Keri Ramsey

2.2k total citations
17 papers, 511 citations indexed

About

Keri Ramsey is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Keri Ramsey has authored 17 papers receiving a total of 511 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Physiology. Recurrent topics in Keri Ramsey's work include Alzheimer's disease research and treatments (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Keri Ramsey is often cited by papers focused on Alzheimer's disease research and treatments (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Keri Ramsey collaborates with scholars based in United States, Netherlands and Germany. Keri Ramsey's co-authors include Winnie S. Liang, Richard J. Caselli, Daniel W. McKeel, Joseph Rogers, Christine M. Hulette, Thomas G. Beach, Dietrich A. Stephan, John C. Morris, Diego Mastroeni and Eric M. Reiman and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Scientific Reports.

In The Last Decade

Keri Ramsey

13 papers receiving 507 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Keri Ramsey United States 9 324 215 94 81 72 17 511
Xianxiao Zhou United States 14 458 1.4× 187 0.9× 83 0.9× 81 1.0× 145 2.0× 34 751
J. Nicholas Cochran United States 12 291 0.9× 316 1.5× 139 1.5× 129 1.6× 91 1.3× 24 617
Meike Hick Germany 11 235 0.7× 375 1.7× 211 2.2× 71 0.9× 54 0.8× 14 565
Benjamin Siddoway United States 11 382 1.2× 116 0.5× 153 1.6× 133 1.6× 73 1.0× 13 613
T.G. Beach United States 1 250 0.8× 151 0.7× 52 0.6× 48 0.6× 121 1.7× 2 464
Natacha Coppieters New Zealand 11 405 1.3× 116 0.5× 44 0.5× 136 1.7× 104 1.4× 18 624
Minerva M. Carrasquillo United States 9 266 0.8× 295 1.4× 41 0.4× 147 1.8× 68 0.9× 13 479
Talisha A. Hunter United States 8 234 0.7× 316 1.5× 53 0.6× 100 1.2× 77 1.1× 8 484
Joo In Jung United States 11 270 0.8× 134 0.6× 63 0.7× 130 1.6× 23 0.3× 11 486

Countries citing papers authored by Keri Ramsey

Since Specialization
Citations

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

Fields of papers citing papers by Keri Ramsey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keri Ramsey

This figure shows the co-authorship network connecting the top 25 collaborators of Keri Ramsey. A scholar is included among the top collaborators of Keri Ramsey 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 Keri Ramsey. Keri Ramsey is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Ramsey, Keri, et al.. (2024). Managing Gastrointestinal Symptoms Resulting from Treatment with Trofinetide for Rett Syndrome: Caregiver and Nurse Perspectives. Advances in Therapy. 41(4). 1305–1317. 3 indexed citations
2.
Belnap, Newell, Keri Ramsey, Alon Abraham, et al.. (2024). Expanded carrier screening for inherited genetic disease using exome and genome sequencing. Journal of Genetic Counseling. 34(2). e1964–e1964.
3.
Ramsey, Keri, Marcus Naymik, Jennifer L. Sloan, et al.. (2024). Duchenne Muscular Dystrophy in Two Half-Brothers Due to Inherited 306 Kb Inverted Insertion of 10p15.1 into Intron 44 of the Dp427m Transcript of the DMD Gene. International Journal of Molecular Sciences. 25(22). 11922–11922.
4.
Belnap, Newell, et al.. (2024). Exploring the Frontier: The Human Microbiome’s Role in Rare Childhood Neurological Diseases and Epilepsy. Brain Sciences. 14(11). 1051–1051. 1 indexed citations
5.
Hernández, Ciria C., Ningning Hu, Wangzhen Shen, et al.. (2023). GABRG2 Variants Associated with Febrile Seizures. Biomolecules. 13(3). 414–414. 11 indexed citations
6.
7.
Narayanan, Vinodh, et al.. (2021). A novel insertion mutation in atlastin 1 is associated with spastic quadriplegia, increased membrane tethering, and aberrant conformational switching. Journal of Biological Chemistry. 298(1). 101438–101438. 6 indexed citations
8.
Halperin, Rebecca F., Apurva M. Hegde, Jessica D. Lang, et al.. (2021). Improved methods for RNAseq-based alternative splicing analysis. Scientific Reports. 11(1). 10740–10740. 26 indexed citations
9.
Belnap, Newell, et al.. (2021). Progressive bilateral nuclear cataracts associated with cerebellar-facial-dental syndrome: case report, literature review, and identification of a new genetic variant. Journal of American Association for Pediatric Ophthalmology and Strabismus. 25(6). 370–373.
10.
11.
Chen, Chun‐An, Harinder Gill, Tanya N. Nelson, et al.. (2020). The expanding clinical phenotype of germline ABL1 ‐associated congenital heart defects and skeletal malformations syndrome. Human Mutation. 41(10). 1738–1744. 11 indexed citations
12.
Okur, Volkan, Ashley Wilson, Erica H. Gerkes, et al.. (2019). Clinical and genetic characterization of individuals with predicted deleterious PHIP variants. Molecular Case Studies. 5(4). a004200–a004200. 18 indexed citations
13.
Guzmán, Yomayra F., et al.. (2017). A gain-of-function mutation in the GRIK2 gene causes neurodevelopmental deficits. Neurology Genetics. 3(1). e129–e129. 35 indexed citations
14.
Rechem, Capucine Van, Brian R. Rood, Sébastien Pinte, et al.. (2009). Scavenger Chemokine (CXC Motif) Receptor 7 (CXCR7) Is a Direct Target Gene of HIC1 (Hypermethylated in Cancer 1). Journal of Biological Chemistry. 284(31). 20927–20935. 66 indexed citations
15.
Liang, Winnie S., Travis Dunckley, Thomas G. Beach, et al.. (2008). Neuronal gene expression in non-demented individuals with intermediate Alzheimer's Disease neuropathology. Neurobiology of Aging. 31(4). 549–566. 63 indexed citations
16.
Alter, Mark D., Daniel B. Rubin, Keri Ramsey, et al.. (2008). Variation in the Large-Scale Organization of Gene Expression Levels in the Hippocampus Relates to Stable Epigenetic Variability in Behavior. PLoS ONE. 3(10). e3344–e3344. 22 indexed citations
17.
Liang, Winnie S., Travis Dunckley, Thomas G. Beach, et al.. (2008). Altered neuronal gene expression in brain regions differentially affected by Alzheimer's disease: a reference data set. Physiological Genomics. 33(2). 240–256. 245 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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