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



Times Cited
  Times     Co-cited
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The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.
David N Louis, Arie Perry, Guido Reifenberger, Andreas von Deimling, Dominique Figarella-Branger, Webster K Cavenee, Hiroko Ohgaki, Otmar D Wiestler, Paul Kleihues, David W Ellison. Acta Neuropathol 2016
30

Assessing copy number aberrations and copy-neutral loss-of-heterozygosity across the genome as best practice: An evidence-based review from the Cancer Genomics Consortium (CGC) working group for chronic lymphocytic leukemia.
Kathy Chun, Gail D Wenger, Alka Chaubey, D P Dash, Rashmi Kanagal-Shamanna, Sibel Kantarci, Ravindra Kolhe, Daniel L Van Dyke, Lu Wang, Daynna J Wolff,[...]. Cancer Genet 2018
11
20



Diagnostic application of high resolution single nucleotide polymorphism array analysis for children with brain tumors.
Jacquelyn J Roth, Mariarita Santi, Lucy B Rorke-Adams, Brian N Harding, Tracy M Busse, Laura S Tooke, Jaclyn A Biegel. Cancer Genet 2014
29
20

Mutational landscape and clonal architecture in grade II and III gliomas.
Hiromichi Suzuki, Kosuke Aoki, Kenichi Chiba, Yusuke Sato, Yusuke Shiozawa, Yuichi Shiraishi, Teppei Shimamura, Atsushi Niida, Kazuya Motomura, Fumiharu Ohka,[...]. Nat Genet 2015
433
20

cIMPACT-NOW update 2: diagnostic clarifications for diffuse midline glioma, H3 K27M-mutant and diffuse astrocytoma/anaplastic astrocytoma, IDH-mutant.
David N Louis, Caterina Giannini, David Capper, Werner Paulus, Dominique Figarella-Branger, M Beatriz Lopes, Tracy T Batchelor, J Gregory Cairncross, Martin van den Bent, Wolfgang Wick,[...]. Acta Neuropathol 2018
131
20

Angiomatous meningiomas have a distinct genetic profile with multiple chromosomal polysomies including polysomy of chromosome 5.
Malak S Abedalthagafi, Parker H Merrill, Wenya Linda Bi, Robert T Jones, Marc L Listewnik, Shakti H Ramkissoon, Aaron R Thorner, Ian F Dunn, Rameen Beroukhim, Brian M Alexander,[...]. Oncotarget 2014
38
20

Analysis of genomic alterations in benign, atypical, and anaplastic meningiomas: toward a genetic model of meningioma progression.
R G Weber, J Boström, M Wolter, M Baudis, V P Collins, G Reifenberger, P Lichter. Proc Natl Acad Sci U S A 1997
304
20

cIMPACT-NOW update 3: recommended diagnostic criteria for "Diffuse astrocytic glioma, IDH-wildtype, with molecular features of glioblastoma, WHO grade IV".
Daniel J Brat, Kenneth Aldape, Howard Colman, Eric C Holland, David N Louis, Robert B Jenkins, B K Kleinschmidt-DeMasters, Arie Perry, Guido Reifenberger, Roger Stupp,[...]. Acta Neuropathol 2018
248
20

cIMPACT-NOW update 5: recommended grading criteria and terminologies for IDH-mutant astrocytomas.
Daniel J Brat, Kenneth Aldape, Howard Colman, Dominique Figrarella-Branger, Gregory N Fuller, Caterina Giannini, Eric C Holland, Robert B Jenkins, Bette Kleinschmidt-DeMasters, Takashi Komori,[...]. Acta Neuropathol 2020
93
20

DNA methylation-based classification of central nervous system tumours.
David Capper, David T W Jones, Martin Sill, Volker Hovestadt, Daniel Schrimpf, Dominik Sturm, Christian Koelsche, Felix Sahm, Lukas Chavez, David E Reuss,[...]. Nature 2018
720
20

Methylation array profiling of adult brain tumours: diagnostic outcomes in a large, single centre.
Zane Jaunmuktane, David Capper, David T W Jones, Daniel Schrimpf, Martin Sill, Monika Dutt, Nirosha Suraweera, Stefan M Pfister, Andreas von Deimling, Sebastian Brandner. Acta Neuropathol Commun 2019
34
20

Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG).
Marilyn M Li, Elizabeth Chao, Edward D Esplin, David T Miller, Katherine L Nathanson, Sharon E Plon, Maren T Scheuner, Douglas R Stewart. Genet Med 2020
25
20

Treatment reduction for children and young adults with low-risk acute lymphoblastic leukaemia defined by minimal residual disease (UKALL 2003): a randomised controlled trial.
Ajay Vora, Nick Goulden, Rachel Wade, Chris Mitchell, Jeremy Hancock, Rachael Hough, Clare Rowntree, Sue Richards. Lancet Oncol 2013
258
10

