Amanda Myers

26.4k total citations · 1 hit paper
56 papers, 3.0k citations indexed

About

Amanda Myers is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Amanda Myers has authored 56 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 26 papers in Physiology and 18 papers in Genetics. Recurrent topics in Amanda Myers's work include Alzheimer's disease research and treatments (26 papers), Genetic Associations and Epidemiology (15 papers) and Bioinformatics and Genomic Networks (12 papers). Amanda Myers is often cited by papers focused on Alzheimer's disease research and treatments (26 papers), Genetic Associations and Epidemiology (15 papers) and Bioinformatics and Genomic Networks (12 papers). Amanda Myers collaborates with scholars based in United States, United Kingdom and Australia. Amanda Myers's co-authors include John Hardy, Anzhelika Engel, Alison Goate, Tanja Jovanović, Kerry J. Ressler, Bekh Bradley, Kristina B. Mercer, Kimberly Kerley, Manuel Ramı́rez and Karen M. Braas and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and PLoS ONE.

In The Last Decade

Amanda Myers

55 papers receiving 3.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Post-traumatic stress disorder is associated with PACAP and the PAC1 receptor

2011 617 citations Kerry J. Ressler, Tanja Jovanović et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amanda Myers United States	25	1.1k	1.0k	597	514	388	56	3.0k
Goran Šimić Croatia	29	1.2k 1.1×	1.3k 1.3×	739 1.2×	222 0.4×	578 1.5×	106	4.1k
David St Clair United Kingdom	40	1.6k 1.4×	738 0.7×	751 1.3×	1.0k 2.0×	230 0.6×	114	4.6k
Sabine Bahn United Kingdom	35	2.2k 1.9×	721 0.7×	631 1.1×	686 1.3×	241 0.6×	74	4.2k
Dan Ehninger Germany	34	1.8k 1.6×	1.1k 1.1×	1.2k 2.0×	889 1.7×	595 1.5×	87	4.7k
Ling‐Qiang Zhu China	41	2.4k 2.1×	1.2k 1.2×	1.0k 1.7×	345 0.7×	672 1.7×	128	4.9k
Barbara J. Caldarone United States	34	1.9k 1.6×	943 0.9×	1.2k 2.1×	177 0.3×	783 2.0×	67	4.0k
Qi Xu China	32	1.3k 1.1×	351 0.3×	637 1.1×	438 0.9×	240 0.6×	133	2.9k
Luisella Bocchio‐Chiavetto Italy	31	814 0.7×	448 0.4×	723 1.2×	244 0.5×	518 1.3×	64	3.1k
Roberto Carlos Agís‐Balboa Spain	27	1.9k 1.6×	565 0.5×	784 1.3×	778 1.5×	323 0.8×	44	3.5k
Francesco Impagnatiello United States	31	1.7k 1.5×	479 0.5×	1.8k 3.1×	618 1.2×	477 1.2×	51	4.4k

Countries citing papers authored by Amanda Myers

Since Specialization

Citations

This map shows the geographic impact of Amanda Myers'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 Amanda Myers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amanda Myers more than expected).

Fields of papers citing papers by Amanda Myers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amanda Myers. 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 Amanda Myers. The network helps show where Amanda Myers may publish in the future.

Co-authorship network of co-authors of Amanda Myers

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda Myers. A scholar is included among the top collaborators of Amanda Myers 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 Amanda Myers. Amanda Myers 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

Leonenko, Ganna, Eftychia Bellou, Amanda Myers, et al.. (2024). Chromosome X-wide association study in case control studies of pathologically confirmed Alzheimer’s disease in a European population. Translational Psychiatry. 14(1). 358–358. 4 indexed citations

Branciamore, Sergio, Grigoriy Gogoshin, Andréi S. Rodin, & Amanda Myers. (2024). Changes in expression of VGF, SPECC1L, HLA-DRA and RANBP3L act with APOE E4 to alter risk for late onset Alzheimer’s disease. Scientific Reports. 14(1). 14954–14954. 1 indexed citations

Baker, Emily, Ganna Leonenko, Karl Michael Schmidt, et al.. (2023). What does heritability of Alzheimer’s disease represent?. PLoS ONE. 18(4). e0281440–e0281440. 22 indexed citations

