A citation-based method for searching scientific literature

S A Miller, D D Dykes, H F Polesky. Nucleic Acids Res 1988
Times Cited: 15643







List of co-cited articles
78 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
11

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
7


MutationTaster2: mutation prediction for the deep-sequencing age.
Jana Marie Schwarz, David N Cooper, Markus Schuelke, Dominik Seelow. Nat Methods 2014
5

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
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

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

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
4

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
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



VarSome: the human genomic variant search engine.
Christos Kopanos, Vasilis Tsiolkas, Alexandros Kouris, Charles E Chapple, Monica Albarca Aguilera, Richard Meyer, Andreas Massouras. Bioinformatics 2019
365
3

SIFT web server: predicting effects of amino acid substitutions on proteins.
Ngak-Leng Sim, Prateek Kumar, Jing Hu, Steven Henikoff, Georg Schneider, Pauline C Ng. Nucleic Acids Res 2012
962
3

De novo identification of differentially methylated regions in the human genome.
Timothy J Peters, Michael J Buckley, Aaron L Statham, Ruth Pidsley, Katherine Samaras, Reginald V Lord, Susan J Clark, Peter L Molloy. Epigenetics Chromatin 2015
329
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

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
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
19
10

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
263
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
18
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
87
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
146
2


SNPassoc: an R package to perform whole genome association studies.
Juan R González, Lluís Armengol, Xavier Solé, Elisabet Guinó, Josep M Mercader, Xavier Estivill, Víctor Moreno. Bioinformatics 2007
521
2

DNA methylation in mammals.
En Li, Yi Zhang. Cold Spring Harb Perspect Biol 2014
369
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

Role of TCF7L2 risk variant and dietary fibre intake on incident type 2 diabetes.
G Hindy, E Sonestedt, U Ericson, X-J Jing, Y Zhou, O Hansson, E Renström, E Wirfält, M Orho-Melander. Diabetologia 2012
42
4

TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program.
Jose C Florez, Kathleen A Jablonski, Nick Bayley, Toni I Pollin, Paul I W de Bakker, Alan R Shuldiner, William C Knowler, David M Nathan, David Altshuler. N Engl J Med 2006
585
2


TCF7L2 rs7903146-macronutrient interaction in obese individuals' responses to a 10-wk randomized hypoenergetic diet.
Katrine Grau, Stephane Cauchi, Claus Holst, Arne Astrup, J Alfredo Martinez, Wim H M Saris, Ellen E Blaak, Jean-Michel Oppert, Peter Arner, Stephan Rössner,[...]. Am J Clin Nutr 2010
37
5

Dietary saturated fat, gender and genetic variation at the TCF7L2 locus predict the development of metabolic syndrome.
Catherine M Phillips, Louisa Goumidi, Sandrine Bertrais, Martyn R Field, Ross McManus, Serge Hercberg, Denis Lairon, Richard Planells, Helen M Roche. J Nutr Biochem 2012
33
6

Interaction between dietary patterns and TCF7L2 polymorphisms on type 2 diabetes mellitus among Uyghur adults in Xinjiang Province, China.
Junxiu Cai, Yan Zhang, Rebiya Nuli, Yangyi Zhang, Manfutong Abudusemaiti, Aizhatiguli Kadeer, Xiaoli Tian, Hui Xiao. Diabetes Metab Syndr Obes 2019
6
33

TCF7L2, dietary carbohydrate, and risk of type 2 diabetes in US women.
Marilyn C Cornelis, Lu Qi, Peter Kraft, Frank B Hu. Am J Clin Nutr 2009
50
4


Glutathione transferases.
John D Hayes, Jack U Flanagan, Ian R Jowsey. Annu Rev Pharmacol Toxicol 2005
2

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
2

VarAFT: a variant annotation and filtration system for human next generation sequencing data.
Jean-Pierre Desvignes, Marc Bartoli, Valérie Delague, Martin Krahn, Morgane Miltgen, Christophe Béroud, David Salgado. Nucleic Acids Res 2018
56
3

From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline.
Geraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, Ryan Poplin, Guillermo Del Angel, Ami Levy-Moonshine, Tadeusz Jordan, Khalid Shakir, David Roazen, Joel Thibault,[...]. Curr Protoc Bioinformatics 2013
2

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
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.