Russell G. Snell

16.7k total citations · 3 hit papers
134 papers, 6.0k citations indexed

About

Russell G. Snell is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Russell G. Snell has authored 134 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 45 papers in Genetics and 41 papers in Cellular and Molecular Neuroscience. Recurrent topics in Russell G. Snell's work include Genetic Neurodegenerative Diseases (37 papers), Genetic and phenotypic traits in livestock (30 papers) and Mitochondrial Function and Pathology (27 papers). Russell G. Snell is often cited by papers focused on Genetic Neurodegenerative Diseases (37 papers), Genetic and phenotypic traits in livestock (30 papers) and Mitochondrial Function and Pathology (27 papers). Russell G. Snell collaborates with scholars based in New Zealand, United Kingdom and United States. Russell G. Snell's co-authors include Richard Spelman, Suzanne J. Reid, Christine A. Ford, Richard J. Wilkins, Garry B. Udy, Prabha A. Ram, Helen W. Davey, Soo-Hee Park, David J. Waxman and Jeremy P. Cheadle and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nucleic Acids Research.

In The Last Decade

Russell G. Snell

129 papers receiving 5.8k citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Requirement of STAT5b for sexual dimorphism of body growth rates and liver gene expression

1997 828 citations Russell G. Snell et al. Proceedings of the National Academy of Sciences profile →
Positional Candidate Cloning of a QTL in Dairy Cattle: Identification of a Missense Mutation in the Bovine DGAT1 Gene with Major Effect on Milk Yield and Composition

2002 781 citations Suzanne J. Reid, Richard Spelman et al. profile →
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

1993 558 citations Russell G. Snell, Marcy E. MacDonald et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Russell G. Snell	2.5k	2.4k	1.5k	683	628	134	6.0k
P. Jones	1.8k 0.7×	891 0.4×	570 0.4×	410 0.6×	473 0.8×	114	6.4k
G. Ferrari	3.4k 1.3×	827 0.3×	1.3k 0.9×	278 0.4×	232 0.4×	83	6.1k
Roland P.S. Kwok	3.8k 1.5×	1.1k 0.4×	732 0.5×	126 0.2×	609 1.0×	46	5.6k
Rainer Schneider	2.9k 1.1×	360 0.1×	928 0.6×	714 1.0×	236 0.4×	90	4.5k
Jerome Schaack	3.9k 1.5×	1.0k 0.4×	689 0.5×	277 0.4×	373 0.6×	108	6.1k
Dirk Bohmann	7.7k 3.0×	999 0.4×	1.4k 0.9×	236 0.3×	980 1.6×	84	10.6k
Yuji Tanaka	2.2k 0.9×	420 0.2×	1.1k 0.7×	778 1.1×	163 0.3×	116	4.7k
William Biggs	6.0k 2.4×	1.2k 0.5×	767 0.5×	74 0.1×	618 1.0×	33	8.1k
Patrick Martin	3.4k 1.3×	1.1k 0.4×	829 0.6×	83 0.1×	387 0.6×	129	5.8k
Isabel Novoa	6.5k 2.5×	674 0.3×	505 0.3×	222 0.3×	442 0.7×	26	11.0k

Countries citing papers authored by Russell G. Snell

Since Specialization

Citations

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

Fields of papers citing papers by Russell G. Snell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Russell G. Snell. 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 Russell G. Snell. The network helps show where Russell G. Snell may publish in the future.

Co-authorship network of co-authors of Russell G. Snell

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

All Works

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20 of 20 papers shown

Li, Jun, Skye R. Rudiger, Jennifer M. Kelly, et al.. (2025). Presenilin 1 hemizygosity has no overt deleterious phenotypic outcomes in sheep: Potential implications for therapeutic targets in Alzheimer's disease. Neurobiology of Aging. 152. 25–33.

Walker, Caroline, Zaneta M. Thayer, Emma Marks, et al.. (2024). Association between maternal depression symptoms and child telomere length. Journal of Psychiatric Research. 174. 319–325.

