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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: May 03, 2024
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Susceptibility to Treatment-Resistant Depression Within Families.
Chih-Ming Cheng et al. JAMA Psychiatry 2024
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Genetic risk for attention-deficit/hyperactivity disorder predicts cognitive decline and development of Alzheimer's disease pathophysiology in cognitively unimpaired older adults.
Douglas T Leffa et al. Mol Psychiatry 2022 28(3) 1248-1255
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A Family Genetic Study of Obsessive Compulsive Disorder in Youth.
Daniel A Geller et al. J Atten Disord 2023 10870547231217091
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Postpartum and non-postpartum depression: a population-based matched case-control study comparing polygenic risk scores for severe mental disorders.
Trine Munk-Olsen et al. Transl Psychiatry 2023 13(1) 346
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Mental health impact of autism on families of children with intellectual and developmental disabilities of genetic origin.
Jeanne Wolstencroft et al. JCPP Adv 2023 3(1) e12128
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A twin study of genetic and environmental contributions to attention-deficit/hyperactivity disorder over time.
Mark J Taylor et al. J Child Psychol Psychiatry 2023
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Evaluation of Birth Weight and Neurodevelopmental Conditions Among Monozygotic and Dizygotic Twins.
Johan Isaksson et al. JAMA Netw Open 2023 6(6) e2321165
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Neuropsychological and quality of life outcomes in PKU patients: expert recommendations of assessment tools in Brazil.
Ida Vanessa Doederlein Schwartz et al. Arq Neuropsiquiatr 2023
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General v. specific vulnerabilities: polygenic risk scores and higher-order psychopathology dimensions in the Adolescent Brain Cognitive Development (ABCD) Study.
Monika A Waszczuk et al. Psychol Med 2023 53(5) 1937-1946
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Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome.
Pritesh Jain et al. Transl Psychiatry 2023 13(1) 69
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Co-occurring conditions in children with Down syndrome and autism: a retrospective study.
Noemi A Spinazzi et al. Journal of neurodevelopmental disorders 2023 15(1) 9
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The incidence and clinical characteristics of fragile X syndrome in China.
Lianni Mei et al. Frontiers in pediatrics 2023 111064104
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Polygenic risk score for attention-deficit/hyperactivity disorder and brain functional networks segregation in a community-based sample.
João Ricardo Sato et al. Genes, brain, and behavior 2023 e12838
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Update on genetics of attention deficit/hyperactivity disorder: current status 2023.
Thorsten M Kranz et al. Current opinion in psychiatry 2023
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Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease.
Sarah U Morton et al. JAMA network open 2023 6(1) e2253191
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Family coaggregation of type 1 diabetes mellitus, major depressive disorder, attention-deficiency hyperactivity disorder and autism spectrum disorder in affected families: a nationwide study.
Hsu Tien-Wei et al. Acta diabetologica 2023
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Candidate diagnostic biomarkers for neurodevelopmental disorders in children and adolescents: a systematic review.
Cortese Samuele et al. World psychiatry : official journal of the World Psychiatric Association (WPA) 2023 22(1) 129-149
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Findings of a Multidisciplinary Assessment of Children Referred for Possible Neurodevelopmental Disorders: Insights from a Retrospective Chart Review Study.
Alenezi Shuliweeh et al. Behavioral sciences (Basel, Switzerland) 2022 12(12)
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Association of Attention-Deficit/Hyperactivity Disorder and Depression Polygenic Scores with Lithium Response: A Consortium for Lithium Genetics Study.
Coombes Brandon J et al. Complex psychiatry 2022 7(3-4) 80-89
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Association between Gut Microbiota and Emotional-Behavioral Symptoms in Children with Attention-Deficit/Hyperactivity Disorder
MJ Lee et al, J Per Medicine, September 29, 2022
Disentangling the influences of parental genetics on offspring's cognition, education, and psychopathology via genetic and phenotypic pathways.
Axelrud Luiza K et al. Journal of child psychology and psychiatry, and allied disciplines 2022
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Autism and ADHD in the Era of Big Data; An Overview of Digital Resources for Patient, Genetic and Clinical Trials Information.
Abomelha Faris M et al. Genes 2022 13(9)
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Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups.
Mattheisen Manuel et al. Nature genetics 2022
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Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder.
Rajagopal Veera M et al. Nature genetics 2022
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A phenome-wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data.
Niarchou Maria et al. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2022
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Associations of a family history of lupus with the risks of lupus and major psychiatric disorders in first-degree relatives.
Lin Po-Chun et al. QJM : monthly journal of the Association of Physicians 2022
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Mendelian randomization analysis for attention deficit/hyperactivity disorder: studying a broad range of exposures and outcomes.
Soler Artigas María et al. International journal of epidemiology 2022
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An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities.
Slaby Isabella et al. Journal of neurodevelopmental disorders 2022 14(1) 37
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Familial risk for bipolar I disorder is associated with erythrocyte omega-3 polyunsaturated fatty acid deficits in youth with attention-deficit hyperactivity disorder.
Mc Namara Robert K et al. Psychiatry research 2022 313114587
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Differences in genetic risk score profiles for drug use disorder, major depression, and ADHD as a function of sex, age at onset, recurrence, mode of ascertainment, and treatment.
Kendler Kenneth S et al. Psychological medicine 2022 1-13
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 03, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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