A citation-based method for searching scientific literature

Karthik A Ganapathi, Karyn M Austin, Chung-Sheng Lee, Anusha Dias, Maggie M Malsch, Robin Reed, Akiko Shimamura. Blood 2007
Times Cited: 98







List of co-cited articles
918 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
461
67

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
223
55

The Shwachman-Diamond SBDS protein localizes to the nucleolus.
Karyn M Austin, Rebecca J Leary, Akiko Shimamura. Blood 2005
92
40

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
73
45

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
85
38

THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION.
H SHWACHMAN, L K DIAMOND, F A OSKI, K T KHAW. J Pediatr 1964
365
29

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
631
26

The Shwachman-Bodian-Diamond syndrome protein family is involved in RNA metabolism.
Alexei Savchenko, Nevan Krogan, John R Cort, Elena Evdokimova, Jocelyne M Lew, Adelinda A Yee, Luis Sánchez-Pulido, Miguel A Andrade, Alexey Bochkarev, James D Watson,[...]. J Biol Chem 2005
82
30

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
174
25

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
84
27

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
598
22

Mutations of the SBDS gene are present in most patients with Shwachman-Diamond syndrome.
Jill R Woloszynek, Robert J Rothbaum, Amy S Rawls, Patrick J Minx, Richard K Wilson, Philip J Mason, Monica Bessler, Daniel C Link. Blood 2004
79
24

Shwachman syndrome: phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar.
H Ginzberg, J Shin, L Ellis, J Morrison, W Ip, Y Dror, M Freedman, L A Heitlinger, M A Belt, M Corey,[...]. J Pediatr 1999
147
19

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
260
19

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
37
48

Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients.
Hanna T Gazda, Mee Rie Sheen, Adrianna Vlachos, Valerie Choesmel, Marie-Françoise O'Donohue, Hal Schneider, Natasha Darras, Catherine Hasman, Colin A Sieff, Peter E Newburger,[...]. Am J Hum Genet 2008
281
18

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
39
46

Shwachman-Diamond syndrome.
Yigal Dror. Pediatr Blood Cancer 2005
75
22


CONGENITAL HYPOPLASIA OF THE EXOCRINE PANCREAS.
M BODIAN, W SHELDON, R LIGHTWOOD. Acta Paediatr 1964
166
16

The Shwachman-Bodian-Diamond syndrome gene encodes an RNA-binding protein that localizes to the pseudopod of Dictyostelium amoebae during chemotaxis.
Deborah Wessels, Thyagarajan Srikantha, Song Yi, Spencer Kuhl, L Aravind, David R Soll. J Cell Sci 2006
39
41

Lentiviral-mediated RNAi inhibition of Sbds in murine hematopoietic progenitors impairs their hematopoietic potential.
Amy S Rawls, Alyssa D Gregory, Jill R Woloszynek, Fulu Liu, Daniel C Link. Blood 2007
34
47

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
304
16

Impaired control of IRES-mediated translation in X-linked dyskeratosis congenita.
Andrew Yoon, Guang Peng, Yves Brandenburger, Ornella Zollo, Wei Xu, Eduardo Rego, Davide Ruggero. Science 2006
294
16



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
280
16

Ribosomopathies: human disorders of ribosome dysfunction.
Anupama Narla, Benjamin L Ebert. Blood 2010
484
16

Defective ribosome assembly in Shwachman-Diamond syndrome.
Chi C Wong, David Traynor, Nicolas Basse, Robert R Kay, Alan J Warren. Blood 2011
98
16

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
631
15

Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia.
M Ridanpää, H van Eenennaam, K Pelin, R Chadwick, C Johnson, B Yuan, W vanVenrooij, G Pruijn, R Salmela, S Rockas,[...]. Cell 2001
301
15

Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Study Group.
Jean Donadieu, Thierry Leblanc, Brigitte Bader Meunier, Mohamed Barkaoui, Odile Fenneteau, Yves Bertrand, Micheline Maier-Redelsperger, Marguerite Micheau, Jean Louis Stephan, Noel Phillipe,[...]. Haematologica 2005
197
15

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
82
18

Ribosomal protein L23 activates p53 by inhibiting MDM2 function in response to ribosomal perturbation but not to translation inhibition.
Mu-Shui Dai, Shelya X Zeng, Yetao Jin, Xiao-Xin Sun, Larry David, Hua Lu. Mol Cell Biol 2004
375
14

Impaired ribosome biogenesis in Diamond-Blackfan anemia.
Valérie Choesmel, Daniel Bacqueville, Jacques Rouquette, Jacqueline Noaillac-Depeyre, Sébastien Fribourg, Aurore Crétien, Thierry Leblanc, Gil Tchernia, Lydie Da Costa, Pierre-Emmanuel Gleizes. Blood 2007
155
14

Does the ribosome translate cancer?
Davide Ruggero, Pier Paolo Pandolfi. Nat Rev Cancer 2003
709
14


Absence of nucleolar disruption after impairment of 40S ribosome biogenesis reveals an rpL11-translation-dependent mechanism of p53 induction.
Stefano Fumagalli, Alessandro Di Cara, Arti Neb-Gulati, Francois Natt, Sandy Schwemberger, Jonathan Hall, George F Babcock, Rosa Bernardi, Pier Paolo Pandolfi, George Thomas. Nat Cell Biol 2009
227
14

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
248
14

Immune function in patients with Shwachman-Diamond syndrome.
Y Dror, H Ginzberg, I Dalal, V Cherepanov, G Downey, P Durie, C M Roifman, M H Freedman. Br J Haematol 2001
64
20


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
179
13

Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia.
Hanna T Gazda, Agnieszka Grabowska, Lilia B Merida-Long, Elzbieta Latawiec, Hal E Schneider, Jeffrey M Lipton, Adrianna Vlachos, Eva Atsidaftos, Sarah E Ball, Karen A Orfali,[...]. Am J Hum Genet 2006
205
13

Shwachman-diamond syndrome.
Yigal Dror, Melvin H Freedman. Br J Haematol 2002
105
12

The chemotaxis defect of Shwachman-Diamond Syndrome leukocytes.
Vesna Stepanovic, Deborah Wessels, Frederick D Goldman, Jeremy Geiger, David R Soll. Cell Motil Cytoskeleton 2004
45
26

Ribosomal protein S17 gene (RPS17) is mutated in Diamond-Blackfan anemia.
Radek Cmejla, Jana Cmejlova, Helena Handrkova, Jiri Petrak, Dagmar Pospisilova. Hum Mutat 2007
174
12

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
294
12


Shwachman's syndrome. A review of 21 cases.
P J Aggett, N P Cavanagh, D J Matthew, J R Pincott, J Sutcliffe, J T Harries. Arch Dis Child 1980
206
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.