A citation-based method for searching scientific literature

Karin Wadt, Jiyeon Choi, Joon-Yong Chung, Jens Kiilgaard, Steffen Heegaard, Krzysztof T Drzewiecki, Jeffrey M Trent, Stephen M Hewitt, Nicholas K Hayward, Anne-Marie Gerdes, Kevin M Brown. Pigment Cell Melanoma Res 2012
Times Cited: 86







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



Times Cited
  Times     Co-cited
Similarity


Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers.
Mohamed H Abdel-Rahman, Robert Pilarski, Colleen M Cebulla, James B Massengill, Benjamin N Christopher, Getachew Boru, Peter Hovland, Frederick H Davidorf. J Med Genet 2011
299
58

Germline mutations in BAP1 predispose to melanocytic tumors.
Thomas Wiesner, Anna C Obenauf, Rajmohan Murali, Isabella Fried, Klaus G Griewank, Peter Ulz, Christian Windpassinger, Werner Wackernagel, Shea Loy, Ingrid Wolf,[...]. Nat Genet 2011
462
56

Germline BAP1 mutations predispose to malignant mesothelioma.
Joseph R Testa, Mitchell Cheung, Jianming Pei, Jennifer E Below, Yinfei Tan, Eleonora Sementino, Nancy J Cox, A Umran Dogan, Harvey I Pass, Sandra Trusa,[...]. Nat Genet 2011
626
55

Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families.
Ching-Ni Jenny Njauw, Ivana Kim, Adriano Piris, Michele Gabree, Michael Taylor, Anne Marie Lane, Margaret M DeAngelis, Evangelos Gragoudas, Lyn M Duncan, Hensin Tsao. PLoS One 2012
171
52

Frequent mutation of BAP1 in metastasizing uveal melanomas.
J William Harbour, Michael D Onken, Elisha D O Roberson, Shenghui Duan, Li Cao, Lori A Worley, M Laurin Council, Katie A Matatall, Cynthia Helms, Anne M Bowcock. Science 2010
882
50

Germline BAP1 mutations predispose to renal cell carcinomas.
Tatiana Popova, Lucie Hebert, Virginie Jacquemin, Sophie Gad, Virginie Caux-Moncoutier, Catherine Dubois-d'Enghien, Bénédicte Richaudeau, Xavier Renaudin, Jason Sellers, André Nicolas,[...]. Am J Hum Genet 2013
178
41

Toward an improved definition of the tumor spectrum associated with BAP1 germline mutations.
Thomas Wiesner, Isabella Fried, Peter Ulz, Elvira Stacher, Helmut Popper, Rajmohan Murali, Heinz Kutzner, Sigurd Lax, Freya Smolle-Jüttner, Jochen B Geigl,[...]. J Clin Oncol 2012
71
43

BAP1 cancer syndrome: malignant mesothelioma, uveal and cutaneous melanoma, and MBAITs.
Michele Carbone, Laura Korb Ferris, Francine Baumann, Andrea Napolitano, Christopher A Lum, Erin G Flores, Giovanni Gaudino, Amy Powers, Peter Bryant-Greenwood, Thomas Krausz,[...]. J Transl Med 2012
190
32

A BAP1 mutation in a Danish family predisposes to uveal melanoma and other cancers.
Lauren G Aoude, Karin Wadt, Anders Bojesen, Dorthe Crüger, Ake Borg, Jeffrey M Trent, Kevin M Brown, Anne-Marie Gerdes, Göran Jönsson, Nicholas K Hayward. PLoS One 2013
46
52

Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases.
Robert Pilarski, Colleen M Cebulla, James B Massengill, Karan Rai, Thereasa Rich, Louise Strong, Barbara McGillivray, Mary-Jill Asrat, Frederick H Davidorf, Mohamed H Abdel-Rahman. Genes Chromosomes Cancer 2014
83
27

Further evidence for germline BAP1 mutations predisposing to melanoma and malignant mesothelioma.
Mitchell Cheung, Jacqueline Talarchek, Karen Schindeler, Eduardo Saraiva, Lynette S Penney, Mark Ludman, Joseph R Testa. Cancer Genet 2013
60
38

