Stefanie Eggers

2.2k citations

25 papers · 728 indexed · h-index 15

Co-authors: Andrew Sinclair Thomas Ohnesorg Stefan J. White Leendert H. J. Looijenga Thomas Illig Katharina Heim Eva Lattka Jerzy Adamski
Topics: Sexual Differentiation and Disorders (10 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers)Urological Disorders and Treatments (5 papers)
Cited by: Genetics Urology Reproductive Medicine
Journals: SHILAP Revista de lepidopterologíaPLoS ONE The American Journal of Human Genetics
Partner nations: Australia United States Netherlands

In The Last Decade

Stefanie Eggers

25 papers receiving 722 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	The cost of proband and trio exome and genome analysis in rare disease: A micro-costing study 2023 ·Genetics in Medicine ·Dylan Mordaunt,(unknown),Sebastian Lunke,Stefanie Eggers,Simon Sadedin,Belinda Chong,Kim Dalziel,Zornitza Stark,Ilias Goranitis	7
2	FGF9 variant in 46, XY DSD patient suggests a role for dimerization in sex determination 2022 ·Clinical Genetics ·Brittany Croft,Anthony D. Bird,Makoto Ono,Stefanie Eggers,Stefan Bagheri‐Fam,Janelle Ryan,(unknown),Jocelyn van den Bergen,Anne Baxendale,Elizabeth M. Thompson,Andrew J. Kueh,Peter G. Stanton,Tim Thomas,Andrew Sinclair,Vincent R. Harley	9
3	Aberrant splicing and transcriptional activity of TPP1 result in CLN2-like disorder 2021 ·European Journal of Medical Genetics ·Guy Helman,(unknown),Marzena Walkiewicz,(unknown),Stefanie Eggers,Joy Yaplito‐Lee,Maria Fuller,(unknown),Victoria Rodriguez‐Casero,Susan M. White,Cas Simons	2
4	Bi-allelic LoF NRROS Variants Impairing Active TGF-β1 Delivery Cause a Severe Infantile-Onset Neurodegenerative Condition with Intracranial Calcification 2020 ·The American Journal of Human Genetics ·Xiaomin Dong,Natalie B. Tan,Katherine B. Howell,Sabina Barresi,Jeremy L. Freeman,Davide Vecchio,Maria Piccione,Francesca Clementina Radio,Daniel G. Calame,Shan Zong,Stefanie Eggers,Ingrid E. Scheffer,Tiong Yang Tan,(unknown),Marco Tartaglia,John Christodoulou,Susan M. White	18
5	Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencing 2019 ·European Journal of Human Genetics ·Lauren Akesson,Stefanie Eggers,(unknown),Belinda Chong,Emma Krzesinski,Natasha J. Brown,Tiong Yang Tan,Christopher M. Richmond,David R. Thorburn,John Christodoulou,Matthew F. Hunter,Sebastian Lunke,Zornitza Stark	14
6	The association between pneumococcal vaccination, ethnicity, and the nasopharyngeal microbiota of children in Fiji 2019 ·Microbiome ·(unknown),Eileen M. Dunne,Moana Mika,Stefanie Eggers,Cattram Nguyen,(unknown),Fiona M. Russell,Kim Mulholland,Markus Hilty,Catherine Satzke	21
7	A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy 2018 ·Epilepsia ·Katherine B. Howell,Stefanie Eggers,Kim Dalziel,Jessica R. Riseley,Simone Mandelstam,Candace T. Myers,Jacinta M. McMahon,Amy Schneider,Gemma L. Carvill,Heather C. Mefford,(unknown),Ingrid E. Scheffer,A. Simon Harvey	64
8	XX Disorder of Sex Development is associated with an insertion on chromosome 9 and downregulation of RSPO1 in dogs (Canis lupus familiaris) 2017 ·PLoS ONE ·Vicki N. Meyers-Wallen,Adam R. Boyko,Charles G. Danko,Jennifer K. Grenier,Jason G. Mezey,Jessica J. Hayward,Laura M. Shannon,Chuan Gao,Afrah Shafquat,Edward J. Rice,Shashikant Pujar,Stefanie Eggers,Thomas Ohnesorg,Andrew Sinclair	13
9	Functional characterization of novel NR5A1 variants reveals multiple complex roles in disorders of sex development 2017 ·Human Mutation ·Gorjana Robevska,Jocelyn A. van den Bergen,Thomas Ohnesorg,Stefanie Eggers,(unknown),Remko Hersmus,Elizabeth M. Thompson,Anne Baxendale,Charles F. Verge,Antony Lafferty,(unknown),(unknown),(unknown),Stefan Riedl,Garry L. Warne,Leendert H. J. Looijenga,Sultana MH Faradz,Katie Ayers,Andrew Sinclair	36
