P Narcisi

969 citations

26 papers · 709 · h-index 15

Impact in

Genetics top 5%
- Connective tissue disorders research
- Dermatological and Skeletal Disorders
Neurology top 5%
- Intracranial Aneurysms: Treatment and Complications

Papers in

Genetics 19
- Connective tissue disorders research 19
- Dermatological and Skeletal Disorders 8
Molecular Biology 8
- Wnt/β-catenin signaling in development and cancer 4

Co-authors: F M Pope (20 shared papers)A C Nicholls (15 shared papers)Allan J. Richards (9 shared papers)Glenn Neil-Dwyer (1 shared paper)John R. Bartlett (1 shared paper)G. Neil‐Dwyer (1 shared paper)J. C. Lloyd (5 shared papers)Anne De Paepe (5 shared papers)
Journals: Journal of Medical Genetics (4 papers)Human Genetics (3 papers)British Journal of Dermatology (3 papers)Human Molecular Genetics (2 papers)Journal of Inherited Metabolic Disease (1 paper)
Partner nations: United Kingdom United States Italy

In The Last Decade

P Narcisi

26 papers receiving 668 citations

Peers

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-authors

The 25 scholars most cited alongside P Narcisi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with P Narcisi Line = papers co-authored together P Narcisi links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	SOME PATIENTS WITH CEREBRAL ANEURYSMS ARE DEFICIENT IN TYPE III COLLAGEN The Lancet ·F M Pope, P Narcisi, G. Neil‐Dwyer, A C Nicholls, John R. Bartlett, B.S. Doshi	1981	112
2	Collagen deficiency and ruptured cerebral aneurysms Journal of neurosurgery ·Glenn Neil-Dwyer, John R. Bartlett, A C Nicholls, P Narcisi, F M Pope	1983	100
3	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 ·P Narcisi, Allan J. Richards, Stanley D. Ferguson, F M Pope	1994	66
4	Type III collagen mutations cause fragile cerebral arteries British Journal of Neurosurgery ·F M Pope, B. E. Kendall, G. I. Slapak, Ravish Kapoor, W. I. McDonald, D. A. S. Compston, R. Mitchell, Daniel Hope, M.W. Millar‐Craig, John Dean, Alan Johnston, Patrick Lynch, Padmini Sarathchandra, P Narcisi, A C Nicholls, Allan J. Richards, J. L. Mackenzie	1991	45
5	Clinical presentations of Ehlers Danlos syndrome type IV. Archives of Disease in Childhood ·F M Pope, P Narcisi, A C Nicholls, Meytal Liberman, J. W. E. Oorthuys	1988	45
6	Type III collagen mutations in Ehlers Danlos Syndrome type IV and other related disorders Clinical and Experimental Dermatology ·F M Pope, A C Nicholls, P Narcisi, Anne Temple, Y. Chia, P Fryer, Anne De Paepe, W. P. GROOTE, Jean R. McEwan, D. A. S. Compston, Hanna W. E. Oorthuys, Jenny Davies, Doreen Dinwoodie	1988	38
7	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 ·A C Nicholls, A. De Paepe, P Narcisi, Raymond Dalgleish, Filip De Keyser, M. Matton, F M Pope	1988	32
8	A single base mutation in the gene for type III collagen (COL3A1) converts glycine 847 to glutamic acid in a family with Ehlers-Danlos syndrome type IV. An unaffected family member is mosaic for the mutation Human Genetics ·Allan J. Richards, Philip N. Ward, P Narcisi, A C Nicholls, J. C. Lloyd, F M Pope	1992	30
9	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 ·Allan J. Richards, J. C. Lloyd, Philip N. Ward, Anne De Paepe, P Narcisi, F M Pope	1991	28
10	Spontaneous carotid cavernous fistula in Ehlers Danlos syndrome. Journal of Neurology Neurosurgery & Psychiatry ·Rachel Fox, F M Pope, P Narcisi, A C Nicholls, B. E. Kendall, M D Hourihan, D. A. S. Compston	1988	26
11	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 ·P Narcisi, Yuli Wu, Gerard Tromp, James J. Earley, Allan J. Richards, F M Pope, Helena Kuivaniemi	1993	25
12	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 ·Allan J. Richards, J. C. Lloyd, P Narcisi, Philip N. Ward, A C Nicholls, Anne De Paepe, F M Pope	1992	23
13	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 ·Lieve Nuytinck, P Narcisi, A C Nicholls, Jean‐Pierre Renard, F M Pope, Anne De Paepe	1992	21
14	Ehlers–Danlos syndrome type IV mimicking non-accidental injury in a child British Journal of Dermatology ·D.L. Roberts, F M Pope, A C Nicholls, P Narcisi	1984	20
15	Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type III British Journal of Dermatology ·Anne De Paepe, A C Nicholls, P Narcisi, Filip De Keyser, J. Quatacker, M. Van Staey, M. Matton, F. Michael Pope	1987	17
16	Safety of magnesium-lidocaine combination for severe head injury: the turin lidomag pilot study Surgical Neurology ·Sergio Canavero, Vincenzo Bonicalzi, P Narcisi	2003	14
17	Detection of type III collagen in skin fibroblasts from patients with Ehlers-Danlos syndrome type IV by immunofluorescence British Journal of Dermatology ·Anne Temple, Perry R. Hinton, P Narcisi, F M Pope	1988	12
18	A T+6 to C+6 mutation in the donor splice site of COL3A1 IVS7 causes exon skipping and results in Ehlers-Danlos syndrome type IV. Journal of Medical Genetics ·J. C. Lloyd, P Narcisi, Allan J. Richards, F M Pope	1993	12
19	Type III Collagen Deficiency with Normal Phenotype Journal of the Royal Society of Medicine ·F M Pope, A C Nicholls, D. E. Dorrance, Anne H. Child, P Narcisi	1983	10
20	The substitution of glycine 661 by arginine in type III collagen produces mutant molecules with different thermal stabilities and causes Ehlers-Danlos syndrome type IV. Journal of Medical Genetics ·Allan J. Richards, P Narcisi, J. C. Lloyd, C. F. Ferguson, F M Pope	1993	8

About P Narcisi

P Narcisi is a scholar working on Genetics, Molecular Biology, Rheumatology, Neurology and Pulmonary and Respiratory Medicine, having authored 26 papers that have together received 709 indexed citations. Recurring topics across this work include Connective tissue disorders research (19 papers), Dermatological and Skeletal Disorders (8 papers), Dupuytren's Contracture and Treatments (6 papers), Wnt/β-catenin signaling in development and cancer (4 papers), Proteoglycans and glycosaminoglycans research (3 papers), Aortic aneurysm repair treatments (3 papers), Peptidase Inhibition and Analysis (2 papers) and Intracranial Aneurysms: Treatment and Complications (2 papers). The work is most often cited by research in Genetics (494 citations), Neurology (217 citations), Rheumatology (186 citations), Immunology and Allergy (44 citations) and Pulmonary and Respiratory Medicine (137 citations). P Narcisi has collaborated with scholars based in United Kingdom, United States and Italy. Frequent 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. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, British Journal of Dermatology, Human Molecular Genetics and Journal of Inherited Metabolic Disease.

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.

Explore authors with similar magnitude of impact

P Narcisi

Impact in

Papers in i

In The Last Decade

P Narcisi

Peers

Countries citing papers authored by P Narcisi

Fields of papers citing papers by P Narcisi

All Works

About P Narcisi

Explore authors with similar magnitude of impact

Papers in