A citation-based method for searching scientific literature

Roberto Valli, Emanuela Maserati, Cristina Marletta, Barbara Pressato, Francesco Lo Curto, Francesco Pasquali. Cancer Genet 2011
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity


Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
Emanuela Maserati, Antonella Minelli, Barbara Pressato, Roberto Valli, Barbara Crescenzi, Maurizio Stefanelli, Giuseppe Menna, Laura Sainati, Furio Poli, Claudio Panarello,[...]. Genes Chromosomes Cancer 2006
33
25

The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
Emanuela Maserati, Barbara Pressato, Roberto Valli, Antonella Minelli, Laura Sainati, Francesco Patitucci, Cristina Marletta, Angela Mastronuzzi, Furio Poli, Francesco Lo Curto,[...]. Br J Haematol 2009
36
25

Shwachman-Diamond syndrome.
Yigal Dror. Pediatr Blood Cancer 2005
74
15

Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells.
Roberto Valli, Cristina Marletta, Barbara Pressato, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. Mol Cytogenet 2011
31
15

Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis.
Barbara Pressato, Roberto Valli, Cristina Marletta, Lydia Mare, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. Br J Haematol 2012
32
15

Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms.
Roberto Valli, Barbara Pressato, Cristina Marletta, Lydia Mare, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. Mol Cytogenet 2013
16
18

Cytogenetic monitoring in Shwachman-Diamond syndrome: a note on clonal progression and a practical warning.
Barbara Pressato, Roberto Valli, Cristina Marletta, Lydia Mare, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. J Pediatr Hematol Oncol 2015
11
27

Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes.
Marilyn L Slovak, David D Smith, Victoria Bedell, Ya-Hsuan Hsu, Margaret O'Donnell, Stephen J Forman, Karl Gaal, Lisa McDaniel, Roger Schultz, Blake C Ballif,[...]. Mol Cytogenet 2010
25
10

High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival.
Daniel T Starczynowski, Suzanne Vercauteren, Adele Telenius, Sandy Sung, Kaoru Tohyama, Angela Brooks-Wilson, John J Spinelli, Connie J Eaves, Allen C Eaves, Douglas E Horsman,[...]. Blood 2008
91
10

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.
B Menten, N Maas, B Thienpont, K Buysse, J Vandesompele, C Melotte, T de Ravel, S Van Vooren, I Balikova, L Backx,[...]. J Med Genet 2006
313
10

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.
Blake C Ballif, Emily A Rorem, Kyle Sundin, Matt Lincicum, Shannon Gaskin, Justine Coppinger, Catherine D Kashork, Lisa G Shaffer, Bassem A Bejjani. Am J Med Genet A 2006
207
10

Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia.
Renu Bajaj, Fang Xu, Bixia Xiang, Katherine Wilcox, Autumn J Diadamo, Rachana Kumar, Alexandra Pietraszkiewicz, Stephanie Halene, Peining Li. Mol Cytogenet 2011
25
10


Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
10

Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromes.
Kathryn A Kolquist, Roger A Schultz, Aubry Furrow, Theresa C Brown, Jin-Yeong Han, Lynda J Campbell, Meaghan Wall, Marilyn L Slovak, Lisa G Shaffer, Blake C Ballif. Cancer Genet 2011
44
10

Prognostic and biologic significance of chromosomal imbalances assessed by comparative genomic hybridization in multiple myeloma.
Norma C Gutiérrez, Juan L García, Jesús M Hernández, Eva Lumbreras, Mariana Castellanos, Ana Rasillo, Gema Mateo, José M Hernández, Sonia Pérez, Alberto Orfao,[...]. Blood 2004
75
10

High-resolution genomic profiles define distinct clinico-pathogenetic subgroups of multiple myeloma patients.
Daniel R Carrasco, Giovanni Tonon, Yongsheng Huang, Yunyu Zhang, Raktim Sinha, Bin Feng, James P Stewart, Fenghuang Zhan, Deepak Khatry, Marina Protopopova,[...]. Cancer Cell 2006
296
10

A compendium of myeloma-associated chromosomal copy number abnormalities and their prognostic value.
Brian A Walker, Paola E Leone, Laura Chiecchio, Nicholas J Dickens, Matthew W Jenner, Kevin D Boyd, David C Johnson, David Gonzalez, Gian Paolo Dagrada, Rebecca K M Protheroe,[...]. Blood 2010
227
10

International Myeloma Working Group molecular classification of multiple myeloma: spotlight review.
R Fonseca, P L Bergsagel, J Drach, J Shaughnessy, N Gutierrez, A K Stewart, G Morgan, B Van Ness, M Chesi, S Minvielle,[...]. Leukemia 2009
562
10

Negative prognostic significance of two or more cytogenetic abnormalities in multiple myeloma patients treated with autologous stem cell transplantation.
H Greslikova, R Zaoralova, H Filkova, P Nemec, A Oltova, R Kupska, P Rudolecka, J Smetana, L Pour, L Zahradova,[...]. Neoplasma 2010
16
12

Prognostic significance of copy-number alterations in multiple myeloma.
Hervé Avet-Loiseau, Cheng Li, Florence Magrangeas, Wilfried Gouraud, Catherine Charbonnel, Jean-Luc Harousseau, Michel Attal, Gerald Marit, Claire Mathiot, Thierry Facon,[...]. J Clin Oncol 2009
189
10

Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
E Maserati, A Minelli, C Olivieri, L Bonvini, A Marchi, M Bozzola, C Danesino, S Scappaticci, F Pasquali. Cancer Genet Cytogenet 2000
24
10

