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Author Details

Maria Niarchou
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
2013
31
14
PMIDPaper TitleJournal TitlePublished Year
36851882Confronting ethical and social issues related to the genetics of musicality.Ann N Y Acad Sci2023
37693435Comorbidity Profiles of Posttraumatic Stress Disorder Across the Medical Phenome.medRxiv2023
37034728Multi-ancestry meta-analysis of tobacco use disorder prioritizes novel candidate risk genes and reveals associations with numerous health outcomes.medRxiv2023
37328826The physical and psychiatric health conditions related to autism genetic scores, across genetic ancestries, sexes and age-groups in electronic health records.J Neurodev Disord2023
36446581Psychopathology in mothers of children with pathogenic Copy Number Variants.J Med Genet2023
36171425Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction.Nat Neurosci2022
35710621Genome-wide association study of musical beat synchronization demonstrates high polygenicity.Nat Hum Behav2022
35841203A phenome-wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data.Am J Med Genet B Neuropsychiatr Genet2022
36545045Identifying High-Risk Comorbidities Associated with Opioid Use Patterns Using Electronic Health Record Prescription Data.Complex Psychiatry2022
33441150Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease.Genome Med2021
33634770Genetic contributions to autism spectrum disorder.Psychol Med2021
34420388Linking the genomic signatures of human beat synchronization and learned song in birds.Philos Trans R Soc Lond B Biol Sci2021
34414577Medical phenome of musicians: an investigation of health records collected on 9803 musically active individuals.Ann N Y Acad Sci2021
34099040Psychometric validation and refinement of the Interoception Sensory Questionnaire (ISQ) in adolescents and adults on the autism spectrum.Mol Autism2021
32015465Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.Mol Psychiatry2021
32066663Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.Transl Psychiatry2020
30458299The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome.J Psychiatr Res2019
30093352Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome.Schizophr Res2019
31445317Corrigendum to "The dimensional structure of psychopathology in 22q11.2 Deletion Syndrome" [J. Psychiatr. Res. 92 (2017) 124-131].J Psychiatr Res2019
30837452Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication.Transl Psychiatry2019
29040797Attention Deficit Hyperactivity Disorder Symptoms and Psychosis in 22q11.2 Deletion Syndrome.Schizophr Bull2018
30289625Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects.Am J Med Genet A2018
28882829Childhood cognitive development in 22q11.2 deletion syndrome: case-control study.Br J Psychiatry2017
28433949The dimensional structure of psychopathology in 22q11.2 Deletion Syndrome.J Psychiatr Res2017
26002411The 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 depression and psychosis.Soc Psychiatry Psychiatr Epidemiol2015
26400629The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome.Am J Med Genet B Neuropsychiatr Genet2015
24115343Psychopathology and cognition in children with 22q11.2 deletion syndrome.Br J Psychiatry2014
24862404Exploring 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.Am J Med Genet B Neuropsychiatr Genet2014
24577245Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.Am J Psychiatry2014
24534796Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.Schizophr Res2014
23632836Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohort.Am J Psychiatry2013
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Collaborators

Co-authored papers 14
Vanderbilt University Medical Center, Tennessee Vanderbilt Genetics Institute
Co-authored papers 9
University of Pennsylvania Perelman School of Medicine
Co-authored papers 7
Children's Hospital of Philadelphia
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Co-authored papers 4
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Co-authored papers 4
University of North Carolina-Chapel Hill
Co-authored papers 3
Duke University School of Medicine
Co-authored papers 3
Institute of Medical Science, University of Toronto
Co-authored papers 3
Vanderbilt University Medical Center
Co-authored papers 2
King's College London
Co-authored papers 2
VA Connecticut Healthcare System
Co-authored papers 2
Center for Genomic Medicine, Massachusetts General Hospital
Co-authored papers 2
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 2
Institute of Molecular Bioscience, The University of Queensland
Co-authored papers 2
Mayo Clinic
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McMaster University & St. Joseph's Healthcare Hamilton
Co-authored papers 1
The Hospital for Sick Children Research Institute
Co-authored papers 1
Johns Hopkins Bloomberg School of Public Health
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Boston Children's Hospital and Harvard Medical School
Co-authored papers 1
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Bakar Computational Health Sciences Institute, University of California san francisco
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Geisinger-Bucknell Autism & Developmental Medicine Institute (D.B.
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University of Wisconsin-Madison
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