A citation-based method for searching scientific literature

Adam S Nelson, Kasiani C Myers. Hematol Oncol Clin North Am 2018
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
38

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
467
38

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features.
Raphael Carapito, Martina Konantz, Catherine Paillard, Zhichao Miao, Angélique Pichot, Magalie S Leduc, Yaping Yang, Katie L Bergstrom, Donald H Mahoney, Deborah L Shardy,[...]. J Clin Invest 2017
70
33

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
33

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
69
33

Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome.
Yigal Dror, Jean Donadieu, Jutta Koglmeier, John Dodge, Sanna Toiviainen-Salo, Outi Makitie, Elizabeth Kerr, Cornelia Zeidler, Akiko Shimamura, Neil Shah,[...]. Ann N Y Acad Sci 2011
106
33

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
27

Somatic mutations and clonal hematopoiesis in congenital neutropenia.
Jun Xia, Christopher A Miller, Jack Baty, Amrita Ramesh, Matthew R M Jotte, Robert S Fulton, Tiphanie P Vogel, Megan A Cooper, Kelly J Walkovich, Vahagn Makaryan,[...]. Blood 2018
54
27

Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome.
Polina Stepensky, Montserrat Chacón-Flores, Katherine H Kim, Omar Abuzaitoun, Arnulfo Bautista-Santos, Natalia Simanovsky, Dritan Siliqi, Davide Altamura, Alfonso Méndez-Godoy, Abril Gijsbers,[...]. J Med Genet 2017
59
27

Clonal evolution in marrows of patients with Shwachman-Diamond syndrome: a prospective 5-year follow-up study.
Yigal Dror, Peter Durie, Hedy Ginzberg, Rebecca Herman, Anu Banerjee, Martin Champagne, Kevin Shannon, David Malkin, Melvin H Freedman. Exp Hematol 2002
61
22

Congenital neutropenia in the era of genomics: classification, diagnosis, and natural history.
Jean Donadieu, Blandine Beaupain, Odile Fenneteau, Christine Bellanné-Chantelot. Br J Haematol 2017
56
22

The Greek Registry of Shwachman Diamond-Syndrome: Molecular and clinical data.
Polyxeni Delaporta, Christalena Sofocleous, Marina Economou, Alexandros Makis, Stavroula Kostaridou, Antonis Kattamis. Pediatr Blood Cancer 2017
10
40


Shwachman-Diamond Syndrome: Molecular Mechanisms and Current Perspectives.
Valentino Bezzerri, Marco Cipolli. Mol Diagn Ther 2019
21
22


Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome.
Andrew J Finch, Christine Hilcenko, Nicolas Basse, Lesley F Drynan, Beatriz Goyenechea, Tobias F Menne, Africa González Fernández, Paul Simpson, Clive S D'Santos, Mark J Arends,[...]. Genes Dev 2011
178
16

Defective ribosome assembly in Shwachman-Diamond syndrome.
Chi C Wong, David Traynor, Nicolas Basse, Robert R Kay, Alan J Warren. Blood 2011
100
16

Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy.
Philip S Rosenberg, Cornelia Zeidler, Audrey A Bolyard, Blanche P Alter, Mary A Bonilla, Laurence A Boxer, Yigal Dror, Sally Kinsey, Daniel C Link, Peter E Newburger,[...]. Br J Haematol 2010
128
16

DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit Maturation.
Hemanth Tummala, Amanda J Walne, Mike Williams, Nicholas Bockett, Laura Collopy, Shirleny Cardoso, Alicia Ellison, Rob Wynn, Thierry Leblanc, Jude Fitzgibbon,[...]. Am J Hum Genet 2016
42
16


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
16

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
16

Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.
S Goobie, M Popovic, J Morrison, L Ellis, H Ginzberg, G R Boocock, N Ehtesham, C Bétard, C G Brewer, N M Roslin,[...]. Am J Hum Genet 2001
85
16

Clinical and molecular pathophysiology of Shwachman-Diamond syndrome: an update.
Kasiani C Myers, Stella M Davies, Akiko Shimamura. Hematol Oncol Clin North Am 2013
58
16

Immunophenotypic analysis of hematopoiesis in patients suffering from Shwachman-Bodian-Diamond Syndrome.
Angela Mercuri, Elisa Cannata, Omar Perbellini, Chiara Cugno, Rita Balter, Ada Zaccaron, Gloria Tridello, Giovanni Pizzolo, Massimiliano De Bortoli, Mauro Krampera,[...]. Eur J Haematol 2015
7
42

EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome.
Shengjiang Tan, Laëtitia Kermasson, Angela Hoslin, Pekka Jaako, Alexandre Faille, Abraham Acevedo-Arozena, Etienne Lengline, Dana Ranta, Maryline Poirée, Odile Fenneteau,[...]. Blood 2019
19
16

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
16

Clinical features and outcomes of patients with Shwachman-Diamond syndrome and myelodysplastic syndrome or acute myeloid leukaemia: a multicentre, retrospective, cohort study.
Kasiani C Myers, Elissa Furutani, Edie Weller, Bradford Siegele, Ashley Galvin, Valerie Arsenault, Blanche P Alter, Farid Boulad, Carlos Bueso-Ramos, Lauri Burroughs,[...]. Lancet Haematol 2020
16
18

