A citation-based method for searching scientific literature

Andrea Desmond, Allison W Kurian, Michele Gabree, Meredith A Mills, Michael J Anderson, Yuya Kobayashi, Nora Horick, Shan Yang, Kristen M Shannon, Nadine Tung, James M Ford, Stephen E Lincoln, Leif W Ellisen. JAMA Oncol 2015
Times Cited: 197



Mary B Daly, Robert Pilarski, Michael Berry, Saundra S Buys, Meagan Farmer, Susan Friedman, Judy E Garber, Noah D Kauff, Seema Khan, Catherine Klein, Wendy Kohlmann, Allison Kurian, Jennifer K Litton, Lisa Madlensky, Sofia D Merajver, Kenneth Offit, Tuya Pal, Gwen Reiser, Kristen Mahoney Shannon, Elizabeth Swisher, Shaveta Vinayak, Nicoleta C Voian, Jeffrey N Weitzel, Myra J Wick, Georgia L Wiesner, Mary Dwyer, Susan Darlow. J Natl Compr Canc Netw 2017
Times Cited: 287




List of shared articles



Times cited

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
21

Multigene Panel Testing for Hereditary Cancer and Genetic Counseling.
Eun-Shin Lee, Jongjin Kim, Wonshik Han. Adv Exp Med Biol 2021
0

Prevalence of hereditary breast and ovarian cancer (HBOC) predisposition gene mutations among 882 HBOC high-risk Chinese individuals.
Di Shao, Shaomin Cheng, Fengming Guo, Changbin Zhu, Yuying Yuan, Kunling Hu, Zhe Wang, Xuan Meng, Xin Jin, Yun Xiong,[...]. Cancer Sci 2020
7

Exon splicing analysis of intronic variants in multigene cancer panel testing for hereditary breast/ovarian cancer.
Jin-Sun Ryu, Hye-Young Lee, Eun Hae Cho, Kyong-Ah Yoon, Min-Kyeong Kim, Jungnam Joo, Eun-Sook Lee, Han-Sung Kang, Seeyoun Lee, Dong Ock Lee,[...]. Cancer Sci 2020
2

Women with breast and uterine cancer are more likely to harbor germline mutations than women with breast or uterine cancer alone: A case for expanded gene testing.
Kelly Fulk, Michael R Milam, Shuwei Li, Amal Yussuf, Mary Helen Black, Elizabeth C Chao, Holly LaDuca, Michael P Stany. Gynecol Oncol 2019
8

Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA report.
Irene Lopez-Perolio, Raphaël Leman, Raquel Behar, Vanessa Lattimore, John F Pearson, Laurent Castéra, Alexandra Martins, Dominique Vaur, Nicolas Goardon, Grégoire Davy,[...]. J Med Genet 2019
9

Multicenter Prospective Cohort Study of the Diagnostic Yield and Patient Experience of Multiplex Gene Panel Testing For Hereditary Cancer Risk.
Gregory E Idos, Allison W Kurian, Charité Ricker, Duveen Sturgeon, Julie O Culver, Kerry E Kingham, Rachel Koff, Nicolette M Chun, Courtney Rowe-Teeter, Alexandra P Lebensohn,[...]. JCO Precis Oncol 2019
2

Optimizing the identification of risk-relevant mutations by multigene panel testing in selected hereditary breast/ovarian cancer families.
Anna Coppa, Arianna Nicolussi, Sonia D'Inzeo, Carlo Capalbo, Francesca Belardinilli, Valeria Colicchia, Marialaura Petroni, Massimo Zani, Sergio Ferraro, Christian Rinaldi,[...]. Cancer Med 2018
16

Multi-gene Panel Testing in Breast Cancer Management.
Christos Fountzilas, Virginia G Kaklamani. Cancer Treat Res 2018
7

Patient communication of cancer genetic test results in a diverse population.
Charité N Ricker, Rachel B Koff, Chenxu Qu, Julie Culver, Duveen Sturgeon, Kerry E Kingham, Katrina Lowstuter, Nicolette M Chun, Courtney Rowe-Teeter, Alexandra Lebensohn,[...]. Transl Behav Med 2018
13