A citation-based method for searching scientific literature

S Le Scouarnec, S M Gribble. Heredity (Edinb) 2012
Times Cited: 57







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



Times Cited
  Times     Co-cited
Similarity


Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors.
A Kallioniemi, O P Kallioniemi, D Sudar, D Rutovitz, J W Gray, F Waldman, D Pinkel. Science 1992
21

Multicolor spectral karyotyping of human chromosomes.
E Schröck, S du Manoir, T Veldman, B Schoell, J Wienberg, M A Ferguson-Smith, Y Ning, D H Ledbetter, I Bar-Am, D Soenksen,[...]. Science 1996
19

Karyotyping human chromosomes by combinatorial multi-fluor FISH.
M R Speicher, S Gwyn Ballard, D C Ward. Nat Genet 1996
863
17

Origins and functional impact of copy number variation in the human genome.
Donald F Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T Daniel Andrews, Chris Barnes, Peter Campbell,[...]. Nature 2010
15

Genome structural variation discovery and genotyping.
Can Alkan, Bradley P Coe, Evan E Eichler. Nat Rev Genet 2011
759
15

Detection of large-scale variation in the human genome.
A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer, Charles Lee. Nat Genet 2004
12

Paired-end mapping reveals extensive structural variation in the human genome.
Jan O Korbel, Alexander Eckehart Urban, Jason P Affourtit, Brian Godwin, Fabian Grubert, Jan Fredrik Simons, Philip M Kim, Dean Palejev, Nicholas J Carriero, Lei Du,[...]. Science 2007
769
12

Sequencing technologies - the next generation.
Michael L Metzker. Nat Rev Genet 2010
12

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
12


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
12

Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
8

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
820
8

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants.
Dalila Pinto, Katayoon Darvishi, Xinghua Shi, Diana Rajan, Diane Rigler, Tom Fitzgerald, Anath C Lionel, Bhooma Thiruvahindrapuram, Jeffrey R Macdonald, Ryan Mills,[...]. Nat Biotechnol 2011
294
8

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
8

Towards a comprehensive structural variation map of an individual human genome.
Andy W Pang, Jeffrey R MacDonald, Dalila Pinto, John Wei, Muhammad A Rafiq, Donald F Conrad, Hansoo Park, Matthew E Hurles, Charles Lee, J Craig Venter,[...]. Genome Biol 2010
182
8

Mapping copy number variation by population-scale genome sequencing.
Ryan E Mills, Klaudia Walter, Chip Stewart, Robert E Handsaker, Ken Chen, Can Alkan, Alexej Abyzov, Seungtai Chris Yoon, Kai Ye, R Keira Cheetham,[...]. Nature 2011
714
8


Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing.
Wei Chen, Reinhard Ullmann, Claudia Langnick, Corinna Menzel, Zofia Wotschofsky, Hao Hu, Andreas Döring, Yuhui Hu, Hui Kang, Andreas Tzschach,[...]. Eur J Hum Genet 2010
46
10

Okihiro syndrome is caused by SALL4 mutations.
Jürgen Kohlhase, Marielle Heinrich, Lucia Schubert, Manuela Liebers, Andreas Kispert, Franco Laccone, Peter Turnpenny, Robin M Winter, William Reardon. Hum Mol Genet 2002
218
8

Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome.
Noriko Miyake, John Chilton, Maria Psatha, Long Cheng, Caroline Andrews, Wai-Man Chan, Krystal Law, Moira Crosier, Susan Lindsay, Michelle Cheung,[...]. Science 2008
104
8

Association of familial Duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22.
P Cullen, C S Rodgers, D F Callen, V M Connolly, H Eyre, P Fells, H Gordon, R M Winter, R V Thakker. Am J Med Genet 1993
49
10

The clinical spectrum of homozygous HOXA1 mutations.
Thomas M Bosley, Ibrahim A Alorainy, Mustafa A Salih, Hesham M Aldhalaan, Khaled K Abu-Amero, Darren T Oystreck, Max A Tischfield, Elizabeth C Engle, Robert P Erickson. Am J Med Genet A 2008
65
8

Duane's syndrome and 22 marker chromosome: a possible cat-eye syndrome.
Carmen Gómez-Lado, Jesús Eirís, José Manuel Martínez-Yriarte, Oscar Blanco, Manuel Castro-Gago. Acta Paediatr 2006
9
55

