A citation-based method for searching scientific literature

Santhosh Dhanraj, Anna Matveev, Hongbing Li, Supanun Lauhasurayotin, Lawrence Jardine, Michaela Cada, Bozana Zlateska, Chetankumar S Tailor, Joseph Zhou, Roberto Mendoza-Londono, Ajoy Vincent, Peter R Durie, Stephen W Scherer, Johanna M Rommens, Elise Heon, Yigal Dror. Blood 2017
Times Cited: 62







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



Times Cited
  Times     Co-cited
Similarity


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
59
69

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
467
53

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
70
50

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
42
69

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
72
30

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
106
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
178
27

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
225
25


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
20

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
332
20

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
69
20

Defective ribosome assembly in Shwachman-Diamond syndrome.
Chi C Wong, David Traynor, Nicolas Basse, Robert R Kay, Alan J Warren. Blood 2011
100
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
58
18

THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION.
H SHWACHMAN, L K DIAMOND, F A OSKI, K T KHAW. J Pediatr 1964
367
17

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome.
Christine Bellanné-Chantelot, Barbara Schmaltz-Panneau, Caroline Marty, Odile Fenneteau, Isabelle Callebaut, Séverine Clauin, Aurélie Docet, Gandhi-Laurent Damaj, Thierry Leblanc, Isabelle Pellier,[...]. Blood 2018
46
21

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
149
14

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
16

GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity.
Michael A Spinner, Lauren A Sanchez, Amy P Hsu, Pamela A Shaw, Christa S Zerbe, Katherine R Calvo, Diane C Arthur, Wenjuan Gu, Christine M Gould, Carmen C Brewer,[...]. Blood 2014
378
14

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
13
69

EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome.
Shengjiang Tan, Laëtitia Kermasson, Angela Hoslin, Pekka Jaako, Alexandre Faille, Abraham Acevedo-Arozena, Etienne Lengline, Dana Ranta, Maryline Poirée, Odile Fenneteau,[...]. Blood 2019
19
47

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
34
23

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
74
12

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
601
12

Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry.
Adrianna Vlachos, Philip S Rosenberg, Eva Atsidaftos, Blanche P Alter, Jeffrey M Lipton. Blood 2012
175
12

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
86
12

Altered translation of GATA1 in Diamond-Blackfan anemia.
Leif S Ludwig, Hanna T Gazda, Jennifer C Eng, Stephen W Eichhorn, Prathapan Thiru, Roxanne Ghazvinian, Tracy I George, Jason R Gotlib, Alan H Beggs, Colin A Sieff,[...]. Nat Med 2014
165
12

A landscape of germ line mutations in a cohort of inherited bone marrow failure patients.
Olivier Bluteau, Marie Sebert, Thierry Leblanc, Régis Peffault de Latour, Samuel Quentin, Elodie Lainey, Lucie Hernandez, Jean-Hugues Dalle, Flore Sicre de Fontbrune, Etienne Lengline,[...]. Blood 2018
119
12

Comparative analysis of Shwachman-Diamond syndrome to other inherited bone marrow failure syndromes and genotype-phenotype correlation.
S K Hashmi, C Allen, R Klaassen, C V Fernandez, R Yanofsky, E Shereck, J Champagne, M Silva, J H Lipton, J Brossard,[...]. Clin Genet 2011
29
27

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
34
23

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
11

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
11

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
11

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
18

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
75
11

Evaluation of energy metabolism and calcium homeostasis in cells affected by Shwachman-Diamond syndrome.
Silvia Ravera, Carlo Dufour, Simone Cesaro, Roberta Bottega, Michela Faleschini, Paola Cuccarolo, Fabio Corsolini, Cesare Usai, Marta Columbaro, Marco Cipolli,[...]. Sci Rep 2016
25
28


Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Haematologica 2018
106
11

Further evidence for the involvement of EFL1 in a Shwachman-Diamond-like syndrome and expansion of the phenotypic features.
Queenie K-G Tan, Heidi Cope, Rebecca C Spillmann, Nicholas Stong, Yong-Hui Jiang, Marie T McDonald, Jennifer A Rothman, Megan W Butler, Donald P Frush, Ralph S Lachman,[...]. Cold Spring Harb Mol Case Stud 2018
13
53

Marrow failure: a window into ribosome biology.
Davide Ruggero, Akiko Shimamura. Blood 2014
67
9

Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.
S Goobie, M Popovic, J Morrison, L Ellis, H Ginzberg, G R Boocock, N Ehtesham, C Bétard, C G Brewer, N M Roslin,[...]. Am J Hum Genet 2001
85
9

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
33

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
285
9

Impaired ribosomal subunit association in Shwachman-Diamond syndrome.
Nicholas Burwick, Scott A Coats, Tomoka Nakamura, Akiko Shimamura. Blood 2012
50
12

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
636
9

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
35

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
9

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
40
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
86
9

Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
292
9


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.