozzi, Alyssa; Embalabala, Rebecca; Niarchou, Maria; Cox, Nancy J.; Creanza, Nicole Journal: Philosophical transactions Issue: Volume 376:Number 1835(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Medical phenome of musicians: an investigation of health records collected on 9803 musically active individuals. Issue 1 (19th August 2021) Authors: Niarchou, Maria; Lin, George T.; Lense, Miriam D.; Gordon, Reyna L.; Davis, Lea K. Journal: Annals of the New York Academy of Sciences Issue: Volume 1505:Issue 1(2021) Page Start: 156 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Psychopathology and cognition in children with 22q11.2 deletion syndrome. (January 2014) Authors: Niarchou, Maria; Zammit, Stanley; van Goozen, Stephanie H. M.; Thapar, Anita; Tierling, Hayley M.; Owen, Michael J.; Van Den Bree, Marianne B. M. Journal: British journal of psychiatry Issue: Volume 204:Number 1(2014) Page Start: 46 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The clinical presentation of attention deficit‐hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome. Issue 8 (24th September 2015) Authors: Niarchou, Maria; Martin, Joanna; Thapar, Anita; Owen, Michael J.; van den Bree, Marianne B. M. Journal: American journal of medical genetics Issue: Volume 168:Issue 8(2015) Page Start: 730 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