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Manolis Kellis

Researcher at Massachusetts Institute of Technology

Publications -  448
Citations -  132627

Manolis Kellis is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Gene & Genome. The author has an hindex of 128, co-authored 405 publications receiving 112181 citations. Previous affiliations of Manolis Kellis include Broad Institute & Epigenomics AG.

Papers
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Journal ArticleDOI

Network Maximal Correlation

TL;DR: Network Maximal Correlation is introduced as a multivariate measure of nonlinear association among random variables and its utility in a data application of learning nonlinear dependencies among genes in a cancer dataset is shown.
Journal ArticleDOI

Integrative construction of regulatory region networks in 127 human reference epigenomes by matrix factorization

TL;DR: It is shown that the unbiased integration of independent data sources suggestive of regulatory interactions produces meaningful associations supported by existing functional and physical evidence, correlating with expected independent biological features.
Posted ContentDOI

Exome-wide age-of-onset analysis reveals exonic variants in ERN1, TACR3 and SPPL2C associated with Alzheimer’s disease

TL;DR: Novel evidence is provided supporting the hypothesis of the potential involvement of the UPR to ER stress in the pathological pathway of AD, and more insights are given into underlying regulatory mechanisms behind the pleiotropic effects of rs12373123 in multiple degenerative diseases including AD and Parkinson’s disease.
Patent

Systems and methods for crowdsourcing, analyzing, and/or matching personal data

TL;DR: In this article, the authors describe a secure system for sharing private data and related systems and methods for incentivizing and validating private data sharing. But they do not discuss how private data providers can register to selectively share private data under controlled sharing conditions.
Posted ContentDOI

A partnership of the lipid scramblase XK and of the lipid transfer protein VPS13A at the plasma membrane

TL;DR: This paper showed that VPS13A can also localize at ER-PM contacts via the binding of its PH domain to a cytosolic loop of XK, that such interaction is regulated by an intramolecular interaction within XK and that both PS13A and XK are highly expressed in the caudate neurons.