A citation-based method for searching scientific literature

Roberto Valli, Barbara Pressato, Cristina Marletta, Lydia Mare, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. Mol Cytogenet 2013
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


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
36
73

Mutations in SBDS are associated with Shwachman-Diamond syndrome.
Graeme R B Boocock, Jodi A Morrison, Maja Popovic, Nicole Richards, Lynda Ellis, Peter R Durie, Johanna M Rommens. Nat Genet 2003
477
52

Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
Emanuela Maserati, Antonella Minelli, Barbara Pressato, Roberto Valli, Barbara Crescenzi, Maurizio Stefanelli, Giuseppe Menna, Laura Sainati, Furio Poli, Claudio Panarello,[...]. Genes Chromosomes Cancer 2006
35
47

Prognostic Mutations in Myelodysplastic Syndrome after Stem-Cell Transplantation.
R Coleman Lindsley, Wael Saber, Brenton G Mar, Robert Redd, Tao Wang, Michael D Haagenson, Peter V Grauman, Zhen-Huan Hu, Stephen R Spellman, Stephanie J Lee,[...]. N Engl J Med 2017
354
42

Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome.
Andrew J Finch, Christine Hilcenko, Nicolas Basse, Lesley F Drynan, Beatriz Goyenechea, Tobias F Menne, Africa González Fernández, Paul Simpson, Clive S D'Santos, Mark J Arends,[...]. Genes Dev 2011
183
36

Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome.
Polina Stepensky, Montserrat Chacón-Flores, Katherine H Kim, Omar Abuzaitoun, Arnulfo Bautista-Santos, Natalia Simanovsky, Dritan Siliqi, Davide Altamura, Alfonso Méndez-Godoy, Abril Gijsbers,[...]. J Med Genet 2017
66
36

The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast.
Tobias F Menne, Beatriz Goyenechea, Nuria Sánchez-Puig, Chi C Wong, Louise M Tonkin, Philip J Ancliff, Renée L Brost, Michael Costanzo, Charles Boone, Alan J Warren. Nat Genet 2007
227
31

The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
Emanuela Maserati, Barbara Pressato, Roberto Valli, Antonella Minelli, Laura Sainati, Francesco Patitucci, Cristina Marletta, Angela Mastronuzzi, Furio Poli, Francesco Lo Curto,[...]. Br J Haematol 2009
41
31

Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome.
Santhosh Dhanraj, Anna Matveev, Hongbing Li, Supanun Lauhasurayotin, Lawrence Jardine, Michaela Cada, Bozana Zlateska, Chetankumar S Tailor, Joseph Zhou, Roberto Mendoza-Londono,[...]. Blood 2017
69
31

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
110
31

Refining the phenotype associated with biallelic DNAJC21 mutations.
G D'Amours, F Lopes, J Gauthier, V Saillour, C Nassif, R Wynn, N Alos, T Leblanc, Y Capri, S Nizard,[...]. Clin Genet 2018
20
31

Release of eIF6 (p27BBP) from the 60S subunit allows 80S ribosome assembly.
Marcello Ceci, Cristina Gaviraghi, Chiara Gorrini, Leonardo A Sala, Nina Offenhäuser, Pier Carlo Marchisio, Stefano Biffo. Nature 2003
302
26

Defective ribosome assembly in Shwachman-Diamond syndrome.
Chi C Wong, David Traynor, Nicolas Basse, Robert R Kay, Alan J Warren. Blood 2011
105
26

The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.
A Minelli, E Maserati, E Nicolis, M Zecca, L Sainati, D Longoni, F Lo Curto, G Menna, F Poli, E De Paoli,[...]. Leukemia 2009
39
26

Clinical and molecular pathophysiology of Shwachman-Diamond syndrome: an update.
Kasiani C Myers, Stella M Davies, Akiko Shimamura. Hematol Oncol Clin North Am 2013
60
26

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
25
26

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features.
Raphael Carapito, Martina Konantz, Catherine Paillard, Zhichao Miao, Angélique Pichot, Magalie S Leduc, Yaping Yang, Katie L Bergstrom, Donald H Mahoney, Deborah L Shardy,[...]. J Clin Invest 2017
80
26

