Eric Powell

2.4k total citations
12 papers, 995 citations indexed

About

Eric Powell is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Eric Powell has authored 12 papers receiving a total of 995 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Rheumatology. Recurrent topics in Eric Powell's work include Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (3 papers) and Neurological diseases and metabolism (2 papers). Eric Powell is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (3 papers) and Neurological diseases and metabolism (2 papers). Eric Powell collaborates with scholars based in United States, Italy and Germany. Eric Powell's co-authors include Stephan Züchner, Eden R. Martin, Jeffery M. Vance, Gary W. Beecham, Ioanna Konidari, Margaret A. Pericak‐Vance, Jonathan L. Haines, William K. Scott, Carlos Singer and Todd L. Edwards and has published in prestigious journals such as Bioinformatics, PLoS ONE and Annals of Neurology.

In The Last Decade

Eric Powell

12 papers receiving 973 citations

Peers

Eric Powell

GENET

NEURO

CMN

PHYSI

Hossein Darvish Iran

Lynsey Bilsland United Kingdom

Stanka Romac Serbia

Tiao Xie United States

Andrée Robaglia‐Schlupp France

Tarja Joensuu Finland

Jay P. Ross Canada

Alexandra Benchoua France

Carine Ciron France

P. F. Chance United States

Hossein Darvish Iran

Eric Powell

609 ×1.4

332 ×1.0

GENET

259 ×0.8

NEURO

270 ×1.1

CMN

113 ×0.6

PHYSI

Citations per year, relative to Eric Powell Eric Powell (= 1×) peers Hossein Darvish

Countries citing papers authored by Eric Powell

Since Specialization

Citations

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

Fields of papers citing papers by Eric Powell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric Powell. 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 Eric Powell. The network helps show where Eric Powell may publish in the future.

Co-authorship network of co-authors of Eric Powell

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

All Works

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12 of 12 papers shown

Gonzalez, Michael, Derek Van Booven, Eric Powell, et al.. (2013). GEnomes Management Application (GEM.app): A New Software Tool for Large-Scale Collaborative Genome Analysis. Human Mutation. 34(6). 842–846. 48 indexed citations

Velinov, Milen, Natalia Dolzhanskaya, Michael Gonzalez, et al.. (2012). Correction: Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families. PLoS ONE. 7(9). 7 indexed citations

Velinov, Milen, Natalia Dolzhanskaya, Michael Gonzalez, et al.. (2012). Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families. PLoS ONE. 7(1). e29729–e29729. 64 indexed citations

Sırmacı, Aslı, Michail Spiliopoulos, Francesco Brancati, et al.. (2011). Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia. The American Journal of Human Genetics. 89(2). 289–294. 170 indexed citations

Powell, Eric, Jiaqiang Huang, Fiorella Speziani, et al.. (2011). Exome sequencing allows for rapid gene identification in a Charcot‐Marie‐Tooth family. Annals of Neurology. 69(3). 464–470. 83 indexed citations

Edwards, Todd L., William K. Scott, Amber Burt, et al.. (2010). Genome‐Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease. Annals of Human Genetics. 74(2). 97–109. 370 indexed citations

Martin, Eden R., Daniel D. Kinnamon, Michael A. Schmidt, et al.. (2010). SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies. Bioinformatics. 26(22). 2803–2810. 49 indexed citations

Naj, Adam C., Gary W. Beecham, Eden R. Martin, et al.. (2010). Dementia Revealed: Novel Chromosome 6 Locus for Late-Onset Alzheimer Disease Provides Genetic Evidence for Folate-Pathway Abnormalities. PLoS Genetics. 6(9). e1001130–e1001130. 114 indexed citations

Naj, Adam C., Gary W. Beecham, Eden R. Martin, et al.. (2010). O1‐03‐03: Dementia revealed: Novel chromosome 6 locus for late‐onset Alzheimer's disease provides genetic evidence for folate‐pathway abnormalities. Alzheimer s & Dementia. 6(4S_Part_3). 2 indexed citations

10.

Hedges, Dale J., Eric Powell, Jia Huang, et al.. (2009). Exome Sequencing of a Multigenerational Human Pedigree. PLoS ONE. 4(12). e8232–e8232. 53 indexed citations

11.

Hedges, Dale J., Eric Powell, Jia Huang, et al.. (2009). Correction: Exome Sequencing of a Multigenerational Human Pedigree. PLoS ONE. 4(12). 2 indexed citations

12.

Powell, Eric, et al.. (2004). Disseminated cutaneous acanthamebiasis: a case report and review of the literature.. PubMed. 73(4). 241–8. 33 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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