Raphael Bernier
Impact in
- Cognitive Neuroscience top 0.1%
- Autism Spectrum Disorder Research
- Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
-
- Autism Spectrum Disorder Research 111
- Genetics 95
- Genetics and Neurodevelopmental Disorders 76
- Genomic variations and chromosomal abnormalities 34
- Genomics and Rare Diseases 25
- Co-authors
- Evan E. Eichler (31 shared papers)Sara Jane Webb (39 shared papers)Carl A. Baker (7 shared papers)Jennifer A. Gerdts (22 shared papers)Holly A.F. Stessman (7 shared papers)Emily Neuhaus (22 shared papers)Géraldine Dawson (18 shared papers)Laura Vives (4 shared papers)
- Journals
- Autism Research (19 papers)Journal of Autism and Developmental Disorders (14 papers)The American Journal of Human Genetics (12 papers)Nature Genetics (7 papers)Nature Communications (7 papers)
- Partner nations
- United StatesNetherlandsFrance
In The Last Decade
Raphael Bernier
179 papers receiving 15.1k citations
Raphael Bernier's Hit Papers
Peers
Comparison fields: 5 of 168
- Cognitive Neuroscience 6.9k
- Genetics 7.8k
- Psychiatry and Mental health 1.1k
- Developmental Neuroscience 315
- Molecular Biology 5.4k
Countries citing papers authored by Raphael Bernier
This map shows the geographic impact of Raphael Bernier'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 Raphael Bernier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Raphael Bernier more than expected).
Fields of papers citing papers by Raphael Bernier
This network shows the impact of papers produced by Raphael Bernier. 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 Raphael Bernier. The network helps show where Raphael Bernier may publish in the future.
Co-authors
The 25 scholars most cited alongside Raphael Bernier, 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 181 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Autism genome-wide copy number variation reveals ubiquitin and neuronal genes Hit paper breakdown → | 2009 | 1178 |
| 2 | Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations Hit paper breakdown → | 2011 | 959 |
| 3 | Common genetic variants on 5p14.1 associate with autism spectrum disorders Hit paper breakdown → | 2009 | 807 |
| 4 | Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders Hit paper breakdown → | 2014 | 755 |
| 5 | Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development Hit paper breakdown → | 2014 | 596 |
| 6 | Excess of rare, inherited truncating mutations in autism Hit paper breakdown → | 2015 | 432 |
| 7 | Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases Hit paper breakdown → | 2017 | 414 |
| 8 | 2018 | 328 | |
| 9 | 2002 | 289 | |
| 10 | 2014 | 271 | |
| 11 | Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes Hit paper breakdown → | 2022 | 265 |
| 12 | 2011 | 262 | |
| 13 | 2013 | 240 | |
| 14 | 2012 | 240 | |
| 15 | 2018 | 239 | |
| 16 | 2018 | 219 | |
| 17 | Long-term Risk of Neuropsychiatric Disease After Exposure to Infection In Utero Hit paper breakdown → | 2019 | 209 |
| 18 | The fetal origins of mental illness Hit paper breakdown → | 2019 | 201 |
| 19 | 2014 | 200 | |
| 20 | 2019 | 190 |
About Raphael Bernier
Raphael Bernier is a scholar working on Cognitive Neuroscience, Genetics, Psychiatry and Mental health, Clinical Psychology and Molecular Biology, having authored 181 papers that have together received 15.6k indexed citations. Recurring topics across this work include Autism Spectrum Disorder Research (111 papers), Genetics and Neurodevelopmental Disorders (76 papers), Genomic variations and chromosomal abnormalities (34 papers), Genomics and Rare Diseases (25 papers), Congenital heart defects research (21 papers), Child Development and Digital Technology (16 papers), Attention Deficit Hyperactivity Disorder (15 papers) and Family and Disability Support Research (12 papers). The work is most often cited by research in Cognitive Neuroscience (6.9k citations), Genetics (7.8k citations), Psychiatry and Mental health (1.1k citations), Developmental Neuroscience (315 citations) and Molecular Biology (5.4k citations). Raphael Bernier has collaborated with scholars based in United States, Netherlands and France. Frequent co-authors include Evan E. Eichler, Sara Jane Webb, Carl A. Baker, Jennifer A. Gerdts, Holly A.F. Stessman, Emily Neuhaus, Géraldine Dawson, Laura Vives, Brian J. O’Roak and Bradley P. Coe. Their work appears in journals such as Autism Research, Journal of Autism and Developmental Disorders, The American Journal of Human Genetics, Nature Genetics and Nature Communications.
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.