Ron C. Michaelis
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 27
- Genomic variations and chromosomal abnormalities 14
- Genetics and Neurodevelopmental Disorders 11
- Genetic Syndromes and Imprinting 8
- Co-authors
- Frank Holloway (10 shared papers)Mary C. Phelan (10 shared papers)Richard J. Schroer (6 shared papers)Cynthia M. Powell (2 shared papers)Roger E. Stevenson (5 shared papers)Cindy Skinner (5 shared papers)Richard D. Harland (6 shared papers)Richard J. Simensen (4 shared papers)
- Journals
- Prenatal Diagnosis (4 papers)Journal of Medical Genetics (4 papers)Pharmacology Biochemistry and Behavior (4 papers)Psychopharmacology (3 papers)Human Genetics (2 papers)
- Partner nations
- United StatesCanadaIsrael
In The Last Decade
Ron C. Michaelis
53 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 117
- Genetics 911
- Cognitive Neuroscience 543
- Cellular and Molecular Neuroscience 306
- Pediatrics, Perinatology and Child Health 217
- Developmental Neuroscience 38
Countries citing papers authored by Ron C. Michaelis
This map shows the geographic impact of Ron C. Michaelis'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 Ron C. Michaelis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ron C. Michaelis more than expected).
Fields of papers citing papers by Ron C. Michaelis
This network shows the impact of papers produced by Ron C. Michaelis. 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 Ron C. Michaelis. The network helps show where Ron C. Michaelis may publish in the future.
Co-authors
The 25 scholars most cited alongside Ron C. Michaelis, 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 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 282 | |
| 2 | 2001 | 122 | |
| 3 | 2007 | 116 | |
| 4 | 2004 | 113 | |
| 5 | 1999 | 84 | |
| 6 | 1998 | 76 | |
| 7 | 2008 | 71 | |
| 8 | 2012 | 50 | |
| 9 | 1996 | 50 | |
| 10 | 1989 | 48 | |
| 11 | 2005 | 48 | |
| 12 | 2005 | 46 | |
| 13 | 1989 | 45 | |
| 14 | 2002 | 39 | |
| 15 | 2002 | 39 | |
| 16 | 1985 | 38 | |
| 17 | Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B. | 1998 | 38 |
| 18 | 1998 | 35 | |
| 19 | 1997 | 29 | |
| 20 | 2001 | 28 |
About Ron C. Michaelis
Ron C. Michaelis is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Cognitive Neuroscience, having authored 54 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (11 papers), Prenatal Screening and Diagnostics (10 papers), Autism Spectrum Disorder Research (8 papers), Neurotransmitter Receptor Influence on Behavior (8 papers), Genetic Syndromes and Imprinting (8 papers), Neuroscience and Neuropharmacology Research (4 papers) and Biochemical Analysis and Sensing Techniques (4 papers). The work is most often cited by research in Genetics (911 citations), Cognitive Neuroscience (543 citations), Cellular and Molecular Neuroscience (306 citations), Pediatrics, Perinatology and Child Health (217 citations) and Developmental Neuroscience (38 citations). Ron C. Michaelis has collaborated with scholars based in United States, Canada and Israel. Frequent co-authors include Frank Holloway, Mary C. Phelan, Richard J. Schroer, Cynthia M. Powell, Roger E. Stevenson, Cindy Skinner, Richard D. Harland, Richard J. Simensen, Steven A. Skinner and Charles E. Schwartz. Their work appears in journals such as Prenatal Diagnosis, Journal of Medical Genetics, Pharmacology Biochemistry and Behavior, Psychopharmacology and Human Genetics.
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.