study cohort cohort

Aliases

1,139 baseline participants, 1,148 persons, 1,953 patients, 14 alcoholic and 13 control cases, 15 probands and family members, 17,355 subjects, 188 subjects, 189 subjects, 19 participants, 2134 families, 23 laboratories cohort, 26 cohorts, 27 cases, 3,112 individuals, 3,315 individuals, 3,378 individuals, 3,816 individuals, 3.2 million individuals, 353 participants, 3589 individuals, 4,385 individuals, 410 subjects, 449 subjects, 50,222 subjects, 535 samples, 5441 individuals, 69 subjects, 766 subjects, Cohort 2, Diabetes Heart Studies, GWAS, N=406 men, Nr, Participants, Participants (n=1023), age at interview cohort, age cohort, clinical population of over 20,000 patients, cohort, cohort 1, cohort 2, cohort 3, cohort 4, cohort 5, cohort 6, cohort [19], cohort studies, cohort-level summary statistics, cohort-sequential approach, cohort1, cohort2, cohort3, cohort4, cohort5, cohort6, cohorts, depressed patients, eight cohorts, entire cohort, first cohort, genome-wide association scan, independent cohort, large cohort, large cohorts, multiple studies, original cohort, other cohorts, our cohorts, our students, our study cohort, participants, patient sample, patients, project, replication cases, replication sample, replication samples, sample, schizophrenia organoids, second cohort, seven studies, six additional cohorts, subjects, subjects from our study, the cohort, the study, these cohorts, this population, this study, total sample, working group dataset, younger panel, youngest cohort

Related entities (139)

Mentioned in (478)

Papers in which this entity is mentioned.

• Infant subcortical brain volumes associated with maternal obesity and diabetes: a large multicohort human study. (2026)
• Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
• Integrative epigenetics and transcriptomics identify aging genes in human blood. (2026)
• Consortium profile: the methylation, imaging and NeuroDevelopment (MIND) consortium. (2026)
• Alcohol use disorder is associated with altered frontomedial phase-amplitude coupling strength during resting state. (2026)
• Whole genome sequencing approach to assess homologous recombination deficiency in a pan-cancer cohort. (2026)
• Validation of the ND-PAE Diagnosis in Children with Heavy Prenatal Alcohol Exposure. (2026)
• Nanopore-based cell-free DNA fragmentation and methylation profiles from the cerebral spinal fluid of patients with lung cancer brain metastases. (2025)
• Feasibility trial of the My Health Coach app for adults with fetal alcohol spectrum disorders. (2025)
• Associations between common genetic variants and income provide insights about the socio-economic health gradient. (2025)
• Extrachromosomal DNA-Driven Oncogene Spatial Heterogeneity and Evolution in Glioblastoma. (2025)
• Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
• Trajectories of genetic risk across dimensions of alcohol use behaviors. (2025)
• Integrated single-cell multiomic profiling of caudate nucleus suggests key mechanisms in alcohol use disorder. (2025)
• Epigenetic timing effects on child developmental outcomes: a longitudinal meta-regression of findings from the Pregnancy And Childhood Epigenetics Consortium. (2025)
• Tumour-wide RNA splicing aberrations generate actionable public neoantigens. (2025)
• Multi-omic quantitative trait loci link tandem repeat size variation to gene regulation in human brain. (2025)
• Maternal and child immune profiles are associated with neurometabolite measures of early-life neuroinflammation in children who are HIV-exposed and uninfected: a South African birth cohort. (2025)
• Genome-wide association testing beyond SNPs. (2025)
• Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
• Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
• Differential reorganization of episodic and semantic memory systems in epilepsy-related mesiotemporal pathology. (2024)
• Prenatal Exposures, Diagnostic Outcomes, and Life Experiences of Children and Youths with Fetal Alcohol Spectrum Disorder. (2024)
• Tumor-informed deep sequencing of ctDNA detects minimal residual disease and predicts relapse in osteosarcoma. (2024)
• Characteristics of the Symptoms of the Proposed ND-PAE Disorder in First Grade Children in a Community Sample. (2024)
• Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (2024)
• Osteosarcoma PDX-Derived Cell Line Models for Preclinical Drug Evaluation Demonstrate Metastasis Inhibition by Dinaciclib through a Genome-Targeted Approach. (2024)
• Normative modelling of brain morphometry across the lifespan with CentileBrain: algorithm benchmarking and model optimisation. (2024)
• DNA methylation at birth and lateral ventricular volume in childhood: a neuroimaging epigenetics study. (2024)
• Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. (2024)
• A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
• The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
• Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders. (2024)
• Adaptive, Externalizing, and Internalizing Behavior of Children with Prenatal Alcohol Exposure: A Comparison of Three Parent-Report Questionnaires. (2024)
• Integrated Single-Cell Multiomic Profiling of Caudate Nucleus Suggests Key Mechanisms in Alcohol Use Disorder. (2024)
• Consortium Profile: The Methylation, Imaging and NeuroDevelopment (MIND) Consortium. (2024)
• Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme. (2024)
• Comprehensive repertoire of the chromosomal alteration and mutational signatures across 16 cancer types from 10,983 cancer patients (2023)
• Predicting tumour content of liquid biopsies from cell-free DNA. (2023)
• Associations among prenatal exposure to gestational diabetes mellitus, brain structure, and child adiposity markers. (2023)
• An overview of DNA methylation-derived trait score methods and applications. (2023)
• Heritable defects in telomere and mitotic function selectively predispose to sarcomas. (2023)
• Gene-alcohol interactions in birth defects. (2023)
• Pervasive Downward Bias in Estimates of Liability-Scale Heritability in Genome-wide Association Study Meta-analysis: A Simple Solution. (2023)
• Alcohol blunts pregnancy-mediated insulin resistance and reduces fetal brain glucose despite elevated fetal gluconeogenesis, and these changes associate with fetal weight outcomes. (2023)
