A citation-based method for searching scientific literature

Isabel Heidegger, Igor Tsaur, Hendrik Borgmann, Christian Surcel, Alexander Kretschmer, Romain Mathieu, Pieter De Visschere, Massimo Valerio, Roderick C N van den Bergh, Piet Ost, Derya Tilki, Giorgio Gandaglia, Guillaume Ploussard. Cancer Treat Rev 2019
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Prostate Cancer, Version 2.2019, NCCN Clinical Practice Guidelines in Oncology.
James L Mohler, Emmanuel S Antonarakis, Andrew J Armstrong, Anthony V D'Amico, Brian J Davis, Tanya Dorff, James A Eastham, Charles A Enke, Thomas A Farrington, Celestia S Higano,[...]. J Natl Compr Canc Netw 2019
506
60

Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
Freddie Bray, Jacques Ferlay, Isabelle Soerjomataram, Rebecca L Siegel, Lindsey A Torre, Ahmedin Jemal. CA Cancer J Clin 2018
40

Population-based estimate of prostate cancer risk for carriers of the HOXB13 missense mutation G84E.
Robert J MacInnis, Gianluca Severi, Laura Baglietto, James G Dowty, Mark A Jenkins, Melissa C Southey, John L Hopper, Graham G Giles. PLoS One 2013
26
40

Family History of Breast or Prostate Cancer and Prostate Cancer Risk.
Lauren Barber, Travis Gerke, Sarah C Markt, Samuel F Peisch, Kathryn M Wilson, Thomas Ahearn, Edward Giovannucci, Giovanni Parmigiani, Lorelei A Mucci. Clin Cancer Res 2018
21
40

Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification.
Rick Kamps, Rita D Brandão, Bianca J van den Bosch, Aimee D C Paulussen, Sofia Xanthoulea, Marinus J Blok, Andrea Romano. Int J Mol Sci 2017
181
40

Genetic testing for hereditary prostate cancer: Current status and limitations.
Jun Tu Zhen, Jamil Syed, Kevin Anh Nguyen, Michael S Leapman, Neeraj Agarwal, Karina Brierley, Xavier Llor, Erin Hofstatter, Brian Shuch. Cancer 2018
32
40

Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer.
Paula Paulo, Sofia Maia, Carla Pinto, Pedro Pinto, Augusta Monteiro, Ana Peixoto, Manuel R Teixeira. PLoS Genet 2018
27
40

Bringing Prostate Cancer Germline Genetics into Clinical Practice.
Sanjay Das, Simpa S Salami, Daniel E Spratt, Samuel D Kaffenberger, Michelle F Jacobs, Todd M Morgan. J Urol 2019
21
40

Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers.
Elizabeth C Page, Elizabeth K Bancroft, Mark N Brook, Melissa Assel, Mona Hassan Al Battat, Sarah Thomas, Natalie Taylor, Anthony Chamberlain, Jennifer Pope, Holly Ni Raghallaigh,[...]. Eur Urol 2019
63
40

Germline mutations in HOXB13 and prostate-cancer risk.
Charles M Ewing, Anna M Ray, Ethan M Lange, Kimberly A Zuhlke, Christiane M Robbins, Waibhav D Tembe, Kathleen E Wiley, Sarah D Isaacs, Dorhyun Johng, Yunfei Wang,[...]. N Engl J Med 2012
371
40

Genetic predisposition to prostate cancer: an update.
Holly Ni Raghallaigh, Rosalind Eeles. Fam Cancer 2021
3
66

Prostate cancer incidence in males with Lynch syndrome.
Sigurdis Haraldsdottir, Heather Hampel, Lai Wei, Christina Wu, Wendy Frankel, Tanios Bekaii-Saab, Albert de la Chapelle, Richard M Goldberg. Genet Med 2014
66
40

Prevalence of Germline Variants in Prostate Cancer and Implications for Current Genetic Testing Guidelines.
Piper Nicolosi, Elisa Ledet, Shan Yang, Scott Michalski, Brandy Freschi, Erin O'Leary, Edward D Esplin, Robert L Nussbaum, Oliver Sartor. JAMA Oncol 2019
91
40

Prevalence of the HOXB13 G84E mutation in Danish men undergoing radical prostatectomy and its correlations with prostate cancer risk and aggressiveness.
Tine M Storebjerg, Søren Høyer, Pia Kirkegaard, Flemming Bro, Torben F Ørntoft, Michael Borre, Karina D Sørensen. BJU Int 2016
22
40

