Keri Ramsey

1.4k total citations
14 papers, 255 citations indexed

About

Keri Ramsey is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Keri Ramsey has authored 14 papers receiving a total of 255 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Keri Ramsey's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and RNA Research and Splicing (3 papers). Keri Ramsey is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and RNA Research and Splicing (3 papers). Keri Ramsey collaborates with scholars based in United States, Canada and Belgium. Keri Ramsey's co-authors include David W. Craig, Vinodh Narayanan, Isabelle Schrauwen, Dietrich Stephan, Gregory G. Heuer, Scott Gottlieb, Erik G. Puffenberger, D. Holmes Morton, David A. Ramsay and Ashley L. Siniard and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Keri Ramsey

14 papers receiving 253 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Keri Ramsey United States	10	163	97	54	43	27	14	255
Fılız Hazan Türkiye	10	183 1.1×	119 1.2×	46 0.9×	32 0.7×	24 0.9×	54	309
Shinobu Fukumura Japan	11	149 0.9×	55 0.6×	43 0.8×	53 1.2×	44 1.6×	29	272
Chris Esapa United Kingdom	8	271 1.7×	92 0.9×	57 1.1×	34 0.8×	48 1.8×	9	320
Andrey Goltsov Russia	9	168 1.0×	65 0.7×	84 1.6×	36 0.8×	19 0.7×	19	314
Omid Aryani Iran	10	186 1.1×	86 0.9×	42 0.8×	58 1.3×	30 1.1×	42	307
Julie A. Jurgens United States	11	148 0.9×	124 1.3×	38 0.7×	25 0.6×	10 0.4×	14	298
Emmanuelle Ranza Switzerland	12	137 0.8×	103 1.1×	19 0.4×	20 0.5×	36 1.3×	22	295
Dalia Ghoneim United States	10	277 1.7×	125 1.3×	59 1.1×	18 0.4×	31 1.1×	15	409
Tuva Barøy Norway	12	221 1.4×	161 1.7×	27 0.5×	24 0.6×	44 1.6×	21	333
Piotr Gasperowicz Poland	12	191 1.2×	74 0.8×	22 0.4×	20 0.5×	42 1.6×	23	312

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

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14 of 14 papers shown

Ramsey, Keri, et al.. (2024). Family and caregiver perspectives on gene therapy for Rett syndrome. SHILAP Revista de lepidopterología. 2. 100045–100045. 2 indexed citations

Belnap, Newell, Marcus Naymik, Jennifer L. Sloan, et al.. (2023). Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: A novel SMS gene variant. SHILAP Revista de lepidopterología. 2. 100017–100017. 2 indexed citations

Wongkittichote, Parith, Tae‐Ik Choi, Dwight D. Koeberl, et al.. (2022). Expanding allelic and phenotypic spectrum of ZC4H2‐related disorder: A novel hypomorphic variant and high prevalence of tethered cord. Clinical Genetics. 103(2). 167–178. 5 indexed citations

Wie, Jinhong, Vinodh Narayanan, Keri Ramsey, et al.. (2020). Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex. Nature Communications. 11(1). 3351–3351. 19 indexed citations

Llaci, Lorida, Keri Ramsey, Newell Belnap, et al.. (2019). Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD). Human Genetics. 138(11-12). 1409–1417. 12 indexed citations

Szelinger, Szabolcs, Newell Belnap, Keri Ramsey, et al.. (2019). Utilizing RNA and outlier analysis to identify an intronic splice‐altering variant inAP4S1in a sibling pair with progressive spastic paraplegia. Human Mutation. 41(2). 412–419. 5 indexed citations

Liktor‐Busa, Erika, Aubin Moutal, Sara S. Parker, et al.. (2018). A novel variant in TAF1 affects gene expression and is associated with X-linked TAF1 intellectual disability syndrome. PubMed. 2(3). NS20180141–NS20180141. 14 indexed citations

Wojcik, Monica H., Kyoko Okada, Sanjay P. Prabhu, et al.. (2018). De novo variant in KIF26B is associated with pontocerebellar hypoplasia with infantile spinal muscular atrophy. American Journal of Medical Genetics Part A. 176(12). 2623–2629. 19 indexed citations

Ramsey, Keri, Newell Belnap, Szabolcs Szelinger, et al.. (2017). Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results. Seminars in Pediatric Neurology. 26. 28–32. 9 indexed citations

10.

Narayanan, Vinodh, et al.. (2016). An atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach. Molecular Genetics and Metabolism Reports. 10. 38–44. 11 indexed citations

11.

Belnap, Newell, Ashley L. Siniard, Szabolcs Szelinger, et al.. (2016). A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia. Molecular Case Studies. 2(5). a000851–a000851. 15 indexed citations

12.

Schrauwen, Isabelle, Szabolcs Szelinger, Ashley L. Siniard, et al.. (2015). A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome. PLoS ONE. 10(7). e0131797–e0131797. 35 indexed citations

13.

Schrauwen, Isabelle, Szabolcs Szelinger, Ashley L. Siniard, et al.. (2015). A De Novo Mutation inTEAD1Causes Non–X-Linked Aicardi Syndrome. Investigative Ophthalmology & Visual Science. 56(6). 3896–3896. 14 indexed citations

14.

Puffenberger, Erik G., Kevin A. Strauss, Keri Ramsey, et al.. (2007). Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5. Brain. 130(7). 1929–1941. 93 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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