A citation-based method for searching scientific literature

Musaffe Tuna, Zhenlin Ju, Marcel Smid, Christopher I Amos, Gordon B Mills. Mol Cancer 2015
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Uniparental disomy in cancer.
Musaffe Tuna, Sakari Knuutila, Gordon B Mills. Trends Mol Med 2009
124
41


Pathogenesis and consequences of uniparental disomy in cancer.
Hideki Makishima, Jaroslaw P Maciejewski. Clin Cancer Res 2011
70
33

Genome-wide analysis of recurrent copy-number alterations and copy-neutral loss of heterozygosity in head and neck squamous cell carcinoma.
Maria Sebastiana Marescalco, Carmela Capizzi, Daniele Filippo Condorelli, Vincenza Barresi. J Oral Pathol Med 2014
22
33

Frequent occurrence of uniparental disomy in colorectal cancer.
Claus Lindbjerg Andersen, Carsten Wiuf, Mogens Kruhøffer, Marianne Korsgaard, Søren Laurberg, Torben Falck Ørntoft. Carcinogenesis 2007
93
25

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies.
Christine O'Keefe, Michael A McDevitt, Jaroslaw P Maciejewski. Blood 2010
154
25


Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies.
Karen Stephens, Molly Weaver, Kathleen A Leppig, Kyoko Maruyama, Peter D Emanuel, Michelle M Le Beau, Kevin M Shannon. Blood 2006
50
25


Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias.
Manoj Raghavan, Debra M Lillington, Spyros Skoulakis, Silvana Debernardi, Tracy Chaplin, Nicola J Foot, T Andrew Lister, Bryan D Young. Cancer Res 2005
222
25

Characterizing Genetic Transitions of Copy Number Alterations and Allelic Imbalances in Oral Tongue Carcinoma Metastasis.
Takuma Morita, Narikazu Uzawa, Kaoru Mogushi, Jun Sumino, Chieko Michikawa, Ken-Ichiro Takahashi, Kunihiro Myo, Toshiyuki Izumo, Kiyoshi Harada. Genes Chromosomes Cancer 2016
7
42

Loss of heterozygosity and copy number abnormality in clear cell renal cell carcinoma discovered by high-density affymetrix 10K single nucleotide polymorphism mapping array.
Marieta I Toma, Marianne Grosser, Alexander Herr, Daniela E Aust, Axel Meye, Christian Hoefling, Susanne Fuessel, Daniela Wuttig, Manfred P Wirth, Gustavo B Baretton. Neoplasia 2008
66
16

Loss of heterozygosity associated with uniparental disomy in breast carcinoma.
Sabita K Murthy, Lisa M DiFrancesco, R Travis Ogilvie, Douglas J Demetrick. Mod Pathol 2002
48
16

High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: four cases of homozygous deletions of the CDKN2A gene.
Helena Carén, Jennie Erichsen, Linda Olsson, Charlotta Enerbäck, Rose-Marie Sjöberg, Jonas Abrahamsson, Per Kogner, Tommy Martinsson. BMC Genomics 2008
68
16

Association between acquired uniparental disomy and homozygous mutations and HER2/ER/PR status in breast cancer.
Musaffe Tuna, Marcel Smid, Dakai Zhu, John W M Martens, Christopher I Amos. PLoS One 2010
13
16

Genome-wide loss of heterozygosity and uniparental disomy in BRCA1/2-associated ovarian carcinomas.
Christine S Walsh, Seishi Ogawa, Daniel R Scoles, Carl W Miller, Norihiko Kawamata, Steven A Narod, H Phillip Koeffler, Beth Y Karlan. Clin Cancer Res 2008
33
16

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias.
Jude Fitzgibbon, Lan-Lan Smith, Manoj Raghavan, Matthew L Smith, Silvana Debernardi, Spyros Skoulakis, Debra Lillington, T Andrew Lister, Bryan D Young. Cancer Res 2005
186
16

Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.
Muy-Teck Teh, Diana Blaydon, Tracy Chaplin, Nicola J Foot, Spyros Skoulakis, Manoj Raghavan, Catherine A Harwood, Charlotte M Proby, Michael P Philpott, Bryan D Young,[...]. Cancer Res 2005
117
16

Pan-cancer patterns of somatic copy number alteration.
Travis I Zack, Stephen E Schumacher, Scott L Carter, Andre D Cherniack, Gordon Saksena, Barbara Tabak, Michael S Lawrence, Cheng-Zhong Zhsng, Jeremiah Wala, Craig H Mermel,[...]. Nat Genet 2013
16

The landscape of somatic copy-number alteration across human cancers.
Rameen Beroukhim, Craig H Mermel, Dale Porter, Guo Wei, Soumya Raychaudhuri, Jerry Donovan, Jordi Barretina, Jesse S Boehm, Jennifer Dobson, Mitsuyoshi Urashima,[...]. Nature 2010
16

Uniparental disomies 7 and 14.
Katrin Hoffmann, Raoul Heller. Best Pract Res Clin Endocrinol Metab 2011
38
16


Patterns of somatic uniparental disomy identify novel tumor suppressor genes in colorectal cancer.
Keyvan Torabi, Rosa Miró, Nora Fernández-Jiménez, Isabel Quintanilla, Laia Ramos, Esther Prat, Javier del Rey, Núria Pujol, J Keith Killian, Paul S Meltzer,[...]. Carcinogenesis 2015
14
16


Human papillomavirus and rising oropharyngeal cancer incidence in the United States.
Anil K Chaturvedi, Eric A Engels, Ruth M Pfeiffer, Brenda Y Hernandez, Weihong Xiao, Esther Kim, Bo Jiang, Marc T Goodman, Maria Sibug-Saber, Wendy Cozen,[...]. J Clin Oncol 2011
16

Cancer statistics, 2015.
Rebecca L Siegel, Kimberly D Miller, Ahmedin Jemal. CA Cancer J Clin 2015
16

Increasing incidence of oral tongue squamous cell carcinoma in young white women, age 18 to 44 years.
Sagar C Patel, William R Carpenter, Seth Tyree, Marion Everett Couch, Mark Weissler, Trevor Hackman, D Neil Hayes, Carol Shores, Bhishamjit S Chera. J Clin Oncol 2011
220
16

Copy number rather than epigenetic alterations are the major dictator of imprinted methylation in tumors.
Alex Martin-Trujillo, Enrique Vidal, Ana Monteagudo-Sánchez, Marta Sanchez-Delgado, Sebastian Moran, Jose Ramon Hernandez Mora, Holger Heyn, Miriam Guitart, Manel Esteller, David Monk. Nat Commun 2017
16
16

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays.
Go Yamamoto, Yasuhito Nannya, Motohiro Kato, Masashi Sanada, Ross L Levine, Norihiko Kawamata, Akira Hangaishi, Mineo Kurokawa, Shigeru Chiba, D Gary Gilliland,[...]. Am J Hum Genet 2007
216
16

Involvement of homologous recombination in carcinogenesis.
Ramune Reliene, Alexander J R Bishop, Robert H Schiestl. Adv Genet 2007
52
16

Loss of heterozygosity occurs via mitotic recombination in Trp53+/- mice and associates with mammary tumor susceptibility of the BALB/c strain.
Anneke C Blackburn, S Christine McLary, Rizwan Naeem, Jason Luszcz, David W Stockton, Lawrence A Donehower, Mansoor Mohammed, John B Mailhes, Tamar Soferr, Stephen P Naber,[...]. Cancer Res 2004
35
16




REporting recommendations for tumor MARKer prognostic studies (REMARK).
Lisa M McShane, Douglas G Altman, Willi Sauerbrei, Sheila E Taube, Massimo Gion, Gary M Clark. Breast Cancer Res Treat 2006
587
16

Genetic imbalances with impact on survival in head and neck cancer patients.
U Bockmühl, K Schlüns, I Küchler, S Petersen, I Petersen. Am J Pathol 2000
117
16

