Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Zarina Shameer"'
Autor:
Yelena Kemel, Diana Mandelker, Mark E. Robson, Karen Cadoo, Michael Francis Walsh, Steven M. Lipkin, Zarina Shameer, Liying Zhang, Vignesh Ravichandran, Kenneth Offit, Zsofia K. Stadler, Vijai Joseph
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
Cancer care professionals are confronted with interpreting results from multiplexed gene sequencing of patients at hereditary risk for cancer. Assessments for variant classification now require orthogonal data searches, requiring aggregation of multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65a4359e4709d3e26a66efe858d6e992
https://doi.org/10.1101/295865
https://doi.org/10.1101/295865
Autor:
Karen Cadoo, Michael Walsh, Yelena Kemel, Joseph Vijai, Steven M. Lipkin, Diana Mandelker, Mark E. Robson, Kenneth Offit, Vignesh Ravichandran, Liying Zhang, Zsofia K. Stadler, Zarina Shameer
Publikováno v:
Genetics in Medicine. 21:1668
An update to the original published conflict of interest for author Liying Zhang, PhD. L.Z. received compensation from Future Technology Research LLC (seminar on precision medicine), Roche Diagnostics Asia Pacific, BGI, Illumina (speaking activities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::734c4e9ea85be2f9609f5a35a8898823
https://doi.org/10.1038/s41436-019-0490-5
https://doi.org/10.1038/s41436-019-0490-5
Autor:
Nikolaus Schultz, Michael F. Berger, Geoffrey Y. Ku, Philip Jonsson, David B. Solit, Barry S. Taylor, David P. Kelsen, Yelena Kemel, Mark E. Robson, Zsofia K. Stadler, Jaclyn F. Hechtman, Vijai Joseph, Liying Zhang, Vignesh Ravichandran, Yelena Y. Janjigian, Yaelle Tuvy, Zarina Shameer, Kenneth Offit, Diana Mandelker, David H. Ilson
Publikováno v:
Journal of Clinical Oncology. 36:12116-12116
12116Background: Although EG cancer is included in Lynch syndrome (LS) and hereditary diffuse gastric cancer (HDGC), the prevalence of HRD-associated germline mutations in patients with EG cancer r...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac064ae822e11cbefb2579f5da354e90
https://doi.org/10.1200/jco.2018.36.15_suppl.12116
https://doi.org/10.1200/jco.2018.36.15_suppl.12116