A citation-based method for searching scientific literature

Prashant Chhabra, Prateek Bhatia, Minu Singh, Deepak Bansal, Richa Jain, Neelam Varma, Amita Trehan. Blood Cells Mol Dis 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
100


Analysis of telomeres in peripheral blood cells from patients with bone marrow failure.
Elisa Pavesi, Federica Avondo, Anna Aspesi, Paola Quarello, Alberto Rocci, Chiara Vimercati, Simona Pigullo, Carlo Dufour, Ugo Ramenghi, Irma Dianzani. Pediatr Blood Cancer 2009
19
50

TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements.
Hong-Yan Du, Elena Pumbo, Jennifer Ivanovich, Ping An, Richard T Maziarz, Ulrike M Reiss, Deborah Chirnomas, Akiko Shimamura, Adrianna Vlachos, Jeffrey M Lipton,[...]. Blood 2009
97
50

Abnormal telomere shortening in leucocytes of children with Shwachman-Diamond syndrome.
Ian Thornley, Yigal Dror, Lilian Sung, Rob F Wynn, Melvin H Freedman. Br J Haematol 2002
41
50


Peripheral blood lymphocyte telomere length as a predictor of response to immunosuppressive therapy in childhood aplastic anemia.
Hirotoshi Sakaguchi, Nobuhiro Nishio, Asahito Hama, Nozomu Kawashima, Xinan Wang, Atsushi Narita, Sayoko Doisaki, Yinyan Xu, Hideki Muramatsu, Nao Yoshida,[...]. Haematologica 2014
31
50

Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia.
Xiaxin Li, François Leteurtre, Vanderson Rocha, Philippe Guardiola, Roland Berger, Marie-Therese Daniel, Maria Helena Noguera, Odile Maarek, Gwenaëlle L E Roux, Pauline de la Salmonière,[...]. Br J Haematol 2003
38
50

Progressive telomere shortening in aplastic anemia.
S E Ball, F M Gibson, S Rizzo, J A Tooze, J C Marsh, E C Gordon-Smith. Blood 1998
196
50

Delayed diagnosis of Shwachman diamond syndrome with short telomeres and a review of cases in Asia.
Shin Yeu Ong, Shao-Tzu Li, Gee Chuan Wong, Aloysius Yew Leng Ho, Chandramouli Nagarajan, Joanne Ngeow. Leuk Res Rep 2018
5
50


Telomere length in inherited bone marrow failure syndromes.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Haematologica 2015
40
50

Guidelines for the diagnosis and management of aplastic anaemia.
Judith C W Marsh, Sarah E Ball, Jamie Cavenagh, Phil Darbyshire, Inderjeet Dokal, Edward C Gordon-Smith, Jane Keidan, Andrew Laurie, Anna Martin, Jane Mercieca,[...]. Br J Haematol 2009
359
50

Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach.
H Hanson, C G Mathew, Z Docherty, C Mackie Ogilvie. Cytogenet Cell Genet 2001
36
50

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
819
50

Clinical exome sequencing: results from 2819 samples reflecting 1000 families.
Daniel Trujillano, Aida M Bertoli-Avella, Krishna Kumar Kandaswamy, Maximilian Er Weiss, Julia Köster, Anett Marais, Omid Paknia, Rolf Schröder, Jose Maria Garcia-Aznar, Martin Werber,[...]. Eur J Hum Genet 2017
181
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
119
50

Late Effects Screening Guidelines after Hematopoietic Cell Transplantation for Inherited Bone Marrow Failure Syndromes: Consensus Statement From the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects After Pediatric HCT.
Andrew C Dietz, Sharon A Savage, Adrianna Vlachos, Parinda A Mehta, Dorine Bresters, Jakub Tolar, Carmem Bonfim, Jean Hugues Dalle, Josu de la Fuente, Roderick Skinner,[...]. Biol Blood Marrow Transplant 2017
19
50


The differential diagnosis and bone marrow evaluation of new-onset pancytopenia.
Elizabeth P Weinzierl, Daniel A Arber. Am J Clin Pathol 2013
57
50

dbSNP: the NCBI database of genetic variation.
S T Sherry, M H Ward, M Kholodov, J Baker, L Phan, E M Smigielski, K Sirotkin. Nucleic Acids Res 2001
50

Clinical approach to marrow failure.
Akiko Shimamura. Hematology Am Soc Hematol Educ Program 2009
14
50


