A citation-based method for searching scientific literature

Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Haematologica 2018
Times Cited: 93







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



Times Cited
  Times     Co-cited
Similarity




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
466
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
168
17

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
194
17

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
234
17

Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
288
13

Fanconi anemia and the development of leukemia.
Blanche P Alter. Best Pract Res Clin Haematol 2014
94
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
248
11

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
115
11

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
11

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome.
Jean Donadieu, Odile Fenneteau, Blandine Beaupain, Sandrine Beaufils, Florence Bellanger, Nizar Mahlaoui, Anne Lambilliotte, Nathalie Aladjidi, Yves Bertrand, Valérie Mialou,[...]. Haematologica 2012
66
16

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
99
11

Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.
M Gross, H Hanenberg, S Lobitz, R Friedl, S Herterich, R Dietrich, B Gruhn, D Schindler, H Hoehn. Cytogenet Genome Res 2002
112
11

Increased risk of colon cancer and osteogenic sarcoma in Diamond-Blackfan anemia.
Adrianna Vlachos, Philip S Rosenberg, Eva Atsidaftos, Jessica Kang, Kenan Onel, Ravi N Sharaf, Blanche P Alter, Jeffrey M Lipton. Blood 2018
31
35

Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry.
Philip S Rosenberg, Blanche P Alter, Wolfram Ebell. Haematologica 2008
122
10

Response to androgen therapy in patients with dyskeratosis congenita.
Payal P Khincha, Ingrid M Wentzensen, Neelam Giri, Blanche P Alter, Sharon A Savage. Br J Haematol 2014
55
18

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
302
10

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
104
10

Outcomes of allogeneic hematopoietic cell transplantation in patients with dyskeratosis congenita.
Shahinaz M Gadalla, Carmem Sales-Bonfim, Jeanette Carreras, Blanche P Alter, Joseph H Antin, Mouhab Ayas, Prasad Bodhi, Jeffrey Davis, Stella M Davies, Eric Deconinck,[...]. Biol Blood Marrow Transplant 2013
66
15

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
594
10

Fanconi anemia and its diagnosis.
Arleen D Auerbach. Mutat Res 2009
323
10

The Fanconi anaemia pathway: new players and new functions.
Raphael Ceccaldi, Prabha Sarangi, Alan D D'Andrea. Nat Rev Mol Cell Biol 2016
314
10


Clinical utility gene card for: Dyskeratosis congenita - update 2015.
Inderjeet Dokal, Tom Vulliamy, Philip Mason, Monica Bessler. Eur J Hum Genet 2015
37
27

Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita.
A C Dietz, P J Orchard, K S Baker, R H Giller, S A Savage, B P Alter, J Tolar. Bone Marrow Transplant 2011
94
9

The genomics of inherited bone marrow failure: from mechanism to the clinic.
Talia Wegman-Ostrosky, Sharon A Savage. Br J Haematol 2017
53
16

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
68
13


Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema.
Susan E Stanley, Dustin L Gable, Christa L Wagner, Thomas M Carlile, Vidya Sagar Hanumanthu, Joshua D Podlevsky, Sara E Khalil, Amy E DeZern, Maria F Rojas-Duran, Carolyn D Applegate,[...]. Sci Transl Med 2016
96
9

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
9


Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients.
Asuka Hira, Hiromasa Yabe, Kenichi Yoshida, Yusuke Okuno, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Jun Nakamura, Seiji Kojima,[...]. Blood 2013
100
9


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
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
121
9

Cancer incidence in persons with Fanconi anemia.
Philip S Rosenberg, Mark H Greene, Blanche P Alter. Blood 2003
308
8

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
108
8


Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita.
Bari J Ballew, Meredith Yeager, Kevin Jacobs, Neelam Giri, Joseph Boland, Laurie Burdett, Blanche P Alter, Sharon A Savage. Hum Genet 2013
141
8

Telomerase mutations in families with idiopathic pulmonary fibrosis.
Mary Y Armanios, Julian J-L Chen, Joy D Cogan, Jonathan K Alder, Roxann G Ingersoll, Cheryl Markin, William E Lawson, Mingyi Xie, Irma Vulto, John A Phillips,[...]. N Engl J Med 2007
791
8

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.
N S Heiss, S W Knight, T J Vulliamy, S M Klauck, S Wiemann, P J Mason, A Poustka, I Dokal. Nat Genet 1998
628
8


Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase.
Erin M Parry, Jonathan K Alder, Xiaodong Qi, Julian J-L Chen, Mary Armanios. Blood 2011
98
8

Dyskeratosis congenita.
Inderjeet Dokal. Hematology Am Soc Hematol Educ Program 2011
168
8

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
455
8

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
185
8

Fanconi anaemia and cancer: an intricate relationship.
Grzegorz Nalepa, D Wade Clapp. Nat Rev Cancer 2018
117
8

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
141
8


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.