A citation-based method for searching scientific literature

Małgorzata Grzanka, Agnieszka Piekiełko-Witkowska. Int J Mol Sci 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity



Treacher Collins syndrome: a clinical and molecular study based on a large series of patients.
Marie Vincent, David Geneviève, Agnès Ostertag, Sandrine Marlin, Didier Lacombe, Dominique Martin-Coignard, Christine Coubes, Albert David, Stanislas Lyonnet, Catheline Vilain,[...]. Genet Med 2016
63
50

Treacher Collins syndrome.
Jill Dixon, Paul Trainor, Michael J Dixon. Orthod Craniofac Res 2007
54
50

Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients.
Chuan Zhang, Lisha An, Huiqin Xue, Shengju Hao, Yousheng Yan, Qinghua Zhang, Xiaohua Jin, Qian Li, Bingbo Zhou, Xuan Feng,[...]. J Clin Lab Anal 2021
6
50

Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.
Ozge Altug Teber, Gabriele Gillessen-Kaesbach, Sven Fischer, Stefan Böhringer, Beate Albrecht, Angelika Albert, Mine Arslan-Kirchner, Eric Haan, Monika Hagedorn-Greiwe, Christof Hammans,[...]. Eur J Hum Genet 2004
97
50

Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome.
Johannes G Dauwerse, Jill Dixon, Saskia Seland, Claudia A L Ruivenkamp, Arie van Haeringen, Lies H Hoefsloot, Dorien J M Peters, Agnes Clement-de Boers, Cornelia Daumer-Haas, Robert Maiwald,[...]. Nat Genet 2011
192
50

Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes.
Piranit Nik Kantaputra, Kanich Tripuwabhrut, Worrachet Intachai, Bruce M Carlson, Natalina Quarto, Chumpol Ngamphiw, Sissades Tongsima, Nuntigar Sonsuwan. Clin Otolaryngol 2020
2
50

The mandibulofacial dysostosis; a new hereditary syndrome.
A FRANCESCHETTI, D KLEIN. Acta Ophthalmol (Copenh) 1949
126
50


Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome.
Chiara Conte, Maria Rosaria D'Apice, Fabrizio Rinaldi, Stefano Gambardella, Federica Sangiuolo, Giuseppe Novelli. BMC Med Genet 2011
20
50

Another face of the Treacher Collins syndrome (TCOF1) gene: identification of additional exons.
Rolando B So, Bianca Gonzales, Dale Henning, Jill Dixon, Michael J Dixon, Benigno C Valdez. Gene 2004
31
50


Gross deletions in TCOF1 are a cause of Treacher-Collins-Franceschetti syndrome.
Michael Bowman, Michael Oldridge, Caroline Archer, Anthony O'Rourke, Joanna McParland, Roel Brekelmans, Anneke Seller, Tracy Lester. Eur J Hum Genet 2012
32
50

First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome.
J Beygo, K Buiting, S Seland, H-J Lüdecke, U Hehr, C Lich, B Prager, D R Lohmann, D Wieczorek. Mol Syndromol 2012
13
50


The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor.
Benigno C Valdez, Dale Henning, Rolando B So, Jill Dixon, Michael J Dixon. Proc Natl Acad Sci U S A 2004
180
50

Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA damage response.
Alberto Ciccia, Jen-Wei Huang, Lior Izhar, Mathew E Sowa, J Wade Harper, Stephen J Elledge. Proc Natl Acad Sci U S A 2014
66
50


Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndrome.
Zhiqiang Yan, Yu Lu, Yanfei Wang, Xiuju Zhang, Hong Duan, Jing Cheng, Huijun Yuan, Dongyi Han. Exp Ther Med 2018
7
50

Basic mechanisms in RNA polymerase I transcription of the ribosomal RNA genes.
Sarah J Goodfellow, Joost C B M Zomerdijk. Subcell Biochem 2013
82
50

High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes.
A Splendore, E O Silva, L G Alonso, A Richieri-Costa, N Alonso, A Rosa, G Carakushanky, D P Cavalcanti, D Brunoni, M R Passos-Bueno. Hum Mutat 2000
77
50

