Emmanouil T Dermitzakis

发表

A complete tool set for molecular QTL discovery and analysis

Olivier Delaneau, Halit Ongen, Andrew A Brown, 2016, Nature Communications.

Inference and quantification of peptidoforms in large sample cohorts by SWATH-MS

Lars Malmström, Ruedi Aebersold, Hannes L Röst, 2017, Nature Biotechnology.

Sex-biased genetic effects on gene regulation in humans

Maria Gutierrez-Arcelus, Mark I McCarthy, Stephen B Montgomery, 2012, Genome research.

Large-Scale Population Study of Human Cell Lines Indicates that Dosage Compensation Is Virtually Complete

Emmanouil T Dermitzakis, Barbara E Stranger, M. Ross, 2007, PLoS genetics.

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

Thomas Meitinger, Michael Inouye, Martin Dichgans, 2010, Nature Genetics.

Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA Sequencing.

Emmanouil T Dermitzakis, Serge Nef, Lee B. Smith, 2018, Cell reports.

Evolutionary Discrimination of Mammalian Conserved Non-Genic Sequences (CNGs)

Alexandre Reymond, Emmanouil T Dermitzakis, E. Kirkness, 2003, Science.

Williams–Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase

Alexandre Reymond, Emmanouil T Dermitzakis, Giuseppe Merla, 2008, European Journal of Human Genetics.

The effect of genetic variation on promoter usage and enhancer activity

Piero Carninci, Olivier Delaneau, Alexandre Fort, 2017, Nature Communications.

The genetics of regulatory variation in the human genome

Emmanouil T Dermitzakis, Barbara E Stranger, E. Dermitzakis, 2005, Human Genomics.

Allelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies

Maria Gutierrez-Arcelus, Emmanouil T Dermitzakis, Tuuli Lappalainen, 2014, Genome Biology.

Correction: Passive and active DNA methylation and the interplay with genetic variation in gene regulation

Maria Gutierrez-Arcelus, Stephen B Montgomery, Alisa Yurovsky, 2013, eLife.

From DNA to RNA to disease and back: The 'central dogma' of regulatory disease variation

Emmanouil T Dermitzakis, Barbara E Stranger, E. Dermitzakis, 2006, Human Genomics.

Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes.

C. V. Jongeneel, Robert Lyle, Emmanouil T Dermitzakis, 2005, Human molecular genetics.

A genome-wide association study of testicular germ cell tumor

Deborah Hughes, Nazneen Rahman, Panagiotis Deloukas, 2009, Nature Genetics.

Biased allelic expression in human primary fibroblast single cells.

Piero Carninci, Olivier Delaneau, Pedro G. Ferreira, 2015, American journal of human genetics.

Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins

Richard Durbin, Matthew N Davies, Andrew Anand Brown, 2014, Nature Genetics.

Cell-type, allelic, and genetic signatures in the human pancreatic beta cell transcriptome

Halit Ongen, Emmanouil T Dermitzakis, Philippe A Halban, 2013, Genome research.

Functional variation and evolution of non-coding DNA.

Emmanouil T Dermitzakis, Barbara E Stranger, C. Bird, 2006, Current opinion in genetics & development.

Quantitative variability of 342 plasma proteins in a human twin population

Ruedi Aebersold, Olga Vitek, Ludovic C. Gillet, 2015 .

Genetic interactions affecting human gene expression identified by variance association mapping

Richard Durbin, Andrew Anand Brown, J Brent Richards, 2014, eLife.

Gene expression changes with age in skin, adipose tissue, blood and brain

Leopold Parts, David A. Knowles, Richard Durbin, 2013, Genome Biology.

Common variants near MC4R are associated with fat mass, weight and risk of obesity

Subhajyoti De, Inês Barroso, Philippe Froguel, 2008, Nature Genetics.

Conserved noncoding sequences are selectively constrained and not mutation cold spots

Laurent Excoffier, Alexandre Reymond, Emmanouil T Dermitzakis, 2006, Nature Genetics.

The functional impact of structural variation in humans.

Matthew E Hurles, Chris Tyler-Smith, Emmanouil T Dermitzakis, 2008, Trends in genetics : TIG.