A citation-based method for searching scientific literature

Usua Oyarbide, Jacek Topczewski, Seth J Corey. Haematologica 2019
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


A zebrafish model for the Shwachman-Diamond syndrome (SDS).
Narayanan Venkatasubramani, Alan N Mayer. Pediatr Res 2008
16
44

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
44

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
44


Severe congenital neutropenias.
Julia Skokowa, David C Dale, Ivo P Touw, Cornelia Zeidler, Karl Welte. Nat Rev Dis Primers 2017
100
33

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
33

Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects.
Nadia Danilova, Kathleen M Sakamoto, Shuo Lin. Br J Haematol 2011
66
33

Live imaging of neutrophil motility in a zebrafish model of WHIM syndrome.
Kevin B Walters, Julie M Green, Jill C Surfus, Sa Kan Yoo, Anna Huttenlocher. Blood 2010
110
33

Ribosomal protein deficiency causes Tp53-independent erythropoiesis failure in zebrafish.
Gnaneshwar V Yadav, Anirban Chakraborty, Tamayo Uechi, Naoya Kenmochi. Int J Biochem Cell Biol 2014
20
33



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
33

Deficiency of ribosomal protein S19 during early embryogenesis leads to reduction of erythrocytes in a zebrafish model of Diamond-Blackfan anemia.
Tamayo Uechi, Yukari Nakajima, Anirban Chakraborty, Hidetsugu Torihara, Sayomi Higa, Naoya Kenmochi. Hum Mol Genet 2008
76
33

Premature aging in telomerase-deficient zebrafish.
Monique Anchelin, Francisca Alcaraz-Pérez, Carlos M Martínez, Manuel Bernabé-García, Victoriano Mulero, María L Cayuela. Dis Model Mech 2013
48
33

Hematopoietic defects in rps29 mutant zebrafish depend upon p53 activation.
Alison M Taylor, Jessica M Humphries, Richard M White, Ryan D Murphey, Caroline E Burns, Leonard I Zon. Exp Hematol 2012
50
33

Ribosomopathies: human disorders of ribosome dysfunction.
Anupama Narla, Benjamin L Ebert. Blood 2010
491
33

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.
Hans Matsson, Edward J Davey, Natalia Draptchinskaia, Isao Hamaguchi, Andreas Ooka, Per Levéen, Erik Forsberg, Stefan Karlsson, Niklas Dahl. Mol Cell Biol 2004
120
33

Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis.
Julia Skokowa, Doris Steinemann, Jenny E Katsman-Kuipers, Cornelia Zeidler, Olga Klimenkova, Maksim Klimiankou, Murat Unalan, Siarhei Kandabarau, Vahagn Makaryan, Renee Beekman,[...]. Blood 2014
88
33

Loss of Sbds in zebrafish leads to neutropenia and pancreas and liver atrophy.
Usua Oyarbide, Arish N Shah, Wilmer Amaya-Mejia, Matthew Snyderman, Margaret J Kell, Daniela S Allende, Eliezer Calo, Jacek Topczewski, Seth J Corey. JCI Insight 2020
4
75

The zebrafish reference genome sequence and its relationship to the human genome.
Kerstin Howe, Matthew D Clark, Carlos F Torroja, James Torrance, Camille Berthelot, Matthieu Muffato, John E Collins, Sean Humphray, Karen McLaren, Lucy Matthews,[...]. Nature 2013
22

Reticular dysgenesis-associated AK2 protects hematopoietic stem and progenitor cell development from oxidative stress.
Alberto Rissone, Katja Gabriele Weinacht, Giancarlo la Marca, Kevin Bishop, Elisa Giocaliere, Jayashree Jagadeesh, Kerstin Felgentreff, Kerry Dobbs, Waleed Al-Herz, Marypat Jones,[...]. J Exp Med 2015
33
22

Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT Pathway.
Ana T Antunes, Yvonne J Goos, Tamara C Pereboom, Dorien Hermkens, Marcin W Wlodarski, Lydie Da Costa, Alyson W MacInnes. PLoS Genet 2015
16
22


Erythropoiesis failure due to RPS19 deficiency is independent of an activated Tp53 response in a zebrafish model of Diamond-Blackfan anaemia.
Hidetsugu Torihara, Tamayo Uechi, Anirban Chakraborty, Minori Shinya, Noriyoshi Sakai, Naoya Kenmochi. Br J Haematol 2011
47
22

A Zebrafish Model of 5q-Syndrome Using CRISPR/Cas9 Targeting RPS14 Reveals a p53-Independent and p53-Dependent Mechanism of Erythroid Failure.
Jason Ear, Jessica Hsueh, Melinda Nguyen, QingHua Zhang, Victoria Sung, Rajesh Chopra, Kathleen M Sakamoto, Shuo Lin. J Genet Genomics 2016
19
22

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
23
22

Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitors.
Sergei Doulatov, Linda T Vo, Elizabeth R Macari, Lara Wahlster, Melissa A Kinney, Alison M Taylor, Jessica Barragan, Manav Gupta, Katherine McGrath, Hsiang-Ying Lee,[...]. Sci Transl Med 2017
65
22

Transparent adult zebrafish as a tool for in vivo transplantation analysis.
Richard Mark White, Anna Sessa, Christopher Burke, Teresa Bowman, Jocelyn LeBlanc, Craig Ceol, Caitlin Bourque, Michael Dovey, Wolfram Goessling, Caroline Erter Burns,[...]. Cell Stem Cell 2008
711
22

