Brittany Croft

469 total citations
13 papers, 289 citations indexed

About

Brittany Croft is a scholar working on Molecular Biology, Genetics and Urology. According to data from OpenAlex, Brittany Croft has authored 13 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 3 papers in Urology. Recurrent topics in Brittany Croft's work include Sexual Differentiation and Disorders (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers) and Sperm and Testicular Function (3 papers). Brittany Croft is often cited by papers focused on Sexual Differentiation and Disorders (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers) and Sperm and Testicular Function (3 papers). Brittany Croft collaborates with scholars based in Australia, United States and France. Brittany Croft's co-authors include Andrew Sinclair, Thomas Ohnesorg, Katie Ayers, Gorjana Robevska, Vincent R. Harley, Ingrid Knarston, Jacqueline Tan, Rajini Sreenivasan, Peter Koopman and Jocelyn van den Bergen and has published in prestigious journals such as Nature Communications, Endocrinology and Human Molecular Genetics.

In The Last Decade

Brittany Croft

13 papers receiving 288 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brittany Croft Australia	9	239	233	71	67	40	13	289
Ingrid Knarston Australia	7	167 0.7×	172 0.7×	37 0.5×	68 1.0×	43 1.1×	8	237
Janelle Ryan Australia	9	212 0.9×	190 0.8×	37 0.5×	71 1.1×	26 0.7×	13	243
Juliana Gabriel Ribeiro de Andrade Brazil	10	155 0.6×	192 0.8×	63 0.9×	43 0.6×	8 0.2×	22	209
Denise R. Archambeault United States	8	99 0.4×	196 0.8×	24 0.3×	109 1.6×	79 2.0×	8	267
Alaa K. Kamel Egypt	9	180 0.8×	138 0.6×	33 0.5×	21 0.3×	11 0.3×	34	227
Sandra Rojo France	4	155 0.6×	147 0.6×	37 0.5×	58 0.9×	12 0.3×	6	200
Capucine Hyon France	12	262 1.1×	210 0.9×	43 0.6×	89 1.3×	64 1.6×	21	376
Tomohide Kidokoro Japan	4	206 0.9×	185 0.8×	11 0.2×	97 1.4×	21 0.5×	6	245
Louisa Ludbrook Australia	8	231 1.0×	223 1.0×	32 0.5×	85 1.3×	19 0.5×	10	270
Nikolay L. Manuylov United States	9	264 1.1×	310 1.3×	14 0.2×	86 1.3×	78 1.9×	10	404

Countries citing papers authored by Brittany Croft

Since Specialization

Citations

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

Fields of papers citing papers by Brittany Croft

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brittany Croft

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

All Works

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13 of 13 papers shown

Bird, Anthony D., Stefan Bagheri‐Fam, Brittany Croft, et al.. (2023). Somatic FGFR2 is Required for Germ Cell Maintenance in the Mouse Ovary. Endocrinology. 164(5). 3 indexed citations

Croft, Brittany, Anthony D. Bird, Makoto Ono, et al.. (2022). FGF9 variant in 46, XY DSD patient suggests a role for dimerization in sex determination. Clinical Genetics. 103(3). 277–287. 9 indexed citations

Zhao, Liang, Yen‐Shan Chen, Ee Ting Ng, et al.. (2021). Generation and mutational analysis of a transgenic mouse model of human SRY. Human Mutation. 43(3). 362–379. 5 indexed citations

Thuresson, Ann‐Charlotte, et al.. (2020). A novel heterozygous variant in FGF9 associated with previously unreported features of multiple synostosis syndrome 3. Clinical Genetics. 99(2). 325–329. 7 indexed citations

Bird, Anthony D., Brittany Croft, Masayo Harada, et al.. (2020). Ovotesticular disorders of sex development in FGF9 mouse models of human synostosis syndromes. Human Molecular Genetics. 29(13). 2148–2161. 9 indexed citations

Jaillard, Sylvie, Rajini Sreenivasan, Gorjana Robevska, et al.. (2019). Analysis of NR5A1 in 142 patients with premature ovarian insufficiency, diminished ovarian reserve, or unexplained infertility. Maturitas. 131. 78–86. 26 indexed citations

Croft, Brittany, Thomas Ohnesorg, Josephine Bowles, et al.. (2019). Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9. Yearbook of pediatric endocrinology. 1 indexed citations

Croft, Brittany, Thomas Ohnesorg, Jacqueline Hewitt, et al.. (2018). Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9. Nature Communications. 9(1). 5319–5319. 117 indexed citations

Knarston, Ingrid, Gorjana Robevska, Jocelyn A. van den Bergen, et al.. (2018). NR5A1gene variants repress the ovarian-specific WNT signaling pathway in 46,XX disorders of sex development patients. Human Mutation. 40(2). 207–216. 26 indexed citations

10.

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

11.

Croft, Brittany, Thomas Ohnesorg, & Andrew Sinclair. (2017). The Role of Copy Number Variants in Disorders of Sex Development. Sexual Development. 12(1-3). 19–29. 39 indexed citations

12.

Croft, Brittany, Katie Ayers, Andrew Sinclair, & Thomas Ohnesorg. (2016). Review disorders of sex development: The evolving role of genomics in diagnosis and gene discovery. Birth Defects Research Part C Embryo Today Reviews. 108(4). 337–350. 21 indexed citations

13.

Ohnesorg, Thomas, Brittany Croft, Jacqueline Tan, & Andrew Sinclair. (2016). Using ROADMAP Data to Identify Enhancers Associated with Disorders of Sex Development. Sexual Development. 10(2). 59–65. 12 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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