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
41


Crystal structure of the eukaryotic 60S ribosomal subunit in complex with initiation factor 6.
Sebastian Klinge, Felix Voigts-Hoffmann, Marc Leibundgut, Sofia Arpagaus, Nenad Ban. Science 2011
248
21

Mechanism of eIF6-mediated inhibition of ribosomal subunit joining.
Marco Gartmann, Michael Blau, Jean-Paul Armache, Thorsten Mielke, Maya Topf, Roland Beckmann. J Biol Chem 2010
80
21

The nucle(ol)ar Tif6p and Efl1p are required for a late cytoplasmic step of ribosome synthesis.
B Senger, D L Lafontaine, J S Graindorge, O Gadal, A Camasses, A Sanni, J M Garnier, M Breitenbach, E Hurt, F Fasiolo. Mol Cell 2001
127
21

A new system for naming ribosomal proteins.
Nenad Ban, Roland Beckmann, Jamie H D Cate, Jonathan D Dinman, François Dragon, Steven R Ellis, Denis L J Lafontaine, Lasse Lindahl, Anders Liljas, Jeffrey M Lipton,[...]. Curr Opin Struct Biol 2014
339
21

Shwachman-Diamond syndrome.
Yigal Dror. Pediatr Blood Cancer 2005
77
21

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome.
Jean Donadieu, Odile Fenneteau, Blandine Beaupain, Sandrine Beaufils, Florence Bellanger, Nizar Mahlaoui, Anne Lambilliotte, Nathalie Aladjidi, Yves Bertrand, Valérie Mialou,[...]. Haematologica 2012
78
21

Cytogenetic monitoring in Shwachman-Diamond syndrome: a note on clonal progression and a practical warning.
Barbara Pressato, Roberto Valli, Cristina Marletta, Lydia Mare, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. J Pediatr Hematol Oncol 2015
12
33

Evaluating chromosomal mosaicism by array comparative genomic hybridization in hematological malignancies: the proposal of a formula.
Roberto Valli, Emanuela Maserati, Cristina Marletta, Barbara Pressato, Francesco Lo Curto, Francesco Pasquali. Cancer Genet 2011
20
21

DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit Maturation.
Hemanth Tummala, Amanda J Walne, Mike Williams, Nicholas Bockett, Laura Collopy, Shirleny Cardoso, Alicia Ellison, Rob Wynn, Thierry Leblanc, Jude Fitzgibbon,[...]. Am J Hum Genet 2016
50
21

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.
Kelly A McGowan, Jun Z Li, Christopher Y Park, Veronica Beaudry, Holly K Tabor, Amit J Sabnis, Weibin Zhang, Helmut Fuchs, Martin Hrabé de Angelis, Richard M Myers,[...]. Nat Genet 2008
269
21

Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene.
Lucia Nacci, Roberto Valli, Rita Maria Pinto, Marco Zecca, Marco Cipolli, Jacopo Morini, Simone Cesaro, Emanuela Boveri, Vittorio Rosti, Paola Corti,[...]. Genes Chromosomes Cancer 2017
7
57

Somatic genetic rescue in Mendelian haematopoietic diseases.
Patrick Revy, Caroline Kannengiesser, Alain Fischer. Nat Rev Genet 2019
34
21

A functional network involved in the recycling of nucleocytoplasmic pre-60S factors.
Alice Lebreton, Cosmin Saveanu, Laurence Decourty, Jean-Christophe Rain, Alain Jacquier, Micheline Fromont-Racine. J Cell Biol 2006
86
15

Eukaryotic initiation factor 6 is rate-limiting in translation, growth and transformation.
Valentina Gandin, Annarita Miluzio, Anna Maria Barbieri, Anne Beugnet, Hiroaki Kiyokawa, Pier Carlo Marchisio, Stefano Biffo. Nature 2008
148
15

Crystal structures of ribosome anti-association factor IF6.
C M Groft, R Beckmann, A Sali, S K Burley. Nat Struct Biol 2000
52
15

