Ryan Murtha
Impact in
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
Papers in
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- Genetic Neurodegenerative Diseases 3
-
- Neurological disorders and treatments 1
- Co-authors
- Vanessa C. Wheeler (2 shared papers)Ricardo Mouro Pinto (2 shared papers)Tammy Gillis (1 shared paper)Seung Kwak (1 shared paper)Jong‐Min Lee (1 shared paper)Marcy E. MacDonald (1 shared paper)Jayalakshmi Srinidhi Mysore (1 shared paper)James F. Gusella (1 shared paper)
- Journals
- Nature (1 paper)Nature Genetics (1 paper)Scientific Reports (1 paper)Human Molecular Genetics (1 paper)JAMA Cardiology (1 paper)
- Partner nations
- United StatesItalyCzechia
In The Last Decade
Ryan Murtha
5 papers receiving 1.7k citations
Ryan Murtha's Hit Papers
Peers
Comparison fields: 5 of 85
- Cognitive Neuroscience 744
- Genetics 1.1k
- Developmental Neuroscience 54
- Molecular Biology 802
- Cellular and Molecular Neuroscience 212
Countries citing papers authored by Ryan Murtha
This map shows the geographic impact of Ryan Murtha'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 Ryan Murtha with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryan Murtha more than expected).
Fields of papers citing papers by Ryan Murtha
This network shows the impact of papers produced by Ryan Murtha. 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 Ryan Murtha. The network helps show where Ryan Murtha may publish in the future.
Co-authors
The 16 scholars most cited alongside Ryan Murtha, 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 | De novo mutations revealed by whole-exome sequencing are strongly associated with autism Hit paper breakdown → | 2012 | 1638 |
| 2 | 2020 | 54 | |
| 3 | 2025 | 24 | |
| 4 | 2019 | 22 | |
| 5 | 2026 | 1 |
About Ryan Murtha
Ryan Murtha is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Cognitive Neuroscience and Genetics, having authored 5 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (3 papers), Mitochondrial Function and Pathology (2 papers), Muscle Physiology and Disorders (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Neurological disorders and treatments (1 paper), Genomics and Rare Diseases (1 paper), DNA Repair Mechanisms (1 paper) and Autism Spectrum Disorder Research (1 paper). The work is most often cited by research in Cognitive Neuroscience (744 citations), Genetics (1.1k citations), Developmental Neuroscience (54 citations), Molecular Biology (802 citations) and Cellular and Molecular Neuroscience (212 citations). Ryan Murtha has collaborated with scholars based in United States, Italy and Czechia. Frequent co-authors include Vanessa C. Wheeler, Ricardo Mouro Pinto, Tammy Gillis, Seung Kwak, Jong‐Min Lee, Marcy E. MacDonald, Jayalakshmi Srinidhi Mysore, James F. Gusella, Marina V. Kovalenko and Jacob M. Loupe. Their work appears in journals such as Nature, Nature Genetics, Scientific Reports, Human Molecular Genetics and JAMA Cardiology.
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.