• Guidelines for Evaluating the Comparability of Down-Sampled GWAS Summary Statistics. (2023)
• Comprehensive analysis of mutational signatures reveals distinct patterns and molecular processes across 27 pediatric cancers. (2023)
• Path analysis of the impact of prenatal alcohol on adult vascular function. (2023)
• Immune selection determines tumor antigenicity and influences response to checkpoint inhibitors. (2023)
• Reducing Prenatal Alcohol Exposure and the Incidence of FASD: Is the Past Prologue? (2023)
• Single-molecule methylation profiles of cell-free DNA in cancer with nanopore sequencing. (2023)
• Prenatal alcohol exposure and cognition at midlife: Evidence of fluid cognition deficits in two cohorts. (2023)
• Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
• DNA methylation and general psychopathology in childhood: an epigenome-wide meta-analysis from the PACE consortium. (2023)
• Brain charts for the human lifespan. (2022)
• Mapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNA. (2022)
• Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation. (2022)
• Alcohol-related dysmorphic features as predictors of neurodevelopmental delay in infants and preschool-aged children: Results from a birth cohort in Ukraine. (2022)
• Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. (2022)
• Single-cell analysis of somatic mutations in human bronchial epithelial cells in relation to aging and smoking. (2022)
• The normative modeling framework for computational psychiatry. (2022)
• Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA. (2022)
• Association of Maternal and Child Anemia With Brain Structure in Early Life in South Africa. (2022)
• Explainable multiview framework for dissecting spatial relationships from highly multiplexed data. (2022)
• Item-Level Genome-Wide Association Study of the Alcohol Use Disorders Identification Test in Three Population-Based Cohorts. (2022)
• Epigenetic profiling of social communication trajectories and co-occurring mental health problems: a prospective, methylome-wide association study. (2022)
• Single-cell analysis of hepatoblastoma identifies tumor signatures that predict chemotherapy susceptibility using patient-specific tumor spheroids. (2022)
• Prenatal depression exposure alters white matter integrity and neurodevelopment in early childhood. (2022)
• A saturated map of common genetic variants associated with human height. (2022)
• A methodological pipeline to generate an epigenetic marker of prenatal exposure to air pollution indicators. (2022)
• Newborn differential DNA methylation and subcortical brain volumes as early signs of severe neurodevelopmental delay in a South African Birth Cohort Study. (2022)
• Estimation of tumor cell total mRNA expression in 15 cancer types predicts disease progression. (2022)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• The impact of micronutrient supplementation in alcohol-exposed pregnancies on reaction time responses of preschoolers in Ukraine. (2022)
• The impact of prenatal alcohol exposure on gray matter volume and cortical surface area of 2 to 3-year-old children in a South African birth cohort. (2022)
• Different FreeSurfer versions might generate different statistical outcomes in case-control comparison studies. (2022)
• Inferring gene expression from cell-free DNA fragmentation profiles. (2022)
• Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data. (2022)
• Construction and validation of a novel gene signature for predicting the prognosis of osteosarcoma. (2022)
• Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
• Subcortical brain volumes in young infants exposed to antenatal maternal depression: Findings from a South African birth cohort. (2022)
• Circulating Tumor DNA as a Biomarker in Patients With Stage III and IV Wilms Tumor: Analysis From a Children's Oncology Group Trial, AREN0533. (2022)
• Association between Maternal Choline, Fetal Brain Development, and Child Neurocognition: Systematic Review and Meta-Analysis of Human Studies. (2022)
• Early structural brain development in infants exposed to HIV and antiretroviral therapy in utero in a South African birth cohort. (2022)
• Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
• Med-BERT: pretrained contextualized embeddings on large-scale structured electronic health records for disease prediction. (2021)
• Partner influence as a factor in maternal alcohol consumption and depressive symptoms, and maternal effects on infant neurodevelopmental outcomes. (2021)
• Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group. (2021)
• Enhanced detection of minimal residual disease by targeted sequencing of phased variants in circulating tumor DNA. (2021)
• Integrated analysis of multimodal single-cell data. (2021)
• Central white matter integrity alterations in 2-3-year-old children following prenatal alcohol exposure. (2021)
• Validity and Reliability of Executive Function Measures in Children With Heavy Prenatal Alcohol Exposure: Correspondence Between Multiple Raters and Laboratory Measures. (2021)
• Association Between Benzodiazepine or Z-Drug Prescriptions and Drug-Related Poisonings Among Patients Receiving Buprenorphine Maintenance: A Case-Crossover Analysis. (2021)
• Epigenome-wide change and variation in DNA methylation in childhood: trajectories from birth to late adolescence. (2021)
• Prospective pan-cancer germline testing using MSK-IMPACT informs clinical translation in 751 patients with pediatric solid tumors. (2021)
• Autosomal sex-associated co-methylated regions predict biological sex from DNA methylation. (2021)
• Integrated Genomic Analysis Identifies Driver Genes and Cisplatin-Resistant Progenitor Phenotype in Pediatric Liver Cancer. (2021)
• An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders. (2021)
• Micro-RNA-125a mediates the effects of hypomethylating agents in chronic myelomonocytic leukemia. (2021)
• A practical guide to cancer subclonal reconstruction from DNA sequencing. (2021)
• Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. (2021)
• Fetal Alcohol Exposure Alters BOLD Activation Patterns in Brain Regions Mediating the Interpretation of Facial Affect. (2021)
