N E Haites

4.9k total citations
72 papers, 3.1k citations indexed

About

N E Haites is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, N E Haites has authored 72 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 20 papers in Genetics and 12 papers in Oncology. Recurrent topics in N E Haites's work include BRCA gene mutations in cancer (12 papers), Genetic factors in colorectal cancer (8 papers) and Ovarian cancer diagnosis and treatment (8 papers). N E Haites is often cited by papers focused on BRCA gene mutations in cancer (12 papers), Genetic factors in colorectal cancer (8 papers) and Ovarian cancer diagnosis and treatment (8 papers). N E Haites collaborates with scholars based in United Kingdom, United States and Sweden. N E Haites's co-authors include John Rawles, Kevin F. Kelly, Howard L. McLeod, Martin McKee, Emma Matthews, Karen Forrest, Edwin van Teijlingen, Diana Eccles, Heather M. Wilson and John T. Price and has published in prestigious journals such as The Lancet, The Journal of Clinical Endocrinology & Metabolism and American Journal of Respiratory and Critical Care Medicine.

In The Last Decade

N E Haites

71 papers receiving 3.0k 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 E Haites United Kingdom 28 1.2k 808 612 429 349 72 3.1k
J. A. Franklyn United Kingdom 41 967 0.8× 885 1.1× 288 0.5× 287 0.7× 473 1.4× 118 5.5k
Bruce W. Eckloff United States 36 1.6k 1.3× 637 0.8× 896 1.5× 571 1.3× 466 1.3× 76 3.5k
Jeffrey A. Jones United States 39 1.3k 1.1× 505 0.6× 750 1.2× 411 1.0× 305 0.9× 130 4.4k
Andrea Lania Italy 41 1.7k 1.4× 758 0.9× 593 1.0× 359 0.8× 303 0.9× 274 6.0k
Akira Hata Japan 41 1.5k 1.3× 1.5k 1.9× 398 0.7× 312 0.7× 213 0.6× 164 6.6k
Kathryn M. Thrailkill United States 36 1.5k 1.2× 582 0.7× 539 0.9× 490 1.1× 284 0.8× 75 3.5k
A C Moses United States 27 1.4k 1.1× 379 0.5× 427 0.7× 185 0.4× 109 0.3× 49 3.1k
Ethan M. Lange United States 37 1.3k 1.1× 1.3k 1.6× 319 0.5× 457 1.1× 243 0.7× 137 3.9k
Joshua A. Bell United Kingdom 35 1.1k 0.9× 549 0.7× 1.5k 2.4× 937 2.2× 531 1.5× 90 4.2k
Tom Grotmol Norway 36 939 0.8× 501 0.6× 1.3k 2.2× 258 0.6× 512 1.5× 134 3.8k