Genes commonly deleted in childhood B-cell precursor acute lymphoblastic leukemia: association with cytogenetics and clinical features.
Claire J Schwab, Lucy Chilton, Heather Morrison, Lisa Jones, Halima Al-Shehhi, Amy Erhorn, Lisa J Russell, Anthony V Moorman, Christine J Harrison. Haematologica 2013
91
10

Toxicity and efficacy of 6-thioguanine versus 6-mercaptopurine in childhood lymphoblastic leukaemia: a randomised trial.
Ajay Vora, Chris D Mitchell, Lynne Lennard, T O B Eden, Sally E Kinsey, John Lilleyman, Sue M Richards. Lancet 2006
104
10

Evaluation of multiplex ligation-dependent probe amplification as a method for the detection of copy number abnormalities in B-cell precursor acute lymphoblastic leukemia.
C J Schwab, L R Jones, H Morrison, S L Ryan, H Yigittop, J P Schouten, C J Harrison. Genes Chromosomes Cancer 2010
85
10

Genetic Basis of Acute Lymphoblastic Leukemia.
Ilaria Iacobucci, Charles G Mullighan. J Clin Oncol 2017
168
10

Masked hypodiploidy: Hypodiploid acute lymphoblastic leukemia (ALL) mimicking hyperdiploid ALL in children: A report from the Children's Oncology Group.
Andrew J Carroll, Mary Shago, Fady M Mikhail, Susana C Raimondi, Betsy A Hirsch, Mignon L Loh, Elizabeth A Raetz, Michael J Borowitz, Brent L Wood, Kelly W Maloney,[...]. Cancer Genet 2019
11
10

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms.
Sharon J Diskin, Mingyao Li, Cuiping Hou, Shuzhang Yang, Joseph Glessner, Hakon Hakonarson, Maja Bucan, John M Maris, Kai Wang. Nucleic Acids Res 2008
224
10

Circular binary segmentation for the analysis of array-based DNA copy number data.
Adam B Olshen, E S Venkatraman, Robert Lucito, Michael Wigler. Biostatistics 2004
10

BLAT--the BLAST-like alignment tool.
W James Kent. Genome Res 2002
10

Prognostic effect of chromosomal abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: results from the UK Medical Research Council ALL97/99 randomised trial.
Anthony V Moorman, Hannah M Ensor, Sue M Richards, Lucy Chilton, Claire Schwab, Sally E Kinsey, Ajay Vora, Chris D Mitchell, Christine J Harrison. Lancet Oncol 2010
223
10


IKZF1plus Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia.
Martin Stanulla, Elif Dagdan, Marketa Zaliova, Anja Möricke, Chiara Palmi, Giovanni Cazzaniga, Cornelia Eckert, Geertruy Te Kronnie, Jean-Pierre Bourquin, Beat Bornhauser,[...]. J Clin Oncol 2018
77
10

Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience.
Évelin Aline Zanardo, Roberta Lelis Dutra, Flavia Balbo Piazzon, Alexandre Torchio Dias, Gil Monteiro Novo-Filho, Amom Mendes Nascimento, Marília Moreira Montenegro, Jullian Gabriel Damasceno, Fabrícia Andreia Rosa Madia, Thaís Virgínia Moura Machado da Costa,[...]. Clinics (Sao Paulo) 2017
7
14

Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases.
Liborio Stuppia, Ivana Antonucci, Giandomenico Palka, Valentina Gatta. Int J Mol Sci 2012
100
10

CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing.
Eric Talevich, A Hunter Shain, Thomas Botton, Boris C Bastian. PLoS Comput Biol 2016
480
10

Bioconductor: open software development for computational biology and bioinformatics.
Robert C Gentleman, Vincent J Carey, Douglas M Bates, Ben Bolstad, Marcel Dettling, Sandrine Dudoit, Byron Ellis, Laurent Gautier, Yongchao Ge, Jeff Gentry,[...]. Genome Biol 2004
10

Validation of the United Kingdom copy-number alteration classifier in 3239 children with B-cell precursor ALL.
Lina Hamadeh, Amir Enshaei, Claire Schwab, Cristina N Alonso, Andishe Attarbaschi, Gisela Barbany, Monique L den Boer, Judith M Boer, Marcin Braun, Luciano Dalla Pozza,[...]. Blood Adv 2019
16
10

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
10

A novel integrated cytogenetic and genomic classification refines risk stratification in pediatric acute lymphoblastic leukemia.
Anthony V Moorman, Amir Enshaei, Claire Schwab, Rachel Wade, Lucy Chilton, Alannah Elliott, Stacey Richardson, Jeremy Hancock, Sally E Kinsey, Christopher D Mitchell,[...]. Blood 2014
119
10

IKZF1 deletion is an independent predictor of outcome in pediatric acute lymphoblastic leukemia treated according to the ALL-BFM 2000 protocol.
Petra Dörge, Barbara Meissner, Martin Zimmermann, Anja Möricke, André Schrauder, Jean-Pierre Bouquin, Denis Schewe, Jochen Harbott, Andrea Teigler-Schlegel, Richard Ratei,[...]. Haematologica 2013
97
10


