A citation-based method for searching scientific literature

Marina Pavanello, Isaac Hy Chan, Amir Ariff, Paul Dp Pharoah, Simon A Gayther, Susan J Ramus. Cancers (Basel) 2020
Times Cited: 5







List of co-cited articles
14 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Inherited Mutations in Women With Ovarian Carcinoma.
Barbara M Norquist, Maria I Harrell, Mark F Brady, Tom Walsh, Ming K Lee, Suleyman Gulsuner, Sarah S Bernards, Silvia Casadei, Qian Yi, Robert A Burger,[...]. JAMA Oncol 2016
353
60

Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D.
Xin Yang, Honglin Song, Goska Leslie, Christoph Engel, Eric Hahnen, Bernd Auber, Judit Horváth, Karin Kast, Dieter Niederacher, Clare Turnbull,[...]. J Natl Cancer Inst 2020
34
60

Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing.
Hsiao-Mei Lu, Shuwei Li, Mary Helen Black, Shela Lee, Robert Hoiness, Sitao Wu, Wenbo Mu, Robert Huether, Jefferey Chen, Srijani Sridhar,[...]. JAMA Oncol 2019
77
60


A Population-Based Study of Genes Previously Implicated in Breast Cancer.
Chunling Hu, Steven N Hart, Rohan Gnanaolivu, Hongyan Huang, Kun Y Lee, Jie Na, Chi Gao, Jenna Lilyquist, Siddhartha Yadav, Nicholas J Boddicker,[...]. N Engl J Med 2021
66
40

Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls.
Jenna Lilyquist, Holly LaDuca, Eric Polley, Brigette Tippin Davis, Hermela Shimelis, Chunling Hu, Steven N Hart, Jill S Dolinsky, Fergus J Couch, David E Goldgar. Gynecol Oncol 2017
53
40

Germline mutations in RAD51D confer susceptibility to ovarian cancer.
Chey Loveday, Clare Turnbull, Emma Ramsay, Deborah Hughes, Elise Ruark, Jessica R Frankum, Georgina Bowden, Bolot Kalmyrzaev, Margaret Warren-Perry, Katie Snape,[...]. Nat Genet 2011
320
40

Literature Review of BARD1 as a Cancer Predisposing Gene with a Focus on Breast and Ovarian Cancers.
Wejdan M Alenezi, Caitlin T Fierheller, Neil Recio, Patricia N Tonin. Genes (Basel) 2020
8
40

Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.
Leila Dorling, Sara Carvalho, Jamie Allen, Anna González-Neira, Craig Luccarini, Cecilia Wahlström, Karen A Pooley, Michael T Parsons, Cristina Fortuno, Qin Wang,[...]. N Engl J Med 2021
87
40

Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer.
Susan J Ramus, Honglin Song, Ed Dicks, Jonathan P Tyrer, Adam N Rosenthal, Maria P Intermaggio, Lindsay Fraser, Aleksandra Gentry-Maharaj, Jane Hayward, Susan Philpott,[...]. J Natl Cancer Inst 2015
215
40

Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population.
Honglin Song, Ed Dicks, Susan J Ramus, Jonathan P Tyrer, Maria P Intermaggio, Jane Hayward, Christopher K Edlund, David Conti, Patricia Harrington, Lindsay Fraser,[...]. J Clin Oncol 2015
168
40

Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer.
Honglin Song, Ed M Dicks, Jonathan Tyrer, Maria Intermaggio, Georgia Chenevix-Trench, David D Bowtell, Nadia Traficante, Aocs Group, James Brenton, Teodora Goranova,[...]. J Med Genet 2021
9
40

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families.
Xin Yang, Goska Leslie, Alicja Doroszuk, Sandra Schneider, Jamie Allen, Brennan Decker, Alison M Dunning, James Redman, James Scarth, Inga Plaskocinska,[...]. J Clin Oncol 2020
99
40

