A citation-based method for searching scientific literature

Kate A McBride, Timothy E Schlub, Mandy L Ballinger, David M Thomas, Martin Hn Tattersall. Asia Pac J Clin Oncol 2016
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Succinate dehydrogenase-deficient renal cell carcinoma: detailed characterization of 11 tumors defining a unique subtype of renal cell carcinoma.
Sean R Williamson, John N Eble, Mahul B Amin, Nilesh S Gupta, Steven C Smith, Lynette M Sholl, Rodolfo Montironi, Michelle S Hirsch, Jason L Hornick. Mod Pathol 2015
117
50

Tubulocystic Carcinoma of the Kidney With Poorly Differentiated Foci: A Frequent Morphologic Pattern of Fumarate Hydratase-deficient Renal Cell Carcinoma.
Steven C Smith, Kiril Trpkov, Ying-Bei Chen, Rohit Mehra, Deepika Sirohi, Chisato Ohe, Andi K Cani, Daniel H Hovelson, Kei Omata, Jonathan B McHugh,[...]. Am J Surg Pathol 2016
76
50

Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.
Reinhard Schneppenheim, Michael C Frühwald, Stefan Gesk, Martin Hasselblatt, Astrid Jeibmann, Uwe Kordes, Markus Kreuz, Ivo Leuschner, Jose Ignacio Martin Subero, Tobias Obser,[...]. Am J Hum Genet 2010
196
50

Monogenic and polygenic determinants of sarcoma risk: an international genetic study.
Mandy L Ballinger, David L Goode, Isabelle Ray-Coquard, Paul A James, Gillian Mitchell, Eveline Niedermayr, Ajay Puri, Joshua D Schiffman, Gillian S Dite, Arcadi Cipponi,[...]. Lancet Oncol 2016
112
50

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
Rachel Pearlman, Wendy L Frankel, Benjamin Swanson, Weiqiang Zhao, Ahmet Yilmaz, Kristin Miller, Jason Bacher, Christopher Bigley, Lori Nelsen, Paul J Goodfellow,[...]. JAMA Oncol 2017
283
50

Simultaneous juvenile polyposis syndrome and neurofibromatosis type 1.
Lodewijk A A Brosens, G Johan Offerhaus, Marcia Irene F Canto, Elizabeth A Montgomery, Francis M Giardiello. Histopathology 2016
8
50

Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.
Hellen Houlleberghs, Anne Goverde, Jarnick Lusseveld, Marleen Dekker, Marco J Bruno, Fred H Menko, Arjen R Mensenkamp, Manon C W Spaander, Anja Wagner, Robert M W Hofstra,[...]. PLoS Genet 2017
13
50


Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology.
Tim Ripperger, Stefan S Bielack, Arndt Borkhardt, Ines B Brecht, Birgit Burkhardt, Gabriele Calaminus, Klaus-Michael Debatin, Hedwig Deubzer, Uta Dirksen, Cornelia Eckert,[...]. Am J Med Genet A 2017
88
50

Increased risk of secondary uterine leiomyosarcoma in hereditary retinoblastoma.
Jasmine H Francis, Ruth A Kleinerman, Johanna M Seddon, David H Abramson. Gynecol Oncol 2012
30
50


High Prevalence of Hereditary Cancer Syndromes in Adolescents and Young Adults With Colorectal Cancer.
Maureen E Mork, Y Nancy You, Jun Ying, Sarah A Bannon, Patrick M Lynch, Miguel A Rodriguez-Bigas, Eduardo Vilar. J Clin Oncol 2015
100
50


DICER1 mutations in familial pleuropulmonary blastoma.
D Ashley Hill, Jennifer Ivanovich, John R Priest, Christina A Gurnett, Louis P Dehner, David Desruisseau, Jason A Jarzembowski, Kathryn A Wikenheiser-Brokamp, Brian K Suarez, Alison J Whelan,[...]. Science 2009
406
50

Succinate dehydrogenase deficient gastrointestinal stromal tumors (GISTs) - a review.
Markku Miettinen, Jerzy Lasota. Int J Biochem Cell Biol 2014
85
50


