A citation-based method for searching scientific literature


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



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  Times     Co-cited
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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
60

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
202
37

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
207
31

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
189
29

Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel.
Hartmut Döhner, Elihu Estey, David Grimwade, Sergio Amadori, Frederick R Appelbaum, Thomas Büchner, Hervé Dombret, Benjamin L Ebert, Pierre Fenaux, Richard A Larson,[...]. Blood 2017
28

Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemia.
Jane E Churpek, Khateriaa Pyrtel, Krishna-Latha Kanchi, Jin Shao, Daniel Koboldt, Christopher A Miller, Dong Shen, Robert Fulton, Michelle O'Laughlin, Catrina Fronick,[...]. Blood 2015
141
27

Disease evolution and outcomes in familial AML with germline CEBPA mutations.
Kiran Tawana, Jun Wang, Aline Renneville, Csaba Bödör, Robert Hills, Chey Loveday, Aleksandar Savic, Frederik W Van Delft, Jennifer Treleaven, Panayiotis Georgiades,[...]. Blood 2015
88
28

Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy.
Carolyn J Owen, Cynthia L Toze, Anna Koochin, Donna L Forrest, Clayton A Smith, Jane M Stevens, Shannon C Jackson, Man-Chiu Poon, Gary D Sinclair, Brian Leber,[...]. Blood 2008
166
26

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
800
24

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
109
23

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
398
21

Proposal for the clinical detection and management of patients and their family members with familial myelodysplastic syndrome/acute leukemia predisposition syndromes.
Jane E Churpek, Rachelle Lorenz, Siya Nedumgottil, Kenan Onel, Olufunmilayo I Olopade, April Sorrell, Carolyn J Owen, Alison A Bertuch, Lucy A Godley. Leuk Lymphoma 2013
56
35

Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignancies.
Michael W Drazer, Sabah Kadri, Madina Sukhanova, Sushant A Patil, Allison H West, Simone Feurstein, Dalein A Calderon, Matthew F Jones, Caroline M Weipert, Christopher K Daugherty,[...]. Blood Adv 2018
47
42

Genomic Classification and Prognosis in Acute Myeloid Leukemia.
Elli Papaemmanuil, Moritz Gerstung, Lars Bullinger, Verena I Gaidzik, Peter Paschka, Nicola D Roberts, Nicola E Potter, Michael Heuser, Felicitas Thol, Niccolo Bolli,[...]. N Engl J Med 2016
20

Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC).
Courtney D DiNardo, Sarah A Bannon, Mark Routbort, Anna Franklin, Maureen Mork, Mary Armanios, Emily M Mace, Jordan S Orange, Meselle Jeff-Eke, Jane E Churpek,[...]. Clin Lymphoma Myeloma Leuk 2016
50
38

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
20

Somatic CEBPA mutations are a frequent second event in families with germline CEBPA mutations and familial acute myeloid leukemia.
Thomas Pabst, Marianne Eyholzer, Simon Haefliger, Julian Schardt, Beatrice U Mueller. J Clin Oncol 2008
118
19

Mutation of CEBPA in familial acute myeloid leukemia.
Matthew L Smith, Jamie D Cavenagh, T Andrew Lister, Jude Fitzgibbon. N Engl J Med 2004
208
19

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
168
18


Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes.
David P Steensma, Rafael Bejar, Siddhartha Jaiswal, R Coleman Lindsley, Mikkael A Sekeres, Robert P Hasserjian, Benjamin L Ebert. Blood 2015
942
17

Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.
Tommaso Pippucci, Anna Savoia, Silverio Perrotta, Núria Pujol-Moix, Patrizia Noris, Giovanni Castegnaro, Alessandro Pecci, Chiara Gnan, Francesca Punzo, Caterina Marconi,[...]. Am J Hum Genet 2011
124
17

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.
Patrizia Noris, Silverio Perrotta, Marco Seri, Alessandro Pecci, Chiara Gnan, Giuseppe Loffredo, Nuria Pujol-Moix, Marco Zecca, Francesca Scognamiglio, Daniela De Rocco,[...]. Blood 2011
168
17

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
149
17

Prognostic impact, concurrent genetic mutations, and gene expression features of AML with CEBPA mutations in a cohort of 1182 cytogenetically normal AML patients: further evidence for CEBPA double mutant AML as a distinctive disease entity.
Erdogan Taskesen, Lars Bullinger, Andrea Corbacioglu, Mathijs A Sanders, Claudia A J Erpelinck, Bas J Wouters, Sonja C van der Poel-van de Luytgaarde, Frederik Damm, Jürgen Krauter, Arnold Ganser,[...]. Blood 2011
250
15

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
15

Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia.
Michael Kirwan, Amanda J Walne, Vincent Plagnol, Mark Velangi, Aloysius Ho, Upal Hossain, Tom Vulliamy, Inderjeet Dokal. Am J Hum Genet 2012
72
20

