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Pharmacogenetics and Genomics|November 1, 2017
Gene-gene interaction between DRD4 and COMT modulates clinical response to clozapine in treatment-resistant schizophreniaVeera M Rajagopal, Anto P Rajkumar, Kuruthukulangara S Jacob, et al.
Translational Psychiatry|October 5, 2019
Exploring genetic variation that influences brain methylation in attention-deficit/hyperactivity disorderLaura Pineda-Cirera, Anu Shivalikanjli, Judit Cabana-Domínguez, et al.
Nature Human Behaviour|December 10, 2024
Neuropsychiatric polygenic scores are weak predictors of professional categoriesGeorgios Voloudakis, Karen Therrien, Simone Tomasi, et al.
Nature Communications|August 25, 2019
Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traitsWen Zhang, Georgios Voloudakis, Veera M Rajagopal, et al.
Biological Psychiatry Global Open Science|November 14, 2025
Multisite, Multiancestry Genome-Wide Association Study Meta-Analysis of Functional Seizure Disorder in a Hospital Sample of 675,680 PatientsSlavina B Goleva, Costin Leu, Yen-Chen Anne Feng, et al.
Nature Communications|January 26, 2021
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorderDitte Demontis, Raymond K Walters, Veera M Rajagopal, et al.
The Lancet. Child & Adolescent Health|January 17, 2021
Identification of genetic loci associated with nocturnal enuresis: a genome-wide association studyCecilie S Jørgensen, Henriette T Horsdal, Veera M Rajagopal, et al.
Molecular Psychiatry|July 25, 2022
Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk lociJoseph D Deak, Hang Zhou, Marco Galimberti, et al.
Psychological Medicine|May 5, 2021
Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort studyKatherine L Musliner, Klaus K Andersen, Esben Agerbo, et al.
Nature Genetics|August 4, 2022
Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorderVeera M Rajagopal, Jinjie Duan, Laura Vilar-Ribó, et al.
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