| 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 | 842 | 2019 |
| A draft human pangenome reference WW Liao, M Asri, J Ebler, D Doerr, M Haukness, G Hickey, S Lu, JK Lucas, ... Nature 617 (7960), 312-324, 2023 | 606 | 2023 |
| Haplotype-resolved diverse human genomes and integrated analysis of structural variation P Ebert, PA Audano, Q Zhu, B Rodriguez-Martin, D Porubsky, MJ Bonder, ... Science 372 (6537), eabf7117, 2021 | 558 | 2021 |
| DNA template strand sequencing of single-cells maps genomic rearrangements at high resolution E Falconer, M Hills, U Naumann, SSS Poon, EA Chavez, AD Sanders, ... Nature methods 9 (11), 1107-1112, 2012 | 223 | 2012 |
| Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads D Porubsky, P Ebert, PA Audano, MR Vollger, WT Harvey, P Marijon, ... Nature biotechnology 39 (3), 302-308, 2021 | 159 | 2021 |
| Semi-automated assembly of high-quality diploid human reference genomes ED Jarvis, G Formenti, A Rhie, A Guarracino, C Yang, J Wood, A Tracey, ... Nature 611 (7936), 519-531, 2022 | 152 | 2022 |
| The prognostic impact of CD163-positive macrophages in follicular lymphoma: a study from the BC cancer agency and the lymphoma study association R Kridel, L Xerri, B Gelas-Dore, K Tan, P Feugier, A Vawda, D Canioni, ... Clinical Cancer Research 21 (15), 3428-3435, 2015 | 141 | 2015 |
| Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads MR Vollger, GA Logsdon, PA Audano, A Sulovari, D Porubsky, P Peluso, ... Annals of human genetics 84 (2), 125-140, 2020 | 138 | 2020 |
| Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility WC Warren, RA Harris, M Haukness, IT Fiddes, SC Murali, J Fernandes, ... Science 370 (6523), eabc6617, 2020 | 135 | 2020 |
| Single-cell template strand sequencing by Strand-seq enables the characterization of individual homologs AD Sanders, E Falconer, M Hills, DCJ Spierings, PM Lansdorp Nature Protocols 12 (6), 1151-1176, 2017 | 131 | 2017 |
| Human-specific tandem repeat expansion and differential gene expression during primate evolution A Sulovari, R Li, PA Audano, D Porubsky, MR Vollger, GA Logsdon, ... Proceedings of the National Academy of Sciences 116 (46), 23243-23253, 2019 | 108 | 2019 |
| Essential role for Ptpn11 in survival of hematopoietic stem and progenitor cells G Chan, LS Cheung, W Yang, M Milyavsky, AD Sanders, S Gu, WX Hong, ... Blood, The Journal of the American Society of Hematology 117 (16), 4253-4261, 2011 | 107 | 2011 |
| Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders D Porubsky, W Höps, H Ashraf, PH Hsieh, B Rodriguez-Martin, F Yilmaz, ... Cell 185 (11), 1986-2005. e26, 2022 | 106 | 2022 |
| Dense and accurate whole-chromosome haplotyping of individual genomes D Porubsky, S Garg, AD Sanders, JO Korbel, V Guryev, PM Lansdorp, ... Nature communications 8 (1), 1293, 2017 | 97 | 2017 |
| Characterizing polymorphic inversions in human genomes by single-cell sequencing AD Sanders, M Hills, D Porubský, V Guryev, E Falconer, PM Lansdorp Genome research 26 (11), 1575-1587, 2016 | 93 | 2016 |
| Single-cell analysis of structural variations and complex rearrangements with tri-channel processing AD Sanders, S Meiers, M Ghareghani, D Porubsky, H Jeong, ... Nature biotechnology 38 (3), 343-354, 2020 | 76 | 2020 |
| Direct chromosome-length haplotyping by single-cell sequencing D Porubský, AD Sanders, N Van Wietmarschen, E Falconer, M Hills, ... Genome research 26 (11), 1565-1574, 2016 | 68 | 2016 |
| Adult spinal cord radial glia display a unique progenitor phenotype A Petit, AD Sanders, TE Kennedy, W Tetzlaff, KJ Glattfelder, RA Dalley, ... PloS one 6 (9), e24538, 2011 | 61 | 2011 |
| Recurrent inversion toggling and great ape genome evolution D Porubsky, AD Sanders, W Höps, PH Hsieh, A Sulovari, R Li, L Mercuri, ... Nature genetics 52 (8), 849-858, 2020 | 60 | 2020 |
| Familial long-read sequencing increases yield of de novo mutations MD Noyes, WT Harvey, D Porubsky, A Sulovari, R Li, NR Rose, ... The American Journal of Human Genetics 109 (4), 631-646, 2022 | 57 | 2022 |