John Chamberlin
Impact in
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- Prenatal Screening and Diagnostics
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- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 6
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 1
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- Single-cell and spatial transcriptomics 2
- Epigenetics and DNA Methylation 1
- DNA Repair Mechanisms 1
- Co-authors
- R.E. Magenis (7 shared papers)E.W. Lovrien (5 shared papers)Timothy F. Brady (2 shared papers)D. James Harris (1 shared paper)Michael L. Begleiter (1 shared paper)Younghee Lee (3 shared papers)Young‐Joo Jin (2 shared papers)Michael G. Brown (1 shared paper)
- Journals
- Human Genetics (3 papers)BMC Medical Genomics (2 papers)NAR Genomics and Bioinformatics (1 paper)Mammalian Genome (1 paper)The Electricity Journal (1 paper)
- Partner nations
- United StatesSouth KoreaEthiopia
In The Last Decade
John Chamberlin
13 papers receiving 271 citations
Peers
Comparison fields: 5 of 74
- Pediatrics, Perinatology and Child Health 114
- Genetics 160
- Plant Science 70
- Developmental Biology 4
- Molecular Biology 106
Countries citing papers authored by John Chamberlin
This map shows the geographic impact of John Chamberlin'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 Chamberlin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Chamberlin more than expected).
Fields of papers citing papers by John Chamberlin
This network shows the impact of papers produced by John Chamberlin. 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 Chamberlin. The network helps show where John Chamberlin may publish in the future.
Co-authors
The 25 scholars most cited alongside John Chamberlin, 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 | 1977 | 75 | |
| 2 | 1980 | 64 | |
| 3 | Parental trisomy 21 mosaicism. | 1982 | 34 |
| 4 | 1981 | 26 | |
| 5 | 2018 | 23 | |
| 6 | Cytogenetic darkroom magic: now you see them, now you don't. | 1976 | 23 |
| 7 | 1979 | 20 | |
| 8 | 2019 | 13 | |
| 9 | 2017 | 7 | |
| 10 | 2020 | 6 | |
| 11 | 1993 | 4 | |
| 12 | 2024 | 4 | |
| 13 | 2024 | 1 | |
| 14 | 2008 | 0 | |
| 15 | 2024 | 0 | |
| 16 | 2008 | 0 |
About John Chamberlin
John Chamberlin is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Plant Science, having authored 16 papers that have together received 300 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (3 papers), Single-cell and spatial transcriptomics (2 papers), Bladder and Urothelial Cancer Treatments (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Epigenetics and DNA Methylation (1 paper), Cancer Genomics and Diagnostics (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (114 citations), Genetics (160 citations), Plant Science (70 citations), Developmental Biology (4 citations) and Molecular Biology (106 citations). John Chamberlin has collaborated with scholars based in United States, South Korea and Ethiopia. Frequent co-authors include R.E. Magenis, E.W. Lovrien, Timothy F. Brady, D. James Harris, Michael L. Begleiter, Younghee Lee, Young‐Joo Jin, Michael G. Brown, Susan Y. Euling and Michelle Angrish. Their work appears in journals such as Human Genetics, BMC Medical Genomics, NAR Genomics and Bioinformatics, Mammalian Genome and The Electricity Journal.
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.