Lucia Brown

1.5k total citations
21 papers, 1.1k citations indexed

About

Lucia Brown is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Lucia Brown has authored 21 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Pediatrics, Perinatology and Child Health and 8 papers in Genetics. Recurrent topics in Lucia Brown's work include Hedgehog Signaling Pathway Studies (7 papers), Prenatal Screening and Diagnostics (7 papers) and Epigenetics and DNA Methylation (5 papers). Lucia Brown is often cited by papers focused on Hedgehog Signaling Pathway Studies (7 papers), Prenatal Screening and Diagnostics (7 papers) and Epigenetics and DNA Methylation (5 papers). Lucia Brown collaborates with scholars based in United States, Australia and United Kingdom. Lucia Brown's co-authors include Stephen Brown, S. Stengel‐Rutkowski, Chih‐Yu Yu, Maximilian Muenke, Dorothy Warburton, Raoul C. M. Hennekam, Elizabeth Roeder, Carol A. Mason, Jun Aruga and Rivka A. Rachel and has published in prestigious journals such as Cell, Nature Genetics and The Journal of Cell Biology.

In The Last Decade

Lucia Brown

20 papers receiving 1.1k citations

Peers

Lucia Brown
Steven Lisgo United Kingdom
Alexandra L. Joyner United States
Dirk A. Kleinjan United Kingdom
Boglárka Banizs United States
Marjorie Withers United States
Bert H.J. Eussen Netherlands
Steven Lisgo United Kingdom
Lucia Brown
Citations per year, relative to Lucia Brown Lucia Brown (= 1×) peers Steven Lisgo

Countries citing papers authored by Lucia Brown

Since Specialization
Citations

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

Fields of papers citing papers by Lucia Brown

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Brown

This figure shows the co-authorship network connecting the top 25 collaborators of Lucia Brown. A scholar is included among the top collaborators of Lucia 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 Lucia Brown. Lucia 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, Lucia, et al.. (2018). Pregnancy-Induced Physiologic Adaptation of the Abdominal Aorta Is Associated with Changes in Gene Expression and Genomic Methylation. Journal of Vascular Research. 55(5). 319–327. 1 indexed citations
2.
Brown, Lucia, Sharon Mount, Ramesh Reddy, et al.. (2013). Recurrent Pregnancy Loss in a Woman With NLRP7 Mutation. International Journal of Gynecological Pathology. 32(4). 399–405. 13 indexed citations
3.
Brown, Lucia, et al.. (2013). Generalized Disturbance of DNA Methylation in the Uterine Decidua in the CBA/J × DBA/2 Mouse Model of Pregnancy Failure1. Biology of Reproduction. 89(5). 120–120. 17 indexed citations
4.
Wright, Katharine M., Lucia Brown, Gregory G. Brown, Peter R. Casson, & Stephen Brown. (2011). Microarray assessment of methylation in individual mouse blastocyst stage embryos shows that in vitro culture may have widespread genomic effects. Human Reproduction. 26(9). 2576–2585. 39 indexed citations
5.
Moldrich, Randal X., Ilan Gobius, Thomas Pollak, et al.. (2010). Molecular regulation of the developing commissural plate. The Journal of Comparative Neurology. 518(18). 3645–3661. 37 indexed citations
6.
Brown, Lucia, Gregory G. Brown, Pamela M. Vacek, & Stephen Brown. (2010). Aneuploidy Detection in Mixed DNA Samples by Methylation-Sensitive Amplification and Microarray Analysis. Clinical Chemistry. 56(5). 805–813. 8 indexed citations
7.
Moldrich, Randal X., Ilan Gobius, Thomas Pollak, et al.. (2010). Molecular regulation of the developing commissural plate. The Journal of Comparative Neurology. 518(18). 2 indexed citations
9.
McGreal, Stanley, et al.. (2009). Housing and Neighbourhood Monitor: UK-Wide Report. Research Explorer (The University of Manchester). 2 indexed citations
10.
Brown, Lucia & Stephen Brown. (2008). Zic2 is expressed in pluripotent cells in the blastocyst and adult brain expression overlaps with makers of neurogenesis. Gene Expression Patterns. 9(1). 43–49. 22 indexed citations
11.
Brown, Lucia, et al.. (2006). Validation of QF-PCR for prenatal aneuploidy screening in the United States. Prenatal Diagnosis. 26(11). 1068–1074. 27 indexed citations
12.
13.
Herrera, Eloı́sa, Lucia Brown, Jun Aruga, et al.. (2003). Zic2 Patterns Binocular Vision by Specifying the Uncrossed Retinal Projection. Cell. 114(5). 545–557. 199 indexed citations
14.
Brown, Lucia, Andreas H. Kottmann, & Stephen Brown. (2003). Immunolocalization of Zic2 expression in the developing mouse forebrain. Gene Expression Patterns. 3(3). 361–367. 41 indexed citations
15.
Brown, Lucia, et al.. (2002). Possible association of NTDs with a polyhistidine tract polymorphism in the ZIC2 gene. American Journal of Medical Genetics. 108(2). 128–131. 26 indexed citations
16.
Brown, Lucia, et al.. (2001). Prenatal diagnosis of a familial Xq deletion in a female fetus: a case report. Prenatal Diagnosis. 21(1). 27–30. 6 indexed citations
17.
Brown, Lucia. (2001). Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination. Human Molecular Genetics. 10(8). 791–796. 142 indexed citations
18.
Sakurai, Takeshi, Marc Lustig, Joanne Babiarz, et al.. (2001). Overlapping functions of the cell adhesion molecules Nr-CAM and L1 in cerebellar granule cell development. The Journal of Cell Biology. 154(6). 1259–1274. 87 indexed citations
19.
Brown, Stephen, Dorothy Warburton, Lucia Brown, et al.. (1998). Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired. Nature Genetics. 20(2). 180–183. 386 indexed citations
20.
Balamuth, D. P., et al.. (1983). Final state branching ratio in theBe7decay. Physical Review C. 27(4). 1724–1727. 3 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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