A citation-based method for searching scientific literature

Lydie Da Costa, Thierry Leblanc, Narla Mohandas. Blood 2020
Times Cited: 14







List of co-cited articles
38 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
256
50

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
35

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
271
28

How I treat Diamond-Blackfan anemia.
Adrianna Vlachos, Ellen Muir. Blood 2010
104
28

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
28

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
21

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
211
21

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
21


Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.
H Moniz, M Gastou, T Leblanc, C Hurtaud, A Crétien, Y Lécluse, H Raslova, J Larghero, L Croisille, M Faubladier,[...]. Cell Death Dis 2012
47
14

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
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
230
14

Calmodulin inhibitors improve erythropoiesis in Diamond-Blackfan anemia.
Alison M Taylor, Elizabeth R Macari, Iris T Chan, Megan C Blair, Sergei Doulatov, Linda T Vo, David M Raiser, Kavitha Siva, Anindita Basak, Mehdi Pirouz,[...]. Sci Transl Med 2020
8
25



Congenital dyserythropoietic anemias.
Achille Iolascon, Immacolata Andolfo, Roberta Russo. Blood 2020
15
14

Ex-vivo expansion of red blood cells: how real for transfusion in humans?
Anna Rita Migliaccio, Elena Masselli, Lilian Varricchio, Carolyn Whitsett. Blood Rev 2012
31
14

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
14


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
14

An overview of pre-ribosomal RNA processing in eukaryotes.
Anthony K Henras, Célia Plisson-Chastang, Marie-Françoise O'Donohue, Anirban Chakraborty, Pierre-Emmanuel Gleizes. Wiley Interdiscip Rev RNA 2015
290
14

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
14

How I manage children with Diamond-Blackfan anaemia.
Marije Bartels, Marc Bierings. Br J Haematol 2019
19
14

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
14

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
14

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
14


Genotype-phenotype associations in Fanconi anemia: A literature review.
Moisés O Fiesco-Roa, Neelam Giri, Lisa J McReynolds, Ana F Best, Blanche P Alter. Blood Rev 2019
45
14

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
14


Acquired and germline predisposition to bone marrow failure: Diagnostic features and clinical implications.
Michael E Kallen, Alina Dulau-Florea, Weixin Wang, Katherine R Calvo. Semin Hematol 2019
25
14

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
14

Diamond-blackfan anemia and growth status: the French registry.
S Chen, J Warszawski, B Bader-Meunier, G Tchernia, L Da Costa, I Marie, J P Dommergues. J Pediatr 2005
17
14

Growth hormone improves short stature in children with Diamond-Blackfan anemia.
Jonathan C Howell, Sarita A Joshi, Lindsey Hornung, Jane Khoury, Richard E Harris, Susan R Rose. Pediatr Blood Cancer 2015
9
22

Favorable outcomes of hematopoietic stem cell transplantation in children and adolescents with Diamond-Blackfan anemia.
Brigitte Strahm, Felicia Loewecke, Charlotte M Niemeyer, Michael Albert, Marc Ansari, Peter Bader, Yves Bertrand, Birgit Burkhardt, Lydie M Da Costa, Alina Ferster,[...]. Blood Adv 2020
6
33

Endocrine Dysfunction in Diamond-Blackfan Anemia (DBA): A Report from the DBA Registry (DBAR).
Amit Lahoti, Yael T Harris, Phyllis W Speiser, Evangelia Atsidaftos, Jeffrey M Lipton, Adrianna Vlachos. Pediatr Blood Cancer 2016
9
22

A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease?
Paola Quarello, Emanuela Garelli, Adriana Carando, Rebecca Cillario, Alfredo Brusco, Elisa Giorgio, Daniela Ferrante, Paola Corti, Marco Zecca, Matteo Luciani,[...]. Br J Haematol 2020
9
22

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
14

clusterProfiler: an R package for comparing biological themes among gene clusters.
Guangchuang Yu, Li-Gen Wang, Yanyan Han, Qing-Yu He. OMICS 2012
7

Gestational ethanol exposure disrupts the expression of FGF8 and Sonic hedgehog during limb patterning.
Kimberly Chrisman, Robert Kenney, Jeremy Comin, Tanya Thal, Lawrence Suchocki, Y Gloria Yueh, David P Gardner. Birth Defects Res A Clin Mol Teratol 2004
34
7

Effects of thalidomide on Fgf8, Bmp4 and Hoxa11 expression in the limb bud in Kbl:JW rabbit embryos.
Yoshinori Kawamura, Teruyoshi Yamashita, Toshiaki Yamauchi, Kiyoshi Matsumoto, Keiichiro Sato. Congenit Anom (Kyoto) 2014
3
33


Microtia: epidemiology and genetics.
Daniela V Luquetti, Carrie L Heike, Anne V Hing, Michael L Cunningham, Timothy C Cox. Am J Med Genet A 2012
142
7

A mutation-specific, single-arm, phase 2 study of dovitinib in patients with advanced malignancies.
Matthew H Taylor, Ajjai S Alva, Timothy Larson, Sebastian Szpakowski, Das Purkaystha, Alpesh Amin, Linda Karpiak, Sarina A Piha-Paul. Oncotarget 2020
1
100


Glucose metabolism disorder is a risk factor in ethanol exposure induced malformation in embryonic brain.
Rui-Rong Tan, Yi-Fang Li, Xiao-Tan Zhang, Yi-Hua Huang, Yan-Ping Wu, Shu-Hua Ouyang, Bun Tsoi, Ruo-Nan Yi, Xuesong Yang, Hiroshi Kurihara,[...]. Food Chem Toxicol 2013
5
20

The role of p53 in developmental syndromes.
Margot E Bowen, Laura D Attardi. J Mol Cell Biol 2019
18
7

Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemia.
K W Gripp, D M McDonald-McGinn, D La Rossa, D McGain, N Federman, A Vlachos, B E Glader, S E McKenzie, J M Lipton, E H Zackai. Am J Med Genet 2001
25
7

Synergistic Effects of FGF-2 with Insulin or IGF-I on the Proliferation of Human Auricular Chondrocytes.
Tsuguharu Takahashi, Toru Ogasawara, Junji Kishimoto, Guangyao Liu, Hirotaka Asato, Takashi Nakatsuka, Eijyu Uchinuma, Kozo Nakamura, Hiroshi Kawaguchi, Tsuyoshi Takato,[...]. Cell Transplant 2005
46
7

Pax6 organizes the anterior eye segment by guiding two distinct neural crest waves.
Masanari Takamiya, Johannes Stegmaier, Andrei Yu Kobitski, Benjamin Schott, Benjamin D Weger, Dimitra Margariti, Angel R Cereceda Delgado, Victor Gourain, Tim Scherr, Lixin Yang,[...]. PLoS Genet 2020
4
25


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.