A citation-based method for searching scientific literature

Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
Times Cited: 1141



Sharon J Diskin, Mingyao Li, Cuiping Hou, Shuzhang Yang, Joseph Glessner, Hakon Hakonarson, Maja Bucan, John M Maris, Kai Wang. Nucleic Acids Res 2008
Times Cited: 220




List of shared articles



Times cited


Large mosaic copy number variations confer autism risk.
Maxwell A Sherman, Rachel E Rodin, Giulio Genovese, Caroline Dias, Alison R Barton, Ronen E Mukamel, Bonnie Berger, Peter J Park, Christopher A Walsh, Po-Ru Loh. Nat Neurosci 2021
3

Copy Number Variants in Four Italian Turkey Breeds.
Maria Giuseppina Strillacci, Stefano Paolo Marelli, Raffaella Milanesi, Luisa Zaniboni, Chiara Punturiero, Silvia Cerolini. Animals (Basel) 2021
0

Genome-wide association study between copy number variants and hoof health traits in Holstein dairy cattle.
Adrien M Butty, Tatiane C S Chud, Diercles F Cardoso, Lucas S F Lopes, Filippo Miglior, Flavio S Schenkel, Angela Cánovas, Irene M Häfliger, Cord Drögemüller, Paul Stothard,[...]. J Dairy Sci 2021
0

Genome-wide detection of CNV regions and their potential association with growth and fatness traits in Duroc pigs.
Yibin Qiu, Rongrong Ding, Zhanwei Zhuang, Jie Wu, Ming Yang, Shenping Zhou, Yong Ye, Qian Geng, Zheng Xu, Sixiu Huang,[...]. BMC Genomics 2021
0

Genome-wide detection of CNVs and their association with performance traits in broilers.
Anna Carolina Fernandes, Vinicius Henrique da Silva, Carolina Purcell Goes, Gabriel Costa Monteiro Moreira, Thaís Fernanda Godoy, Adriana Mércia Guaratini Ibelli, Jane de Oliveira Peixoto, Maurício Egídio Cantão, Mônica Corrêa Ledur, Fernanda Marcondes de Rezende,[...]. BMC Genomics 2021
0

Concordance of copy number abnormality detection using SNP arrays and Multiplex Ligation-dependent Probe Amplification (MLPA) in acute lymphoblastic leukaemia.
Matthew Bashton, Robin Hollis, Sarra Ryan, Claire J Schwab, John Moppett, Christine J Harrison, Anthony V Moorman, Amir Enshaei. Sci Rep 2020
0


Recurrent Rare Copy Number Variants Increase Risk for Esotropia.
Mary C Whitman, Silvio Alessandro Di Gioia, Wai-Man Chan, Alon Gelber, Brandon M Pratt, Jessica L Bell, Thomas E Collins, James A Knowles, Christopher Armoskus, Michele Pato,[...]. Invest Ophthalmol Vis Sci 2020
0

Contrasting DCIS and invasive breast cancer by subtype suggests basal-like DCIS as distinct lesions.
Helga Bergholtz, Tonje G Lien, David M Swanson, Arnoldo Frigessi, Maria Grazia Daidone, Jörg Tost, Fredrik Wärnberg, Therese Sørlie. NPJ Breast Cancer 2020
0

Contribution of de novo and inherited rare CNVs to very preterm birth.
Hilary S Wong, Megan Wadon, Alexandra Evans, George Kirov, Neena Modi, Michael C O'Donovan, Anita Thapar. J Med Genet 2020
1

High confidence copy number variants identified in Holstein dairy cattle from whole genome sequence and genotype array data.
Adrien M Butty, Tatiane C S Chud, Filippo Miglior, Flavio S Schenkel, Arun Kommadath, Kirill Krivushin, Jason R Grant, Irene M Häfliger, Cord Drögemüller, Angela Cánovas,[...]. Sci Rep 2020
3

Contrasting DCIS and invasive breast cancer by subtype suggests basal-like DCIS as distinct lesions.
Helga Bergholtz, Tonje G Lien, David M Swanson, Arnoldo Frigessi, Maria Grazia Daidone, Jörg Tost, Fredrik Wärnberg, Therese Sørlie. NPJ Breast Cancer 2020
1