A citation-based method for searching scientific literature

Maryam Rafati, Elaheh Seyyedaboutorabi, Mohammad R Ghadirzadeh, Yaser Heshmati, Homeira Adibi, Zarrintaj Keihanidoust, Mohammad R Eshraghian, Gholam Reza Javadi, Jila Dastan, Alireza Mosavi-Jarrahi, Azadeh Hoseini, Marzieh Purhoseini, Saeed R Ghaffari. Mol Cytogenet 2012
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Microdeletion and microduplication syndromes.
Anja Weise, Kristin Mrasek, Elisabeth Klein, Milene Mulatinho, Juan C Llerena, David Hardekopf, Sona Pekova, Samarth Bhatt, Nadezda Kosyakova, Thomas Liehr. J Histochem Cytochem 2012
79
50



Microdeletion and microduplication syndromes.
Lisenka E L M Vissers, Paweł Stankiewicz. Methods Mol Biol 2012
41
50

CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
Francesco Brancati, Giuseppe Barrano, Jennifer L Silhavy, Sarah E Marsh, Lorena Travaglini, Stephanie L Bielas, Maria Amorini, Dominika Zablocka, Hulya Kayserili, Lihadh Al-Gazali,[...]. Am J Hum Genet 2007
105
25

CEP290, a gene with many faces: mutation overview and presentation of CEP290base.
Frauke Coppieters, Steve Lefever, Bart P Leroy, Elfride De Baere. Hum Mutat 2010
175
25

Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki-Lupski duplication syndrome.
Zhe Sun, Pengfei Liu, Xueyuan Jia, Marjorie A Withers, Li Jin, James R Lupski, Feng Zhang. Hum Mol Genet 2013
12
25


Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
156
25

Array CGH in human leukemia: from somatics to genetics.
L T van der Veken, A Buijs. Cytogenet Genome Res 2011
7
25

Short telomeres on human chromosome 17p.
U M Martens, J M Zijlmans, S S Poon, W Dragowska, J Yui, E A Chavez, R K Ward, P M Lansdorp. Nat Genet 1998
284
25

OligoArray: genome-scale oligonucleotide design for microarrays.
Jean-Marie Rouillard, Christopher J Herbert, Michael Zuker. Bioinformatics 2002
107
25

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker,[...]. Nat Genet 2010
417
25

A tiling resolution DNA microarray with complete coverage of the human genome.
Adrian S Ishkanian, Chad A Malloff, Spencer K Watson, Ronald J DeLeeuw, Bryan Chi, Bradley P Coe, Antoine Snijders, Donna G Albertson, Daniel Pinkel, Marco A Marra,[...]. Nat Genet 2004
467
25


Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
815
25



Assembly of microarrays for genome-wide measurement of DNA copy number.
A M Snijders, N Nowak, R Segraves, S Blackwood, N Brown, J Conroy, G Hamilton, A K Hindle, B Huey, K Kimura,[...]. Nat Genet 2001
634
25


Screening of human placentas for chromosomal mosaicism using comparative genomic hybridization.
V S Lestou, B L Lomax, I J Barrett, D K Kalousek. Teratology 1999
29
25

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
Nick Craddock, Matthew E Hurles, Niall Cardin, Richard D Pearson, Vincent Plagnol, Samuel Robson, Damjan Vukcevic, Chris Barnes, Donald F Conrad, Eleni Giannoulatou,[...]. Nature 2010
574
25


Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances.
S Solinas-Toldo, S Lampel, S Stilgenbauer, J Nickolenko, A Benner, H Döhner, T Cremer, P Lichter. Genes Chromosomes Cancer 1997
649
25

The chromosome number in humans: a brief history.
Stanley M Gartler. Nat Rev Genet 2006
18
25

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.
D Pinkel, R Segraves, D Sudar, S Clark, I Poole, D Kowbel, C Collins, W L Kuo, C Chen, Y Zhai,[...]. Nat Genet 1998
25

