Frances K. Wiseman

2.2k total citations · 1 hit paper
38 papers, 1.1k citations indexed

About

Frances K. Wiseman is a scholar working on Public Health, Environmental and Occupational Health, Molecular Biology and Genetics. According to data from OpenAlex, Frances K. Wiseman has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Public Health, Environmental and Occupational Health, 14 papers in Molecular Biology and 14 papers in Genetics. Recurrent topics in Frances K. Wiseman's work include Down syndrome and intellectual disability research (22 papers), Alzheimer's disease research and treatments (12 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Frances K. Wiseman is often cited by papers focused on Down syndrome and intellectual disability research (22 papers), Alzheimer's disease research and treatments (12 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Frances K. Wiseman collaborates with scholars based in United Kingdom, United States and France. Frances K. Wiseman's co-authors include Elizabeth Fisher, Victor L. J. Tybulewicz, John Hardy, André Strydom, Dean Nižetić, Annette Karmiloff‐Smith, Tamara Al‐Janabi, Kate Alford, Jean Manson and Enrico Cancellotti and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Frances K. Wiseman

35 papers receiving 1.1k 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.

A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome

2015 376 citations Frances K. Wiseman, Tamara Al‐Janabi et al. Nature reviews. Neuroscience profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Frances K. Wiseman United Kingdom	16	450	429	284	225	161	38	1.1k
Eric Doran United States	20	704 1.6×	421 1.0×	585 2.1×	163 0.7×	139 0.9×	45	1.5k
Mustafa Ayberk Kurt Türkiye	16	162 0.4×	238 0.6×	281 1.0×	128 0.6×	131 0.8×	31	857
Jean Maurice Delabar France	23	1.0k 2.3×	851 2.0×	214 0.8×	808 3.6×	50 0.3×	48	1.9k
Verónica Vidal Spain	15	311 0.7×	201 0.5×	163 0.6×	170 0.8×	67 0.4×	36	658
Shiping Li China	18	55 0.1×	281 0.7×	173 0.6×	40 0.2×	127 0.8×	41	872
Emilia Gatto Argentina	20	69 0.2×	418 1.0×	154 0.5×	79 0.4×	132 0.8×	90	1.3k
John Kauwe United States	24	54 0.1×	659 1.5×	834 2.9×	359 1.6×	261 1.6×	53	1.7k
Alica M. Goldman United States	19	156 0.3×	564 1.3×	214 0.8×	340 1.5×	48 0.3×	26	1.5k
Séverine Trabado France	21	121 0.3×	424 1.0×	123 0.4×	275 1.2×	13 0.1×	70	1.4k

Countries citing papers authored by Frances K. Wiseman

Since Specialization

Citations

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

Fields of papers citing papers by Frances K. Wiseman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Frances K. Wiseman. 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 Frances K. Wiseman. The network helps show where Frances K. Wiseman may publish in the future.

Co-authorship network of co-authors of Frances K. Wiseman

This figure shows the co-authorship network connecting the top 25 collaborators of Frances K. Wiseman. A scholar is included among the top collaborators of Frances K. Wiseman 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 Frances K. Wiseman. Frances K. Wiseman 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

Fertan, Emre, Yu P. Zhang, Georg Meisl, et al.. (2025). SynPull: An advanced method for studying neurodegeneration-related aggregates in synaptosomes using super-resolution microscopy. Cell chemical biology. 32(2). 338–351.e4. 3 indexed citations

Banks, Gareth, Tatiana V. Lipina, Rasneer Sonia Bains, et al.. (2025). Multi-modal comparative phenotyping of knock-in mouse models of frontotemporal dementia/amyotrophic lateral sclerosis. Disease Models & Mechanisms. 18(8). 1 indexed citations

Mumford, Paige, Wendy Heywood, Jenny Hällqvist, et al.. (2025). Apolipoprotein E abundance is elevated in the brains of individuals with Down syndrome–Alzheimer’s disease. Acta Neuropathologica. 149(1). 49–49.

Mumford, Paige, Justin Tosh, Eleni Gkanatsiou, et al.. (2023). Genetic mapping of APP and amyloid‐β biology modulation by trisomy 21. Alzheimer s & Dementia. 19(S1).

