Louisa Ludbrook

406 total citations
10 papers, 270 citations indexed

About

Louisa Ludbrook is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Louisa Ludbrook has authored 10 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Reproductive Medicine. Recurrent topics in Louisa Ludbrook's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Sexual Differentiation and Disorders (9 papers) and Sperm and Testicular Function (7 papers). Louisa Ludbrook is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Sexual Differentiation and Disorders (9 papers) and Sperm and Testicular Function (7 papers). Louisa Ludbrook collaborates with scholars based in Australia, United States and United Kingdom. Louisa Ludbrook's co-authors include Vincent R. Harley, Pascal Bernard, Sabine Kelly, Stefan Bagheri‐Fam, Helena Sim, Ryohei Sekido, Robin Lovell‐Badge, Janelle Ryan, Dagmar Wilhelm and Andrew H. A. Clayton and has published in prestigious journals such as PLoS ONE, Endocrinology and Molecular Endocrinology.

In The Last Decade

Louisa Ludbrook

10 papers receiving 269 citations

Peers

Louisa Ludbrook

GENET

MB

RM

UROLO

PHEOH

Sandra Rojo France

Tomohide Kidokoro Japan

S. Alexandra Garcia-Moreno United States

Ingrid Knarston Australia

Denise R. Archambeault United States

Yung Ming Lin Taiwan

Alaa K. Kamel Egypt

Maria Rosa Maduro United States

Mayo Kodani Japan

Eske Bendsen Denmark

Sandra Rojo France

Louisa Ludbrook

155 ×0.7

GENET

147 ×0.7

MB

58 ×0.7

RM

37 ×1.2

UROLO

12 ×0.6

PHEOH

Citations per year, relative to Louisa Ludbrook Louisa Ludbrook (= 1×) peers Sandra Rojo

Countries citing papers authored by Louisa Ludbrook

Since Specialization

Citations

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

Fields of papers citing papers by Louisa Ludbrook

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louisa Ludbrook

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

All Works

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10 of 10 papers shown

1.

Sreenivasan, Rajini, Louisa Ludbrook, Kevin C. Knower, et al.. (2018). Mutant NR5A1/SF-1 in patients with disorders of sex development shows defective activation of theSOX9TESCO enhancer. Human Mutation. 39(12). 1861–1874. 14 indexed citations

2.

Ludbrook, Louisa, et al.. (2016). Dataset of differentially expressed genes from SOX9 over-expressing NT2/D1 cells. Data in Brief. 9. 194–198. 3 indexed citations

3.

Lavery, Rowena, Terje Svingen, Sabine Kelly, et al.. (2016). SOX9 regulates expression of the male fertility gene Ets variant factor 5 (ETV5) during mammalian sex development. The International Journal of Biochemistry & Cell Biology. 79. 41–51. 15 indexed citations

4.

Ludbrook, Louisa, Pascal Bernard, Stefan Bagheri‐Fam, et al.. (2012). Excess DAX1 Leads to XY Ovotesticular Disorder of Sex Development (DSD) in Mice by Inhibiting Steroidogenic Factor-1 (SF1) Activation of the Testis Enhancer of SRY-box-9 (Sox9). Endocrinology. 153(4). 1948–1958. 53 indexed citations

5.

Ludbrook, Louisa & Vincent R. Harley. (2011). Genetic Mechanisms Underlying 46,XY DSD with Gonadal Dysgenesis. Advances in experimental medicine and biology. 707. 87–88. 1 indexed citations

6.

Knower, Kevin C., Sabine Kelly, Louisa Ludbrook, et al.. (2011). Failure of SOX9 Regulation in 46XY Disorders of Sex Development with SRY, SOX9 and SF1 Mutations. PLoS ONE. 6(3). e17751–e17751. 53 indexed citations

7.

Ryan, Janelle, Louisa Ludbrook, Dagmar Wilhelm, et al.. (2010). Analysis of Gene Function in Cultured Embryonic Mouse Gonads Using Nucleofection. Sexual Development. 5(1). 7–15. 12 indexed citations

8.

Bernard, Pascal, Louisa Ludbrook, Gloria Queipo, et al.. (2006). A familial missense mutation in the hinge region of DAX1 associated with late-onset AHC in a prepubertal female. Molecular Genetics and Metabolism. 88(3). 272–279. 20 indexed citations

9.

Sim, Helena, Kieran Rimmer, Sabine Kelly, et al.. (2005). Defective Calmodulin-Mediated Nuclear Transport of the Sex-Determining Region of the Y Chromosome (SRY) in XY Sex Reversal. Molecular Endocrinology. 19(7). 1884–1892. 46 indexed citations

10.

Ludbrook, Louisa & Vincent R. Harley. (2004). Sex determination: a ‘window’ of DAX1 activity. Trends in Endocrinology and Metabolism. 15(3). 116–121. 53 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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