Improving diagnostic precision, care and syndrome definitions using comprehensive next-generation sequencing for the inherited bone marrow failure syndromes.
Ibrahim Ghemlas, Hongbing Li, Bozana Zlateska, Robert Klaassen, Conrad V Fernandez, Rochelle A Yanofsky, John Wu, Yves Pastore, Mariana Silva, Jeff H Lipton,[...]. J Med Genet 2015
52
50

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
97
50

Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies.
Massimo Bogliolo, Roser Pujol, Miriam Aza-Carmona, Núria Muñoz-Subirana, Benjamin Rodriguez-Santiago, José Antonio Casado, Paula Rio, Christopher Bauser, Judith Reina-Castillón, Marcos Lopez-Sanchez,[...]. J Med Genet 2020
12
50

Dyskeratosis congenita.
Inderjeet Dokal. Hematology Am Soc Hematol Educ Program 2011
173
50

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
50

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
50


Aplastic anemia and clonal evolution: germ line and somatic genetics.
Akiko Shimamura. Hematology Am Soc Hematol Educ Program 2016
22
50

Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.
Daniela De Rocco, Roberta Bottega, Enrico Cappelli, Simona Cavani, Maria Criscuolo, Elena Nicchia, Fabio Corsolini, Chiara Greco, Adriana Borriello, Johanna Svahn,[...]. Haematologica 2014
28
50

Clinical and Counseling Experiences of Early Adopters of Whole Exome Sequencing.
Shubhangi Arora, Eden Haverfield, Gabriele Richard, Susanne B Haga, Rachel Mills. J Genet Couns 2016
11
50

Genetic Counselor Recommendations for Cancer Predisposition Evaluation and Surveillance in the Pediatric Oncology Patient.
Harriet Druker, Kristin Zelley, Rose B McGee, Sarah R Scollon, Wendy K Kohlmann, Katherine A Schneider, Kami Wolfe Schneider. Clin Cancer Res 2017
50
50

Genetic diagnosis in recently transfused patients.
Ana C Mardini, Fabiana Q Mayer, Rodrigo Rodenbusch, Ursula Matte, Maria L Saraiva-Pereira. Diagn Mol Pathol 2013
1
100

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
50

Cancer genetic counseling for childhood cancer predisposition is associated with improved levels of knowledge and high satisfaction in parents.
Olivia A Juarez, Bojana B Pencheva, Cecelia Bellcross, Kami W Schneider, Joyce Turner, Christopher C Porter. J Genet Couns 2021
1
100

Incidence of Fanconi anaemia in phenotypically normal aplastic anaemia patients in West Bengal.
Atreyee Dutta, Rajib De, Tuphan Kanti Dolai, Pritha Pal, Shanoli Ghosh, Pradip Kumar Mitra, Ajanta Halder. Hematology 2018
2
50

MutationTaster2: mutation prediction for the deep-sequencing age.
Jana Marie Schwarz, David N Cooper, Markus Schuelke, Dominik Seelow. Nat Methods 2014
50


Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes.
Piers Blombery, Lucy Fox, Georgina L Ryland, Ella R Thompson, Jennifer Lickiss, Michelle McBean, Satwica Yerneni, David Hughes, Anthea Greenway, Francoise Mechinaud,[...]. Haematologica 2021
7
50

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
45
50

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
50

Severe aplastic anemia: allogeneic bone marrow transplantation as first-line treatment.
George E Georges, Kris Doney, Rainer Storb. Blood Adv 2018
39
50

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017
70
50

A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.
Sarah Scollon, Amanda Knoth Anglin, Martha Thomas, Joyce T Turner, Kami Wolfe Schneider. J Genet Couns 2017
28
50

Diagnosis and treatment of pediatric acquired aplastic anemia (AAA): an initial survey of the North American Pediatric Aplastic Anemia Consortium (NAPAAC).
David A Williams, Carolyn Bennett, Alison Bertuch, Monica Bessler, Thomas Coates, Seth Corey, Yigal Dror, James Huang, Jeffrey Lipton, Timothy S Olson,[...]. Pediatr Blood Cancer 2014
19
50

Genomic characterization of the inherited bone marrow failure syndromes.
Payal P Khincha, Sharon A Savage. Semin Hematol 2013
41
50


Aplastic anaemia in childhood: prognosis and approach to therapy.
B Windass, M R Vowels, D O Hughes, L White. Med J Aust 1987
13
50


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.