• A Comprehensive Circulating Tumor DNA Assay for Detection of Translocation and Copy-Number Changes in Pediatric Sarcomas. (2021)
• Therapeutic Implications of Germline Testing in Patients With Advanced Cancers. (2021)
• Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
• Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
• Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. (2021)
• Genetic association study of childhood aggression across raters, instruments, and age. (2021)
• Use of Telemedicine for the Physical Examination of Children With Fetal Alcohol Spectrum Disorders. (2021)
• Pan-cancer analysis of longitudinal metastatic tumors reveals genomic alterations and immune landscape dynamics associated with pembrolizumab sensitivity. (2021)
• Gestational age and birth growth parameters as early predictors of fetal alcohol spectrum disorders. (2021)
• gene network in the prefrontal cortex is associated with total brain volume in childhood. (2020)
• Interpretation of risk loci from genome-wide association studies of Alzheimer's disease. (2020)
• Neuroimaging young children and associations with neurocognitive development in a South African birth cohort study. (2020)
• Genome-wide association analysis of opioid use disorder: A novel approach using clinical data. (2020)
• Validity of automated FreeSurfer segmentation compared to manual tracing in detecting prenatal alcohol exposure-related subcortical and corpus callosal alterations in 9- to 11-year-old children. (2020)
• Fetal alcohol spectrum disorder predisposes to metabolic abnormalities in adulthood. (2020)
• Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
• B cells and tertiary lymphoid structures promote immunotherapy response. (2020)
• Immuno-genomic landscape of osteosarcoma. (2020)
• Pan-cancer analysis of whole genomes. (2020)
• Multi-cancer analysis of clonality and the timing of systemic spread in paired primary tumors and metastases. (2020)
• Sibling comparisons elucidate the associations between educational attainment polygenic scores and alcohol, nicotine and cannabis. (2020)
• Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis. (2020)
• Ewing sarcoma with FEV gene rearrangements is a rare subset with predilection for extraskeletal locations and aggressive behavior. (2020)
• Longitudinal development of hippocampal subregions from early- to mid-childhood. (2020)
• Extrachromosomal DNA is associated with oncogene amplification and poor outcome across multiple cancers. (2020)
• Diverse noncoding mutations contribute to deregulation of cis-regulatory landscape in pediatric cancers. (2020)
• Amygdala-Prefrontal Structural Connectivity Mediates the Relationship between Prenatal Depression and Behavior in Preschool Boys. (2020)
• A Prospective Comparison of Bipolar I and II Subjects With and Without Comorbid Alcohol Dependence From the COGA Dataset. (2020)
• Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. (2020)
• Multivariate models of brain volume for identification of children and adolescents with fetal alcohol spectrum disorder. (2020)
• Alcohol Use in Pregnancy and Miscarriage: A Systematic Review and Meta-Analysis. (2019)
• Cost-effectiveness of electronic- and clinician-delivered screening, brief intervention and referral to treatment for women in reproductive health centers. (2019)
• Single-Cell RNA-Seq Reveals AML Hierarchies Relevant to Disease Progression and Immunity. (2019)
• Gestational age and socioeconomic status as mediators for the impact of prenatal alcohol exposure on development at 6 months. (2019)
• The mutational footprints of cancer therapies. (2019)
• Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. (2019)
• Determining cell type abundance and expression from bulk tissues with digital cytometry. (2019)
• Neurodevelopment of HIV-exposed uninfected children in South Africa: outcomes from an observational birth cohort study. (2019)
• htsget: a protocol for securely streaming genomic data. (2019)
• The Network of Cancer Genes (NCG): a comprehensive catalogue of known and candidate cancer genes from cancer sequencing screens. (2019)
• Global DNA Methylation and Histone Posttranslational Modifications in Human and Nonhuman Primate Brain in Association with Prenatal Alcohol Exposure. (2019)
• Prenatal Particulate Air Pollution and DNA Methylation in Newborns: An Epigenome-Wide Meta-Analysis. (2019)
• Neuroanatomical Changes Underlying Vertical HIV Infection in Adolescents. (2019)
• How I diagnose and manage Philadelphia chromosome-like acute lymphoblastic leukemia. (2019)
• Implementation of prevention of mother-to-child transmission (PMTCT) in South Africa: outcomes from a population-based birth cohort study in Paarl, Western Cape. (2019)
• Risk and protective factors for child development: An observational South African birth cohort. (2019)
• Barriers to and Facilitators of the Use of Mobile Health Apps From a Security Perspective: Mixed-Methods Study. (2019)
• Epigenetics and depression
. (2019)
• Forty Years of Assessing Neurodevelopmental and Behavioral Effects of Prenatal Alcohol Exposure in Infants: What Have We Learned? (2019)
• Psychosocial moderation of polygenic risk for cannabis involvement: the role of trauma exposure and frequency of religious service attendance. (2019)
• Mega-Analysis of Gray Matter Volume in Substance Dependence: General and Substance-Specific Regional Effects. (2019)
• Maternal health and birth outcomes in a South African birth cohort study. (2019)
• Genome-wide cell-free DNA fragmentation in patients with cancer. (2019)
• Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. (2019)
• RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (2019)
• Best practices for bioinformatic characterization of neoantigens for clinical utility. (2019)
• Longitudinally Mapping Childhood Socioeconomic Status Associations with Cortical and Subcortical Morphology. (2019)
• Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• Collider scope: when selection bias can substantially influence observed associations. (2018)
• mSignatureDB: a database for deciphering mutational signatures in human cancers. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. (2018)
• Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours. (2018)
• Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors. (2018)
• Structural brain development: A review of methodological approaches and best practices. (2018)
• Drakenstein Child Health Study (DCHS): investigating determinants of early child development and cognition. (2018)
• Widespread Selection for Oncogenic Mutant Allele Imbalance in Cancer. (2018)
• Genome-wide association study identifies a novel locus for cannabis dependence. (2018)
• Genome doubling shapes the evolution and prognosis of advanced cancers. (2018)
• Oxytocin Receptor Gene Variant Interacts with Intervention Delivery Format in Predicting Intervention Outcomes for Youth with Conduct Problems. (2018)
• DNA methylation as a predictor of fetal alcohol spectrum disorder. (2018)
• Immune diversity sheds light on missing variation in worldwide genetic diversity panels. (2018)
• Extending the Human Connectome Project across ages: Imaging protocols for the Lifespan Development and Aging projects. (2018)
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
• Prenatal Alcohol Exposure: Profiling Developmental DNA Methylation Patterns in Central and Peripheral Tissues. (2018)
• Longitudinal development of hippocampal subregions from childhood to adulthood. (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)
• Glucocorticoid Receptor (NR3C1) Gene Polymorphism Moderate Intervention Effects on the Developmental Trajectory of African-American Adolescent Alcohol Abuse. (2018)
• Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes (2018)
• Predicting T cell recognition of MHC class I restricted neoepitopes. (2018)
• Cortical Abnormalities Associated With Pediatric and Adult Obsessive-Compulsive Disorder: Findings From the ENIGMA Obsessive-Compulsive Disorder Working Group. (2018)
• Perinatal HIV Infection or Exposure Is Associated With Low -Acetylaspartate and Glutamate in Basal Ganglia at Age 9 but Not 7 Years. (2018)
• Trajectories of maternal depressive symptoms during pregnancy and the first 12 months postpartum and child externalizing and internalizing behavior at three years. (2018)
• PDGFRA gene, maternal binge drinking and obstructive heart defects. (2018)
• Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium. (2018)
• Altered brain morphometry in 7-year old HIV-infected children on early ART. (2018)
• Copy number signatures and mutational processes in ovarian carcinoma. (2018)
• Influences of prenatal and postnatal maternal depression on amygdala volume and microstructure in young children. (2017)
• The Use of Cardiac Orienting Responses as an Early and Scalable Biomarker of Alcohol-Related Neurodevelopmental Impairment. (2017)
• CRAVAT 4: Cancer-Related Analysis of Variants Toolkit. (2017)
• Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden. (2017)
• Vitamin D Deficiency in Pregnant Ukrainian Women: Effects of Alcohol Consumption on Vitamin D Status. (2017)
• OncoKB: A Precision Oncology Knowledge Base. (2017)
• Mapping White Matter Microstructure in the One Month Human Brain. (2017)
• HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures. (2017)
• The evolution of tumour phylogenetics: principles and practice. (2017)
• Universal Patterns of Selection in Cancer and Somatic Tissues. (2017)
• Cerebral organoids reveal early cortical maldevelopment in schizophrenia-computational anatomy and genomics, role of FGFR1. (2017)
• Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure. (2017)
• Human Brain Abnormalities Associated With Prenatal Alcohol Exposure and Fetal Alcohol Spectrum Disorder. (2017)
• Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. (2017)
• The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
• Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients. (2017)
• Benchmark Dose Modeling Estimates of the Concentrations of Inorganic Arsenic That Induce Changes to the Neonatal Transcriptome, Proteome, and Epigenome in a Pregnancy Cohort. (2017)
• Machine learning shows association between genetic variability in and cerebral connectivity in preterm infants. (2017)
• Quantifying cortical development in typically developing toddlers and young children, 1-6 years of age. (2017)
• Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (2017)
• BECon: a tool for interpreting DNA methylation findings from blood in the context of brain. (2017)
• Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants. (2017)
• Time-specific and cumulative effects of exposure to parental externalizing behavior on risk for young adult alcohol use disorder. (2017)
• De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
• Reductions in Corpus Callosum Volume Partially Mediate Effects of Prenatal Alcohol Exposure on IQ. (2017)
• Alterations of resting state functional network connectivity in the brain of nicotine and alcohol users. (2017)
• Fetal sex is associated with maternal stimulated cytokine production, but not serum cytokine levels, in human pregnancy. (2017)
• The impact of structural variation on human gene expression. (2017)
• Neural correlates of language variability in preschool-aged boys with autism spectrum disorder. (2017)
• A Decision Tree to Identify Children Affected by Prenatal Alcohol Exposure. (2016)
• "Did you ever drink more?" A detailed description of pregnant women's drinking patterns. (2016)
• Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. (2016)
• The developmental relationship between DHEA and visual attention is mediated by structural plasticity of cortico-amygdalar networks. (2016)
• Timing control of gait: a study of essential tremor patients vs. age-matched controls. (2016)
• Parental divorce and initiation of alcohol use in early adolescence. (2016)
• Gray matter maturation and cognition in children with different APOE ε genotypes. (2016)
• KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)
• The effects of prenatal HIV exposure on language functioning in Kenyan children: establishing an evaluative framework. (2016)
• Abnormal Eating Behaviors Are Common in Children with Fetal Alcohol Spectrum Disorder. (2016)
• Reference-based phasing using the Haplotype Reference Consortium panel. (2016)
• The diffusion tensor imaging (DTI) component of the NIH MRI study of normal brain development (PedsDTI). (2016)
