Neil Humphreys

3.6k total citations · 1 hit paper
43 papers, 2.6k citations indexed

About

Neil Humphreys is a scholar working on Immunology, Physiology and Molecular Biology. According to data from OpenAlex, Neil Humphreys has authored 43 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Immunology, 13 papers in Physiology and 10 papers in Molecular Biology. Recurrent topics in Neil Humphreys's work include Parasites and Host Interactions (9 papers), Asthma and respiratory diseases (8 papers) and IL-33, ST2, and ILC Pathways (7 papers). Neil Humphreys is often cited by papers focused on Parasites and Host Interactions (9 papers), Asthma and respiratory diseases (8 papers) and IL-33, ST2, and ILC Pathways (7 papers). Neil Humphreys collaborates with scholars based in United Kingdom, Germany and Italy. Neil Humphreys's co-authors include Richard K. Grencis, Allison J. Bancroft, Thomas E. Lane, Jacques Van Snick, Matthew R. Hepworth, Foo Y. Liew, Damo Xu, Jean‐Christophe Renauld, Cath Booth and Laura Cliffe and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Neil Humphreys

42 papers receiving 2.5k citations

Hit Papers

Paternal microbiome perturbations impact offspring fitness 2024 2026 2025 2024 20 40 60
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.

  1. Paternal microbiome perturbations impact offspring fitness
    2024 72 citations Ayele Argaw-Denboba, Thomas Schmidt et al. Nature profile →

Peers

Neil Humphreys
Margaret Mentink‐Kane United States
Niamh E. Mangan Australia
Peter C. Cook United Kingdom
De’Broski R. Herbert United States
Ahmed Metwali United States
Arthur Blum United States
Naoki Arizono Japan
Philip Smith United Kingdom
Matthias Hesse United States
G. F. J. NEWLANDS United Kingdom
Margaret Mentink‐Kane United States
Neil Humphreys
Citations per year, relative to Neil Humphreys Neil Humphreys (= 1×) peers Margaret Mentink‐Kane

Countries citing papers authored by Neil Humphreys

Since Specialization
Citations

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

Fields of papers citing papers by Neil Humphreys

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neil Humphreys

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

All Works

20 of 20 papers shown
1.
Ganter, Kerstin, et al.. (2025). Genetic gradual reduction of OGT activity unveils the essential role of O-GlcNAc in the mouse embryo. PLoS Genetics. 21(1). e1011507–e1011507. 2 indexed citations
2.
Argaw-Denboba, Ayele, Thomas Schmidt, Monica Di Giacomo, et al.. (2024). Paternal microbiome perturbations impact offspring fitness. Nature. 629(8012). 652–659. 72 indexed citations breakdown →
3.
Endesh, Naima, Eulashini Chuntharpursat‐Bon, Charlotte Revill, et al.. (2023). Independent endothelial functions of PIEZO1 and TRPV4 in hepatic portal vein and predominance of PIEZO1 in mechanical and osmotic stress. Liver International. 43(9). 2026–2038. 20 indexed citations
4.
Chen, Fuhui, David Novo, Çiğdem Selli, et al.. (2023). RAC1B function is essential for breast cancer stem cell maintenance and chemoresistance of breast tumor cells. Oncogene. 42(9). 679–692. 8 indexed citations
5.
Chuntharpursat‐Bon, Eulashini, Oleksandr V. Povstyan, Melanie J. Ludlow, et al.. (2023). PIEZO1 and PECAM1 interact at cell-cell junctions and partner in endothelial force sensing. Communications Biology. 6(1). 358–358. 57 indexed citations
6.
Downton, Polly, James Bagnall, Hazel England, et al.. (2023). Overexpression of IκB⍺ modulates NF-κB activation of inflammatory target gene expression. Frontiers in Molecular Biosciences. 10. 1187187–1187187. 10 indexed citations
7.
Mokrosiński, Jacek, Katherine Lawler, Julia M. Keogh, et al.. (2023). A rare human variant that disrupts GPR10 signalling causes weight gain in mice. Nature Communications. 14(1). 1450–1450. 7 indexed citations
8.
Hunter, Louise, Antony Adamson, Polly Downton, et al.. (2020). Nuclear receptor REVERBα is a state-dependent regulator of liver energy metabolism. Proceedings of the National Academy of Sciences. 117(41). 25869–25879. 39 indexed citations
9.
Grabert, Kathleen, Anuj Sehgal, Katharine M. Irvine, et al.. (2020). A Transgenic Line That Reports CSF1R Protein Expression Provides a Definitive Marker for the Mouse Mononuclear Phagocyte System. The Journal of Immunology. 205(11). 3154–3166. 60 indexed citations
10.
Pinteaux, Emmanuel, Wesam H. Abdulaal, Ilgiz A. Mufazalov, et al.. (2020). Cell-specific conditional deletion of interleukin-1 (IL-1) ligands and its receptors: a new toolbox to study the role of IL-1 in health and disease. Journal of Molecular Medicine. 98(7). 923–930. 6 indexed citations
11.
Yang, Nan, Nicola J. Smyllie, Michal Dudek, et al.. (2020). Quantitative live imaging of Venus::BMAL1 in a mouse model reveals complex dynamics of the master circadian clock regulator. PLoS Genetics. 16(4). e1008729–e1008729. 19 indexed citations
12.
Hemmings, Karen E., Nadira Yuldasheva, Azhar Maqbool, et al.. (2019). Fibroblast-specific deletion of IL-1 receptor-1 reduces adverse cardiac remodeling following myocardial infarction. JCI Insight. 4(17). 57 indexed citations
13.
Minshawi, Faisal, Michael White, Werner Müller, et al.. (2019). Human TNF-Luc reporter mouse: A new model to quantify inflammatory responses. Scientific Reports. 9(1). 193–193. 12 indexed citations
14.
Roostalu, Urmas, et al.. (2017). Distinct Cellular Mechanisms Underlie Smooth Muscle Turnover in Vascular Development and Repair. Circulation Research. 122(2). 267–281. 51 indexed citations
15.
Lázaro, Irene de, et al.. (2014). Generation of induced pluripotent stem cells from virus-free in vivo reprogramming of BALB/c mouse liver cells. Biomaterials. 35(29). 8312–8320. 10 indexed citations
16.
Dhungana, Hiramani, Tarja Malm, Ádám Dénes, et al.. (2013). Aging aggravates ischemic stroke-induced brain damage in mice with chronic peripheral infection. Aging Cell. 12(5). 842–850. 35 indexed citations
17.
Massacand, Joanna C., Reto Meier, Neil Humphreys, et al.. (2009). Helminth products bypass the need for TSLP in Th2 immune responses by directly modulating dendritic cell function. Proceedings of the National Academy of Sciences. 106(33). 13968–13973. 148 indexed citations
18.
Cliffe, Laura, et al.. (2005). Accelerated Intestinal Epithelial Cell Turnover: A New Mechanism of Parasite Expulsion. Science. 308(5727). 1463–1465. 326 indexed citations
19.
Bancroft, Allison J., Neil Humphreys, John J. Worthington, Hiroki Yoshida, & Richard K. Grencis. (2004). WSX-1: A Key Role in Induction of Chronic Intestinal Nematode Infection. The Journal of Immunology. 172(12). 7635–7641. 50 indexed citations
20.
Bancroft, Allison J., Kathryn J. Else, Neil Humphreys, & Richard K. Grencis. (2001). The effect of challenge and trickle Trichuris muris infections on the polarisation of the immune response. International Journal for Parasitology. 31(14). 1627–1637. 69 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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