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Ebiomedicine|October 21, 2019
Re-evaluating genetic variants identified in candidate gene studies of breast cancer risk using data from nearly 280,000 women of Asian and European ancestryYaohua Yang, Xiang Shu, Xiao-Ou Shu, et al.Nature Communications|December 23, 2015
Patterns and functional implications of rare germline variants across 12 cancer typesCharles Lu, Mingchao Xie, Michael C Wendl, et al.Nature Communications|April 18, 2018
Greenland records of aerosol source and atmospheric lifetime changes from the Eemian to the HoloceneS Schüpbach, H Fischer, M Bigler, et al.BMC Medicine|July 4, 2015
Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosisMarcelo Sobral-Leite, Jelle Wesseling, Vincent T H B M Smit, et al.International Journal of Epidemiology|January 10, 2018
Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association ConsortiumAnja Rudolph, Minsun Song, Mark N Brook, et al.Genome Medicine|May 8, 2026
The contribution of rare germline variants to the immune landscape of breast cancerFelipe Rojas-Rodríguez, Sander Canisius, Renske Keeman, et al.Oncotarget|February 10, 2017
TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancerRainer Fagerholm, Sofia Khan, Marjanka K Schmidt, et al.Nature Medicine|March 25, 2026
Enhanced dynamic risk stratification of smoldering multiple myelomaFloris Chabrun, Daniel E Schwartz, Susanna Gentile, et al.Nature Genetics|June 10, 2022
Genomic analysis defines clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancerEsther H Lips, Tapsi Kumar, Anargyros Megalios, et al.Ebiomedicine|August 20, 2015
Crowdsourcing the General Public for Large Scale Molecular Pathology Studies in CancerFrancisco J Candido Dos Reis, Stuart Lynn, H Raza Ali, et al.Pageof 179