Søren Brunak
Professor
Brunak Group
Blegdamsvej 3B
2200 København N
ORCID: 0000-0003-0316-5866
31 - 34 out of 34Page size: 10
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Leveraging European infrastructures to access 1 million human genomes by 2022
Saunders, G., Baudis, M., Becker, R., Beltran, S., Béroud, C., Birney, E., Brooksbank, C., Brunak, S., Van den Bulcke, M., Drysdale, R., Capella-Gutierrez, S., Flicek, P., Florindi, F., Goodhand, P., Gut, I., Heringa, J., Holub, P., Hooyberghs, J., Juty, N., Keane, T. M. & 21 others, , 2019, In: Nature Reviews. Genetics. 20, p. 693-701 9 p.Research output: Contribution to journal › Review › Research › peer-review
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Population-wide analysis of differences in disease progression patterns in men and women
Westergaard, David, Moseley, P., Sørup, Freja Karuna Hemmingsen, Baldi, P. & Brunak, Søren, 2019, In: Nature Communications. 10, 1, 14 p., 666.Research output: Contribution to journal › Journal article › Research › peer-review
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Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration
Wilman, H. R., Parisinos, C. A., Atabaki-Pasdar, N., Kelly, M., Thomas, E. L., Neubauer, S., Jennison, C., Ehrhardt, B., Baum, P., Schoelsch, C., Freijer, J., Grempler, R., Graefe-Mody, U., Hennige, A., Dings, C., Lehr, T., Scherer, N., Sihinecich, I., Pattou, F., Raverdi, V. & 31 others, , 2019, In: Journal of Hepatology. 71, 3, p. 594-602 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
Infrastruktur for klinik og forskning i Nationalt Genom Center
Ørntoft, T. F., Brunak, Søren, Jespergaard, C., Heickendorff, L., Grønkjær, K. & Løngreen, P., 1 Apr 2019, In: Ugeskrift for Laeger. 181, 7AResearch output: Contribution to journal › Journal article › Communication
ID: 12895347
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Identification of odorant-receptor interactions by global mapping of the human odorome
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2863
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Porcine transcriptome analysis based on 97 non-normalized cDNA libraries and assembly of 1,021,891 expressed sequence tags
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1245
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A human gut microbial gene catalogue established by metagenomic sequencing
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