A citation-based method for searching scientific literature

Ana R Cardoso, Manuela Oliveira, Antonio Amorim, Luisa Azevedo. Hum Genomics 2016
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Mechanisms underlying structural variant formation in genomic disorders.
Claudia M B Carvalho, James R Lupski. Nat Rev Genet 2016
292
40

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
30

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
714
20

Mechanisms for human genomic rearrangements.
Wenli Gu, Feng Zhang, James R Lupski. Pathogenetics 2008
390
20

A map of human genome variation from population-scale sequencing.
Gonçalo R Abecasis, David Altshuler, Adam Auton, Lisa D Brooks, Richard M Durbin, Richard A Gibbs, Matt E Hurles, Gil A McVean. Nature 2010
20


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
20



The impact of retrotransposons on human genome evolution.
Richard Cordaux, Mark A Batzer. Nat Rev Genet 2009
972
20

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
20

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
20

An integrated map of structural variation in 2,504 human genomes.
Peter H Sudmant, Tobias Rausch, Eugene J Gardner, Robert E Handsaker, Alexej Abyzov, John Huddleston, Yan Zhang, Kai Ye, Goo Jun, Markus Hsi-Yang Fritz,[...]. Nature 2015
20

Return to the Sea, Get Huge, Beat Cancer: An Analysis of Cetacean Genomes Including an Assembly for the Humpback Whale (Megaptera novaeangliae).
Marc Tollis, Jooke Robbins, Andrew E Webb, Lukas F K Kuderna, Aleah F Caulin, Jacinda D Garcia, Martine Bèrubè, Nader Pourmand, Tomas Marques-Bonet, Mary J O'Connell,[...]. Mol Biol Evol 2019
36
20

Mechanisms of change in gene copy number.
P J Hastings, James R Lupski, Susan M Rosenberg, Grzegorz Ira. Nat Rev Genet 2009
745
20

APOL1 risk variants, race, and progression of chronic kidney disease.
Afshin Parsa, W H Linda Kao, Dawei Xie, Brad C Astor, Man Li, Chi-yuan Hsu, Harold I Feldman, Rulan S Parekh, John W Kusek, Tom H Greene,[...]. N Engl J Med 2013
474
10

FSGS Recurrence in Adults after Renal Transplantation.
Michael Rudnicki. Biomed Res Int 2016
28
10


Copy Number Variation at the APOL1 Locus.
Rupam Ruchi, Giulio Genovese, Jessica Lee, Victoria T Charoonratana, Andrea J Bernhardy, Seth L Alper, Jeffrey B Kopp, Ravi Thadhani, David J Friedman, Martin R Pollak. PLoS One 2015
13
10

Structural variation in the human genome: the impact of copy number variants on clinical diagnosis.
Laia Rodriguez-Revenga, Montserrat Mila, Carla Rosenberg, Allen Lamb, Charles Lee. Genet Med 2007
50
10

FSGS: Diagnosis and Diagnostic Work-Up.
Ben Sprangers, Björn Meijers, Gerald Appel. Biomed Res Int 2016
19
10

Familial clustering of end-stage renal disease in blacks with HIV-associated nephropathy.
B I Freedman, J M Soucie, S M Stone, S Pegram. Am J Kidney Dis 1999
127
10

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.
Shay Tzur, Saharon Rosset, Revital Shemer, Guennady Yudkovsky, Sara Selig, Ayele Tarekegn, Endashaw Bekele, Neil Bradman, Walter G Wasser, Doron M Behar,[...]. Hum Genet 2010
414
10


KDOQI US commentary on the 2012 KDIGO clinical practice guideline for the evaluation and management of CKD.
Lesley A Inker, Brad C Astor, Chester H Fox, Tamara Isakova, James P Lash, Carmen A Peralta, Manjula Kurella Tamura, Harold I Feldman. Am J Kidney Dis 2014
774
10

Collapsing glomerulopathy in a young woman with APOL1 risk alleles following acute parvovirus B19 infection: a case report investigation.
Whitney Besse, Sherry Mansour, Karan Jatwani, Cynthia C Nast, Ursula C Brewster. BMC Nephrol 2016
25
10

Gene copy number variation in male breast cancer by aCGH.
Stefania Tommasi, Anita Mangia, Giuseppina Iannelli, Patrizia Chiarappa, Elena Rossi, Laura Ottini, Marcella Mottolese, Wainer Zoli, Orsetta Zuffardi, Angelo Paradiso. Anal Cell Pathol (Amst) 2010
17
10

Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis--a review.
M M Löwik, P J Groenen, E N Levtchenko, L A Monnens, L P van den Heuvel. Eur J Pediatr 2009
78
10

Human apolipoprotein L1 (ApoL1) in cancer and chronic kidney disease.
Chien-An A Hu, Edward I Klopfer, Patricio E Ray. FEBS Lett 2012
46
10

