Vidya Ramesh

522 total citations
5 papers, 386 citations indexed

About

Vidya Ramesh is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Vidya Ramesh has authored 5 papers receiving a total of 386 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Genetics. Recurrent topics in Vidya Ramesh's work include Genetics and Neurodevelopmental Disorders (3 papers), Epigenetics and DNA Methylation (2 papers) and Amyotrophic Lateral Sclerosis Research (1 paper). Vidya Ramesh is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Epigenetics and DNA Methylation (2 papers) and Amyotrophic Lateral Sclerosis Research (1 paper). Vidya Ramesh collaborates with scholars based in Germany, United Kingdom and France. Vidya Ramesh's co-authors include François Guillemot, Diogo S. Castro, Daniela Drechsel, Charles J. Hunt, Noel J. Buckley, Carlos Parras, Angela Bithell, Ben Martynoga, Emilie Pacary and Dirk Dolle and has published in prestigious journals such as Genes & Development, PLoS ONE and Glia.

In The Last Decade

Vidya Ramesh

5 papers receiving 378 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vidya Ramesh Germany	4	317	142	66	53	41	5	386
Tessa Walcher Germany	5	271 0.9×	128 0.9×	53 0.8×	87 1.6×	49 1.2×	5	430
Ariane Baudhuin United States	9	250 0.8×	85 0.6×	92 1.4×	71 1.3×	47 1.1×	9	511
Mireia Moreno‐Estellés Spain	8	301 0.9×	87 0.6×	70 1.1×	66 1.2×	38 0.9×	13	438
Anjana Nityanandam United States	9	323 1.0×	135 1.0×	127 1.9×	52 1.0×	49 1.2×	12	502
Frada Berenshteyn United States	5	355 1.1×	69 0.5×	92 1.4×	90 1.7×	23 0.6×	6	446
Dhananjay Yellajoshyula United States	9	272 0.9×	81 0.6×	87 1.3×	47 0.9×	36 0.9×	13	353
Anke Schardt Germany	8	241 0.8×	136 1.0×	101 1.5×	28 0.5×	36 0.9×	8	422
Yujin Harada Japan	5	207 0.7×	182 1.3×	53 0.8×	34 0.6×	65 1.6×	5	293
Matthew G. Andrusiak Canada	10	274 0.9×	74 0.5×	63 1.0×	31 0.6×	55 1.3×	11	399
Vivian M. Lee United States	8	328 1.0×	87 0.6×	102 1.5×	64 1.2×	93 2.3×	13	456

Countries citing papers authored by Vidya Ramesh

Since Specialization

Citations

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

Fields of papers citing papers by Vidya Ramesh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vidya Ramesh

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

All Works

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5 of 5 papers shown

1.

Ramesh, Vidya, Karen Burr, Biju Viswanath, et al.. (2025). The Fragile X Messenger Ribonucleoprotein 1 Regulates the Morphology and Maturation of Human and Rat Oligodendrocytes. Glia. 73(6). 1203–1220. 1 indexed citations

2.

Ramesh, Vidya, et al.. (2024). Neuronal Circuit Dysfunction in Amyotrophic Lateral Sclerosis. Cells. 13(10). 792–792. 3 indexed citations

3.

Ramesh, Vidya, Efil Bayam, Filippo M. Cernilogar, et al.. (2016). Loss of Uhrf1 in neural stem cells leads to activation of retroviral elements and delayed neurodegeneration. Genes & Development. 30(19). 2199–2212. 49 indexed citations

4.

Seibt, Julie, Olivier Armant, Anne Le Digarcher, et al.. (2012). Expression at the Imprinted Dlk1-Gtl2 Locus Is Regulated by Proneural Genes in the Developing Telencephalon. PLoS ONE. 7(11). e48675–e48675. 23 indexed citations

5.

Castro, Diogo S., Ben Martynoga, Carlos Parras, et al.. (2011). A novel function of the proneural factor Ascl1 in progenitor proliferation identified by genome-wide characterization of its targets. Genes & Development. 25(9). 930–945. 310 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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