A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
25

The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.
Daniel A Arber, Attilio Orazi, Robert Hasserjian, Jürgen Thiele, Michael J Borowitz, Michelle M Le Beau, Clara D Bloomfield, Mario Cazzola, James W Vardiman. Blood 2016
25

Fanconi anemia and the development of leukemia.
Blanche P Alter. Best Pract Res Clin Haematol 2014
97
22

Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.
Siobán B Keel, Angela Scott, Marilyn Sanchez-Bonilla, Phoenix A Ho, Suleyman Gulsuner, Colin C Pritchard, Janis L Abkowitz, Mary-Claire King, Tom Walsh, Akiko Shimamura. Haematologica 2016
59
19

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
19

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
16



Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms.
Chantana Polprasert, Isabell Schulze, Mikkael A Sekeres, Hideki Makishima, Bartlomiej Przychodzen, Naoko Hosono, Jarnail Singh, Richard A Padgett, Xiaorong Gu, James G Phillips,[...]. Cancer Cell 2015
185
16


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

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

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
12

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
12

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions.
Samuel Quentin, Wendy Cuccuini, Raphael Ceccaldi, Olivier Nibourel, Corinne Pondarre, Marie-Pierre Pagès, Nadia Vasquez, Catherine Dubois d'Enghien, Jérôme Larghero, Régis Peffault de Latour,[...]. Blood 2011
108
12

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
202
12

Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells.
Raphael Ceccaldi, Kalindi Parmar, Enguerran Mouly, Marc Delord, Jung Min Kim, Marie Regairaz, Marika Pla, Nadia Vasquez, Qing-Shuo Zhang, Corinne Pondarre,[...]. Cell Stem Cell 2012
194
12

The Fanconi anaemia pathway: new players and new functions.
Raphael Ceccaldi, Prabha Sarangi, Alan D D'Andrea. Nat Rev Mol Cell Biol 2016
341
12

How I treat acquired aplastic anemia.
Andrea Bacigalupo. Blood 2017
142
12

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
12

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.
Maya Lewinsohn, Anna L Brown, Luke M Weinel, Connie Phung, George Rafidi, Ming K Lee, Andreas W Schreiber, Jinghua Feng, Milena Babic, Chan-Eng Chong,[...]. Blood 2016
99
12

Donor cell leukemia arising from preleukemic clones with a novel germline DDX41 mutation after allogenic hematopoietic stem cell transplantation.
S Kobayashi, A Kobayashi, Y Osawa, S Nagao, K Takano, Y Okada, N Tachi, M Teramoto, T Kawamura, T Horiuchi,[...]. Leukemia 2017
33
12

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms.
Bianca Tesi, Josef Davidsson, Matthias Voss, Elisa Rahikkala, Tim D Holmes, Samuel C C Chiang, Jonna Komulainen-Ebrahim, Sorina Gorcenco, Alexandra Rundberg Nilsson, Tim Ripperger,[...]. Blood 2017
86
12

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents.
Marcin W Wlodarski, Shinsuke Hirabayashi, Victor Pastor, Jan Starý, Henrik Hasle, Riccardo Masetti, Michael Dworzak, Markus Schmugge, Marry van den Heuvel-Eibrink, Marek Ussowicz,[...]. Blood 2016
174
12

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.
Satoshi Narumi, Naoko Amano, Tomohiro Ishii, Noriyuki Katsumata, Koji Muroya, Masanori Adachi, Katsuaki Toyoshima, Yukichi Tanaka, Ryuji Fukuzawa, Kenichi Miyako,[...]. Nat Genet 2016
129
12

Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L.
Dong-Hui Chen, Jennifer E Below, Akiko Shimamura, Sioban B Keel, Mark Matsushita, John Wolff, Youngmee Sul, Emily Bonkowski, Maria Castella, Toshiyasu Taniguchi,[...]. Am J Hum Genet 2016
77
12

The genomics of inherited bone marrow failure: from mechanism to the clinic.
Talia Wegman-Ostrosky, Sharon A Savage. Br J Haematol 2017
57
12

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
12


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
16

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
9

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
9

Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia.
Hiroki Yamaguchi, Rodrigo T Calado, Hinh Ly, Sachiko Kajigaya, Gabriela M Baerlocher, Stephen J Chanock, Peter M Lansdorp, Neal S Young. N Engl J Med 2005
486
9

