A citation-based method for searching scientific literature

Christina A Castellani, Melkaye G Melka, Andrea E Wishart, M Elizabeth O Locke, Zain Awamleh, Richard L O'Reilly, Shiva M Singh. BMC Bioinformatics 2014
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


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
36

Genomic characteristics of cattle copy number variations.
Yali Hou, George E Liu, Derek M Bickhart, Maria Francesca Cardone, Kai Wang, Eui-Soo Kim, Lakshmi K Matukumalli, Mario Ventura, Jiuzhou Song, Paul M VanRaden,[...]. BMC Genomics 2011
142
36

Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins.
Li Jiang, Jicai Jiang, Jie Yang, Xuan Liu, Jiying Wang, Haifei Wang, Xiangdong Ding, Jianfeng Liu, Qin Zhang. BMC Genomics 2013
59
36

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
27

The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation.
Armand Valsesia, Aurélien Macé, Sébastien Jacquemont, Jacques S Beckmann, Zoltán Kutalik. Front Genet 2013
37
27

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
655
27

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
27

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
27

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
27

Structural variation in the human genome.
Lars Feuk, Andrew R Carson, Stephen W Scherer. Nat Rev Genet 2006
27

Characterising and predicting haploinsufficiency in the human genome.
Ni Huang, Insuk Lee, Edward M Marcotte, Matthew E Hurles. PLoS Genet 2010
418
18

Genome-wide algorithm for detecting CNV associations with diseases.
Yaji Xu, Bo Peng, Yunxin Fu, Christopher I Amos. BMC Bioinformatics 2011
7
28

A genome-wide detection of copy number variations using SNP genotyping arrays in swine.
Jiying Wang, Jicai Jiang, Weixuan Fu, Li Jiang, Xiangdong Ding, Jian-Feng Liu, Qin Zhang. BMC Genomics 2012
71
18

Cytoplasmic 5'-3' exonuclease Xrn1p is also a genome-wide transcription factor in yeast.
Daniel A Medina, Antonio Jordán-Pla, Gonzalo Millán-Zambrano, Sebastián Chávez, Mordechai Choder, José E Pérez-Ortín. Front Genet 2014
156
18

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms.
Sharon J Diskin, Mingyao Li, Cuiping Hou, Shuzhang Yang, Joseph Glessner, Hakon Hakonarson, Maja Bucan, John M Maris, Kai Wang. Nucleic Acids Res 2008
229
18

Mouse segmental duplication and copy number variation.
Xinwei She, Ze Cheng, Sebastian Zöllner, Deanna M Church, Evan E Eichler. Nat Genet 2008
165
18

Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.
Jeanette E Eckel-Passow, Elizabeth J Atkinson, Sooraj Maharjan, Sharon L R Kardia, Mariza de Andrade. BMC Bioinformatics 2011
40
18

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.
Da Wei Huang, Brad T Sherman, Richard A Lempicki. Nat Protoc 2009
18

Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives.
Min Zhao, Qingguo Wang, Quan Wang, Peilin Jia, Zhongming Zhao. BMC Bioinformatics 2013
267
18

A novel mutation in the maternally imprinted PEG3 domain results in a loss of MIMT1 expression and causes abortions and stillbirths in cattle (Bos taurus).
Krzysztof Flisikowski, Heli Venhoranta, Joanna Nowacka-Woszuk, Stephanie D McKay, Antti Flyckt, Juhani Taponen, Robert Schnabel, Hermann Schwarzenbacher, Izabela Szczerbal, Hannes Lohi,[...]. PLoS One 2010
43
18

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
18

Genome structural variation discovery and genotyping.
Can Alkan, Bradley P Coe, Evan E Eichler. Nat Rev Genet 2011
759
18


Genetic diversity and population structure among six cattle breeds in South Africa using a whole genome SNP panel.
Sithembile O Makina, Farai C Muchadeyi, Este van Marle-Köster, Michael D MacNeil, Azwihangwisi Maiwashe. Front Genet 2014
38
18

Analysis of copy number variations among diverse cattle breeds.
George E Liu, Yali Hou, Bin Zhu, Maria Francesca Cardone, Lu Jiang, Angelo Cellamare, Apratim Mitra, Leeson J Alexander, Luiz L Coutinho, Maria Elena Dell'Aquila,[...]. Genome Res 2010
186
18

Copy number variation in the cattle genome.
George E Liu, Derek M Bickhart. Funct Integr Genomics 2012
32
18

Common polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease risk.
Meike Heurich, Ruben Martínez-Barricarte, Nigel J Francis, Dawn L Roberts, Santiago Rodríguez de Córdoba, B Paul Morgan, Claire L Harris. Proc Natl Acad Sci U S A 2011
148
18

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies.
Aude Servais, Laure-Hélène Noël, Lubka T Roumenina, Moglie Le Quintrec, Stephanie Ngo, Marie-Agnès Dragon-Durey, Marie-Alice Macher, Julien Zuber, Alexandre Karras, François Provot,[...]. Kidney Int 2012
317
18

Dense deposit disease.
Richard J H Smith, Claire L Harris, Matthew C Pickering. Mol Immunol 2011
60
18

Complement analysis in the 21st century.
Tom Eirik Mollnes, T Sakari Jokiranta, Lennart Truedsson, Bo Nilsson, Santiago Rodriguez de Cordoba, Michael Kirschfink. Mol Immunol 2007
85
18


Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.
Elena Bresin, Erica Rurali, Jessica Caprioli, Pilar Sanchez-Corral, Veronique Fremeaux-Bacchi, Santiago Rodriguez de Cordoba, Sheila Pinto, Timothy H J Goodship, Marta Alberti, David Ribes,[...]. J Am Soc Nephrol 2013
220
18


Biomarkers of terminal complement activation confirm the diagnosis of aHUS and differentiate aHUS from TTP.
Spero R Cataland, V Michael Holers, Susan Geyer, Shangbin Yang, Haifeng M Wu. Blood 2014
98
18

C3 glomerulonephritis associated with complement factor B mutation.
Sanjeev Sethi, Richard J H Smith, John J Dillon, Fernando C Fervenza. Am J Kidney Dis 2015
8
25

Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome.
Anna Richards, M Kathryn Liszewski, David Kavanagh, Celia J Fang, Elizabeth Moulton, Veronique Fremeaux-Bacchi, Giuseppe Remuzzi, Marina Noris, Timothy H J Goodship, John P Atkinson. Mol Immunol 2007
96
18

C3 glomerulopathy: consensus report.
Matthew C Pickering, Vivette D D'Agati, Carla M Nester, Richard J Smith, Mark Haas, Gerald B Appel, Charles E Alpers, Ingeborg M Bajema, Camille Bedrosian, Michael Braun,[...]. Kidney Int 2013
323
18

Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II).
C Licht, S Heinen, M Józsi, I Löschmann, R E Saunders, S J Perkins, R Waldherr, C Skerka, M Kirschfink, B Hoppe,[...]. Kidney Int 2006
145
18

Soluble c5b-9 as a biomarker for complement activation in atypical hemolytic uremic syndrome.
Fengxiao Bu, Nicole C Meyer, Yuzhou Zhang, Nicolo Ghiringhelli Borsa, Christie Thomas, Carla Nester, Richard J H Smith. Am J Kidney Dis 2015
27
18

Complement activation: the missing link between ADAMTS-13 deficiency and microvascular thrombosis of thrombotic microangiopathies.
Maria Piedad Ruiz-Torres, Federica Casiraghi, Miriam Galbusera, Daniela Macconi, Sara Gastoldi, Marta Todeschini, Francesca Porrati, Daniela Belotti, Enrico Maria Pogliani, Marina Noris,[...]. Thromb Haemost 2005
73
18

Eculizumab in severe Shiga-toxin-associated HUS.
Anne-Laure Lapeyraque, Michal Malina, Véronique Fremeaux-Bacchi, Tobias Boppel, Michael Kirschfink, Mehdi Oualha, François Proulx, Marie-José Clermont, Françoise Le Deist, Patrick Niaudet,[...]. N Engl J Med 2011
279
18

Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics.
Lianne M Geerdink, Dineke Westra, Joanna A E van Wijk, Eiske M Dorresteijn, Marc R Lilien, Jean-Claude Davin, Martin Kömhoff, Koen Van Hoeck, Amerins van der Vlugt, Lambertus P van den Heuvel,[...]. Pediatr Nephrol 2012
103
18

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome.
Marie-Agnès Dragon-Durey, Chantal Loirat, Sylvie Cloarec, Marie-Alice Macher, Jacques Blouin, Hubert Nivet, Laurence Weiss, Wolf Herman Fridman, Véronique Frémeaux-Bacchi. J Am Soc Nephrol 2005
343
18

Complement activation in thrombotic thrombocytopenic purpura.
M Réti, P Farkas, D Csuka, K Rázsó, Á Schlammadinger, M L Udvardy, K Madách, G Domján, C Bereczki, G S Reusz,[...]. J Thromb Haemost 2012
97
18

Dynamics of complement activation in aHUS and how to monitor eculizumab therapy.
Marina Noris, Miriam Galbusera, Sara Gastoldi, Paolo Macor, Federica Banterla, Elena Bresin, Claudio Tripodo, Serena Bettoni, Roberta Donadelli, Elisabetta Valoti,[...]. Blood 2014
187
18

Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome.
Fengxiao Bu, Tara Maga, Nicole C Meyer, Kai Wang, Christie P Thomas, Carla M Nester, Richard J H Smith. J Am Soc Nephrol 2014
129
18

Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement.
Sanjeev Sethi, Fernando C Fervenza, Yuzhou Zhang, Samih H Nasr, Nelson Leung, Julie Vrana, Carl Cramer, Carla M Nester, Richard J H Smith. Clin J Am Soc Nephrol 2011
106
18

Hypocomplementemia and leukocytosis in diarrhea-associated hemolytic uremic syndrome.
W L Robson, A K Leung, G H Fick, A I McKenna. Nephron 1992
63
18

Causes of alternative pathway dysregulation in dense deposit disease.
Yuzhou Zhang, Nicole C Meyer, Kai Wang, Carla Nishimura, Kathy Frees, Michael Jones, Louis M Katz, Sanjeev Sethi, Richard J H Smith. Clin J Am Soc Nephrol 2012
126
18

Autoantibody stabilization of the classical pathway C3 convertase leading to C3 deficiency and Neisserial sepsis: C4 nephritic factor revisited.
Elizabeth C Miller, Nicole M Chase, Peter Densen, Mary K Hintermeyer, James T Casper, John P Atkinson. Clin Immunol 2012
19
18


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.