BAP1: a novel ubiquitin hydrolase which binds to the BRCA1 RING finger and enhances BRCA1-mediated cell growth suppression.
D E Jensen, M Proctor, S T Marquis, H P Gardner, S I Ha, L A Chodosh, A M Ishov, N Tommerup, H Vissing, Y Sekido,[...]. Oncogene 1998
507
24

Hereditary uveal melanoma: a report of a germline mutation in BAP1.
Veronica Höiom, Daniel Edsgärd, Hildur Helgadottir, Hanna Eriksson, Charlotta All-Ericsson, Rainer Tuominen, Ivayla Ivanova, Joakim Lundeberg, Olof Emanuelsson, Johan Hansson. Genes Chromosomes Cancer 2013
39
53

BAP1 loss defines a new class of renal cell carcinoma.
Samuel Peña-Llopis, Silvia Vega-Rubín-de-Celis, Arnold Liao, Nan Leng, Andrea Pavía-Jiménez, Shanshan Wang, Toshinari Yamasaki, Leah Zhrebker, Sharanya Sivanand, Patrick Spence,[...]. Nat Genet 2012
594
23

The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma.
Matthew Bott, Marie Brevet, Barry S Taylor, Shigeki Shimizu, Tatsuo Ito, Lu Wang, Jenette Creaney, Richard A Lake, Maureen F Zakowski, Boris Reva,[...]. Nat Genet 2011
450
23

BAP1 and cancer.
Michele Carbone, Haining Yang, Harvey I Pass, Thomas Krausz, Joseph R Testa, Giovanni Gaudino. Nat Rev Cancer 2013
385
23

A novel germline mutation in BAP1 predisposes to familial clear-cell renal cell carcinoma.
Megan N Farley, Laura S Schmidt, Jessica L Mester, Samuel Pena-Llopis, Andrea Pavia-Jimenez, Alana Christie, Cathy D Vocke, Christopher J Ricketts, James Peterson, Lindsay Middelton,[...]. Mol Cancer Res 2013
105
23

A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma.
K A W Wadt, L G Aoude, P Johansson, A Solinas, A Pritchard, O Crainic, M T Andersen, J F Kiilgaard, S Heegaard, L Sunde,[...]. Clin Genet 2015
66
30

Germline BAP1 mutations predispose also to multiple basal cell carcinomas.
A de la Fouchardière, O Cabaret, L Savin, P Combemale, H Schvartz, C Penet, V Bonadona, N Soufir, B Bressac-de Paillerets. Clin Genet 2015
67
25

Well-differentiated papillary mesothelioma: clustering in a Portuguese family with a germline BAP1 mutation.
C Ribeiro, S Campelos, C S Moura, J C Machado, A Justino, B Parente. Ann Oncol 2013
37
37

Frequent inactivation of the BAP1 gene in epithelioid-type malignant mesothelioma.
Yoshie Yoshikawa, Ayuko Sato, Tohru Tsujimura, Mitsuru Emi, Tomonori Morinaga, Kazuya Fukuoka, Shusai Yamada, Aki Murakami, Nobuyuki Kondo, Seiji Matsumoto,[...]. Cancer Sci 2012
123
15

Germline mutation of Bap1 accelerates development of asbestos-induced malignant mesothelioma.
Jinfei Xu, Yuwaraj Kadariya, Mitchell Cheung, Jianming Pei, Jacqueline Talarchek, Eleonora Sementino, Yinfei Tan, Craig W Menges, Kathy Q Cai, Samuel Litwin,[...]. Cancer Res 2014
88
15

A distinct subset of atypical Spitz tumors is characterized by BRAF mutation and loss of BAP1 expression.
Thomas Wiesner, Rajmohan Murali, Isabella Fried, Lorenzo Cerroni, Klaus Busam, Heinz Kutzner, Boris C Bastian. Am J Surg Pathol 2012
175
13