High frequency of somatic frameshift BHD gene mutations in Birt-Hogg-Dubé-associated renal tumors.
Cathy D Vocke, Youfeng Yang, Christian P Pavlovich, Laura S Schmidt, Michael L Nickerson, Carlos A Torres-Cabala, Maria J Merino, McClellan M Walther, Berton Zbar, W Marston Linehan. J Natl Cancer Inst 2005
155
8


Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome.
Michael L Nickerson, Michelle B Warren, Jorge R Toro, Vera Matrosova, Gladys Glenn, Maria L Turner, Paul Duray, Maria Merino, Peter Choyke, Christian P Pavlovich,[...]. Cancer Cell 2002
588
8

Detection of chromosomal aberrations in renal tumors: a comparative study of conventional cytogenetics and virtual karyotyping with single-nucleotide polymorphism microarrays.
Federico A Monzon, Karla Alvarez, Zoran Gatalica, Julia A Bridge, Marilu Nelson, Hyun-Jung Kim, Jill M Hagenkord. Arch Pathol Lab Med 2009
12
8

Immunohistochemical characterization of renal tumors in patients with Birt-Hogg-Dubé syndrome.
Yasuhiro Iribe, Naoto Kuroda, Yoji Nagashima, Masahiro Yao, Reiko Tanaka, Hiroko Gotoda, Fumi Kawakami, Yoshiaki Imamura, Yasushi Nakamura, Midori Ando,[...]. Pathol Int 2015
12
8

High-resolution DNA copy number and gene expression analyses distinguish chromophobe renal cell carcinomas and renal oncocytomas.
Maria V Yusenko, Roland P Kuiper, Tamas Boethe, Börje Ljungberg, Ad Geurts van Kessel, Gyula Kovacs. BMC Cancer 2009
148
8

A transmembrane accessory subunit that modulates kainate-type glutamate receptors.
Wei Zhang, Fannie St-Gelais, Chad P Grabner, Jonathan C Trinidad, Akio Sumioka, Megumi Morimoto-Tomita, Kwang S Kim, Christoph Straub, Alma L Burlingame, James R Howe,[...]. Neuron 2009
151
8

Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes.
Steffen Durinck, Eric W Stawiski, Andrea Pavía-Jiménez, Zora Modrusan, Payal Kapur, Bijay S Jaiswal, Na Zhang, Vanina Toffessi-Tcheuyap, Thong T Nguyen, Kanika Bajaj Pahuja,[...]. Nat Genet 2015
211
8


Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families.
A C Houweling, L M Gijezen, M A Jonker, M B A van Doorn, R A Oldenburg, K Y van Spaendonck-Zwarts, E M Leter, T A van Os, N C T van Grieken, E H Jaspars,[...]. Br J Cancer 2011
91
8

Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome.
Berton Zbar, W Gregory Alvord, Gladys Glenn, Maria Turner, Christian P Pavlovich, Laura Schmidt, McClellan Walther, Peter Choyke, Gregor Weirich, Stephen M Hewitt,[...]. Cancer Epidemiol Biomarkers Prev 2002
338
8

Cytogenetic analysis of a series of 13 renal oncocytomas.
Valerie Lindgren, Gladell P Paner, Atilla Omeroglu, Steven C Campbell, W Bedford Waters, Robert C Flanigan, Maria M Picken. J Urol 2004
43
8

Altered metabolic pathways in clear cell renal cell carcinoma: A meta-analysis and validation study focused on the deregulated genes and their associated networks.
Apostolos Zaravinos, Myrtani Pieri, Nikos Mourmouras, Natassa Anastasiadou, Ioanna Zouvani, Dimitris Delakas, Constantinos Deltas. Oncoscience 2014
31
8

Clinical genomics of renal epithelial tumors.
Jill M Hagenkord, Zoran Gatalica, Eric Jonasch, Federico A Monzon. Cancer Genet 2011
55
8


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.