Lauren E. Ethridge

3.0k total citations · 1 hit paper
45 papers, 1.9k citations indexed

About

Lauren E. Ethridge is a scholar working on Cognitive Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, Lauren E. Ethridge has authored 45 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Cognitive Neuroscience, 19 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Lauren E. Ethridge's work include Genetics and Neurodevelopmental Disorders (19 papers), Autism Spectrum Disorder Research (15 papers) and Neural dynamics and brain function (13 papers). Lauren E. Ethridge is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), Autism Spectrum Disorder Research (15 papers) and Neural dynamics and brain function (13 papers). Lauren E. Ethridge collaborates with scholars based in United States, China and United Kingdom. Lauren E. Ethridge's co-authors include John A. Sweeney, Matthew W. Mosconi, Brett A. Clementz, Jun Wang, Godfrey D. Pearlson, Matcheri S. Keshavan, Carol A. Tamminga, Jordan P. Hamm, Yukari Takarae and Jamie Barstein and has published in prestigious journals such as Nature Medicine, Nature Communications and Journal of Neuroscience.

In The Last Decade

Lauren E. Ethridge

37 papers receiving 1.9k citations

Hit Papers

Identification of Distinct Psychosis Biotypes Using Brain... 2015 2026 2018 2022 2015 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lauren E. Ethridge United States 19 1.4k 631 511 353 268 45 1.9k
Rebekka Lencer Germany 30 1.1k 0.8× 173 0.3× 758 1.5× 308 0.9× 404 1.5× 114 2.5k
Jordan P. Hamm United States 28 1.6k 1.1× 136 0.2× 425 0.8× 257 0.7× 736 2.7× 49 2.2k
Tobias Renner Germany 20 605 0.4× 226 0.4× 786 1.5× 191 0.5× 292 1.1× 47 1.4k
Matthew W. Mosconi United States 27 2.4k 1.7× 897 1.4× 788 1.5× 396 1.1× 273 1.0× 68 2.9k
Brett A. Clementz United States 17 920 0.7× 183 0.3× 842 1.6× 218 0.6× 206 0.8× 28 1.7k
Roberto Galvez United States 17 856 0.6× 560 0.9× 146 0.3× 581 1.6× 613 2.3× 37 1.8k
Deana Crocetti United States 25 1.4k 1.0× 255 0.4× 888 1.7× 150 0.4× 247 0.9× 57 2.1k
Taina Nieminen‐von Wendt Finland 23 1.3k 0.9× 360 0.6× 434 0.8× 216 0.6× 76 0.3× 35 1.7k
Toshio Munesue Japan 25 1.1k 0.8× 245 0.4× 269 0.5× 100 0.3× 81 0.3× 62 1.7k
Caroline E. Robertson United States 15 1.4k 1.0× 260 0.4× 250 0.5× 197 0.6× 239 0.9× 31 1.6k

Countries citing papers authored by Lauren E. Ethridge

Since Specialization
Citations

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

Fields of papers citing papers by Lauren E. Ethridge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lauren E. Ethridge. 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 Lauren E. Ethridge. The network helps show where Lauren E. Ethridge may publish in the future.

