Benjamin M. Neale
Impact in
- Genetics top 0.01%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Genetic diversity and population structure
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Cancer Research top 0.5%
- Cancer-related molecular mechanisms research
Papers in
- Genetics 116
- Genetic Associations and Epidemiology 90
- Genetic Mapping and Diversity in Plants and Animals 31
- Genomics and Rare Diseases 30
- Genetic and phenotypic traits in livestock 20
- Genetics and Neurodevelopmental Disorders 17
- Genomic variations and chromosomal abnormalities 16
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- Attention Deficit Hyperactivity Disorder 12
- Co-authors
- Mark J. DalyPak C. ShamShaun PurcellPaul I. W. de BakkerManuel A. R. FerreiraJulian MallerPamela SklarKatherine EO Todd-Brown
- Journals
- Nature Genetics (18 papers)European Neuropsychopharmacology (16 papers)The American Journal of Human Genetics (12 papers)Molecular Psychiatry (10 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (8 papers)
- Partner nations
- United StatesUnited KingdomNetherlands
In The Last Decade
Benjamin M. Neale
159 papers receiving 41.6k citations
Hit Papers
Peers
Comparison fields: 5 of 204
- Genetics 24.7k
- Cancer Research 2.7k
- Molecular Biology 12.4k
- Biological Psychiatry 446
- Psychiatry and Mental health 2.3k
Countries citing papers authored by Benjamin M. Neale
This map shows the geographic impact of Benjamin M. Neale'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 Benjamin M. Neale with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Benjamin M. Neale more than expected).
Fields of papers citing papers by Benjamin M. Neale
This network shows the impact of papers produced by Benjamin M. Neale. 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 Benjamin M. Neale. The network helps show where Benjamin M. Neale may publish in the future.
Co-authors
The 25 scholars most cited alongside Benjamin M. Neale, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2023 | 11 | |
| 2 | 2023 | 4 | |
| 3 | 2023 | 14 | |
| 4 | 2021 | 10 | |
| 5 | 2021 | 5 | |
| 6 | 2021 | 2 | |
| 7 | 2021 | 4 | |
| 8 | 2021 | 9 | |
| 9 | 2020 | 148 | |
| 10 | A global overview of pleiotropy and genetic architecture in complex traits Hit paper breakdown → | 2019 | 670 |
| 11 | 2019 | 61 | |
| 12 | 2018 | 54 | |
| 13 | 2018 | 40 | |
| 14 | 2018 | 73 | |
| 15 | 2015 | 14 | |
| 16 | 2013 | 21 | |
| 17 | 2005 | 6 | |
| 18 | 2005 | 8 | |
| 19 | 2003 | 72 | |
| 20 | 2003 | 2 |
About Benjamin M. Neale
Benjamin M. Neale is a scholar working on Genetics, Psychiatry and Mental health, Molecular Biology, Cognitive Neuroscience and Clinical Psychology, having authored 165 papers that have together received 42.0k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (90 papers), Genetic Mapping and Diversity in Plants and Animals (31 papers), Genomics and Rare Diseases (30 papers), Genetic and phenotypic traits in livestock (20 papers), Genetics and Neurodevelopmental Disorders (17 papers), Genomic variations and chromosomal abnormalities (16 papers), Bioinformatics and Genomic Networks (15 papers) and Attention Deficit Hyperactivity Disorder (12 papers). The work is most often cited by research in Genetics (24.7k citations), Cancer Research (2.7k citations), Molecular Biology (12.4k citations), Biological Psychiatry (446 citations) and Psychiatry and Mental health (2.3k citations). Benjamin M. Neale has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Mark J. Daly, Pak C. Sham, Shaun Purcell, Paul I. W. de Bakker, Manuel A. R. Ferreira, Julian Maller, Pamela Sklar, Katherine EO Todd-Brown, D.B. Bender and Ron Do. Their work appears in journals such as Nature Genetics, European Neuropsychopharmacology, The American Journal of Human Genetics, Molecular Psychiatry and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.
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.