A citation-based method for searching scientific literature

Maname Benyelles, Marie-Françoise O'Donohue, Laëtitia Kermasson, Elodie Lainey, Raphael Borie, Chantal Lagresle-Peyrou, Hilario Nunes, Clarisse Cazelles, Cécile Fourrage, Emmanuelle Ollivier, Ambroise Marcais, Anne-Sophie Gamez, Fanny Morice-Picard, Denis Caillaud, Nicolas Pottier, Christelle Ménard, Ibrahima Ba, Alicia Fernandes, Bruno Crestani, Jean-Pierre de Villartay, Pierre-Emmanuel Gleizes, Isabelle Callebaut, Caroline Kannengiesser, Patrick Revy. Hum Mol Genet 2020
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita.
Tom Vulliamy, Richard Beswick, Michael Kirwan, Anna Marrone, Martin Digweed, Amanda Walne, Inderjeet Dokal. Proc Natl Acad Sci U S A 2008
205
44

Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in mice.
Jun He, Sandra Navarrete, Murek Jasinski, Tom Vulliamy, Inderjeet Dokal, Monica Bessler, Philip J Mason. Oncogene 2002
71
33

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.
N S Heiss, S W Knight, T J Vulliamy, S M Klauck, S Wiemann, P J Mason, A Poustka, I Dokal. Nat Genet 1998
628
33

H/ACA small RNA dysfunctions in disease reveal key roles for noncoding RNA modifications in hematopoietic stem cell differentiation.
Cristian Bellodi, Mary McMahon, Adrian Contreras, Dayle Juliano, Noam Kopmar, Tomoka Nakamura, David Maltby, Alma Burlingame, Sharon A Savage, Akiko Shimamura,[...]. Cell Rep 2013
72
33


Pseudouridine profiling reveals regulated mRNA pseudouridylation in yeast and human cells.
Thomas M Carlile, Maria F Rojas-Duran, Boris Zinshteyn, Hakyung Shin, Kristen M Bartoli, Wendy V Gilbert. Nature 2014
461
22


Transcriptome-wide mapping reveals widespread dynamic-regulated pseudouridylation of ncRNA and mRNA.
Schraga Schwartz, Douglas A Bernstein, Maxwell R Mumbach, Marko Jovanovic, Rebecca H Herbst, Brian X León-Ricardo, Jesse M Engreitz, Mitchell Guttman, Rahul Satija, Eric S Lander,[...]. Cell 2014
433
22




Site-specific ribose methylation of preribosomal RNA: a novel function for small nucleolar RNAs.
Z Kiss-László, Y Henry, J P Bachellerie, M Caizergues-Ferrer, T Kiss. Cell 1996
601
22

GAR1 is an essential small nucleolar RNP protein required for pre-rRNA processing in yeast.
J P Girard, H Lehtonen, M Caizergues-Ferrer, F Amalric, D Tollervey, B Lapeyre. EMBO J 1992
239
22


Nhp2p and Nop10p are essential for the function of H/ACA snoRNPs.
A Henras, Y Henry, C Bousquet-Antonelli, J Noaillac-Depeyre, J P Gélugne, M Caizergues-Ferrer. EMBO J 1998
177
22

An essential yeast protein, CBF5p, binds in vitro to centromeres and microtubules.
W Jiang, K Middleton, H J Yoon, C Fouquet, J Carbon. Mol Cell Biol 1993
152
22

Dyskeratosis congenita and cancer in mice deficient in ribosomal RNA modification.
Davide Ruggero, Silvia Grisendi, Francesco Piazza, Eduardo Rego, Francesca Mari, Pulivarthi H Rao, Carlos Cordon-Cardo, Pier Paolo Pandolfi. Science 2003
302
22


Germline NPM1 mutations lead to altered rRNA 2'-O-methylation and cause dyskeratosis congenita.
Daphna Nachmani, Anne H Bothmer, Silvia Grisendi, Aldo Mele, Dietmar Bothmer, Jonathan D Lee, Emanuele Monteleone, Ke Cheng, Yang Zhang, Assaf C Bester,[...]. Nat Genet 2019
27
22

Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10.
Amanda J Walne, Tom Vulliamy, Anna Marrone, Richard Beswick, Michael Kirwan, Yuka Masunari, Fat-Hia Al-Qurashi, Mahmoud Aljurf, Inderjeet Dokal. Hum Mol Genet 2007
203
22

Reconstitution and structural analysis of the yeast box H/ACA RNA-guided pseudouridine synthase.
Shuang Li, Jingqi Duan, Dandan Li, Bing Yang, Mengqiu Dong, Keqiong Ye. Genes Dev 2011
50
22

Crystal structure of a Cbf5-Nop10-Gar1 complex and implications in RNA-guided pseudouridylation and dyskeratosis congenita.
Rumana Rashid, Bo Liang, Daniel L Baker, Osama A Youssef, Yang He, Kathleen Phipps, Rebecca M Terns, Michael P Terns, Hong Li. Mol Cell 2006
126
22

Human Telomerase RNA Processing and Quality Control.
Chi-Kang Tseng, Hui-Fang Wang, Allison M Burns, Morgan R Schroeder, Martina Gaspari, Peter Baumann. Cell Rep 2015
76
22

Alternative lengthening of telomeres: models, mechanisms and implications.
Anthony J Cesare, Roger R Reddel. Nat Rev Genet 2010
562
22

The human telomerase RNA component, hTR, activates the DNA-dependent protein kinase to phosphorylate heterogeneous nuclear ribonucleoprotein A1.
Nicholas S Y Ting, Brant Pohorelic, Yaping Yu, Susan P Lees-Miller, Tara L Beattie. Nucleic Acids Res 2009
42
22

