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Peter H Sudmant
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A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
87172010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82132012
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
23322015
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
23292014
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
21012012
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
14862014
Great ape genetic diversity and population history
J Prado-Martinez, PH Sudmant, JM Kidd, H Li, JL Kelley, ...
Nature 499 (7459), 471-475, 2013
9312013
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
8412015
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
7802010
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
7072011
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
6922012
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
4452012
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
4322014
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
3822015
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
3532015
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
3012011
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
2852014
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
2812014
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
2442012
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
1932019
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