Clinical and molecular pathophysiology of Shwachman-Diamond syndrome: an update.
Kasiani C Myers, Stella M Davies, Akiko Shimamura. Hematol Oncol Clin North Am 2013
56
10

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
59
10


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
63
10

Refining the phenotype associated with biallelic DNAJC21 mutations.
G D'Amours, F Lopes, J Gauthier, V Saillour, C Nassif, R Wynn, N Alos, T Leblanc, Y Capri, S Nizard,[...]. Clin Genet 2018
12
16

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
52
10

Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.
Roberto Valli, Elena De Paoli, Lucia Nacci, Annalisa Frattini, Francesco Pasquali, Emanuela Maserati. Pediatr Blood Cancer 2017
10
20

Human female meiosis revised: new insights into the mechanisms of chromosome segregation and aneuploidies from advanced genomics and time-lapse imaging.
Antonio Capalbo, Eva R Hoffmann, Danilo Cimadomo, Filippo Maria Ubaldi, Laura Rienzi. Hum Reprod Update 2017
72
10


Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature.
Roberto Valli, Francesca De Bernardi, Annalisa Frattini, Luca Volpi, Maurizio Bignami, Fabio Facchetti, Francesco Pasquali, Paolo Castelnuovo, Emanuela Maserati. Genes Chromosomes Cancer 2015
11
18


Chromosomal changes characterize head and neck cancer with poor prognosis.
Verena L Bauer, Herbert Braselmann, Michael Henke, Dominik Mattern, Axel Walch, Kristian Unger, Michael Baudis, Silke Lassmann, Reinhard Huber, Johannes Wienberg,[...]. J Mol Med (Berl) 2008
27
5

Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR.
G Porta, E Maserati, E Mattarucchi, A Minelli, B Pressato, R Valli, M Zecca, M E Bernardo, F Lo Curto, F Locatelli,[...]. Leukemia 2007
11
9

Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH.
Nicholas J Neill, Beth S Torchia, Bassem A Bejjani, Lisa G Shaffer, Blake C Ballif. Mol Cytogenet 2010
45
5

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.
Gurdeep S Sagoo, Adam S Butterworth, Simon Sanderson, Charles Shaw-Smith, Julian P T Higgins, Hilary Burton. Genet Med 2009
146
5

Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
M De Gregori, R Ciccone, P Magini, T Pramparo, S Gimelli, J Messa, F Novara, A Vetro, E Rossi, P Maraschio,[...]. J Med Genet 2007
186
5

Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.
Sau W Cheung, Chad A Shaw, Daryl A Scott, Ankita Patel, Trilochan Sahoo, Carlos A Bacino, Amber Pursley, Jiangzhen Li, Robert Erickson, Andrea L Gropman,[...]. Am J Med Genet A 2007
129
5

Multiple putative oncogenes at the chromosome 20q amplicon contribute to colorectal adenoma to carcinoma progression.
B Carvalho, C Postma, S Mongera, E Hopmans, S Diskin, M A van de Wiel, W van Criekinge, O Thas, A Matthäi, M A Cuesta,[...]. Gut 2009
173
5

Clinical utility of contemporary molecular cytogenetics.
Bassem A Bejjani, Lisa G Shaffer. Annu Rev Genomics Hum Genet 2008
53
5

Development of new postnatal diagnostic methods for chromosome disorders.
Lisa G Shaffer, Bassem A Bejjani. Semin Fetal Neonatal Med 2011
1
100

Detection of large-scale variation in the human genome.
A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer, Charles Lee. Nat Genet 2004
5

Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.
Elia Mattarucchi, Milena Marsoni, Alberto Passi, Francesco Lo Curto, Francesco Pasquali, Giovanni Porta. J Mol Diagn 2006
5
20

Myelodysplastic syndrome in children and adolescents.
Charlotte M Niemeyer, Irith Baumann. Semin Hematol 2008
37
5

Unbalanced 6p translocation as primary karyotypic anomaly in secondary acute nonlymphocytic leukemia.
M Mancini, C Mecucci, M Cedrone, M B Rondinelli, M A Aloe-Spiriti, G Alimena. Cancer Genet Cytogenet 1992
4
25

The short arm of chromosome 6 is nonrandomly rearranged in secondary myelodysplastic syndromes.
C Mecucci, J L Michaux, A Louwagie, M Boogaerts, H Van den Berghe. Cancer Genet Cytogenet 1988
37
5

Allogeneic hematopoetic stem cell transplantation in pediatric myelodysplastic syndromes: improved outcomes for de novo disease.
Jeffrey R Andolina, Morris Kletzel, William T Tse, David A Jacobsohn, Reggie E Duerst, Jennifer Schneiderman, Irene Helenowski, Alfred Rademaker, Sonali Chaudhury. Pediatr Transplant 2011
7
14

Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia.
R La Starza, A Aventin, C Matteucci, B Crescenzi, S Romoli, N Testoni, V Pierini, S Ciolli, C Sambani, A Locasciulli,[...]. Leukemia 2006
7
14

Risk of secondary leukemia after a solid tumor in childhood according to the dose of epipodophyllotoxins and anthracyclines: a case-control study by the Société Française d'Oncologie Pédiatrique.
Marie-Cécile Le Deley, Thierry Leblanc, Akthar Shamsaldin, Marie-Anne Raquin, Brigitte Lacour, Danièle Sommelet, Agnès Chompret, Jean-Michel Cayuela, Chantal Bayle, Alain Bernheim,[...]. J Clin Oncol 2003
139
5


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.