David E. Godler
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 51
- Genetics and Neurodevelopmental Disorders 43
- Genetic Syndromes and Imprinting 11
- Genomic variations and chromosomal abnormalities 8
- Genomics and Rare Diseases 2
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- Epigenetics and DNA Methylation 16
- Congenital heart defects research 5
- Co-authors
- David J. Amor (26 shared papers)Minh Bui (27 shared papers)Howard R. Slater (18 shared papers)David Francis (25 shared papers)Claudine M. Kraan (13 shared papers)Danuta Z. Loesch (9 shared papers)Freya Gehling (6 shared papers)Randi J. Hagerman (6 shared papers)
- Journals
- Genes (5 papers)Scientific Reports (4 papers)Genetics in Medicine (3 papers)International Journal of Molecular Sciences (3 papers)Clinical Chemistry (3 papers)
- Partner nations
- AustraliaUnited StatesChile
In The Last Decade
David E. Godler
54 papers receiving 793 citations
Peers
Comparison fields: 5 of 53
- Genetics 707
- Cognitive Neuroscience 421
- Molecular Biology 431
- Cellular and Molecular Neuroscience 54
- Pediatrics, Perinatology and Child Health 33
Countries citing papers authored by David E. Godler
This map shows the geographic impact of David E. Godler'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 David E. Godler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David E. Godler more than expected).
Fields of papers citing papers by David E. Godler
This network shows the impact of papers produced by David E. Godler. 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 David E. Godler. The network helps show where David E. Godler may publish in the future.
Co-authors
The 25 scholars most cited alongside David E. Godler, 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 90 | |
| 2 | 2011 | 65 | |
| 3 | 2018 | 53 | |
| 4 | 2014 | 40 | |
| 5 | 2011 | 37 | |
| 6 | 2012 | 33 | |
| 7 | 2015 | 27 | |
| 8 | 2015 | 27 | |
| 9 | 2018 | 24 | |
| 10 | 2015 | 23 | |
| 11 | 2009 | 23 | |
| 12 | 2017 | 23 | |
| 13 | 2016 | 20 | |
| 14 | 2013 | 20 | |
| 15 | 2018 | 19 | |
| 16 | 2012 | 18 | |
| 17 | 2019 | 15 | |
| 18 | 2015 | 15 | |
| 19 | 2018 | 15 | |
| 20 | 2015 | 14 |
About David E. Godler
David E. Godler is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Cellular and Molecular Neuroscience and Genetics, having authored 55 papers that have together received 805 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (43 papers), Autism Spectrum Disorder Research (25 papers), Epigenetics and DNA Methylation (16 papers), Genetic Syndromes and Imprinting (11 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetic Neurodegenerative Diseases (5 papers), Congenital heart defects research (5 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Genetics (707 citations), Cognitive Neuroscience (421 citations), Molecular Biology (431 citations), Cellular and Molecular Neuroscience (54 citations) and Pediatrics, Perinatology and Child Health (33 citations). David E. Godler has collaborated with scholars based in Australia, United States and Chile. Frequent co-authors include David J. Amor, Minh Bui, Howard R. Slater, David Francis, Claudine M. Kraan, Danuta Z. Loesch, Freya Gehling, Randi J. Hagerman, Kim Cornish and Carolyn Rogers. Their work appears in journals such as Genes, Scientific Reports, Genetics in Medicine, International Journal of Molecular Sciences and Clinical Chemistry.
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.