A citation-based method for searching scientific literature

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
Times Cited: 25







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



Times Cited
  Times     Co-cited
Similarity


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
68

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
56

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
40

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
36

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
36

Defective ribosome assembly in Shwachman-Diamond syndrome.
Chi C Wong, David Traynor, Nicolas Basse, Robert R Kay, Alan J Warren. Blood 2011
105
32

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
32

Mitotic spindle destabilization and genomic instability in Shwachman-Diamond syndrome.
Karyn M Austin, Mohan L Gupta, Scott A Coats, Asmin Tulpule, Gustavo Mostoslavsky, Alejandro B Balazs, Richard C Mulligan, George Daley, David Pellman, Akiko Shimamura. J Clin Invest 2008
88
28

Ribosomopathies: human disorders of ribosome dysfunction.
Anupama Narla, Benjamin L Ebert. Blood 2010
508
28

Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes.
Noemi A Zambetti, Eric M J Bindels, Paulina M H Van Strien, Marijke G Valkhof, Maria N Adisty, Remco M Hoogenboezem, Mathijs A Sanders, Johanna M Rommens, Ivo P Touw, Marc H G P Raaijmakers. Haematologica 2015
37
28

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
28


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
28

Impaired ribosomal subunit association in Shwachman-Diamond syndrome.
Nicholas Burwick, Scott A Coats, Tomoka Nakamura, Akiko Shimamura. Blood 2012
50
24

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
24

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
24

Shwachman-Bodian Diamond syndrome is a multi-functional protein implicated in cellular stress responses.
Heather L Ball, Bing Zhang, J Jacob Riches, Rikesh Gandhi, Jing Li, Johanna M Rommens, Jeremy S Myers. Hum Mol Genet 2009
44
24

Loss of the mouse ortholog of the shwachman-diamond syndrome gene (Sbds) results in early embryonic lethality.
Siyi Zhang, Mingjun Shi, Chi-Chung Hui, Johanna M Rommens. Mol Cell Biol 2006
77
24

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
24

Deficiency of Sbds in the mouse pancreas leads to features of Shwachman-Diamond syndrome, with loss of zymogen granules.
Marina E Tourlakis, Jian Zhong, Rikesh Gandhi, Siyi Zhang, Lingling Chen, Peter R Durie, Johanna M Rommens. Gastroenterology 2012
29
24

THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION.
H SHWACHMAN, L K DIAMOND, F A OSKI, K T KHAW. J Pediatr 1964
371
24

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
292
24

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
24

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen.
Benjamin L Ebert, Jennifer Pretz, Jocelyn Bosco, Cindy Y Chang, Pablo Tamayo, Naomi Galili, Azra Raza, David E Root, Eyal Attar, Steven R Ellis,[...]. Nature 2008
647
24

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
24

SBDS-deficient cells undergo accelerated apoptosis through the Fas-pathway.
Piya Rujkijyanont, Ken-Ichiro Watanabe, Chhaya Ambekar, Hanming Wang, Aaron Schimmer, Joseph Beyene, Yigal Dror. Haematologica 2008
38
20

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
198
20

Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cells.
Shilpee Dutt, Anupama Narla, Katherine Lin, Ann Mullally, Nirmalee Abayasekara, Christine Megerdichian, Frederick H Wilson, Treeve Currie, Arati Khanna-Gupta, Nancy Berliner,[...]. Blood 2011
274
20

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
20

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
20

SBDS-Deficient Cells Have an Altered Homeostatic Equilibrium due to Translational Inefficiency Which Explains their Reduced Fitness and Provides a Logical Framework for Intervention.
Piera Calamita, Annarita Miluzio, Arianna Russo, Elisa Pesce, Sara Ricciardi, Farhat Khanim, Cristina Cheroni, Roberta Alfieri, Marilena Mancino, Chiara Gorrini,[...]. PLoS Genet 2017
24
20

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
19
26

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
20


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
20

SBDS expression and localization at the mitotic spindle in human myeloid progenitors.
Claudia Orelio, Paul Verkuijlen, Judy Geissler, Timo K van den Berg, Taco W Kuijpers. PLoS One 2009
27
16

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
16

A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome.
Jillian L Barlow, Lesley F Drynan, Duncan R Hewett, Luke R Holmes, Silvia Lorenzo-Abalde, Alison L Lane, Helen E Jolin, Richard Pannell, Angela J Middleton, See Heng Wong,[...]. Nat Med 2010
251
16

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
123
16

Transcriptome analysis reveals a ribosome constituents disorder involved in the RPL5 downregulated zebrafish model of Diamond-Blackfan anemia.
Yang Wan, Qian Zhang, Zhaojun Zhang, Binfeng Song, Xiaomin Wang, Yingchi Zhang, Qiong Jia, Tao Cheng, Xiaofan Zhu, Anskar Yu-Hung Leung,[...]. BMC Med Genomics 2016
24
16

Shwachman-Diamond syndrome: a review of the clinical presentation, molecular pathogenesis, diagnosis, and treatment.
Lauri Burroughs, Ann Woolfrey, Akiko Shimamura. Hematol Oncol Clin North Am 2009
87
16

A Ribosomopathy Reveals Decoding Defective Ribosomes Driving Human Dysmorphism.
Nahuel A Paolini, Martin Attwood, Samuel B Sondalle, Carolina Marques Dos Santos Vieira, Anita M van Adrichem, Franca M di Summa, Marie-Françoise O'Donohue, Pierre-Emmanuel Gleizes, Swaksha Rachuri, Joseph W Briggs,[...]. Am J Hum Genet 2017
45
16

The Shwachman-Diamond SBDS protein localizes to the nucleolus.
Karyn M Austin, Rebecca J Leary, Akiko Shimamura. Blood 2005
94
16

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia.
N Draptchinskaia, P Gustavsson, B Andersson, M Pettersson, T N Willig, I Dianzani, S Ball, G Tchernia, J Klar, H Matsson,[...]. Nat Genet 1999
610
16

Mesenchymal Inflammation Drives Genotoxic Stress in Hematopoietic Stem Cells and Predicts Disease Evolution in Human Pre-leukemia.
Noemi A Zambetti, Zhen Ping, Si Chen, Keane J G Kenswil, Maria A Mylona, Mathijs A Sanders, Remco M Hoogenboezem, Eric M J Bindels, Maria N Adisty, Paulina M H Van Strien,[...]. Cell Stem Cell 2016
188
16

Variable clinical presentation of Shwachman-Diamond syndrome: update from the North American Shwachman-Diamond Syndrome Registry.
Kasiani C Myers, Audrey Anna Bolyard, Barbara Otto, Trisha E Wong, Amanda T Jones, Richard E Harris, Stella M Davies, David C Dale, Akiko Shimamura. J Pediatr 2014
80
16

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
16


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
59
16

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
20


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.