Gerton Lunter

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Chris PontingChair of Medical Bioinformatics, University of EdinburghVerified email at igmm.ed.ac.uk
Andy RimmerWellcome Trues Centre For Human Genetics, OxfordVerified email at well.ox.ac.uk
Johannes TrückMD DPhil | University Children's Hospital Zurich, SwitzerlandVerified email at kispi.uzh.ch
Jacob GalsonAlchemab Therapeutics Ltd & University of ZurichVerified email at alchemab.com
Daniel G MacArthurGarvan Institute of Medical Research, Murdoch Children's Research InstituteVerified email at garvan.org.au
Istvan MiklosRenyi InstituteVerified email at ramet.elte.hu
Rory BowdenWalter and Eliza Hall Institute of Medical ResearchVerified email at wehi.edu.au
Professor Sir Andrew PollardUniversity of OxfordVerified email at paediatrics.ox.ac.uk
Zamin IqbalProfessor of Algorithmic and Microbial Genomics, University of BathVerified email at bath.ac.uk
Iain MathiesonUniversity of PennsylvaniaVerified email at mail.med.upenn.edu
Andreas HegerCGAT / WIMM / University of OxfordVerified email at imm.ox.ac.uk
Ian HolmesProfessor, Computational Biology and Bioengineering, UC BerkeleyVerified email at berkeley.edu
Kenneth B HoehnGeisel School of Medicine at DartmouthVerified email at dartmouth.edu
Alexei J. DrummondProfessor of Computational Biology, University of AucklandVerified email at cs.auckland.ac.nz
Oliver PybusUniversity of Oxford / Royal Veterinary CollegeVerified email at zoo.ox.ac.uk
Thomas MailundAssociate Professor of Bioinformatics, Aarhus UniversityVerified email at birc.au.dk
Sha (Joe) ZhuRoche ShanghaiVerified email at roche.com
Elise RuarkThe Institute of Cancer ResearchVerified email at icr.ac.uk
Mikkel Heide SchierupProfessor, Bioinformatics Research Centre, Aarhus UniversityVerified email at birc.au.dk
Asger HobolthProfessor, Department of Mathematics, Aarhus UniversityVerified email at math.au.dk

Gerton Lunter

Full Professor, Groningen University

Verified email at umcg.nl

Population genetics computational biology next-gen sequencing Bayesian statistics


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
The variant call format and VCFtools P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ... Bioinformatics 27 (15), 2156-2158, 2011	14706	2011
A map of human genome variation from population scale sequencing DM Altshuler, ES Lander, L Ambrogio, T Bloom, K Cibulskis, TJ Fennell, ... Nature 467 (7319), 1061-1073, 2010	8924*	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8505	2012
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	1429	2012
Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads G Lunter, M Goodson Genome research 21 (6), 936-939, 2011	1416	2011
Integrating mapping-, assembly-and haplotype-based approaches for calling variants in clinical sequencing applications A Rimmer, H Phan, I Mathieson, Z Iqbal, SRF Twigg, WGS500 Consortium, ... Nature genetics 46 (8), 912-918, 2014	1185	2014
Functionality or transcriptional noise? Evidence for selection within long noncoding RNAs J Ponjavic, CP Ponting, G Lunter Genome research 17 (5), 556-565, 2007	867	2007
Insights into hominid evolution from the gorilla genome sequence A Scally, JY Dutheil, LDW Hillier, GE Jordan, I Goodhead, J Herrero, ... Nature 483 (7388), 169-175, 2012	837	2012
1000 Genomes Project Analysis Group. 2011 P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ... The variant call format and VCFtools. Bioinformatics 27 (15), 2156-2158, 2011	747	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	745	2011
Comparative and demographic analysis of orang-utan genomes DP Locke, LDW Hillier, WC Warren, KC Worley, LV Nazareth, DM Muzny, ... Nature 469 (7331), 529-533, 2011	714	2011
The bonobo genome compared with the chimpanzee and human genomes K Prüfer, K Munch, I Hellmann, K Akagi, JR Miller, B Walenz, S Koren, ... Nature 486 (7404), 527-531, 2012	674	2012
Dindel: accurate indel calls from short-read data CA Albers, G Lunter, DG MacArthur, G McVean, WH Ouwehand, R Durbin Genome research 21 (6), 961-973, 2011	564	2011
The human pancreatic islet transcriptome: expression of candidate genes for type 1 diabetes and the impact of pro-inflammatory cytokines DL Eizirik, M Sammeth, T Bouckenooghe, G Bottu, G Sisino, ... PLoS genetics 8 (3), e1002552, 2012	533	2012
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel O Delaneau, J Marchini Nature communications 5 (1), 3934, 2014	478	2014
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders JC Taylor, HC Martin, S Lise, J Broxholme, JB Cazier, A Rimmer, ... Nature genetics 47 (7), 717-726, 2015	448	2015
Genomic and transcriptional co-localization of protein-coding and long non-coding RNA pairs in the developing brain J Ponjavic, PL Oliver, G Lunter, CP Ponting PLoS genetics 5 (8), e1000617, 2009	393	2009
Accelerated Evolution of the Prdm9 Speciation Gene across Diverse Metazoan Taxa PL Oliver, L Goodstadt, JJ Bayes, Z Birtle, KC Roach, N Phadnis, ... PLoS genetics 5 (12), e1000753, 2009	338	2009
A fine-scale chimpanzee genetic map from population sequencing A Auton, A Fledel-Alon, S Pfeifer, O Venn, L Ségurel, T Street, EM Leffler, ... science 336 (6078), 193-198, 2012	331	2012
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes SB Montgomery, DL Goode, E Kvikstad, CA Albers, ZD Zhang, XJ Mu, ... Genome research 23 (5), 749-761, 2013	290	2013

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