Diagnosing hereditary cancer predisposition in men with prostate cancer.
Mary Pritzlaff, Yuan Tian, Patrick Reineke, A J Stuenkel, Kyle Allen, Stephanie Gutierrez, Michelle Jackson, Jill S Dolinsky, Holly LaDuca, Jianfeng Xu,[...]. Genet Med 2020
14
40

Role of Genetic Testing for Inherited Prostate Cancer Risk: Philadelphia Prostate Cancer Consensus Conference 2017.
Veda N Giri, Karen E Knudsen, William K Kelly, Wassim Abida, Gerald L Andriole, Chris H Bangma, Justin E Bekelman, Mitchell C Benson, Amie Blanco, Arthur Burnett,[...]. J Clin Oncol 2018
99
40

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland.
P Lichtenstein, N V Holm, P K Verkasalo, A Iliadou, J Kaprio, M Koskenvuo, E Pukkala, A Skytthe, K Hemminki. N Engl J Med 2000
40

Polygenic hazard score to guide screening for aggressive prostate cancer: development and validation in large scale cohorts.
Tyler M Seibert, Chun Chieh Fan, Yunpeng Wang, Verena Zuber, Roshan Karunamuni, J Kellogg Parsons, Rosalind A Eeles, Douglas F Easton, ZSofia Kote-Jarai, Ali Amin Al Olama,[...]. BMJ 2018
73
40

Familial renal cancer as an indicator of hereditary leiomyomatosis and renal cell cancer syndrome.
Victoria M Raymond, Casey M Herron, Thomas J Giordano, Stephen B Gruber. Fam Cancer 2012
12
20

Clinical Syndromes and Genetic Screening Strategies of Pheochromocytoma and Paraganglioma.
Peihua Liu, Minghao Li, Xiao Guan, Anze Yu, Qiao Xiao, Cikui Wang, Yixi Hu, Feizhou Zhu, Hongling Yin, Xiaoping Yi,[...]. J Kidney Cancer VHL 2018
10
20


Tuberous sclerosis complex.
Monica P Islam, E Steve Roach. Handb Clin Neurol 2015
18
20

Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes.
Shan Lin, Jia-Bin Zeng, Gui-Xian Zhao, Zhen-Zhen Yang, Hui-Ping Huang, Min-Ting Lin, Zhi-Ying Wu, Ning Wang, Wan-Jin Chen, Ling Fang. Seizure 2019
5
20

The Cancer Genome Atlas of renal cell carcinoma: findings and clinical implications.
W Marston Linehan, Christopher J Ricketts. Nat Rev Urol 2019
113
20

Metabolome-guided genomics to identify pathogenic variants in isocitrate dehydrogenase, fumarate hydratase, and succinate dehydrogenase genes in pheochromocytoma and paraganglioma.
Susan Richter, Laura Gieldon, Ying Pang, Mirko Peitzsch, Thanh Huynh, Rocio Leton, Bruna Viana, Tonino Ercolino, Anastasios Mangelis, Elena Rapizzi,[...]. Genet Med 2019
36
20

FLCN: The causative gene for Birt-Hogg-Dubé syndrome.
Laura S Schmidt, W Marston Linehan. Gene 2018
49
20


Met in urological cancers.
Yasuyoshi Miyata, Akihiro Asai, Kensuke Mitsunari, Tomohiro Matsuo, Kojiro Ohba, Yasushi Mochizuki, Hideki Sakai. Cancers (Basel) 2014
14
20

Clinical Features, Genetics and Potential Therapeutic Approaches for Birt-Hogg-Dubé Syndrome.
Laura S Schmidt, W Marston Linehan. Expert Opin Orphan Drugs 2015
25
20

The mTOR signalling pathway in human cancer.
Helena Pópulo, José Manuel Lopes, Paula Soares. Int J Mol Sci 2012
445
20

Lynch Syndrome in Urologic Malignancies - What Does the Urologist Need to Know?
Hanan Goldberg, Christopher J D Wallis, Zachary Klaassen, Thenappan Chandrasekar, Neil Fleshner, Alexandre R Zlotta. Urology 2019
3
33


Urinary Bladder Paragangliomas: How Immunohistochemistry Can Assist to Identify Patients With SDHB Germline and Somatic Mutations.
Alessio Giubellino, Karlena Lara, Victoria Martucci, Than Huynh, Piyush Agarwal, Karel Pacak, Maria J Merino. Am J Surg Pathol 2015
11
20

Good Laboratory Standards for Clinical Next-Generation Sequencing Cancer Panel Tests.
Jihun Kim, Woong-Yang Park, Nayoung K D Kim, Se Jin Jang, Sung-Min Chun, Chang-Ohk Sung, Jene Choi, Young-Hyeh Ko, Yoon-La Choi, Hyo Sup Shim,[...]. J Pathol Transl Med 2017
20
20