The Saccharomyces cerevisiae 60 S ribosome biogenesis factor Tif6p is regulated by Hrr25p-mediated phosphorylation.
Partha Ray, Uttiya Basu, Anirban Ray, Romit Majumdar, Haiteng Deng, Umadas Maitra. J Biol Chem 2008
27
15

Integrity of the P-site is probed during maturation of the 60S ribosomal subunit.
Cyril Bussiere, Yaser Hashem, Sucheta Arora, Joachim Frank, Arlen W Johnson. J Cell Biol 2012
56
15

Clonal evolution in marrows of patients with Shwachman-Diamond syndrome: a prospective 5-year follow-up study.
Yigal Dror, Peter Durie, Hedy Ginzberg, Rebecca Herman, Anu Banerjee, Martin Champagne, Kevin Shannon, David Malkin, Melvin H Freedman. Exp Hematol 2002
61
15

Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome.
Yigal Dror, Jean Donadieu, Jutta Koglmeier, John Dodge, Sanna Toiviainen-Salo, Outi Makitie, Elizabeth Kerr, Cornelia Zeidler, Akiko Shimamura, Neil Shah,[...]. Ann N Y Acad Sci 2011
109
15

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
271
15

Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman-Diamond Syndrome.
Camille Shammas, Tobias F Menne, Christine Hilcenko, Stephen R Michell, Beatriz Goyenechea, Graeme R B Boocock, Peter R Durie, Johanna M Rommens, Alan J Warren. J Biol Chem 2005
86
15

Defining the pathway of cytoplasmic maturation of the 60S ribosomal subunit.
Kai-Yin Lo, Zhihua Li, Cyril Bussiere, Stefan Bresson, Edward M Marcotte, Arlen W Johnson. Mol Cell 2010
136
15

Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS.
O Mäkitie, L Ellis, P R Durie, J A Morrison, E B Sochett, J M Rommens, W G Cole. Clin Genet 2004
79
15

Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome.
Barbara Crescenzi, Roberta La Starza, Constantina Sambani, Agapi Parcharidou, Valentina Pierini, Valeria Nofrini, Lucia Brandimarte, Caterina Matteucci, Franco Aversa, Massimo Fabrizio Martelli,[...]. Br J Haematol 2009
16
18

Hematologic abnormalities in Shwachman Diamond syndrome: lack of genotype-phenotype relationship.
Taco W Kuijpers, Mariel Alders, Anton T J Tool, Clemens Mellink, Dirk Roos, Raoul C M Hennekam. Blood 2005
61
15

THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION.
H SHWACHMAN, L K DIAMOND, F A OSKI, K T KHAW. J Pediatr 1964
371
15

Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
E Maserati, A Minelli, C Olivieri, L Bonvini, A Marchi, M Bozzola, C Danesino, S Scappaticci, F Pasquali. Cancer Genet Cytogenet 2000
25
15

Shwachman-Bodian-Diamond syndrome (SBDS) protein deficiency impairs translation re-initiation from C/EBPα and C/EBPβ mRNAs.
Kyungmin In, Mohamad A Zaini, Christine Müller, Alan J Warren, Marieke von Lindern, Cornelis F Calkhoven. Nucleic Acids Res 2016
18
16

Haematopoietic stem cells require a highly regulated protein synthesis rate.
Robert A J Signer, Jeffrey A Magee, Adrian Salic, Sean J Morrison. Nature 2014
336
15

Ribosomal biogenesis genes play an essential and p53-independent role in zebrafish pancreas development.
Elayne Provost, Karen A Wehner, Xiangang Zhong, Foram Ashar, Elizabeth Nguyen, Rachel Green, Michael J Parsons, Steven D Leach. Development 2012
54
15

Diamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28.
Karen W Gripp, Cynthia Curry, Ann Haskins Olney, Claudio Sandoval, Jamie Fisher, Jessica Xiao-Ling Chong, Lisa Pilchman, Rebecca Sahraoui, Deborah L Stabley, Katia Sol-Church. Am J Med Genet A 2014
79
15


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.