Eric H. Powell

2.4k citations

16 papers · 2.0k · 1 hit paper · h-index 13

Impact in

Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders
- Nerve injury and regeneration
Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments

Papers in

Cellular and Molecular Neuroscience 6
- Hereditary Neurological Disorders 5
- Nerve injury and regeneration 1
Genetics 4
- Genomics and Rare Diseases 4

Co-authors: Stephan L. Zuchner (7 shared papers)Eden R. Martin (5 shared papers)Gary W. Beecham (4 shared papers)Jeffery M. Vance (4 shared papers)Ioanna Konidari (4 shared papers)Margaret A. Pericak‐Vance (4 shared papers)William K. Scott (3 shared papers)Jonathan L. Haines (3 shared papers)
Journals: The American Journal of Human Genetics (4 papers)PLoS ONE (2 papers)Annals of Human Genetics (1 paper)PLoS Genetics (1 paper)Alzheimer s & Dementia (1 paper)
Partner nations: United States United Kingdom Germany

In The Last Decade

Eric H. Powell

16 papers receiving 1.9k citations

Eric H. Powell's Hit Papers

align trajectories log scale

dSarm/Sarm1 Is Required for Activation of an Injury-Induced Axon Death Pathway 2012 · 553 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2012 Science

Peers

Countries citing papers authored by Eric H. Powell

Since Specialization

Citations

This map shows the geographic impact of Eric H. 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 H. 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 H. Powell more than expected).

Fields of papers citing papers by Eric H. Powell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Eric H. Powell, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eric H. Powell Line = papers co-authored together Eric H. Powell links everyone, so they are left out of the graph.

All Works

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16 of 16 papers shown

#	Work
1	dSarm/Sarm1 Is Required for Activation of an Injury-Induced Axon Death Pathway Science ·Jeannette M. Osterloh, Jing Hui Yang, Timothy M. Rooney, A. Nicole Fox, Róbert Adalbert, Eric H. Powell, Amy E. Sheehan, Michelle A. Avery Hit paper breakdown →	2012	553
2	Genome‐Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease Annals of Human Genetics ·Todd L. Edwards, William K. Scott, Cherylyn Almonte, Amber Burt, Eric H. Powell, Gary W. Beecham, Liyong Wang, Stephan L. Zuchner	2010	408
3	Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia The American Journal of Human Genetics ·Aslı Sırmacı, Michail Spiliopoulos, Francesco Brancati, Eric H. Powell, Duygu Duman, Alexander J. Abrams, Güney Bademci, Emanuele Agolini	2011	214
4	Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes Nature Genetics ·Andrea Cortese, Yi Zhu, Adriana P. Rebelo, Sara Negri, Steve C. Courel, Lisa Abreu, Chelsea J. Bacon, Yunhong Bai	2020	133
5	Dementia Revealed: Novel Chromosome 6 Locus for Late-Onset Alzheimer Disease Provides Genetic Evidence for Folate-Pathway Abnormalities PLoS Genetics ·Adam Christian Naj, Gary W. Beecham, Eden R. Martin, Paul J. Gallins, Eric H. Powell, Ioanna Konidari, Patrice L. Whitehead, Guiqing Cai	2010	132
6	Exome sequencing allows for rapid gene identification in a Charcot‐Marie‐Tooth family Annals of Neurology ·Gladys Montenegro, Eric H. Powell, Jiaqiang Huang, Fiorella Speziani, Yvonne J. K. Edwards, Gary W. Beecham, William F. Hulme, Carly E. Siskind	2011	100
7	GEnomes Management Application (GEM.app): A New Software Tool for Large-Scale Collaborative Genome Analysis Human Mutation ·Michael Gonzalez, Rafael F. Acosta Lebrigio, Derek Van Booven, Rick H. Ulloa, Eric H. Powell, Fiorella Speziani, Mustafa Tekin, Rebecca Schüle	2013	70
8	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 ·Milen T. Velinov, Natalia Dolzhanskaya, Michael Gonzalez, Eric H. Powell, Ioanna Konidari, William F. Hulme, John F. Staropoli, Winnie W. Xin	2012	69
9	Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2 The American Journal of Human Genetics ·Petra Laššuthová, Adriana P. Rebelo, Gianina Ravenscroft, Phillipa J. Lamont, Mark R. Davis, Fiore Manganelli, Shawna M. E. Feely, Chelsea J. Bacon	2018	64
10	Exome Sequencing of a Multigenerational Human Pedigree PLoS ONE ·Dale J. Hedges, Eric H. Powell, Cherylyn Almonte, Jia Huang, Benjamin Boese, Mike F. Schmidt, Margaret A. Pericak‐Vance, Eden R. Martin	2009	61
11	SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies Bioinformatics ·Eden R. Martin, Daniel D. Kinnamon, Michael A. Schmidt, Eric H. Powell, Stephan L. Zuchner +1 other	2010	56
12	Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia The American Journal of Human Genetics ·Mohammad Ali Farazi Fard, Adriana P. Rebelo, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Ina Gehweiler, Selina Reich, Jennifer Reichbauer	2019	51
13	Disseminated cutaneous acanthamebiasis: a case report and review of the literature. PubMed ·Michael Paltiel, Eric H. Powell, Jane Lynch, Ciro R. Martins +1 other	2004	34
14	Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia The American Journal of Human Genetics ·Mohammad Ali Farazi Fard, Adriana P. Rebelo, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Ina Gehweiler, Selina Reich, Jennifer Reichbauer	2019	9
15	The GENESIS database and tools: A decade of discovery in Mendelian genomics Experimental Neurology ·Matt Christopher Danzi, Eric H. Powell, Adriana P. Rebelo, Maike Franziska Dohrn, Danique Beijer, Sarah Fazal, Isaac R. L. Xu, Jessica M. Medina	2024	4
16	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 ·Adam Christian Naj, Gary W. Beecham, Eden R. Martin, Paul J. Gallins, Eric H. Powell, Ioanna Konidari, Patrice L. Whitehead, Guiqing Cai	2010	2

About Eric H. Powell

Eric H. Powell is a scholar working on Cellular and Molecular Neuroscience, Genetics, Endocrinology, Neurology and Physiology, having authored 16 papers that have together received 2.0k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (5 papers), Genomics and Rare Diseases (4 papers), Genomics and Phylogenetic Studies (1 paper), Legionella and Acanthamoeba research (1 paper), Parkinson's Disease Mechanisms and Treatments (1 paper), Lysosomal Storage Disorders Research (1 paper) and Nerve injury and regeneration (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (356 citations), Neurology (352 citations), Genetics (258 citations), Geriatrics and Gerontology (23 citations) and Endocrinology (23 citations). Eric H. Powell has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Stephan L. Zuchner, Eden R. Martin, Gary W. Beecham, Jeffery M. Vance, Ioanna Konidari, Margaret A. Pericak‐Vance, William K. Scott, Jonathan L. Haines, Carlos Singer and Liyong Wang. Their work appears in journals such as The American Journal of Human Genetics, PLoS ONE, Annals of Human Genetics, PLoS Genetics and Alzheimer s & Dementia.

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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Eric H. Powell

Eric H. Powell's Hit Papers

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Fields of papers citing papers by Eric H. Powell

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About Eric H. Powell

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