normal controls cohort
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Mentioned in (20)
Papers in which this entity is mentioned.
- Splicing neoantigen discovery with SNAF reveals shared targets for cancer immunotherapy. (2024)
- Cell-Free DNA Fragmentomics: The Novel Promising Biomarker. (2023)
- Enter the Matrix: Factorization Uncovers Knowledge from Omics. (2018)
- Meta-Analyses of Externalizing Disorders: Genetics or Prenatal Alcohol Exposure? (2018)
- Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. (2017)
- Differential Recruitment of Brain Regions During Response Inhibition in Children Prenatally Exposed to Alcohol. (2017)
- Maternal choline supplementation in a sheep model of first trimester binge alcohol fails to protect against brain volume reductions in peripubertal lambs. (2016)
- Integrated digital error suppression for improved detection of circulating tumor DNA. (2016)
- Maternal risk factors for fetal alcohol spectrum disorders in a province in Italy. (2014)
- Adaptive behaviour in children and adolescents with foetal alcohol spectrum disorders: a comparison with specific learning disability and typical development. (2012)
- Fetal alcohol spectrum disorders: neuropsychological and behavioral features. (2011)
- Impaired delay and trace eyeblink conditioning in school-age children with fetal alcohol syndrome. (2011)
- Biobehavioral markers of adverse effect in fetal alcohol spectrum disorders. (2011)
- DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing. (2010)
- Population differences in dysmorphic features among children with fetal alcohol spectrum disorders. (2010)
- The plausibility of maternal nutritional status being a contributing factor to the risk for fetal alcohol spectrum disorders: the potential influence of zinc status as an example. (2010)
- Differentiating prenatal exposure to methamphetamine and alcohol versus alcohol and not methamphetamine using tensor-based brain morphometry and discriminant analysis. (2010)
- Brain signatures of monetary loss and gain: outcome-related potentials in a single outcome gambling task. (2009)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
- Accurate and reliable high-throughput detection of copy number variation in the human genome. (2006)
Merged raw entities (4)
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 |
|---|---|---|---|
| normal controls | cohort | 55 | 110 |
| normal subjects | cohort | 27 | 41 |
| normal individuals | cohort | 10 | 12 |
| normals | cohort | 3 | 3 |