Andrew R. Jackson

2.4k total citations
9 papers, 375 citations indexed

About

Andrew R. Jackson is a scholar working on Molecular Biology, Genetics and Computer Networks and Communications. According to data from OpenAlex, Andrew R. Jackson has authored 9 papers receiving a total of 375 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Computer Networks and Communications. Recurrent topics in Andrew R. Jackson's work include Genomics and Rare Diseases (3 papers), Genomics and Phylogenetic Studies (3 papers) and Chromosomal and Genetic Variations (2 papers). Andrew R. Jackson is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genomics and Phylogenetic Studies (3 papers) and Chromosomal and Genetic Variations (2 papers). Andrew R. Jackson collaborates with scholars based in United States, Canada and Russia. Andrew R. Jackson's co-authors include Aleksandar Milosavljevic, Sameer Paithankar, Cristian Coarfa, Fuli Yu, Danny Challis, Uday S. Evani, Jin Yu, Richard A. Gibbs, R. Alan Harris and Malcolm G. Baines and has published in prestigious journals such as Nature Communications, Genome Research and BMC Bioinformatics.

In The Last Decade

Andrew R. Jackson

9 papers receiving 365 citations

Peers

Andrew R. Jackson

MB

GENET

CR

PS

IMMUN

Yongzhuang Liu China

Jian Tajbakhsh United States

Nikhil R. Podduturi United States

Michal Galdzicki United States

Marta Bleda Spain

Zachary Zappala United States

Charles Tilford United States

Stas Volik United States

Yanmei Dou China

M. Q. Zhang United States

Yongzhuang Liu China

Andrew R. Jackson

409 ×1.4

MB

323 ×2.2

GENET

147 ×1.5

CR

89 ×2.3

PS

20 ×1.2

IMMUN

Citations per year, relative to Andrew R. Jackson Andrew R. Jackson (= 1×) peers Yongzhuang Liu

Countries citing papers authored by Andrew R. Jackson

Since Specialization

Citations

This map shows the geographic impact of Andrew R. Jackson'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 Andrew R. Jackson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew R. Jackson more than expected).

Fields of papers citing papers by Andrew R. Jackson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew R. Jackson. 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 Andrew R. Jackson. The network helps show where Andrew R. Jackson may publish in the future.

Co-authorship network of co-authors of Andrew R. Jackson

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew R. Jackson. A scholar is included among the top collaborators of Andrew R. Jackson 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 Andrew R. Jackson. Andrew R. Jackson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

1.

Patel, Ronak Y., Andrew R. Jackson, Chris Bizon, et al.. (2018). ClinGen Allele Registry links information about genetic variants. Human Mutation. 39(11). 1690–1701. 25 indexed citations

2.

Amin, Viren, R. Alan Harris, Vitor Onuchic, et al.. (2015). Epigenomic footprints across 111 reference epigenomes reveal tissue-specific epigenetic regulation of lincRNAs. Nature Communications. 6(1). 6370–6370. 57 indexed citations

3.

Nielsen, Cydney, Henriette O’Geen, Xiaoqin Xu, et al.. (2012). Spark: A navigational paradigm for genomic data exploration. Genome Research. 22(11). 2262–2269. 24 indexed citations

4.

Challis, Danny, Jin Yu, Uday S. Evani, et al.. (2012). An integrative variant analysis suite for whole exome next-generation sequencing data. BMC Bioinformatics. 13(1). 8–8. 160 indexed citations

5.

Evani, Uday S., Danny Challis, Jin Yu, et al.. (2012). Atlas2 Cloud: a framework for personal genome analysis in the cloud. BMC Genomics. 13(S6). 39 indexed citations

6.

Evani, Uday S., Danny Challis, Jin Yu, et al.. (2011). Enabling Atlas2 personal genome analysis on the cloud. 26. 117–120. 1 indexed citations

7.

Milosavljevic, Aleksandar, R. Alan Harris, Erica Sodergren, et al.. (2005). Pooled genomic indexing of rhesus macaque. Genome Research. 15(2). 292–301. 12 indexed citations

8.

Jackson, Andrew R., et al.. (2004). Pash: Efficient Genome-Scale Sequence Anchoring by Positional Hashing. Genome Research. 14(4). 672–678. 27 indexed citations

9.

Munro, Sandra B., Alain Duclos, Andrew R. Jackson, Malcolm G. Baines, & Orest W. Blaschuk. (1996). Characterization of Cadherins Expressed by Murine Thymocytes. Cellular Immunology. 169(2). 309–312. 30 indexed citations

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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