• The Essential Role of Growth Deficiency in the Diagnosis of Fetal Alcohol Spectrum Disorder. (2016)
• Pre- and Post-Natal Maternal Depressive Symptoms in Relation with Infant Frontal Function, Connectivity, and Behaviors. (2016)
• High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs. (2016)
• Sexual Dimorphism in White Matter Developmental Trajectories Using Tract-Based Spatial Statistics. (2016)
• The Influence of Extrinsic Reinforcement on Children with Heavy Prenatal Alcohol Exposure. (2016)
• Association between alcohol consumption during pregnancy and risks of congenital heart defects in offspring: meta-analysis of epidemiological observational studies. (2016)
• Landscape of somatic mutations in 560 breast cancer whole-genome sequences. (2016)
• Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer. (2016)
• Age at first use and later substance use disorder: Shared genetic and environmental pathways for nicotine, alcohol, and cannabis. (2016)
• A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease. (2016)
• Associations between mobility, cognition and callosal integrity in people with parkinsonism. (2016)
• Prenatal exposure to cannabis and maternal and child health outcomes: a systematic review and meta-analysis. (2016)
• DNA methylation signature of human fetal alcohol spectrum disorder. (2016)
• Rapid Ngn2-induction of excitatory neurons from hiPSC-derived neural progenitor cells. (2016)
• FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing. (2016)
• Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. (2016)
• Outcome of Patients With Recurrent Osteosarcoma Enrolled in Seven Phase II Trials Through Children's Cancer Group, Pediatric Oncology Group, and Children's Oncology Group: Learning From the Past to Move Forward. (2016)
• Trajectories of cortical thickness maturation in normal brain development--The importance of quality control procedures. (2016)
• Feedback from Outcome Measures and Treatment Effectiveness, Treatment Efficiency, and Collaborative Practice: A Systematic Review. (2016)
• Effect of Marriage on Risk for Onset of Alcohol Use Disorder: A Longitudinal and Co-Relative Analysis in a Swedish National Sample. (2016)
• Development and clinical application of an integrative genomic approach to personalized cancer therapy. (2016)
• Dietary Nutrient Intake in School-Aged Children With Heavy Prenatal Alcohol Exposure. (2016)
• Antenatal depression, treatment with selective serotonin reuptake inhibitors, and neonatal brain structure: A propensity-matched cohort study. (2016)
• The role of romantic relationship status in pathways of risk for emerging adult alcohol use. (2016)
• "Did you ever drink more?" A detailed description of pregnant women's drinking patterns. (2016)
• Prognostic value of inflammation-based scores in patients with osteosarcoma. (2016)
• Quantifying Clonal and Subclonal Passenger Mutations in Cancer Evolution. (2016)
• Genomic Characterization of Brain Metastases Reveals Branched Evolution and Potential Therapeutic Targets. (2015)
• Integrating basic research with prevention/intervention to reduce risky substance use among college students. (2015)
• Early onset alcohol use and self-harm: a discordant twin analysis. (2015)
• Recurrent somatic mutations in regulatory regions of human cancer genomes. (2015)
• Integrative clinical genomics of advanced prostate cancer. (2015)
• Fetal sex-based differences in maternal hormones, angiogenic factors, and immune mediators during pregnancy and the postpartum period. (2015)
• Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia. (2015)
• An introductory review of parallel independent component analysis (p-ICA) and a guide to applying p-ICA to genetic data and imaging phenotypes to identify disease-associated biological pathways and systems in common complex disorders. (2015)
• Learning-based prediction of gestational age from ultrasound images of the fetal brain. (2015)
• Early-pregnancy vitamin D deficiency and risk of preterm birth subtypes. (2015)
• A Genome-Wide Association Study of a Biomarker of Nicotine Metabolism. (2015)
• Computer-Delivered Screening and Brief Intervention for Alcohol Use in Pregnancy: A Pilot Randomized Trial. (2015)
• Parietal dysfunction during number processing in children with fetal alcohol spectrum disorders. (2015)
• Cortical maturation and myelination in healthy toddlers and young children. (2015)
• Vitamin D deficiency in early pregnancy. (2015)
• Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth. (2015)
• Gender modulates the development of theta event related oscillations in adolescents and young adults. (2015)
• A study of the effects of prenatal alcohol exposure on white matter microstructural integrity at birth. (2015)
• CONSERTING: integrating copy-number analysis with structural-variation detection. (2015)
• Hypomania after augmenting venlafaxine and olanzapine with sarcosine in a patient with schizophrenia: a case study. (2015)
• Germline Mutations in Predisposition Genes in Pediatric Cancer. (2015)
• Profiling tissue-resident T cell repertoires by RNA sequencing. (2015)
• Prenatal Alcohol Exposure and Congenital Heart Defects: A Meta-Analysis. (2015)
• Robust enumeration of cell subsets from tissue expression profiles. (2015)
• SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations. (2015)
• Comparison of RNA-seq and microarray-based models for clinical endpoint prediction. (2015)
• Prenatal ethanol exposure alters adult hippocampal VGLUT2 expression with concomitant changes in promoter DNA methylation, H3K4 trimethylation and miR-467b-5p levels. (2015)
• Describing and predicting developmental profiles of externalizing problems from childhood to adulthood. (2015)
• Prenatal drug exposure affects neonatal brain functional connectivity. (2015)
• Comprehensive genomic profiles of small cell lung cancer. (2015)
• Gonadectomy before puberty increases the number of neurons and glia in the medial prefrontal cortex of female, but not male, rats. (2015)
• Inappropriate feeding behaviors and dietary intakes in children with fetal alcohol spectrum disorder or probable prenatal alcohol exposure. (2014)
• Effects of methylphenidate in children with attention deficit hyperactivity disorder: a near-infrared spectroscopy study with CANTAB®. (2014)