10	Hormonal evaluation in relation to phenotype and genotype in 286 patients with a disorder of sex development from Indonesia 2016 ·Clinical Endocrinology ·Achmad Zulfa Juniarto,Yvonne G. van der Zwan,(unknown),(unknown),Stefanie Eggers,Remko Hersmus,Axel P. N. Themmen,Hennie T. Brüggenwirth,Katja P. Wolffenbuttel,Andrew Sinclair,Stefan J. White,Leendert H. J. Looijenga,Frank H. de Jong,Sultana MH Faradz,Stenvert L. S. Drop	24
11	Functionally distinct roles for different miR-155 expression levels through contrasting effects on gene expression, in acute myeloid leukaemia 2016 ·Leukemia ·Nisha Narayan,(unknown),Belinda Phipson,Simon N. Willis,Gabriela Brumatti,Stefanie Eggers,Najoua Lalaoui,Lauren M. Brown,(unknown),Ray C. Bartolo,Zhou Li,Daniel Catchpoole,Richard Saffery,Alicia Oshlack,Gregory J. Goodall,Paul G. Ekert	44
12	MethPat: a tool for the analysis and visualisation of complex methylation patterns obtained by massively parallel sequencing 2016 ·BMC Bioinformatics ·Nicholas C. Wong,Bernard J. Pope,Ida Candiloro,Darren Korbie,Matt Trau,Stephen Q. Wong,Thomas Mikeska,Xinmin Zhang,(unknown),Stefanie Eggers,Stephen R. Doyle,Alexander Dobrovic	15
13	Whole exome sequencing combined with linkage analysis identifies a novel 3 bp deletion in NR5A1 2014 ·European Journal of Human Genetics ·Stefanie Eggers,Katherine R. Smith,Melanie Bahlo,Leendert H. J. Looijenga,Stenvert L. S. Drop,(unknown),Vincent R. Harley,Peter Koopman,Sultana MH Faradz,Andrew Sinclair	25
14	Copy number variation associated with meiotic arrest in idiopathic male infertility 2014 ·Fertility and Sterility ·Stefanie Eggers,Kathleen DeBoer,Jocelyn van den Bergen,Lavinia Gordon,Stefan J. White,Duangporn Jamsai,Robert I. McLachlan,Andrew Sinclair,Moira K. O’Bryan	32
15	Genetic regulation of mammalian gonad development 2014 ·Nature Reviews Endocrinology ·Stefanie Eggers,Thomas Ohnesorg,Andrew Sinclair	142
16	Mammalian sex determination—insights from humans and mice 2012 ·Chromosome Research ·Stefanie Eggers,Andrew Sinclair	112
17	CITED2 mutations potentially cause idiopathic premature ovarian failure 2012 ·Translational research ·Dora Janeth Fonseca,(unknown),(unknown),R. Braham,Stefanie Eggers,Erin Turbitt,Stefan J. White,Sonia Grover,Garry L. Warne,Margaret Zacharin,(unknown),Hanène Landolsi,Hatem Elghezal,Saad Hasan Mohammed Ali,Carlos Martín Restrepo,Marc Fellous,Andrew Sinclair,Peter Koopman,Paul Laissue	12
18	Detecting DNaseI-Hypersensitivity Sites with MLPA 2011 ·Methods in molecular biology ·Thomas Ohnesorg,Stefanie Eggers,Stefan J. White	2
19	A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1 2009 ·Journal of Lipid Research ·Eva Lattka,Stefanie Eggers,Gabriele Moeller,Katharina Heim,Malory Weber,Divya Mehta,Holger Prokisch,Thomas Illig,Jerzy Adamski	65
20	Rapid high-throughput analysis of DNaseI hypersensitive sites using a modified Multiplex Ligation-dependent Probe Amplification approach 2009 ·BMC Genomics ·Thomas Ohnesorg,Stefanie Eggers,Wouter N. Leonhard,Andrew Sinclair,Stefan J. White	6

About Stefanie Eggers

Stefanie Eggers is a scholar working on Urology, Genetics and Reproductive Medicine, having authored 25 papers that have together received 728 indexed citations. Recurring topics across this 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). The work is most often cited by research in Genetics (450 citations), Urology (99 citations) and Reproductive Medicine (100 citations). Stefanie Eggers has collaborated with scholars based in Australia, United States and Netherlands. Frequent co-authors include Andrew Sinclair, Thomas Ohnesorg, Stefan J. White, Leendert H. J. Looijenga, Thomas Illig, Katharina Heim, Eva Lattka, Jerzy Adamski, Malory Weber and Divya Mehta. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

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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