A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010 | 8817 | 2010 |
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8329 | 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 | 2431 | 2015 |
The complete genome sequence of a Neanderthal from the Altai Mountains K Prüfer, F Racimo, N Patterson, F Jay, S Sankararaman, S Sawyer, ... Nature 505 (7481), 43-49, 2014 | 2422 | 2014 |
A high-coverage genome sequence from an archaic Denisovan individual M Meyer, M Kircher, MT Gansauge, H Li, F Racimo, S Mallick, ... Science 338 (6104), 222-226, 2012 | 2187 | 2012 |
Ancient human genomes suggest three ancestral populations for present-day Europeans I Lazaridis, N Patterson, A Mittnik, G Renaud, S Mallick, K Kirsanow, ... Nature 513 (7518), 409-413, 2014 | 1548 | 2014 |
Great ape genetic diversity and population history J Prado-Martinez, PH Sudmant, JM Kidd, H Li, JL Kelley, ... Nature 499 (7459), 471-475, 2013 | 953 | 2013 |
Resolving the complexity of the human genome using single-molecule sequencing MJP Chaisson, J Huddleston, MY Dennis, PH Sudmant, M Malig, ... Nature 517 (7536), 608-611, 2015 | 860 | 2015 |
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 | 800 | 2010 |
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 | 719 | 2011 |
Copy number variation detection and genotyping from exome sequence data N Krumm, PH Sudmant, A Ko, BJ O'Roak, M Malig, BP Coe, AR Quinlan, ... Genome research 22 (8), 1525-1532, 2012 | 713 | 2012 |
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication MY Dennis, X Nuttle, PH Sudmant, F Antonacci, TA Graves, M Nefedov, ... Cell 149 (4), 912-922, 2012 | 468 | 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 | 451 | 2014 |
Global diversity, population stratification, and selection of human copy-number variation PH Sudmant, S Mallick, BJ Nelson, F Hormozdiari, N Krumm, ... Science 349 (6253), aab3761, 2015 | 396 | 2015 |
Mountain gorilla genomes reveal the impact of long-term population decline and inbreeding Y Xue, J Prado-Martinez, PH Sudmant, V Narasimhan, Q Ayub, M Szpak, ... Science 348 (6231), 242-245, 2015 | 368 | 2015 |
Haplotype-resolved genome sequencing of a Gujarati Indian individual JO Kitzman, AP MacKenzie, A Adey, JB Hiatt, RP Patwardhan, ... Nature biotechnology 29 (1), 59-63, 2011 | 305 | 2011 |
Reconstructing complex regions of genomes using long-read sequencing technology J Huddleston, S Ranade, M Malig, F Antonacci, M Chaisson, L Hon, ... Genome research 24 (4), 688-696, 2014 | 290 | 2014 |
Low copy number of the salivary amylase gene predisposes to obesity M Falchi, JS El-Sayed Moustafa, P Takousis, F Pesce, A Bonnefond, ... Nature genetics 46 (5), 492-497, 2014 | 289 | 2014 |
Estimating the human mutation rate using autozygosity in a founder population CD Campbell, JX Chong, M Malig, A Ko, BL Dumont, L Han, L Vives, ... Nature genetics 44 (11), 1277-1281, 2012 | 251 | 2012 |
Blood-brain barrier dysfunction in aging induces hyperactivation of TGFβ signaling and chronic yet reversible neural dysfunction VV Senatorov Jr, AR Friedman, DZ Milikovsky, J Ofer, R Saar-Ashkenazy, ... Science Translational Medicine 11 (521), eaaw8283, 2019 | 212 | 2019 |