A citation-based method for searching scientific literature

John N Griffin, Samuel B Sondalle, Andrew Robson, Emily K Mis, Gerald Griffin, Saurabh S Kulkarni, Engin Deniz, Susan J Baserga, Mustafa K Khokha. Development 2018
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Impaired ribosome biogenesis: mechanisms and relevance to cancer and aging.
Zsofia Turi, Matthew Lacey, Martin Mistrik, Pavel Moudry. Aging (Albany NY) 2019
39
33

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons.
Alexandre Bolze, Bertrand Boisson, Barbara Bosch, Alexander Antipenko, Matthieu Bouaziz, Paul Sackstein, Malik Chaker-Margot, Vincent Barlogis, Tracy Briggs, Elena Colino,[...]. Proc Natl Acad Sci U S A 2018
18
33

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia.
Alexandre Bolze, Nizar Mahlaoui, Minji Byun, Bridget Turner, Nikolaus Trede, Steven R Ellis, Avinash Abhyankar, Yuval Itan, Etienne Patin, Samuel Brebner,[...]. Science 2013
120
33


Nucleolar stress with and without p53.
Allison James, Yubo Wang, Himanshu Raje, Raphyel Rosby, Patrick DiMario. Nucleus 2014
152
22

The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome.
Kristin E Noack Watt, Annita Achilleos, Cynthia L Neben, Amy E Merrill, Paul A Trainor. PLoS Genet 2016
47
22

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
22

Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function.
Natalie C Jones, Megan L Lynn, Karin Gaudenz, Daisuke Sakai, Kazushi Aoto, Jean-Phillipe Rey, Earl F Glynn, Lacey Ellington, Chunying Du, Jill Dixon,[...]. Nat Med 2008
283
22

The ribosome biogenesis protein Esf1 is essential for pharyngeal cartilage formation in zebrafish.
Jian-Yang Chen, Xungang Tan, Zheng-Hua Wang, Yun-Zhang Liu, Jian-Feng Zhou, Xiao-Zhi Rong, Ling Lu, Yun Li. FEBS J 2018
8
25

Diverse Regulators of Human Ribosome Biogenesis Discovered by Changes in Nucleolar Number.
Katherine I Farley-Barnes, Kathleen L McCann, Lisa M Ogawa, Janie Merkel, Yulia V Surovtseva, Susan J Baserga. Cell Rep 2018
40
22

The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus.
John N Griffin, Samuel B Sondalle, Florencia Del Viso, Susan J Baserga, Mustafa K Khokha. PLoS Genet 2015
27
22

Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction.
K Nicole Weaver, Kristin E Noack Watt, Robert B Hufnagel, Joaquin Navajas Acedo, Luke L Linscott, Kristen L Sund, Patricia L Bender, Rainer König, Charles M Lourenco, Ute Hehr,[...]. Am J Hum Genet 2015
37
22

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
22

Fanconi anemia protein FANCI functions in ribosome biogenesis.
Samuel B Sondalle, Simonne Longerich, Lisa M Ogawa, Patrick Sung, Susan J Baserga. Proc Natl Acad Sci U S A 2019
18
22

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
22

Genome-wide RNAi Screening Identifies Protein Modules Required for 40S Subunit Synthesis in Human Cells.
Lukas Badertscher, Thomas Wild, Christian Montellese, Leila T Alexander, Lukas Bammert, Marie Sarazova, Michael Stebler, Gabor Csucs, Thomas U Mayer, Nicola Zamboni,[...]. Cell Rep 2015
55
22

The complexity of human ribosome biogenesis revealed by systematic nucleolar screening of Pre-rRNA processing factors.
Lionel Tafforeau, Christiane Zorbas, Jean-Louis Langhendries, Sahra-Taylor Mullineux, Vassiliki Stamatopoulou, Romain Mullier, Ludivine Wacheul, Denis L J Lafontaine. Mol Cell 2013
251
22

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
22

Treacher Collins Syndrome: the genetics of a craniofacial disease.
Sameep Kadakia, Samuel N Helman, Arvind K Badhey, Masoud Saman, Yadranko Ducic. Int J Pediatr Otorhinolaryngol 2014
39
22

Tissue-selective effects of nucleolar stress and rDNA damage in developmental disorders.
Eliezer Calo, Bo Gu, Margot E Bowen, Fardin Aryan, Antoine Zalc, Jialiang Liang, Ryan A Flynn, Tomek Swigut, Howard Y Chang, Laura D Attardi,[...]. Nature 2018
61
22

tp53-dependent and independent signaling underlies the pathogenesis and possible prevention of Acrofacial Dysostosis-Cincinnati type.
Kristin E N Watt, Cynthia L Neben, Shawn Hall, Amy E Merrill, Paul A Trainor. Hum Mol Genet 2018
6
33

Tissue specific roles for the ribosome biogenesis factor Wdr43 in zebrafish development.
Chengtian Zhao, Viktoria Andreeva, Yann Gibert, Melissa LaBonty, Victoria Lattanzi, Shubhangi Prabhudesai, Yi Zhou, Leonard Zon, Kathleen L McCann, Susan Baserga,[...]. PLoS Genet 2014
26
22

Mutations in RPSA and NKX2-3 link development of the spleen and intestinal vasculature.
Chantal Kerkhofs, Servi J C Stevens, Saul N Faust, William Rae, Anthony P Williams, Peter Wurm, Rune Østern, Paul Fockens, Christiane Würfel, Martin Laass,[...]. Hum Mutat 2020
6
33

