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Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genesR E Ellsworth, D C Jamison, J W Touchman, et al.
Nature Genetics|December 14, 2011
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromesTimothy A Graubert, Dong Shen, Li Ding, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|May 9, 2009
National hand hygiene campaigns in Europe, 2000-2009A P Magiorakos, C Suetens, L Boyd, et al.
Nature Communications|September 19, 2018
Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancerAlex H Wagner, Siddhartha Devarakonda, Zachary L Skidmore, et al.
Nature Biotechnology|March 24, 2015
Clearance of persistent hepatitis C virus infection in humanized mice using a claudin-1-targeting monoclonal antibodyLaurent Mailly, Fei Xiao, Joachim Lupberger, et al.
Cancer Discovery|September 17, 2014
Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutationsFranck Tirode, Didier Surdez, Xiaotu Ma, et al.
The Journal of Clinical Investigation|March 26, 2011
Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progressionLukas D Wartman, David E Larson, Zhifu Xiang, et al.
Nature Communications|September 6, 2018
The prognostic effects of somatic mutations in ER-positive breast cancerObi L Griffith, Nicholas C Spies, Meenakshi Anurag, et al.
Cancer Cell|February 5, 2010
Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1Roel G W Verhaak, Katherine A Hoadley, Elizabeth Purdom, et al.
Plos Genetics|February 6, 2014
Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS lociSusan K Service, Tanya M Teslovich, Christian Fuchsberger, et al.
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