Judith Brown

4.7k total citations
22 papers, 752 citations indexed

About

Judith Brown is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Judith Brown has authored 22 papers receiving a total of 752 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Plant Science. Recurrent topics in Judith Brown's work include Chromosomal and Genetic Variations (6 papers), Genetic Associations and Epidemiology (3 papers) and BRCA gene mutations in cancer (3 papers). Judith Brown is often cited by papers focused on Chromosomal and Genetic Variations (6 papers), Genetic Associations and Epidemiology (3 papers) and BRCA gene mutations in cancer (3 papers). Judith Brown collaborates with scholars based in United States, United Kingdom and Australia. Judith Brown's co-authors include Rachel J. O’Neill, Douglas F. Easton, Yuichiro Itoh, Kathy Kampf, Arthur P. Arnold, Sarah Mitchell, Jean Leyland, Tina Audley, Ruth Warren and Karen A. Pooley and has published in prestigious journals such as PLoS ONE, Development and Cancer Research.

In The Last Decade

Judith Brown

22 papers receiving 732 citations

Peers

Judith Brown
Otto Jolanki United States
Karen Fitch United States
Yunjiang Qiu United States
Nick Sampas United States
Jonathan Lim United States
N. Alice Yamada United States
Moira Crosier United Kingdom
Judith Brown
Citations per year, relative to Judith Brown Judith Brown (= 1×) peers Tomasz Gambin

Countries citing papers authored by Judith Brown

Since Specialization
Citations

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

Fields of papers citing papers by Judith Brown

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Brown

This figure shows the co-authorship network connecting the top 25 collaborators of Judith Brown. A scholar is included among the top collaborators of Judith 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 Judith Brown. Judith 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, Judith, et al.. (2024). Vibration mitigation of a model aircraft with high-aspect-ratio wings using two-dimensional nonlinear vibration absorbers. International Journal of Non-Linear Mechanics. 167. 104878–104878. 5 indexed citations
2.
Brown, Judith, et al.. (2022). A two-dimensional nonlinear vibration absorber using elliptical impacts and sliding. Mechanical Systems and Signal Processing. 189. 110068–110068. 14 indexed citations
3.
Baple, Emma L., Ashley J. Russo, Judith Brown, et al.. (2017). An Amish founder mutation disrupts a PI(3)P-WHAMM-Arp2/3 complex–driven autophagosomal remodeling pathway. Molecular Biology of the Cell. 28(19). 2492–2507. 19 indexed citations
4.
Decker, Brennan, Jamie Allen, Craig Luccarini, et al.. (2017). Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks. Journal of Medical Genetics. 54(11). 732–741. 62 indexed citations
5.
Ramos, Érica, Adauto Lima Cardoso, Judith Brown, et al.. (2016). The repetitive DNA element BncDNA, enriched in the B chromosome of the cichlid fish Astatotilapia latifasciata, transcribes a potentially noncoding RNA. Chromosoma. 126(2). 313–323. 32 indexed citations
6.
Germain, Noélle D., Alex Plocik, Heather R. Glatt-Deeley, et al.. (2014). Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1. Molecular Autism. 5(1). 44–44. 75 indexed citations
7.
Varghese, Jajini S., Paula L. Smith, Elizabeth Folkerd, et al.. (2012). The Heritability of Mammographic Breast Density and Circulating Sex-Hormone Levels: Two Independent Breast Cancer Risk Factors. Cancer Epidemiology Biomarkers & Prevention. 21(12). 2167–2175. 18 indexed citations
8.
Prescott, Jennifer, Deborah J. Thompson, Peter Kraft, et al.. (2012). Genome-Wide Association Study of Circulating Estradiol, Testosterone, and Sex Hormone-Binding Globulin in Postmenopausal Women. PLoS ONE. 7(6). e37815–e37815. 45 indexed citations
9.
Brown, Judith, Sarah Mitchell, & Rachel J. O’Neill. (2011). Making a long story short: noncoding RNAs and chromosome change. Heredity. 108(1). 42–49. 30 indexed citations
10.
Brown, Judith, et al.. (2011). Retroelement Demethylation Associated with Abnormal Placentation in Mus musculus × Mus caroli Hybrids1. Biology of Reproduction. 86(3). 88–88. 15 indexed citations
11.
Brown, Judith, et al.. (2011). Centromere Conversion and Retention in Somatic Cell Hybrids. Cytogenetic and Genome Research. 134(3). 182–190. 1 indexed citations
12.
Ferreri, Gianni C, Judith Brown, Craig Obergfell, et al.. (2011). Recent Amplification of the Kangaroo Endogenous Retrovirus, KERV, Limited to the Centromere. Journal of Virology. 85(10). 4761–4771. 30 indexed citations
13.
Brown, Judith & Rachel J. O’Neill. (2010). Chromosomes, Conflict, and Epigenetics: Chromosomal Speciation Revisited. Annual Review of Genomics and Human Genetics. 11(1). 291–316. 123 indexed citations
14.
Pooley, Karen A., Jonathan P. Tyrer, Mitul Shah, et al.. (2010). No Association between TERT-CLPTM1L Single Nucleotide Polymorphism rs401681 and Mean Telomere Length or Cancer Risk. Cancer Epidemiology Biomarkers & Prevention. 19(7). 1862–1865. 32 indexed citations
15.
Kataoka, Masako, Antonis C. Antoniou, Ruth Warren, et al.. (2009). Genetic Models for the Familial Aggregation of Mammographic Breast Density. Cancer Epidemiology Biomarkers & Prevention. 18(4). 1277–1284. 12 indexed citations
16.
Brown, Judith, D.A. Golden, & Rachel J. O’Neill. (2008). Methylation perturbations in retroelements within the genome of a Mus interspecific hybrid correlate with double minute chromosome formation. Genomics. 91(3). 267–273. 13 indexed citations
17.
Smilowitz, Henry M., Jakob Weissenberger, Joachim Weis, et al.. (2007). Orthotopic transplantation of v-src–expressing glioma cell lines into immunocompetent mice: establishment of a new transplantable in vivo model for malignant glioma. Journal of neurosurgery. 106(4). 652–659. 32 indexed citations
18.
Mitchell, Gillian, Antonis C. Antoniou, Ruth Warren, et al.. (2006). Mammographic Density and Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers. Cancer Research. 66(3). 1866–1872. 90 indexed citations
19.
Carvalho‐Silva, Denise, Rachel J. O’Neill, Judith Brown, et al.. (2004). Molecular characterization and evolution of X and Y-borne ATRX homologues in American marsupials. Chromosome Research. 12(8). 795–804. 10 indexed citations
20.
Brown, Judith, Judith A. Cebra‐Thomas, Jeffrey D. Bleil, Paul M. Wassarman, & Lee M. Silver. (1989). A premature acrosome reaction is programmed by mouse t haplotypes during sperm differentiation and could play a role in transmission ratio distortion. Development. 106(4). 769–773. 16 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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