Ascia Eskin

4.8k total citations
33 papers, 1.9k citations indexed

About

Ascia Eskin is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Ascia Eskin has authored 33 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 6 papers in Genetics and 6 papers in Genetics. Recurrent topics in Ascia Eskin's work include Muscle Physiology and Disorders (7 papers), Glioma Diagnosis and Treatment (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Ascia Eskin is often cited by papers focused on Muscle Physiology and Disorders (7 papers), Glioma Diagnosis and Treatment (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Ascia Eskin collaborates with scholars based in United States, Singapore and France. Ascia Eskin's co-authors include Stanley F. Nelson, Linda M. Liau, Robert M. Prins, Horacio Soto, William H. Yong, Vera Konkankit, Sylvia K. Odesa, Zugen Chen, Hane Lee and Barry Merriman and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Circulation.

In The Last Decade

Ascia Eskin

33 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ascia Eskin United States 22 957 547 358 358 348 33 1.9k
Stéphan Saïkali France 23 701 0.7× 769 1.4× 205 0.6× 372 1.0× 303 0.9× 61 1.9k
Björn Scheffler Germany 30 1.4k 1.5× 998 1.8× 219 0.6× 511 1.4× 483 1.4× 82 3.4k
Violeta Silva-Vargas United States 16 2.0k 2.0× 445 0.8× 226 0.6× 500 1.4× 595 1.7× 17 3.7k
Joseph Najbauer United States 26 1.4k 1.4× 618 1.1× 246 0.7× 366 1.0× 852 2.4× 41 2.6k
Siddhartha S. Mitra United States 23 960 1.0× 837 1.5× 921 2.6× 308 0.9× 613 1.8× 52 2.5k
A. Jonas Ekstrand Sweden 12 1.1k 1.2× 634 1.2× 179 0.5× 362 1.0× 795 2.3× 16 2.3k
Yonehiro Kanemura Japan 31 1.6k 1.7× 985 1.8× 251 0.7× 355 1.0× 342 1.0× 175 3.5k
Giuseppe Lamorte Italy 22 1.5k 1.5× 526 1.0× 245 0.7× 441 1.2× 804 2.3× 44 2.5k
Roland H. Friedel United States 34 1.5k 1.6× 224 0.4× 349 1.0× 249 0.7× 367 1.1× 61 2.9k
Abhik Ray‐Chaudhury United States 22 943 1.0× 285 0.5× 123 0.3× 557 1.6× 226 0.6× 55 1.8k

Countries citing papers authored by Ascia Eskin

Since Specialization
Citations

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

Fields of papers citing papers by Ascia Eskin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ascia Eskin

