Anthony P. Fejes

2.6k total citations
15 papers, 1.2k citations indexed

About

Anthony P. Fejes is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Anthony P. Fejes has authored 15 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Genetics and 1 paper in Genetics. Recurrent topics in Anthony P. Fejes's work include RNA modifications and cancer (4 papers), RNA and protein synthesis mechanisms (4 papers) and Genomics and Rare Diseases (3 papers). Anthony P. Fejes is often cited by papers focused on RNA modifications and cancer (4 papers), RNA and protein synthesis mechanisms (4 papers) and Genomics and Rare Diseases (3 papers). Anthony P. Fejes collaborates with scholars based in Canada, United States and France. Anthony P. Fejes's co-authors include Steven J.M. Jones, Matthew N. Bainbridge, Richard Varhol, Marco A. Marra, Mikhail Bilenky, Gordon Robertson, Ryan D. Morin, Martin Hirst, Martin Krzywinski and Trevor J. Pugh and has published in prestigious journals such as Nucleic Acids Research, Bioinformatics and Journal of Molecular Biology.

In The Last Decade

Anthony P. Fejes

15 papers receiving 1.2k citations

Peers

Countries citing papers authored by Anthony P. Fejes

Since Specialization

Citations

This map shows the geographic impact of Anthony P. Fejes's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Anthony P. Fejes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anthony P. Fejes more than expected).

Fields of papers citing papers by Anthony P. Fejes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anthony P. Fejes. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Anthony P. Fejes. The network helps show where Anthony P. Fejes may publish in the future.

Co-authorship network of co-authors of Anthony P. Fejes

This figure shows the co-authorship network connecting the top 25 collaborators of Anthony P. Fejes. A scholar is included among the top collaborators of Anthony P. Fejes based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Anthony P. Fejes. Anthony P. Fejes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool 2018 ·BMC Bioinformatics ·Steven Flygare, Edgar J. Hernández, Lon Phan, Barry Moore, Man Li, Anthony P. Fejes, Hao Hu, Karen Eilbeck, Chad Huff, Lynn B. Jorde, Martin G. Reese, Mark Yandell	25
2	DaVIE: Database for the Visualization and Integration of Epigenetic data 2014 ·Frontiers in Genetics ·Anthony P. Fejes, Meaghan J. Jones, Michael S. Kobor	5
3	Identifying cancer mutation targets across thousands of samples: MuteProc, a high throughput mutation analysis pipeline 2013 ·BMC Bioinformatics ·Alireza Hadj Khodabakhshi, Anthony P. Fejes, İnanç Birol, Steven J.M. Jones	1
4	GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome 2012 ·The American Journal of Human Genetics ·Dan Doherty, Albert E. Chudley, Gail Coghlan, Gisele E. Ishak, A. Micheil Innes, Edmond G. Lemire, R. Curtis Rogers, Aizeddin A. Mhanni, Ian G. Phelps, Steven J.M. Jones, Shing H. Zhan, Anthony P. Fejes, Hashem Shahin, Moien Kanaan, Hatice Akay, Mustafa Tekin, Barbara L. Triggs‐Raine, Teresa Zelinski	2
5	GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome 2012 ·The American Journal of Human Genetics ·Dan Doherty, Albert E. Chudley, Gail Coghlan, Gisele E. Ishak, A. Micheil Innes, Edmond G. Lemire, R. Curtis Rogers, Aizeddin A. Mhanni, Ian G. Phelps, Steven J.M. Jones, Shing H. Zhan, Anthony P. Fejes, Hashem Shahin, Moien Kanaan, Hatice Akay, Mustafa Tekin, Barbara L. Triggs‐Raine, Teresa Zelinski	81
6	Recurrent targets of aberrant somatic hypermutation in lymphoma 2012 ·Oncotarget ·Alireza Hadj Khodabakhshi, Ryan D. Morin, Anthony P. Fejes, Andrew J. Mungall, Karen Mungall, Madison Bolger-Munro, Nathalie A. Johnson, Joseph M. Connors, Randy D. Gascoyne, Marco A. Marra, İnanç Birol, Steven J.M. Jones	95
7	Gene expression profiling of oxidative stress response of C. elegans aging defective AMPK mutants using massively parallel transcriptome sequencing 2011 ·BMC Research Notes ·Heesun Shin, Hyojin Lee, Anthony P. Fejes, David L. Baillie, Hyeon‐Sook Koo, Steven J.M. Jones	30
8	Mutations in EZH2 Cause Weaver Syndrome 2011 ·The American Journal of Human Genetics ·William T. Gibson, Rebecca L. Hood, Shing H. Zhan, Dennis E. Bulman, Anthony P. Fejes, Richard A. Moore, Andrew J. Mungall, Patrice Eydoux, Riyana Babul‐Hirji, Jianghong An, Marco A. Marra, David Chitayat, Kym M. Boycott, David D. Weaver, Steven J.M. Jones	196
9	Human variation database: an open-source database template for genomic discovery 2011 ·Bioinformatics ·Anthony P. Fejes, Alireza Hadj Khodabakhshi, İnanç Birol, Steven J.M. Jones	6
10	De novo motif identification improves the accuracy of predicting transcription factor binding sites in ChIP-Seq data analysis 2010 ·Nucleic Acids Research ·Valentina Boeva, Didier Surdez, (unknown), Franck Tirode, Anthony P. Fejes, Olivier Delattre, Emmanuel Barillot	52
11	Genome-wide relationship between histone H3 lysine 4 mono- and tri-methylation and transcription factor binding 2008 ·Genome Research ·A. Gordon Robertson, Mikhail Bilenky, Angela Tam, Yongjun Zhao, Thomas Zeng, Nina Thiessen, Timothée Cezard, Anthony P. Fejes, Elizabeth D. Wederell, Rebecca Cullum, Ghia Euskirchen, Martin Krzywinski, İnanç Birol, M Snyder, Pamela A. Hoodless, Martin Hirst, Marco A. Marra, Steven J.M. Jones	139
12	Profiling the HeLa S3 Transcriptome using Randomly Primed cDNA and Massively Parallel Short-Read Sequencing 2008 ·BioTechniques ·Ryan D. Morin, Matthew N. Bainbridge, Anthony P. Fejes, Martin Hirst, Martin Krzywinski, Trevor J. Pugh, Helen McDonald, Richard Varhol, Steven J.M. Jones, Marco A. Marra	246
13	FindPeaks 3.1: a tool for identifying areas of enrichment from massively parallel short-read sequencing technology 2008 ·Bioinformatics ·Anthony P. Fejes, Gordon Robertson, Mikhail Bilenky, Richard Varhol, Matthew N. Bainbridge, Steven J.M. Jones	215
14	A New Algorithm for RNA Secondary Structure Design 2003 ·Journal of Molecular Biology ·Mirela Andronescu, Anthony P. Fejes, Frank Hutter, Holger H. Hoos, Anne Condon	117
15	Shotgun proteomic analysis of a chromatophore-enriched preparation from the purple phototrophic bacterium Rhodopseudomonas palustris 2003 ·Photosynthesis Research ·Anthony P. Fejes, Eugene C. Yi, David R. Goodlett, J. Thomas Beatty	14

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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