Co-authorship network of co-authors of Lauren E. Ethridge

This figure shows the co-authorship network connecting the top 25 collaborators of Lauren E. Ethridge. A scholar is included among the top collaborators of Lauren E. Ethridge 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 Lauren E. Ethridge. Lauren E. Ethridge 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.
2.
Gelegen, Çiğdem, et al.. (2026). A human electrophysiological signature of Fragile X pathophysiology is shared in V1 of Fmr1-/y mice. Nature Communications. 17(1). 1497–1497.
4.
Smith, Michelle, Elizabeth Berry‐Kravis, Allison Durkin, et al.. (2025). Phenotypic variation in neural sensory processing by deletion size, age, and sex in Phelan-McDermid syndrome. Journal of Neurodevelopmental Disorders. 17(1). 51–51.
5.
Ewen, Joshua B., Claudio Babiloni, Gary S. Collins, et al.. (2025). The GREENBEAN checklist for reporting studies evaluating the effectiveness of EEG-based biomarkers. Clinical Neurophysiology. 176. 2110777–2110777.
6.
Schmitt, Lauren, Lauren E. Ethridge, Paul S. Horn, et al.. (2024). Results from a Double-Blind, Randomized, Placebo-Controlled, Single-Dose, Crossover Trial of Lovastatin or Minocycline in Fragile X Syndrome. Journal of Child and Adolescent Psychopharmacology. 35(4). 211–221.
7.
8.
Schmitt, Lauren, et al.. (2023). Neuropsychiatric feature-based subgrouping reveals neural sensory processing spectrum in female FMR1 premutation carriers: A pilot study. Frontiers in Integrative Neuroscience. 17. 898215–898215.
9.
Pedapati, Ernest V., Lauren Schmitt, Lauren E. Ethridge, et al.. (2022). Neocortical localization and thalamocortical modulation of neuronal hyperexcitability contribute to Fragile X Syndrome. Communications Biology. 5(1). 442–442. 24 indexed citations
11.
Jonak, Carrie R., Ernest V. Pedapati, Lauren Schmitt, et al.. (2022). Baclofen-associated neurophysiologic target engagement across species in fragile X syndrome. Journal of Neurodevelopmental Disorders. 14(1). 52–52. 13 indexed citations
12.
Schmitt, Lauren, Kelli C. Dominick, Ernest V. Pedapati, et al.. (2022). Evidence for Three Subgroups of Female FMR1 Premutation Carriers Defined by Distinct Neuropsychiatric Features: A Pilot Study. Frontiers in Integrative Neuroscience. 15. 797546–797546. 5 indexed citations
13.
Berry‐Kravis, Elizabeth, Joseph D. Buxbaum, Lauren E. Ethridge, et al.. (2021). Shifted phase of EEG cross-frequency coupling in individuals with Phelan-McDermid syndrome. Molecular Autism. 12(1). 29–29. 11 indexed citations
14.
Berry‐Kravis, Elizabeth, et al.. (2021). Inhibition of phosphodiesterase-4D in adults with fragile X syndrome: a randomized, placebo-controlled, phase 2 clinical trial. Nature Medicine. 27(5). 862–870. 85 indexed citations
15.
Schmitt, Lauren, et al.. (2019). Developmental Effects on Auditory Neural Oscillatory Synchronization Abnormalities in Autism Spectrum Disorder. Frontiers in Integrative Neuroscience. 13. 34–34. 26 indexed citations
16.
Wang, Jun, Lauren E. Ethridge, Matthew W. Mosconi, et al.. (2017). A resting EEG study of neocortical hyperexcitability and altered functional connectivity in fragile X syndrome. Journal of Neurodevelopmental Disorders. 9(1). 11–11. 112 indexed citations
17.
Wang, Jun, Jamie Barstein, Lauren E. Ethridge, et al.. (2013). Resting state EEG abnormalities in autism spectrum disorders. Journal of Neurodevelopmental Disorders. 5(1). 24–24. 367 indexed citations
18.
Ethridge, Lauren E., Jordan P. Hamm, Ann Summerfelt, et al.. (2012). Neural Activations During Auditory Oddball Processing Discriminating Schizophrenia and Psychotic Bipolar Disorder. Biological Psychiatry. 72(9). 766–774. 54 indexed citations
19.
Ethridge, Lauren E., Stephen M. Malone, William G. Iacono, & Brett A. Clementz. (2012). Genetic influences on composite neural activations supporting visual target identification. Biological Psychology. 92(2). 329–341. 4 indexed citations
20.
Ethridge, Lauren E., Shefali Brahmbhatt, Yuan Gao, Jennifer E. McDowell, & Brett A. Clementz. (2009). Consider the context: Blocked versus interleaved presentation of antisaccade trials. Psychophysiology. 46(5). 1100–1107. 25 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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