A citation-based method for searching scientific literature

Francesca Scionti, Maria Teresa Di Martino, Licia Pensabene, Valentina Bruni, Daniela Concolino. High Throughput 2018
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity



Shifting the focus toward rare variants in schizophrenia to close the gap from genotype to phenotype.
M Leonor Bustamante, Luisa Herrera, Pablo A Gaspar, Rodrigo Nieto, Alejandro Maturana, María José Villar, Valeria Salinas, Hernán Silva. Am J Med Genet B Neuropsychiatr Genet 2017
11
40

Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics.
Ina Giegling, Ladislav Hosak, Rainald Mössner, Alessandro Serretti, Frank Bellivier, Stephan Claes, David A Collier, Alejo Corrales, Lynn E DeLisi, Carla Gallo,[...]. World J Biol Psychiatry 2017
32
40

Understanding the Basics of NGS: From Mechanism to Variant Calling.
Dale Muzzey, Eric A Evans, Caroline Lieber. Curr Genet Med Rep 2015
35
40

Chromosome abnormalities, mental retardation and the search for genes in bipolar disorder and schizophrenia.
D H R Blackwood, T Thiagarajah, P Malloy, B S Pickard, W J Muir. Neurotox Res 2008
13
40

The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
Dorothy Warburton, Michael Ronemus, Jennie Kline, Vaidehi Jobanputra, Ismee Williams, Kwame Anyane-Yeboa, Wendy Chung, Lan Yu, Nancy Wong, Danielle Awad,[...]. Hum Genet 2014
78
20

Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.
Dimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, Sarah Bowdin, Nasim Monfared, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Giovanna Pellecchia, Ryan K C Yuen, Michael J Szego,[...]. NPJ Genom Med 2016
174
20

Microarray analysis for constitutional cytogenetic abnormalities.
Lisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, Betsy Hirsch, Brynn Levy, Christa Lese Martin, James T Mascarello, Kathleen W Rao. Genet Med 2007
49
20

Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangements.
Vaidehi Jobanputra, Jonathan Sebat, Jennifer Troge, Wendy Chung, Kwame Anyane-Yeboa, Michael Wigler, Dorothy Warburton. Genet Med 2005
26
20


Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions.
Yanjie Fan, Yanming Wu, Lili Wang, Yu Wang, Zhuwen Gong, Wenjuan Qiu, Jingmin Wang, Huiwen Zhang, Xing Ji, Jun Ye,[...]. BMC Med Genomics 2018
10
20

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
20

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.
Jm Friedman, Shelin Adam, Laura Arbour, Linlea Armstrong, Agnes Baross, Patricia Birch, Cornelius Boerkoel, Susanna Chan, David Chai, Allen D Delaney,[...]. BMC Genomics 2009
27
20

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
20



Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
20

Reducing system noise in copy number data using principal components of self-self hybridizations.
Yoon-ha Lee, Michael Ronemus, Jude Kendall, B Lakshmi, Anthony Leotta, Dan Levy, Diane Esposito, Vladimir Grubor, Kenny Ye, Michael Wigler,[...]. Proc Natl Acad Sci U S A 2012
7
20

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.
Jenny C Taylor, Hilary C Martin, Stefano Lise, John Broxholme, Jean-Baptiste Cazier, Andy Rimmer, Alexander Kanapin, Gerton Lunter, Simon Fiddy, Chris Allan,[...]. Nat Genet 2015
194
20

UPD detection using homozygosity profiling with a SNP genotyping microarray.
Peter Papenhausen, Stuart Schwartz, Hiba Risheg, Elisabeth Keitges, Inder Gadi, Rachel D Burnside, Vikram Jaswaney, John Pappas, Romela Pasion, Kenneth Friedman,[...]. Am J Med Genet A 2011
88
20

Genomic runs of homozygosity record population history and consanguinity.
Mirna Kirin, Ruth McQuillan, Christopher S Franklin, Harry Campbell, Paul M McKeigue, James F Wilson. PLoS One 2010
245
20

Assuring the quality of next-generation sequencing in clinical laboratory practice.
Amy S Gargis, Lisa Kalman, Meredith W Berry, David P Bick, David P Dimmock, Tina Hambuch, Fei Lu, Elaine Lyon, Karl V Voelkerding, Barbara A Zehnbauer,[...]. Nat Biotechnol 2012
313
20

