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A comprehensive comparison on cell-type composition inference for spatial transcriptomics data

artículo científico publicado en 2022

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences

scientific article published on 11 September 2020

Age-related DNA hydroxymethylation is enriched for gene expression and immune system processes in human peripheral blood

artículo científico publicado en 2019

CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration

artículo científico publicado en 2006

CUE: CpG impUtation ensemble for DNA methylation levels across the human methylation450 (HM450) and EPIC (HM850) BeadChip platforms

scientific article published on 04 October 2020

Cell-type-specific 3D epigenomes in the developing human cortex

artículo científico publicado en 2020

Common genetic variation near MC4R is associated with waist circumference and insulin resistance

artículo científico publicado en 2008

Common variants at 30 loci contribute to polygenic dyslipidemia

artículo científico publicado en 2009

Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.

artículo científico publicado en 2017

From GWAS variant to function: A study of ∼148,000 variants for blood cell traits

artículo científico publicado en 2022

Generalized multi-SNP mediation intersection-union test

artículo científico publicado en 2020

Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

artículo científico publicado en 2017

Genome-wide detection and characterization of positive selection in human populations

artículo científico publicado en 2007

Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways

artículo científico publicado en 2009

HPRep: Quantifying Reproducibility in HiChIP and PLAC-Seq Datasets

artículo científico publicado en 2021

MAPS: Model-based analysis of long-range chromatin interactions from PLAC-seq and HiChIP experiments

artículo científico publicado en 2019

MRLocus: Identifying causal genes mediating a trait through Bayesian estimation of allelic heterogeneity

artículo científico publicado en 2021

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

artículo científico publicado en 2010

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

artículo científico publicado en 2008

Parallel characterization of cis-regulatory elements for multiple genes using CRISPRpath

artículo científico publicado en 2021

Putative association between a new polymorphism in exon 3 (Arg109Cys) of the pancreatic colipase gene and type 2 diabetes mellitus in two independent Caucasian study populations

artículo científico publicado en 2005

SAME-clustering: Single-cell Aggregated Clustering via Mixture Model Ensemble

artículo científico publicado en 2020

Single-cell dual-omics reveals the transcriptomic and epigenomic diversity of cardiac non-myocytes

artículo científico publicado en 2022

TWO-SIGMA: A novel two-component single cell model-based association method for single-cell RNA-seq data

artículo científico publicado en 2020

The Association of Epigenetic Age Acceleration and Multimorbidity at Age 90 in the Women’s Health Initiative

artículo científico publicado en 2022

The genome of a songbird

artículo científico publicado en 2010

Transcriptome-wide association analysis of brain structures yields insights into pleiotropy with complex neuropsychiatric traits

artículo científico publicado en 2021

Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits

artículo científico publicado en 2022

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

artículo científico publicado en 2019

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

artículo científico publicado en 2019