A citation-based method for searching scientific literature

Getabalew Engidaye, Mulugeta Melku, Bamlaku Enawgaw. EJIFCC 2019
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


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
45

An update on the pathogenesis and diagnosis of Diamond-Blackfan anemia.
Lydie Da Costa, Anupama Narla, Narla Mohandas. F1000Res 2018
38
45

Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.
Adrianna Vlachos, Sarah Ball, Niklas Dahl, Blanche P Alter, Sujit Sheth, Ugo Ramenghi, Joerg Meerpohl, Stefan Karlsson, Johnson M Liu, Thierry Leblanc,[...]. Br J Haematol 2008
256
45

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
45

How I treat Diamond-Blackfan anemia.
Adrianna Vlachos, Ellen Muir. Blood 2010
104
36

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
36

RPS19 mutations in patients with Diamond-Blackfan anemia.
Maria Francesca Campagnoli, Ugo Ramenghi, Marta Armiraglio, Paola Quarello, Emanuela Garelli, Adriana Carando, Federica Avondo, Elisa Pavesi, Sébastien Fribourg, Pierre-Emmanuel Gleizes,[...]. Hum Mutat 2008
75
36

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
27

Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience.
Lydie Da Costa, Marie-Françoise O'Donohue, Birgit van Dooijeweert, Katarzyna Albrecht, Sule Unal, Ugo Ramenghi, Thierry Leblanc, Irma Dianzani, Hannah Tamary, Marije Bartels,[...]. Eur J Med Genet 2018
33
27

Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature.
Maria Francesca Campagnoli, Emanuela Garelli, Paola Quarello, Adriana Carando, Stefania Varotto, Bruno Nobili, Daniela Longoni, Vanna Pecile, Marco Zecca, Carlo Dufour,[...]. Haematologica 2004
76
27

Target enrichment and high-throughput sequencing of 80 ribosomal protein genes to identify mutations associated with Diamond-Blackfan anaemia.
Gareth Gerrard, Mikel Valgañón, Hui En Foong, Dalia Kasperaviciute, Deena Iskander, Laurence Game, Michael Müller, Timothy J Aitman, Irene Roberts, Josu de la Fuente,[...]. Br J Haematol 2013
34
27

The Genetic Landscape of Diamond-Blackfan Anemia.
Jacob C Ulirsch, Jeffrey M Verboon, Shideh Kazerounian, Michael H Guo, Daniel Yuan, Leif S Ludwig, Robert E Handsaker, Nour J Abdulhay, Claudia Fiorini, Giulio Genovese,[...]. Am J Hum Genet 2019
9
33

Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression.
T N Willig, N Draptchinskaia, I Dianzani, S Ball, C Niemeyer, U Ramenghi, K Orfali, P Gustavsson, E Garelli, A Brusco,[...]. Blood 1999
152
27

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
27

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
27

Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation.
Lisa Mirabello, Payal P Khincha, Steven R Ellis, Neelam Giri, Seth Brodie, Settara C Chandrasekharappa, Frank X Donovan, Weiyin Zhou, Belynda D Hicks, Joseph F Boland,[...]. J Med Genet 2017
55
27

Increased risk of colon cancer and osteogenic sarcoma in Diamond-Blackfan anemia.
Adrianna Vlachos, Philip S Rosenberg, Eva Atsidaftos, Jessica Kang, Kenan Onel, Ravi N Sharaf, Blanche P Alter, Jeffrey M Lipton. Blood 2018
36
27

The ribosomal basis of Diamond-Blackfan Anemia: mutation and database update.
Ilenia Boria, Emanuela Garelli, Hanna T Gazda, Anna Aspesi, Paola Quarello, Elisa Pavesi, Daniela Ferrante, Joerg J Meerpohl, Mutlu Kartal, Lydie Da Costa,[...]. Hum Mutat 2010
150
27

Diamond-Blackfan anemia: diagnosis, treatment, and molecular pathogenesis.
Jeffrey M Lipton, Steven R Ellis. Hematol Oncol Clin North Am 2009
106
27


The Genetic Landscape of Diamond-Blackfan Anemia.
Jacob C Ulirsch, Jeffrey M Verboon, Shideh Kazerounian, Michael H Guo, Daniel Yuan, Leif S Ludwig, Robert E Handsaker, Nour J Abdulhay, Claudia Fiorini, Giulio Genovese,[...]. Am J Hum Genet 2018
85
27