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
Karoline B Kuchenbaecker, John L Hopper, Daniel R Barnes, Kelly-Anne Phillips, Thea M Mooij, Marie-José Roos-Blom, Sarah Jervis, Flora E van Leeuwen, Roger L Milne, Nadine Andrieu,[...]. JAMA 2017
867
40

Clinicopathological and molecular genetic analysis of HNPCC in China.
Ding-Cun Luo, Qi Cai, Meng-Hong Sun, Yao-Zhong Ni, Shi-Chang Ni, Zhe-Jing Chen, Xiao-Yang Li, Chong-Wei Tao, Xue-Miao Zhang, Da-Ren Shi. World J Gastroenterol 2005
9
20

Single-center study of Lynch syndrome screening in colorectal polyps.
FangChao Zhu, Da Pan, Hui Zhang, Qiong Ye, PeiSong Xu, Jie Pan. Hered Cancer Clin Pract 2019
7
20

Phenotypic characteristics of hereditary non-polyposis colorectal cancer by the Amsterdam criteria: an Asian perspective.
Min-Hoe Chew, Poh-Koon Koh, Kheng-Hong Ng, Jit-Fong Lim, Kok-Sun Ho, Boon-Swee Ooi, Choong-Leong Tang, Kong-Weng Eu. ANZ J Surg 2008
12
20

Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients.
Muhammad Usman Rashid, Humaira Naeemi, Noor Muhammad, Asif Loya, Jan Lubiński, Anna Jakubowska, Muhammed Aasim Yusuf. Hered Cancer Clin Pract 2019
3
33

Cancer-risk by family history and mismatch-repair mutation in Lynch syndrome.
Inês Marques-de-Sá, Rui Castro, Inês Pita, Mário Dinis-Ribeiro, Catarina Brandão. Scand J Gastroenterol 2020
2
50

A new mutL homolog 1 c.1896+5G>A germline mutation detected in a Lynch syndrome-associated lung and gastric double primary cancer patient.
Xuyuan Chen, Xiang Li, Hongsen Liang, Lichun Wei, Qiang Cui, Ming Yao, Xu Wu. Mol Genet Genomic Med 2019
5
20

Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families.
Tadeusz Dębniak, Tomasz Gromowski, Rodney J Scott, Jacek Gronwald, Tomasz Huzarski, Tomasz Byrski, Grzegorz Kurzawski, Dagmara Dymerska, Bohdan Górski, Katarzyna Paszkowska-Szczur,[...]. Hered Cancer Clin Pract 2015
8
20

Identification of novel Lynch syndrome mutations in Chinese patients with endometriod endometrial cancer.
Caixia Ren, Yan Liu, Yuxiang Wang, Yan Tang, Yawei Wei, Congrong Liu, Hongquan Zhang. Cancer Biol Med 2020
2
50

MSH6 immunohistochemical heterogeneity in colorectal cancer: comparative sequencing from different tumor areas.
Wei Chen, Rachel Pearlman, Heather Hampel, Colin C Pritchard, Michael Markow, Christina Arnold, Deborah Knight, Wendy L Frankel. Hum Pathol 2020
8
20

Screening for hereditary cancers in patients with endometrial cancer reveals a high frequency of germline mutations in cancer predisposition genes.
Wenjuan Tian, Rui Bi, Yulan Ren, Hongsheng He, Shanfu Shi, Boer Shan, Wentao Yang, Qing Wang, Huaying Wang. Int J Cancer 2019
8
20

Mutation spectrum of germline cancer susceptibility genes among unselected Chinese colorectal cancer patients.
Rui Gong, Yuan He, Xiao-Yun Liu, Hai-Yun Wang, Li-Yue Sun, Xin-Hua Yang, Bin Li, Xin-Kai Cao, Zu-Lu Ye, Ling-Heng Kong,[...]. Cancer Manag Res 2019
7
20


