A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure.
Emidio Capriotti, Piero Fariselli, Rita Casadio. Nucleic Acids Res 2005
837
100

SNAP: predict effect of non-synonymous polymorphisms on function.
Yana Bromberg, Burkhard Rost. Nucleic Acids Res 2007
520
100


SIFT: Predicting amino acid changes that affect protein function.
Pauline C Ng, Steven Henikoff. Nucleic Acids Res 2003
100

Proteomics-Based Approach Identifies Altered ER Domain Properties by ALS-Linked VAPB Mutation.
Tomoyuki Yamanaka, Risa Nishiyama, Tomomi Shimogori, Nobuyuki Nukina. Sci Rep 2020
8
50

Analysis of the TP53 Deleterious Single Nucleotide Polymorphisms Impact on Estrogen Receptor Alpha-p53 Interaction: A Machine Learning Approach.
Kumaraswamy Naidu Chitrala, Mitzi Nagarkatti, Prakash Nagarkatti, Suneetha Yeguvapalli. Int J Mol Sci 2019
3
50

Current status of clinical proteogenomics in lung cancer.
Toshihide Nishimura, Haruhiko Nakamura, Ákos Végvári, György Marko-Varga, Naoki Furuya, Hisashi Saji. Expert Rev Proteomics 2019
10
50

U2AF65 enhances milk synthesis and growth of bovine mammary epithelial cells by positively regulating the mTOR-SREBP-1c signalling pathway.
Yanbo Yu, Zhen Zhen, Hao Qi, Xiaohan Yuan, Xuejun Gao, Minghui Zhang. Cell Biochem Funct 2019
7
50

Jumonji domain-containing protein 6 protein and its role in cancer.
Jing Yang, Siyuan Chen, Yanfei Yang, Xuelei Ma, Bin Shao, Shengyong Yang, Yuquan Wei, Xiawei Wei. Cell Prolif 2020
11
50

Chapter 11: Genome-wide association studies.
William S Bush, Jason H Moore. PLoS Comput Biol 2012
505
50

Ranking non-synonymous single nucleotide polymorphisms based on disease concepts.
Hashem A Shihab, Julian Gough, Matthew Mort, David N Cooper, Ian N M Day, Tom R Gaunt. Hum Genomics 2014
88
50

Computational analysis of functional single nucleotide polymorphisms associated with SLC26A4 gene.
Mirza Jawad Ul Hasnain, Muhammad Shoaib, Salman Qadri, Bakhtawar Afzal, Tehreem Anwar, Syed Hassan Abbas, Amina Sarwar, Hafiz Muhammad Talha Malik, Muhammad Tariq Pervez. PLoS One 2020
5
50

Linkage of early-onset familial breast cancer to chromosome 17q21.
J M Hall, M K Lee, B Newman, J E Morrow, L A Anderson, B Huey, M C King. Science 1990
50

Mass spectrometry-based protein-protein interaction networks for the study of human diseases.
Alicia L Richards, Manon Eckhardt, Nevan J Krogan. Mol Syst Biol 2021
23
50

Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.
Joachim Schessl, Yaqun Zou, Meagan J McGrath, Belinda S Cowling, Baijayanta Maiti, Steven S Chin, Caroline Sewry, Roberta Battini, Ying Hu, Denny L Cottle,[...]. J Clin Invest 2008
113
50

Jmjd6 catalyses lysyl-hydroxylation of U2AF65, a protein associated with RNA splicing.
Celia J Webby, Alexander Wolf, Natalia Gromak, Mathias Dreger, Holger Kramer, Benedikt Kessler, Michael L Nielsen, Corinna Schmitz, Danica S Butler, John R Yates,[...]. Science 2009
269
50

The coming age of complete, accurate, and ubiquitous proteomes.
Matthias Mann, Nils A Kulak, Nagarjuna Nagaraj, Jürgen Cox. Mol Cell 2013
254
50

A second generation human haplotype map of over 3.1 million SNPs.
Kelly A Frazer, Dennis G Ballinger, David R Cox, David A Hinds, Laura L Stuve, Richard A Gibbs, John W Belmont, Andrew Boudreau, Paul Hardenbol, Suzanne M Leal,[...]. Nature 2007
50


JMJD6 is a histone arginine demethylase.
Bingsheng Chang, Yue Chen, Yingming Zhao, Richard K Bruick. Science 2007
424
50

p21: A Two-Faced Genome Guardian.
Alexandros G Georgakilas, Olga A Martin, William M Bonner. Trends Mol Med 2017
219
50

Structural basis for polypyrimidine tract recognition by the essential pre-mRNA splicing factor U2AF65.
E Allen Sickmier, Katherine E Frato, Haihong Shen, Shanthi R Paranawithana, Michael R Green, Clara L Kielkopf. Mol Cell 2006
133
50

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
50

Predicting the functional consequences of non-synonymous single nucleotide polymorphisms in IL8 gene.
Tikam Chand Dakal, Deepak Kala, Gourav Dhiman, Vinod Yadav, Andrey Krokhotin, Nikolay V Dokholyan. Sci Rep 2017
34
50

Analysis of genetic inheritance in a family quartet by whole-genome sequencing.
Jared C Roach, Gustavo Glusman, Arian F A Smit, Chad D Huff, Robert Hubley, Paul T Shannon, Lee Rowen, Krishna P Pant, Nathan Goodman, Michael Bamshad,[...]. Science 2010
688
50