Familial FSGS.
Martin R Pollak. Adv Chronic Kidney Dis 2014
35
10

International standardization of criteria for the histologic diagnosis of renal allograft rejection: the Banff working classification of kidney transplant pathology.
K Solez, R A Axelsen, H Benediktsson, J F Burdick, A H Cohen, R B Colvin, B P Croker, D Droz, M S Dunnill, P F Halloran. Kidney Int 1993
10


Association of APOL1 variants with mild kidney disease in the first-degree relatives of African American patients with non-diabetic end-stage renal disease.
Barry I Freedman, Carl D Langefeld, Jolyn Turner, Marina Núñez, Kevin P High, Mitzie Spainhour, Pamela J Hicks, Donald W Bowden, Amber M Reeves-Daniel, Mariana Murea,[...]. Kidney Int 2012
54
10

Clinical Features and Histology of Apolipoprotein L1-Associated Nephropathy in the FSGS Clinical Trial.
Jeffrey B Kopp, Cheryl A Winkler, Xiongce Zhao, Milena K Radeva, Jennifer J Gassman, Vivette D D'Agati, Cynthia C Nast, Changli Wei, Jochen Reiser, Lisa M Guay-Woodford,[...]. J Am Soc Nephrol 2015
79
10

Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction.
Zhen Ai, Ming Li, Wenting Liu, Jia-Nee Foo, Omniah Mansouri, Peiran Yin, Qian Zhou, Xueqing Tang, Xiuqing Dong, Shaozhen Feng,[...]. Sci Transl Med 2016
21
10

APOL1 nephropathy: from gene to mechanisms of kidney injury.
Etty Kruzel-Davila, Walter G Wasser, Sharon Aviram, Karl Skorecki. Nephrol Dial Transplant 2016
63
10

Glomerular diseases: FSGS.
Bhadran Bose, Daniel Cattran. Clin J Am Soc Nephrol 2014
42
10

Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.
Gemma Bullich, Daniel Trujillano, Sheila Santín, Stephan Ossowski, Santiago Mendizábal, Gloria Fraga, Álvaro Madrid, Gema Ariceta, José Ballarín, Roser Torra,[...]. Eur J Hum Genet 2015
56
10

Focal segmental glomerulosclerosis.
Vivette D D'Agati, Frederick J Kaskel, Ronald J Falk. N Engl J Med 2011
456
10

APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy.
Jeffrey B Kopp, George W Nelson, Karmini Sampath, Randall C Johnson, Giulio Genovese, Ping An, David Friedman, William Briggs, Richard Dart, Stephen Korbet,[...]. J Am Soc Nephrol 2011
505
10

Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake.
Lisa C Willcocks, Paul A Lyons, Menna R Clatworthy, James I Robinson, Wanling Yang, Stephen A Newland, Vincent Plagnol, Naomi N McGovern, Alison M Condliffe, Edwin R Chilvers,[...]. J Exp Med 2008
175
10

Capturing chromosome conformation.
Job Dekker, Karsten Rippe, Martijn Dekker, Nancy Kleckner. Science 2002
10


Mapping long-range promoter contacts in human cells with high-resolution capture Hi-C.
Borbala Mifsud, Filipe Tavares-Cadete, Alice N Young, Robert Sugar, Stefan Schoenfelder, Lauren Ferreira, Steven W Wingett, Simon Andrews, William Grey, Philip A Ewels,[...]. Nat Genet 2015
526
10

Disruption of neurexin 1 associated with autism spectrum disorder.
Hyung-Goo Kim, Shotaro Kishikawa, Anne W Higgins, Ihn-Sik Seong, Diana J Donovan, Yiping Shen, Eric Lally, Lauren A Weiss, Juliane Najm, Kerstin Kutsche,[...]. Am J Hum Genet 2008
406
10

Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project.
Anne W Higgins, Fowzan S Alkuraya, Amy F Bosco, Kerry K Brown, Gail A P Bruns, Diana J Donovan, Robert Eisenman, Yanli Fan, Chantal G Farra, Heather L Ferguson,[...]. Am J Hum Genet 2008
76
10

Organization and function of the 3D genome.
Boyan Bonev, Giacomo Cavalli. Nat Rev Genet 2016
405
10

Constitutional rearrangement of the architectural factor HMGA2: a novel human phenotype including overgrowth and lipomas.
Azra H Ligon, Steven D P Moore, Melissa A Parisi, Matthew E Mealiffe, David J Harris, Heather L Ferguson, Bradley J Quade, Cynthia C Morton. Am J Hum Genet 2005
98
10

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
10

A role for noncoding variation in schizophrenia.
Panos Roussos, Amanda C Mitchell, Georgios Voloudakis, John F Fullard, Venu M Pothula, Jonathan Tsang, Eli A Stahl, Anastasios Georgakopoulos, Douglas M Ruderfer, Alexander Charney,[...]. Cell Rep 2014
154
10


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.