Gabor T Marth

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Richard DurbinDept of Genetics, University of CambridgeVerified email at cam.ac.uk
Goncalo AbecasisUniversity of Michigan School of Public HealthVerified email at umich.edu
Nils HomerFulcrum GenomicsVerified email at fulcrumgenomics.com
Erik GarrisonAssociate Professor, University of Tennessee Health Science CenterVerified email at uthsc.edu
Aaron QuinlanProfessor of Human Genetics, U. of Utah; https://github.com/arq5x/vitae/raw/master/quinlan.cv.pdfVerified email at genetics.utah.edu
Heng LiDana-Farber Cancer Institute & Harvard UniversityVerified email at jimmy.harvard.edu
Mark DePristoBigHat BiosciencesVerified email at bighatbio.com
Adam Auton23andMeVerified email at 23andme.com
Michael StrombergIlluminaVerified email at bc.edu
Andrew R. FarrellUniversity of GlasgowVerified email at chem.gla.ac.uk
Gerton LunterFull Professor, Groningen UniversityVerified email at umcg.nl
Mark YandellProfessor of Human Genetics, University of UtahVerified email at genetics.utah.edu
Kees AlbersScenic BiotechVerified email at scenicbiotech.com
Wan-Ping LeeUniversity of PennsylvaniaVerified email at pennmedicine.upenn.edu
Marc-Jan GubbelsProfessorVerified email at bc.edu
Pui-Yan KwokHenry Bachrach Distinguished Professor, University of California, San FranciscoVerified email at ucsf.edu
Karen EilbeckProfessor, Biomedical Informatics, University of UtahVerified email at genetics.utah.edu
Miriam KonkelClemson UniversityVerified email at clemson.edu
Alexander Eckehart UrbanAssociate Professor of Psychiatry and Behavioral Sciences, and of Genetics, Stanford UniversityVerified email at stanford.edu
Paul FlicekThe Jackson Laboratory, University of CambridgeVerified email at jax.org

Gabor T Marth

Professor of Human Genetics, University of Utah

Verified email at genetics.utah.edu - Homepage

Computational Biology


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The sequence alignment/map format and SAMtools H Li, B Handsaker, A Wysoker, T Fennell, J Ruan, N Homer, G Marth, ... bioinformatics 25 (16), 2078-2079, 2009	55813	2009
A global reference for human genetic variation AGR 1000 Genomes Project Consortium, Auton A, Brooks LD, Durbin RM, Garrison ... Nature 526 (7571), 68-74, 2015	15095	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	13089	2011
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	8783	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8312	2012
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms International SNP Map Working Group Cold Spring Harbor Laboratories ... Nature 409 (6822), 928-933, 2001	4441	2001
Haplotype-based variant detection from short-read sequencing E Garrison, G Marth arXiv preprint arXiv:1207.3907, 2012	4437*	2012
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	2408	2015
ART: a next-generation sequencing read simulator W Huang, L Li, JR Myers, GT Marth Bioinformatics 28 (4), 593-594, 2012	1508	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	1290	2011
BamTools: a C++ API and toolkit for analyzing and managing BAM files DW Barnett, EK Garrison, AR Quinlan, MP Strömberg, GT Marth Bioinformatics 27 (12), 1691-1692, 2011	941	2011
Multi-platform discovery of haplotype-resolved structural variation in human genomes MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ... Nature communications 10 (1), 1784, 2019	771	2019
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	716	2011
A general approach to single-nucleotide polymorphism discovery GT Marth, I Korf, MD Yandell, RT Yeh, Z Gu, H Zakeri, NO Stitziel, ... Nature genetics 23 (4), 452-456, 1999	707	1999
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	677	2011
Subgroup 1000 Genome Project Data Processing. 2009. The Sequence Alignment/Map format and SAMtools H Li, B Handsaker, A Wysoker, T Fennell, J Ruan, N Homer, G Marth, ... Bioinformatics 25 (16), 2078-2079, 2009	592	2009
Whole-genome sequencing and variant discovery in C. elegans LDW Hillier, GT Marth, AR Quinlan, D Dooling, G Fewell, D Barnett, P Fox, ... Nature methods 5 (2), 183-188, 2008	587	2008
SpeedSeq: ultra-fast personal genome analysis and interpretation C Chiang, RM Layer, GG Faust, MR Lindberg, DB Rose, EP Garrison, ... Nature methods 12 (10), 966-968, 2015	541	2015
Human diallelic insertion/deletion polymorphisms JL Weber, D David, J Heil, Y Fan, C Zhao, G Marth The American Journal of Human Genetics 71 (4), 854-862, 2002	464	2002
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. MJ Delaneau O, GP Consortium Nat Commun. 5 (3934), 2014	445	2014

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