Bone marrow failure and the telomeropathies.
Danielle M Townsley, Bogdan Dumitriu, Neal S Young. Blood 2014
151
9

Diagnosis of myelodysplastic syndrome among a cohort of 119 patients with fanconi anemia: morphologic and cytogenetic characteristics.
Adina M Cioc, John E Wagner, Margaret L MacMillan, Todd DeFor, Betsy Hirsch. Am J Clin Pathol 2010
54
9

The genetics of dyskeratosis congenita.
Philip J Mason, Monica Bessler. Cancer Genet 2011
88
9

Allogeneic hematopoietic stem cell transplantation in Fanconi anemia: the European Group for Blood and Marrow Transplantation experience.
Régis Peffault de Latour, Raphael Porcher, Jean-Hugues Dalle, Mahmoud Aljurf, Elisabeth T Korthof, Johanna Svahn, Roelof Willemze, Cristina Barrenetxea, Valerie Mialou, Jean Soulier,[...]. Blood 2013
110
9

How I manage patients with Fanconi anaemia.
Carlo Dufour. Br J Haematol 2017
26
11

Fanconi anemia: a model disease for studies on human genetics and advanced therapeutics.
Massimo Bogliolo, Jordi Surrallés. Curr Opin Genet Dev 2015
117
9

TNF-alpha and IFN-gamma are overexpressed in the bone marrow of Fanconi anemia patients and TNF-alpha suppresses erythropoiesis in vitro.
Carlo Dufour, Anna Corcione, Johanna Svahn, Riccardo Haupt, Vincenzo Poggi, Albert Nandor Béka'ssy, Rosanna Scimè, Angela Pistorio, Vito Pistoia. Blood 2003
174
9

Current concepts in the pathophysiology and treatment of aplastic anemia.
Neal S Young, Rodrigo T Calado, Phillip Scheinberg. Blood 2006
548
9

Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia.
Tetsuichi Yoshizato, Bogdan Dumitriu, Kohei Hosokawa, Hideki Makishima, Kenichi Yoshida, Danielle Townsley, Aiko Sato-Otsubo, Yusuke Sato, Delong Liu, Hiromichi Suzuki,[...]. N Engl J Med 2015
319
9

Outcome of aplastic anaemia in children. A study by the severe aplastic anaemia and paediatric disease working parties of the European group blood and bone marrow transplant.
Carlo Dufour, Marta Pillon, Gerard Sociè, Alicia Rovò, Elisa Carraro, Andrea Bacigalupo, Rosi Oneto, Jakob Passweg, Antonio Risitano, Andrè Tichelli,[...]. Br J Haematol 2015
64
9



GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome.
Amy P Hsu, Kirby D Johnson, E Liana Falcone, Rajendran Sanalkumar, Lauren Sanchez, Dennis D Hickstein, Jennifer Cuellar-Rodriguez, Jacob E Lemieux, Christa S Zerbe, Emery H Bresnick,[...]. Blood 2013
150
9

Eltrombopag Added to Standard Immunosuppression for Aplastic Anemia.
Danielle M Townsley, Phillip Scheinberg, Thomas Winkler, Ronan Desmond, Bogdan Dumitriu, Olga Rios, Barbara Weinstein, Janet Valdez, Jennifer Lotter, Xingmin Feng,[...]. N Engl J Med 2017
215
9

Association of telomere length of peripheral blood leukocytes with hematopoietic relapse, malignant transformation, and survival in severe aplastic anemia.
Phillip Scheinberg, James N Cooper, Elaine M Sloand, Colin O Wu, Rodrigo T Calado, Neal S Young. JAMA 2010
137
9

GATA2 deficiency and related myeloid neoplasms.
Marcin W Wlodarski, Matthew Collin, Marshall S Horwitz. Semin Hematol 2017
67
9

Outcome of haematopoietic stem cell transplantation in dyskeratosis congenita.
Francesca Fioredda, Simona Iacobelli, Elisabeth T Korthof, Cora Knol, Anja van Biezen, Dorine Bresters, Paul Veys, Ayami Yoshimi, Franca Fagioli, Brune Mats,[...]. Br J Haematol 2018
27
11


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.