A citation-based method for searching scientific literature




Diana Mandelker, Liying Zhang, Yelena Kemel, Zsofia K Stadler, Vijai Joseph, Ahmet Zehir, Nisha Pradhan, Angela Arnold, Michael F Walsh, Yirong Li, Anoop R Balakrishnan, Aijazuddin Syed, Meera Prasad, Khedoudja Nafa, Maria I Carlo, Karen A Cadoo, Meg Sheehan, Megan H Fleischut, Erin Salo-Mullen, Magan Trottier, Steven M Lipkin, Anne Lincoln, Semanti Mukherjee, Vignesh Ravichandran, Roy Cambria, Jesse Galle, Wassim Abida, Marcia E Arcila, Ryma Benayed, Ronak Shah, Kenneth Yu, Dean F Bajorin, Jonathan A Coleman, Steven D Leach, Maeve A Lowery, Julio Garcia-Aguilar, Philip W Kantoff, Charles L Sawyers, Maura N Dickler, Leonard Saltz, Robert J Motzer, Eileen M O'Reilly, Howard I Scher, Jose Baselga, David S Klimstra, David B Solit, David M Hyman, Michael F Berger, Marc Ladanyi, Mark E Robson, Kenneth Offit. JAMA 2017
Times Cited: 169




List of shared articles



Times cited

Germline testing for homologous recombination repair genes-opportunities and challenges.
Steffen Hirsch, Laura Gieldon, Christian Sutter, Nicola Dikow, Christian P Schaaf. Genes Chromosomes Cancer 2021
2

Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer Syndrome.
N Jewel Samadder, Douglas Riegert-Johnson, Lisa Boardman, Deborah Rhodes, Myra Wick, Scott Okuno, Katie L Kunze, Michael Golafshar, Pedro L S Uson, Luke Mountjoy,[...]. JAMA Oncol 2021
11


Current Approaches to Germline Cancer Genetic Testing.
Elena M Stoffel, John M Carethers. Annu Rev Med 2020
2

Evolving Significance of Tumor-Normal Sequencing in Cancer Care.
Diana Mandelker, Ozge Ceyhan-Birsoy. Trends Cancer 2020
2

Germline alterations in patients with biliary tract cancers: A spectrum of significant and previously underappreciated findings.
Hannah Maynard, Zsofia K Stadler, Michael F Berger, David B Solit, Michele Ly, Maeve A Lowery, Diana Mandelker, Liying Zhang, Emmett Jordan, Imane El Dika,[...]. Cancer 2020
6

Diagnostic yield of multigene panel testing in an Israeli cohort: enrichment of low-penetrance variants.
Rinat Bernstein-Molho, Eitan Friedman, Inbal Kedar, Yael Laitman, Tanir M Allweis, Einav Nili Gal-Yam, Hagit Baris Feldman, Albert Grinshpun, Naama Halpern, Shulamit Hartmajer,[...]. Breast Cancer Res Treat 2020
0

Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG).
Marilyn M Li, Elizabeth Chao, Edward D Esplin, David T Miller, Katherine L Nathanson, Sharon E Plon, Maren T Scheuner, Douglas R Stewart. Genet Med 2020
17

Detection of germline variants using expanded multigene panels in patients with localized pancreatic cancer.
Ashley N Krepline, Jennifer L Geurts, Idayat Akinola, Kathleen K Christians, Callisia N Clarke, Ben George, Paul S Ritch, Abdul H Khan, William A Hall, Beth A Erickson,[...]. HPB (Oxford) 2020
0