| A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010 | 8921 | 2010 |
| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8555 | 2012 |
| From FastQ data to high‐confidence variant calls: the genome analysis toolkit best practices pipeline GA Van der Auwera, MO Carneiro, C Hartl, R Poplin, G Del Angel, ... Current protocols in bioinformatics 43 (1), 11.10. 1-11.10. 33, 2013 | 5894 | 2013 |
| Scaling accurate genetic variant discovery to tens of thousands of samples R Poplin BioRxiv, 2017 | 1541 | 2017 |
| The genetic architecture of type 2 diabetes C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ... Nature 536 (7614), 41-47, 2016 | 1294 | 2016 |
| Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations TJ Pugh, SD Weeraratne, TC Archer, DA Pomeranz Krummel, D Auclair, ... Nature 488 (7409), 106-110, 2012 | 859 | 2012 |
| The advantages of SMRT sequencing RJ Roberts, MO Carneiro, MC Schatz Genome biology 14, 1-4, 2013 | 746 | 2013 |
| 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 | 460 | 2014 |
| 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 | 370 | 2012 |
| Pacific biosciences sequencing technology for genotyping and variation discovery in human data MO Carneiro, C Russ, MG Ross, SB Gabriel, C Nusbaum, MA DePristo BMC genomics 13, 1-7, 2012 | 351 | 2012 |
| Deleterious-and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing Y Xue, Y Chen, Q Ayub, N Huang, EV Ball, M Mort, AD Phillips, K Shaw, ... The American Journal of Human Genetics 91 (6), 1022-1032, 2012 | 320 | 2012 |
| Adaptive landscapes and protein evolution M Carneiro, DL Hartl Proceedings of the National Academy of Sciences 107 (suppl_1), 1747-1751, 2010 | 145 | 2010 |
| Current protocols in bioinformatics GA Van der Auwera (No Title), 11.10. 1, 2013 | 84 | 2013 |
| Population Genomic Inferences from Sparse High-Throughput Sequencing of Two Populations of Drosophila melanogaster TB Sackton, RJ Kulathinal, CM Bergman, AR Quinlan, EB Dopman, ... Genome biology and evolution 1, 449-465, 2009 | 66 | 2009 |
| A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk A Manning, HM Highland, J Gasser, X Sim, T Tukiainen, P Fontanillas, ... Diabetes 66 (7), 2019-2032, 2017 | 54 | 2017 |
| Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers RV Sanghvi, CJ Buhay, BC Powell, EA Tsai, MO Dorschner, CS Hong, ... Genetics in Medicine 20 (8), 855-866, 2018 | 33 | 2018 |
| Sequence data and association statistics from 12,940 type 2 diabetes cases and controls J Flannick, C Fuchsberger, A Mahajan, TM Teslovich, V Agarwala, ... Scientific data 4 (1), 1-22, 2017 | 32 | 2017 |
| Accelerating variant calling M Carneiro Broad Institute, Intel Genomic Sequencing Pipeline Workshop, Powerpoint …, 2013 | 30 | 2013 |
| Semiconductor-based DNA sequencing of histone modification states CS Cheng, K Rai, M Garber, A Hollinger, D Robbins, S Anderson, ... Nature communications 4 (1), 2672, 2013 | 20 | 2013 |
| Model transcriptional networks with continuously varying expression levels MO Carneiro, CH Taubes, DL Hartl BMC evolutionary biology 11, 1-8, 2011 | 11 | 2011 |
Michael C. SchatzBloomberg Distinguished Professor, Johns Hopkins UniversityVerified email at cs.jhu.edu