Severe congenital neutropenias.
Julia Skokowa, David C Dale, Ivo P Touw, Cornelia Zeidler, Karl Welte. Nat Rev Dis Primers 2017
100
18

Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.
RuNan Wang, Kenichi Yoshida, Tsutomu Toki, Takafumi Sawada, Tamayo Uechi, Yusuke Okuno, Aiko Sato-Otsubo, Kazuko Kudo, Isamu Kamimaki, Rika Kanezaki,[...]. Br J Haematol 2015
61
18

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
18

Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families.
Lisa Mirabello, Elizabeth R Macari, Lea Jessop, Steven R Ellis, Timothy Myers, Neelam Giri, Alison M Taylor, Katherine E McGrath, Jessica M Humphries, Bari J Ballew,[...]. Blood 2014
64
18



How I manage children with Diamond-Blackfan anaemia.
Marije Bartels, Marc Bierings. Br J Haematol 2019
19
18

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
18

Untangling the phenotypic heterogeneity of Diamond Blackfan anemia.
Jason E Farrar, Niklas Dahl. Semin Hematol 2011
32
18

Cancer Biogenesis in Ribosomopathies.
Sergey O Sulima, Kim R Kampen, Kim De Keersmaecker. Cells 2019
24
18

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
62
18

Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia.
Jason E Farrar, Michelle Nater, Emi Caywood, Michael A McDevitt, Jeanne Kowalski, Clifford M Takemoto, C Conover Talbot, Paul Meltzer, Diane Esposito, Alan H Beggs,[...]. Blood 2008
171
18

The genetics of dyskeratosis congenita.
Philip J Mason, Monica Bessler. Cancer Genet 2011
88
18

Identification of mutations in the ribosomal protein L5 (RPL5) and ribosomal protein L11 (RPL11) genes in Czech patients with Diamond-Blackfan anemia.
Radek Cmejla, Jana Cmejlova, Helena Handrkova, Jiri Petrak, Kvetoslava Petrtylova, Vladimir Mihal, Jan Stary, Zdena Cerna, Yahia Jabali, Dagmar Pospisilova. Hum Mutat 2009
73
18

Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations.
Ram Ajore, David Raiser, Marie McConkey, Magnus Jöud, Bernd Boidol, Brenton Mar, Gordon Saksena, David M Weinstock, Scott Armstrong, Steven R Ellis,[...]. EMBO Mol Med 2017
52
18

The Czech National Diamond-Blackfan Anemia Registry: clinical data and ribosomal protein mutations update.
Dagmar Pospisilova, Jana Cmejlova, Barbora Ludikova, Jan Stary, Zdena Cerna, Jiri Hak, Pavel Timr, Kvetoslava Petrtylova, Jan Blatny, Samuel Vokurka,[...]. Blood Cells Mol Dis 2012
18
18

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
18

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
18

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
18

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
18


RNA and protein evidence for haplo-insufficiency in Diamond-Blackfan anaemia patients with RPS19 mutations.
Hanna T Gazda, Rong Zhong, Lilia Long, Edyta Niewiadomska, Jeffrey M Lipton, Anna Ploszynska, Jan M Zaucha, Adrianna Vlachos, Evangelia Atsidaftos, David H Viskochil,[...]. Br J Haematol 2004
84
18


Mutations in the ribosomal protein genes in Japanese patients with Diamond-Blackfan anemia.
Yuki Konno, Tsutomu Toki, Satoru Tandai, Gang Xu, Runan Wang, Kiminori Terui, Shouichi Ohga, Toshiro Hara, Asahito Hama, Seiji Kojima,[...]. Haematologica 2010
31
18


Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implications.
Wei Wang, Subhasree Nag, Xu Zhang, Ming-Hai Wang, Hui Wang, Jianwei Zhou, Ruiwen Zhang. Med Res Rev 2015
98
18


Clinical and laboratory evidence for a trilineage haematopoietic defect in patients with refractory Diamond-Blackfan anaemia.
N Giri, E Kang, J F Tisdale, D Follman, M Rivera, G N Schwartz, S Kim, N S Young, M E Rick, C E Dunbar. Br J Haematol 2000
58
18

Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia.
Leana Doherty, Mee Rie Sheen, Adrianna Vlachos, Valerie Choesmel, Marie-Françoise O'Donohue, Catherine Clinton, Hal E Schneider, Colin A Sieff, Peter E Newburger, Sarah E Ball,[...]. Am J Hum Genet 2010
162
18


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.