N E Haites
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Reproductive Medicine top 2%
- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 29
- BRCA gene mutations in cancer 18
- Genomics and Rare Diseases 4
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- Hereditary Neurological Disorders 7
- Genetic Neurodegenerative Diseases 3
- Co-authors
- John M Rawles (4 shared papers)Howard L. McLeod (4 shared papers)Edwin van Teijlingen (1 shared paper)Diana Eccles (6 shared papers)Heather M. Wilson (2 shared papers)Zosia Miedzybrodzka (8 shared papers)Henry Charles Kitchener (5 shared papers)John T. Price (1 shared paper)
- Journals
- Journal of Medical Genetics (11 papers)British Journal of Cancer (5 papers)Disease Markers (3 papers)Occupational and Environmental Medicine (3 papers)European Journal of Cancer (3 papers)
- Partner nations
- United KingdomItalyUnited States
In The Last Decade
N E Haites
80 papers receiving 4k citations
Peers
Comparison fields: 5 of 129
- Genetics 1.2k
- Reproductive Medicine 257
- Neurology 246
- Cellular and Molecular Neuroscience 280
- Cancer Research 202
Countries citing papers authored by N E Haites
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
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-authors
The 25 scholars most cited alongside N E Haites, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 81 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 579 | |
| 2 | 1998 | 340 | |
| 3 | 2003 | 306 | |
| 4 | 2007 | 235 | |
| 5 | Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident. | 1997 | 229 |
| 6 | 1994 | 169 | |
| 7 | p53 mutation is a common genetic event in ovarian carcinoma. | 1993 | 158 |
| 8 | 2006 | 137 | |
| 9 | 2001 | 128 | |
| 10 | 1999 | 115 | |
| 11 | 2002 | 104 | |
| 12 | 2007 | 95 | |
| 13 | 1996 | 93 | |
| 14 | 1998 | 90 | |
| 15 | 1986 | 84 | |
| 16 | 1995 | 81 | |
| 17 | Early loss of heterozygosity on 17q in ovarian cancer. The Abe Ovarian Cancer Genetics Group. | 1992 | 80 |
| 18 | 1988 | 76 | |
| 19 | 1993 | 73 | |
| 20 | 1990 | 62 |
About N E Haites
N E Haites is a scholar working on Genetics, Cellular and Molecular Neuroscience, Reproductive Medicine, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 81 papers that have together received 4.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (18 papers), Hereditary Neurological Disorders (7 papers), Ovarian cancer diagnosis and treatment (6 papers), Genomics and Rare Diseases (4 papers), Retinal Development and Disorders (4 papers), Hormonal Regulation and Hypertension (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Genetics (1.2k citations), Reproductive Medicine (257 citations), Neurology (246 citations), Cellular and Molecular Neuroscience (280 citations) and Cancer Research (202 citations). N E Haites has collaborated with scholars based in United Kingdom, Italy and United States. Frequent co-authors include John M Rawles, Howard L. McLeod, Edwin van Teijlingen, Diana Eccles, Heather M. Wilson, Zosia Miedzybrodzka, Henry Charles Kitchener, John T. Price, A. Kidd and Patrick H. Rooney. Their work appears in journals such as Journal of Medical Genetics, British Journal of Cancer, Disease Markers, Occupational and Environmental Medicine and European Journal of Cancer.
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.