N. C. Nevin

5.6k total citations · 1 hit paper
160 papers, 3.0k citations indexed

About

N. C. Nevin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, N. C. Nevin has authored 160 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 38 papers in Pediatrics, Perinatology and Child Health and 37 papers in Molecular Biology. Recurrent topics in N. C. Nevin's work include Prenatal Screening and Diagnostics (15 papers), Folate and B Vitamins Research (15 papers) and Fetal and Pediatric Neurological Disorders (13 papers). N. C. Nevin is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Folate and B Vitamins Research (15 papers) and Fetal and Pediatric Neurological Disorders (13 papers). N. C. Nevin collaborates with scholars based in United Kingdom, Ireland and United States. N. C. Nevin's co-authors include Mary J. Seller, R. W. Smithells, Andrew Read, S Sheppard, D W Fielding, C J Schorah, R Harris, Colin A. Graham, Jennifer Wild and S. Walker and has published in prestigious journals such as Nature, The Lancet and JAMA.

In The Last Decade

N. C. Nevin

153 papers receiving 2.8k citations

Hit Papers

align trajectories

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.

FURTHER EXPERIENCE OF VITAMIN SUPPLEMENTATION FOR PREVENTION OF NEURAL TUBE DEFECT RECURRENCES

1983 354 citations N. C. Nevin et al. profile →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Smoking and Orofacial Clefts: A United Kingdom–Based Case-Control Study 2004 ·The Cleft Palate-Craniofacial Journal ·Julian Little, (unknown), (unknown), M. Ian Gilmour, Peter Mossey, Jill Clayton‐Smith, M. L. Connor, Lisa Crampin, David Fitzpatrick, Alan Fryer, (unknown), Alison L. Hill, N. C. Nevin, Joyce E. A. Russell, Margo Whiteford	83
2	The KBG syndrome, characteristic dental findings: a case report 2001 ·International Journal of Paediatric Dentistry ·Paul Dowling, Padhraig S. Fleming, Robert J. Gorlin, Marissa King, N. C. Nevin, Meriel McEntagart	12
3	Insurance considerations for individuals with a high risk of breast cancer in Europe:Some recommendations 2000 ·Research Explorer (The University of Manchester) ·Patrick J. Morrison, C. M. Steel, N. C. Nevin, D. Gareth Evans, Diana Eccles, Hans F. A. Vasen, Pål Møller, Shirley Hodgson, Dominique Stoppa‐Lyonnet, Jenny C. Chang, Maria A. Caligo, Edith Oláh, (unknown)	3
4	A Second Family with Probable CRAC (Colorectal Adenomata and Carcinoma) Syndrome—A New Familial Cancer 1999 ·Disease Markers ·Patrick J. Morrison, (unknown), N. C. Nevin	2
5	Frontonasal dysostosis in two successive generations 1999 ·American Journal of Medical Genetics ·N. C. Nevin, Alan G. Leonard, Barry M. Jones	22
6	Mutations in Keratin K9 in Kindreds with Epidermolytic Palmoplantar Keratoderma and Epidemiology in Northern Ireland 1998 ·Journal of Investigative Dermatology ·(unknown), Alan D. Irvine, Kevin E. McKenna, Colin S. Munro, N. C. Nevin, Frances J.D. Smith, Jouni Uitto, W.H. Irwin McLean	30
7	Early amniocentesis: effect of removing a reduced volume of amniotic fluid on pregnancy outcome 1998 ·Prenatal Diagnosis ·(unknown), (unknown), (unknown), Margaret Harper, Fiona Stewart, (unknown), N. C. Nevin, (unknown)	9
8	A Novel Mutation in the Helix Termination Peptide of Keratin 5 Causing Epidermolysis Bullosa Simplex Dowling–Meara 1997 ·Journal of Investigative Dermatology ·Alan D. Irvine, Kevin E. McKenna, Anne Bingham, N. C. Nevin, (unknown)	17
9	Klinefelter Syndrome and Non-Hodgkin Lymphoma 1997 ·Cancer Genetics and Cytogenetics ·Mervyn Humphreys, (unknown), Curly Morris, N. C. Nevin	12
10	Fluorescent multiplex microsatellites used to define haplotypes associated with 75 CFTR mutations from the UK on 437 CF chromosomes 1996 ·Human Mutation ·David J. Hughes, Andrew J. Wallace, Joanne Taylor, May Tassabehji, (unknown), Alison Hill, N. C. Nevin, Colin A. Graham	8
11	T-cell receptor alpha, beta, gamma, and delta chain gene microsatellites show no association with multiple sclerosis 1996 ·Neurology ·Aidan Droogan, C W Kirk, SA Hawkins, S A McMillan, N. C. Nevin, Colin A. Graham	17
12	Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approach. 1995 ·Europe PMC (PubMed Central) ·Johannes Zschocke, CA Graham, (unknown), N. C. Nevin	48
13	Three novel mutations in the EGF precursor homology domain of the low-density lipoprotein receptor gene in Northern Irish patients with familial hypercholesterolemia 1995 ·Human Mutation ·(unknown), Maurice O’Kane, Ian Young, (unknown), N. C. Nevin, Colin A. Graham	10
14	X-linked clinical anophthalmos Localization of the gene to Xq27-Xq28 1991 ·Ophthalmic Paediatrics and Genetics ·Colin A. Graham, R M Redmond, N. C. Nevin	37
15	Facio‐cardio‐renal (Eastman‐Bixler) syndrome 1991 ·American Journal of Medical Genetics ·N. C. Nevin, (unknown), D. J. Carson	3
16	Early amniocentesis: Experience of 222 consecutive patients, 1987–1988 1990 ·Prenatal Diagnosis ·(unknown), N. C. Nevin, James Dornan, (unknown), (unknown)	53
17	Congenital Anomalies in Twins in Northern Ireland. II: Neural Tube Defects, 1974-1979 1989 ·Acta geneticae medicae et gemellologiae twin research ·Julian Little, N. C. Nevin	10
18	Prevention and avoidance of congenital malformations 1988 ·Philosophical transactions of the Royal Society of London. Series B, Biological sciences ·N. C. Nevin	4
19	A family with the testicular feminisation syndrome 1976 ·Irish Journal of Medical Science (1971 -) ·N. C. Nevin, (unknown), (unknown), (unknown)	1
20	Introduction to Medical Genetics 1966 ·BMJ ·N. C. Nevin	3

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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