Distinct clinical phenotype and genetic testing strategy for Lynch syndrome in China based on a large colorectal cancer cohort.
Lin Dong, Xianglan Jin, Wenmiao Wang, Qiurong Ye, Weihua Li, Susheng Shi, Lei Guo, Jianming Ying, Shuangmei Zou. Int J Cancer 2020
5
20

TYMS/KRAS/BRAF molecular profiling predicts survival following adjuvant chemotherapy in colorectal cancer.
Anastasios Ntavatzikos, Aris Spathis, Paul Patapis, Nikolaos Machairas, Georgia Vourli, George Peros, Iordanis Papadopoulos, Ioannis Panayiotides, Anna Koumarianou. World J Gastrointest Oncol 2019
8
20

Mismatch repair gene mutation analysis and colonoscopy surveillance in Chinese Lynch syndrome families.
Lei Fu, Jian-qiu Sheng, Xiao-ou Li, Peng Jin, Hong Mu, Min Han, Ji-sheng Huang, Zi-qin Sun, Ai-qin Li, Zi-tao Wu,[...]. Cell Oncol (Dordr) 2013
7
20

Variants of DNA mismatch repair genes derived from 33,998 Chinese individuals with and without cancer reveal their highly ethnic-specific nature.
Li Zhang, Shanmuga Priya Bhaskaran, Teng Huang, Hui Dong, Khyati Chandratre, Xiaobing Wu, Zixin Qin, Xiaoyu Wang, Wenming Cao, Tianhui Chen,[...]. Eur J Cancer 2020
5
20

Comparison of screening strategies for Lynch syndrome in patients with newly diagnosed endometrial cancer: a prospective cohort study in China.
Xiaopei Chao, Lei Li, Ming Wu, Shuiqing Ma, Xianjie Tan, Sen Zhong, Yalan Bi, Jinghe Lang. Cancer Commun (Lond) 2019
14
20

Clinical and genetic characteristics of Chinese hereditary nonpolyposis colorectal cancer families.
Xu-Lin Wang, Ying Yuan, Su-Zhan Zhang, Shan-Rong Cai, Yan-Qin Huang, Qiang Jiang, Shu Zheng. World J Gastroenterol 2006
20
20

Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree.
Tahir Zaib, Chunhui Zhang, Komal Saleem, Lidan Xu, Qian Qin, Yusi Wang, Wei Ji, Hanif Khan, Hanfei Yu, Siqi Zhu,[...]. Dis Markers 2020
1
100

Penetrance of Colorectal Cancer Among Mismatch Repair Gene Mutation Carriers: A Meta-Analysis.
Cathy Wang, Yan Wang, Kevin S Hughes, Giovanni Parmigiani, Danielle Braun. JNCI Cancer Spectr 2020
4
25

Clinicopathological features in endometrial carcinoma associated with Lynch syndrome in China.
Yingmei Wang, Fengxia Xue, Russell R Broaddus, Xia Tao, Su-su Xie, Yanbin Zhu. Int J Gynecol Cancer 2009
15
20

Importance of gastric cancer for the diagnosis and surveillance of Japanese Lynch syndrome patients.
Tsuneo Ikenoue, Masami Arai, Chikashi Ishioka, Takeo Iwama, Satoshi Kaneko, Nagahide Matsubara, Yoshihiro Moriya, Tadashi Nomizu, Kokichi Sugano, Kazuo Tamura,[...]. J Hum Genet 2019
8
20

Clinicopathologic features of endometrial cancer with mismatch repair deficiency.
Sushmita Gordhandas, Ryan M Kahn, Charlotte Gamble, Nizam Talukdar, Brandon Maddy, Becky Baltich Nelson, Gulce Askin, Paul J Christos, Kevin Holcomb, Thomas A Caputo,[...]. Ecancermedicalscience 2020
2
50

Clinicopathological and genetic features of Chinese hereditary nonpolyposis colorectal cancer (HNPCC).
Fangqi Liu, Li Yang, Xiaoyan Zhou, Weiqi Sheng, Sanjun Cai, Lei Liu, Peng Nan, Ye Xu. Med Oncol 2014
14
20

