Dan Doherty
Impact in
- Genetics top 0.5%
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Developmental Neuroscience top 2%
- Neurogenesis and neuroplasticity mechanisms
Papers in
- Genetics 71
- Genetic and Kidney Cyst Diseases 45
- Genomics and Rare Diseases 18
- Genetics and Neurodevelopmental Disorders 15
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- Fetal and Pediatric Neurological Disorders 23
- Neonatal and fetal brain pathology 3
- Co-authors
- Ian A. Glass (16 shared papers)Melissa A. Parisi (10 shared papers)Kimberly A. Aldinger (6 shared papers)Gisele E. Ishak (15 shared papers)Diana R. O’Day (7 shared papers)Ian G. Phelps (15 shared papers)Jennifer C. Dempsey (18 shared papers)Jay Shendure (4 shared papers)
- Journals
- The American Journal of Human Genetics (20 papers)Journal of Medical Genetics (7 papers)Genetics in Medicine (4 papers)Science (3 papers)Human Genetics and Genomics Advances (2 papers)
- Partner nations
- United StatesNetherlandsUnited Kingdom
In The Last Decade
Dan Doherty
105 papers receiving 7k citations
Dan Doherty's Hit Papers
Peers
Comparison fields: 5 of 109
- Genetics 3.7k
- Developmental Neuroscience 193
- Pediatrics, Perinatology and Child Health 784
- Molecular Biology 1.8k
- Cognitive Neuroscience 516
Countries citing papers authored by Dan Doherty
This map shows the geographic impact of Dan Doherty'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 Dan Doherty with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dan Doherty more than expected).
Fields of papers citing papers by Dan Doherty
This network shows the impact of papers produced by Dan Doherty. 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 Dan Doherty. The network helps show where Dan Doherty may publish in the future.
Co-authors
The 25 scholars most cited alongside Dan Doherty, 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 107 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders Hit paper breakdown → | 2012 | 1026 |
| 2 | A human cell atlas of fetal gene expression Hit paper breakdown → | 2020 | 503 |
| 3 | 2020 | 274 | |
| 4 | 2007 | 266 | |
| 5 | 2015 | 227 | |
| 6 | 2015 | 206 | |
| 7 | 2012 | 205 | |
| 8 | 2008 | 204 | |
| 9 | 2007 | 185 | |
| 10 | 2013 | 179 | |
| 11 | 2009 | 166 | |
| 12 | 2011 | 161 | |
| 13 | 2009 | 143 | |
| 14 | 2014 | 140 | |
| 15 | 2017 | 139 | |
| 16 | 2021 | 139 | |
| 17 | 2021 | 138 | |
| 18 | 2009 | 117 | |
| 19 | 2012 | 115 | |
| 20 | 2017 | 103 |
About Dan Doherty
Dan Doherty is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience, Clinical Biochemistry and Molecular Biology, having authored 107 papers that have together received 7.1k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (45 papers), Fetal and Pediatric Neurological Disorders (23 papers), Genomics and Rare Diseases (18 papers), Genetics and Neurodevelopmental Disorders (15 papers), Single-cell and spatial transcriptomics (4 papers), Cerebrospinal fluid and hydrocephalus (4 papers), Hereditary Neurological Disorders (3 papers) and Neonatal and fetal brain pathology (3 papers). The work is most often cited by research in Genetics (3.7k citations), Developmental Neuroscience (193 citations), Pediatrics, Perinatology and Child Health (784 citations), Molecular Biology (1.8k citations) and Cognitive Neuroscience (516 citations). Dan Doherty has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Ian A. Glass, Melissa A. Parisi, Kimberly A. Aldinger, Gisele E. Ishak, Diana R. O’Day, Ian G. Phelps, Jennifer C. Dempsey, Jay Shendure, Phillip F. Chance and Kathleen J. Millen. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics, Genetics in Medicine, Science and Human Genetics and Genomics Advances.
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.