Histopathology of melanocytic lesions in a family with an inherited BAP1 mutation.
Sally J O'Shea, Angana Mitra, Jennifer L Graham, Ruth Charlton, Julian Adlard, Will Merchant, Julia A Newton-Bishop. J Cutan Pathol 2016
8
50

Synchronous small bowel and atypical primary leiomyosarcoma of inferior vena cava in a patient with RB1 mutation.
Sachin S Saboo, Nikhil Ramaiya, Heather Jacene, Irene Rainville, Lisa Diller, Jason L Hornick, Suzanne George. Abdom Imaging 2014
3
50

Multiplex genetic cancer testing identifies pathogenic mutations in TP53 and CDH1 in a patient with bilateral breast and endometrial adenocarcinoma.
Ellen Heitzer, Sigurd Lax, Ingrid Lafer, Stephanie M Müller, Gunda Pristauz, Peter Ulz, Stephan Jahn, Christoph Högenauer, Edgar Petru, Michael R Speicher,[...]. BMC Med Genet 2013
12
50

Pleuropulmonary Blastoma: Evolution of an Entity as an Entry into a Familial Tumor Predisposition Syndrome.
Louis P Dehner, Yoav H Messinger, Kris Ann P Schultz, Gretchen M Williams, Kathryn Wikenheiser-Brokamp, D Ashley Hill. Pediatr Dev Pathol 2015
36
50

Hereditary Renal Cell Carcinoma Syndromes: Clinical, Pathologic, and Genetic Features.
Adebowale J Adeniran, Brian Shuch, Peter A Humphrey. Am J Surg Pathol 2015
32
50

Characterizing genetic variants for clinical action.
Erin M Ramos, Corina Din-Lovinescu, Jonathan S Berg, Lisa D Brooks, Audrey Duncanson, Michael Dunn, Peter Good, Tim J P Hubbard, Gail P Jarvik, Christopher O'Donnell,[...]. Am J Med Genet C Semin Med Genet 2014
33
50

Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad.
Florian Haller, Evgeny A Moskalev, Fabio R Faucz, Sarah Barthelmeß, Stefan Wiemann, Matthias Bieg, Guillaume Assie, Jerome Bertherat, Inga-Marie Schaefer, Claudia Otto,[...]. Endocr Relat Cancer 2014
112
50

Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood.
Maria Isabel Achatz, Christopher C Porter, Laurence Brugières, Harriet Druker, Thierry Frebourg, William D Foulkes, Christian P Kratz, Roland P Kuiper, Jordan R Hansford, Hector Salvador Hernandez,[...]. Clin Cancer Res 2017
48
50

Extending the phenotypes associated with DICER1 mutations.
William D Foulkes, Amin Bahubeshi, Nancy Hamel, Barbara Pasini, Sofia Asioli, Gareth Baynam, Catherine S Choong, Adrian Charles, Richard P Frieder, Megan K Dishop,[...]. Hum Mutat 2011
121
50


Communication and technology in genetic counseling for familial cancer.
H T Lynch, C Snyder, M Stacey, B Olson, S K Peterson, S Buxbaum, T Shaw, P M Lynch. Clin Genet 2014
15
50

New malignancies following childhood cancer in the United States, 1973-2002.
Peter D Inskip, Rochelle E Curtis. Int J Cancer 2007
121
50


The hereditary nature of small cell carcinoma of the ovary, hypercalcemic type: two new familial cases.
Leora Witkowski, Nancy Donini, Rebecca Byler-Dann, James A Knost, Steffen Albrecht, Andrew Berchuck, W Glenn McCluggage, Martin Hasselblatt, William D Foulkes. Fam Cancer 2017
13
50

Occurrence of other malignancies in patients with gastrointestinal stromal tumors.
Abbas Agaimy, Peter H Wünsch, Leslie H Sobin, Jerzy Lasota, Markku Miettinen. Semin Diagn Pathol 2006
158
50