Germline mutations in MLH1, MSH2 and MSH6 in Korean hereditary non-polyposis colorectal cancer families.
Young-Kyoung Shin, Seung-Chul Heo, Joo-Ho Shin, Sung-Hye Hong, Ja-Lok Ku, Byong-Chul Yoo, Il-Jin Kim, Jae-Gahb Park. Hum Mutat 2004
30
20

Characteristics of colorectal carcinoma patients with PMS2 defects detected by immunohistochemistry.
Zhijun Zeng, Qijia Yan, Guodong Chen, Xiaoli Zhang, Jia Huang, Kai Fu, Xiuda Peng, Shuai Xiao. Eur J Cancer Prev 2021
1
100

Patients with unexplained mismatch repair deficiency are interested in updated genetic testing.
Jessica Omark, Eduardo Vilar, Y Nancy You, Leslie Dunnington, Sarah Noblin, Blair Stevens, Maureen Mork. Hered Cancer Clin Pract 2020
3
33

Clinicopathologic features of endometrial cancer in Chinese patients younger than 50 years with a family history of cancer.
Yuan He, Xiang Tao, Feifei Huang, Nan Jia, Yan Du, Jinming Yu, Weiwei Feng. Medicine (Baltimore) 2018
7
20

Protein expression-based classification of gastric cancer by immunohistochemistry of tissue microarray.
Chong Zhao, Zhiqiang Feng, Hongzhen He, Dan Zang, Hong Du, Hongli Huang, Yanlei Du, Jie He, Yongjian Zhou, Yuqiang Nie. PLoS One 2020
2
50

Investigating the Link between Lynch Syndrome and Breast Cancer.
Megan Sheehan, Brandie Heald, Courtney Yanda, Erinn Downs Kelly, Stephen Grobmyer, Charis Eng, Matthew Kalady, Holly Pederson. Eur J Breast Health 2020
5
20

Diagnostics of Mutations in MMR/EPCAM Genes and Their Role in the Treatment and Care of Patients with Lynch Syndrome.
Joanna Sobocińska, Tomasz Kolenda, Anna Teresiak, Natalia Badziąg-Leśniak, Magda Kopczyńska, Kacper Guglas, Anna Przybyła, Violetta Filas, Elżbieta Bogajewska-Ryłko, Katarzyna Lamperska,[...]. Diagnostics (Basel) 2020
4
25

Recent Advances in Lynch Syndrome: Diagnosis, Treatment, and Cancer Prevention.
Matthew B Yurgelun, Heather Hampel. Am Soc Clin Oncol Educ Book 2018
28
20

Mismatch repair gene mutations in Chinese HNPCC patients.
J Q Sheng, L Fu, Z Q Sun, J S Huang, M Han, H Mu, H Zhang, Y Z Zhang, M Z Zhang, A Q Li,[...]. Cytogenet Genome Res 2008
13
20

The ATPase motif in RAD51D is required for resistance to DNA interstrand crosslinking agents and interaction with RAD51C.
Aaron M Gruver, Kristi A Miller, Changanamkandath Rajesh, Phillip G Smiraldo, Saravanan Kaliyaperumal, Rachel Balder, Katie M Stiles, Joanna S Albala, Douglas L Pittman. Mutagenesis 2005
23
20

Splicing profile by capture RNA-seq identifies pathogenic germline variants in tumor suppressor genes.
Tyler Landrith, Bing Li, Ashley A Cass, Blair R Conner, Holly LaDuca, Danielle B McKenna, Kara N Maxwell, Susan Domchek, Nichole A Morman, Christopher Heinlen,[...]. NPJ Precis Oncol 2020
10
20

Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15.
Eugenia Fraile-Bethencourt, Alberto Valenzuela-Palomo, Beatriz Díez-Gómez, María José Caloca, Susana Gómez-Barrero, Eladio A Velasco. Front Genet 2019
8
20


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.