Jill M. Brown

3.4k total citations
43 papers, 2.2k citations indexed

About

Jill M. Brown is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Jill M. Brown has authored 43 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 11 papers in Hematology and 10 papers in Genetics. Recurrent topics in Jill M. Brown's work include Genomics and Chromatin Dynamics (12 papers), Genomic variations and chromosomal abnormalities (9 papers) and Acute Myeloid Leukemia Research (8 papers). Jill M. Brown is often cited by papers focused on Genomics and Chromatin Dynamics (12 papers), Genomic variations and chromosomal abnormalities (9 papers) and Acute Myeloid Leukemia Research (8 papers). Jill M. Brown collaborates with scholars based in United Kingdom, Germany and United States. Jill M. Brown's co-authors include Veronica J. Buckle, Douglas R. Higgs, Jim R. Hughes, W. G. Wood, Francisco J. Iborra, Lothar Schermelleh, James Davies, Robert E. Kearney, Joyce E. Reittie and Ann Atzberger and has published in prestigious journals such as Nature, Science and Nature Medicine.

In The Last Decade

Jill M. Brown

41 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jill M. Brown United Kingdom 24 1.7k 412 359 291 241 43 2.2k
Éric Soler France 23 1.3k 0.8× 230 0.6× 169 0.5× 206 0.7× 134 0.6× 42 1.7k
Lars Velten Germany 13 1.4k 0.8× 116 0.3× 189 0.5× 746 2.6× 237 1.0× 26 2.3k
Alicia N. Schep United States 10 1.6k 0.9× 146 0.4× 90 0.3× 103 0.4× 362 1.5× 12 1.9k
Marie-Françoise O’Donohue France 29 2.6k 1.5× 210 0.5× 134 0.4× 42 0.1× 243 1.0× 53 2.9k
Violaine Saint‐André France 9 2.5k 1.5× 295 0.7× 143 0.4× 134 0.5× 438 1.8× 11 3.0k
Felix Kokocinski Germany 16 1.2k 0.7× 361 0.9× 151 0.4× 72 0.2× 384 1.6× 22 2.0k
Yilong Li United States 16 1.7k 1.0× 352 0.9× 225 0.6× 39 0.1× 305 1.3× 26 2.0k
Kimmo Palin Finland 19 2.2k 1.3× 412 1.0× 231 0.6× 37 0.1× 267 1.1× 36 3.1k
John LaCava United States 21 2.2k 1.3× 109 0.3× 481 1.3× 44 0.2× 194 0.8× 49 2.5k
Anton Valouev United States 20 2.6k 1.5× 500 1.2× 429 1.2× 43 0.1× 375 1.6× 25 3.0k

Countries citing papers authored by Jill M. Brown

Since Specialization
Citations

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

Fields of papers citing papers by Jill M. Brown

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jill M. Brown

This figure shows the co-authorship network connecting the top 25 collaborators of Jill M. Brown. A scholar is included among the top collaborators of Jill M. 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 Jill M. Brown. Jill M. Brown 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.
Brown, Jill M., Ron Schweßinger, Simon J. McGowan, et al.. (2025). Exploring the size limits of Bionano optical genome mapping to resolve alternative structures of linked interspersed chromosomal duplications. Genome Medicine. 17(1). 141–141. 1 indexed citations
2.
Ochs, Fena, Aleksander Szczurek, Jill M. Brown, et al.. (2024). Sister chromatid cohesion is mediated by individual cohesin complexes. Science. 383(6687). 1122–1130. 16 indexed citations
3.
Jeziorska, Danuta M., Edward Tunnacliffe, Jill M. Brown, et al.. (2022). On-microscope staging of live cells reveals changes in the dynamics of transcriptional bursting during differentiation. Nature Communications. 13(1). 6641–6641. 7 indexed citations
4.
Downes, Damien J., Caroline Scott, Jelena Telenius, et al.. (2022). The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin. Nature Communications. 13(1). 3485–3485. 29 indexed citations
5.
Oldenkamp, Roel, Jill M. Brown, David Miguel Susano Pinto, et al.. (2020). Chromatin arranges in chains of mesoscale domains with nanoscale functional topography independent of cohesin. Science Advances. 6(39). 121 indexed citations
6.
Waithe, Dominic, et al.. (2020). Object detection networks and augmented reality for cellular detection in fluorescence microscopy. The Journal of Cell Biology. 219(10). 20 indexed citations
7.
Rhodes, James, Angelika Feldmann, Benjamín Hernández-Rodríguez, et al.. (2020). Cohesin Disrupts Polycomb-Dependent Chromosome Interactions in Embryonic Stem Cells. Cell Reports. 30(3). 820–835.e10. 121 indexed citations
8.
Ochs, Fena, Gopal Karemore, Jill M. Brown, et al.. (2019). Stabilization of chromatin topology safeguards genome integrity. Nature. 574(7779). 571–574. 129 indexed citations
9.
Cheong, Pak Leng, Aude-Anaïs Olijnik, Jill M. Brown, et al.. (2018). Robust CRISPR/Cas9 Genome Editing of the HUDEP-2 Erythroid Precursor Line Using Plasmids and Single-Stranded Oligonucleotide Donors. Methods and Protocols. 1(3). 28–28. 17 indexed citations
10.
Oudelaar, A. Marieke, James Davies, Lars L. P. Hanssen, et al.. (2018). Single-allele chromatin interactions identify regulatory hubs in dynamic compartmentalized domains. Nature Genetics. 50(12). 1744–1751. 134 indexed citations
11.
Kowalczyk, Monika S., Jim R. Hughes, David Garrick, et al.. (2012). Intragenic Enhancers Act as Alternative Promoters. Molecular Cell. 45(4). 447–458. 194 indexed citations
12.
Schödel, Johannes, Chiara Bardella, Lina K. Sciesielski, et al.. (2012). Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression. Nature Genetics. 44(4). 420–425. 114 indexed citations
13.
Renella, Raffaele, Nigel Roberts, Jill M. Brown, et al.. (2011). Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1α localization in erythroblasts. Blood. 117(25). 6928–6938. 34 indexed citations
14.
Brown, Jill M. & Veronica J. Buckle. (2010). Detection of Nascent RNA Transcripts by Fluorescence In Situ Hybridization. Methods in molecular biology. 659. 33–50. 15 indexed citations
15.
Renella, Raffaele, Nigel Roberts, Jacqueline A. Sharpe, et al.. (2008). A Transgenic Mouse Model for Congenital Dyserythropoietic Anemia Type I. Blood. 112(11). 3455–3455. 2 indexed citations
16.
Brown, Jill M., et al.. (2002). Identification of a dup(5)(p15.3) by multicolor banding. Clinical Genetics. 61(4). 277–282. 4 indexed citations
17.
Saracoglu, Kaan, Jill M. Brown, Robert E. Kearney, et al.. (2001). New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization. Cytometry. 44(1). 7–15. 33 indexed citations
18.
Brown, Jill M., Sharon W. Horsley, Christine Jung, et al.. (2000). Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL. European Journal of Human Genetics. 8(12). 903–910. 28 indexed citations
19.
Goodship, JA, Sally Ann Lynch, & Jill M. Brown. (1994). Comparison of facial features of DiGeorge syndrome (DGS) due to deletion 10p13-10pter with DGS due to 22q11 deletion. The American Journal of Human Genetics. 55. 4 indexed citations
20.
Brown, Jill M.. (1992). Application of Molecular Genetics to the Diagnosis of Inherited Diseases: Edited by K E Davies. pp 90. Royal College of Physicians, London. 1990. Biochemical Education. 20(2). 6 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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