Audrey H. Lynn
Impact in
- Developmental Biology top 5%
- Genetics top 5%
- Genetic Mapping and Diversity in Plants and Animals
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 4
- Nutrition, Genetics, and Disease 2
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- DNA Repair Mechanisms 7
- Mitochondrial Function and Pathology 5
- Genomics and Chromatin Dynamics 4
- Co-authors
- Terry J Hassold (5 shared papers)G. Valentin Börner (1 shared paper)Patricia A. Hunt (3 shared papers)Terry Ashley (1 shared paper)Aravinda Chakravarti (8 shared papers)Kara E. Koehler (2 shared papers)LuAnn M. Judis (2 shared papers)Stuart H. Schwartz (2 shared papers)
- Journals
- Alzheimer s & Dementia (6 papers)Human Genetics and Genomics Advances (2 papers)Annals of Neurology (2 papers)Genomics (2 papers)Chromosome Research (1 paper)
- Partner nations
- United StatesSwitzerlandCanada
In The Last Decade
Audrey H. Lynn
29 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 98
- Developmental Biology 58
- Genetics 491
- Molecular Biology 1.0k
- Rheumatology 137
- Plant Science 307
Countries citing papers authored by Audrey H. Lynn
This map shows the geographic impact of Audrey H. Lynn'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 Audrey H. Lynn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Audrey H. Lynn more than expected).
Fields of papers citing papers by Audrey H. Lynn
This network shows the impact of papers produced by Audrey H. Lynn. 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 Audrey H. Lynn. The network helps show where Audrey H. Lynn may publish in the future.
Co-authors
The 25 scholars most cited alongside Audrey H. Lynn, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 240 | |
| 2 | 1997 | 237 | |
| 3 | 2002 | 225 | |
| 4 | 2004 | 139 | |
| 5 | 1997 | 120 | |
| 6 | 2002 | 95 | |
| 7 | Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3. | 1996 | 92 |
| 8 | Genetic epidemiology of rheumatoid arthritis. | 1995 | 74 |
| 9 | 2010 | 72 | |
| 10 | 2004 | 55 | |
| 11 | 2005 | 55 | |
| 12 | 1997 | 41 | |
| 13 | 2004 | 31 | |
| 14 | A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination. | 1995 | 30 |
| 15 | 1996 | 26 | |
| 16 | 2007 | 19 | |
| 17 | 1998 | 17 | |
| 18 | 2025 | 14 | |
| 19 | 2024 | 7 | |
| 20 | 1996 | 6 |
About Audrey H. Lynn
Audrey H. Lynn is a scholar working on Genetics, Molecular Biology, Cell Biology, Pediatrics, Perinatology and Child Health and Physiology, having authored 31 papers that have together received 1.6k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (7 papers), Mitochondrial Function and Pathology (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Chromatin Dynamics (4 papers), Prenatal Screening and Diagnostics (3 papers), Chromosomal and Genetic Variations (3 papers), Alzheimer's disease research and treatments (3 papers) and Nutrition, Genetics, and Disease (2 papers). The work is most often cited by research in Developmental Biology (58 citations), Genetics (491 citations), Molecular Biology (1.0k citations), Rheumatology (137 citations) and Plant Science (307 citations). Audrey H. Lynn has collaborated with scholars based in United States, Switzerland and Canada. Frequent co-authors include Terry J Hassold, G. Valentin Börner, Patricia A. Hunt, Terry Ashley, Aravinda Chakravarti, Kara E. Koehler, LuAnn M. Judis, Stuart H. Schwartz, Ernest Ricky Chan and Allen D. Seftel. Their work appears in journals such as Alzheimer s & Dementia, Human Genetics and Genomics Advances, Annals of Neurology, Genomics and Chromosome Research.
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.