A citation-based method for searching scientific literature

Rongyue Wang, Tingying Lei, Fang Fu, Ru Li, Xiangyi Jing, Xin Yang, Juan Liu, Dongzhi Li, Can Liao. Pediatr Neonatol 2019
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
22

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
22

RNA cytosine methylation by Dnmt2 and NSun2 promotes tRNA stability and protein synthesis.
Francesca Tuorto, Reinhard Liebers, Tanja Musch, Matthias Schaefer, Sarah Hofmann, Stefanie Kellner, Michaela Frye, Mark Helm, Georg Stoecklin, Frank Lyko. Nat Struct Mol Biol 2012
259
22

Defects in tRNA Anticodon Loop 2'-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1.
Michael P Guy, Marie Shaw, Catherine L Weiner, Lynne Hobson, Zornitza Stark, Katherine Rose, Vera M Kalscheuer, Jozef Gecz, Eric M Phizicky. Hum Mutat 2015
68
22

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
920
22

Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers,[...]. Nat Genet 2014
323
22

Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
Felippe Borlot, Brigid M Regan, Anne S Bassett, D James Stavropoulos, Danielle M Andrade. JAMA Neurol 2017
38
11

De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy.
Mehdi Zarrei, Darcy L Fehlings, Karizma Mawjee, Lauren Switzer, Bhooma Thiruvahindrapuram, Susan Walker, Daniele Merico, Guillermo Casallo, Mohammed Uddin, Jeffrey R MacDonald,[...]. Genet Med 2018
37
11

Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing.
Joanna Wiszniewska, Weimin Bi, Chad Shaw, Pawel Stankiewicz, Sung-Hae L Kang, Amber N Pursley, Seema Lalani, Patricia Hixson, Tomasz Gambin, Chun-hui Tsai,[...]. Eur J Hum Genet 2014
79
11

Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction.
Hui Zhu, Shaobin Lin, Linhuan Huang, Zhiming He, Xuan Huang, Yi Zhou, Qun Fang, Yanmin Luo. Prenat Diagn 2016
16
11

The clinical significance of small copy number variants in neurodevelopmental disorders.
Reza Asadollahi, Beatrice Oneda, Pascal Joset, Silvia Azzarello-Burri, Deborah Bartholdi, Katharina Steindl, Marie Vincent, Joana Cobilanschi, Heinrich Sticht, Rosa Baldinger,[...]. J Med Genet 2014
55
11

Single-nucleotide polymorphism array (SNP-A) improves the identification of chromosomal abnormalities by metaphase cytogenetics in myelodysplastic syndrome.
Fernanda Borges da Silva, João Agostinho Machado-Neto, Virginia Helena Leira Lipoli Bertini, Elvira Deolinda Rodrigues Pereira Velloso, Cristina Alonso Ratis, Rodrigo T Calado, Belinda Pinto Simões, Eduardo Magalhães Rego, Fabiola Traina. J Clin Pathol 2017
9
11

Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities.
Heather Mason-Suares, Wayne Kim, Leslie Grimmett, Eli S Williams, Vanessa L Horner, Dawn Kunig, Ian S Goldlust, Bai-Lin Wu, Yiping Shen, David T Miller,[...]. Genet Med 2013
20
11


Clinical relevance of small copy-number variants in chromosomal microarray clinical testing.
Dana Hollenbeck, Crescenda L Williams, Kathryn Drazba, Maria Descartes, Bruce R Korf, S Lane Rutledge, Edward J Lose, Nathaniel H Robin, Andrew J Carroll, Fady M Mikhail. Genet Med 2017
12
11

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
11

The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population.
Sarah M Al-Qattan, Salma M Wakil, Shamsa Anazi, Anas M Alazami, Nisha Patel, Ranad Shaheen, Hanan E Shamseldin, Samya T Hagos, Haya M AlDossari, Mustafa A Salih,[...]. Genet Med 2015
13
11

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
11

Optimization of probe length and the number of probes per gene for optimal microarray analysis of gene expression.
Cheng-Chung Chou, Chun-Houh Chen, Te-Tsui Lee, Konan Peck. Nucleic Acids Res 2004
122
11

Gene expression in diagnosis.
A Berns. Nature 2000
30
11




High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?
Laura Bernardini, Viola Alesi, Sara Loddo, Antonio Novelli, Irene Bottillo, Agatino Battaglia, Maria Cristina Digilio, Giuseppe Zampino, Adam Ertel, Paolo Fortina,[...]. Eur J Hum Genet 2010
39
11

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.
Laura K Conlin, Brian D Thiel, Carsten G Bonnemann, Livija Medne, Linda M Ernst, Elaine H Zackai, Matthew A Deardorff, Ian D Krantz, Hakon Hakonarson, Nancy B Spinner. Hum Mol Genet 2010
265
11


DNA methylome of familial breast cancer identifies distinct profiles defined by mutation status.
James M Flanagan, Sibylle Cocciardi, Nic Waddell, Cameron N Johnstone, Anna Marsh, Stephen Henderson, Peter Simpson, Leonard da Silva, Kumkum Khanna, Sunil Lakhani,[...]. Am J Hum Genet 2010
65
11

Genomic microarrays in mental retardation: a practical workflow for diagnostic applications.
David A Koolen, Rolph Pfundt, Nicole de Leeuw, Jayne Y Hehir-Kwa, Willy M Nillesen, Ineke Neefs, Ine Scheltinga, Erik Sistermans, Dominique Smeets, Han G Brunner,[...]. Hum Mutat 2009
112
11

