Galina Erikson

3.6k total citations · 1 hit paper
23 papers, 1.4k citations indexed

About

Galina Erikson is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Galina Erikson has authored 23 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Galina Erikson's work include Genomics and Chromatin Dynamics (5 papers), Genomics and Rare Diseases (4 papers) and Neuroinflammation and Neurodegeneration Mechanisms (3 papers). Galina Erikson is often cited by papers focused on Genomics and Chromatin Dynamics (5 papers), Genomics and Rare Diseases (4 papers) and Neuroinflammation and Neurodegeneration Mechanisms (3 papers). Galina Erikson collaborates with scholars based in United States, Germany and Switzerland. Galina Erikson's co-authors include Maxim N. Shokhirev, Matthew M. Boisvert, Nicola J. Allen, Ali Torkamani, Eric J. Topol, William C. Ferguson, Valentina Lo Sardo, Kristin K. Baldwin, Pradeep Reddy and Juan Carlos Izpisúa Belmonte and has published in prestigious journals such as Cell, Nucleic Acids Research and Nature Medicine.

In The Last Decade

Galina Erikson

22 papers receiving 1.4k 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.

The Aging Astrocyte Transcriptome from Multiple Regions of the Mouse Brain

2018 487 citations Matthew M. Boisvert, Galina Erikson et al. Cell Reports profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Galina Erikson United States	15	759	372	234	220	172	23	1.4k
Matheus B. Victor United States	12	877 1.2×	386 1.0×	324 1.4×	359 1.6×	68 0.4×	16	1.4k
Devon S. Svoboda Canada	9	784 1.0×	165 0.4×	159 0.7×	120 0.5×	113 0.7×	13	1.2k
Angelo Raggioli Germany	6	488 0.6×	437 1.2×	229 1.0×	168 0.8×	66 0.4×	8	1.2k
Mark E. Hester United States	20	1.1k 1.4×	308 0.8×	241 1.0×	390 1.8×	194 1.1×	32	1.9k
Bula J. Bhattacharyya United States	19	804 1.1×	176 0.5×	249 1.1×	399 1.8×	147 0.9×	30	1.5k
Makoto Horiuchi United States	22	740 1.0×	416 1.1×	164 0.7×	415 1.9×	240 1.4×	44	1.6k
Carlos Río United States	14	850 1.1×	275 0.7×	303 1.3×	677 3.1×	136 0.8×	32	2.1k
José P. López‐Atalaya Spain	27	1.2k 1.5×	365 1.0×	127 0.5×	427 1.9×	399 2.3×	46	2.0k
Roeben N. Munji United States	9	633 0.8×	634 1.7×	136 0.6×	282 1.3×	110 0.6×	11	1.5k
Kun Leng United States	9	485 0.6×	343 0.9×	229 1.0×	113 0.5×	50 0.3×	16	905

Countries citing papers authored by Galina Erikson

Since Specialization

Citations

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

Fields of papers citing papers by Galina Erikson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Galina Erikson

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

Shukeir, Nicholas, Reagan W. Ching, Galina Erikson, et al.. (2025). The isoflavone genistein selectively stimulates major satellite repeat transcription in mouse heterochromatin. Epigenetics & Chromatin. 18(1). 58–58.

Ching, Reagan W., et al.. (2025). Forced expression of MSR repeat transcripts above a threshold limit breaks heterochromatin organisation. Nature Communications. 16(1). 6420–6420. 1 indexed citations

Shrestha, Shristi, Galina Erikson, James Lyon, et al.. (2022). Aging compromises human islet beta cell function and identity by decreasing transcription factor activity and inducing ER stress. Science Advances. 8(40). eabo3932–eabo3932. 39 indexed citations

Sen, Arko, et al.. (2021). Discovering single nucleotide variants and indels from bulk and single-cell ATAC-seq. Nucleic Acids Research. 49(14). 7986–7994. 9 indexed citations

