Stephen Brown

583 total citations
8 papers, 249 citations indexed

About

Stephen Brown is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Stephen Brown has authored 8 papers receiving a total of 249 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Infectious Diseases. Recurrent topics in Stephen Brown's work include Epigenetics and DNA Methylation (2 papers), Developmental Biology and Gene Regulation (2 papers) and RNA modifications and cancer (1 paper). Stephen Brown is often cited by papers focused on Epigenetics and DNA Methylation (2 papers), Developmental Biology and Gene Regulation (2 papers) and RNA modifications and cancer (1 paper). Stephen Brown collaborates with scholars based in United States, Lebanon and United Kingdom. Stephen Brown's co-authors include Pierre C. Jelenc, James A. Knowles, Dorothy Warburton, Maria de Fátima Bonaldo, Marcelo B. Soares, Ling Qiu, Lee N. Lawton, Kirsten M. Timms, M. Ali Ansari‐Lari and Richard A. Gibbs and has published in prestigious journals such as Gene, Journal of Visualized Experiments and Prenatal Diagnosis.

In The Last Decade

Stephen Brown

8 papers receiving 246 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephen Brown United States 6 168 114 99 89 45 8 249
Stephan Iglseder Austria 5 75 0.4× 32 0.3× 45 0.5× 101 1.1× 11 0.2× 7 233
Florence Renaldo France 11 28 0.2× 69 0.6× 59 0.6× 205 2.3× 36 0.8× 19 339
Susan M. Baddeley United Kingdom 7 56 0.3× 223 2.0× 70 0.7× 47 0.5× 19 0.4× 7 368
Cary A. Jones United States 8 27 0.2× 176 1.5× 150 1.5× 131 1.5× 61 1.4× 8 363
Andrew J. Stempel United States 9 26 0.2× 81 0.7× 21 0.2× 113 1.3× 14 0.3× 14 327
Burcu Ayoglu Sweden 7 42 0.3× 23 0.2× 39 0.4× 157 1.8× 17 0.4× 12 236
Maja Dembić Denmark 9 51 0.3× 15 0.1× 64 0.6× 208 2.3× 12 0.3× 22 319
Manuel San United States 5 53 0.3× 257 2.3× 46 0.5× 46 0.5× 9 0.2× 6 385
Gaurav Gadhvi United States 6 77 0.5× 93 0.8× 16 0.2× 59 0.7× 8 0.2× 16 206
Connie Ha United States 3 18 0.1× 50 0.4× 66 0.7× 91 1.0× 14 0.3× 3 308

Countries citing papers authored by Stephen Brown

Since Specialization
Citations

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

Fields of papers citing papers by Stephen Brown

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephen Brown

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

All Works

8 of 8 papers shown
1.
Brown, Stephen, et al.. (2017). ACTA2 mutation and postpartum hemorrhage: a case report. BMC Medical Genetics. 18(1). 143–143. 6 indexed citations
2.
3.
Handley, Mark T., André Mégarbané, Alison Meynert, et al.. (2014). Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome. Molecular Genetics & Genomic Medicine. 2(4). 319–325. 15 indexed citations
4.
Brown, Ashly, et al.. (2009). A Practical Approach to Genetic Inducible Fate Mapping: A Visual Guide to Mark and Track Cells <em>In Vivo</em>. Journal of Visualized Experiments. 13 indexed citations
5.
Baxi, Laxmi, et al.. (2009). Recurrent Cystic Hygroma with Hydrops. Fetal Diagnosis and Therapy. 25(1). 127–129. 7 indexed citations
7.
Timms, Kirsten M., M. Ali Ansari‐Lari, Wendy L. Morris, Stephen Brown, & Richard A. Gibbs. (1998). The genomic organization of Isopeptidase T-3 (ISOT-3), a new member of the ubiquitin specific protease family (UBP). Gene. 217(1-2). 101–106. 20 indexed citations
8.
Lawton, Lee N., Maria de Fátima Bonaldo, Pierre C. Jelenc, et al.. (1997). Identification of a novel member of the TGF-beta superfamily highly expressed in human placenta. Gene. 203(1). 17–26. 182 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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