SETD2 alterations impair DNA damage recognition and lead to resistance to chemotherapy in leukemia.
Brenton G Mar, S Haihua Chu, Josephine D Kahn, Andrei V Krivtsov, Richard Koche, Cecilia A Castellano, Jacob L Kotlier, Rebecca L Zon, Marie E McConkey, Jonathan Chabon,[...]. Blood 2017
52
10

Major prognostic value of complex karyotype in addition to TP53 and IGHV mutational status in first-line chronic lymphocytic leukemia.
Yannick Le Bris, Stéphanie Struski, Romain Guièze, Caroline Rouvellat, Naïs Prade, Xavier Troussard, Olivier Tournilhac, Marie C Béné, Eric Delabesse, Loïc Ysebaert. Hematol Oncol 2017
18
10

Genomic aberrations and survival in chronic lymphocytic leukemia.
H Döhner, S Stilgenbauer, A Benner, E Leupolt, A Kröber, L Bullinger, K Döhner, M Bentz, P Lichter. N Engl J Med 2000
10

Molecular allelokaryotyping of early-stage, untreated chronic lymphocytic leukemia.
Sören Lehmann, Seishi Ogawa, Sophie D Raynaud, Masashi Sanada, Yasuhito Nannya, Michel Ticchioni, Christian Bastard, Norihiko Kawamata, H Phillip Koeffler. Cancer 2008
57
10

Whole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemia.
Shelly R Gunn, Mansoor S Mohammed, Mercedes E Gorre, Philip D Cotter, Jaeweon Kim, David W Bahler, Sergey N Preobrazhensky, Russell A Higgins, Aswani R Bolla, Sahar H Ismail,[...]. J Mol Diagn 2008
61
10

Array-based genomic screening at diagnosis and during follow-up in chronic lymphocytic leukemia.
Rebeqa Gunnarsson, Larry Mansouri, Anders Isaksson, Hanna Göransson, Nicola Cahill, Mattias Jansson, Markus Rasmussen, Jeanette Lundin, Stefan Norin, Anne Mette Buhl,[...]. Haematologica 2011
69
10

Genomic disruption of the histone methyltransferase SETD2 in chronic lymphocytic leukaemia.
H Parker, M J J Rose-Zerilli, M Larrayoz, R Clifford, J Edelmann, S Blakemore, J Gibson, J Wang, V Ljungström, T K Wojdacz,[...]. Leukemia 2016
44
10

Chromosomal translocations and karyotype complexity in chronic lymphocytic leukemia: a systematic reappraisal of classic cytogenetic data.
Panagiotis Baliakas, Michalis Iskas, Anne Gardiner, Zadie Davis, Karla Plevova, Florence Nguyen-Khac, Jitka Malcikova, Achilles Anagnostopoulos, Sharron Glide, Sarah Mould,[...]. Am J Hematol 2014
80
10

Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition.
Jan A Burger, Dan A Landau, Amaro Taylor-Weiner, Ivana Bozic, Huidan Zhang, Kristopher Sarosiek, Lili Wang, Chip Stewart, Jean Fan, Julia Hoellenriegel,[...]. Nat Commun 2016
180
10

Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia.
S J L Knight, C Yau, R Clifford, A T Timbs, E Sadighi Akha, H M Dréau, A Burns, C Ciria, D G Oscier, A R Pettitt,[...]. Leukemia 2012
47
10

Clinical staging of chronic lymphocytic leukemia.
K R Rai, A Sawitsky, E P Cronkite, A D Chanana, R N Levy, B S Pasternack. Blood 1975
10

Clinicopathological features and outcomes of progression of CLL on the BCL2 inhibitor venetoclax.
Mary Ann Anderson, Constantine Tam, Thomas E Lew, Surender Juneja, Manu Juneja, David Westerman, Meaghan Wall, Stephen Lade, Alexandra Gorelik, David C S Huang,[...]. Blood 2017
94
10

SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage.
Ruth Clifford, Tania Louis, Pauline Robbe, Sam Ackroyd, Adam Burns, Adele T Timbs, Glen Wright Colopy, Helene Dreau, Francois Sigaux, Jean Gabriel Judde,[...]. Blood 2014
136
10

Complex karyotypes and KRAS and POT1 mutations impact outcome in CLL after chlorambucil-based chemotherapy or chemoimmunotherapy.
Carmen Diana Herling, Marion Klaumünzer, Cristiano Krings Rocha, Janine Altmüller, Holger Thiele, Jasmin Bahlo, Sandra Kluth, Giuliano Crispatzu, Marco Herling, Joanna Schiller,[...]. Blood 2016
74
10

13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia.
H Parker, M J J Rose-Zerilli, A Parker, T Chaplin, R Wade, A Gardiner, M Griffiths, A Collins, B D Young, D G Oscier,[...]. Leukemia 2011
74
10


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.