Mumford, Paige, Suzanna Noy, Karen Cleverley, et al.. (2023). Cathepsin B abundance, activity and microglial localisation in Alzheimer’s disease-Down syndrome and early onset Alzheimer’s disease; the role of elevated cystatin B. Acta Neuropathologica Communications. 11(1). 132–132. 9 indexed citations

Mumford, Paige, et al.. (2022). Rodent Modeling of Alzheimer's Disease in Down Syndrome: In vivo and ex vivo Approaches. Frontiers in Neuroscience. 16. 909669–909669. 13 indexed citations

Mumford, Paige, Justin Tosh, Eleni Gkanatsiou, et al.. (2022). Genetic Mapping of APP and Amyloid-β Biology Modulation by Trisomy 21. Journal of Neuroscience. 42(33). 6453–6468. 10 indexed citations

Cleverley, Karen, Weaverly Colleen Lee, Paige Mumford, et al.. (2021). A novel knockout mouse for the small EDRK-rich factor 2 (Serf2) showing developmental and other deficits. Mammalian Genome. 32(2). 94–103. 6 indexed citations

Whittaker, Heather, Suzanna Noy, Karen Cleverley, et al.. (2021). The effects of Cstb duplication on APP/amyloid-β pathology and cathepsin B activity in a mouse model. PLoS ONE. 16(7). e0242236–e0242236. 2 indexed citations

10.

Ma, Da, M. Jorge Cardoso, María A. Zuluaga, et al.. (2020). Substantially thinner internal granular layer and reduced molecular layer surface in the cerebellar cortex of the Tc1 mouse model of down syndrome – a comprehensive morphometric analysis with active staining contrast-enhanced MRI. NeuroImage. 223. 117271–117271. 4 indexed citations

11.

Chang, Pishan, Daniel Bush, Stéphanie Schorge, et al.. (2020). Altered Hippocampal-Prefrontal Neural Dynamics in Mouse Models of Down Syndrome. Cell Reports. 30(4). 1152–1163.e4. 27 indexed citations

12.

Watson-Scales, Sheona, Bernadett Kalmár, Eva Lana‐Elola, et al.. (2018). Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration. PLoS Genetics. 14(5). e1007383–e1007383. 28 indexed citations

13.

Wiseman, Frances K., et al.. (2016). Tc1 mouse model of trisomy-21 dissociates properties of short- and long-term recognition memory. Neurobiology of Learning and Memory. 130. 118–128. 13 indexed citations

14.

Powell, Nick, Marc Modat, M. Jorge Cardoso, et al.. (2016). Fully-Automated μMRI Morphometric Phenotyping of the Tc1 Mouse Model of Down Syndrome. PLoS ONE. 11(9). e0162974–e0162974. 13 indexed citations

15.

Wiseman, Frances K., Tamara Al‐Janabi, John Hardy, et al.. (2015). A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome. Nature reviews. Neuroscience. 16(9). 564–574. 376 indexed citations breakdown →

16.

Ma, Da, M. Jorge Cardoso, Marc Modat, et al.. (2014). Automatic Structural Parcellation of Mouse Brain MRI Using Multi-Atlas Label Fusion. PLoS ONE. 9(1). e86576–e86576. 52 indexed citations

17.

Pope, Benjamin D., Tamir Chandra, Matthew Hoare, et al.. (2012). Replication-timing boundaries facilitate cell-type and species-specific regulation of a rearranged human chromosome in mouse. Human Molecular Genetics. 21(19). 4162–4170. 23 indexed citations

18.

Cleary, Jon O., Frances K. Wiseman, Anthony N. Price, et al.. (2011). Structural correlates of active-staining following magnetic resonance microscopy in the mouse brain. NeuroImage. 56(3). 974–983. 25 indexed citations

19.

Wiseman, Frances K., Kate Alford, Victor L. J. Tybulewicz, & Elizabeth Fisher. (2009). Down syndrome--recent progress and future prospects. Human Molecular Genetics. 18(R1). R75–R83. 163 indexed citations

20.

Cancellotti, Enrico, Rona Barron, Matthew Bishop, et al.. (2006). The role of host PrP in Transmissible Spongiform Encephalopathies. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1772(6). 673–680. 22 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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