Patterns of homozygosity in patients with uniparental disomy: detection rate and suggested reporting thresholds for SNP microarrays.
Nicole Hoppman, Kandelaria Rumilla, Emily Lauer, Hutton Kearney, Erik Thorland. Genet Med 2018
11
20

A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data.
Brett Trost, Susan Walker, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Jeffrey R MacDonald, Wilson W L Sung, Sergio L Pereira, Joe Whitney, Ada J S Chan, Giovanna Pellecchia,[...]. Am J Hum Genet 2018
78
20

A clinical evaluation tool for SNP arrays, especially for autosomal recessive conditions in offspring of consanguineous parents.
Klaas J Wierenga, Zhijie Jiang, Amy C Yang, John J Mulvihill, Nicholas F Tsinoremas. Genet Med 2013
47
20

Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions.
Tiong Yang Tan, Oliver James Dillon, Zornitza Stark, Deborah Schofield, Khurshid Alam, Rupendra Shrestha, Belinda Chong, Dean Phelan, Gemma R Brett, Emma Creed,[...]. JAMA Pediatr 2017
146
20

Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis.
Aparna Prasad, Matthew A Sdano, Rena J Vanzo, Patricia A Mowery-Rushton, Moises A Serrano, Charles H Hensel, E Robert Wassman. BMC Med Genet 2018
11
20

SMASH, a fragmentation and sequencing method for genomic copy number analysis.
Zihua Wang, Peter Andrews, Jude Kendall, Beicong Ma, Inessa Hakker, Linda Rodgers, Michael Ronemus, Michael Wigler, Dan Levy. Genome Res 2016
14
20


An overview on the role of FLT3-tyrosine kinase receptor in acute myeloid leukemia: biology and treatment.
Tiziana Grafone, Michela Palmisano, Chiara Nicci, Sergio Storti. Oncol Rev 2012
87
20

Activating somatic and germline TERT promoter variants in myeloid malignancies.
Valeria Nofrini, Caterina Matteucci, Fabrizia Pellanera, Paolo Gorello, Danika Di Giacomo, Anair Graciela Lema Fernandez, Carlotta Nardelli, Tamara Iannotti, Lucia Brandimarte, Silvia Arniani,[...]. Leukemia 2021
3
33

Clinical Validation of a Next-Generation Sequencing Genomic Oncology Panel via Cross-Platform Benchmarking against Established Amplicon Sequencing Assays.
Sabah Kadri, Bradley C Long, Ibro Mujacic, Chao J Zhen, Michelle N Wurst, Shruti Sharma, Nadia McDonald, Nifang Niu, Sonia Benhamed, Jigyasa H Tuteja,[...]. J Mol Diagn 2017
61
20

Gene expression profiling of acute myeloid leukemia with translocation t(8;16)(p11;p13) and MYST3-CREBBP rearrangement reveals a distinctive signature with a specific pattern of HOX gene expression.
Mireia Camós, Jordi Esteve, Pedro Jares, Dolors Colomer, María Rozman, Neus Villamor, Dolors Costa, Ana Carrió, Josep Nomdedéu, Emili Montserrat,[...]. Cancer Res 2006
99
20

The impact of therapy-related acute myeloid leukemia (AML) on outcome in 2853 adult patients with newly diagnosed AML.
Sabine Kayser, Konstanze Döhner, Jürgen Krauter, Claus-Henning Köhne, Heinz A Horst, Gerhard Held, Marie von Lilienfeld-Toal, Sibylla Wilhelm, Andrea Kündgen, Katharina Götze,[...]. Blood 2011
255
20

Prognostic Role of Gene Mutations in Chronic Myelomonocytic Leukemia Patients Treated With Hypomethylating Agents.
Matthieu Duchmann, Fevzi F Yalniz, Alessandro Sanna, David Sallman, Catherine C Coombs, Aline Renneville, Olivier Kosmider, Thorsten Braun, Uwe Platzbecker, Lise Willems,[...]. EBioMedicine 2018
41
20

Acute myeloid leukemia with t(8;16)(p11.2;p13.3)/KAT6A-CREBBP in adults.
Wei Xie, Shimin Hu, Jie Xu, Zhining Chen, L Jeffrey Medeiros, Guilin Tang. Ann Hematol 2019
10
20

