Stefanie Eggers

2.2k total citations
25 papers, 728 citations indexed

About

Stefanie Eggers is a scholar working on Molecular Biology, Genetics and Urology. According to data from OpenAlex, Stefanie Eggers has authored 25 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Genetics and 5 papers in Urology. Recurrent topics in Stefanie Eggers's work include Sexual Differentiation and Disorders (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers) and Urological Disorders and Treatments (5 papers). Stefanie Eggers is often cited by papers focused on Sexual Differentiation and Disorders (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers) and Urological Disorders and Treatments (5 papers). Stefanie Eggers collaborates with scholars based in Australia, United States and Netherlands. Stefanie Eggers's co-authors include Andrew Sinclair, Thomas Ohnesorg, Stefan J. White, Leendert H. J. Looijenga, Holger Prokisch, Sultana MH Faradz, Eva Lattka, Malory Weber, Thomas Illig and Jerzy Adamski and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Stefanie Eggers

25 papers receiving 722 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefanie Eggers Australia 15 466 450 100 99 83 25 728
Deidre M Mattiske Australia 14 361 0.8× 103 0.2× 77 0.8× 51 0.5× 97 1.2× 27 581
Yunmin Li United States 16 617 1.3× 589 1.3× 196 2.0× 32 0.3× 37 0.4× 25 871
Alastair S. H. Goldman United Kingdom 21 1.1k 2.5× 436 1.0× 75 0.8× 19 0.2× 102 1.2× 41 1.5k
Winnie Shum United States 19 421 0.9× 77 0.2× 318 3.2× 31 0.3× 55 0.7× 30 866
I. Fontaine France 15 276 0.6× 249 0.6× 301 3.0× 17 0.2× 29 0.3× 28 707
Andrew J. Childs United Kingdom 19 631 1.4× 344 0.8× 288 2.9× 28 0.3× 71 0.9× 32 1.1k
Bertha Chávez Mexico 19 488 1.0× 395 0.9× 157 1.6× 117 1.2× 14 0.2× 49 824
Qunsheng Dai United States 14 329 0.7× 187 0.4× 227 2.3× 11 0.1× 50 0.6× 17 667
Yvonne A.R. White United States 10 464 1.0× 127 0.3× 302 3.0× 18 0.2× 29 0.3× 11 849
Xinchang Zhou China 7 376 0.8× 351 0.8× 341 3.4× 29 0.3× 48 0.6× 9 920

Countries citing papers authored by Stefanie Eggers

Since Specialization
Citations

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

Fields of papers citing papers by Stefanie Eggers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefanie Eggers

This figure shows the co-authorship network connecting the top 25 collaborators of Stefanie Eggers. A scholar is included among the top collaborators of Stefanie Eggers 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 Stefanie Eggers. Stefanie Eggers 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.
Mordaunt, Dylan, Sebastian Lunke, Stefanie Eggers, et al.. (2023). The cost of proband and trio exome and genome analysis in rare disease: A micro-costing study. Genetics in Medicine. 26(4). 101058–101058. 7 indexed citations
2.
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
3.
Helman, Guy, Marzena Walkiewicz, Stefanie Eggers, et al.. (2021). Aberrant splicing and transcriptional activity of TPP1 result in CLN2-like disorder. European Journal of Medical Genetics. 64(8). 104259–104259. 2 indexed citations
4.
Dong, Xiaomin, Natalie B. Tan, Katherine B. Howell, et al.. (2020). Bi-allelic LoF NRROS Variants Impairing Active TGF-β1 Delivery Cause a Severe Infantile-Onset Neurodegenerative Condition with Intracranial Calcification. The American Journal of Human Genetics. 106(4). 559–569. 18 indexed citations
5.
Akesson, Lauren, Stefanie Eggers, Belinda Chong, et al.. (2019). Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencing. European Journal of Human Genetics. 27(12). 1821–1826. 14 indexed citations
6.
Dunne, Eileen M., Moana Mika, Stefanie Eggers, et al.. (2019). The association between pneumococcal vaccination, ethnicity, and the nasopharyngeal microbiota of children in Fiji. Microbiome. 7(1). 106–106. 21 indexed citations
7.
Howell, Katherine B., Stefanie Eggers, Kim Dalziel, et al.. (2018). A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy. Epilepsia. 59(6). 1177–1187. 64 indexed citations
8.
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
9.
Robevska, Gorjana, Jocelyn A. van den Bergen, Thomas Ohnesorg, et al.. (2017). Functional characterization of novel NR5A1 variants reveals multiple complex roles in disorders of sex development. Human Mutation. 39(1). 124–139. 36 indexed citations
10.
Meyers-Wallen, Vicki N., Adam R. Boyko, Charles G. Danko, et al.. (2017). XX Disorder of Sex Development is associated with an insertion on chromosome 9 and downregulation of RSPO1 in dogs (Canis lupus familiaris). PLoS ONE. 12(10). e0186331–e0186331. 13 indexed citations
11.
Juniarto, Achmad Zulfa, Yvonne G. van der Zwan, Stefanie Eggers, et al.. (2016). Hormonal evaluation in relation to phenotype and genotype in 286 patients with a disorder of sex development from Indonesia. Clinical Endocrinology. 85(2). 247–257. 24 indexed citations
12.
Narayan, Nisha, Belinda Phipson, Simon N. Willis, et al.. (2016). Functionally distinct roles for different miR-155 expression levels through contrasting effects on gene expression, in acute myeloid leukaemia. Leukemia. 31(4). 808–820. 44 indexed citations
13.
Wong, Nicholas C., Bernard J. Pope, Ida Candiloro, et al.. (2016). MethPat: a tool for the analysis and visualisation of complex methylation patterns obtained by massively parallel sequencing. BMC Bioinformatics. 17(1). 98–98. 15 indexed citations
14.
Eggers, Stefanie, Katherine R. Smith, Melanie Bahlo, et al.. (2014). Whole exome sequencing combined with linkage analysis identifies a novel 3 bp deletion in NR5A1. European Journal of Human Genetics. 23(4). 486–493. 25 indexed citations
15.
Eggers, Stefanie, Thomas Ohnesorg, & Andrew Sinclair. (2014). Genetic regulation of mammalian gonad development. Nature Reviews Endocrinology. 10(11). 673–683. 142 indexed citations
16.
Eggers, Stefanie, Kathleen DeBoer, Jocelyn van den Bergen, et al.. (2014). Copy number variation associated with meiotic arrest in idiopathic male infertility. Fertility and Sterility. 103(1). 214–219. 32 indexed citations
17.
Eggers, Stefanie & Andrew Sinclair. (2012). Mammalian sex determination—insights from humans and mice. Chromosome Research. 20(1). 215–238. 112 indexed citations
18.
Fonseca, Dora Janeth, R. Braham, Stefanie Eggers, et al.. (2012). CITED2 mutations potentially cause idiopathic premature ovarian failure. Translational research. 160(5). 384–388. 12 indexed citations
19.
Ohnesorg, Thomas, Stefanie Eggers, Wouter N. Leonhard, Andrew Sinclair, & Stefan J. White. (2009). Rapid high-throughput analysis of DNaseI hypersensitive sites using a modified Multiplex Ligation-dependent Probe Amplification approach. BMC Genomics. 10(1). 412–412. 6 indexed citations
20.
Lattka, Eva, Stefanie Eggers, Gabriele Moeller, et al.. (2009). A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1. Journal of Lipid Research. 51(1). 182–191. 65 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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