A citation-based method for searching scientific literature

Simone Feurstein, Ayodeji Adegunsoye, Danijela Mojsilovic, Rekha Vij, Allison H West DePersia, Padma Sheila Rajagopal, Afaf Osman, Robert H Collins, Raymond H Kim, Steven D Gore, Peter Greenberg, Lucy A Godley, Zejuan Li, Daniela Del Gaudio, Hari Prasanna Subramanian, Soma Das, Tom Walsh, Suleyman Gulsuner, Jeremy P Segal, Aliya N Husain, Sandeep Gurbuxani, Mary-Claire King, Mary E Strek, Jane E Churpek. Blood Adv 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Germline variants drive myelodysplastic syndrome in young adults.
Simone Feurstein, Jane E Churpek, Tom Walsh, Sioban Keel, Marja Hakkarainen, Thomas Schroeder, Ulrich Germing, Stefanie Geyh, Michael Heuser, Felicitas Thol,[...]. Leukemia 2021
4
75

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
41
75

Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis.
Jonathan K Alder, Susan E Stanley, Christa L Wagner, Makenzie Hamilton, Vidya Sagar Hanumanthu, Mary Armanios. Chest 2015
88
50

Cancer spectrum and outcomes in the Mendelian short telomere syndromes.
Kristen E Schratz, Lisa Haley, Sonye K Danoff, Amanda L Blackford, Amy E DeZern, Christopher D Gocke, Amy S Duffield, Mary Armanios. Blood 2020
14
50

Somatic reversion events point towards RPL4 as a novel disease gene in a condition resembling Diamond-Blackfan anemia.
Marjolijn C J Jongmans, Illja J Diets, Paola Quarello, Emanuela Garelli, Roland P Kuiper, Rolph Pfundt. Haematologica 2018
11
50

Germline predisposition in myeloid neoplasms: Unique genetic and clinical features of GATA2 deficiency and SAMD9/SAMD9L syndromes.
Sushree S Sahoo, Emilia J Kozyra, Marcin W Wlodarski. Best Pract Res Clin Haematol 2020
10
50

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
78
50

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
19
50

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
174
50


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
139
50

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
41
50

Incidental detection of germline variants of potential clinical significance by massively parallel sequencing in haematological malignancies.
Costas K Yannakou, Kate Jones, Georgina L Ryland, Ella R Thompson, Gareth Reid, Michelle McBean, Alison Trainer, David Westerman, Piers Blombery. J Clin Pathol 2018
14
50

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
130
50

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
158
50

Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer.
Deepak Singhal, Christopher N Hahn, Simone Feurstein, Li Yan A Wee, Luke Moma, Monika M Kutyna, Rakchha Chhetri, Leila Eshraghi, Andreas W Schreiber, Jinghua Feng,[...]. Leukemia 2021
3
66

Bone marrow failure and the telomeropathies.
Danielle M Townsley, Bogdan Dumitriu, Neal S Young. Blood 2014
145
50

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
111
50

Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7.
Akiko Nagamachi, Hirotaka Matsui, Hiroya Asou, Yuko Ozaki, Daisuke Aki, Akinori Kanai, Keiyo Takubo, Toshio Suda, Takuro Nakamura, Linda Wolff,[...]. Cancer Cell 2013
75
50

Diagnostic utility of telomere length testing in a hospital-based setting.
Jonathan K Alder, Vidya Sagar Hanumanthu, Margaret A Strong, Amy E DeZern, Susan E Stanley, Clifford M Takemoto, Ludmila Danilova, Carolyn D Applegate, Stephen G Bolton, David W Mohr,[...]. Proc Natl Acad Sci U S A 2018
71
50


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
50

RUNX1 germline variants in RUNX1-mutant AML: how frequent?
Martijn P T Ernst, François G Kavelaars, Bob Löwenberg, Peter J M Valk, Marc H G P Raaijmakers. Blood 2021
3
66

High frequency of germline RUNX1 mutations in patients with RUNX1-mutated AML.
Laura Simon, Jean-François Spinella, Chi-Yuan Yao, Vincent-Philippe Lavallée, Isabel Boivin, Geneviève Boucher, Eric Audemard, Marie-Eve Bordeleau, Sébastien Lemieux, Josée Hébert,[...]. Blood 2020
14
50

Accurate germline RUNX1 variant interpretation and its clinical significance.
Simone Feurstein, Liying Zhang, Courtney D DiNardo. Blood Adv 2020
3
66

Improving the detection of patients with inherited predispositions to hematologic malignancies using next-generation sequencing-based leukemia prognostication panels.
Courtney D DiNardo, Mark J Routbort, Sarah A Bannon, Christopher B Benton, Koichi Takahashi, Steve M Kornblau, Rajyalakshmi Luthra, Rashmi Kanagal-Shamanna, L Jeffrey Medeiros, Guillermo Garcia-Manero,[...]. Cancer 2018
19
50


