Simon G. Gregory

53.7k total citations · 4 hit papers
171 papers, 7.0k citations indexed

About

Simon G. Gregory is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Simon G. Gregory has authored 171 papers receiving a total of 7.0k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Molecular Biology, 33 papers in Cancer Research and 27 papers in Genetics. Recurrent topics in Simon G. Gregory's work include Cancer Genomics and Diagnostics (13 papers), RNA Research and Splicing (12 papers) and Genomic variations and chromosomal abnormalities (9 papers). Simon G. Gregory is often cited by papers focused on Cancer Genomics and Diagnostics (13 papers), RNA Research and Splicing (12 papers) and Genomic variations and chromosomal abnormalities (9 papers). Simon G. Gregory collaborates with scholars based in United States, United Kingdom and Germany. Simon G. Gregory's co-authors include Margaret A. Pericak‐Vance, Mariano A. García-Blanco, Elizabeth R. Hauser, Allison E. Ashley‐Koch, Jessica J. Connelly, Svati H. Shah, Aaron J. Towers, Jason Gibson, William E. Kraus and Cordelia F. Langford and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

Simon G. Gregory

163 papers receiving 6.9k citations

Hit Papers

LMNA, encoding lamin A/C, is mutated in partial lipodystr... 2000 2026 2008 2017 2000 2011 2020 2022 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simon G. Gregory United States 44 3.0k 1.1k 994 732 620 171 7.0k
Holger M. Reichardt Germany 52 2.5k 0.8× 1.7k 1.5× 2.7k 2.8× 636 0.9× 531 0.9× 135 10.1k
Tomoshige Kino United States 51 3.1k 1.0× 2.2k 2.0× 1.0k 1.0× 1.3k 1.8× 498 0.8× 161 9.2k
Sulev Kõks Estonia 37 2.0k 0.7× 826 0.8× 1.1k 1.1× 416 0.6× 286 0.5× 277 5.4k
Christine Bôle‐Feysot France 39 2.4k 0.8× 1.2k 1.1× 911 0.9× 386 0.5× 380 0.6× 123 5.9k
Margaret E. Wierman United States 46 1.7k 0.6× 1.5k 1.4× 629 0.6× 424 0.6× 597 1.0× 147 6.4k
Bart C.J.M. Fauser Netherlands 83 2.7k 0.9× 2.1k 1.9× 2.3k 2.3× 316 0.4× 511 0.8× 299 26.1k
Masahiro Toda Japan 40 1.4k 0.5× 947 0.9× 773 0.8× 355 0.5× 647 1.0× 281 5.4k
Henrik Daa Schrøder Denmark 51 3.8k 1.3× 571 0.5× 383 0.4× 766 1.0× 1.3k 2.0× 297 9.5k
Tamir Ben‐Hur Israel 44 3.6k 1.2× 494 0.5× 687 0.7× 457 0.6× 665 1.1× 182 9.4k
Thomas Rülicke Austria 62 6.5k 2.1× 1.2k 1.1× 2.8k 2.8× 1.0k 1.4× 733 1.2× 206 13.5k

Countries citing papers authored by Simon G. Gregory

Since Specialization
Citations

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

Fields of papers citing papers by Simon G. Gregory

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Simon G. Gregory. 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 Simon G. Gregory. The network helps show where Simon G. Gregory may publish in the future.