Novel insertion in exon 5 of the TCOF1 gene in twin sisters with Treacher Collins syndrome.
Bożena Anna Marszałek-Kruk, Piotr Wójcicki, Robert Smigiel, Wiesław H Trzeciak. J Appl Genet 2012
6
50

Characterization of the nucleolar gene product, treacle, in Treacher Collins syndrome.
C Isaac, K L Marsh, W A Paznekas, J Dixon, M J Dixon, E W Jabs, U T Meier. Mol Biol Cell 2000
73
50

TCOF1 mutation database: novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature.
Alessandra Splendore, Roberto D Fanganiello, Cibele Masotti, Lucas S C Morganti, M Rita Passos-Bueno. Hum Mutat 2005
30
50

Mutation screening of Chinese Treacher Collins syndrome patients identified novel TCOF1 mutations.
Ying Chen, Luo Guo, Chen-Long Li, Jing Shan, Hai-Song Xu, Jie-Ying Li, Shan Sun, Shao-Juan Hao, Lei Jin, Gang Chai,[...]. Mol Genet Genomics 2018
7
50

Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome.
Jing Liu, Pengsiyuan Lin, Jialun Pang, Zhengjun Jia, Ying Peng, Hui Xi, Lingqian Wu, Zhuo Li, Hua Wang. Mol Genet Genomic Med 2020
4
50

TCOF1 pathogenic variants identified by Whole-exome sequencing in Chinese Treacher Collins syndrome families and hearing rehabilitation effect.
Xinmiao Fan, Yibei Wang, Yue Fan, Huiqian Du, Nana Luo, Shuyang Zhang, Xiaowei Chen. Orphanet J Rare Dis 2019
9
50


POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4.
Elodie Sanchez, Béryl Laplace-Builhé, Frédéric Tran Mau-Them, Eric Richard, Alice Goldenberg, Tomi L Toler, Thomas Guignard, Vincent Gatinois, Marie Vincent, Catherine Blanchet,[...]. Genet Med 2020
22
50

A novel nonsense mutation in the TCOF1 gene in one Chinese newborn with Treacher Collins syndrome.
Haisheng Zeng, Mingyu Xie, Jianbo Li, Haoqiang Xie, Xiaomei Lu. Int J Pediatr Otorhinolaryngol 2021
2
50

SNHG12 promotes carcinogenesis of human renal cell cancer via functioning as a competing endogenous RNA and sponging miR-30a-3p.
Hongyuan Yu, Junlong Liu, Zhe Zhang, Yuyan Zhu, Jianbin Bi, Chuize Kong. J Cell Mol Med 2021
2
50

HIF activation by pH-dependent nucleolar sequestration of VHL.
Karim Mekhail, Lakshman Gunaratnam, Marie-Eve Bonicalzi, Stephen Lee. Nat Cell Biol 2004
183
50

LncRNA SNHG3 promotes clear cell renal cell carcinoma proliferation and migration by upregulating TOP2A.
Chong Zhang, Yan Qu, Haibing Xiao, Wen Xiao, Jing Liu, Yunhui Gao, Manping Li, Juntian Liu. Exp Cell Res 2019
20
50


Discovery and validation of the prognostic value of the lncRNAs encoding snoRNAs in patients with clear cell renal cell carcinoma.
Wuping Yang, Kenan Zhang, Lei Li, Kaifang Ma, Baoan Hong, Yanqing Gong, Kan Gong. Aging (Albany NY) 2020
11
50

Dissecting miRNA gene repression on single cell level with an advanced fluorescent reporter system.
Nicolas Lemus-Diaz, Kai O Böker, Ignacio Rodriguez-Polo, Michael Mitter, Jasmin Preis, Maximilian Arlt, Jens Gruber. Sci Rep 2017
8
50