Jiang, Andrew, Russell G. Snell, & Klaus Lehnert. (2024). ICARUS v3, a massively scalable web server for single-cell RNA-seq analysis of millions of cells. Bioinformatics. 40(4). 3 indexed citations

Lopdell, Thomas, Claire Prowse-Wilkins, Sarah Knowles, et al.. (2024). A common regulatory haplotype doubles lactoferrin concentration in milk. Genetics Selection Evolution. 56(1). 22–22. 3 indexed citations

Jiang, Andrew, Linya You, Renée R. Handley, et al.. (2024). Single nuclei RNA-seq reveals a medium spiny neuron glutamate excitotoxicity signature prior to the onset of neuronal death in an ovine Huntington’s disease model. Human Molecular Genetics. 33(17). 1524–1539. 4 indexed citations

Jiang, Andrew, Renée R. Handley, Klaus Lehnert, & Russell G. Snell. (2023). From Pathogenesis to Therapeutics: A Review of 150 Years of Huntington’s Disease Research. International Journal of Molecular Sciences. 24(16). 13021–13021. 68 indexed citations

Broadhurst, Marita, et al.. (2023). Successful editing and maintenance of lactogenic gene expression in primary bovine mammary epithelial cells. In Vitro Cellular & Developmental Biology - Animal. 3 indexed citations

Jiang, Andrew, Linya You, Russell G. Snell, & Klaus Lehnert. (2022). Delineation of complex gene expression patterns in single cell RNA-seq data with ICARUS v2.0. NAR Genomics and Bioinformatics. 5(2). lqad032–lqad032. 5 indexed citations

Jiang, Andrew, Klaus Lehnert, Linya You, & Russell G. Snell. (2022). ICARUS, an interactive web server for single cell RNA-seq analysis. Nucleic Acids Research. 50(W1). W427–W433. 23 indexed citations

10.

Sugrue, Victoria J, Joseph A. Zoller, Pritika Narayan, et al.. (2021). Castration delays epigenetic aging and feminizes DNA methylation at androgen-regulated loci. eLife. 10. 42 indexed citations

11.

Poquérusse, Jessie, et al.. (2021). Novel PRMT7 mutation in a rare case of dysmorphism and intellectual disability. Journal of Human Genetics. 67(1). 19–26. 9 indexed citations

12.

Cleuren, Yamila N. Torres, et al.. (2020). Natural cryptic variation in epigenetic modulation of an embryonic gene regulatory network. Proceedings of the National Academy of Sciences. 117(24). 13637–13646. 14 indexed citations

13.

López‐Villalobos, N., Stephen R. Davis, Sarah Berry, et al.. (2020). Genetic correlations of milk fatty acid contents predicted from milk mid-infrared spectra in New Zealand dairy cattle. Journal of Dairy Science. 103(8). 7238–7248. 13 indexed citations

14.

López‐Villalobos, N., et al.. (2020). Advantage of including Genomic Information to Predict Breeding Values for Lactation Yields of Milk, Fat, and Protein or Somatic Cell Score in a New Zealand Dairy Goat Herd. Animals. 11(1). 24–24. 4 indexed citations

15.

Lopdell, Thomas, Christine Couldrey, Kathryn Tiplady, et al.. (2018). Widespread cis -regulation of RNA editing in a large mammal. RNA. 25(3). 319–335. 6 indexed citations

16.

Ly, Kien, Callum Wilson, Klaus Lehnert, et al.. (2018). Modelling brain dopamine-serotonin vesicular transport disease in Caenorhabditis elegans. Disease Models & Mechanisms. 11(11). 4 indexed citations

17.

Harland, Chad, et al.. (2018). GWAS of novel protein coding variants discovered through whole genome sequencing of dairy cattle. Proceedings of the World Congress on Genetics Applied to Livestock Production. 421. 1 indexed citations

18.

Lopdell, Thomas, Kathryn Tiplady, Maksim Struchalin, et al.. (2017). DNA and RNA-sequence based GWAS highlights membrane-transport genes as key modulators of milk lactose content. BMC Genomics. 18(1). 968–968. 45 indexed citations

19.

Handley, Renée R., Stefano Patassini, Skye R. Rudiger, et al.. (2011). Characterisation of a transgenic ovine model of Huntington’s disease. Clinical Genetics. 1 indexed citations

20.

Rees, Mark I., Kristin Baer, Hamish E. Ward, et al.. (2001). A missense mutation of human Gephyrin (GPHN) is associated with Hyperekplexia and transcript isoform analysis re-defines the genomic structure of GPHN. ORCA Online Research @Cardiff (Cardiff University). 1 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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