Atypical tuberous sclerosis complex presenting as familial renal cell carcinoma with leiomyomatous stroma.
Ismaël Bah, Somayyeh Fahiminiya, Louis R Bégin, Nancy Hamel, Maria D D'Agostino, Simon Tanguay, William D Foulkes. J Pathol Clin Res 2018
8
20

A Review of Von Hippel-Lindau Syndrome.
Neha Varshney, Amanuel A Kebede, Harry Owusu-Dapaah, Jason Lather, Manu Kaushik, Jasneet S Bhullar. J Kidney Cancer VHL 2017
59
20


Birt-Hogg-Dubé syndrome in two Chinese families with mutations in the FLCN gene.
Xiaocan Hou, Yuan Zhou, Yun Peng, Rong Qiu, Kun Xia, Beisha Tang, Wei Zhuang, Hong Jiang. BMC Med Genet 2018
7
20

Targeting HIF-2 α in clear cell renal cell carcinoma: A promising therapeutic strategy.
Olga Martínez-Sáez, Pablo Gajate Borau, Teresa Alonso-Gordoa, Javier Molina-Cerrillo, Enrique Grande. Crit Rev Oncol Hematol 2017
56
20

Mismatch repair deficiency assessment by immunohistochemistry: for Lynch syndrome screening and beyond.
Hui-Li Wong, Michael Christie, Lucy Gately, Jeanne Tie, Belinda Lee, Christine Semira, Sheau Wen Lok, Rachel Wong, Peter Gibbs. Future Oncol 2018
11
20

Screening for familial and hereditary prostate cancer.
Henry T Lynch, Omofolasade Kosoko-Lasaki, Stephen W Leslie, Marc Rendell, Trudy Shaw, Carrie Snyder, Anthony V D'Amico, Sarah Buxbaum, William B Isaacs, Stacy Loeb,[...]. Int J Cancer 2016
24
20

The incidence of consecutive manifestations in Von Hippel-Lindau disease.
Anouk N A van der Horst-Schrivers, Wim J Sluiter, Roeliene C Kruizinga, Rachel S van Leeuwaarde, Rachel Giles, Maran J W Olderode-Berends, Thera P Links. Fam Cancer 2019
7
20

A germline mutation in PBRM1 predisposes to renal cell carcinoma.
Patrick R Benusiglio, Sophie Couvé, Brigitte Gilbert-Dussardier, Sophie Deveaux, Hélène Le Jeune, Mélanie Da Costa, Gaëlle Fromont, Françoise Memeteau, Mokrane Yacoub, Isabelle Coupier,[...]. J Med Genet 2015
22
20

Non-founder BRCA1 mutations in Russian breast cancer patients.
Aglaya G Iyevleva, Evgeny N Suspitsin, Karin Kroeze, Tatiana V Gorodnova, Anna P Sokolenko, Konstantin G Buslov, Dmitry A Voskresenskiy, Alexandr V Togo, Sergey P Kovalenko, Nienke van der Stoep,[...]. Cancer Lett 2010
24
20

Men with a susceptibility to prostate cancer and the role of genetic based screening.
Rosalind Eeles, Holly Ni Raghallaigh. Transl Androl Urol 2018
14
20

Familial Kidney Cancer: Implications of New Syndromes and Molecular Insights.
Maria I Carlo, A Ari Hakimi, Grant D Stewart, Gennady Bratslavsky, James Brugarolas, Ying-Bei Chen, W Marston Linehan, Eamonn R Maher, Maria J Merino, Kenneth Offit,[...]. Eur Urol 2019
36
20

Clinical and genetic characteristics of chinese patients with Birt-Hogg-Dubé syndrome.
Yaping Liu, Zhiyan Xu, Ruie Feng, Yongzhong Zhan, Jun Wang, Guozhen Li, Xue Li, Weihong Zhang, Xiaowen Hu, Xinlun Tian,[...]. Orphanet J Rare Dis 2017
15
20

Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma.
W Marston Linehan, Paul T Spellman, Christopher J Ricketts, Chad J Creighton, Suzanne S Fei, Caleb Davis, David A Wheeler, Bradley A Murray, Laura Schmidt, Cathy D Vocke,[...]. N Engl J Med 2016
645
20


Germline mutations of renal cancer predisposition genes and clinical relevance in Chinese patients with sporadic, early-onset disease.
Junlong Wu, Hongkai Wang, Christopher J Ricketts, Youfeng Yang, Maria J Merino, Hailiang Zhang, Guohai Shi, Hualei Gan, W Marston Linehan, Yao Zhu,[...]. Cancer 2019
11
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.