Countries citing papers authored by N E Haites

Since Specialization
Citations

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

Fields of papers citing papers by N E Haites

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N E Haites

This figure shows the co-authorship network connecting the top 25 collaborators of N E Haites. A scholar is included among the top collaborators of N E Haites 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 E Haites. N E Haites 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.
Dick, Finlay, Giuseppe De Palma, Ahmad Ahmadi, et al.. (2007). Environmental risk factors for Parkinson’s disease and parkinsonism: the Geoparkinson study. Occupational and Environmental Medicine. 64(10). 666–672. 214 indexed citations
2.
Tayeb, Mohammed T., Caroline Clark, N E Haites, et al.. (2003). CYP3A4 and VDR gene polymorphisms and the risk of prostate cancer in men with benign prostate hyperplasia. British Journal of Cancer. 88(6). 928–932. 46 indexed citations
3.
Κroupis, Christos, Irene Konstantopoulou, Lydia Ioannidou-Mouzaka, et al.. (2002). Germ line BRCA1 & BRCA2 mutations in Greek breast/ovarian cancer families: 5382insC is the most frequent mutation observed. Cancer Letters. 185(1). 61–70. 39 indexed citations
4.
Haites, N E. (2002). Sources of DNA for studying gene–nutrition interactions. European Journal of Cancer Prevention. 11(1). 101–103. 3 indexed citations
5.
McFadyen, Morag, Margaret Cruickshank, I.D. Miller, et al.. (2001). Cytochrome P450 CYP1B1 over-expression in primary and metastatic ovarian cancer. British Journal of Cancer. 85(2). 242–246. 126 indexed citations
6.
Kidd, A., et al.. (2001). Breast cancer in two sisters with Friedreich's ataxia. European Journal of Surgical Oncology. 27(5). 512–514. 13 indexed citations
7.
Semple, Sean, Finlay Dick, John W. Cherrie, et al.. (2000). Impairment of colour vision in workers exposed to organic solvents. Occupational and Environmental Medicine. 57(9). 582–587. 26 indexed citations
8.
Payne, Shay, et al.. (2000). Immunohistochemical detection of a germline BRCA1 mutation in a breast and ovarian cancer family. The Breast. 9(5). 286–291. 2 indexed citations
9.
CHRISTIE, G. L., P Helms, Sue Ross, et al.. (1999). Asthma, Wheezy Bronchitis, and Atopy across Two Generations. American Journal of Respiratory and Critical Care Medicine. 159(1). 125–129. 27 indexed citations
10.
Eccles, Diana, et al.. (1999). Management of Hereditary Breast Cancer. Disease Markers. 15(1-3). 187–189. 15 indexed citations
11.
Evans, D. Gareth, Elaine Anderson, Fiona Lalloo, et al.. (1999). Utilisation of Prophylactic Mastectomy in 10 European Centres. Disease Markers. 15(1-3). 148–151. 20 indexed citations
12.
Stanković, Tatjana, A. Kidd, Amanda Sutcliffe, et al.. (1998). ATM Mutations and Phenotypes in Ataxia-Telangiectasia Families in the British Isles: Expression of Mutant ATM and the Risk of Leukemia, Lymphoma, and Breast Cancer. The American Journal of Human Genetics. 62(2). 334–345. 281 indexed citations
13.
Vasen, Hans F. A., N E Haites, D. Gareth Evans, et al.. (1998). Current policies for surveillance and management in women at risk of breast and ovarian cancer: a survey among 16 European family cancer clinics. European Journal of Cancer. 34(12). 1922–1926. 84 indexed citations
14.
Price, John T., Heather M. Wilson, & N E Haites. (1996). Epidermal growth factor (EGF) Increases the in vitro invasion, motility and adhesion interactions of the primary renal carcinoma cell line, A704. European Journal of Cancer. 32(11). 1977–1982. 89 indexed citations
15.
Bell, C., et al.. (1992). Autosomal dominant retinitis pigmentosa (ADRP): a rhodopsin mutation in a Scottish family.. Journal of Medical Genetics. 29(9). 667–668. 23 indexed citations
16.
Miedzybrodzka, Zosia, Kevin F. Kelly, M. J. Davidson, et al.. (1992). Prenatal diagnosis for the cystic fibrosis mutation 1717‐1, G→A using arms. Prenatal Diagnosis. 12(10). 845–849. 2 indexed citations
17.
Cruickshank, Derek, N E Haites, Stewart Anderson, et al.. (1992). The multidisciplinary management of a family with epithelial ovarian cancer. BJOG An International Journal of Obstetrics & Gynaecology. 99(3). 226–231. 8 indexed citations
18.
Suthers, G K, John C. Mulley, Marie‐Antoinette Voelckel, et al.. (1991). Linkage homogeneity near the fragile X locus in normal and fragile X families. Genomics. 10(3). 576–582. 11 indexed citations
19.
Clark, Caroline, Kevin Kelly, Nicholas M. A. Smith, et al.. (1991). Prenatal diagnosis for dystrophia myotonica using the polymerase chain reaction. Prenatal Diagnosis. 11(7). 467–470. 2 indexed citations
20.
Haites, N E, et al.. (1989). Linkage in a family with X‐linked Charcot‐Marie‐Tooth disease. Clinical Genetics. 35(6). 399–403. 26 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by J. A. Franklyn Breakdown of academic impact, for papers by Bruce W. Eckloff Breakdown of academic impact, for papers by Jeffrey A. Jones Breakdown of academic impact, for papers by Andrea Lania Breakdown of academic impact, for papers by Akira Hata Breakdown of academic impact, for papers by Kathryn M. Thrailkill Breakdown of academic impact, for papers by A C Moses Breakdown of academic impact, for papers by Ethan M. Lange Breakdown of academic impact, for papers by Joshua A. Bell Breakdown of academic impact, for papers by Tom Grotmol
Rankless by CCL
2026