Статии с изисквания за обществен достъп - Peter H SudmantНаучете повече
Налице някъде: 69
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
Изисквания: Swiss National Science Foundation, US National Institutes of Health, Howard …
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute, British …
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
Изисквания: US National Institutes of Health, German Research Foundation, European …
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute, German …
Great ape genetic diversity and population history
J Prado-Martinez, PH Sudmant, JM Kidd, H Li, JL Kelley, ...
Nature 499 (7459), 471-475, 2013
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute, Danish …
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute
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
Изисквания: US National Institutes of Health
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute
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
Изисквания: US National Institutes of Health, UK Biotechnology and Biological Sciences …
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute, Autism …
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute, Wellcome …
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute, UK …
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute
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
Изисквания: US National Institutes of Health, Canadian Institutes of Health Research …
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
Изисквания: US National Institutes of Health, Howard Hughes Medical Institute
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
Изисквания: US National Science Foundation, US National Institutes of Health
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