N C Nevin

1.4k total citations
32 papers, 851 citations indexed

About

N C Nevin is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, N C Nevin has authored 32 papers receiving a total of 851 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Genetics and 6 papers in Surgery. Recurrent topics in N C Nevin's work include Connective tissue disorders research (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Cleft Lip and Palate Research (4 papers). N C Nevin is often cited by papers focused on Connective tissue disorders research (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Cleft Lip and Palate Research (4 papers). N C Nevin collaborates with scholars based in United Kingdom, United States and Italy. N C Nevin's co-authors include Patrick J. Morrison, Helen Mulholland, J. Slack, Elaine Hicks, T. R. J. Tubman, B. Craig, J. Morrison, J.M. Beare, J.A. Dodge and P. C. Elmes and has published in prestigious journals such as Brain, Journal of Neurology Neurosurgery & Psychiatry and British Journal of Dermatology.

In The Last Decade

N C Nevin

32 papers receiving 781 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N C Nevin United Kingdom 18 332 324 198 118 110 32 851
Yoshihisa Fukushima Japan 15 92 0.3× 148 0.5× 150 0.8× 90 0.8× 144 1.3× 80 733
Mark B. Zimering United States 17 222 0.7× 398 1.2× 111 0.6× 88 0.7× 279 2.5× 57 1.3k
C. Adamsbaum France 17 177 0.5× 223 0.7× 181 0.9× 43 0.4× 42 0.4× 57 712
P Fleury Netherlands 14 165 0.5× 214 0.7× 48 0.2× 55 0.5× 39 0.4× 44 698
Jan Bruder United States 20 210 0.6× 411 1.3× 256 1.3× 40 0.3× 85 0.8× 51 1.4k
Siddharth Banka United Kingdom 18 480 1.4× 339 1.0× 104 0.5× 33 0.3× 67 0.6× 55 991
Abdollah Sadeghi‐Nejad United States 20 220 0.7× 295 0.9× 151 0.8× 21 0.2× 56 0.5× 46 925
Pinki Munot United Kingdom 15 103 0.3× 259 0.8× 104 0.5× 113 1.0× 56 0.5× 51 718
Shih‐Shan Lang United States 19 177 0.5× 157 0.5× 280 1.4× 139 1.2× 150 1.4× 80 1.1k
Antony Lafferty Australia 16 367 1.1× 558 1.7× 548 2.8× 44 0.4× 112 1.0× 30 1.6k

Countries citing papers authored by N C Nevin

Since Specialization
Citations

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

Fields of papers citing papers by N C Nevin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N C Nevin. 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 N C Nevin. The network helps show where N C Nevin may publish in the future.

Co-authorship network of co-authors of N C Nevin

This figure shows the co-authorship network connecting the top 25 collaborators of N C Nevin. A scholar is included among the top collaborators of N C Nevin 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 N C Nevin. N C Nevin 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.
Hughes, Jonathan H., N C Nevin, & P. Morrison. (2001). Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.. PubMed. 70(1). 47–50. 3 indexed citations
2.
Nevin, N C. (2000). What has happened to gene therapy?. European Journal of Pediatrics. 159(S3). S240–S242. 2 indexed citations
3.
Dean, G, N C Nevin, Margareta Mikkelsen, et al.. (2000). Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland. Occupational and Environmental Medicine. 57(12). 793–804. 18 indexed citations
4.
McNicholl, Feargal, et al.. (1999). Hereditary benign telangiectasia--first family in Northern Ireland.. PubMed. 68(2). 106–7. 6 indexed citations
5.
Nevin, N C, Paul S. Thomas, R. I. Davis, & G H Cowie. (1999). Melorheostosis in a family with autosomal dominant osteopoikilosis. American Journal of Medical Genetics. 82(5). 409–414. 25 indexed citations
6.
Morrison, Patrick J., C. M. Steel, Hans F. A. Vasen, et al.. (1999). Insurance Implications for Individuals with a High Risk of Breast and Ovarian Cancer in Europe. Disease Markers. 15(1-3). 159–165. 10 indexed citations
7.
Morrison, Patrick J., et al.. (1998). Laryngeal atresia or stenosis presenting as second‐trimester fetal ascites—diagnosis and pathology in three independent cases. Prenatal Diagnosis. 18(9). 963–967. 1 indexed citations
8.
Nevin, N C, Helen Mulholland, & PS Thomas. (1996). Congenital hypertrichosis, cardiomegaly and mild osteochondrodysplasia. American Journal of Medical Genetics. 66(1). 33–38. 20 indexed citations
9.
Hicks, Elaine, et al.. (1996). The prevalence of inherited neuromuscular disease in Northern Ireland. Neuromuscular Disorders. 6(1). 69–73. 68 indexed citations
10.
Irvine, Alan D., et al.. (1996). An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis.. Journal of Medical Genetics. 33(11). 972–974. 20 indexed citations
11.
Morrison, Patrick J., et al.. (1995). The epidemiology of Huntington's disease in Northern Ireland.. Journal of Medical Genetics. 32(7). 524–530. 46 indexed citations
12.
Ton, Carl C.T., Robert F. Mueller, Maria Luiza Petzl‐Erler, et al.. (1994). Absence of PAX6 Gene Mutations in Gillespie Syndrome (Partial Aniridia, Cerebellar Ataxia, and Mental Retardation). Genomics. 19(1). 145–148. 43 indexed citations
13.
Morrison, Patrick J. & N C Nevin. (1994). Serum iron, total iron binding capacity and ferritin in early huntington disease patients. Irish Journal of Medical Science (1971 -). 163(5). 236–237. 15 indexed citations
14.
Stewart, Fiona, N C Nevin, & R. Stephen Brown. (1993). Axial mesodermal dysplasia spectrum. American Journal of Medical Genetics. 45(4). 426–429. 24 indexed citations
15.
MacMillan, J., Patrick J. Morrison, N C Nevin, et al.. (1993). Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea.. Journal of Medical Genetics. 30(12). 1012–1013. 31 indexed citations
16.
Hughes, Alison, et al.. (1993). Autosomal dominant polycystic kidney disease with minimal clinical expression unlinked to the PKD1 locus. Nephrology Dialysis Transplantation. 8(6). 491–494. 5 indexed citations
17.
Morrison, Patrick J. & N C Nevin. (1993). Huntington disease in County Donegal: epidemiological trends over four decades.. PubMed. 62(2). 141–4. 8 indexed citations
18.
Nevin, N C, J.A. Dodge, & I. V. Allen. (1972). Two cases of trisomy D associated with adrenal tumours.. Journal of Medical Genetics. 9(1). 119–122. 17 indexed citations
19.
Nevin, N C & J. Slack. (1968). Hyperlipidaemic xanthomatosis. II. Mode of inheritance in 55 families with essential hyperlipidaemia and xanthomatosis.. Journal of Medical Genetics. 5(1). 9–28. 39 indexed citations
20.
Nevin, N C, J. N. Cumings, & Florence McKeown. (1967). REFSUM'S SYNDROME HEREDOPATHIA ATACTICA POLYNEURITIFORMIS. Brain. 90(2). 419–428. 19 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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