DICER1 mutation and tumors associated with a familial tumor predisposition syndrome: practical considerations.
Eduardo J Bardón-Cancho, Ana Haro-Díaz, Francisco J Alonso-García-de la Rosa, Jorge Huerta-Aragonés, Marina García-Morín, Felipe González-Martínez, Carmen Garrido-Colino. Fam Cancer 2017
7
50


Multiple sporadic gastrointestinal stromal tumours arising at different gastrointestinal sites: pattern of involvement of the muscularis propria as a clue to independent primary GISTs.
Abbas Agaimy, Bruno Märkl, Hans Arnholdt, Peter H Wünsch, Luigi M Terracciano, Stephan Dirnhofer, Arndt Hartmann, Luigi Tornillo, Michel P Bihl. Virchows Arch 2009
26
50

Comprehensive screening for mutations associated with colorectal cancer in unselected cases reveals penetrant and nonpenetrant mutations.
Cornelia Kraus, Tilman T Rau, Philipp Lux, Katharina Erlenbach-Wünsch, Sabine Löhr, Mandy Krumbiegel, Christian T Thiel, Robert Stöhr, Abbas Agaimy, Roland S Croner,[...]. Int J Cancer 2015
18
50

Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients.
Anthony J Gill, Ondrej Hes, Thomas Papathomas, Monika Šedivcová, Puay Hoon Tan, Abbas Agaimy, Per Arne Andresen, Andrew Kedziora, Adele Clarkson, Christopher W Toon,[...]. Am J Surg Pathol 2014
164
50

Survey of prenatal testing for genetic disorders in Japan: Recent report.
Takahiro Nobuzane, Takahiro Yamada, Kiyonori Miura, Hideaki Sawai, Hideaki Masuzaki, Yoshiki Kudo. J Obstet Gynaecol Res 2016
4
50


Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
335
50

Population screening in the age of genomic medicine.
Muin J Khoury, Linda L McCabe, Edward R B McCabe. N Engl J Med 2003
244
50


Knowledge, attitudes and behavior of physicians regarding predictive genetic tests for breast and colorectal cancer.
Carolina Marzuillo, Corrado De Vito, Stefania Boccia, Maddalena D'Addario, Elvira D'Andrea, Paola Santini, Antonio Boccia, Paolo Villari. Prev Med 2013
35
50

A Survey of Texas Health Educators' Family Health History-based Practice.
Lei-Shih Chen, Patricia Goodson, Eunju Jung, Olufemi Popoola, Oi-Man Kwok, Amber Muenzenberger. Am J Health Behav 2015
3
50

Influence of genetic discrimination perceptions and knowledge on cancer genetics referral practice among clinicians.
Katrina J Lowstuter, Sharon Sand, Kathleen R Blazer, Deborah J MacDonald, Kimberly C Banks, Carol A Lee, Barbara U Schwerin, Margaret Juarez, Gwen C Uman, Jeffrey N Weitzel. Genet Med 2008
46
50



A critical view of the general public's awareness and physicians' opinion of the trends and potential pitfalls of genetic testing in Greece.
Yuan Mai, Theodora Koromila, Aggeliki Sagia, David N Cooper, Georgios Vlachopoulos, George Lagoumintzis, Panagoula Kollia, Konstantinos Poulas, Vlassios Stathakopoulos, George P Patrinos. Per Med 2011
34
50

Genomics. Deflating the genomic bubble.
James P Evans, Eric M Meslin, Theresa M Marteau, Timothy Caulfield. Science 2011
108
50

Physician Attitudes toward Adopting Genome-Guided Prescribing through Clinical Decision Support.
Casey Lynnette Overby, Angelika Ludtke Erwin, Noura S Abul-Husn, Stephen B Ellis, Stuart A Scott, Aniwaa Owusu Obeng, Joseph L Kannry, George Hripcsak, Erwin P Bottinger, Omri Gottesman. J Pers Med 2014
29
50

After the revolution? Ethical and social challenges in 'personalized genomic medicine'
Eric T Juengst, Richard A Settersten, Jennifer R Fishman, Michelle L McGowan. Per Med 2012
25
50


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.