Oliver Stegle

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John MarioniGenentechDirección de correo verificada de gene.com
Karsten BorgwardtDirector, Max Planck Institute of BiochemistryDirección de correo verificada de biochem.mpg.de
Wolf ReikHead, Epigenetics Programme, Babraham Institute Cambridge, UKDirección de correo verificada de babraham.ac.uk
Sarah A. TeichmannUniversity of CambridgeDirección de correo verificada de cam.ac.uk
Christoph LippertProfessor, Hasso Plattner Institute, Universität PotsdamDirección de correo verificada de hpi.de
Francesco Paolo CasaleHelmholtz Pioneer Campus, Institute of AI for Health, Helmholtz Zentrum MünchenDirección de correo verificada de helmholtz-muenchen.de
Gunnar RätschProfessor, ETH ZürichDirección de correo verificada de inf.ethz.ch
Marc Jan BonderPostdoctoral researcher UMCGDirección de correo verificada de umcg.nl
Leopold PartsFaculty at Wellcome Sanger Institute; Senior Researcher (part-time) at University of TartuDirección de correo verificada de sanger.ac.uk
Richard DurbinDept of Genetics, University of CambridgeDirección de correo verificada de cam.ac.uk
Ricard ArgelaguetAltos LabsDirección de correo verificada de altoslabs.com
Detlef WeigelMax Planck Institute for Biology TübingenDirección de correo verificada de weigelworld.org
Stephen ClarkAltos Labs Cambridge InstituteDirección de correo verificada de altoslabs.com
John WinnPrincipal Researcher, Machine Learning Group, Microsoft Research CambridgeDirección de correo verificada de microsoft.com
Neil D. LawrenceUniversity of CambridgeDirección de correo verificada de cl.cam.ac.uk
Richard MottWeldon Professor of Computational Genetics, University College London, UKDirección de correo verificada de ucl.ac.uk
Magnus NordborgGregor Mendel Institute, Austrian Academy of SciencesDirección de correo verificada de gmi.oeaw.ac.at
Bernhard SchölkopfDirector, Max Planck Institute for Intelligent Systems & ELLIS Institute Tübingen; Professor at ETHDirección de correo verificada de tuebingen.mpg.de
Ewan BirneyDirector, EMBL-EBIDirección de correo verificada de ebi.ac.uk
David MacKayProfessor of Natural Philosophy, Cavendish Laboratory, University of CambridgeDirección de correo verificada de mrao.cam.ac.uk

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Oliver Stegle

German Cancer Research Center (DKFZ) & EMBL Heidelberg

Dirección de correo verificada de dkfz.de - Página principal

Systems Genetics Single-cell genomics Computational Biology Statistical Genomics


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	16253	2015
An integrated map of structural variation in 2,504 human genomes PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ... Nature 526 (7571), 75-81, 2015	2537	2015
The human cell atlas A Regev, SA Teichmann, ES Lander, I Amit, C Benoist, E Birney, ... elife 6, e27041, 2017	2269	2017
Transcriptome and genome sequencing uncovers functional variation in humans T Lappalainen, M Sammeth, MR Friedländer, PAC ‘t Hoen, J Monlong, ... Nature 501 (7468), 506-511, 2013	2128	2013
Pan-cancer analysis of whole genomes Nature 578 (7793), 82-93, 2020	2023*	2020
Deep learning for computational biology C Angermueller, T Pärnamaa, L Parts, O Stegle Molecular systems biology 12 (7), 878, 2016	1693	2016
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression U Võsa, A Claringbould, HJ Westra, MJ Bonder, P Deelen, B Zeng, ... Nature genetics 53 (9), 1300-1310, 2021	1625*	2021
Severe COVID-19 is marked by a dysregulated myeloid cell compartment J Schulte-Schrepping, N Reusch, D Paclik, K Baßler, S Schlickeiser, ... Cell 182 (6), 1419-1440. e23, 2020	1401	2020
Computational and analytical challenges in single-cell transcriptomics O Stegle, SA Teichmann, JC Marioni Nature Reviews Genetics 16 (3), 133-145, 2015	1323	2015
Computational analysis of cell-to-cell heterogeneity in single-cell RNA-sequencing data reveals hidden subpopulations of cells F Buettner, KN Natarajan, FP Casale, V Proserpio, A Scialdone, FJ Theis, ... Nature biotechnology 33 (2), 155-160, 2015	1298	2015
Single-cell genome-wide bisulfite sequencing for assessing epigenetic heterogeneity SA Smallwood, HJ Lee, C Angermueller, F Krueger, H Saadeh, J Peat, ... Nature methods 11 (8), 817-820, 2014	1201	2014
Eleven grand challenges in single-cell data science D Lähnemann, J Köster, E Szczurek, DJ McCarthy, SC Hicks, ... Genome biology 21, 1-35, 2020	1154	2020
Whole-genome sequencing of multiple Arabidopsis thaliana populations J Cao, K Schneeberger, S Ossowski, T Günther, S Bender, J Fitz, ... Nature Genetics 43 (10), 956-963, 2011	1112	2011
Lineage-specific genome architecture links enhancers and non-coding disease variants to target gene promoters BM Javierre, OS Burren, SP Wilder, R Kreuzhuber, SM Hill, S Sewitz, ... Cell 167 (5), 1369-1384. e19, 2016	1063	2016
Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses O Stegle, L Parts, M Piipari, J Winn, R Durbin Nature protocols 7 (3), 500-507, 2012	1037	2012
Multi‐Omics Factor Analysis—a framework for unsupervised integration of multi‐omics data sets R Argelaguet, B Velten, D Arnol, S Dietrich, T Zenz, JC Marioni, F Buettner, ... Molecular systems biology 14 (6), e8124, 2018	1011	2018
A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium. SMIII Consortium Nature Biotechnology 32 (9), 903-914, 2014	883	2014
Comprehensive analysis of alternative splicing across tumors from 8,705 patients A Kahles, KV Lehmann, NC Toussaint, M Hüser, SG Stark, ... Cancer cell 34 (2), 211-224. e6, 2018	825	2018
Spontaneous epigenetic variation in the Arabidopsis thaliana methylome C Becker, J Hagmann, J Müller, D Koenig, O Stegle, K Borgwardt, ... Nature 480 (7376), 245-249, 2011	795	2011
Parallel single-cell sequencing links transcriptional and epigenetic heterogeneity C Angermueller, SJ Clark, HJ Lee, IC Macaulay, MJ Teng, TX Hu, ... Nature methods 13 (3), 229-232, 2016	771	2016

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