A citation-based method for searching scientific literature

Adrianna Vlachos, Philip S Rosenberg, Eva Atsidaftos, Blanche P Alter, Jeffrey M Lipton. Blood 2012
Times Cited: 171







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



Times Cited
  Times     Co-cited
Similarity


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
249
43

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
277
34

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
595
33

How I treat Diamond-Blackfan anemia.
Adrianna Vlachos, Ellen Muir. Blood 2010
99
27

Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia.
Vijay G Sankaran, Roxanne Ghazvinian, Ron Do, Prathapan Thiru, Jo-Anne Vergilio, Alan H Beggs, Colin A Sieff, Stuart H Orkin, David G Nathan, Eric S Lander,[...]. J Clin Invest 2012
208
25

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
74
33


Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia.
Hanna T Gazda, Milena Preti, Mee Rie Sheen, Marie-Françoise O'Donohue, Adrianna Vlachos, Stella M Davies, Antonis Kattamis, Leana Doherty, Michael Landowski, Christopher Buros,[...]. Hum Mutat 2012
105
21

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
259
20

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
59
32

Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.
Blanche P Alter, Neelam Giri, Sharon A Savage, June A Peters, Jennifer T Loud, Lisa Leathwood, Ann G Carr, Mark H Greene, Philip S Rosenberg. Br J Haematol 2010
195
18

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
157
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
26


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
148
17

Recommendations on hematopoietic stem cell transplantation for inherited bone marrow failure syndromes.
R Peffault de Latour, C Peters, B Gibson, B Strahm, A Lankester, C D de Heredia, D Longoni, F Fioredda, F Locatelli, I Yaniv,[...]. Bone Marrow Transplant 2015
43
39

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
33
51

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
16

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
169
16

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
158
16

Haematopoietic stem cell transplantation for Diamond Blackfan anaemia: a report from the Italian Association of Paediatric Haematology and Oncology Registry.
Franca Fagioli, Paola Quarello, Marco Zecca, Edoardo Lanino, Paola Corti, Claudio Favre, Mimmo Ripaldi, Ugo Ramenghi, Franco Locatelli, Arcangelo Prete. Br J Haematol 2014
31
51

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
94
17

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
29

Erythrocyte adenosine deaminase: diagnostic value for Diamond-Blackfan anaemia.
John H Fargo, Christian P Kratz, Neelam Giri, Sharon A Savage, Carolyn Wong, Karen Backer, Blanche P Alter, Bertil Glader. Br J Haematol 2013
44
34

Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
288
15

Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia.
Michael Landowski, Marie-Françoise O'Donohue, Christopher Buros, Roxanne Ghazvinian, Nathalie Montel-Lehry, Adrianna Vlachos, Colin A Sieff, Peter E Newburger, Edyta Niewiadomska, Michal Matysiak,[...]. Hum Genet 2013
75
20

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
76
19

Ribosomopathies: human disorders of ribosome dysfunction.
Anupama Narla, Benjamin L Ebert. Blood 2010
479
14

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
626
14


Ribosomal protein gene deletions in Diamond-Blackfan anemia.
Jason E Farrar, Adrianna Vlachos, Eva Atsidaftos, Hannah Carlson-Donohoe, Thomas C Markello, Robert J Arceci, Steven R Ellis, Jeffrey M Lipton, David M Bodine. Blood 2011
91
15

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
13

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
70
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
12

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
16

Role of ribosomal protein mutations in tumor development (Review).
Kaveh M Goudarzi, Mikael S Lindström. Int J Oncol 2016
74
16

Exploiting pre-rRNA processing in Diamond Blackfan anemia gene discovery and diagnosis.
Jason E Farrar, Paola Quarello, Ross Fisher, Kelly A O'Brien, Anna Aspesi, Sara Parrella, Adrianna L Henson, Nancy E Seidel, Eva Atsidaftos, Supraja Prakash,[...]. Am J Hematol 2014
36
33

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
15

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
458
12

The ribosomal protein gene RPL5 is a haploinsufficient tumor suppressor in multiple cancer types.
Laura Fancello, Kim R Kampen, Isabel J F Hofman, Jelle Verbeeck, Kim De Keersmaecker. Oncotarget 2017
47
25

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
36

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
130
12

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
260
11

Hematopoietic stem cell transplantation for Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry.
A Vlachos, N Federman, C Reyes-Haley, J Abramson, J M Lipton. Bone Marrow Transplant 2001
60
18

Severe iron overload in Blackfan-Diamond anemia: a case-control study.
Simona Roggero, Paola Quarello, Tiziana Vinciguerra, Filomena Longo, Antonio Piga, Ugo Ramenghi. Am J Hematol 2009
33
33

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
50
22

Diamond-Blackfan anemia: diagnosis, treatment, and molecular pathogenesis.
Jeffrey M Lipton, Steven R Ellis. Hematol Oncol Clin North Am 2009
103
11


Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations.
Paola Quarello, Emanuela Garelli, Adriana Carando, Alfredo Brusco, Roberto Calabrese, Carlo Dufour, Daniela Longoni, Aldo Misuraca, Luciana Vinti, Anna Aspesi,[...]. Haematologica 2010
54
18

Fanconi anemia and the development of leukemia.
Blanche P Alter. Best Pract Res Clin Haematol 2014
94
10


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.