Expression signature of six-snoRNA serves as novel non-invasive biomarker for diagnosis and prognosis prediction of renal clear cell carcinoma.
Yanyun Zhao, Yuanyuan Yan, Rong Ma, Xuemei Lv, Liwen Zhang, Jinlong Wang, Wenjing Zhu, Lan Zhao, Longyang Jiang, Lin Zhao,[...]. J Cell Mol Med 2020
10
50

RNA-Seq of the nucleolus reveals abundant SNORD44-derived small RNAs.
Baoyan Bai, Srinivasan Yegnasubramanian, Sarah J Wheelan, Marikki Laiho. PLoS One 2014
16
50

Immobilization of proteins in the nucleolus by ribosomal intergenic spacer noncoding RNA.
Timothy E Audas, Mathieu D Jacob, Stephen Lee. Mol Cell 2012
157
50


Assembly of the nucleolus: in need of revision.
Maria Carmo-Fonseca. EMBO J 2015
9
50

Dynamic localisation of mature microRNAs in Human nucleoli is influenced by exogenous genetic materials.
Zhou Fang Li, Yi Min Liang, Pui Ngan Lau, Wei Shen, Dai Kui Wang, Wing Tai Cheung, Chun Jason Xue, Lit Man Poon, Yun Wah Lam. PLoS One 2013
43
50

A phase II trial of AS1411 (a novel nucleolin-targeted DNA aptamer) in metastatic renal cell carcinoma.
Jonathan E Rosenberg, Richard M Bambury, Eliezer M Van Allen, Harry A Drabkin, Primo N Lara, Andrea L Harzstark, Nikhil Wagle, Robert A Figlin, Gregory W Smith, Levi A Garraway,[...]. Invest New Drugs 2014
179
50

EAU guidelines on renal cell carcinoma: 2014 update.
Borje Ljungberg, Karim Bensalah, Steven Canfield, Saeed Dabestani, Fabian Hofmann, Milan Hora, Markus A Kuczyk, Thomas Lam, Lorenzo Marconi, Axel S Merseburger,[...]. Eur Urol 2015
50

DDX31 regulates the p53-HDM2 pathway and rRNA gene transcription through its interaction with NPM1 in renal cell carcinomas.
Tomoya Fukawa, Masaya Ono, Taisuke Matsuo, Hisanori Uehara, Tsuneharu Miki, Yusuke Nakamura, Hiro-omi Kanayama, Toyomasa Katagiri. Cancer Res 2012
26
50

A Pan-cancer Analysis of the Expression and Clinical Relevance of Small Nucleolar RNAs in Human Cancer.
Jing Gong, Yajuan Li, Chun-Jie Liu, Yu Xiang, Chunlai Li, Youqiong Ye, Zhao Zhang, David H Hawke, Peter K Park, Lixia Diao,[...]. Cell Rep 2017
105
50

SNORD63 and SNORD96A as the non-invasive diagnostic biomarkers for clear cell renal cell carcinoma.
Xiaoling Shang, Xingguo Song, Kangyu Wang, Miao Yu, Shanshan Ding, Xiaohan Dong, Li Xie, Xianrang Song. Cancer Cell Int 2021
3
50

New Roles for the Nucleolus in Health and Disease.
Lorena Núñez Villacís, Mei S Wong, Laura L Ferguson, Nadine Hein, Amee J George, Katherine M Hannan. Bioessays 2018
34
50

Directed proteomic analysis of the human nucleolus.
Jens S Andersen, Carol E Lyon, Archa H Fox, Anthony K L Leung, Yun Wah Lam, Hanno Steen, Matthias Mann, Angus I Lamond. Curr Biol 2002
713
50

Insulin/IGF1-PI3K-dependent nucleolar localization of a glycolytic enzyme--phosphoglycerate mutase 2, is necessary for proper structure of nucleolus and RNA synthesis.
Agnieszka Gizak, Marcin Grenda, Piotr Mamczur, Janusz Wisniewski, Filip Sucharski, Jerzy Silberring, James A McCubrey, Jacek R Wisniewski, Dariusz Rakus. Oncotarget 2015
7
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.