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
14

Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia.
Christopher N Hahn, Chan-Eng Chong, Catherine L Carmichael, Ella J Wilkins, Peter J Brautigan, Xiao-Chun Li, Milena Babic, Ming Lin, Amandine Carmagnac, Young K Lee,[...]. Nat Genet 2011
374
14

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
85
16

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
126
14

Genetic predisposition to leukemia and other hematologic malignancies.
Simone Feurstein, Michael W Drazer, Lucy A Godley. Semin Oncol 2016
39
35

Clinical utility of gene panel-based testing for hereditary myelodysplastic syndrome/acute leukemia predisposition syndromes.
L Guidugli, A K Johnson, G Alkorta-Aranburu, V Nelakuditi, K Arndt, J E Churpek, L A Godley, D Townsley, N S Young, C Fitzpatrick,[...]. Leukemia 2017
33
42

First report of multiple CEBPA mutations contributing to donor origin of leukemia relapse after allogeneic hematopoietic stem cell transplantation.
Haowen Xiao, Jimin Shi, Yi Luo, Yamin Tan, Jingsong He, Wanzhuo Xie, Lifei Zhang, Yingjia Wang, Lizhen Liu, Kangni Wu,[...]. Blood 2011
44
31

Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.
Timothy J Ley, Christopher Miller, Li Ding, Benjamin J Raphael, Andrew J Mungall, A Gordon Robertson, Katherine Hoadley, Timothy J Triche, Peter W Laird, Jack D Baty,[...]. N Engl J Med 2013
13

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
85
15


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
97
13

Myelodysplastic Syndromes, Version 2.2017, NCCN Clinical Practice Guidelines in Oncology.
Peter L Greenberg, Richard M Stone, Aref Al-Kali, Stefan K Barta, Rafael Bejar, John M Bennett, Hetty Carraway, Carlos M De Castro, H Joachim Deeg, Amy E DeZern,[...]. J Natl Compr Canc Netw 2017
201
13

A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies.
A Buijs, P Poddighe, R van Wijk, W van Solinge, E Borst, L Verdonck, A Hagenbeek, P Pearson, H Lokhorst. Blood 2001
90
13

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
66
18

Familial myelodysplastic syndromes: a review of the literature.
Elena Liew, Carolyn Owen. Haematologica 2011
99
12

Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia.
I Antony-Debré, N Duployez, M Bucci, S Geffroy, J-B Micol, A Renneville, N Boissel, N Dhédin, D Réa, B Nelken,[...]. Leukemia 2016
65
18

Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.
Veronique Latger-Cannard, Christophe Philippe, Alexandre Bouquet, Veronique Baccini, Marie-Christine Alessi, Annick Ankri, Anne Bauters, Sophie Bayart, Pascale Cornillet-Lefebvre, Sylvie Daliphard,[...]. Orphanet J Rare Dis 2016
55
21

Myeloid neoplasms with germline DDX41 mutation.
Jesse J C Cheah, Christopher N Hahn, Devendra K Hiwase, Hamish S Scott, Anna L Brown. Int J Hematol 2017
42
28

Clinical effect of point mutations in myelodysplastic syndromes.
Rafael Bejar, Kristen Stevenson, Omar Abdel-Wahab, Naomi Galili, Björn Nilsson, Guillermo Garcia-Manero, Hagop Kantarjian, Azra Raza, Ross L Levine, Donna Neuberg,[...]. N Engl J Med 2011
11

Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy-related leukemia.
Jane E Churpek, Rafael Marquez, Barbara Neistadt, Kimberly Claussen, Ming K Lee, Matthew M Churpek, Dezheng Huo, Howard Weiner, Mekhala Bannerjee, Lucy A Godley,[...]. Cancer 2016
87
12

ANKRD26-related thrombocytopenia and myeloid malignancies.
Patrizia Noris, Remi Favier, Marie-Christine Alessi, Amy E Geddis, Shinji Kunishima, Paula G Heller, Paola Giordano, Karen Y Niederhoffer, James B Bussel, Gian Marco Podda,[...]. Blood 2013
93
11

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).
Pia Ostergaard, Michael A Simpson, Fiona C Connell, Colin G Steward, Glen Brice, Wesley J Woollard, Dimitra Dafou, Tatjana Kilo, Sarah Smithson, Peter Lunt,[...]. Nat Genet 2011
315
11

Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy.
Katarzyna Rojek, Eric Nickels, Barbara Neistadt, Rafael Marquez, Amittha Wickrema, Andrew Artz, Koen van Besien, Richard A Larson, Ming K Lee, Jeremy P Segal,[...]. Biol Blood Marrow Transplant 2016
26
42


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.