Joan Atkin
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
- Pharmacological Effects and Toxicity Studies
Papers in
- Genetics 14
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 3
- Genetic Syndromes and Imprinting 3
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- Prenatal Screening and Diagnostics 6
- Co-authors
- Gail E. Herman (3 shared papers)Thomas W. Prior (3 shared papers)Bruce E. Maley (1 shared paper)MIROSLAVA B. NIKITOVITCH-WINER (1 shared paper)Kandamurugu Manickam (2 shared papers)Matthew Pastore (2 shared papers)Liz Varga (1 shared paper)Kim L. McBride (1 shared paper)
- Journals
- European Journal of Medical Genetics (2 papers)Nature Genetics (2 papers)Human Molecular Genetics (2 papers)Human Mutation (1 paper)Ophthalmic Genetics (1 paper)
- Partner nations
- United StatesCanadaNetherlands
In The Last Decade
Joan Atkin
26 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 92
- Genetics 677
- Pediatrics, Perinatology and Child Health 325
- Neurology 152
- Molecular Biology 672
- Developmental Biology 19
Countries citing papers authored by Joan Atkin
This map shows the geographic impact of Joan Atkin'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 Joan Atkin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joan Atkin more than expected).
Fields of papers citing papers by Joan Atkin
This network shows the impact of papers produced by Joan Atkin. 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 Joan Atkin. The network helps show where Joan Atkin may publish in the future.
Co-authors
The 25 scholars most cited alongside Joan Atkin, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1988 | 261 | |
| 2 | 2016 | 240 | |
| 3 | 2012 | 232 | |
| 4 | 2010 | 197 | |
| 5 | 2015 | 158 | |
| 6 | 1987 | 89 | |
| 7 | 2009 | 74 | |
| 8 | 2001 | 50 | |
| 9 | 1985 | 47 | |
| 10 | 2011 | 45 | |
| 11 | 2016 | 29 | |
| 12 | 1983 | 22 | |
| 13 | 1998 | 21 | |
| 14 | 2005 | 20 | |
| 15 | 2003 | 18 | |
| 16 | 2012 | 16 | |
| 17 | 1984 | 15 | |
| 18 | 2008 | 15 | |
| 19 | 2010 | 14 | |
| 20 | 2005 | 13 |
About Joan Atkin
Joan Atkin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Clinical Biochemistry and Genetics, having authored 26 papers that have together received 1.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Epigenetics and DNA Methylation (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genetic Syndromes and Imprinting (3 papers), Congenital heart defects research (3 papers), Genomics and Chromatin Dynamics (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). The work is most often cited by research in Genetics (677 citations), Pediatrics, Perinatology and Child Health (325 citations), Neurology (152 citations), Molecular Biology (672 citations) and Developmental Biology (19 citations). Joan Atkin has collaborated with scholars based in United States, Canada and Netherlands. Frequent co-authors include Gail E. Herman, Thomas W. Prior, Bruce E. Maley, MIROSLAVA B. NIKITOVITCH-WINER, Kandamurugu Manickam, Matthew Pastore, Liz Varga, Kim L. McBride, James F. Reynolds and Shivanand R. Patil. Their work appears in journals such as European Journal of Medical Genetics, Nature Genetics, Human Molecular Genetics, Human Mutation and Ophthalmic 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.