Audrey Lynn
Impact in
- Genetics top 5%
- Genetic Mapping and Diversity in Plants and Animals
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 10%
- DNA Repair Mechanisms
- Genomics and Chromatin Dynamics
- CRISPR and Genetic Engineering
- Amyloidosis: Diagnosis, Treatment, Outcomes
Papers in
-
- DNA Repair Mechanisms 8
- Mitochondrial Function and Pathology 4
- Genomics and Chromatin Dynamics 4
- Epigenetics and DNA Methylation 2
- Genetics 6
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Terry Hassold (5 shared papers)G. Valentin Börner (1 shared paper)Patricia A. Hunt (3 shared papers)Aravinda Chakravarti (9 shared papers)Kara E. Koehler (2 shared papers)Terry Ashley (1 shared paper)LuAnn Judis (2 shared papers)Stuart Schwartz (2 shared papers)
- Journals
- Annals of Neurology (2 papers)Alzheimer s & Dementia (2 papers)Genomics (2 papers)Annual Review of Genomics and Human Genetics (1 paper)Genetics (1 paper)
- Partner nations
- United StatesSwitzerlandGreece
In The Last Decade
Audrey Lynn
22 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 90
- Genetics 398
- Molecular Biology 821
- Plant Science 310
- Cell Biology 112
- Pediatrics, Perinatology and Child Health 110
Countries citing papers authored by Audrey Lynn
This map shows the geographic impact of Audrey 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 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 Lynn more than expected).
Fields of papers citing papers by Audrey Lynn
This network shows the impact of papers produced by Audrey 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 Lynn. The network helps show where Audrey Lynn may publish in the future.
Co-authors
The 25 scholars most cited alongside Audrey 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 233 | |
| 2 | 2002 | 220 | |
| 3 | 2004 | 129 | |
| 4 | 1997 | 110 | |
| 5 | 2002 | 96 | |
| 6 | Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3. | 1996 | 87 |
| 7 | Genetic epidemiology of rheumatoid arthritis. | 1995 | 70 |
| 8 | 2010 | 68 | |
| 9 | 2005 | 49 | |
| 10 | 2004 | 48 | |
| 11 | 2000 | 40 | |
| 12 | 1997 | 40 | |
| 13 | A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination. | 1995 | 29 |
| 14 | 2004 | 28 | |
| 15 | 1996 | 26 | |
| 16 | 2007 | 19 | |
| 17 | 1998 | 16 | |
| 18 | 2024 | 6 | |
| 19 | 1996 | 6 | |
| 20 | 1996 | 2 |
About Audrey Lynn
Audrey Lynn is a scholar working on Molecular Biology, Genetics, Plant Science, Pediatrics, Perinatology and Child Health and Cell Biology, having authored 22 papers that have together received 1.3k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (8 papers), Genomic variations and chromosomal abnormalities (5 papers), Mitochondrial Function and Pathology (4 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (4 papers), Alzheimer's disease research and treatments (3 papers), Prenatal Screening and Diagnostics (3 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Genetics (398 citations), Molecular Biology (821 citations), Plant Science (310 citations), Cell Biology (112 citations) and Pediatrics, Perinatology and Child Health (110 citations). Audrey Lynn has collaborated with scholars based in United States, Switzerland and Greece. Frequent co-authors include Terry Hassold, G. Valentin Börner, Patricia A. Hunt, Aravinda Chakravarti, Kara E. Koehler, Terry Ashley, LuAnn Judis, Stuart Schwartz, E. Ricky Chan and Stylianos E. Antonarakis. Their work appears in journals such as Annals of Neurology, Alzheimer s & Dementia, Genomics, Annual Review of Genomics and Human Genetics and 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.