Shwachman-Diamond syndrome: a review of the clinical presentation, molecular pathogenesis, diagnosis, and treatment.
Lauri Burroughs, Ann Woolfrey, Akiko Shimamura. Hematol Oncol Clin North Am 2009
86
11

Ribosomopathies: human disorders of ribosome dysfunction.
Anupama Narla, Benjamin L Ebert. Blood 2010
491
11

Activation of the tumor suppressor p53 upon impairment of ribosome biogenesis.
Sladana Bursac, Maja Cokaric Brdovcak, Giulio Donati, Sinisa Volarevic. Biochim Biophys Acta 2014
95
11

The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA.
Karthik A Ganapathi, Karyn M Austin, Chung-Sheng Lee, Anusha Dias, Maggie M Malsch, Robin Reed, Akiko Shimamura. Blood 2007
99
11

The genetics of dyskeratosis congenita.
Philip J Mason, Monica Bessler. Cancer Genet 2011
88
11

The Shwachman-Diamond SBDS protein localizes to the nucleolus.
Karyn M Austin, Rebecca J Leary, Akiko Shimamura. Blood 2005
93
11

Diverse diseases from a ubiquitous process: the ribosomopathy paradox.
Joy Armistead, Barbara Triggs-Raine. FEBS Lett 2014
64
11


Severe congenital neutropenias.
Julia Skokowa, David C Dale, Ivo P Touw, Cornelia Zeidler, Karl Welte. Nat Rev Dis Primers 2017
100
11

TCIRG1-associated congenital neutropenia.
Vahagn Makaryan, Elisabeth A Rosenthal, Audrey Anna Bolyard, Merideth L Kelley, Jennifer E Below, Michael J Bamshad, Kathryn M Bofferding, Joshua D Smith, Kati Buckingham, Laurence A Boxer,[...]. Hum Mutat 2014
24
11

Hematologic Manifestations of Deficiency of Adenosine Deaminase 2 (DADA2) and Response to Tumor Necrosis Factor Inhibition in DADA2-Associated Bone Marrow Failure.
Thomas F Michniacki, Mark Hannibal, Charles W Ross, David G Frame, Adam S DuVall, Rami Khoriaty, Mark T Vander Lugt, Kelly J Walkovich. J Clin Immunol 2018
26
11

Immune function in patients with Shwachman-Diamond syndrome.
Y Dror, H Ginzberg, I Dalal, V Cherepanov, G Downey, P Durie, C M Roifman, M H Freedman. Br J Haematol 2001
64
11

The Severe Chronic Neutropenia International Registry: 10-Year Follow-up Report.
David C Dale, Audrey Anna Bolyard, Beate G Schwinzer, Gusal Pracht, Mary Ann Bonilla, Laurence Boxer, Melvin H Freedman, Jean Donadieu, George Kannourakis, Blanche P Alter,[...]. Support Cancer Ther 2006
79
11

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
Christoph Klein, Magda Grudzien, Giridharan Appaswamy, Manuela Germeshausen, Inga Sandrock, Alejandro A Schäffer, Chozhavendan Rathinam, Kaan Boztug, Beate Schwinzer, Nima Rezaei,[...]. Nat Genet 2007
312
11

Allogeneic Hematopoietic Cell Transplantation Using Treosulfan-Based Conditioning for Treatment of Marrow Failure Disorders.
Lauri M Burroughs, Akiko Shimamura, Julie-An Talano, Jennifer A Domm, Kelsey K Baker, Colleen Delaney, Haydar Frangoul, David A Margolis, K Scott Baker, Eneida R Nemecek,[...]. Biol Blood Marrow Transplant 2017
27
11

A congenital neutrophil defect syndrome associated with mutations in VPS45.
Thierry Vilboux, Atar Lev, May Christine V Malicdan, Amos J Simon, Päivi Järvinen, Tomas Racek, Jacek Puchalka, Raman Sood, Blake Carrington, Kevin Bishop,[...]. N Engl J Med 2013
77
11

Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia.
K Devriendt, A S Kim, G Mathijs, S G Frints, M Schwartz, J J Van Den Oord, G E Verhoef, M A Boogaerts, J P Fryns, D You,[...]. Nat Genet 2001
293
11

Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease.
Paolo A Hernandez, Robert J Gorlin, John N Lukens, Shoichiro Taniuchi, Joze Bohinjec, Fleur Francois, Mary E Klotman, George A Diaz. Nat Genet 2003
439
11

JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia.
Kaan Boztug, Päivi M Järvinen, Elisabeth Salzer, Tomas Racek, Sebastian Mönch, Wojciech Garncarz, E Michael Gertz, Alejandro A Schäffer, Aristotelis Antonopoulos, Stuart M Haslam,[...]. Nat Genet 2014
74
11

Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.
Rachel Emma Dickinson, Helen Griffin, Venetia Bigley, Louise N Reynard, Rafiqul Hussain, Muzlifah Haniffa, Jeremy H Lakey, Thahira Rahman, Xiao-Nong Wang, Naomi McGovern,[...]. Blood 2011
277
11

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
25
11

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
789
11


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.