Expansion of the CHN1 strabismus phenotype.
Noriko Miyake, Joseph L Demer, Sherin Shaaban, Caroline Andrews, Wai-Man Chan, Stephen P Christiansen, David G Hunter, Elizabeth C Engle. Invest Ophthalmol Vis Sci 2011
30
16

Clinical characterization of the HOXA1 syndrome BSAS variant.
T M Bosley, M A Salih, I A Alorainy, D T Oystreck, M Nester, K K Abu-Amero, M A Tischfield, E C Engle. Neurology 2007
52
9

Chromosome 22 marker in a child with Duane syndrome and urogenital abnormalities.
M G Tibiletti, E Sala, D Colombo, S Arlati, T Varisco, G La Placa. Ann Genet 1996
15
33

Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family.
Raidah Al-Baradie, Koki Yamada, Cynthia St Hilaire, Wai-Man Chan, Caroline Andrews, Nathalie McIntosh, Motoi Nakano, E Jean Martonyi, William R Raymond, Sada Okumura,[...]. Am J Hum Genet 2002
202
8

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development.
Max A Tischfield, Thomas M Bosley, Mustafa A M Salih, Ibrahim A Alorainy, Emin C Sener, Michael J Nester, Darren T Oystreck, Wai-Man Chan, Caroline Andrews, Robert P Erickson,[...]. Nat Genet 2005
182
8

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
8

The new cytogenetics: blurring the boundaries with molecular biology.
Michael R Speicher, Nigel P Carter. Nat Rev Genet 2005
231
8

Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer.
H Telenius, N P Carter, C E Bebb, M Nordenskjöld, B A Ponder, A Tunnacliffe. Genomics 1992
8

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.
D Pinkel, T Straume, J W Gray. Proc Natl Acad Sci U S A 1986
8

Describing sequencing results of structural chromosome rearrangements with a suggested next-generation cytogenetic nomenclature.
Zehra Ordulu, Kristen E Wong, Benjamin B Currall, Andrew R Ivanov, Shahrin Pereira, Sara Althari, James F Gusella, Michael E Talkowski, Cynthia C Morton. Am J Hum Genet 2014
34
14

Copy number variation in human health, disease, and evolution.
Feng Zhang, Wenli Gu, Matthew E Hurles, James R Lupski. Annu Rev Genomics Hum Genet 2009
701
7

Structural variation in the human genome and its role in disease.
Paweł Stankiewicz, James R Lupski. Annu Rev Med 2010
676
7

The pitfalls of platform comparison: DNA copy number array technologies assessed.
Christina Curtis, Andy G Lynch, Mark J Dunning, Inmaculada Spiteri, John C Marioni, James Hadfield, Suet-Feung Chin, James D Brenton, Simon Tavaré, Carlos Caldas. BMC Genomics 2009
76
7

Duane syndrome in the setting of chromosomal duplications.
Sarah B Smith, Elias I Traboulsi. Am J Ophthalmol 2010
13
30


Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene.
G Calabrese, L Stuppia, E Morizio, P Guanciali Franchi, F Pompetti, R Mingarelli, T Marsilio, M Rocchi, P E Gallenga, G Palka,[...]. Eur J Hum Genet 1998
44
9

Structural variation in the human genome.
Lars Feuk, Andrew R Carson, Stephen W Scherer. Nat Rev Genet 2006
7

Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency and/or congenital malformations.
Caroline Schluth-Bolard, Audrey Labalme, Marie-Pierre Cordier, Marianne Till, Gwenaël Nadeau, Hélène Tevissen, Gaétan Lesca, Nadia Boutry-Kryza, Sylvie Rossignol, Delphine Rocas,[...]. J Med Genet 2013
68
7


New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling.
H J Tanke, J Wiegant, R P van Gijlswijk, V Bezrookove, H Pattenier, R J Heetebrij, E G Talman, A K Raap, J Vrolijk. Eur J Hum Genet 1999
149
7

Two novel CHN1 mutations in 2 families with Duane retraction syndrome.
Wai-Man Chan, Noriko Miyake, Lily Zhu-Tam, Caroline Andrews, Elizabeth C Engle. Arch Ophthalmol 2011
21
19

Mutations in KIF21A are responsible for CFEOM1 worldwide.
Elias I Traboulsi, Elizabeth C Engle. Ophthalmic Genet 2004
14
28


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
7




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.