• The influence of sex steroids on structural brain maturation in adolescence. (2014)
• Polymorphisms in ABC transporter genes and concentrations of mercury in newborns--evidence from two Mediterranean birth cohorts. (2014)
• RADIA: RNA and DNA integrated analysis for somatic mutation detection. (2014)
• White matter development and early cognition in babies and toddlers. (2014)
• Maternal smoking during pregnancy and infant stress response: test of a prenatal programming hypothesis. (2014)
• Maternal vitamin D status and the risk of mild and severe preeclampsia. (2014)
• Cognitive ability changes and dynamics of cortical thickness development in healthy children and adolescents. (2014)
• The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
• Exciting fear in adolescence: does pubertal development alter threat processing? (2014)
• Effects of prenatal alcohol exposure on testosterone and pubertal development. (2014)
• Puberty in the corpus callosum. (2014)
• The effects of intracranial volume adjustment approaches on multiple regional MRI volumes in healthy aging and Alzheimer's disease. (2014)
• Maternal obesity and tobacco use modify the impact of genetic variants on the occurrence of conotruncal heart defects. (2014)
• Dynamic analyses of alternative polyadenylation from RNA-seq reveal a 3'-UTR landscape across seven tumour types. (2014)
• Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. (2014)
• In utero exposure to alcohol and puberty in boys: a pregnancy cohort study. (2014)
• Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. (2014)
• Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study. (2014)
• An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage. (2014)
• Clonal evolution in hematological malignancies and therapeutic implications. (2014)
• A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. (2014)
• mHealth: a mechanism to deliver more accessible, more effective mental health care. (2014)
• Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
• A general approach for haplotype phasing across the full spectrum of relatedness. (2014)
• Prenatal exposure to binge pattern of alcohol consumption: mental health and learning outcomes at age 11. (2014)
• Embryonic alcohol exposure impairs associative learning performance in adult zebrafish. (2014)
• DNA-Mutation Inventory to Refine and Enhance Cancer Treatment (DIRECT): a catalog of clinically relevant cancer mutations to enable genome-directed anticancer therapy. (2013)
• Association of PER2 genotype and stressful life events with alcohol drinking in young adults. (2013)
• Contribution of brain size to IQ and educational underperformance in extremely preterm adolescents. (2013)
• A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. (2013)
• Somatic rearrangements across cancer reveal classes of samples with distinct patterns of DNA breakage and rearrangement-induced hypermutability. (2013)
• Topological properties of large-scale structural brain networks in children with familial risk for reading difficulties. (2013)
• Why mental arithmetic counts: brain activation during single digit arithmetic predicts high school math scores. (2013)
• Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
• Inadequate intake of nutrients essential for neurodevelopment in children with fetal alcohol spectrum disorders (FASD). (2013)
• A mega-analysis of genome-wide association studies for major depressive disorder. (2013)
• A simple consensus approach improves somatic mutation prediction accuracy. (2013)
• Functional brain imaging across development. (2013)
• Comparing growth trajectories of risk behaviors from late adolescence through young adulthood: an accelerated design. (2013)
• Is there a viability-vulnerability tradeoff? Sex differences in fetal programming. (2013)
• Longitudinal MRI reveals altered trajectory of brain development during childhood and adolescence in fetal alcohol spectrum disorders. (2013)
• ACMG clinical laboratory standards for next-generation sequencing. (2013)
• Extreme binge drinking among 12th-grade students in the United States: prevalence and predictors. (2013)
• Smartphones for smarter delivery of mental health programs: a systematic review. (2013)
• Magnetic resonance imaging of the newborn brain: automatic segmentation of brain images into 50 anatomical regions. (2013)
• Preconceptional motivational interviewing interventions to reduce alcohol-exposed pregnancy risk. (2013)
• GABRA2 markers moderate the subjective effects of alcohol. (2013)
• A comparative analysis of algorithms for somatic SNV detection in cancer. (2013)
• Preliminary evidence for a gene-environment interaction in predicting alcohol use disorders in adolescents. (2013)
• The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
• Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
• Association of PER2 genotype and stressful life events with alcohol drinking in young adults. (2013)
• Central precocious puberty caused by mutations in the imprinted gene MKRN3. (2013)
• Fetal alcohol-related growth restriction from birth through young adulthood and moderating effects of maternal prepregnancy weight. (2013)
• Choline status and neurodevelopmental outcomes at 5 years of age in the Seychelles Child Development Nutrition Study. (2013)
• Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder. (2013)
• Brief FASD prevention intervention: physicians' skills demonstrated in a clinical trial in Russia. (2013)
• Quantification of multiple-sclerosis-related brain atrophy in two heterogeneous MRI datasets using mixed-effects modeling. (2013)
• Multiple behavioural impulsivity tasks predict prospective alcohol involvement in adolescents. (2013)
• Statistical analysis of longitudinal neuroimage data with Linear Mixed Effects models. (2013)
• Cognition assessment using the NIH Toolbox. (2013)
• Adequacy of maternal iron status protects against behavioral, neuroanatomical, and growth deficits in fetal alcohol spectrum disorders. (2012)
• Sex differences in white matter development during adolescence: a DTI study. (2012)
• Along-tract statistics allow for enhanced tractography analysis. (2012)
• Impulsiveness and insula activation during reward anticipation are associated with genetic variants in GABRA2 in a family sample enriched for alcoholism. (2012)
