Patrick M. Nolan

9.4k total citations · 1 hit paper
108 papers, 5.2k citations indexed

About

Patrick M. Nolan is a scholar working on Molecular Biology, Endocrine and Autonomic Systems and Cellular and Molecular Neuroscience. According to data from OpenAlex, Patrick M. Nolan has authored 108 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 37 papers in Endocrine and Autonomic Systems and 31 papers in Cellular and Molecular Neuroscience. Recurrent topics in Patrick M. Nolan's work include Circadian rhythm and melatonin (37 papers), Neurobiology and Insect Physiology Research (12 papers) and Sleep and Wakefulness Research (10 papers). Patrick M. Nolan is often cited by papers focused on Circadian rhythm and melatonin (37 papers), Neurobiology and Insect Physiology Research (12 papers) and Sleep and Wakefulness Research (10 papers). Patrick M. Nolan collaborates with scholars based in United Kingdom, United States and Italy. Patrick M. Nolan's co-authors include Gareth Banks, Alun R. Barnard, Sofia I.H. Godinho, Sara Wells, Ciaran M. Regan, R.W. Bell, Luca Busino, Michele Pagano, Steve D. M. Brown and Maja Bućan and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Patrick M. Nolan

105 papers receiving 5.1k citations

Hit Papers

align trajectories

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.

Overexpression of Fto leads to increased food intake and results in obesity

2010 556 citations Lee Moir, Gareth Banks et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Patrick M. Nolan United Kingdom	36	2.3k	1.5k	1.2k	767	699	108	5.2k
Masatsugu Ueda Japan	37	2.3k 1.0×	1.5k 1.0×	758 0.6×	837 1.1×	942 1.3×	169	6.0k
Erno Vreugdenhil Netherlands	46	2.3k 1.0×	557 0.4×	2.2k 1.8×	833 1.1×	612 0.9×	112	8.1k
Vivek Kumar United States	22	1.4k 0.6×	2.2k 1.4×	579 0.5×	487 0.6×	1.0k 1.5×	58	4.0k
Nirinjini Naidoo United States	33	756 0.3×	1.3k 0.9×	952 0.8×	249 0.3×	618 0.9×	56	3.8k
Maja Bućan United States	40	4.1k 1.7×	456 0.3×	804 0.7×	2.8k 3.7×	858 1.2×	102	7.3k
Jesse Gray United States	21	3.1k 1.3×	991 0.6×	1.1k 0.9×	513 0.7×	445 0.6×	35	5.4k
Shun Yamaguchi Japan	30	1.2k 0.5×	3.3k 2.1×	1.8k 1.5×	189 0.2×	1.3k 1.9×	74	5.8k
Louis J. Ptáček United States	63	6.7k 2.8×	3.0k 2.0×	4.0k 3.5×	981 1.3×	1.2k 1.7×	179	12.4k
Qun‐Yong Zhou United States	30	1.5k 0.7×	1.4k 0.9×	1.8k 1.5×	446 0.6×	518 0.7×	55	4.4k
Morten Møller Denmark	41	2.6k 1.1×	2.3k 1.5×	2.1k 1.8×	226 0.3×	616 0.9×	174	5.8k

Countries citing papers authored by Patrick M. Nolan

Since Specialization

Citations

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

Fields of papers citing papers by Patrick M. Nolan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick M. Nolan. 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 Patrick M. Nolan. The network helps show where Patrick M. Nolan may publish in the future.

Co-authorship network of co-authors of Patrick M. Nolan

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick M. Nolan. A scholar is included among the top collaborators of Patrick M. Nolan 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 Patrick M. Nolan. Patrick M. Nolan 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

Banks, Gareth, et al.. (2025). Zinc finger homeobox-3 (ZFHX3) orchestrates genome-wide daily gene expression in the suprachiasmatic nucleus. eLife. 14. 1 indexed citations

Banks, Gareth, et al.. (2023). Dynamic modulation of genomic enhancer elements in the suprachiasmatic nucleus, the site of the mammalian circadian clock. Genome Research. 33(5). 673–688. 3 indexed citations