Wuchty, Stefan, Amanda Myers, Manuel Ramirez‐Restrepo, et al.. (2021). Integration of peripheral transcriptomics, genomics, and interactomics following trauma identifies causal genes for symptoms of post-traumatic stress and major depression. Molecular Psychiatry. 26(7). 3077–3092. 16 indexed citations

Escott‐Price, Valentina, Emily Baker, Maryam Shoai, et al.. (2019). Genetic analysis suggests high misassignment rates in clinical Alzheimer's cases and controls. Neurobiology of Aging. 77. 178–182. 10 indexed citations

Huentelman, Matt, Matthew De Both, Ignazio S. Piras, et al.. (2019). Common BACE2 Polymorphisms are Associated with Altered Risk for Alzheimer’s Disease and CSF Amyloid Biomarkers in APOE ε4 Non-Carriers. Scientific Reports. 9(1). 9640–9640. 16 indexed citations

Giraldo, Margarita, Francisco Lopera, Ashley L. Siniard, et al.. (2013). Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease. Neurobiology of Aging. 34(8). 2077.e11–2077.e18. 116 indexed citations

Swaminathan, Shanker, Matthew J. Huentelman, Jason J. Corneveaux, et al.. (2012). Analysis of Copy Number Variation in Alzheimer’s Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals. PLoS ONE. 7(12). e50640–e50640. 55 indexed citations

Lim, Andrew, Anne‐Marie Chang, Joshua Shulman, et al.. (2012). A common polymorphism near PER1 and the timing of human behavioral rhythms. Annals of Neurology. 72(3). 324–334. 32 indexed citations

10.

Myers, Amanda. (2012). AD Gene 3-D: Moving Past Single Layer Genetic Information to Map Novel Loci Involved in Alzheimer's Disease. Journal of Alzheimer s Disease. 33(s1). S15–S22. 4 indexed citations

11.

Jager, Philip L. De, Joshua Shulman, Lori B. Chibnik, et al.. (2011). A genome-wide scan for common variants affecting the rate of age-related cognitive decline. Neurobiology of Aging. 33(5). 1017.e1–1017.e15. 136 indexed citations

12.

Myers, Amanda. (2011). The age of the “ome”: Genome, transcriptome and proteome data set collection and analysis. Brain Research Bulletin. 88(4). 294–301. 7 indexed citations

13.

Liang, Winnie S., Kewei Chen, Wendy Lee, et al.. (2010). Association between GAB2 haplotype and higher glucose metabolism in Alzheimer's disease-affected brain regions in cognitively normal APOEε4 carriers. NeuroImage. 54(3). 1896–1902. 16 indexed citations

14.

Hamshere, Marian L., Peter Holmans, Dimitrios Avramopoulos, et al.. (2007). Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Human Molecular Genetics. 16(22). 2703–2712. 35 indexed citations

15.

Hardy, John, Alan Pittman, Amanda Myers, et al.. (2006). Tangle Diseases and the Tau Haplotypes. Alzheimer Disease & Associated Disorders. 20(1). 60–62. 6 indexed citations

16.

Hardy, John, Amanda Myers, & Fabienne Wavrant‐De Vrièze. (2004). Problems and Solutions in the Genetic Analysis of Late-Onset Alzheimer’s Disease. Neurodegenerative Diseases. 1(4-5). 213–217. 10 indexed citations

17.

Evans, E. Whitney, Hon‐Chung Fung, John C. Steele, et al.. (2004). The tau H2 haplotype is almost exclusively Caucasian in origin. Neuroscience Letters. 369(3). 183–185. 90 indexed citations

18.

Fung, Hon‐Chung, E. Whitney Evans, Jaime Duckworth, et al.. (2004). The architecture of the tau haplotype block in different ethnicities. Neuroscience Letters. 377(2). 81–84. 10 indexed citations

19.

Joyce, Jeffrey N., Amanda Myers, & Eugenia V. Gurevich. (1998). Dopamine D2 receptor bands in normal human temporal cortex are absent in Alzheimer's disease. Brain Research. 784(1-2). 7–17. 40 indexed citations

20.

Lendon, Corinne, Amanda Myers, Alistair Cumming, Alison Goate, & David St Clair. (1997). A polymorphism in the presenilin 1 gene does not modify risk for Alzheimer's disease in a cohort with sporadic early onset. Neuroscience Letters. 228(3). 212–214. 18 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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