Audrey Lynn

2.0k total citations
22 papers, 1.3k citations indexed

About

Audrey Lynn is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Audrey Lynn has authored 22 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Plant Science. Recurrent topics in Audrey Lynn's work include DNA Repair Mechanisms (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Mitochondrial Function and Pathology (4 papers). Audrey Lynn is often cited by papers focused on DNA Repair Mechanisms (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Mitochondrial Function and Pathology (4 papers). Audrey Lynn collaborates with scholars based in United States, Switzerland and Greece. Audrey Lynn's co-authors include Terry Hassold, G. Valentin Börner, Patricia A. Hunt, Aravinda Chakravarti, Terry Ashley, Kara E. Koehler, Stuart Schwartz, E. Ricky Chan, LuAnn Judis and Stylianos E. Antonarakis and has published in prestigious journals such as Science, Annals of Neurology and American Journal of Epidemiology.

In The Last Decade

Audrey Lynn

21 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Audrey Lynn United States	17	852	430	329	120	117	22	1.3k
Alastair S. H. Goldman United Kingdom	21	1.1k 1.3×	436 1.0×	408 1.2×	171 1.4×	195 1.7×	41	1.5k
Abdelhamid Barakat Morocco	23	774 0.9×	491 1.1×	83 0.3×	88 0.7×	84 0.7×	132	1.6k
Donncha S. Dunican United Kingdom	17	1.6k 1.9×	388 0.9×	148 0.4×	106 0.9×	64 0.5×	21	1.8k
Ramaiah Nagaraja United States	20	1.1k 1.3×	609 1.4×	211 0.6×	83 0.7×	32 0.3×	44	1.5k
Sharon L. Wenger United States	24	790 0.9×	985 2.3×	243 0.7×	231 1.9×	47 0.4×	83	1.6k
Jesús del Mazo Spain	24	1.2k 1.4×	356 0.8×	258 0.8×	139 1.2×	129 1.1×	77	1.7k
Irina Stancheva United Kingdom	23	1.8k 2.1×	626 1.5×	115 0.3×	103 0.9×	48 0.4×	28	2.0k
Daniel M. Messerschmidt Singapore	18	1.5k 1.7×	437 1.0×	139 0.4×	341 2.8×	111 0.9×	30	1.9k
Giovanna Floridia Italy	19	1.3k 1.5×	1.4k 3.3×	494 1.5×	208 1.7×	61 0.5×	48	1.9k
Panayiotis A. Ioannou Australia	22	774 0.9×	489 1.1×	224 0.7×	108 0.9×	41 0.4×	44	1.4k

Countries citing papers authored by Audrey Lynn

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Audrey Lynn

This figure shows the co-authorship network connecting the top 25 collaborators of Audrey Lynn. A scholar is included among the top collaborators of Audrey Lynn based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Audrey Lynn. Audrey Lynn is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lynn, Audrey, Kristy Miskimen, Yeunjoo E. Song, et al.. (2024). Genome‐wide association studies identify novel loci in rapidly progressive Alzheimer's disease. Alzheimer s & Dementia. 20(3). 2034–2046. 5 indexed citations

Wang, Ping, Audrey Lynn, Yeunjoo E. Song, & Jonathan L. Haines. (2022). Distinct features of rapidly progressive Alzheimer’s disease. Alzheimer s & Dementia. 18(S7).

Acheson, Louise S., Catharine Wang, Stephen J. Zyzanski, et al.. (2010). Family history and perceptions about risk and prevention for chronic diseases in primary care: A report from the Family Healthware™ Impact Trial. Genetics in Medicine. 12(4). 212–218. 68 indexed citations

Strohl, Kingman P., Audrey Lynn, Lee Friedman, et al.. (2007). Sleep-Related Epilepsy in the A/J Mouse. SLEEP. 30(2). 169–176. 18 indexed citations

Lynn, Audrey, et al.. (2007). ZMM proteins during meiosis: Crossover artists at work. Chromosome Research. 15(5). 591–605. 230 indexed citations

Lynn, Audrey, et al.. (2005). Sex, Not Genotype, Determines Recombination Levels in Mice. The American Journal of Human Genetics. 77(4). 670–675. 48 indexed citations

Neilson, Derek, Heidi S. Feiler, Kirk C. Wilhelmsen, et al.. (2004). Autosomal dominant acute necrotizing encephalopathy maps to 2q12.1‐2q13. Annals of Neurology. 55(2). 291–294. 28 indexed citations

Lynn, Audrey, Terry Ashley, & Terry Hassold. (2004). VARIATION IN HUMAN MEIOTIC RECOMBINATION. Annual Review of Genomics and Human Genetics. 5(1). 317–349. 128 indexed citations

Koehler, Kara E., et al.. (2002). Genetic Control of Mammalian Meiotic Recombination. I. Variation in Exchange Frequencies Among Males From Inbred Mouse Strains. Genetics. 162(1). 297–306. 94 indexed citations

10.

Lynn, Audrey, Carl Kashuk, Michael B. Petersen, et al.. (2000). Patterns of Meiotic Recombination on the Long Arm of Human Chromosome 21. Genome Research. 10(9). 1319–1332. 40 indexed citations

11.

Potier, Marie‐Claude, Annie Dutriaux, Georgia Karadima, et al.. (1998). Two Sequence-Ready Contigs Spanning the Two Copies of a 200-kb Duplication on Human 21q: Partial Sequence and Polymorphisms. Genomics. 51(3). 417–426. 16 indexed citations

12.

Petersen, Robert B., Hershel Goren, Michael Cohen, et al.. (1997). Transthyretin amyloidosis: A new mutation associated with dementia. Annals of Neurology. 41(3). 307–313. 110 indexed citations

13.

Petersen, Michael B., Catherine Tomasetto, Audrey Lynn, & Aravinda Chakravarti. (1997). A Pvull polymorphism detected by a cDNA clone of the gene encoding the human spasmolytic protein (SML1 gene), one of three members of the trefoil peptide gene family clustered on chromosome 21q22.3. Clinical Genetics. 52(4). 247–248. 1 indexed citations

14.

Chen, Haiming, Colette Rossier, Yusuke Nakamura, et al.. (1997). Cloning of a Novel Homeobox-Containing Gene,PKNOX1,and Mapping to Human Chromosome 21q22.3. Genomics. 41(2). 193–200. 40 indexed citations

15.

Kwoh, C. Kent, et al.. (1996). Age, Sex, and the Familial Risk of Rheumatoid Arthritis. American Journal of Epidemiology. 144(1). 15–24. 26 indexed citations

16.

Cohen, Tirza, Barbara McGillivray, Judith G. Hall, et al.. (1996). Segregation analysis of microcephaly. American Journal of Medical Genetics. 65(3). 226–234. 6 indexed citations

17.

Cohen, Tirza, Barbara McGillivray, Judith G. Hall, et al.. (1996). Segregation analysis of microcephaly. American Journal of Medical Genetics. 65(3). 226–234. 2 indexed citations

18.

Chen, Haiming, Colette Rossier, Maria D. Lalioti, et al.. (1996). Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3.. PubMed. 59(1). 66–75. 87 indexed citations

19.

Christie, Derek Pierre, Arnaud Gos, Audrey Lynn, et al.. (1995). A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.. PubMed. 57(2). 388–94. 29 indexed citations

20.

Lynn, Audrey, et al.. (1995). Genetic epidemiology of rheumatoid arthritis.. PubMed. 57(1). 150–9. 70 indexed citations

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.

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