Nolan, Patrick M., Gareth Banks, Liz Bentley, et al.. (2023). A missense mutation in zinc finger homeobox‐3 ( ZFHX3 ) impedes growth and alters metabolism and hypothalamic gene expression in mice. The FASEB Journal. 37(10). e23189–e23189. 5 indexed citations

Banks, Gareth, et al.. (2022). Shift work-like patterns effect on female and male mouse behavior. SHILAP Revista de lepidopterología. 13. 100082–100082. 6 indexed citations

Hughes, Steven, Jessica K. Edwards, Carina A. Pothecary, et al.. (2021). Zfhx3 modulates retinal sensitivity and circadian responses to light. The FASEB Journal. 35(9). e21802–e21802. 5 indexed citations

Banks, Gareth, Mathilde C. C. Guillaumin, Ines Heise, et al.. (2020). Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficits. Science Advances. 6(33). eabb3567–eabb3567. 11 indexed citations

Codner, Gemma, et al.. (2019). The guanine nucleotide exchange factor, Spata13, influences social behaviour and nocturnal activity. Mammalian Genome. 30(3-4). 54–62. 6 indexed citations

Stewart, Michelle, Petrina Lau, Gareth Banks, et al.. (2019). Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities. Disease Models & Mechanisms. 12(2). 19 indexed citations

Schmidt‐Hieber, Christoph, Fernando J. Sialana, Lorenza Ciani, et al.. (2019). Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons. PLoS Biology. 17(9). e3000414–e3000414. 16 indexed citations

10.

Rodgers, Jessica, Steven Hughes, Carina A. Pothecary, et al.. (2015). Characterisation of a novel ENU-induced spectral tuning mutation in melanopsin. Investigative Ophthalmology & Visual Science. 56(7). 5574–5574. 1 indexed citations

11.

Edwards, Jessica K., et al.. (2012). Generation of mouse mutants as tools in dissecting the molecular clock. Progress in brain research. 199. 247–265. 1 indexed citations

12.

Muers, Mary, Jacqueline A. Sharpe, David Garrick, et al.. (2007). Defining the Cause of Skewed X-Chromosome Inactivation in X-Linked Mental Retardation by Use of a Mouse Model. The American Journal of Human Genetics. 80(6). 1138–1149. 24 indexed citations

13.

Busino, Luca, Florian Bassermann, Alessio Maiolica, et al.. (2007). SCF ^Fbxl3 Controls the Oscillation of the Circadian Clock by Directing the Degradation of Cryptochrome Proteins. Science. 316(5826). 900–904. 415 indexed citations

14.

Tsipouri, Vicky, John A. Curtin, Patrick M. Nolan, et al.. (2004). Three novel pigmentation mutants generated by genome‐wide random ENU mutagenesis in the mouse. Comparative and Functional Genomics. 5(2). 123–127. 2 indexed citations

15.

Tsipouri, Vicky, John A. Curtin, Patrick M. Nolan, et al.. (2004). Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse: Short Communications. Comparative and Functional Genomics. 5(2). 123–127.

16.

Ooi, Aikseng, et al.. (2004). Screening for novel ENU‐induced rhythm, entrainment and activity mutants. Genes Brain & Behavior. 3(4). 196–205. 30 indexed citations

17.

Davies, K E, et al.. (2003). Functional studies of Af4 in the robotic mouse.. The American Journal of Human Genetics. 73. 179–179. 3 indexed citations

18.

Alavi, Alireza, Amy E. Kiernan, Patrick M. Nolan, et al.. (2001). The Wheels Mutation in the Mouse Causes Vascular, Hindbrain, and Inner Ear Defects. Developmental Biology. 234(1). 244–260. 32 indexed citations

19.

Potter, Allyson C., Lucie Vizor, Phillip Oliver, et al.. (2000). Evaluation of neurological mouse mutants caused by ENU mutagenesis. European Journal of Neuroscience. 12. 171–171. 9 indexed citations

20.

Shashoua, Victor E., et al.. (1992). Dibutyryl cyclic AMP stimulates expression of ependymin mRNA and the synthesis and release of the protein into the culture medium by neuroblastoma cells (NB2a/d1). Journal of Neuroscience Research. 32(2). 239–244. 9 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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