John B. Moeschler
- Genetics top 1%
- Genomic variations and chromosomal abnormalities 21
- Genetics and Neurodevelopmental Disorders 17
- Genomics and Rare Diseases 9
- Genetic Syndromes and Imprinting 9
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- Prenatal Screening and Diagnostics 15
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research 6
- Clinical Biochemistry top 5%
- Molecular Biology top 10%
- Congenital heart defects research 8
- Epigenetics and DNA Methylation 6
- Co-authors
- Michael ShevellJohn M. GrahamMarilyn C. JonesJohn M. OpitzJoan M. StolerRizwan HamidBeth A. TariniEmily Chen
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
John B. Moeschler
61 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 123
- Genetics 1.7k
- Pediatrics, Perinatology and Child Health 558
- Cognitive Neuroscience 399
- Clinical Biochemistry 109
- Molecular Biology 995
Countries citing papers authored by John B. Moeschler
This map shows the geographic impact of John B. Moeschler'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 John B. Moeschler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John B. Moeschler more than expected).
Fields of papers citing papers by John B. Moeschler
This network shows the impact of papers produced by John B. Moeschler. 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 John B. Moeschler. The network helps show where John B. Moeschler may publish in the future.
Co-authorship network
The 25 scholars most cited alongside John B. Moeschler, 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 | 2014 | 93 | |
| 2 | 2014 | 352 | |
| 3 | 2011 | 168 | |
| 4 | 2011 | 4 | |
| 5 | 2009 | 27 | |
| 6 | 2009 | 13 | |
| 7 | 2008 | 57 | |
| 8 | 2008 | 37 | |
| 9 | 2007 | 152 | |
| 10 | 2007 | 78 | |
| 11 | 2006 | 166 | |
| 12 | 1997 | 266 | |
| 13 | 1993 | 24 | |
| 14 | 1993 | 16 | |
| 15 | 1991 | 11 | |
| 16 | 1990 | 7 | |
| 17 | 1989 | 18 | |
| 18 | 1989 | 11 | |
| 19 | Further delineation of the 10p deletion syndrome. | 1984 | 13 |
| 20 | 1981 | 24 |
About John B. Moeschler
John B. Moeschler is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 62 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Genetics and Neurodevelopmental Disorders (17 papers), Prenatal Screening and Diagnostics (15 papers), Genomics and Rare Diseases (9 papers), Genetic Syndromes and Imprinting (9 papers), Congenital heart defects research (8 papers), Autism Spectrum Disorder Research (6 papers) and Epigenetics and DNA Methylation (6 papers). The work is most often cited by research in Genetics (1.7k citations), Pediatrics, Perinatology and Child Health (558 citations) and Cognitive Neuroscience (399 citations). John B. Moeschler has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Michael Shevell, John M. Graham, Marilyn C. Jones, John M. Opitz, Joan M. Stoler, Rizwan Hamid, Beth A. Tarini, Emily Chen, Robert A. Saul and Debra Freedenberg. Their work appears in journals such as Nature Genetics, Neurology and PEDIATRICS.
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.