P Narcisi

969 total citations
26 papers, 709 citations indexed

About

P Narcisi is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, P Narcisi has authored 26 papers receiving a total of 709 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Rheumatology. Recurrent topics in P Narcisi's work include Connective tissue disorders research (19 papers), Dermatological and Skeletal Disorders (8 papers) and Dupuytren's Contracture and Treatments (6 papers). P Narcisi is often cited by papers focused on Connective tissue disorders research (19 papers), Dermatological and Skeletal Disorders (8 papers) and Dupuytren's Contracture and Treatments (6 papers). P Narcisi collaborates with scholars based in United Kingdom, United States and Italy. P Narcisi's co-authors include F M Pope, A C Nicholls, Allan J. Richards, Glenn Neil-Dwyer, John R. Bartlett, John R. Bartlett, G. Neil‐Dwyer, J. C. Lloyd, Anne De Paepe and Philip N. Ward and has published in prestigious journals such as The Lancet, Human Molecular Genetics and Journal of neurosurgery.

In The Last Decade

P Narcisi

26 papers receiving 668 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P Narcisi United Kingdom 15 494 217 186 174 137 26 709
Hariyadarshi Pannu United States 16 597 1.2× 178 0.8× 174 0.9× 172 1.0× 777 5.7× 16 1.2k
Hiroyuki Akagawa Japan 13 161 0.3× 300 1.4× 306 1.6× 105 0.6× 140 1.0× 36 603
Jacqueline D. Peacock United States 12 102 0.2× 42 0.2× 86 0.5× 299 1.7× 122 0.9× 16 628
Mark J. Stephan United States 15 263 0.5× 26 0.1× 40 0.2× 279 1.6× 142 1.0× 23 762
Isabella Mammi Italy 13 121 0.2× 169 0.8× 58 0.3× 113 0.6× 76 0.6× 29 551
Alyson Morse Australia 15 126 0.3× 56 0.3× 76 0.4× 294 1.7× 31 0.2× 28 641
Sarah Tansley United Kingdom 18 172 0.3× 136 0.6× 887 4.8× 332 1.9× 117 0.9× 50 1.6k
Fleur S van Dijk Netherlands 7 310 0.6× 24 0.1× 54 0.3× 91 0.5× 166 1.2× 12 487
Miki Tomoeda Japan 11 51 0.1× 39 0.2× 86 0.5× 234 1.3× 82 0.6× 19 575
Hanne Hove Denmark 14 286 0.6× 117 0.5× 44 0.2× 200 1.1× 187 1.4× 40 619

Countries citing papers authored by P Narcisi

Since Specialization
Citations

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

Fields of papers citing papers by P Narcisi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P Narcisi

This figure shows the co-authorship network connecting the top 25 collaborators of P Narcisi. A scholar is included among the top collaborators of P Narcisi 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 Narcisi. P Narcisi 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.
Lamorte, Alessandro, et al.. (2016). The Sierra Leone Ultrasound Rainbow4Africa Project (SLURP): an observational study of ultrasound effectiveness in developing countries. Critical Ultrasound Journal. 8(1). 14–14. 3 indexed citations
2.
Canavero, Sergio, Vincenzo Bonicalzi, & P Narcisi. (2003). Safety of magnesium-lidocaine combination for severe head injury: the turin lidomag pilot study. Surgical Neurology. 60(2). 165–169. 14 indexed citations
3.
Merlo, Marco, et al.. (2001). Personal experience of the treatment of ruptured aortic aneurysms. The prognostic evaluation of some parameters.. PubMed. 49(3). 179–87. 6 indexed citations
4.
Richards, Allan J., et al.. (1994). Two new mutations affecting the donor splice site of COL3A1 IVS37 and causing skipping of exon 37 in patients with Ehlers—Danlos syndrome type IV. Human Molecular Genetics. 3(10). 1901–1902. 7 indexed citations
5.
Narcisi, P, et al.. (1994). A family with Ehlers — Danlos syndrome type III/articular hypermobility syndrome has a glycine 637 to serine substitution in type III collagen. Human Molecular Genetics. 3(9). 1617–1620. 66 indexed citations
6.
Narcisi, P, Yuli Wu, Gerard Tromp, et al.. (1993). Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers–Danlos syndrome type IV. American Journal of Medical Genetics. 46(3). 278–283. 25 indexed citations
7.
Paepe, Anne De, et al.. (1992). Study of a type III collagen protein defect in a patient with ecchymotic EDS: importance of the analysis of non-cutaneous connective tissues. Ghent University Academic Bibliography (Ghent University). 1 indexed citations
8.
Richards, Allan J., J. C. Lloyd, P Narcisi, et al.. (1992). A 27-bp deletion from one allele of the type III collagen gene (COL3A1) in a large family with Ehlers-Danlos syndrome type IV. Human Genetics. 88(3). 325–330. 23 indexed citations
9.
Nuytinck, Lieve, P Narcisi, A C Nicholls, et al.. (1992). Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IV.. Journal of Medical Genetics. 29(6). 375–380. 21 indexed citations
10.
11.
Pope, F M, B. E. Kendall, Ravish Kapoor, et al.. (1991). Type III collagen mutations cause fragile cerebral arteries. British Journal of Neurosurgery. 5(6). 551–574. 45 indexed citations
12.
Richards, Allan J., J. C. Lloyd, Philip N. Ward, et al.. (1991). Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IV.. Journal of Medical Genetics. 28(7). 458–463. 28 indexed citations
13.
Pope, F M, et al.. (1989). Prenatal diagnosis and prevention of inherited abnormalities of collagen. Journal of Inherited Metabolic Disease. 12(S1). 135–173. 7 indexed citations
14.
Temple, Anne, Perry R. Hinton, P Narcisi, & F M Pope. (1988). Detection of type III collagen in skin fibroblasts from patients with Ehlers-Danlos syndrome type IV by immunofluorescence. British Journal of Dermatology. 118(1). 17–26. 12 indexed citations
15.
Nicholls, A C, A. De Paepe, P Narcisi, et al.. (1988). Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigree. Human Genetics. 78(3). 276–281. 32 indexed citations
16.
Pope, F M, P Narcisi, A C Nicholls, et al.. (1988). Spontaneous carotid cavernous fistula in Ehlers Danlos syndrome.. Journal of Neurology Neurosurgery & Psychiatry. 51(7). 984–986. 26 indexed citations
17.
Pope, F M, A C Nicholls, P Narcisi, et al.. (1988). Type III collagen mutations in Ehlers Danlos Syndrome type IV and other related disorders. Clinical and Experimental Dermatology. 13(5). 285–302. 38 indexed citations
18.
Gawkrodger, David J., et al.. (1985). . Archives of Dermatology. 121(5). 636–641. 1 indexed citations
19.
Neil-Dwyer, Glenn, John R. Bartlett, A C Nicholls, P Narcisi, & F M Pope. (1983). Collagen deficiency and ruptured cerebral aneurysms. Journal of neurosurgery. 59(1). 16–20. 100 indexed citations
20.
Pope, F M, et al.. (1981). SOME PATIENTS WITH CEREBRAL ANEURYSMS ARE DEFICIENT IN TYPE III COLLAGEN. The Lancet. 317(8227). 973–975. 112 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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