Vadodaria, Krishna C., Ana P. D. Mendes, Arianna Mei, et al.. (2021). Altered Neuronal Support and Inflammatory Response in Bipolar Disorder Patient-Derived Astrocytes. Stem Cell Reports. 16(4). 825–835. 26 indexed citations

Montavon, Thomas, Nicholas Shukeir, Galina Erikson, et al.. (2021). Complete loss of H3K9 methylation dissolves mouse heterochromatin organization. Nature Communications. 12(1). 4359–4359. 66 indexed citations

Onishi‐Seebacher, Megumi, Galina Erikson, Daniel Ryan, et al.. (2021). Repeat to gene expression ratios in leukemic blast cells can stratify risk prediction in acute myeloid leukemia. BMC Medical Genomics. 14(1). 166–166. 13 indexed citations

Santos, Renata, Sara B. Linker, Shani Stern, et al.. (2021). Deficient LEF1 expression is associated with lithium resistance and hyperexcitability in neurons derived from bipolar disorder patients. Molecular Psychiatry. 26(6). 2440–2456. 35 indexed citations

Beyret, Ergin, Hsin‐Kai Liao, Mako Yamamoto, et al.. (2019). Single-dose CRISPR–Cas9 therapy extends lifespan of mice with Hutchinson–Gilford progeria syndrome. Nature Medicine. 25(3). 419–422. 104 indexed citations

10.

Amatya, Debha N., Sara B. Linker, Ana P. D. Mendes, et al.. (2019). Dynamical Electrical Complexity Is Reduced during Neuronal Differentiation in Autism Spectrum Disorder. Stem Cell Reports. 13(3). 474–484. 9 indexed citations

11.

Amaral, Maria Luisa, Galina Erikson, & Maxim N. Shokhirev. (2018). BART: bioinformatics array research tool. BMC Bioinformatics. 19(1). 296–296. 26 indexed citations

12.

Benegiamo, Giorgia, Ludovic S. Mure, Galina Erikson, et al.. (2018). The RNA-Binding Protein NONO Coordinates Hepatic Adaptation to Feeding. Cell Metabolism. 27(2). 404–418.e7. 84 indexed citations

13.

Boisvert, Matthew M., Galina Erikson, Maxim N. Shokhirev, & Nicola J. Allen. (2018). The Aging Astrocyte Transcriptome from Multiple Regions of the Mouse Brain. Cell Reports. 22(1). 269–285. 487 indexed citations breakdown →

14.

DelGiorno, Kathleen E., Tejia Zhang, Randall P. French, et al.. (2017). Reprogramming pancreatic stellate cells via p53 activation: A putative target for pancreatic cancer therapy. PLoS ONE. 12(12). e0189051–e0189051. 29 indexed citations

15.

Erikson, Galina, Dale L. Bodian, Manuel Rueda, et al.. (2016). Whole-Genome Sequencing of a Healthy Aging Cohort. Cell. 165(4). 1002–1011. 131 indexed citations

16.

Cabana‐Domínguez, Judit, Carlos Roncero, Lara Grau‐López, et al.. (2016). A Highly Polymorphic Copy Number Variant in the NSF Gene is Associated with Cocaine Dependence. Scientific Reports. 6(1). 31033–31033. 7 indexed citations

17.

Pham, Phillip, et al.. (2015). Scripps Genome ADVISER: Annotation and Distributed Variant Interpretation SERver. PLoS ONE. 10(2). e0116815–e0116815. 10 indexed citations

18.

Bloss, Cinnamon S., Ashley A. Scott‐Van Zeeland, Sarah E. Topol, et al.. (2015). A genome sequencing program for novel undiagnosed diseases. Genetics in Medicine. 17(12). 995–1001. 20 indexed citations

19.

Erikson, Galina, et al.. (2014). SG-ADVISER CNV: copy-number variant annotation and interpretation. Genetics in Medicine. 17(9). 714–718. 25 indexed citations

20.

Belani, Rajesh, et al.. (2014). ASXL1 and DNMT3A mutation in a cytogenetically normal B3 thymoma. Oncogenesis. 3(7). e111–e111. 11 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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