• Blood cell origin of circulating microRNAs: a cautionary note for cancer biomarker studies. (2012)
• Neuroimaging of child abuse: a critical review. (2012)
• Theta oscillations are sensitive to both early and late conflict processing stages: effects of alcohol intoxication. (2012)
• Persistent dose-dependent changes in brain structure in young adults with low-to-moderate alcohol exposure in utero. (2012)
• Phosphatidylethanol (PEth) as a biomarker of alcohol consumption in HIV-positive patients in sub-Saharan Africa. (2012)
• Whole brain susceptibility mapping using compressed sensing. (2012)
• Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. (2012)
• Head circumference at birth and exposure to tobacco, alcohol and illegal drugs during early pregnancy. (2012)
• Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. (2012)
• Managing incidental findings and research results in genomic research involving biobanks and archived data sets. (2012)
• Maternal intake of methyl-donor nutrients and child cognition at 3 years of age. (2012)
• Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior. (2012)
• Plasma cytokine levels in children with autistic disorder and unrelated siblings. (2012)
• Fractional anisotropy of water diffusion in cerebral white matter across the lifespan. (2012)
• Implication of European-derived adiposity loci in African Americans. (2012)
• Chronic cocaine exposure during pregnancy increases postpartum neuroendocrine stress responses. (2012)
• Effects of heavy prenatal alcohol exposure and iron deficiency anemia on child growth and body composition through age 9 years. (2012)
• Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. (2012)
• Genome-wide association study of primary open angle glaucoma risk and quantitative traits. (2012)
• Alcohol intake in pregnancy increases the child's risk of atopic dermatitis. the COPSAC prospective birth cohort study of a high risk population. (2012)
• Ultrasensitive detection of rare mutations using next-generation targeted resequencing. (2012)
• Patient-derived tumour xenografts as models for oncology drug development. (2012)
• Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion. (2012)
• Ethanol exposure during pregnancy persistently attenuates cranially directed blood flow in the developing fetus: evidence from ultrasound imaging in a murine second trimester equivalent model. (2012)
• Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
• VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012)
• A prospective cohort study of the prevalence of growth, facial, and central nervous system abnormalities in children with heavy prenatal alcohol exposure. (2012)
• Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
• Number processing in adolescents with prenatal alcohol exposure and ADHD: differences in the neurobehavioral phenotype. (2011)
• A comparison of approaches to account for uncertainty in analysis of imputed genotypes. (2011)
• Whole brain diffeomorphic metric mapping via integration of sulcal and gyral curves, cortical surfaces, and images. (2011)
• Prevalence of children with severe fetal alcohol spectrum disorders in communities near Rome, Italy: new estimated rates are higher than previous estimates. (2011)
• DSM-IV to DSM-5: the impact of proposed revisions on diagnosis of alcohol use disorders. (2011)
• Recruitment and retention strategies for minority or poor clinical research participants: lessons from the Healthy Aging in Neighborhoods of Diversity across the Life Span study. (2011)
• Early adolescent cocaine use as determined by hair analysis in a prenatal cocaine exposure cohort. (2011)
• MicroRNA expression in abdominal and gluteal adipose tissue is associated with mRNA expression levels and partly genetically driven. (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)
• A population-based twin study of the genetic and environmental relationship of major depression, regular tobacco use and nicotine dependence. (2011)
• Opioid dependence latent structure: two classes with differing severity? (2011)
• Prenatal and postnatal cocaine exposure predict teen cocaine use. (2011)
• Brain imaging correlates of verbal working memory in children following traumatic brain injury. (2011)
• Alcohol consumption and non-communicable diseases: epidemiology and policy implications. (2011)
• Haplotype block structure of the genomic region of the mu opioid receptor gene. (2011)
• Psychiatric comorbidity in methamphetamine dependence. (2011)
• Basal forebrain involvement in low-functioning autistic children: a voxel-based morphometry study. (2011)
• Maternal salivary cortisol differs by fetal sex during the second half of pregnancy. (2011)
• Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions. (2011)
• S100B and APP promote a gliocentric shift and impaired neurogenesis in Down syndrome neural progenitors. (2011)
• Memory for the order of events in specific sequences: contributions of the hippocampus and medial prefrontal cortex. (2011)
• Hippocampal volumetry for lateralization of temporal lobe epilepsy: automated versus manual methods. (2011)
• Differential effects of intraventricular hemorrhage and white matter injury on preterm cerebellar growth. (2011)
• Up-regulation of microRNAs in brain of human alcoholics. (2011)
• Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. (2011)
• The neuronal transporter gene SLC6A15 confers risk to major depression. (2011)
• Molecular insights into the pathogenesis of Alzheimer's disease and its relationship to normal aging. (2011)
• CA1 neurons in the human hippocampus are critical for autobiographical memory, mental time travel, and autonoetic consciousness. (2011)
• Are there effects of intrauterine cocaine exposure on delinquency during early adolescence? A preliminary report. (2011)
• Diffusion tensor imaging of the cerebellum and eyeblink conditioning in fetal alcohol spectrum disorder. (2011)
• Adolescent initiation of licit and illicit substance use: Impact of intrauterine exposures and post-natal exposure to violence. (2011)
• Genome-wide scan for self-rating of the effects of alcohol in American Indians. (2010)
• Verbal and nonverbal memory in adults prenatally exposed to alcohol. (2010)
