Stephan Sanders
Impact in
- Genetics top 0.02%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- Cognitive Neuroscience top 0.05%
- Autism Spectrum Disorder Research
Papers in
- Genetics 108
- Genetics and Neurodevelopmental Disorders 59
- Genomic variations and chromosomal abnormalities 42
- Genomics and Rare Diseases 36
- Genetic Associations and Epidemiology 16
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- Autism Spectrum Disorder Research 62
- Co-authors
- Jack A. Kosmicki (3 shared papers)Bernie Devlin (13 shared papers)Grace Schwartz (4 shared papers)Kyle Kai‐How Farh (2 shared papers)Siavash Fazel Darbandi (4 shared papers)Serafim Batzoglou (1 shared paper)David A. Knowles (1 shared paper)Juan David Arbelaez Velez (1 shared paper)
- Journals
- The American Journal of Human Genetics (19 papers)Science (14 papers)Nature Genetics (10 papers)Nature (10 papers)Neuron (7 papers)
- Partner nations
- United StatesUnited KingdomFrance
In The Last Decade
Stephan Sanders
193 papers receiving 33.8k citations
Stephan Sanders's Hit Papers
Peers
Comparison fields: 5 of 199
- Genetics 16.7k
- Cognitive Neuroscience 10.5k
- Biological Psychiatry 790
- Developmental Neuroscience 966
- Molecular Biology 14.7k
Countries citing papers authored by Stephan Sanders
This map shows the geographic impact of Stephan Sanders'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 Stephan Sanders with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephan Sanders more than expected).
Fields of papers citing papers by Stephan Sanders
This network shows the impact of papers produced by Stephan Sanders. 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 Stephan Sanders. The network helps show where Stephan Sanders may publish in the future.
Co-authors
The 25 scholars most cited alongside Stephan Sanders, 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 204 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Synaptic, transcriptional and chromatin genes disrupted in autism Hit paper breakdown → | 2014 | 2082 |
| 2 | The contribution of de novo coding mutations to autism spectrum disorder Hit paper breakdown → | 2014 | 1929 |
| 3 | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Hit paper breakdown → | 2013 | 1775 |
| 4 | Predicting Splicing from Primary Sequence with Deep Learning Hit paper breakdown → | 2019 | 1755 |
| 5 | De novo mutations revealed by whole-exome sequencing are strongly associated with autism Hit paper breakdown → | 2012 | 1638 |
| 6 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia Hit paper breakdown → | 2022 | 1614 |
| 7 | Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism Hit paper breakdown → | 2020 | 1519 |
| 8 | Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci Hit paper breakdown → | 2015 | 1030 |
| 9 | Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Hit paper breakdown → | 2011 | 1012 |
| 10 | Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders Hit paper breakdown → | 2019 | 965 |
| 11 | Most genetic risk for autism resides with common variation Hit paper breakdown → | 2014 | 910 |
| 12 | Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder Hit paper breakdown → | 2018 | 892 |
| 13 | De novo mutations in histone-modifying genes in congenital heart disease Hit paper breakdown → | 2013 | 741 |
| 14 | A framework for the interpretation of de novo mutation in human disease Hit paper breakdown → | 2014 | 704 |
| 15 | Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism Hit paper breakdown → | 2013 | 699 |
| 16 | Comprehensive functional genomic resource and integrative model for the human brain Hit paper breakdown → | 2018 | 647 |
| 17 | De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies Hit paper breakdown → | 2015 | 622 |
| 18 | Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways Hit paper breakdown → | 2015 | 620 |
| 19 | Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands Hit paper breakdown → | 2017 | 615 |
| 20 | Integrative functional genomic analysis of human brain development and neuropsychiatric risks Hit paper breakdown → | 2018 | 560 |
About Stephan Sanders
Stephan Sanders is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Biological Psychiatry and Pediatrics, Perinatology and Child Health, having authored 204 papers that have together received 34.6k indexed citations. Recurring topics across this work include Autism Spectrum Disorder Research (62 papers), Genetics and Neurodevelopmental Disorders (59 papers), Genomic variations and chromosomal abnormalities (42 papers), Genomics and Rare Diseases (36 papers), Congenital heart defects research (20 papers), Genetic Associations and Epidemiology (16 papers), Genomics and Chromatin Dynamics (15 papers) and RNA and protein synthesis mechanisms (13 papers). The work is most often cited by research in Genetics (16.7k citations), Cognitive Neuroscience (10.5k citations), Biological Psychiatry (790 citations), Developmental Neuroscience (966 citations) and Molecular Biology (14.7k citations). Stephan Sanders has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Jack A. Kosmicki, Bernie Devlin, Grace Schwartz, Kyle Kai‐How Farh, Siavash Fazel Darbandi, Serafim Batzoglou, David A. Knowles, Juan David Arbelaez Velez, Eric D. Chow and Yang Li. Their work appears in journals such as The American Journal of Human Genetics, Science, Nature Genetics, Nature and Neuron.
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.