Long-term follow-up of four patients with Langer-Giedion syndrome: clinical course and complications.
Albert Schinzel, Mariluce Riegel, Alessandra Baumer, Andrea Superti-Furga, Lilia M A Moreira, Layla D E Santo, Patricia P Schiper, José Henrique Dantas Carvalho, Andres Giedion. Am J Med Genet A 2013
10
25

Multicolor FISH probe sets and their applications.
T Liehr, H Starke, A Weise, H Lehrer, U Claussen. Histol Histopathol 2004
41
25

RNA-DNA hybrids at the cytological level.
H A John, M L Birnstiel, K W Jones. Nature 1969
354
25

A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).
A Nietzel, M Rocchi, H Starke, A Heller, W Fiedler, I Wlodarska, I F Loncarevic, V Beensen, U Claussen, T Liehr. Hum Genet 2001
115
25

Mechanisms for Structural Variation in the Human Genome.
Benjamin B Currall, C Chiang, Michael E Talkowski, Cynthia C Morton. Curr Genet Med Rep 2013
15
25

Genomic disorders: complexity at multiple levels.
Santhosh Girirajan. Genome Med 2013
4
25


Prenatal diagnosis by array-CGH.
L Rickman, H Fiegler, N P Carter, M Bobrow. Eur J Med Genet 2005
42
25

Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today's genomic array era?
Weimin Bi, Caroline Borgan, Amber N Pursley, Patricia Hixson, Chad A Shaw, Carlos A Bacino, Seema R Lalani, Ankita Patel, Pawel Stankiewicz, James R Lupski,[...]. Genet Med 2013
39
25


Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.
Paola Evangelidou, Angelos Alexandrou, Maria Moutafi, Marios Ioannides, Pavlos Antoniou, George Koumbaris, Ioannis Kallikas, Voula Velissariou, Carolina Sismani, Philippos C Patsalis. Biomed Res Int 2013
25
25

Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects.
James R Priest, Santhosh Girirajan, Tiffany H Vu, Aaron Olson, Evan E Eichler, Michael A Portman. Am J Med Genet A 2012
30
25

An integrated map of genetic variation from 1,092 human genomes.
Goncalo R Abecasis, Adam Auton, Lisa D Brooks, Mark A DePristo, Richard M Durbin, Robert E Handsaker, Hyun Min Kang, Gabor T Marth, Gil A McVean. Nature 2012
25

Diagnostic interpretation of array data using public databases and internet sources.
Nicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, Nigel P Carter, Lars Feuk, Helen V Firth, Robert M Kuhn, David H Ledbetter, Christa Lese Martin, Conny M A van Ravenswaaij-Arts,[...]. Hum Mutat 2012
70
25

Array comparative genomic hybridization detects chromosomal abnormalities in hematological cancers that are not detected by conventional cytogenetics.
Lina Shao, Sung-Hae L Kang, Jian Li, Patricia Hixson, Jesalyn Taylor, Svetlana A Yatsenko, Chad A Shaw, Aleksandar Milosavljevic, Chung-Che Chang, Sau Wai Cheung,[...]. J Mol Diagn 2010
18
25

The promise of whole-exome sequencing in medical genetics.
Bahareh Rabbani, Mustafa Tekin, Nejat Mahdieh. J Hum Genet 2014
239
25

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
130
25


A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.
Paul Daniel Brady, Barbara Delle Chiaie, Gabrielle Christenhusz, Kris Dierickx, Kris Van Den Bogaert, Bjorn Menten, Sandra Janssens, Paul Defoort, Ellen Roets, Elke Sleurs,[...]. Genet Med 2014
46
25

Diagnosis of fetal trisomy 21 in first trimester.
B Brambati, G Simoni. Lancet 1983
74
25

Whole-exome/genome sequencing and genomics.
Wayne W Grody, Barry H Thompson, Louanne Hudgins. Pediatrics 2013
23
25

Chemical differentiation along metaphase chromosomes.
T Caspersson, S Farber, G E Foley, J Kudynowski, E J Modest, E Simonsson, U Wagh, L Zech. Exp Cell Res 1968
399
25


Genome screening by comparative genomic hybridization.
F Forozan, R Karhu, J Kononen, A Kallioniemi, O P Kallioniemi. Trends Genet 1997
208
25


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.