Prevalence of germline BAP1 mutation in a population-based sample of uveal melanoma cases.
Lauren G Aoude, Claire M Vajdic, Anne Kricker, Bruce Armstrong, Nicholas K Hayward. Pigment Cell Melanoma Res 2013
43
27

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.
Iñaki Comino-Méndez, Francisco J Gracia-Aznárez, Francesca Schiavi, Iñigo Landa, Luis J Leandro-García, Rocío Letón, Emiliano Honrado, Rocío Ramos-Medina, Daniela Caronia, Guillermo Pita,[...]. Nat Genet 2011
360
13

BAP1 germline mutation in two first grade family members with uveal melanoma.
David A Maerker, Michael Zeschnigk, Jasmin Nelles, Dietmar R Lohmann, Karl Worm, Anja K Bosserhoff, Rosemarie Krupar, Herbert Jägle. Br J Ophthalmol 2014
24
50

Tumours associated with BAP1 mutations.
Rajmohan Murali, Thomas Wiesner, Richard A Scolyer. Pathology 2013
175
13

Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases.
K Rai, R Pilarski, C M Cebulla, M H Abdel-Rahman. Clin Genet 2016
118
13

Loss of the tumor suppressor BAP1 causes myeloid transformation.
Anwesha Dey, Dhaya Seshasayee, Rajkumar Noubade, Dorothy M French, Jinfeng Liu, Mira S Chaurushiya, Donald S Kirkpatrick, Victoria C Pham, Jennie R Lill, Corey E Bakalarski,[...]. Science 2012
273
12

The kinesin KIF1Bbeta acts downstream from EglN3 to induce apoptosis and is a potential 1p36 tumor suppressor.
Susanne Schlisio, Rajappa S Kenchappa, Liesbeth C W Vredeveld, Rani E George, Rodney Stewart, Heidi Greulich, Kristina Shahriari, Nguyen V Nguyen, Pascal Pigny, Patricia L Dahia,[...]. Genes Dev 2008
251
12

High Incidence of Somatic BAP1 alterations in sporadic malignant mesothelioma.
Masaki Nasu, Mitsuru Emi, Sandra Pastorino, Mika Tanji, Amy Powers, Hugh Luk, Francine Baumann, Yu-An Zhang, Adi Gazdar, Shreya Kanodia,[...]. J Thorac Oncol 2015
180
12

Clinical Characteristics of Uveal Melanoma in Patients With Germline BAP1 Mutations.
Mrinali P Gupta, Anne Marie Lane, Margaret M DeAngelis, Katie Mayne, Margaux Crabtree, Evangelos S Gragoudas, Ivana K Kim. JAMA Ophthalmol 2015
71
15

Mutations in GNA11 in uveal melanoma.
Catherine D Van Raamsdonk, Klaus G Griewank, Michelle B Crosby, Maria C Garrido, Swapna Vemula, Thomas Wiesner, Anna C Obenauf, Werner Wackernagel, Gary Green, Nancy Bouvier,[...]. N Engl J Med 2010
913
11

BRCA1-associated protein-1 is a tumor suppressor that requires deubiquitinating activity and nuclear localization.
Karen H Ventii, Narra S Devi, Kenneth L Friedrich, Tatiana A Chernova, Mourad Tighiouart, Erwin G Van Meir, Keith D Wilkinson. Cancer Res 2008
231
11

Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB.
Johanna C Scheuermann, Andrés Gaytán de Ayala Alonso, Katarzyna Oktaba, Nga Ly-Hartig, Robert K McGinty, Sven Fraterman, Matthias Wilm, Tom W Muir, Jürg Müller. Nature 2010
503
11

Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomas.
José Gaal, Nelly Burnichon, Esther Korpershoek, Isabelle Roncelin, Jérôme Bertherat, Pierre-François Plouin, Ronald R de Krijger, Anne-Paule Gimenez-Roqueplo, Winand N M Dinjens. J Clin Endocrinol Metab 2010
96
11

