A citation-based method for searching scientific literature

S A Miller, D D Dykes, H F Polesky. Nucleic Acids Res 1988
Times Cited: 12832







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



Times Cited
  Times     Co-cited
Similarity


Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
7

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
7


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
6

DNA methylation arrays as surrogate measures of cell mixture distribution.
Eugene Andres Houseman, William P Accomando, Devin C Koestler, Brock C Christensen, Carmen J Marsit, Heather H Nelson, John K Wiencke, Karl T Kelsey. BMC Bioinformatics 2012
5

Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays.
Martin J Aryee, Andrew E Jaffe, Hector Corrada-Bravo, Christine Ladd-Acosta, Andrew P Feinberg, Kasper D Hansen, Rafael A Irizarry. Bioinformatics 2014
4

Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
Freddie Bray, Jacques Ferlay, Isabelle Soerjomataram, Rebecca L Siegel, Lindsey A Torre, Ahmedin Jemal. CA Cancer J Clin 2018
4

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
4

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
4

Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration.
Helga Thorvaldsdóttir, James T Robinson, Jill P Mesirov. Brief Bioinform 2013
3

Trimmomatic: a flexible trimmer for Illumina sequence data.
Anthony M Bolger, Marc Lohse, Bjoern Usadel. Bioinformatics 2014
3

MutationTaster2: mutation prediction for the deep-sequencing age.
Jana Marie Schwarz, David N Cooper, Markus Schuelke, Dominik Seelow. Nat Methods 2014
3




A new statistical method for haplotype reconstruction from population data.
M Stephens, N J Smith, P Donnelly. Am J Hum Genet 2001
3

Haploview: analysis and visualization of LD and haplotype maps.
J C Barrett, B Fry, J Maller, M J Daly. Bioinformatics 2005
3

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
3

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
3

Association between human leukocyte antigen-G 14-bp insertion/deletion polymorphism and cancer risk: a meta-analysis and systematic review.
Yu-Zheng Ge, Qian Ge, Ming-Hao Li, Guo-Mei Shi, Xiao Xu, Lu-Wei Xu, Zheng Xu, Tian-Ze Lu, Ran Wu, Liu-Hua Zhou,[...]. Hum Immunol 2014
18
11

Human leukocyte antigen-G overexpression predicts poor clinical outcomes in low-grade gliomas.
Xing Fan, Yinyan Wang, Chuanbao Zhang, Xing Liu, Zenghui Qian, Tao Jiang. J Neuroimmunol 2016
6
33

A functional role of HLA-G expression in human gliomas: an alternative strategy of immune escape.
Heinz Wiendl, Meike Mitsdoerffer, Valeska Hofmeister, Jörg Wischhusen, Antje Bornemann, Richard Meyermann, Elisabeth H Weiss, Arthur Melms, Michael Weller. J Immunol 2002
238
2

Tumor border sharpness correlates with HLA-G expression in low-grade gliomas.
Yinyan Wang, Xing Fan, Hongming Li, Zhiguo Lin, Hongbo Bao, Shaowu Li, Lei Wang, Tianzi Jiang, Yong Fan, Tao Jiang. J Neuroimmunol 2015
17
11


Transcriptional and posttranscriptional regulations of the HLA-G gene.
Erick C Castelli, Luciana C Veiga-Castelli, Layale Yaghi, Philippe Moreau, Eduardo A Donadi. J Immunol Res 2014
85
2

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland,[...]. Genet Med 2020
103
2

Common genetic vulnerability for nicotine and alcohol dependence in men.
W R True, H Xian, J F Scherrer, P A Madden, K K Bucholz, A C Heath, S A Eisen, M J Lyons, J Goldberg, M Tsuang. Arch Gen Psychiatry 1999
298
2

Genetic susceptibility to heroin addiction: a candidate gene association study.
O Levran, D Londono, K O'Hara, D A Nielsen, E Peles, J Rotrosen, P Casadonte, S Linzy, M Randesi, J Ott,[...]. Genes Brain Behav 2008
143
2

Association of OPRK1 gene polymorphisms with opioid dependence in addicted men undergoing methadone treatment in an Iranian population.
Ali Albonaim, Hedyeh Fazel, Alireza Sharafshah, Vahid Omarmeli, Sajjad Rezaei, Farzam Ajamian, Parvaneh Keshavarz. J Addict Dis 2017
9
22

Neurobiological mechanisms involved in nicotine dependence and reward: participation of the endogenous opioid system.
Fernando Berrendero, Patricia Robledo, José Manuel Trigo, Elena Martín-García, Rafael Maldonado. Neurosci Biobehav Rev 2010
86
2