• Effect of motivational interviewing on reduction of alcohol use. (2010)
• Genetic control over the resting brain. (2010)
• Neuronal LRP1 knockout in adult mice leads to impaired brain lipid metabolism and progressive, age-dependent synapse loss and neurodegeneration. (2010)
• The development of the corpus callosum in the healthy human brain. (2010)
• New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. (2010)
• A tract-specific framework for white matter morphometry combining macroscopic and microscopic tract features. (2010)
• Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample. (2010)
• Liver and adipose expression associated SNPs are enriched for association to type 2 diabetes. (2010)
• Obesity is linked with lower brain volume in 700 AD and MCI patients. (2010)
• Prenatal alcohol exposure and chronic mild stress differentially alter depressive- and anxiety-like behaviors in male and female offspring. (2010)
• Novelty P3 reductions in depression: characterization using principal components analysis (PCA) of current source density (CSD) waveforms. (2010)
• Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction. (2010)
• Infant Symbolic Play as an Early Indicator of Fetal Alcohol-Related Deficit. (2010)
• Mothers' maximum drinks ever consumed in 24 hours predicts mental health problems in adolescent offspring. (2010)
• A prospective study of fetuses with isolated ventriculomegaly investigated by antenatal sonography and in utero MR imaging. (2010)
• Neuroimaging study designs, computational analyses and data provenance using the LONI pipeline. (2010)
• Genome-wide association studies in diverse populations. (2010)
• The relationship between self-reported drinking and BAC level in emergency room injury cases: is it a straight line? (2010)
• In vivo magnetic resonance spectroscopy: basic methodology and clinical applications. (2010)
• Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. (2010)
• Prenatal exposure to airborne polycyclic aromatic hydrocarbons and children's intelligence at 5 years of age in a prospective cohort study in Poland. (2010)
• A review of estrogen receptor alpha gene (ESR1) polymorphisms, mood, and cognition. (2010)
• Gene--environment-wide association studies: emerging approaches. (2010)
• Prenatal Maternal Stress Associated with ADHD and Autistic Traits in early Childhood. (2010)
• Genome-wide association study of bipolar disorder in European American and African American individuals. (2009)
• Functional CRH variation increases stress-induced alcohol consumption in primates. (2009)
• Genetic structure of Europeans: a view from the North-East. (2009)
• Expansion of the human mu-opioid receptor gene architecture: novel functional variants. (2009)
• Accurate and robust brain image alignment using boundary-based registration. (2009)
• Meta-analysis in genome-wide association studies. (2009)
• Functional brain networks develop from a "local to distributed" organization. (2009)
• Individual and situational factors that influence the efficacy of personalized feedback substance use interventions for mandated college students. (2009)
• Executive cognitive functions and impulsivity as correlates of risk taking and problem behavior in preadolescents. (2009)
• Dense genomewide linkage scan for alcohol dependence in African Americans: significant linkage on chromosome 10. (2009)
• Parental alcoholism and offspring behavior problems: findings in Australian children of twins. (2009)
• Can we identify genes for alcohol consumption in samples ascertained for heterogeneous purposes? (2009)
• Marker selection for genetic case-control association studies. (2009)
• Neuroimaging of children following prenatal drug exposure. (2009)
• Neuroimaging of children following prenatal drug exposure. (2009)
• Parental alcoholism and offspring behavior problems: findings in Australian children of twins. (2009)
• Altered white matter integrity in adolescent binge drinkers. (2009)
• Superior parietal cortex is critical for the manipulation of information in working memory. (2009)
• A neural network critical for spelling. (2009)
• In vivo hippocampal measurement and memory: a comparison of manual tracing and automated segmentation in a large community-based sample. (2009)
• Children with and without gestational cocaine exposure: a neurocognitive systems analysis. (2009)
• Genome-wide and candidate gene association study of cigarette smoking behaviors. (2009)
• Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia. (2008)
• Alterations in ethyl alcohol pharmacokinetics during oral consumption of malt liquor beverages in African Americans. (2008)
• Toward a global view of alcohol, tobacco, cannabis, and cocaine use: findings from the WHO World Mental Health Surveys. (2008)
• Childhood or adolescent parental divorce/separation, parental history of alcohol problems, and offspring lifetime alcohol dependence. (2008)
• Adrenomedullin signaling is necessary for murine lymphatic vascular development. (2008)
• Neuropsychological study of FASD in a sample of American Indian children: processing simple versus complex information. (2008)
• Elevated inflammation levels in depressed adults with a history of childhood maltreatment. (2008)
• Fetal alcohol spectrum disorders and their persisting sequelae in adult life. (2008)
• The performance of elements of a 'level of response to alcohol'-based model of drinking behaviors in 13-year-olds. (2008)
• Association of a single nucleotide polymorphism in neuronal acetylcholine receptor subunit alpha 5 (CHRNA5) with smoking status and with 'pleasurable buzz' during early experimentation with smoking. (2008)
• Fatty acid ethyl esters in meconium: are they biomarkers of fetal alcohol exposure and effect? (2006)
• Too much or too little step width variability is associated with a fall history in older persons who walk at or near normal gait speed. (2005)
• Fetal alcohol spectrum disorder: Canadian guidelines for diagnosis. (2005)
• A genome-wide scan to identify loci for smoking rate in the Framingham Heart Study population. (2003)
• Prenatal alcohol exposure, birthweight, and measures of child size from birth to age 14 years. (1994)

Merged raw entities (96)

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