Nathan P. Achilly

587 total citations
6 papers, 204 citations indexed

About

Nathan P. Achilly is a scholar working on Molecular Biology, Cognitive Neuroscience and Rheumatology. According to data from OpenAlex, Nathan P. Achilly has authored 6 papers receiving a total of 204 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Cognitive Neuroscience and 2 papers in Rheumatology. Recurrent topics in Nathan P. Achilly's work include Genetics and Neurodevelopmental Disorders (2 papers), Folate and B Vitamins Research (2 papers) and Autism Spectrum Disorder Research (2 papers). Nathan P. Achilly is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Folate and B Vitamins Research (2 papers) and Autism Spectrum Disorder Research (2 papers). Nathan P. Achilly collaborates with scholars based in United States, Switzerland and Canada. Nathan P. Achilly's co-authors include Huda Y. Zoghbi, Wei Wang, Jennifer L. Sloan, Charles P. Venditti, Gunter Scharer, Tamim H. Shaikh, Curtis R. Coughlin, Elizabeth A. Geiger, Brian Fowler and Irini Manoli and has published in prestigious journals such as Nature, Journal of Neurophysiology and The American Journal of Human Genetics.

In The Last Decade

Nathan P. Achilly

6 papers receiving 203 citations

Peers

Nathan P. Achilly
Ganka Douglas United States
Leanne Moynihan United Kingdom
Shujie Yu China
Ernest C. Steele United States
A. T. Pagnamenta United Kingdom
Ganka Douglas United States
Nathan P. Achilly
Citations per year, relative to Nathan P. Achilly Nathan P. Achilly (= 1×) peers Ganka Douglas

Countries citing papers authored by Nathan P. Achilly

Since Specialization
Citations

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

Fields of papers citing papers by Nathan P. Achilly

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nathan P. Achilly. 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 Nathan P. Achilly. The network helps show where Nathan P. Achilly may publish in the future.

Co-authorship network of co-authors of Nathan P. Achilly

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

All Works

6 of 6 papers shown
1.
Achilly, Nathan P., Ling-jie He, Shogo Ohmae, et al.. (2021). Deleting Mecp2 from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice. eLife. 10. 21 indexed citations
2.
Achilly, Nathan P., Wei Wang, & Huda Y. Zoghbi. (2021). Presymptomatic training mitigates functional deficits in a mouse model of Rett syndrome. Nature. 592(7855). 596–600. 50 indexed citations
3.
Sloan, Jennifer L., Nathan P. Achilly, Trevor Blake, et al.. (2020). The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphology. Human Molecular Genetics. 29(13). 2109–2123. 23 indexed citations
4.
Achilly, Nathan P.. (2015). Properties of VIP+ synapses in the suprachiasmatic nucleus highlight their role in circadian rhythm. Journal of Neurophysiology. 115(6). 2701–2704. 5 indexed citations
5.
Morlet, Thierry, Mindy Rabinowitz, Eric A. Sherman, et al.. (2013). A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans. The Laryngoscope. 124(3). E95–103. 15 indexed citations
6.
Yu, Hung‐Chun, Jennifer L. Sloan, Gunter Scharer, et al.. (2013). An X-Linked Cobalamin Disorder Caused by Mutations in Transcriptional Coregulator HCFC1. The American Journal of Human Genetics. 93(3). 506–514. 90 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026