Inference on germline BAP1 mutations and asbestos exposure from the analysis of familial and sporadic mesothelioma in a high-risk area.
Marta Betti, Elisabetta Casalone, Daniela Ferrante, Antonio Romanelli, Federica Grosso, Simonetta Guarrera, Luisella Righi, Simona Vatrano, Giuseppe Pelosi, Roberta Libener,[...]. Genes Chromosomes Cancer 2015
43
23

Germline BAP1 mutation in a family with high incidence of multiple primary cancers and a potential gene-environment interaction.
Mitchell Cheung, Yuwaraj Kadariya, Jacqueline Talarchek, Jianming Pei, Jill A Ohar, Omar R Kayaleh, Joseph R Testa. Cancer Lett 2015
31
32

Frequent somatic mutations of GNAQ in uveal melanoma and blue naevi.
Catherine D Van Raamsdonk, Vladimir Bezrookove, Gary Green, Jürgen Bauer, Lona Gaugler, Joan M O'Brien, Elizabeth M Simpson, Gregory S Barsh, Boris C Bastian. Nature 2009
983
10

Frequent mutations of genes encoding ubiquitin-mediated proteolysis pathway components in clear cell renal cell carcinoma.
Guangwu Guo, Yaoting Gui, Shengjie Gao, Aifa Tang, Xueda Hu, Yi Huang, Wenlong Jia, Zesong Li, Minghui He, Liang Sun,[...]. Nat Genet 2011
225
10


SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma.
Huai-Xiang Hao, Oleh Khalimonchuk, Margit Schraders, Noah Dephoure, Jean-Pierre Bayley, Henricus Kunst, Peter Devilee, Cor W R J Cremers, Joshua D Schiffman, Brandon G Bentz,[...]. Science 2009
510
10

Uveal melanoma: trends in incidence, treatment, and survival.
Arun D Singh, Mary E Turell, Allan K Topham. Ophthalmology 2011
616
10

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
Satoru Yokoyama, Susan L Woods, Glen M Boyle, Lauren G Aoude, Stuart MacGregor, Victoria Zismann, Michael Gartside, Anne E Cust, Rizwan Haq, Mark Harland,[...]. Nature 2011
277
10

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Thomas Strub, Mahaut de Lichy, Karine Bille, Philippe Dessen, Benoit d'Hayer, Hamida Mohamdi, Audrey Remenieras,[...]. Nature 2011
326
10

New syndrome of paraganglioma and somatostatinoma associated with polycythemia.
Karel Pacak, Ivana Jochmanova, Tamara Prodanov, Chunzhang Yang, Maria J Merino, Tito Fojo, Josef T Prchal, Arthur S Tischler, Ronald M Lechan, Zhengping Zhuang. J Clin Oncol 2013
101
10

A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas.
Patricia L M Dahia, Ken N Ross, Matthew E Wright, César Y Hayashida, Sandro Santagata, Marta Barontini, Andrew L Kung, Gabriela Sanso, James F Powers, Arthur S Tischler,[...]. PLoS Genet 2005
335
10

SDH mutations establish a hypermethylator phenotype in paraganglioma.
Eric Letouzé, Cosimo Martinelli, Céline Loriot, Nelly Burnichon, Nasséra Abermil, Chris Ottolenghi, Maxime Janin, Mélanie Menara, An Thach Nguyen, Paule Benit,[...]. Cancer Cell 2013
449
10

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma.
Yuejuan Qin, Li Yao, Elizabeth E King, Kalyan Buddavarapu, Romina E Lenci, E Sandra Chocron, James D Lechleiter, Meghan Sass, Neil Aronin, Francesca Schiavi,[...]. Nat Genet 2010
280
10

Tumor suppressor and deubiquitinase BAP1 promotes DNA double-strand break repair.
Helen Yu, Helen Pak, Ian Hammond-Martel, Mehdi Ghram, Amélie Rodrigue, Salima Daou, Haithem Barbour, Luc Corbeil, Josée Hébert, Elliot Drobetsky,[...]. Proc Natl Acad Sci U S A 2014
212
10


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.