Emmanouil T. Dermitzakis

According to our database, Emmanouil T. Dermitzakis authored at least 9 papers between 2002 and 2017.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of three.

2017

The impact of rare variation on gene expression across tissues.

Xin Li, Yungil Kim, Emily K. Tsang, Joe R. Davis, Farhan N. Damani, Colby Chiang, Gaelen T. Hess, Zachary Zappala, Benjamin J. Strober, Alexandra J. Scott, Amy Li, Andrea Ganna, Michael C. Bassik, Jason D. Merker, François Aguet, Kristin G. Ardlie, Beryl B. Cummings, Ellen T. Gelfand, Gad Getz, Kane Hadley, Robert E. Handsaker, Katherine H. Huang, Seva Kashin, Konrad J. Karczewski, Monkol Lek, Xiao Li, Daniel G. MacArthur, Jared L. Nedzel, Duyen T. Nguyen, Michael S. Noble, Ayellet V. Segrè, Casandra A. Trowbridge, Taru Tukiainen, Nathan S. Abell, Brunilda Balliu, Ruth Barshir, Omer Basha, Alexis J. Battle, Gireesh K. Bogu, Andrew Brown, Christopher D. Brown, Stephane E. Castel, Lin S. Chen, Donald F. Conrad, Nancy J. Cox, Olivier Delaneau, Emmanouil T. Dermitzakis, Barbara E. Engelhardt, Eleazar Eskin, Pedro G. Ferreira, Laure Frésard, Eric R. Gamazon, Diego Garrido-Martín, Ariel D. H. Gewirtz, Genna Gliner, Michael J. Gloudemans, Roderic Guigó, Ira M. Hall, Buhm Han, Yuan He, Farhad Hormozdiari, Cedric Howald, Hae Kyung Im, Brian Jo, Eun Yong Kang, Sarah Kim-Hellmuth, Tuuli Lappalainen, Gen Li, Boxiang Liu, Serghei Mangul, Mark I. McCarthy, Ian C. McDowell, Pejman Mohammadi, Jean Monlong, Stephen B. Montgomery

Nat., 2017

MBV: a method to solve sample mislabeling and detect technical bias in large combined genotype and sequencing assay datasets.

Alexandre Fort, Nikolaos I. Panousis, Marco Garieri, Stylianos E. Antonarakis, Tuuli Lappalainen, Emmanouil T. Dermitzakis, Olivier Delaneau

Bioinform., 2017

2016

Fast and efficient QTL mapper for thousands of molecular phenotypes.

Halit Ongen, Alfonso Buil, Andrew Anand Brown, Emmanouil T. Dermitzakis, Olivier Delaneau

Bioinform., 2016

2015

Assessing allele-specific expression across multiple tissues from RNA-seq read data.

Matti Pirinen, Tuuli Lappalainen, Noah A. Zaitlen, Emmanouil T. Dermitzakis, Peter Donnelly, Mark I. McCarthy, Manuel A. Rivas

Bioinform., 2015

2014

Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data.

Sebastian M. Waszak, Helena Kilpinen, Andreas R. Gschwind, Andrea Orioli, Sunil K. Raghav, Robert M. Witwicki, Eugenia Migliavacca, Alisa Yurovsky, Tuuli Lappalainen, Nouria Hernandez, Alexandre Reymond, Emmanouil T. Dermitzakis, Bart Deplancke

Bioinform., 2014

2012

Analysis of case-control association studies with known risk variants.

Noah Zaitlen, Bogdan Pasaniuc, Nick Patterson, Samuela Pollack, Benjamin Voight, Leif Groop, David Altshuler, Brian E. Henderson, Laurence N. Kolonel, Loic Le Marchand, Kevin Waters, Christopher A. Haiman, Barbara E. Stranger, Emmanouil T. Dermitzakis, Peter Kraft, Alkes L. Price

Bioinform., 2012

2010

Data analysis issues for allele-specific expression using Illumina's GoldenGate assay.

Matthew E. Ritchie, Matthew S. Forrest, Antigone S. Dimas, Caroline Daelemans, Emmanouil T. Dermitzakis, Panagiotis Deloukas, Simon Tavaré

BMC Bioinform., 2010

Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies.

Tsun-Po Yang, Claude Beazley, Stephen B. Montgomery, Antigone S. Dimas, Maria Gutierrez-Arcelus, Barbara E. Stranger, Panos Deloukas, Emmanouil T. Dermitzakis

Bioinform., 2010

2002

Trisomic Phase Inference.

Andrew G. Clark, Emmanouil T. Dermitzakis, Stylianos E. Antonarakis

Proceedings of the Computational Methods for SNPs and Haplotype Inference, 2002