Stephanie Fehr

899 total citations
10 papers, 641 citations indexed

About

Stephanie Fehr is a scholar working on Genetics, Clinical Psychology and Cognitive Neuroscience. According to data from OpenAlex, Stephanie Fehr has authored 10 papers receiving a total of 641 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Clinical Psychology and 4 papers in Cognitive Neuroscience. Recurrent topics in Stephanie Fehr's work include Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (4 papers). Stephanie Fehr is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (4 papers). Stephanie Fehr collaborates with scholars based in Australia, United Kingdom and Canada. Stephanie Fehr's co-authors include Helen Leonard, Jenny Downs, Nicholas de Klerk, Simon Williams, John Christodoulou, Gladys Ho, Ami Bebbington, David Forbes, Gabriel M. Ronen and Natasha Nassar and has published in prestigious journals such as Neurology, Drug and Alcohol Dependence and Pediatric Research.

In The Last Decade

Stephanie Fehr

10 papers receiving 633 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephanie Fehr Australia 8 584 235 188 152 103 10 641
Daniel Moreno‐De‐Luca United States 9 413 0.7× 389 1.7× 179 1.0× 63 0.4× 106 1.0× 16 677
Assunção Ataíde Portugal 8 433 0.7× 501 2.1× 196 1.0× 50 0.3× 157 1.5× 8 691
S. A. Ravan United States 6 527 0.9× 546 2.3× 163 0.9× 75 0.5× 77 0.7× 6 661
Walter E. Kaufmann United States 15 867 1.5× 661 2.8× 313 1.7× 325 2.1× 97 0.9× 24 1.0k
Suzanne Geerts United States 9 697 1.2× 508 2.2× 189 1.0× 325 2.1× 97 0.9× 10 744
S. L. Donnelly United States 7 549 0.9× 543 2.3× 229 1.2× 51 0.3× 74 0.7× 9 793
Teresa S. Miguel Portugal 9 358 0.6× 404 1.7× 159 0.8× 44 0.3× 140 1.4× 11 597
Giorgio Pini Italy 14 474 0.8× 348 1.5× 159 0.8× 174 1.1× 32 0.3× 36 591
Ny Hoang Canada 10 477 0.8× 215 0.9× 162 0.9× 42 0.3× 42 0.4× 20 608
Laura Nations United States 7 201 0.3× 223 0.9× 127 0.7× 74 0.5× 53 0.5× 8 398

Countries citing papers authored by Stephanie Fehr

Since Specialization
Citations

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

Fields of papers citing papers by Stephanie Fehr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Fehr

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

All Works

10 of 10 papers shown
1.
Fehr, Stephanie, Jenny Downs, Gladys Ho, et al.. (2016). Functional abilities in children and adults with the CDKL5 disorder. American Journal of Medical Genetics Part A. 170(11). 2860–2869. 74 indexed citations
2.
Fehr, Stephanie, Kingsley Wong, Richard Chin, et al.. (2016). Seizure variables and their relationship to genotype and functional abilities in the CDKL5 disorder. Neurology. 87(21). 2206–2213. 78 indexed citations
3.
Fehr, Stephanie, Helen Leonard, Gladys Ho, et al.. (2015). There is variability in the attainment of developmental milestones in the CDKL5 disorder. Journal of Neurodevelopmental Disorders. 7(1). 2–2. 73 indexed citations
4.
Fehr, Stephanie. (2015). The natural history of the CDKL5 disorder: development of an international database. UWA Profiles and Research Repository (University of Western Australia). 1 indexed citations
5.
Fehr, Stephanie, Meredith Wilson, Jenny Downs, et al.. (2012). The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy. European Journal of Human Genetics. 21(3). 266–273. 209 indexed citations
6.
Fehr, Stephanie, Ami Bebbington, Natasha Nassar, et al.. (2011). Trends in the Diagnosis of Rett Syndrome in Australia. Pediatric Research. 70(3). 313–319. 117 indexed citations
7.
Vogel, Marc, Kenneth M. Dürsteler‐MacFarland, Marc Walter, et al.. (2011). Prolonged use of benzodiazepines is associated with childhood trauma in opioid-maintained patients. Drug and Alcohol Dependence. 119(1-2). 93–98. 18 indexed citations
8.
Bao, Xinhua, Hui Lü, Hong Pan, et al.. (2011). What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?. Clinical Genetics. 82(6). 526–533. 5 indexed citations
9.
Fehr, Stephanie, et al.. (2011). Altered Attainment of Developmental Milestones Influences the Age of Diagnosis of Rett Syndrome. Journal of Child Neurology. 26(8). 980–987. 36 indexed citations
10.
Fehr, Stephanie, Jenny Downs, Ami Bebbington, & Helen Leonard. (2010). Atypical presentations and specific genotypes are associated with a delay in diagnosis in females with Rett syndrome. American Journal of Medical Genetics Part A. 152A(10). 2535–2542. 30 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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2026