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

All Works

20 of 20 papers shown
1.
Wilkes, Mark C., Hee‐Don Chae, Alma‐Martina Cepika, et al.. (2023). SATB1 Chromatin Loops Regulate Megakaryocyte/Erythroid Progenitor Expansion by Facilitating HSP70 and GATA1 Induction. Stem Cells. 41(6). 560–569. 1 indexed citations
2.
Wilkes, Mark C., Alma‐Martina Cepika, Ascia Eskin, et al.. (2022). Downregulation of SATB1 by miRNAs reduces megakaryocyte/erythroid progenitor expansion in preclinical models of Diamond–Blackfan anemia. Experimental Hematology. 111. 66–78. 5 indexed citations
3.
Chia, Poh Hui, Franklin L. Zhong, Shinsuke Niwa, et al.. (2018). A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability. eLife. 7. 44 indexed citations
4.
Garrett, Matthew C., Jantzen Sperry, Daniel Braas, et al.. (2018). Metabolic characterization of isocitrate dehydrogenase (IDH) mutant and IDH wildtype gliomaspheres uncovers cell type-specific vulnerabilities. SHILAP Revista de lepidopterología. 6(1). 4–4. 51 indexed citations
5.
Barseghyan, Hayk, Ascia Eskin, Matthew S. Bramble, et al.. (2018). Identification of novel candidate genes for 46,XY disorders of sex development (DSD) using a C57BL/6J-Y POS mouse model. Biology of Sex Differences. 9(1). 8–8. 21 indexed citations
6.
Bramble, Matthew S., Allen Lipson, Tuck C. Ngun, et al.. (2016). A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing. Human Reproduction. 31(4). 905–914. 63 indexed citations
7.
Kramerova, Irina, Natalia Ermolova, Ascia Eskin, et al.. (2016). Failure to up-regulate transcription of genes necessary for muscle adaptation underlies limb girdle muscular dystrophy 2A (calpainopathy). Human Molecular Genetics. 25(11). 2194–2207. 29 indexed citations
8.
Bramble, Matthew S., Allen Lipson, Ascia Eskin, et al.. (2016). Sex-Specific Effects of Testosterone on the Sexually Dimorphic Transcriptome and Epigenome of Embryonic Neural Stem/Progenitor Cells. Scientific Reports. 6(1). 36916–36916. 33 indexed citations
9.
Shboul, Mohammad, Valério Taverniti, Carine Bonnard, et al.. (2015). Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects. Human Molecular Genetics. 24(11). 3163–3171. 25 indexed citations
10.
Brown, Robert, Hane Lee, Ascia Eskin, et al.. (2015). Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders. European Journal of Human Genetics. 24(1). 113–119. 2 indexed citations
11.
Eyre, Harris A., Ascia Eskin, Stanley F. Nelson, et al.. (2015). Genomic predictors of remission to antidepressant treatment in geriatric depression using genome‐wide expression analyses: a pilot study. International Journal of Geriatric Psychiatry. 31(5). 510–517. 16 indexed citations
12.
Patananan, Alexander N., et al.. (2014). Ethanol-induced differential gene expression and acetyl-CoA metabolism in a longevity model of the nematode Caenorhabditis elegans. Experimental Gerontology. 61. 20–30. 21 indexed citations
13.
Swaggart, Kayleigh A., Alexis R. Demonbreun, Andy H. Vo, et al.. (2014). Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair. Proceedings of the National Academy of Sciences. 111(16). 6004–6009. 111 indexed citations
14.
Tanaka, Karo, Ascia Eskin, Fabrice Chareyre, et al.. (2013). Therapeutic Potential of HSP90 Inhibition for Neurofibromatosis Type 2. Clinical Cancer Research. 19(14). 3856–3870. 28 indexed citations
15.
Pope, Whitney B., Leili Mirsadraei, Albert Lai, et al.. (2012). Differential Gene Expression in Glioblastoma Defined by ADC Histogram Analysis: Relationship to Extracellular Matrix Molecules and Survival. American Journal of Neuroradiology. 33(6). 1059–1064. 58 indexed citations
16.
Liu, Yue, Fei Ye, Kazunari Yamada, et al.. (2011). Autocrine Endothelin-3/Endothelin Receptor B Signaling Maintains Cellular and Molecular Properties of Glioblastoma Stem Cells. Molecular Cancer Research. 9(12). 1668–1685. 30 indexed citations
17.
Kim, Won, Richard C. Koya, Ascia Eskin, et al.. (2011). Decitabine immunosensitizes human gliomas to NY-ESO-1 specific T lymphocyte targeting through the Fas/Fas Ligand pathway. Journal of Translational Medicine. 9(1). 192–192. 39 indexed citations
18.
Prins, Robert M., Horacio Soto, Vera Konkankit, et al.. (2010). Gene Expression Profile Correlates with T-Cell Infiltration and Relative Survival in Glioblastoma Patients Vaccinated with Dendritic Cell Immunotherapy. Clinical Cancer Research. 17(6). 1603–1615. 334 indexed citations
19.
Clark, Michael J., Nils Homer, Brian D. O’Connor, et al.. (2010). U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line. PLoS Genetics. 6(1). e1000832–e1000832. 214 indexed citations
20.
Eskin, Ascia, Jun Dong, Stanley F. Nelson, et al.. (2009). Stem cell associated gene expression in glioblastoma multiforme: relationship to survival and the subventricular zone. Journal of Neuro-Oncology. 96(3). 359–367. 81 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026