families cohort

Aliases

Family studies, families, families studied, family, family studies, family study, family-based approach, family-based data, family-based design, large extended families, pedigrees, previous family study

Related entities (9)

Mentioned in (28)

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)
• 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)
• Prospective pan-cancer germline testing using MSK-IMPACT informs clinical translation in 751 patients with pediatric solid tumors. (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)
• 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)
• Gestational age and socioeconomic status as mediators for the impact of prenatal alcohol exposure on development at 6 months. (2019)
• Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes. (2018)
• Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (2017)
• Clinical Assessment and Diagnosis of Germline Predisposition to Hematopoietic Malignancies: The University of Chicago Experience. (2017)
• Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth. (2015)
• Genetic linkage analysis in the age of whole-genome sequencing. (2015)
• Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
• ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. (2013)
• Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (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)
• Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
• Gene-environment interaction in psychological traits and disorders. (2011)
• Functioning of alcohol use disorder criteria among men and women with arrests for driving under the influence of alcohol. (2011)
• Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
• Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts. (2010)
• PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
• Co-occurring risk factors for alcohol dependence and habitual smoking: update on findings from the Collaborative Study on the Genetics of Alcoholism. (2006)
• Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN

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