Mutant Proteomics of Lung Adenocarcinomas Harboring Different EGFR Mutations.
Toshihide Nishimura, Ákos Végvári, Haruhiko Nakamura, Harubumi Kato, Hisashi Saji. Front Oncol 2020
2
50

Detecting protein variants by mass spectrometry: a comprehensive study in cancer cell-lines.
Javier A Alfaro, Alexandr Ignatchenko, Vladimir Ignatchenko, Ankit Sinha, Paul C Boutros, Thomas Kislinger. Genome Med 2017
23
50


Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.
R Wooster, S L Neuhausen, J Mangion, Y Quirk, D Ford, N Collins, K Nguyen, S Seal, T Tran, D Averill. Science 1994
50

Proteogenomics connects somatic mutations to signalling in breast cancer.
Philipp Mertins, D R Mani, Kelly V Ruggles, Michael A Gillette, Karl R Clauser, Pei Wang, Xianlong Wang, Jana W Qiao, Song Cao, Francesca Petralia,[...]. Nature 2016
787
50

Proteomics screen to reveal molecular changes mediated by C722G missense mutation in CHRM2 gene.
Dongyan Hou, Ying Chen, Jiamei Liu, Lin Xu, Zhiyong Zhang, Juan Zhang, Hua Wang, Xin Wang, Jin Chen, Rongrui Zhao,[...]. J Proteomics 2013
4
50

WS-SNPs&GO: a web server for predicting the deleterious effect of human protein variants using functional annotation.
Emidio Capriotti, Remo Calabrese, Piero Fariselli, Pier Luigi Martelli, Russ B Altman, Rita Casadio. BMC Genomics 2013
121
50

JMJD6 promotes colon carcinogenesis through negative regulation of p53 by hydroxylation.
Feng Wang, Lin He, Peiwei Huangyang, Jing Liang, Wenzhe Si, Ruorong Yan, Xiao Han, Shumeng Liu, Bin Gui, Wanjin Li,[...]. PLoS Biol 2014
71
50

p53 mutations in human cancers.
M Hollstein, D Sidransky, B Vogelstein, C C Harris. Science 1991
50

TP53 mutations in human cancers: origins, consequences, and clinical use.
Magali Olivier, Monica Hollstein, Pierre Hainaut. Cold Spring Harb Perspect Biol 2010
904
50

Predicting functional effect of human missense mutations using PolyPhen-2.
Ivan Adzhubei, Daniel M Jordan, Shamil R Sunyaev. Curr Protoc Hum Genet 2013
50

JMJD6 is a tumorigenic factor and therapeutic target in neuroblastoma.
Matthew Wong, Yuting Sun, Zhichao Xi, Giorgio Milazzo, Rebecca C Poulos, Christoph Bartenhagen, Jessica L Bell, Chelsea Mayoh, Nicholas Ho, Andrew E Tee,[...]. Nat Commun 2019
25
50


Role of JMJD6 in Breast Tumourigenesis.
Coralie Poulard, Juliette Rambaud, Emilie Lavergne, Julien Jacquemetton, Jack-Michel Renoir, Olivier Trédan, Sylvie Chabaud, Isabelle Treilleux, Laura Corbo, Muriel Le Romancer. PLoS One 2015
33
50

Common polymorphic inversions at 17q21.31 and 8p23.1 associate with cancer prognosis.
Carlos Ruiz-Arenas, Alejandro Cáceres, Victor Moreno, Juan R González. Hum Genomics 2019
2
50

Single ribosomal protein mutations in antibiotic-resistant bacteria analyzed by mass spectrometry.
S K Wilcox, G S Cavey, J D Pearson. Antimicrob Agents Chemother 2001
32
50

PANTHER: a library of protein families and subfamilies indexed by function.
Paul D Thomas, Michael J Campbell, Anish Kejariwal, Huaiyu Mi, Brian Karlak, Robin Daverman, Karen Diemer, Anushya Muruganujan, Apurva Narechania. Genome Res 2003
50

Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study.
Chaimaa Ait El Cadi, Al Mehdi Krami, Hicham Charoute, Zouhair Elkarhat, Najat Sifeddine, Hamid Lakhiari, Hassan Rouba, Abdelhamid Barakat, Halima Nahili. Biomed Res Int 2020
2
50

Control of pre-mRNA splicing by the general splicing factors PUF60 and U2AF(65).
Michelle L Hastings, Eric Allemand, Dominik M Duelli, Michael P Myers, Adrian R Krainer. PLoS One 2007
86
50

Exploring the effect of nsSNPs in human YPEL3 gene in cellular senescence.
Abhishek Singh, Mukesh Thakur, Sujeet Kumar Singh, Lalit Kumar Sharma, Kailash Chandra. Sci Rep 2020
3
50


Assessing the function of genetic variants in candidate gene association studies.
Timothy R Rebbeck, Margaret Spitz, Xifeng Wu. Nat Rev Genet 2004
128
50

PANTHER version 10: expanded protein families and functions, and analysis tools.
Huaiyu Mi, Sagar Poudel, Anushya Muruganujan, John T Casagrande, Paul D Thomas. Nucleic Acids Res 2016
593
50


Molecular mechanisms underlying the potentially adverse effects of folate.
Kyle C Strickland, Natalia I Krupenko, Sergey A Krupenko. Clin Chem Lab Med 2013
44
50


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.