Human Mu Opioid Receptor (OPRM1 A118G) polymorphism is associated with brain mu-opioid receptor binding potential in smokers.
Riju Ray, Kosha Ruparel, Andrew Newberg, E Paul Wileyto, James W Loughead, Chaitanya Divgi, Julie A Blendy, Jean Logan, Jon-Kar Zubieta, Caryn Lerman. Proc Natl Acad Sci U S A 2011
91
2



Assessment of paraoxonase 1 activity and malondialdehyde levels in patients with rheumatoid arthritis.
Gulden Baskol, Huseyin Demir, Mevlut Baskol, Eser Kilic, Filiz Ates, Derya Kocer, Sabahattin Muhtaroglu. Clin Biochem 2005
52
3


Effect of the molecular polymorphisms of human paraoxonase (PON1) on the rate of hydrolysis of paraoxon.
B Mackness, M I Mackness, S Arrol, W Turkie, P N Durrington. Br J Pharmacol 1997
136
2

[Low paraoxonase and arylesterase plasma activities in Mexican patients with coronary artery disease].
Ricardo Gamboa, Juan Carlos Regalado, Claudia Huesca-Gómez, Carlos Posadas-Romero, Juan Verdejo Paris, Gilberto Vargas-Alarcón, Oscar Pérez-Méndez. Arch Cardiol Mex 2008
12
16

Paraoxonase 1 gene polymorphisms and enzyme activities in coronary artery disease and its relationship to serum lipids and glycemia.
Osvaldo Fridman, Luis Gariglio, Stephanie Riviere, Rafael Porcile, Alicia Fuchs, Miguel Potenzoni. Arch Cardiol Mex 2016
8
25


Comparison of Beta-value and M-value methods for quantifying methylation levels by microarray analysis.
Pan Du, Xiao Zhang, Chiang-Ching Huang, Nadereh Jafari, Warren A Kibbe, Lifang Hou, Simon M Lin. BMC Bioinformatics 2010
927
2



PROMO: detection of known transcription regulatory elements using species-tailored searches.
Xavier Messeguer, Ruth Escudero, Domènec Farré, Oscar Núñez, Javier Martínez, M Mar Albà. Bioinformatics 2002
756
2

Annotation of functional variation in personal genomes using RegulomeDB.
Alan P Boyle, Eurie L Hong, Manoj Hariharan, Yong Cheng, Marc A Schaub, Maya Kasowski, Konrad J Karczewski, Julie Park, Benjamin C Hitz, Shuai Weng,[...]. Genome Res 2012
2

Pilon: an integrated tool for comprehensive microbial variant detection and genome assembly improvement.
Bruce J Walker, Thomas Abeel, Terrance Shea, Margaret Priest, Amr Abouelliel, Sharadha Sakthikumar, Christina A Cuomo, Qiandong Zeng, Jennifer Wortman, Sarah K Young,[...]. PLoS One 2014
2

The variant call format and VCFtools.
Petr Danecek, Adam Auton, Goncalo Abecasis, Cornelis A Albers, Eric Banks, Mark A DePristo, Robert E Handsaker, Gerton Lunter, Gabor T Marth, Stephen T Sherry,[...]. Bioinformatics 2011
2

Detection of nonneutral substitution rates on mammalian phylogenies.
Katherine S Pollard, Melissa J Hubisz, Kate R Rosenbloom, Adam Siepel. Genome Res 2010
2

2010 Rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative.
Daniel Aletaha, Tuhina Neogi, Alan J Silman, Julia Funovits, David T Felson, Clifton O Bingham, Neal S Birnbaum, Gerd R Burmester, Vivian P Bykerk, Marc D Cohen,[...]. Arthritis Rheum 2010
2

Appropriate waist circumference cut-off points among Iranian adults: the first report of the Iranian National Committee of Obesity.
Fereidoun Azizi, Davood Khalili, Hassan Aghajani, Alireza Esteghamati, Farhad Hosseinpanah, Alireza Delavari, Bagher Larijani, Parvin Mirmiran, Yadollah Mehrabi, Roya Kelishadi,[...]. Arch Iran Med 2010
92
2

Prevention of non-communicable disease in a population in nutrition transition: Tehran Lipid and Glucose Study phase II.
Fereidoun Azizi, Arash Ghanbarian, Amir Abbas Momenan, Farzad Hadaegh, Parvin Mirmiran, Mehdi Hedayati, Yadollah Mehrabi, Saleh Zahedi-Asl. Trials 2009
454
2


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.