Bernd Timmermann

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Martin KerickInstituto de Parasitología y Biomedicina López-Neyra (CSIC)Verifisert e-postadresse på ipb.csic.es
Stefan MundlosInstitut für Medizinische Genetik und Humangenetik, CharitéVerifisert e-postadresse på molgen.mpg.de
Sven KlagesMax Planck Institute for Molecular Genetics, Berlin, GermanyVerifisert e-postadresse på molgen.mpg.de
Gil McVeanProfessor of Statistical Genetics, University of OxfordVerifisert e-postadresse på bdi.ox.ac.uk
Ralf HerwigGroup Leader, Max Planck Institute for molecular Genetics, BerlinVerifisert e-postadresse på molgen.mpg.de
Markus RalserCharité Berlin & University of OxfordVerifisert e-postadresse på charite.de
Prof. Dr. med., Dipl. Phys. Peter KrawitzInstitute for Genomic Statistics and BioinformaticsVerifisert e-postadresse på uni-bonn.de
Katerina KraftPostdoc, StanfordVerifisert e-postadresse på stanford.edu
Alexander MeissnerMax Planck Institute for Molecular Genetics/ Harvard UniversityVerifisert e-postadresse på molgen.mpg.de
Goncalo AbecasisUniversity of Michigan School of Public HealthVerifisert e-postadresse på umich.edu
Richard DurbinDept of Genetics, University of CambridgeVerifisert e-postadresse på cam.ac.uk
Dario G. LupiañezBerlin Institute for Medical Systems Biology (BIMSB)Verifisert e-postadresse på mdc-berlin.de
Peter RobinsonProfessor of Computational Biology, The Jackson Laboratory for Genomic MedicineVerifisert e-postadresse på jax.org
Helene KretzmerDepartment of Genome Regulation, Max Planck Institute for Molecular GeneticsVerifisert e-postadresse på molgen.mpg.de
Paul FlicekThe Jackson Laboratory, University of CambridgeVerifisert e-postadresse på jax.org
Laura ClarkeBenchSci ltdVerifisert e-postadresse på ebi.ac.uk
Mark GersteinProfessor of Biomedical Informatics, Yale UniversityVerifisert e-postadresse på yale.edu
Jay ShendureProfessor of Genome Sciences, University of WashingtonVerifisert e-postadresse på uw.edu
Evan EichlerProfessor of Genome Sciences, University of WashingtonVerifisert e-postadresse på gs.washington.edu
Ulrich StelzlUniversity of GrazVerifisert e-postadresse på uni-graz.at

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Bernd Timmermann

Max Planck Institute for Molecular Genetics, Berlin, Germany

Verifisert e-postadresse på molgen.mpg.de - Startside

Genome Research Next Generation Sequencing Cancer Model Organism


Tittel Sorter etter sitater Sorter etter år Sorter etter tittel	Sitert av Sitert av	År
A global reference for human genetic variation. 1000 Genomes Project Consortium Nature 526 (7571), 68-74, 2015	13743*	2015
The variant call format and VCFtools P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ... Bioinformatics 27 (15), 2156-2158, 2011	11671	2011
A map of human genome variation from population-scale sequencing. 1000 Genomes Project Consortium Nature 467 (7319), 1061-73, 2010	8518*	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56-65, 2012	8086*	2012
An integrated map of structural variation in 2,504 human genomes. PH Sudmant, T Rausch, Gardner, EJ, RE Handsaker, A Abyzov, ... Nature 526 (7571), 75-81, 2015	2239	2015
Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions DG Lupiáñez, K Kraft, V Heinrich, P Krawitz, F Brancati, E Klopocki, ... Cell 161 (5), 1012-1025, 2015	1977	2015
A systematic survey of loss-of-function variants in human protein-coding genes DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ... Science 335 (6070), 823-828, 2012	1317	2012
Mapping copy number variation by population-scale genome sequencing RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ... Nature 470 (7332), 59-65, 2011	1229	2011
COVID-19 severity correlates with airway epithelium–immune cell interactions identified by single-cell analysis RL Chua, S Lukassen, S Trump, BP Hennig, D Wendisch, F Pott, ... Nature biotechnology 38 (8), 970-979, 2020	948	2020
Diversity of human copy number variation and multicopy genes PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ... Science 330 (6004), 641-646, 2010	756	2010
Variation in genome-wide mutation rates within and between human families DF Conrad, JEM Keebler, MA DePristo, SJ Lindsay, Y Zhang, F Casals, ... Nature Genetics 201, 1, 2011	673*	2011
Demographic history and rare allele sharing among human populations S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ... Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011	663	2011
Formation of new chromatin domains determines pathogenicity of genomic duplications. MS Franke M, Ibrahim DM, Andrey G, Schwarzer W, Heinrich V, Schöpflin R ... Nature 538 (7624), 265-269, 2016	639	2016
Classic selective sweeps were rare in recent human evolution. RD Hernandez, JL Kelley, E Elyashiv, SC Melton, A Auton, G McVean, ... Science 331 (6019), 920-4, 2011	522	2011
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. O Delaneau, J Marchini, 1000 Genomes Project Consortium Nat Commun. 5 (3934), 2014	422	2014
Integrative annotation of variants from 1092 humans: application to cancer genomics. E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ... Science 342 (6154), 1235587, 2013	408	2013
Identifying recent adaptations in large-scale genomic data. SR Grossman, KG Andersen, I Shlyakhter, S Tabrizi, S Winnicki, A Yen, ... Cell. 2013 Feb 14;152(4):703-13. 152 (4), 703-13, 2013	406	2013
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences GD Poznik, Y Xue, FL Mendez, TF Willems, A Massaia, MA Wilson Sayres, ... Nature genetics 48 (6), 593-599, 2016	332	2016
A comprehensive map of mobile element insertion polymorphisms in humans. C Stewart, D Kural, MP Strömberg, JA Walker, MK Konkel, AM Stütz, ... PLoS Genet. 7 (8), e1002236, 2011	319	2011
The 1000 Genomes Project: data management and community access L Clarke, X Zheng-Bradley, R Smith, E Kulesha, C Xiao, I Toneva, ... nature methods 9 (5), 459-462, 2012	310	2012

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