Penelope Roques

7.2k total citations · 1 hit paper
11 papers, 1.7k citations indexed

About

Penelope Roques is a scholar working on Molecular Biology, Physiology and Computational Theory and Mathematics. According to data from OpenAlex, Penelope Roques has authored 11 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Physiology and 2 papers in Computational Theory and Mathematics. Recurrent topics in Penelope Roques's work include Alzheimer's disease research and treatments (8 papers), Bioinformatics and Genomic Networks (6 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (4 papers). Penelope Roques is often cited by papers focused on Alzheimer's disease research and treatments (8 papers), Bioinformatics and Genomic Networks (6 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (4 papers). Penelope Roques collaborates with scholars based in United Kingdom, United States and France. Penelope Roques's co-authors include Martin N. Rossor, Marie‐Christine Chartier‐Harlin, John Hardy, Michael Mullan, David J. Hughes, Alison Goate, Liana Fidani, Fiona Crawford, Henry Houlden and Andrew Warren and has published in prestigious journals such as Nature, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Penelope Roques

11 papers receiving 1.7k citations

Hit Papers

Early-onset Alzheimer's disease caused by mutations at co... 1991 2026 2002 2014 1991 250 500 750
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. Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene
    1991 913 citations Marie‐Christine Chartier‐Harlin, Fiona Crawford et al. Nature profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Penelope Roques United Kingdom 11 1.4k 786 367 324 282 11 1.7k
P. A. Locke United States 9 1.3k 0.9× 665 0.8× 501 1.4× 266 0.8× 213 0.8× 11 1.9k
Lena Lilius Sweden 19 1.7k 1.2× 1.1k 1.4× 297 0.8× 389 1.2× 366 1.3× 42 2.2k
G. W. Small United States 7 1.2k 0.8× 548 0.7× 523 1.4× 245 0.8× 216 0.8× 9 1.8k
Yoshio Namba Japan 16 1.3k 0.9× 778 1.0× 225 0.6× 349 1.1× 189 0.7× 28 1.9k
Leah Sartorius United States 8 937 0.7× 528 0.7× 174 0.5× 344 1.1× 200 0.7× 10 1.4k
Steven G. Younkin United States 12 1.0k 0.7× 616 0.8× 207 0.6× 260 0.8× 178 0.6× 14 1.4k
Cécile Dumanchin France 12 1.4k 1.0× 988 1.3× 239 0.7× 378 1.2× 322 1.1× 17 2.2k
June White United States 10 908 0.7× 622 0.8× 219 0.6× 211 0.7× 184 0.7× 14 1.2k
K S Kosik United States 11 1.4k 1.0× 1.1k 1.4× 153 0.4× 484 1.5× 250 0.9× 16 2.1k

Countries citing papers authored by Penelope Roques

Since Specialization
Citations

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

Fields of papers citing papers by Penelope Roques

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Penelope Roques

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

All Works

11 of 11 papers shown
1.
Harvey, Richard, Penelope Roques, Nick C. Fox, & Martin N. Rossor. (1998). CANDID?counselling and diagnosis in dementia: a national telemedicine service supporting the care of younger patients with dementia. International Journal of Geriatric Psychiatry. 13(6). 381–388. 32 indexed citations
2.
Harvey, Richard, David W. Ellison, John Hardy, et al.. (1998). Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucineright-arrowserine (L250S) substitution at codon 250 of the presenilin 1 gene. Journal of Neurology Neurosurgery & Psychiatry. 64(1). 44–49. 46 indexed citations
3.
Rossor, Martin N., Nick C. Fox, Peter A. Freeborough, & Penelope Roques. (1997). Slowing the progression of Alzheimer disease: monitoring progression.. PubMed. 11 Suppl 5. S6–9. 11 indexed citations
4.
Kennedy, Angus, R. S. J. Frackowiak, Sarah Newman, et al.. (1995). Deficits in cerebral glucose metabolism demonstrated by positron emission tomography in individuals at risk of familial Alzheimer's disease. Neuroscience Letters. 186(1). 17–20. 195 indexed citations
5.
Houlden, Henry, Richard Crook, Karen Duff, et al.. (1995). Apolipoprotein E alleles but neither apolipoprotein B nor apolipoprotein AI/CIII alleles are associated with late onset, familial Alzheimer's disease. Neuroscience Letters. 188(3). 202–204. 11 indexed citations
6.
Crawford, Fiona, Aaron Osborne, Patricia Jaramillo, et al.. (1995). Evidence that the APOE locus influences rate of disease progression in late onset familial Alzheimer's Disease but is not causative. American Journal of Medical Genetics. 60(1). 1–6. 57 indexed citations
7.
Houlden, Henry, Richard Crook, John Hardy, et al.. (1994). Confirmation that familial clustering and age of onset in late onset Alzheimer's disease are determined at the apolipoprotein E locus. Neuroscience Letters. 174(2). 222–224. 35 indexed citations
8.
Chartier‐Harlin, Marie‐Christine, Jordi Pérez‐Tur, Thierry Brousseau, et al.. (1994). Apolipoprotein E, ɛ4 allele as a major risk factor for sporadic early and late-onset forms of Alzheimer's disease: analysis of the 19q13.2 chromosomal region. Human Molecular Genetics. 3(4). 569–574. 345 indexed citations
9.
Fidani, Liana, Karen Rooke, Marie‐Christine Chartier‐Harlin, et al.. (1992). Screening for mutations in the open reading frame and promoter of the β-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val→lle. Human Molecular Genetics. 1(3). 165–168. 62 indexed citations
10.
Chartier‐Harlin, Marie‐Christine, Fiona Crawford, Henry Houlden, et al.. (1991). Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene. Nature. 353(6347). 844–846. 913 indexed citations breakdown →
11.
Crawford, Fiona, John Hardy, Michael Mullan, et al.. (1991). Sequencing of exons 16 and 17 of the β-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the β-amyloid sequence. Neuroscience Letters. 133(1). 1–2. 30 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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