Isolated congenital asplenia: a French nationwide retrospective survey of 20 cases.
Nizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, Alexandre Bolze, Cheng-Lung Ku, Olivier Tournilhac, Brigitte Gilbert-Dussardier, Brigitte Pautard, Philippe Durand, Denis Devictor,[...]. J Pediatr 2011
39
22

Expression of ribosomopathy genes during Xenopus tropicalis embryogenesis.
Andrew Robson, Nick D L Owens, Susan J Baserga, Mustafa K Khokha, John N Griffin. BMC Dev Biol 2016
14
22

Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits.
Marie-Françoise O'Donohue, Valérie Choesmel, Marlène Faubladier, Gwennaële Fichant, Pierre-Emmanuel Gleizes. J Cell Biol 2010
131
22

Gene ontology: tool for the unification of biology. The Gene Ontology Consortium.
M Ashburner, C A Ball, J A Blake, D Botstein, H Butler, J M Cherry, A P Davis, K Dolinski, S S Dwight, J T Eppig,[...]. Nat Genet 2000
22

Evidence for a precursor of the high-affinity metastasis-associated murine laminin receptor.
C N Rao, V Castronovo, M C Schmitt, U M Wewer, A P Claysmith, L A Liotta, M E Sobel. Biochemistry 1989
215
22

ITGA6 and RPSA synergistically promote pancreatic cancer invasion and metastasis via PI3K and MAPK signaling pathways.
Yunhao Wu, Xiaodong Tan, Peng Liu, Yifan Yang, Yinpeng Huang, Xinlu Liu, Xiangli Meng, Boqiang Yu, Mengwei Wu, Haoyi Jin. Exp Cell Res 2019
25
22


Cancer Biogenesis in Ribosomopathies.
Sergey O Sulima, Kim R Kampen, Kim De Keersmaecker. Cells 2019
24
11



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
11

Mechanism of eIF6 release from the nascent 60S ribosomal subunit.
Félix Weis, Emmanuel Giudice, Mark Churcher, Li Jin, Christine Hilcenko, Chi C Wong, David Traynor, Robert R Kay, Alan J Warren. Nat Struct Mol Biol 2015
105
11

Prevalence of dental anomalies, ectopic eruption and associated oral malformations in subjects with Treacher Collins syndrome.
Gisele da Silva Dalben, Beatriz Costa, Marcia Ribeiro Gomide. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006
20
11

Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia.
Kim De Keersmaecker, Zeynep Kalender Atak, Ning Li, Carmen Vicente, Stephanie Patchett, Tiziana Girardi, Valentina Gianfelici, Ellen Geerdens, Emmanuelle Clappier, Michaël Porcu,[...]. Nat Genet 2013
266
11

In Vivo Senescence in the Sbds-Deficient Murine Pancreas: Cell-Type Specific Consequences of Translation Insufficiency.
Marina E Tourlakis, Siyi Zhang, Heather L Ball, Rikesh Gandhi, Hongrui Liu, Jian Zhong, Julie S Yuan, Cynthia J Guidos, Peter R Durie, Johanna M Rommens. PLoS Genet 2015
23
11

Rare ribosomopathies: insights into mechanisms of cancer.
Anna Aspesi, Steven R Ellis. Nat Rev Cancer 2019
37
11

Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning.
Nadya Kondrashov, Aya Pusic, Craig R Stumpf, Kunihiko Shimizu, Andrew C Hsieh, Junko Ishijima, Toshihiko Shiroishi, Maria Barna. Cell 2011
341
11

Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability.
Roberto Valli, Antonella Minelli, Marta Galbiati, Giovanna D'Amico, Annalisa Frattini, Giuseppe Montalbano, Abdul W Khan, Giovanni Porta, Giorgia Millefanti, Carla Olivieri,[...]. Br J Haematol 2019
12
11

Ribosomopathies: There's strength in numbers.
Eric W Mills, Rachel Green. Science 2017
167
11

A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting.
Adam P Ross, M Adela Mansilla, Youngshik Choe, Simon Helminski, Richard Sturm, Roy L Maute, Scott R May, Kamil K Hozyasz, Piotr Wójcicki, Adrianna Mostowska,[...]. PLoS One 2013
6
16

Small and Large Ribosomal Subunit Deficiencies Lead to Distinct Gene Expression Signatures that Reflect Cellular Growth Rate.
Ze Cheng, Christopher Frederick Mugler, Abdurrahman Keskin, Stefanie Hodapp, Leon Yen-Lee Chan, Karsten Weis, Philipp Mertins, Aviv Regev, Marko Jovanovic, Gloria Ann Brar. Mol Cell 2019
41
11

Ear malformations, hearing loss and hearing rehabilitation in children with Treacher Collins syndrome.
Francisco Rosa, Miguel Bebiano Coutinho, João Pinto Ferreira, Cecilia Almeida Sousa. Acta Otorrinolaringol Esp 2016
8
12


Small nucleoli are a cellular hallmark of longevity.
Varnesh Tiku, Chirag Jain, Yotam Raz, Shuhei Nakamura, Bree Heestand, Wei Liu, Martin Späth, H Eka D Suchiman, Roman-Ulrich Müller, P Eline Slagboom,[...]. Nat Commun 2017
97
11

BMS1 is mutated in aplasia cutis congenita.
Alexander G Marneros. PLoS Genet 2013
28
11

Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms.
Roberto Valli, Barbara Pressato, Cristina Marletta, Lydia Mare, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. Mol Cytogenet 2013
17
11

Ribosome biogenesis in the yeast Saccharomyces cerevisiae.
John L Woolford, Susan J Baserga. Genetics 2013
431
11


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.