A citation-based method for searching scientific literature

Lisa J McReynolds, Sharon A Savage. Hematology Am Soc Hematol Educ Program 2017
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
57

Age-related clonal hematopoiesis associated with adverse outcomes.
Siddhartha Jaiswal, Pierre Fontanillas, Jason Flannick, Alisa Manning, Peter V Grauman, Brenton G Mar, R Coleman Lindsley, Craig H Mermel, Noel Burtt, Alejandro Chavez,[...]. N Engl J Med 2014
42

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
42

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

Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence.
Giulio Genovese, Anna K Kähler, Robert E Handsaker, Johan Lindberg, Samuel A Rose, Samuel F Bakhoum, Kimberly Chambert, Eran Mick, Benjamin M Neale, Menachem Fromer,[...]. N Engl J Med 2014
28

The genetics of myelodysplastic syndrome: from clonal haematopoiesis to secondary leukaemia.
Adam S Sperling, Christopher J Gibson, Benjamin L Ebert. Nat Rev Cancer 2017
287
28

Lenalidomide induces ubiquitination and degradation of CK1α in del(5q) MDS.
Jan Krönke, Emma C Fink, Paul W Hollenbach, Kyle J MacBeth, Slater N Hurst, Namrata D Udeshi, Philip P Chamberlain, D R Mani, Hon Wah Man, Anita K Gandhi,[...]. Nature 2015
409
28

Revertant somatic mosaicism by mitotic recombination in dyskeratosis congenita.
Marjolijn C J Jongmans, Eugene T P Verwiel, Yvonne Heijdra, Tom Vulliamy, Eveline J Kamping, Jayne Y Hehir-Kwa, Ernie M H F Bongers, Rolph Pfundt, Liesbeth van Emst, Frank N van Leeuwen,[...]. Am J Hum Genet 2012
69
28

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
28

RUNX1 Mutations in Inherited and Sporadic Leukemia.
Dana C Bellissimo, Nancy A Speck. Front Cell Dev Biol 2017
35
28

Germline Genetic Predisposition to Hematologic Malignancy.
Elissa Furutani, Akiko Shimamura. J Clin Oncol 2017
39
28

Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity.
Michael Y Zhang, Siobán B Keel, Tom Walsh, Ming K Lee, Suleyman Gulsuner, Amanda C Watts, Colin C Pritchard, Stephen J Salipante, Michael R Jeng, Inga Hofmann,[...]. Haematologica 2015
71
28

Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia.
Federica Melazzini, Flavia Palombo, Alessandra Balduini, Daniela De Rocco, Caterina Marconi, Patrizia Noris, Chiara Gnan, Tommaso Pippucci, Valeria Bozzi, Michela Faleschini,[...]. Haematologica 2016
51
28

Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions.
Christopher C Porter, Todd E Druley, Ayelet Erez, Roland P Kuiper, Kenan Onel, Joshua D Schiffman, Kami Wolfe Schneider, Sarah R Scollon, Hamish S Scott, Louise C Strong,[...]. Clin Cancer Res 2017
44
28

Somatic mosaicism in Fanconi anemia: evidence of genotypic reversion in lymphohematopoietic stem cells.
J J Gregory, J E Wagner, P C Verlander, O Levran, S D Batish, C R Eide, A Steffenhagen, B Hirsch, A D Auerbach. Proc Natl Acad Sci U S A 2001
142
28

Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study.
Takaya Moriyama, Monika L Metzger, Gang Wu, Rina Nishii, Maoxiang Qian, Meenakshi Devidas, Wenjian Yang, Cheng Cheng, Xueyuan Cao, Emily Quinn,[...]. Lancet Oncol 2015
97
28

Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7.
Victor B Pastor, Sushree S Sahoo, Jessica Boklan, Georg C Schwabe, Ebru Saribeyoglu, Brigitte Strahm, Dirk Lebrecht, Matthias Voss, Yenan T Bryceson, Miriam Erlacher,[...]. Haematologica 2018
49
28

Fanconi anemia and the development of leukemia.
Blanche P Alter. Best Pract Res Clin Haematol 2014
97
28

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
28

Bone marrow pathologic abnormalities in familial platelet disorder with propensity for myeloid malignancy and germline RUNX1 mutation.
Rashmi Kanagal-Shamanna, Sanam Loghavi, Courtney D DiNardo, L Jeffrey Medeiros, Guillermo Garcia-Manero, Elias Jabbour, Mark J Routbort, Rajyalakshmi Luthra, Carlos E Bueso-Ramos, Joseph D Khoury. Haematologica 2017
32
28

Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome.
Christian P Kratz, Maria Isabel Achatz, Laurence Brugières, Thierry Frebourg, Judy E Garber, Mary-Louise C Greer, Jordan R Hansford, Katherine A Janeway, Wendy K Kohlmann, Rose McGee,[...]. Clin Cancer Res 2017
202
28

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
28

Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort.
Phuong L Mai, Ana F Best, June A Peters, Rosamma M DeCastro, Payal P Khincha, Jennifer T Loud, Renée C Bremer, Philip S Rosenberg, Sharon A Savage. Cancer 2016
193
28

GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity.
Michael A Spinner, Lauren A Sanchez, Amy P Hsu, Pamela A Shaw, Christa S Zerbe, Katherine R Calvo, Diane C Arthur, Wenjuan Gu, Christine M Gould, Carmen C Brewer,[...]. Blood 2014
378
28

Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy.
Michael Y Zhang, Jane E Churpek, Siobán B Keel, Tom Walsh, Ming K Lee, Keith R Loeb, Suleyman Gulsuner, Colin C Pritchard, Marilyn Sanchez-Bonilla, Jeffrey J Delrow,[...]. Nat Genet 2015
200
28

Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia.
Leila Noetzli, Richard W Lo, Alisa B Lee-Sherick, Michael Callaghan, Patrizia Noris, Anna Savoia, Madhvi Rajpurkar, Kenneth Jones, Katherine Gowan, Carlo Balduini,[...]. Nat Genet 2015
159
28

The genomic landscape of pediatric myelodysplastic syndromes.
Jason R Schwartz, Jing Ma, Tamara Lamprecht, Michael Walsh, Shuoguo Wang, Victoria Bryant, Guangchun Song, Gang Wu, John Easton, Chimene Kesserwan,[...]. Nat Commun 2017
61
28


Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia.
Sabine Topka, Joseph Vijai, Michael F Walsh, Lauren Jacobs, Ann Maria, Danylo Villano, Pragna Gaddam, Gang Wu, Rose B McGee, Emily Quinn,[...]. PLoS Genet 2015
80
28

Germline variants in ETV6 underlie reduced platelet formation, platelet dysfunction and increased levels of circulating CD34+ progenitors.
Marjorie Poggi, Matthias Canault, Marie Favier, Ernest Turro, Paul Saultier, Dorsaf Ghalloussi, Veronique Baccini, Lea Vidal, Anna Mezzapesa, Nadjim Chelghoum,[...]. Haematologica 2017
43
28

Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
292
28

Monosomy 7 in Pediatric Myelodysplastic Syndromes.
Marcin W Wlodarski, Sushree S Sahoo, Charlotte M Niemeyer. Hematol Oncol Clin North Am 2018
9
28


Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans.
Federica Buonocore, Peter Kühnen, Jenifer P Suntharalingham, Ignacio Del Valle, Martin Digweed, Harald Stachelscheid, Noushafarin Khajavi, Mohammed Didi, Angela F Brady, Oliver Blankenstein,[...]. J Clin Invest 2017
72
28

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
28

Hematopoietic cell transplantation in Fanconi anemia: current evidence, challenges and recommendations.
Christen L Ebens, Margaret L MacMillan, John E Wagner. Expert Rev Hematol 2017
41
28


How I treat MDS and AML in Fanconi anemia.
Régis Peffault de Latour, Jean Soulier. Blood 2016
37
28

Cancer predisposition syndromes associated with myeloid malignancy.
Emily Quinn, Kim E Nichols. Semin Hematol 2017
5
40

Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome.
Polina Stepensky, Montserrat Chacón-Flores, Katherine H Kim, Omar Abuzaitoun, Arnulfo Bautista-Santos, Natalia Simanovsky, Dritan Siliqi, Davide Altamura, Alfonso Méndez-Godoy, Abril Gijsbers,[...]. J Med Genet 2017
59
28

Inherited TP53 Mutations and the Li-Fraumeni Syndrome.
Tanya Guha, David Malkin. Cold Spring Harb Perspect Med 2017
66
28

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
28


The 'Shp'ing news: SH2 domain-containing tyrosine phosphatases in cell signaling.
Benjamin G Neel, Haihua Gu, Lily Pao. Trends Biochem Sci 2003
849
28

Germline Mutations in Predisposition Genes in Pediatric Cancer.
Jinghui Zhang, Michael F Walsh, Gang Wu, Michael N Edmonson, Tanja A Gruber, John Easton, Dale Hedges, Xiaotu Ma, Xin Zhou, Donald A Yergeau,[...]. N Engl J Med 2015
539
28


High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.
Claude Preudhomme, Aline Renneville, Violaine Bourdon, Nathalie Philippe, Catherine Roche-Lestienne, Nicolas Boissel, Nathalie Dhedin, Jean-Marie André, Pascale Cornillet-Lefebvre, André Baruchel,[...]. Blood 2009
123
28

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
W J Song, M G Sullivan, R D Legare, S Hutchings, X Tan, D Kufrin, J Ratajczak, I C Resende, C Haworth, R Hock,[...]. Nat Genet 1999
789
28

Loss of Runx1 perturbs adult hematopoiesis and is associated with a myeloproliferative phenotype.
Joseph D Growney, Hirokazu Shigematsu, Zhe Li, Benjamin H Lee, Jennifer Adelsperger, Rebecca Rowan, David P Curley, Jeffery L Kutok, Koichi Akashi, Ifor R Williams,[...]. Blood 2005
341
28

Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation.
Marjolijn C J Jongmans, Ineke van der Burgt, Peter M Hoogerbrugge, Kees Noordam, Helger G Yntema, Willy M Nillesen, Roland P Kuiper, Marjolijn J L Ligtenberg, Ad Geurts van Kessel, J Han J M van Krieken,[...]. Eur J Hum Genet 2011
92
28


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.