case cohort cohort

Aliases

1472 case, case samples, case subjects, cases

Related entities (3)

Mentioned in (14)

Papers in which this entity is mentioned.

• Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
• Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
• Genome-wide association analysis of opioid use disorder: A novel approach using clinical data. (2020)
• : batch effect adjustment for RNA-seq count data. (2020)
• Integrating single-cell transcriptomic data across different conditions, technologies, and species. (2018)
• Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways. (2014)
• Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. (2013)
• Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. (2012)
• Association of CHRNA4 polymorphisms with smoking behavior in two populations. (2011)
• Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
• Tackling the widespread and critical impact of batch effects in high-throughput data. (2010)
• Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. (2007)

Merged raw entities (3)

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