Author details

Full Name

Elior Rahmani

Affiliation

ORCID

Career Start Year

2014

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36711575	Phenotypic subtyping via contrastive learning.	bioRxiv	2023
38045283	SLIViT: a general AI framework for clinical-feature diagnosis from limited 3D biomedical-imaging data.	Res Sq	2023
37732190	Genome-wide association study and genomic risk prediction of age-related macular degeneration in Israel.	medRxiv	2023
36303752	The Effect of Model Directionality on Cell-Type-Specific Differential DNA Methylation Analysis.		2021
32620816	Enhancing droplet-based single-nucleus RNA-seq resolution using the semi-supervised machine learning classifier DIEM.	Sci Rep	2020
32106291	Association of a Variant in VWA3A with Response to Anti-Vascular Endothelial Growth Factor Treatment in Neovascular AMD.	Investigative Ophthalmology and Visual Science	2020
32332754	Accurate estimation of cell composition in bulk expression through robust integration of single-cell information.	Nat Commun	2020
32493922	Publisher Correction: Accurate estimation of cell composition in bulk expression through robust integration of single-cell information.	Nat Commun	2020
32925908	The causal effect of obesity on prediabetes and insulin resistance reveals the important role of adipose tissue in insulin resistance.	PLoS Genet	2020
31300005	CONFINED: distinguishing biological from technical sources of variation by leveraging multiple methylation datasets.		2019
31366909	Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology.	Nature Communications	2019
30464216	Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests.	Nat Commun	2018
29932739	Using Stochastic Approximation Techniques to Efficiently Construct Confidence Intervals for Heritability.	Journal of Computational Biology	2018
30241486	BayesCCE: a Bayesian framework for estimating cell-type composition from DNA methylation without the need for methylation reference.		2018
28177067	GLINT: a user-friendly toolset for the analysis of high-throughput DNA-methylation array data.		2017
28881982	Association testing of bisulfite-sequencing methylation data via a Laplace approximation.		2017
29025915	RL-SKAT: An Exact and Efficient Score Test for Heritability and Set Tests.	Genetics	2017
28245214	Correcting for cell-type heterogeneity in DNA methylation: a comprehensive evaluation.	Nat Methods	2017
28149326	Genome-wide methylation data mirror ancestry information.	Epigenetics Chromatin	2017
27723282	Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes.	Arthritis Rheumatol	2017
27018579	Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies.	Nat Methods	2016
24931983	EPIQ-efficient detection of SNP-SNP epistatic interactions for quantitative traits.	Bioinformatics	2014