Mutational analysis of therapy-related myelodysplastic syndromes and acute myelogenous leukemia.
Alan H Shih, Stephen S Chung, Emily K Dolezal, Su-Jiang Zhang, Omar I Abdel-Wahab, Christopher Y Park, Stephen D Nimer, Ross L Levine, Virginia M Klimek. Haematologica 2013
79
20

AML with translocation t(8;16)(p11;p13) demonstrates unique cytomorphological, cytogenetic, molecular and prognostic features.
T Haferlach, A Kohlmann, H-U Klein, C Ruckert, M Dugas, P M Williams, W Kern, S Schnittger, U Bacher, H Löffler,[...]. Leukemia 2009
57
20

Acquired mutations in ASXL1 in acute myeloid leukemia: prevalence and prognostic value.
Marta Pratcorona, Saman Abbas, Mathijs A Sanders, Jasper E Koenders, François G Kavelaars, Claudia A J Erpelinck-Verschueren, Annelieke Zeilemakers, Bob Löwenberg, Peter J M Valk. Haematologica 2012
89
20

Epidemiological, genetic, and clinical characterization by age of newly diagnosed acute myeloid leukemia based on an academic population-based registry study (AMLSG BiO).
Gabriele Nagel, D Weber, E Fromm, S Erhardt, M Lübbert, W Fiedler, T Kindler, J Krauter, P Brossart, A Kündgen,[...]. Ann Hematol 2017
65
20

Association between TERT promoter polymorphisms and acute myeloid leukemia risk and prognosis.
Mohamed Ali Mosrati, Kerstin Willander, Ingrid Jakobsen Falk, Monica Hermanson, Martin Höglund, Dick Stockelberg, Yuan Wei, Kourosh Lotfi, Peter Söderkvist. Oncotarget 2015
40
20

Acute Myeloid Leukemia, Version 3.2017, NCCN Clinical Practice Guidelines in Oncology.
Margaret R O'Donnell, Martin S Tallman, Camille N Abboud, Jessica K Altman, Frederick R Appelbaum, Daniel A Arber, Vijaya Bhatt, Dale Bixby, William Blum, Steven E Coutre,[...]. J Natl Compr Canc Netw 2017
231
20

FLT3 mutations in acute myeloid leukemia: what is the best approach in 2013?
Mark Levis. Hematology Am Soc Hematol Educ Program 2013
161
20

Role of TP53 mutations in the origin and evolution of therapy-related acute myeloid leukaemia.
Terrence N Wong, Giridharan Ramsingh, Andrew L Young, Christopher A Miller, Waseem Touma, John S Welch, Tamara L Lamprecht, Dong Shen, Jasreet Hundal, Robert S Fulton,[...]. Nature 2015
411
20

Acute Myeloid Leukemia with Co-mutated ASXL1 and SRSF2 Exhibits Monocytic Differentiation and has a Mutational Profile Overlapping with Chronic Myelomonocytic Leukemia.
Steven M Johnson, Daniel R Richardson, Jonathan Galeotti, Sonia Esparza, Anqi Zhu, Yuri Fedoriw, Karen E Weck, Matthew C Foster, Catherine C Coombs, Joshua F Zeidner,[...]. Hemasphere 2019
4
25

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein.
J Borrow, V P Stanton, J M Andresen, R Becher, F G Behm, R S Chaganti, C I Civin, C Disteche, I Dubé, A M Frischauf,[...]. Nat Genet 1996
606
20

Prognostic significance of FLT3 ITD and D835 mutations in AML patients.
Mohammad Hasan Sheikhha, Abida Awan, Khalid Tobal, John Ahman Liu Yin. Hematol J 2003
50
20

Acute myeloid leukemia with translocation t(8;16) presents with features which mimic acute promyelocytic leukemia and is associated with poor prognosis.
Adi Diab, Lynette Zickl, Omar Abdel-Wahab, Suresh Jhanwar, Manjit A Gulam, Katherine S Panageas, Jay P Patel, Joseph Jurcic, Peter Maslak, Elisabeth Paietta,[...]. Leuk Res 2013
21
20

RAS, FLT3, and TP53 mutations in therapy-related myeloid malignancies with abnormalities of chromosomes 5 and 7.
Lucy E Side, Nicole P Curtiss, Kathryn Teel, Christian Kratz, Pauline W Wang, Richard A Larson, Michelle M Le Beau, Kevin M Shannon. Genes Chromosomes Cancer 2004
40
20



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.