A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
75

cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs.
Lachlan J M Coin, Julian E Asher, Robin G Walters, Julia S El-Sayed Moustafa, Adam J de Smith, Rob Sladek, David J Balding, Philippe Froguel, Alexandra I F Blakemore. Nat Methods 2010
36
75

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
75

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.
Joshua M Korn, Finny G Kuruvilla, Steven A McCarroll, Alec Wysoker, James Nemesh, Simon Cawley, Earl Hubbell, Jim Veitch, Patrick J Collins, Katayoon Darvishi,[...]. Nat Genet 2008
597
75

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.
Stefano Colella, Christopher Yau, Jennifer M Taylor, Ghazala Mirza, Helen Butler, Penny Clouston, Anne S Bassett, Anneke Seller, Christopher C Holmes, Jiannis Ragoussis. Nucleic Acids Res 2007
418
50

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
50

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
50

A robust statistical method for case-control association testing with copy number variation.
Chris Barnes, Vincent Plagnol, Tomas Fitzgerald, Richard Redon, Jonathan Marchini, David Clayton, Matthew E Hurles. Nat Genet 2008
129
50

Optimal Sparse Segment Identification with Application in Copy Number Variation Analysis.
X Jessie Jeng, T Tony Cai, Hongzhe Li. J Am Stat Assoc 2010
21
50

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
50

Markov Models for inferring copy number variations from genotype data on Illumina platforms.
Hui Wang, Jan H Veldink, Hylke Blauw, Leonard H van den Berg, Roel A Ophoff, Chiara Sabatti. Hum Hered 2009
9
50

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
944
50

Microduplications of 16p11.2 are associated with schizophrenia.
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
489
50

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
Maja Bucan, Brett S Abrahams, Kai Wang, Joseph T Glessner, Edward I Herman, Lisa I Sonnenblick, Ana I Alvarez Retuerto, Marcin Imielinski, Dexter Hadley, Jonathan P Bradfield,[...]. PLoS Genet 2009
284
50

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
50

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Peter Szatmari, Andrew D Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Xiao-Qing Liu, John B Vincent, Jennifer L Skaug, Ann P Thompson, Lili Senman,[...]. Nat Genet 2007
962
50

Novel copy number variants in children with autism and additional developmental anomalies.
L K Davis, K J Meyer, D S Rudd, A L Librant, E A Epping, V C Sheffield, T H Wassink. J Neurodev Disord 2009
30
50

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
50

De novo gene disruptions in children on the autistic spectrum.
Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta,[...]. Neuron 2012
931
50

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
50

A first-generation linkage disequilibrium map of human chromosome 22.
Elisabeth Dawson, Gonçalo R Abecasis, Suzannah Bumpstead, Yuan Chen, Sarah Hunt, David M Beare, Jagjit Pabial, Thomas Dibling, Emma Tinsley, Susan Kirby,[...]. Nature 2002
282
25

Fine-scale structural variation of the human genome.
Eray Tuzun, Andrew J Sharp, Jeffrey A Bailey, Rajinder Kaul, V Anne Morrison, Lisa M Pertz, Eric Haugen, Hillary Hayden, Donna Albertson, Daniel Pinkel,[...]. Nat Genet 2005
718
25

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.
N Patil, A J Berno, D A Hinds, W A Barrett, J M Doshi, C R Hacker, C R Kautzer, D H Lee, C Marjoribanks, D P McDonough,[...]. Science 2001
739
25

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
Daisuke Komura, Fan Shen, Shumpei Ishikawa, Karen R Fitch, Wenwei Chen, Jane Zhang, Guoying Liu, Sigeo Ihara, Hiroshi Nakamura, Matthew E Hurles,[...]. Genome Res 2006
142
25

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.
Daniel A Peiffer, Jennie M Le, Frank J Steemers, Weihua Chang, Tony Jenniges, Francisco Garcia, Kirt Haden, Jiangzhen Li, Chad A Shaw, John Belmont,[...]. Genome Res 2006
375
25

An algorithm for inferring complex haplotypes in a region of copy-number variation.
Mamoru Kato, Yusuke Nakamura, Tatsuhiko Tsunoda. Am J Hum Genet 2008
16
25

Accuracy of CNV Detection from GWAS Data.
Dandan Zhang, Yudong Qian, Nirmala Akula, Ney Alliey-Rodriguez, Jinsong Tang, Elliot S Gershon, Chunyu Liu. PLoS One 2011
60
25

Common deletion polymorphisms in the human genome.
Steven A McCarroll, Tracy N Hadnott, George H Perry, Pardis C Sabeti, Michael C Zody, Jeffrey C Barrett, Stephanie Dallaire, Stacey B Gabriel, Charles Lee, Mark J Daly,[...]. Nat Genet 2006
534
25

Haplotype block partition with limited resources and applications to human chromosome 21 haplotype data.
Kui Zhang, Fengzhu Sun, Michael S Waterman, Ting Chen. Am J Hum Genet 2003
37
25

