P Roques

1.2k total citations
11 papers, 453 citations indexed

About

P Roques is a scholar working on Physiology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, P Roques has authored 11 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Physiology, 3 papers in Genetics and 2 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in P Roques's work include Alzheimer's disease research and treatments (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). P Roques is often cited by papers focused on Alzheimer's disease research and treatments (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). P Roques collaborates with scholars based in United Kingdom, France and Netherlands. P Roques's co-authors include Martin N. Rossor, John Hardy, Michael Mullan, P. L. Lantos, Robert Williamson, Angus Kennedy, E. K. Warrington, R. S. J. Frackowiak, Irene Stratton and Jeremy Brown and has published in prestigious journals such as The Lancet, Brain and Annals of the New York Academy of Sciences.

In The Last Decade

P Roques

11 papers receiving 434 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P Roques United Kingdom	8	287	140	111	97	83	11	453
Donald Schmechel United States	3	195 0.7×	121 0.9×	77 0.7×	62 0.6×	21 0.3×	4	323
Aki Kugo Japan	9	155 0.5×	88 0.6×	142 1.3×	26 0.3×	93 1.1×	11	393
Nicoletta Smirne Italy	11	162 0.6×	120 0.9×	81 0.7×	36 0.4×	93 1.1×	20	322
Jean-François Foncin France	8	197 0.7×	237 1.7×	33 0.3×	42 0.4×	44 0.5×	12	386
Mary Ann A. DeMichele‐Sweet United States	13	288 1.0×	113 0.8×	270 2.4×	84 0.9×	33 0.4×	15	512
Valentina Nesci Italy	12	156 0.5×	209 1.5×	123 1.1×	44 0.5×	38 0.5×	23	470
Isabel Barroeta Spain	8	215 0.7×	131 0.9×	118 1.1×	26 0.3×	48 0.6×	24	453
Katie Peppercorn New Zealand	13	207 0.7×	125 0.9×	67 0.6×	29 0.3×	81 1.0×	22	412
Sarah Moghadam United States	7	166 0.6×	82 0.6×	62 0.6×	51 0.5×	28 0.3×	7	411
Paulina R. Davis United States	7	351 1.2×	153 1.1×	146 1.3×	72 0.7×	56 0.7×	8	576

Countries citing papers authored by P Roques

Since Specialization

Citations

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

Fields of papers citing papers by P Roques

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P Roques

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

All Works

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11 of 11 papers shown

Kennedy, Angus, Scott Newman, R. S. J. Frackowiak, et al.. (1995). Chromosome 14 linked familial Alzheimer's disease. Brain. 118(1). 185–205. 72 indexed citations

Lantos, P. L., et al.. (1994). Lewy bodies in the brain of two members of a family with the 717 (Val to Ile) mutation of the amyloid precursor protein gene. Neuroscience Letters. 172(1-2). 77–79. 38 indexed citations

Crook, Richard, et al.. (1993). The Cystatin-C gene is not linked to early onset familial Alzheimer's disease. Neuroscience Letters. 154(1-2). 81–83. 7 indexed citations

Kennedy, Angus, Sarah Newman, Andrew McCaddon, et al.. (1993). Familial Alzheimer's disease A pedigree with a mis-sense mutation in the amyloid precursor protein gene (amyloid precursor protein 717 valine → glycine). Brain. 116(2). 309–324. 61 indexed citations

Brown, Jeremy, P. L. Lantos, Irene Stratton, P Roques, & Martin N. Rossor. (1993). Familial progressive supranuclear palsy.. Journal of Neurology Neurosurgery & Psychiatry. 56(5). 473–476. 42 indexed citations

Kennedy, Angus, Stanton Newman, Pippa Tyrrell, et al.. (1992). Imaging in dementia: Longitudinal studies using positron emission tomography. Neurobiology of Aging. 13. S13–S14. 4 indexed citations

Mullan, Michael, L. Giuffra, John Hardy, et al.. (1991). Clinical and Pathologic Features of Chromosome 21‐Linked Familial Alzheimer's Disease. Annals of the New York Academy of Sciences. 640(1). 177–180. 2 indexed citations

Hardy, John, et al.. (1990). Genetics of Alzheimer's disease.. PubMed. 51. 197–8. 9 indexed citations

Mullan, Michael, et al.. (1989). PREDISPOSING LOCUS FOR ALZHEIMER'S DISEASE ON CHROMOSOME 21. The Lancet. 333(8634). 352–355. 168 indexed citations

10.

Guicheney, Pascale, J Barrat, B. de Lignières, et al.. (1988). Platelet serotonin content and plasma tryptophan in peri‐ and postmenopausal women: variations with plasma oestrogen levels and depressive symptoms. European Journal of Clinical Investigation. 18(3). 297–304. 45 indexed citations

11.

Léger, Damien, B. de Lignières, P Roques, et al.. (1988). Platelet serotonin content and plasma tryptophan in peri- and post-menopausal women: Variations with plasma oestrogen levels and depressive symptoms. Maturitas. 10(4). 356–356. 5 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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