A citation-based method for searching scientific literature

Talia Wegman-Ostrosky, Sharon A Savage. Br J Haematol 2017
Times Cited: 57







List of co-cited articles
488 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
19

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
15

A 20-year perspective on the International Fanconi Anemia Registry (IFAR).
David I Kutler, Bhuvanesh Singh, Jaya Satagopan, Sat Dev Batish, Marianne Berwick, Philip F Giampietro, Helmut Hanenberg, Arleen D Auerbach. Blood 2003
478
14

Comparison of chromosome breakage in non-mosaic and mosaic patients with Fanconi anemia, relatives, and patients with other inherited bone marrow failure syndromes.
John H Fargo, Andrzej Rochowski, Neelam Giri, Sharon A Savage, Susan B Olson, Blanche P Alter. Cytogenet Genome Res 2014
25
32

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
14

Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita.
Blanche P Alter, Gabriela M Baerlocher, Sharon A Savage, Stephen J Chanock, Babette B Weksler, Judith P Willner, June A Peters, Neelam Giri, Peter M Lansdorp. Blood 2007
237
12


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
12

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
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

Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry.
Philip S Rosenberg, Blanche P Alter, Wolfram Ebell. Haematologica 2008
125
10

Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry.
Hannah Tamary, Daniella Nishri, Joanne Yacobovich, Rama Zilber, Orly Dgany, Tanya Krasnov, Shraga Aviner, Polina Stepensky, Shoshana Ravel-Vilk, Menachem Bitan,[...]. Haematologica 2010
46
13

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
10

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
10

Fanconi anemia and its diagnosis.
Arleen D Auerbach. Mutat Res 2009
333
10


Cancer incidence in persons with Fanconi anemia.
Philip S Rosenberg, Mark H Greene, Blanche P Alter. Blood 2003
315
8

Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.
Blanche P Alter, Philip S Rosenberg, Lawrence C Brody. J Med Genet 2007
159
8

Erythrocyte adenosine deaminase: diagnostic value for Diamond-Blackfan anaemia.
John H Fargo, Christian P Kratz, Neelam Giri, Sharon A Savage, Carolyn Wong, Karen Backer, Blanche P Alter, Bertil Glader. Br J Haematol 2013
44
11

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
8

Old and new tools in the clinical diagnosis of inherited bone marrow failure syndromes.
Allison H West, Jane E Churpek. Hematology Am Soc Hematol Educ Program 2017
16
31


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
8

In-vivo dominant immune responses in aplastic anaemia: molecular tracking of putatively pathogenetic T-cell clones by TCR beta-CDR3 sequencing.
Antonio M Risitano, Jaroslaw P Maciejewski, Spencer Green, Magdalena Plasilova, Weihua Zeng, Neal S Young. Lancet 2004
174
8

Clonal hematopoiesis in patients with dyskeratosis congenita.
Nieves Perdigones, Juan C Perin, Irene Schiano, Peter Nicholas, Jaclyn A Biegel, Philip J Mason, Daria V Babushok, Monica Bessler. Am J Hematol 2016
25
20

The Fanconi Anemia Pathway Maintains Genome Stability by Coordinating Replication and Transcription.
Rebekka A Schwab, Jadwiga Nieminuszczy, Fenil Shah, Jamie Langton, David Lopez Martinez, Chih-Chao Liang, Martin A Cohn, Richard J Gibbons, Andrew J Deans, Wojciech Niedzwiedz. Mol Cell 2015
195
7

Telomere length is associated with disease severity and declines with age in dyskeratosis congenita.
Blanche P Alter, Philip S Rosenberg, Neelam Giri, Gabriela M Baerlocher, Peter M Lansdorp, Sharon A Savage. Haematologica 2012
119
7

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
7

Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome.
Santhosh Dhanraj, Anna Matveev, Hongbing Li, Supanun Lauhasurayotin, Lawrence Jardine, Michaela Cada, Bozana Zlateska, Chetankumar S Tailor, Joseph Zhou, Roberto Mendoza-Londono,[...]. Blood 2017
62
7

Serum pancreatic enzymes define the pancreatic phenotype in patients with Shwachman-Diamond syndrome.
Wan F Ip, Annie Dupuis, Lynda Ellis, Satti Beharry, Jodi Morrison, Michael O Stormon, Mary Corey, Johanna M Rommens, Peter R Durie. J Pediatr 2002
57
7

Recommendations on hematopoietic stem cell transplantation for inherited bone marrow failure syndromes.
R Peffault de Latour, C Peters, B Gibson, B Strahm, A Lankester, C D de Heredia, D Longoni, F Fioredda, F Locatelli, I Yaniv,[...]. Bone Marrow Transplant 2015
46
8

How I treat Diamond-Blackfan anemia.
Adrianna Vlachos, Ellen Muir. Blood 2010
104
7

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
9

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
7

Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes.
Hideki Muramatsu, Yusuke Okuno, Kenichi Yoshida, Yuichi Shiraishi, Sayoko Doisaki, Atsushi Narita, Hirotoshi Sakaguchi, Nozomu Kawashima, Xinan Wang, Yinyan Xu,[...]. Genet Med 2017
40
10

How I treat MDS and AML in Fanconi anemia.
Régis Peffault de Latour, Jean Soulier. Blood 2016
37
10


Molecular pathogenesis and clinical management of Fanconi anemia.
Younghoon Kee, Alan D D'Andrea. J Clin Invest 2012
165
7

Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia.
Kerstin Knies, Shojiro Inano, María J Ramírez, Masamichi Ishiai, Jordi Surrallés, Minoru Takata, Detlev Schindler. J Clin Invest 2017
105
7


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
7

Somatic mutations identify a subgroup of aplastic anemia patients who progress to myelodysplastic syndrome.
Austin G Kulasekararaj, Jie Jiang, Alexander E Smith, Azim M Mohamedali, Syed Mian, Shreyans Gandhi, Joop Gaken, Barbara Czepulkowski, Judith C W Marsh, Ghulam J Mufti. Blood 2014
137
7

Telomere diseases.
Rodrigo T Calado, Neal S Young. N Engl J Med 2009
517
7

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
14

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
7

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
7

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
134
7

The inherited bone marrow failure syndromes.
S Deborah Chirnomas, Gary M Kupfer. Pediatr Clin North Am 2013
26
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
86
7


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.