Copy-number variation and association studies of human disease.
Steven A McCarroll, David M Altshuler. Nat Genet 2007
412
25

Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
Marguerite R Irvin, Nathan E Wineinger, Treva K Rice, Nicholas M Pajewski, Edmond K Kabagambe, Charles C Gu, Jim Pankow, Kari E North, Jemma B Wilk, Barry I Freedman,[...]. PLoS One 2011
34
25


Bayesian EM algorithm for scoring polymorphic deletions from SNP data and application to a common CNV on 8q24.
Sebastian Zöllner, Gang Su, William C L Stewart, Yi Chen, Melvin G McInnis, Margit Burmeister. Genet Epidemiol 2009
6
25

Genome wide association identifies PPFIA1 as a candidate gene for acute lung injury risk following major trauma.
Jason D Christie, Mark M Wurfel, Rui Feng, Grant E O'Keefe, Jonathan Bradfield, Lorraine B Ware, David C Christiani, Carolyn S Calfee, Mitchell J Cohen, Michael Matthay,[...]. PLoS One 2012
53
25

The structure of haplotype blocks in the human genome.
Stacey B Gabriel, Stephen F Schaffner, Huy Nguyen, Jamie M Moore, Jessica Roy, Brendan Blumenstiel, John Higgins, Matthew DeFelice, Amy Lochner, Maura Faggart,[...]. Science 2002
25


Inferring combined CNV/SNP haplotypes from genotype data.
Shu-Yi Su, Julian E Asher, Marjo-Riita Jarvelin, Phillipe Froguel, Alexandra I F Blakemore, David J Balding, Lachlan J M Coin. Bioinformatics 2010
27
25

High-resolution haplotype structure in the human genome.
M J Daly, J D Rioux, S F Schaffner, T J Hudson, E S Lander. Nat Genet 2001
25

Comparing CNV detection methods for SNP arrays.
Laura Winchester, Christopher Yau, Jiannis Ragoussis. Brief Funct Genomic Proteomic 2009
141
25


Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome.
Jan O Korbel, Alexander Eckehart Urban, Fabian Grubert, Jiang Du, Thomas E Royce, Peter Starr, Guoneng Zhong, Beverly S Emanuel, Sherman M Weissman, Michael Snyder,[...]. Proc Natl Acad Sci U S A 2007
62
25

A high-resolution survey of deletion polymorphism in the human genome.
Donald F Conrad, T Daniel Andrews, Nigel P Carter, Matthew E Hurles, Jonathan K Pritchard. Nat Genet 2006
476
25

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
25

Large-scale copy number polymorphism in the human genome.
Jonathan Sebat, B Lakshmi, Jennifer Troge, Joan Alexander, Janet Young, Pär Lundin, Susanne Månér, Hillary Massa, Megan Walker, Maoyen Chi,[...]. Science 2004
25

Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.
Lude Franke, Carolien G F de Kovel, Yurii S Aulchenko, Gosia Trynka, Alexandra Zhernakova, Karen A Hunt, Hylke M Blauw, Leonard H van den Berg, Roel Ophoff, Panagiotis Deloukas,[...]. Am J Hum Genet 2008
31
25

Copy number variation: new insights in genome diversity.
Jennifer L Freeman, George H Perry, Lars Feuk, Richard Redon, Steven A McCarroll, David M Altshuler, Hiroyuki Aburatani, Keith W Jones, Chris Tyler-Smith, Matthew E Hurles,[...]. Genome Res 2006
505
25

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
Douglas F Levinson, Jubao Duan, Sang Oh, Kai Wang, Alan R Sanders, Jianxin Shi, Nancy Zhang, Bryan J Mowry, Ann Olincy, Farooq Amin,[...]. Am J Psychiatry 2011
321
25

Copy number variation at 1q21.1 associated with neuroblastoma.
Sharon J Diskin, Cuiping Hou, Joseph T Glessner, Edward F Attiyeh, Marci Laudenslager, Kristopher Bosse, Kristina Cole, Yaël P Mossé, Andrew Wood, Jill E Lynch,[...]. Nature 2009
269
25

famCNV: copy number variant association for quantitative traits in families.
Hariklia Eleftherohorinou, Johanna C Andersson-Assarsson, Robin G Walters, Julia S El-Sayed Moustafa, Lachlan Coin, Peter Jacobson, Lena M S Carlsson, Alexandra I F Blakemore, Philippe Froguel, Andrew J Walley,[...]. Bioinformatics 2011
8
25

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
Maria Teresa Landi, Nilanjan Chatterjee, Kai Yu, Lynn R Goldin, Alisa M Goldstein, Melissa Rotunno, Lisa Mirabello, Kevin Jacobs, William Wheeler, Meredith Yeager,[...]. Am J Hum Genet 2009
412
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.