A citation-based method for searching scientific literature

Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C Rivera, María L Guzmán, Gabriela M Repetto. J Pediatr (Rio J) 2015
Times Cited: 6







List of co-cited articles
12 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
66

Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil.
G S Vianna, P F V Medeiros, A F Alves, T O Silva, F S Jehee. Genet Mol Res 2016
7
50

Considering specific clinical features as evidence of pathogenic copy number variants.
Egle Preiksaitiene, Alma Molytė, Jurate Kasnauskiene, Zivile Ciuladaite, Algirdas Utkus, Philippos C Patsalis, Vaidutis Kučinskas. J Appl Genet 2014
12
33

Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.
A C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, M R Passos-Bueno, J Knijnenburg, K Szuhai, W Sloos, J F Mazzeu, F Kok, C Cheroki,[...]. Cytogenet Genome Res 2006
86
33

Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics.
Joris R Vermeesch, Paul D Brady, Damien Sanlaville, Klaas Kok, Rosalind J Hastings. Hum Mutat 2012
54
33

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
533
33

New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
Gerarda Cappuccio, Francesco Vitiello, Alberto Casertano, Paolo Fontana, Rita Genesio, Dario Bruzzese, Virginia Maria Ginocchio, Angela Mormile, Lucio Nitsch, Generoso Andria,[...]. Ital J Pediatr 2016
10
33

Phenotype profiling of patients with intellectual disability and copy number variations.
Mónica Roselló, Francisco Martínez, Sandra Monfort, Sonia Mayo, Silvestre Oltra, Carmen Orellana. Eur J Paediatr Neurol 2014
10
33

Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
M Shoukier, N Klein, B Auber, J Wickert, J Schröder, B Zoll, P Burfeind, I Bartels, E A Alsat, M Lingen,[...]. Clin Genet 2013
45
33

Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.
E Di Gregorio, E Riberi, E F Belligni, E Biamino, M Spielmann, U Ala, A Calcia, I Bagnasco, D Carli, G Gai,[...]. Clin Genet 2017
24
33

Analysis of chromosomal abnormalities by CGH-array in patients with dysmorphic and intellectual disability with normal karyotype.
Rodrigo Pratte-Santos, Katyanne Heringer Ribeiro, Thainá Altoe Santos, Terezinha Sarquis Cintra. Einstein (Sao Paulo) 2016
4
50

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
40

Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics.
C J Curry, R E Stevenson, D Aughton, J Byrne, J C Carey, S Cassidy, C Cunniff, J M Graham, M C Jones, M M Kaback,[...]. Am J Med Genet 1997
251
16

Chromosomal microarray interpretation: what is a child neurologist to do?
Alex R Paciorkowski, Min Fang. Pediatr Neurol 2009
15
16


Microdeletion and microduplication 17q21.31 plus an additional CNV, in patients with intellectual disability, identified by array-CGH.
Sophia Kitsiou-Tzeli, Helen Frysira, Krinio Giannikou, Areti Syrmou, Konstantina Kosma, Georgia Kakourou, Eleni Leze, Christalena Sofocleous, Emmanuel Kanavakis, Maria Tzetis. Gene 2012
22
16

The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function.
David Warde-Farley, Sylva L Donaldson, Ovi Comes, Khalid Zuberi, Rashad Badrawi, Pauline Chao, Max Franz, Chris Grouios, Farzana Kazi, Christian Tannus Lopes,[...]. Nucleic Acids Res 2010
16

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
411
16

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome.
Sarah B Ng, Abigail W Bigham, Kati J Buckingham, Mark C Hannibal, Margaret J McMillin, Heidi I Gildersleeve, Anita E Beck, Holly K Tabor, Gregory M Cooper, Heather C Mefford,[...]. Nat Genet 2010
847
16

The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.
David A Koolen, Rolph Pfundt, Katrin Linda, Gea Beunders, Hermine E Veenstra-Knol, Jessie H Conta, Ana Maria Fortuna, Gabriele Gillessen-Kaesbach, Sarah Dugan, Sara Halbach,[...]. Eur J Hum Genet 2016
47
16

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.
T H Shaikh, H Kurahashi, S C Saitta, A M O'Hare, P Hu, B A Roe, D A Driscoll, D M McDonald-McGinn, E H Zackai, M L Budarf,[...]. Hum Mol Genet 2000
377
16

Chromatin modifications remodel cardiac gene expression.
Prabhu Mathiyalagan, Samuel T Keating, Xiao-Jun Du, Assam El-Osta. Cardiovasc Res 2014
35
16

miRWalk--database: prediction of possible miRNA binding sites by "walking" the genes of three genomes.
Harsh Dweep, Carsten Sticht, Priyanka Pandey, Norbert Gretz. J Biomed Inform 2011
16

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.
Elisabeth E Mlynarski, Molly B Sheridan, Michael Xie, Tingwei Guo, Silvia E Racedo, Donna M McDonald-McGinn, Xiaowu Gai, Eva W C Chow, Jacob Vorstman, Ann Swillen,[...]. Am J Hum Genet 2015
46
16

Structural analysis of the KANSL1/WDR5/KANSL2 complex reveals that WDR5 is required for efficient assembly and chromatin targeting of the NSL complex.
Jorge Dias, Nhuong Van Nguyen, Plamen Georgiev, Aline Gaub, Janine Brettschneider, Stephen Cusack, Jan Kadlec, Asifa Akhtar. Genes Dev 2014
53
16

ParseCNV integrative copy number variation association software with quality tracking.
Joseph T Glessner, Jin Li, Hakon Hakonarson. Nucleic Acids Res 2013
43
16

Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome.
Tingwei Guo, Jonathan H Chung, Tao Wang, Donna M McDonald-McGinn, Wendy R Kates, Wanda Hawuła, Karlene Coleman, Elaine Zackai, Beverly S Emanuel, Bernice E Morrow. Am J Hum Genet 2015
36
16

The UCSC Genome Browser Database: update 2006.
A S Hinrichs, D Karolchik, R Baertsch, G P Barber, G Bejerano, H Clawson, M Diekhans, T S Furey, R A Harte, F Hsu,[...]. Nucleic Acids Res 2006
643
16

De novo mutations in histone-modifying genes in congenital heart disease.
Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D Overton, Angela Romano-Adesman, Robert D Bjornson, Roger E Breitbart, Kerry K Brown,[...]. Nature 2013
532
16

Cytoscape: a software environment for integrated models of biomolecular interaction networks.
Paul Shannon, Andrew Markiel, Owen Ozier, Nitin S Baliga, Jonathan T Wang, Daniel Ramage, Nada Amin, Benno Schwikowski, Trey Ideker. Genome Res 2003
16

Visualization and Analysis of MiRNA-Targets Interactions Networks.
Luis E León, Sebastián D Calligaris. Methods Mol Biol 2017
8
16

Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease.
Qian Jiang, Yen-Yi Ho, Li Hao, Courtney Nichols Berrios, Aravinda Chakravarti. PLoS One 2011
47
16

Copy-number variation and association studies of human disease.
Steven A McCarroll, David M Altshuler. Nat Genet 2007
408
16

Clinical interpretation of CNVs with cross-species phenotype data.
Sebastian Köhler, Uwe Schoeneberg, Johanna Christina Czeschik, Sandra C Doelken, Jayne Y Hehir-Kwa, Jonas Ibn-Salem, Christopher J Mungall, Damian Smedley, Melissa A Haendel, Peter N Robinson. J Med Genet 2014
13
16

A significant effect of the TSPY1 copy number on spermatogenesis efficiency and the phenotypic expression of the gr/gr deletion.
Ying Shen, Yuanlong Yan, Yunqiang Liu, Sizhong Zhang, Dong Yang, Peng Zhang, Lei Li, Yan Wang, Yongxin Ma, Dachang Tao,[...]. Hum Mol Genet 2013
10
16

Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum.
Federica Natacci, Enrico Alfei, Lucia Tararà, Stefano D'Arrigo, Orsetta Zuffardi, Barbara Gentilin, Chiara Pantaleoni. Eur J Paediatr Neurol 2016
5
20

A human phenome-interactome network of protein complexes implicated in genetic disorders.
Kasper Lage, E Olof Karlberg, Zenia M Størling, Páll I Olason, Anders G Pedersen, Olga Rigina, Anders M Hinsby, Zeynep Tümer, Flemming Pociot, Niels Tommerup,[...]. Nat Biotechnol 2007
619
16



Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome.
Chantal Sellier, Vicki J Hwang, Ravi Dandekar, Blythe Durbin-Johnson, Nicolas Charlet-Berguerand, Bradley P Ander, Frank R Sharp, Kathleen Angkustsiri, Tony J Simon, Flora Tassone. PLoS One 2014
40
16

A systematic review on screening for Fabry disease: prevalence of individuals with genetic variants of unknown significance.
L van der Tol, B E Smid, B J H M Poorthuis, M Biegstraaten, R H Lekanne Deprez, G E Linthorst, C E M Hollak. J Med Genet 2014
115
16

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.
Elisabeth E Mlynarski, Michael Xie, Deanne Taylor, Molly B Sheridan, Tingwei Guo, Silvia E Racedo, Donna M McDonald-McGinn, Eva W C Chow, Jacob Vorstman, Ann Swillen,[...]. Hum Genet 2016
27
16

22q11 deletion syndrome: current perspective.
Bülent Hacıhamdioğlu, Duygu Hacıhamdioğlu, Kenan Delil. Appl Clin Genet 2015
40
16

Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2.
Paula Sandrin-Garcia, Dagma V M Abramides, Lúcia R Martelli, Ester S Ramos, Antônio Richieri-Costa, Geraldo A S Passos. Mol Cell Biochem 2007
17
16

Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.
David A Koolen, Jamie M Kramer, Kornelia Neveling, Willy M Nillesen, Heather L Moore-Barton, Frances V Elmslie, Annick Toutain, Jeanne Amiel, Valérie Malan, Anne Chun-Hui Tsai,[...]. Nat Genet 2012
135
16

Genotype-phenotype correlation in 22q11.2 deletion syndrome.
Elena Michaelovsky, Amos Frisch, Miri Carmel, Miriam Patya, Omer Zarchi, Tamar Green, Lina Basel-Vanagaite, Abraham Weizman, Doron Gothelf. BMC Med Genet 2012
62
16

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Lisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, Jane A Hurst, Bert B A de Vries, Irene M Janssen, Walter A van der Vliet, Erik H L P G Huys, Pieter J de Jong, Ben C J Hamel,[...]. Nat Genet 2004
769
16


dmGWAS: dense module searching for genome-wide association studies in protein-protein interaction networks.
Peilin Jia, Siyuan Zheng, Jirong Long, Wei Zheng, Zhongming Zhao. Bioinformatics 2011
179
16

Subunit composition and substrate specificity of a MOF-containing histone acetyltransferase distinct from the male-specific lethal (MSL) complex.
Yong Cai, Jingji Jin, Selene K Swanson, Michael D Cole, Seung Hyuk Choi, Laurence Florens, Michael P Washburn, Joan W Conaway, Ronald C Conaway. J Biol Chem 2010
147
16


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.