families cohort
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Related entities (34)
Mentioned in (96)
Papers in which this entity is mentioned.
- Alcohol Use Disorder Polygenic Score Compared With Family History and ADH1B. (2024)
- Childhood trauma is associated with developmental trajectories of EEG coherence, alcohol-related outcomes, and PTSD symptoms. (2024)
- Punitive legal responses to prenatal drug use in the United States: A survey of state policies and systematic review of their public health impacts. (2024)
- Larger-scale feasibility trial of the families moving forward (FMF) connect mobile health intervention for caregivers raising children with fetal alcohol spectrum disorders. (2024)
- Genetic nurture effects for alcohol use disorder. (2023)
- The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. (2022)
- Mother-child similarity in brain morphology: A comparison of structural characteristics of the brain's reading network. (2022)
- Prospective pan-cancer germline testing using MSK-IMPACT informs clinical translation in 751 patients with pediatric solid tumors. (2021)
- Early Adolescent Substance Use Before and During the COVID-19 Pandemic: A Longitudinal Survey in the ABCD Study Cohort. (2021)
- Initial Feasibility of the "Families Moving Forward Connect" Mobile Health Intervention for Caregivers of Children With Fetal Alcohol Spectrum Disorders: Mixed Method Evaluation Within a Systematic User-Centered Design Approach. (2021)
- Current Socioeconomic Status Correlates With Brain Volumes in Healthy Children and Adolescents but Not in Children With Prenatal Alcohol Exposure. (2020)
- Association of Prenatal Alcohol Exposure With Psychological, Behavioral, and Neurodevelopmental Outcomes in Children From the Adolescent Brain Cognitive Development Study. (2020)
- Sibling comparisons elucidate the associations between educational attainment polygenic scores and alcohol, nicotine and cannabis. (2020)
- A Mobile Health Intervention for Fetal Alcohol Spectrum Disorders (Families Moving Forward Connect): Development and Qualitative Evaluation of Design and Functionalities. (2020)
- A Prospective Comparison of Bipolar I and II Subjects With and Without Comorbid Alcohol Dependence From the COGA Dataset. (2020)
- Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
- "I'm Doing My Part, I Just Need Help From the Community": Intervention Implications of Foster and Adoptive Parents' Experiences Raising Children and Young Adults With FASD. (2019)
- Gestational age and socioeconomic status as mediators for the impact of prenatal alcohol exposure on development at 6 months. (2019)
- The relationship between biological and psychosocial risk factors and resting-state functional connectivity in 2-month-old Bangladeshi infants: A feasibility and pilot study. (2019)
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. (2019)
- Prevalence of fetal alcohol spectrum disorder among special subpopulations: a systematic review and meta-analysis. (2019)
- Longitudinally Mapping Childhood Socioeconomic Status Associations with Cortical and Subcortical Morphology. (2019)
- Psychiatric Genomics: An Update and an Agenda. (2018)
- Oxytocin Receptor Gene Variant Interacts with Intervention Delivery Format in Predicting Intervention Outcomes for Youth with Conduct Problems. (2018)
- Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes. (2018)
- Factors Associated With Successful MRI Scanning in Unsedated Young Children. (2018)
- Time-varying effects of income on hippocampal volume trajectories in adolescent girls. (2018)
- Neurotrophins in the Brain: Interaction With Alcohol Exposure During Development. (2017)
- Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
- Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (2017)
- Findings from the Families on Track Intervention Pilot Trial for Children with Fetal Alcohol Spectrum Disorders and Their Families. (2017)
- Parent-Mediated Intervention Training Delivered Remotely for Children With Autism Spectrum Disorder Living Outside of Urban Areas: Systematic Review. (2017)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- Clinical Assessment and Diagnosis of Germline Predisposition to Hematopoietic Malignancies: The University of Chicago Experience. (2017)
- Testing Causal Effects of Maternal Smoking During Pregnancy on Offspring's Externalizing and Internalizing Behavior. (2016)
- Social cognition as an RDoC domain. (2016)
- The effects of prenatal HIV exposure on language functioning in Kenyan children: establishing an evaluative framework. (2016)
- Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. (2016)
- The association between parental attributions of misbehavior and parenting practices in caregivers raising children with prenatal alcohol exposure: A mixed-methods study. (2016)
- The heritability of alcohol use disorders: a meta-analysis of twin and adoption studies. (2015)
- The National Birth Defects Prevention Study: A review of the methods. (2015)
- Parental Separation and Offspring Alcohol Involvement: Findings from Offspring of Alcoholic and Drug Dependent Twin Fathers. (2015)
- Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth. (2015)
- Describing and predicting developmental profiles of externalizing problems from childhood to adulthood. (2015)
- Genetic linkage analysis in the age of whole-genome sequencing. (2015)
- Heritability and molecular-genetic basis of the P3 event-related brain potential: a genome-wide association study. (2014)
- Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
- Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study. (2014)
- Epigenetics, microRNA, and addiction. (2014)
- Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways. (2014)
- Differential sensitivity to prevention programming: a dopaminergic polymorphism-enhanced prevention effect on protective parenting and adolescent substance use. (2014)
- Effects of prenatal alcohol and cigarette exposure on offspring substance use in multiplex, alcohol-dependent families. (2014)
- Prevention of problem behavior through annual family check-ups in early childhood: intervention effects from home to early elementary school. (2014)
- ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. (2013)
- Linear mixed-effects modeling approach to FMRI group analysis. (2013)
- Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
- Women's Knowledge, Views, and Experiences Regarding Alcohol Use and Pregnancy: Opportunities to Improve Health Messages. (2013)
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
- Central precocious puberty caused by mutations in the imprinted gene MKRN3. (2013)
- The genomic landscape of hypodiploid acute lymphoblastic leukemia. (2013)
- Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
- Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome. (2012)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- The genetic basis of addictive disorders. (2012)
- Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
- Pharmacogenetics of smoking cessation: role of nicotine target and metabolism genes. (2012)
- High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- Gene-environment interaction in psychological traits and disorders. (2011)
- Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls. (2011)
- The investigation into CYP2E1 in relation to the level of response to alcohol through a combination of linkage and association analysis. (2011)
- Maternal risk factors for fetal alcohol spectrum disorders: not as simple as it might seem. (2011)
- Functioning of alcohol use disorder criteria among men and women with arrests for driving under the influence of alcohol. (2011)
- Prenatal and postnatal cocaine exposure predict teen cocaine use. (2011)
- The contribution of parental alcohol use disorders and other psychiatric illness to the risk of alcohol use disorders in the offspring. (2011)
- Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
- Genetic control over the resting brain. (2010)
- Modeling the interplay of multilevel risk factors for future academic and behavior problems: a person-centered approach. (2010)
- Statistical analysis strategies for association studies involving rare variants. (2010)
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. (2010)
- Sleep Health Issues for Children with FASD: Clinical Considerations. (2010)
- The impact of maternal age on the effects of prenatal alcohol exposure on attention. (2010)
- Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts. (2010)
- Paternal alcoholism, negative parenting, and the mediating role of marital satisfaction. (2009)
- Finding the missing heritability of complex diseases. (2009)
- Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
- An exploration of attitudes among black Americans towards psychiatric genetic research. (2009)
- Discrimination and racial disparities in health: evidence and needed research. (2009)
- Deviant P300 amplitude development in males is associated with paternal externalizing psychopathology. (2008)
- Neurodevelopmental trajectories of the human cerebral cortex. (2008)
- Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
- Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. (2007)
- Co-occurring risk factors for alcohol dependence and habitual smoking: update on findings from the Collaborative Study on the Genetics of Alcoholism. (2006)
- A genome-wide scan to identify loci for smoking rate in the Framingham Heart Study population. (2003)
- Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN
Merged raw entities (16)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| families | cohort | 55 | 63 |
| family | cohort | 17 | 39 |
| family studies | cohort | 12 | 13 |
| family study | cohort | 5 | 5 |
| family | phenotype | 4 | 4 |
| family-based cohort | cohort | 4 | 4 |
| family-based studies | cohort | 4 | 4 |
| family cohort | cohort | 4 | 4 |
| extended families | cohort | 3 | 3 |
| study families | cohort | 3 | 3 |
| family-based design | cohort | 1 | 1 |
| families studied | cohort | — | — |
| family-based approach | cohort | — | — |
| family-based data | cohort | — | — |
| large extended families | cohort | — | — |
| previous family study | cohort | — | — |