Bernie Devlin
Impact in
- Genetics top 0.01%
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Mapping and Diversity in Plants and Animals
- Cognitive Neuroscience top 0.05%
- Autism Spectrum Disorder Research
Papers in
- Genetics 146
- Genetic Associations and Epidemiology 69
- Genomic variations and chromosomal abnormalities 52
- Genetics and Neurodevelopmental Disorders 30
- Genomics and Rare Diseases 26
- Genetic Mapping and Diversity in Plants and Animals 18
- Genetic and phenotypic traits in livestock 18
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- Autism Spectrum Disorder Research 53
- Co-authors
- Kathryn Roeder (89 shared papers)Neil Risch (17 shared papers)Silviu‐Alin Bacanu (20 shared papers)Mária Kovács (4 shared papers)Norman C. Ellstrand (8 shared papers)Larry Wasserman (6 shared papers)Stephen W. Scherer (1 shared paper)Lambertus Klei (37 shared papers)
- Journals
- The American Journal of Human Genetics (21 papers)Nature Genetics (15 papers)Biological Psychiatry (14 papers)Genetic Epidemiology (13 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (12 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Bernie Devlin
257 papers receiving 41.3k citations
Bernie Devlin's Hit Papers
Peers
Comparison fields: 5 of 196
- Genetics 22.0k
- Cognitive Neuroscience 12.0k
- Biological Psychiatry 667
- Developmental Neuroscience 916
- Molecular Biology 15.2k
Countries citing papers authored by Bernie Devlin
This map shows the geographic impact of Bernie Devlin'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 Bernie Devlin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernie Devlin more than expected).
Fields of papers citing papers by Bernie Devlin
This network shows the impact of papers produced by Bernie Devlin. 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 Bernie Devlin. The network helps show where Bernie Devlin may publish in the future.
Co-authors
The 25 scholars most cited alongside Bernie Devlin, 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 262 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genomic Control for Association Studies Hit paper breakdown → | 1999 | 2513 |
| 2 | Synaptic, transcriptional and chromatin genes disrupted in autism Hit paper breakdown → | 2014 | 2082 |
| 3 | Functional impact of global rare copy number variation in autism spectrum disorders Hit paper breakdown → | 2010 | 1652 |
| 4 | De novo mutations revealed by whole-exome sequencing are strongly associated with autism Hit paper breakdown → | 2012 | 1638 |
| 5 | Identification of common genetic risk variants for autism spectrum disorder Hit paper breakdown → | 2019 | 1602 |
| 6 | Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism Hit paper breakdown → | 2020 | 1519 |
| 7 | Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma Hit paper breakdown → | 2000 | 1421 |
| 8 | Patterns and rates of exonic de novo mutations in autism spectrum disorders Hit paper breakdown → | 2012 | 1378 |
| 9 | Autism genome-wide copy number variation reveals ubiquitin and neuronal genes Hit paper breakdown → | 2009 | 1178 |
| 10 | Mapping autism risk loci using genetic linkage and chromosomal rearrangements Hit paper breakdown → | 2007 | 1155 |
| 11 | Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci Hit paper breakdown → | 2015 | 1030 |
| 12 | Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Hit paper breakdown → | 2011 | 1012 |
| 13 | Most genetic risk for autism resides with common variation Hit paper breakdown → | 2014 | 910 |
| 14 | A Comparison of Linkage Disequilibrium Measures for Fine-Scale Mapping Hit paper breakdown → | 1995 | 881 |
| 15 | Gene expression elucidates functional impact of polygenic risk for schizophrenia Hit paper breakdown → | 2016 | 806 |
| 16 | Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap Hit paper breakdown → | 2018 | 763 |
| 17 | Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders Hit paper breakdown → | 2014 | 755 |
| 18 | A framework for the interpretation of de novo mutation in human disease Hit paper breakdown → | 2014 | 704 |
| 19 | Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism Hit paper breakdown → | 2013 | 699 |
| 20 | 2010 | 501 |
About Bernie Devlin
Bernie Devlin is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Clinical Psychology and Ecology, Evolution, Behavior and Systematics, having authored 262 papers that have together received 42.9k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (69 papers), Autism Spectrum Disorder Research (53 papers), Genomic variations and chromosomal abnormalities (52 papers), Genetics and Neurodevelopmental Disorders (30 papers), Genomics and Rare Diseases (26 papers), Genetic Mapping and Diversity in Plants and Animals (18 papers), Genetic and phenotypic traits in livestock (18 papers) and Gene expression and cancer classification (18 papers). The work is most often cited by research in Genetics (22.0k citations), Cognitive Neuroscience (12.0k citations), Biological Psychiatry (667 citations), Developmental Neuroscience (916 citations) and Molecular Biology (15.2k citations). Bernie Devlin has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Kathryn Roeder, Neil Risch, Silviu‐Alin Bacanu, Mária Kovács, Norman C. Ellstrand, Larry Wasserman, Stephen W. Scherer, Lambertus Klei, Andrew G. Stephenson and Robert E. Ferrell. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, Biological Psychiatry, Genetic Epidemiology 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.