A GCSFR/CSF3R zebrafish mutant models the persistent basal neutrophil deficiency of severe congenital neutropenia.
Vahid Pazhakh, Sharon Clark, M Cristina Keightley, Graham J Lieschke. Sci Rep 2017
17
22

Establishment of a congenital amegakaryocytic thrombocytopenia model and a thrombocyte-specific reporter line in zebrafish.
Q Lin, Y Zhang, R Zhou, Y Zheng, L Zhao, M Huang, X Zhang, A Y H Leung, W Zhang, Y Zhang. Leukemia 2017
11
22

The zebrafish granulocyte colony-stimulating factors (Gcsfs): 2 paralogous cytokines and their roles in hematopoietic development and maintenance.
David L Stachura, Ondrej Svoboda, Clyde A Campbell, Raquel Espín-Palazón, Ryan P Lau, Leonard I Zon, Petr Bartunek, David Traver. Blood 2013
67
22

Innate immune system activation in zebrafish and cellular models of Diamond Blackfan Anemia.
Nadia Danilova, Mark Wilkes, Elena Bibikova, Min-Young Youn, Kathleen M Sakamoto, Shuo Lin. Sci Rep 2018
15
22

Loss of the homologous recombination gene rad51 leads to Fanconi anemia-like symptoms in zebrafish.
Jan Gregor Botthof, Ewa Bielczyk-Maczyńska, Lauren Ferreira, Ana Cvejic. Proc Natl Acad Sci U S A 2017
14
22

Zebrafish granulocyte colony-stimulating factor receptor signaling promotes myelopoiesis and myeloid cell migration.
Clifford Liongue, Chris J Hall, Bree A O'Connell, Phil Crosier, Alister C Ward. Blood 2009
86
22

How I treat Diamond-Blackfan anemia.
Adrianna Vlachos, Ellen Muir. Blood 2010
104
22

Cross talk between TP53 and c-Myc in the pathophysiology of Diamond-Blackfan anemia: Evidence from RPL11-deficient in vivo and in vitro models.
Anirban Chakraborty, Tamayo Uechi, Yukari Nakajima, Hanna T Gazda, Marie-Françoise O'Donohue, Pierre-Emmanuel Gleizes, Naoya Kenmochi. Biochem Biophys Res Commun 2018
4
50

Analysis of WASp function during the wound inflammatory response--live-imaging studies in zebrafish larvae.
Ana Cvejic, Chris Hall, Magdalena Bak-Maier, Maria Vega Flores, Phil Crosier, Michael J Redd, Paul Martin. J Cell Sci 2008
57
22

Telomeres in aging and disease: lessons from zebrafish.
Madalena C Carneiro, Inês Pimenta de Castro, Miguel Godinho Ferreira. Dis Model Mech 2016
52
22

Modelling of human Wiskott-Aldrich syndrome protein mutants in zebrafish larvae using in vivo live imaging.
Rebecca A Jones, Yi Feng, Austen J Worth, Adrian J Thrasher, Siobhan O Burns, Paul Martin. J Cell Sci 2013
16
22


L-Leucine improves the anemia and developmental defects associated with Diamond-Blackfan anemia and del(5q) MDS by activating the mTOR pathway.
Elspeth M Payne, Maria Virgilio, Anupama Narla, Hong Sun, Michelle Levine, Barry H Paw, Nancy Berliner, A Thomas Look, Benjamin L Ebert, Arati Khanna-Gupta. Blood 2012
98
22

Mice with ribosomal protein S19 deficiency develop bone marrow failure and symptoms like patients with Diamond-Blackfan anemia.
Pekka Jaako, Johan Flygare, Karin Olsson, Ronan Quere, Mats Ehinger, Adrianna Henson, Steven Ellis, Axel Schambach, Christopher Baum, Johan Richter,[...]. Blood 2011
91
22

Many ribosomal protein genes are cancer genes in zebrafish.
Adam Amsterdam, Kirsten C Sadler, Kevin Lai, Sarah Farrington, Roderick T Bronson, Jacqueline A Lees, Nancy Hopkins. PLoS Biol 2004
321
22

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
22

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
22

Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.
Rajiv K Khajuria, Mathias Munschauer, Jacob C Ulirsch, Claudia Fiorini, Leif S Ludwig, Sean K McFarland, Nour J Abdulhay, Harrison Specht, Hasmik Keshishian, D R Mani,[...]. Cell 2018
143
22


HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
Christoph Klein, Magda Grudzien, Giridharan Appaswamy, Manuela Germeshausen, Inga Sandrock, Alejandro A Schäffer, Chozhavendan Rathinam, Kaan Boztug, Beate Schwinzer, Nima Rezaei,[...]. Nat Genet 2007
312
22

Gene correction of HAX1 reversed Kostmann disease phenotype in patient-specific induced pluripotent stem cells.
Erik Pittermann, Nico Lachmann, Glenn MacLean, Stephan Emmrich, Mania Ackermann, Gudrun Göhring, Brigitte Schlegelberger, Karl Welte, Axel Schambach, Dirk Heckl,[...]. Blood Adv 2017
12
22

Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy.
Philip S Rosenberg, Cornelia Zeidler, Audrey A Bolyard, Blanche P Alter, Mary A Bonilla, Laurence A Boxer, Yigal Dror, Sally Kinsey, Daniel C Link, Peter E Newburger,[...]. Br J Haematol 2010
128
22


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.