TERRA and hnRNPA1 orchestrate an RPA-to-POT1 switch on telomeric single-stranded DNA.
Rachel Litman Flynn, Richard C Centore, Roderick J O'Sullivan, Rekha Rai, Alice Tse, Zhou Songyang, Sandy Chang, Jan Karlseder, Lee Zou. Nature 2011
221
22

Human Ku70/80 interacts directly with hTR, the RNA component of human telomerase.
Nicholas S Y Ting, Yaping Yu, Brant Pohorelic, Susan P Lees-Miller, Tara L Beattie. Nucleic Acids Res 2005
72
22

DNA-PKcs phosphorylates hnRNP-A1 to facilitate the RPA-to-POT1 switch and telomere capping after replication.
Jiangdong Sui, Yu-Fen Lin, Kangling Xu, Kyung-Jong Lee, Dong Wang, Benjamin P C Chen. Nucleic Acids Res 2015
27
22

NHP2 downregulation counteracts hTR-mediated activation of the DNA damage response at ALT telomeres.
Maya Raghunandan, Dan Geelen, Eva Majerova, Anabelle Decottignies. EMBO J 2021
2
100

Senescence and immortalization: role of telomeres and telomerase.
Jerry W Shay, Woodring E Wright. Carcinogenesis 2005
469
22


Telomerase-independent regulation of ATR by human telomerase RNA.
Martijn Kedde, Carlos le Sage, Anja Duursma, Eitan Zlotorynski, Bart van Leeuwen, Wouter Nijkamp, Roderick Beijersbergen, Reuven Agami. J Biol Chem 2006
53
22

Somatic genetic rescue in hematopoietic cells in GATA2 deficiency.
Luiz Fernando B Catto, Gustavo Borges, André L Pinto, Diego V Clé, Fernando Chahud, Barbara A Santana, Flavia S Donaires, Rodrigo T Calado. Blood 2020
6
33

Universal Patterns of Selection in Cancer and Somatic Tissues.
Iñigo Martincorena, Keiran M Raine, Moritz Gerstung, Kevin J Dawson, Kerstin Haase, Peter Van Loo, Helen Davies, Michael R Stratton, Peter J Campbell. Cell 2017
379
22

Pathogenic TERT promoter variants in telomere diseases.
Fernanda Gutierrez-Rodrigues, Flávia S Donaires, André Pinto, Alana Vicente, Laura W Dillon, Diego V Clé, Barbara A Santana, Mehdi Pirooznia, Maria Del Pilar F Ibanez, Danielle M Townsley,[...]. Genet Med 2019
11
22

Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis.
Barbara Pressato, Roberto Valli, Cristina Marletta, Lydia Mare, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. Br J Haematol 2012
32
22

Somatic mutations in telomerase promoter counterbalance germline loss-of-function mutations.
Lindley Maryoung, Yangbo Yue, Ashley Young, Chad A Newton, Cindy Barba, Nicolai S C van Oers, Richard C Wang, Christine Kim Garcia. J Clin Invest 2017
28
22

Somatic mutation in cancer and normal cells.
Iñigo Martincorena, Peter J Campbell. Science 2015
436
22

Somatic genetic rescue in Mendelian haematopoietic diseases.
Patrick Revy, Caroline Kannengiesser, Alain Fischer. Nat Rev Genet 2019
23
22

Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome.
Alyssa L Kennedy, Kasiani C Myers, James Bowman, Christopher J Gibson, Nicholas D Camarda, Elissa Furutani, Gwen M Muscato, Robert H Klein, Kaitlyn Ballotti, Shanshan Liu,[...]. Nat Commun 2021
6
33

An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation.
Tangui Le Guen, Fabien Touzot, Isabelle André-Schmutz, Chantal Lagresle-Peyrou, Benoit France, Laetitia Kermasson, Nathalie Lambert, Capucine Picard, Patrick Nitschke, Wassila Carpentier,[...]. J Allergy Clin Immunol 2015
38
22

Population dynamics of normal human blood inferred from somatic mutations.
Henry Lee-Six, Nina Friesgaard Øbro, Mairi S Shepherd, Sebastian Grossmann, Kevin Dawson, Miriam Belmonte, Robert J Osborne, Brian J P Huntly, Inigo Martincorena, Elizabeth Anderson,[...]. Nature 2018
159
22

Somatic mutations and clonal hematopoiesis in congenital neutropenia.
Jun Xia, Christopher A Miller, Jack Baty, Amrita Ramesh, Matthew R M Jotte, Robert S Fulton, Tiphanie P Vogel, Megan A Cooper, Kelly J Walkovich, Vahagn Makaryan,[...]. Blood 2018
48
22

Specific small nucleolar RNA expression profiles in acute leukemia.
W Valleron, E Laprevotte, E-F Gautier, C Quelen, C Demur, E Delabesse, X Agirre, F Prósper, T Kiss, P Brousset. Leukemia 2012
78
11



Nucleotide sequence determination and secondary structure of Xenopus U3 snRNA.
C Jeppesen, B Stebbins-Boaz, S A Gerbi. Nucleic Acids Res 1988
75
11

The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing.
Shivendra Kishore, Amit Khanna, Zhaiyi Zhang, Jingyi Hui, Piotr J Balwierz, Mihaela Stefan, Carol Beach, Robert D Nicholls, Mihaela Zavolan, Stefan Stamm. Hum Mol Genet 2010
183
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.