Germline pathogenic variants in transcription factors predisposing to pediatric acute myeloid leukemia: results from the French ELAM02 trial.
Laurène Fenwarth, Nicolas Duployez, Alice Marceau-Renaut, Wadih Abou Chahla, Stéphane Ducassou, Virginie Gandemer, Marlène Pasquet, Thierry Leblanc, Pascale Schneider, Carine Domenech,[...]. Haematologica 2021
2
100

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
95
50

Strategy for identification of a potential inherited leukemia predisposition in a 299 patient's cohort with tumor-only sequencing data.
Almudena Aguilera-Diaz, María José Larrayoz, Sara Palomino-Echeverría, Iria Vazquez, Beñat Ariceta, Amagoia Mañú, Zuriñe Blasco-Iturri, Teresa Bernal Del Castillo, Matxalen Olivares Salaverri, Maria Teresa Olave Rubio,[...]. Leuk Res 2020
2
100

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
71
50

Clinical significance of somatic mutation in unexplained blood cytopenia.
Luca Malcovati, Anna Gallì, Erica Travaglino, Ilaria Ambaglio, Ettore Rizzo, Elisabetta Molteni, Chiara Elena, Virginia Valeria Ferretti, Silvia Catricalà, Elisa Bono,[...]. Blood 2017
179
50

Development of a New Monochrome Multiplex qPCR Method for Relative Telomere Length Measurement in Cancer.
Paige N Dahlgren, Kanokwan Bishop, Shatovisha Dey, Brittney-Shea Herbert, Hiromi Tanaka. Neoplasia 2018
10
25

Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.
Richard J Allen, Joanne Porte, Rebecca Braybrooke, Carlos Flores, Tasha E Fingerlin, Justin M Oldham, Beatriz Guillen-Guio, Shwu-Fan Ma, Tsukasa Okamoto, Alison E John,[...]. Lancet Respir Med 2017
107
25


CTC1 Mutations in a patient with dyskeratosis congenita.
Rachel B Keller, Katelyn E Gagne, G Naheed Usmani, George K Asdourian, David A Williams, Inga Hofmann, Suneet Agarwal. Pediatr Blood Cancer 2012
83
25



Targeting telomerase-expressing cancer cells.
Michel M Ouellette, Woodring E Wright, Jerry W Shay. J Cell Mol Med 2011
50
25



Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC.
Tom Vulliamy, Anna Marrone, Richard Szydlo, Amanda Walne, Philip J Mason, Inderjeet Dokal. Nat Genet 2004
317
25

Pirfenidone for idiopathic pulmonary fibrosis: analysis of pooled data from three multinational phase 3 trials.
Paul W Noble, Carlo Albera, Williamson Z Bradford, Ulrich Costabel, Roland M du Bois, Elizabeth A Fagan, Robert S Fishman, Ian Glaspole, Marilyn K Glassberg, Lisa Lancaster,[...]. Eur Respir J 2016
195
25

Interaction profiling identifies the human nuclear exosome targeting complex.
Michal Lubas, Marianne S Christensen, Maiken S Kristiansen, Michal Domanski, Lasse G Falkenby, Søren Lykke-Andersen, Jens S Andersen, Andrzej Dziembowski, Torben Heick Jensen. Mol Cell 2011
249
25

Short telomere length and its correlation with gene mutations in myelodysplastic syndrome.
Sang Mee Hwang, Seon Young Kim, Jung Ah Kim, Hee-Sue Park, Si Nae Park, Kyongok Im, Kwantae Kim, Sung-Min Kim, Dong Soon Lee. J Hematol Oncol 2016
16
25

Obesity, cigarette smoking, and telomere length in women.
A M Valdes, T Andrew, J P Gardner, M Kimura, E Oelsner, L F Cherkas, A Aviv, T D Spector. Lancet 2005
928
25

Association of immune abnormalities with telomere shortening in autosomal-dominant dyskeratosis congenita.
Matt Knudson, Shashikant Kulkarni, Zuhair K Ballas, Monica Bessler, Frederick Goldman. Blood 2005
55
25

Danazol Treatment for Telomere Diseases.
Danielle M Townsley, Bogdan Dumitriu, Delong Liu, Angélique Biancotto, Barbara Weinstein, Christina Chen, Nathan Hardy, Andrew D Mihalek, Shilpa Lingala, Yun Ju Kim,[...]. N Engl J Med 2016
164
25

Unusual complications after bone marrow transplantation for dyskeratosis congenita.
V Rocha, A Devergie, G Socié, P Ribaud, H Espérou, N Parquet, E Gluckman. Br J Haematol 1998
86
25

Telomere shortening in familial and sporadic pulmonary fibrosis.
Jennifer T Cronkhite, Chao Xing, Ganesh Raghu, Kelly M Chin, Fernando Torres, Randall L Rosenblatt, Christine Kim Garcia. Am J Respir Crit Care Med 2008
314
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.