Co-authorship network of co-authors of Simon G. Gregory

This figure shows the co-authorship network connecting the top 25 collaborators of Simon G. Gregory. A scholar is included among the top collaborators of Simon G. Gregory 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 Simon G. Gregory. Simon G. Gregory 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.
SoRelle, Elliott D., Gillian Q. Horn, Laura A. Cooney, et al.. (2025). Early multiple sclerosis activity associated with TBX21+CD21loCXCR3+ B cell expansion resembling EBV-induced phenotypes. JCI Insight. 10(12). 1 indexed citations
2.
Petty, Amy J., Adela R. Cardones, Yingai J. Jin, et al.. (2025). Insights into Keratinocyte and Immunologic Landscape in Cutaneous Graft-Versus-Host Disease through Single-Cell Transcriptomics. JID Innovations. 5(4). 100373–100373.
3.
Du, Kuo, David S. Umbaugh, Liuyang Wang, et al.. (2025). Targeting senescent hepatocytes for treatment of metabolic dysfunction-associated steatotic liver disease and multi-organ dysfunction. Nature Communications. 16(1). 3038–3038. 11 indexed citations
4.
Kolevzon, A lexander, Bryan H. King, Christopher J. McDougle, et al.. (2025). Predictors of Placebo Response in the Study of Oxytocin in Autism to Improve Reciprocal Social Behaviors. Journal of Child and Adolescent Psychopharmacology. 35(4). 202–210.
5.
Hammouda, M. Ben, Wanying Miao, Yingai J. Jin, et al.. (2024). UBE2N Is Essential for Maintenance of Skin Homeostasis and Suppression of Inflammation. Journal of Investigative Dermatology. 144(12). 2742–2753. 2 indexed citations
6.
Newman, Benjamin T., Stephanie N. Giamberardino, Simon G. Gregory, et al.. (2024). Epigenetic age acceleration predicts subject‐specific white matter degeneration in the human brain. Aging Cell. 24(4). e14426–e14426.
7.
Hirano, Minato, Gaddiel Galarza-Muñoz, Liuyang Wang, et al.. (2023). The RNA helicase DDX39B activates FOXP3 RNA splicing to control T regulatory cell fate. eLife. 12. 18 indexed citations
8.
Leuthner, Tess C., Brendan F. Kohrn, Christina M. Bergemann, et al.. (2022). Resistance of mitochondrial DNA to cadmium and Aflatoxin B1 damage-induced germline mutation accumulation in C. elegans. Nucleic Acids Research. 50(15). 8626–8642. 17 indexed citations
9.
Gupta, Santosh, Susan Halabi, Gabor Kemeny, et al.. (2021). Circulating Tumor Cell Genomic Evolution and Hormone Therapy Outcomes in Men with Metastatic Castration-Resistant Prostate Cancer. Molecular Cancer Research. 19(6). 1040–1050. 19 indexed citations
10.
Yahara, Yasuhito, Tomasa Barrientos, Yuning J. Tang, et al.. (2020). Erythromyeloid progenitors give rise to a population of osteoclasts that contribute to bone homeostasis and repair. Nature Cell Biology. 22(1). 49–59. 134 indexed citations
11.
Gupta, Santosh, Jing Li, Gabor Kemeny, et al.. (2016). Whole Genomic Copy Number Alterations in Circulating Tumor Cells from Men with Abiraterone or Enzalutamide-Resistant Metastatic Castration-Resistant Prostate Cancer. Clinical Cancer Research. 23(5). 1346–1357. 52 indexed citations
12.
Markunas, Christina A., Eric F. Lock, Karen Soldano, et al.. (2014). Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics. BMC Medical Genomics. 7(1). 39–39. 23 indexed citations
13.
Zeng, Yi, Ling Zhao, Qihua Tan, et al.. (2013). Interactions between Social/ behavioral factors and ADRB2 genotypes may be associated with health at advanced ages in China. BMC Geriatrics. 13(1). 91–91. 10 indexed citations
14.
Lin, Ningjing, Chunhui Di, Jinrong Fu, et al.. (2012). Deletion or Epigenetic Silencing of AJAP1 on 1p36 in Glioblastoma. Molecular Cancer Research. 10(2). 208–217. 33 indexed citations
15.
Feng, Jie, Jianyi Zhang, Ming Liu, et al.. (2011). Association of mtDNA haplogroup F with healthy longevity in the female Chuang population, China. Experimental Gerontology. 46(12). 987–993. 28 indexed citations
16.
Evsyukova, Irina Y., Jason A. Somarelli, Simon G. Gregory, & Mariano A. García-Blanco. (2010). Alternative splicing in multiple sclerosis and other autoimmune diseases. RNA Biology. 7(4). 462–473. 62 indexed citations
17.
Buckley, Patrick G., Uwe Menzel, Tiit Mathiesen, et al.. (2005). Comprehensive DNA Copy Number Profiling of Meningioma Using a Chromosome 1 Tiling Path Microarray Identifies Novel Candidate Tumor Suppressor Loci. Cancer Research. 65(7). 2653–2661. 38 indexed citations
18.
Wicker, Linda S., Giselle Chamberlain, Kara Hunter, et al.. (2004). Fine Mapping, Gene Content, Comparative Sequencing, and Expression Analyses Support Ctla4 and Nramp1 as Candidates for Idd5.1 and Idd5.2 in the Nonobese Diabetic Mouse. The Journal of Immunology. 173(1). 164–173. 91 indexed citations
19.
Mallon, Ann‐Marie, Laurens Wilming, James Gilbert, et al.. (2004). Organization and Evolution of a Gene-Rich Region of the Mouse Genome: A 12.7-Mb Region Deleted in the Del(13)Svea36H Mouse. Genome Research. 14(10a). 1888–1901. 23 indexed citations
20.
Gregory, Simon G., Mark D. Vaudin, Richard Wooster, et al.. (1998). Report of the fourth international workshop on human chromosome 1 mapping 1998. Cytogenetic and Genome Research. 83(3-4). 147–175. 7 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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