New microdeletion and microduplication syndromes: A comprehensive review.
Julián Nevado, Rafaella Mergener, María Palomares-Bralo, Karen Regina Souza, Elena Vallespín, Rocío Mena, Víctor Martínez-Glez, María Ángeles Mori, Fernando Santos, Sixto García-Miñaur,[...]. Genet Mol Biol 2014
54
11

Exonic deletions of AUTS2 in Chinese patients with developmental delay and intellectual disability.
Yanjie Fan, Wenjuan Qiu, Lili Wang, Xuefan Gu, Yongguo Yu. Am J Med Genet A 2016
7
14

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
11

American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing.
Catherine W Rehder, Karen L David, Betsy Hirsch, Helga V Toriello, Carolyn M Wilson, Hutton M Kearney. Genet Med 2013
59
11

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
12
11

A copy number variation map of the human genome.
Mehdi Zarrei, Jeffrey R MacDonald, Daniele Merico, Stephen W Scherer. Nat Rev Genet 2015
368
11


Optimization of oligonucleotide-based DNA microarrays.
Angela Relógio, Christian Schwager, Alexandra Richter, Wilhelm Ansorge, Juan Valcárcel. Nucleic Acids Res 2002
183
11

Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis.
Ilse Feenstra, Nicolien Hanemaaijer, Birgit Sikkema-Raddatz, Helger Yntema, Trijnie Dijkhuizen, Dorien Lugtenberg, Joke Verheij, Andrew Green, Roel Hordijk, William Reardon,[...]. Eur J Hum Genet 2011
31
11

DMET™ (Drug Metabolism Enzymes and Transporters): a pharmacogenomic platform for precision medicine.
Mariamena Arbitrio, Maria Teresa Di Martino, Francesca Scionti, Giuseppe Agapito, Pietro Hiram Guzzi, Mario Cannataro, Pierfrancesco Tassone, Pierosandro Tagliaferri. Oncotarget 2016
29
11

Screening for intellectual disability using high-resolution CMA technology in a retrospective cohort from Central Brazil.
Rodrigo Roncato Pereira, Irene Plaza Pinto, Lysa Bernardes Minasi, Aldaires Vieira de Melo, Damiana Mirian da Cruz e Cunha, Alex Silva Cruz, Cristiano Luiz Ribeiro, Cláudio Carlos da Silva, Daniela de Melo e Silva, Aparecido Divino da Cruz. PLoS One 2014
5
20

A public antibody lineage that potently inhibits malaria infection through dual binding to the circumsporozoite protein.
Joshua Tan, Brandon K Sack, David Oyen, Isabelle Zenklusen, Luca Piccoli, Sonia Barbieri, Mathilde Foglierini, Chiara Silacci Fregni, Jessica Marcandalli, Said Jongo,[...]. Nat Med 2018
84
11


Prenatal exposure to benzophenone-3 (BP-3) induces apoptosis, disrupts estrogen receptor expression and alters the epigenetic status of mouse neurons.
Agnieszka Wnuk, Joanna Rzemieniec, Ewa Litwa, Władysław Lasoń, Małgorzata Kajta. J Steroid Biochem Mol Biol 2018
21
11

Norcantharidin modulates the miR-30a/Metadherin/AKT signaling axis to suppress proliferation and metastasis of stromal tumor cells in giant cell tumor of bone.
Feiyan Chen, Siqun Wang, Yibing Wei, Jianguo Wu, Gangyong Huang, Jie Chen, Jingsheng Shi, Jun Xia. Biomed Pharmacother 2018
8
12

Sensitive Genotyping of Foodborne-Associated Human Noroviruses and Hepatitis A Virus Using an Array-Based Platform.
Beatriz Quiñones, Bertram G Lee, Todd J Martinsky, Jaszemyn C Yambao, Paul K Haje, Mark Schena. Sensors (Basel) 2017
6
16

Sox9 transcriptionally regulates Wnt signaling in intestinal epithelial stem cells in hypomethylated crypts in the diabetic state.
Can-Ze Huang, Ji-Hao Xu, Wa Zhong, Zhong-Sheng Xia, Si-Yi Wang, Di Cheng, Jie-Yao Li, Ting-Feng Wu, Qi-Kui Chen, Tao Yu. Stem Cell Res Ther 2017
12
11

Comparative transcriptomic analysis of the roots of intercropped peanut and maize reveals novel insights into peanut iron nutrition.
Jing Dai, Wei Qiu, Nanqi Wang, Hiromi Nakanishi, Yuanmei Zuo. Plant Physiol Biochem 2018
5
20

Tyrosine Kinase Inhibition in HPV-related Squamous Cell Carcinoma Reveals Beneficial Expression of cKIT and Src.
Benedikt Kramer, Marcel Kneissle, Richard Birk, Nicole Rotter, Christoph Aderhold. Anticancer Res 2018
6
16

Analysis of G-Protein Coupled Receptor 30 (GPR30) on Endothelial Inflammation.
Subhadeep Chakrabarti, Sandra T Davidge. Methods Mol Biol 2016
10
11


DNA microarray-based mutation discovery and genotyping.
David Gresham. Methods Mol Biol 2011
1
100


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.