Author details

Full Name

Brunilda Balliu

Affiliation

ORCID

Career Start Year

2012

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36999049	RNA-seq data science: From raw data to effective interpretation.	Front Genet	2023
37986808	Transcriptomics and chromatin accessibility in multiple African population samples.	bioRxiv	2023
37464048	Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region.	Nat Med	2023
37452040	Increased body mass index is linked to systemic inflammation through altered chromatin co-accessibility in human preadipocytes.	Nat Commun	2023
35130266	Evaluating supervised and unsupervised background noise correction in human gut microbiome data.	PLoS Computational Biology	2022
35389781	Single-cell RNA-seq reveals cell type-specific molecular and genetic associations to lupus.	Science	2022
36171194	Multi-context genetic modeling of transcriptional regulation resolves novel disease loci.	Nat Commun	2022
36085083	Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.	Genome Med	2022
36384576	Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.	Genome Med	2022
35292083	Integration of genetic colocalizations with physiological and pharmacological perturbations identifies cardiometabolic disease genes.	Genome Med	2022
34582792	An integrated approach to identify environmental modulators of genetic risk factors for complex traits.	Am J Hum Genet	2021
33314708	Association of image-defined risk factors with clinical features, histopathology, and outcomes in neuroblastoma.	Cancer Med	2021
34446078	Technology dictates algorithms: recent developments in read alignment.	Genome Biol	2021
32912333	Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx.	Genome Biol	2020
32470399	Molecular Choreography of Acute Exercise.	Cell	2020
32913072	The impact of sex on gene expression across human tissues.	Science	2020
31123710	Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms.	Commun Biol	2019
31684996	Genetic regulation of gene expression and splicing during a 10-year period of human aging.	Genome Biol	2019
30693553	Powerful testing via hierarchical linkage disequilibrium in haplotype association studies.	Biometrical Journal	2019
29977664	Distinctive facial features in idiopathic Moyamoya disease in Caucasians: a first systematic analysis.	PeerJ	2018
29083406	Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.	Nat Genet	2017
27980622	Gene coexpression network analysis for family studies based on a meta-analytic approach.	BMC Proceedings	2016
27197214	Impact of the X Chromosome and sex on regulatory variation.	Genome Res	2016
26865367	A Novel Test for Detecting SNP-SNP Interactions in Case-Only Trio Studies.	Genetics	2016
25620726	A retrospective likelihood approach for efficient integration of multiple omics factors in case-control association studies.	Genetic Epidemiology	2015
25112186	Testing genetic association with rare and common variants in family data.	Genet Epidemiol	2014
25405460	Classification and visualization based on derived image features: application to genetic syndromes.	PLoS ONE	2014
25519415	Gene analysis for longitudinal family data using random-effects models.	BMC Proceedings	2014
25519382	Combining information from linkage and association mapping for next-generation sequencing longitudinal family data.	BMC Proceedings	2014
23652375	CHEK2*1100delC homozygosity in the Netherlands--prevalence and risk of breast and lung cancer.	Eur J Hum Genet	2014
22851506	Combining family and twin data in association studies to estimate the noninherited maternal antigens effect.	Genetic Epidemiology	2012