Andrea Schneider

4.6k total citations
110 papers, 3.2k citations indexed

About

Andrea Schneider is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Andrea Schneider has authored 110 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Genetics, 62 papers in Cognitive Neuroscience and 44 papers in Molecular Biology. Recurrent topics in Andrea Schneider's work include Genetics and Neurodevelopmental Disorders (84 papers), Autism Spectrum Disorder Research (61 papers) and Congenital heart defects research (15 papers). Andrea Schneider is often cited by papers focused on Genetics and Neurodevelopmental Disorders (84 papers), Autism Spectrum Disorder Research (61 papers) and Congenital heart defects research (15 papers). Andrea Schneider collaborates with scholars based in United States, Germany and Canada. Andrea Schneider's co-authors include Randi J. Hagerman, David Hessl, Flora Tassone, Danh V. Nguyen, Susan M. Rivera, David Hessl, Elizabeth Berry‐Kravis, Weerasak Chonchaiya, Andreea L. Seritan and Paul J. Hagerman and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and NeuroImage.

In The Last Decade

Andrea Schneider

104 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrea Schneider United States 30 2.4k 1.9k 1.4k 339 296 110 3.2k
Andrea Beckel‐Mitchener United States 14 1.0k 0.4× 1.4k 0.7× 984 0.7× 315 0.9× 238 0.8× 20 2.6k
Annette K. Taylor United States 40 4.1k 1.7× 3.2k 1.7× 2.6k 1.8× 311 0.9× 257 0.9× 77 5.5k
Éric Lemonnier France 23 1.1k 0.5× 1.5k 0.8× 597 0.4× 596 1.8× 412 1.4× 56 2.5k
Linda M. Brzustowicz United States 36 1.8k 0.8× 894 0.5× 2.3k 1.6× 508 1.5× 342 1.2× 91 4.5k
Jeannie Visootsak United States 26 2.0k 0.8× 1.1k 0.6× 1.2k 0.9× 172 0.5× 173 0.6× 54 2.7k
Masatsugu Tsujii Japan 28 998 0.4× 1.7k 0.9× 718 0.5× 323 1.0× 690 2.3× 68 3.1k
W. Ted Brown United States 31 2.5k 1.1× 1.6k 0.8× 1.5k 1.1× 262 0.8× 95 0.3× 97 3.4k
Louise W. Gane United States 24 3.5k 1.5× 2.1k 1.1× 2.2k 1.5× 543 1.6× 114 0.4× 42 3.9k
Tracey L. Petryshen United States 28 1.1k 0.5× 637 0.3× 1.2k 0.8× 621 1.8× 555 1.9× 50 3.2k
Anne Philippe France 22 1.2k 0.5× 1.4k 0.8× 591 0.4× 186 0.5× 328 1.1× 53 2.4k

Countries citing papers authored by Andrea Schneider

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Schneider

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Schneider

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Schneider. A scholar is included among the top collaborators of Andrea Schneider 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 Andrea Schneider. Andrea Schneider 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.
Tassone, Flora, Andrea Schneider, James A. Bourgeois, et al.. (2025). Premutation Females with preFXTAS. International Journal of Molecular Sciences. 26(6). 2825–2825.
2.
Hung, Mei, James A. Bourgeois, Kyoungmi Kim, et al.. (2024). Psychiatric Manifestations in Early to Middle Stages of Fragile X-Associated Tremor-Ataxia Syndrome (FXTAS). Journal of Neuropsychiatry. 37(1). 20–28. 1 indexed citations
3.
Espinal, Glenda, Blythe Durbin‐Johnson, Andrea Schneider, et al.. (2024). FMR1 Protein Expression Correlates with Intelligence Quotient in Both Peripheral Blood Mononuclear Cells and Fibroblasts from Individuals with an FMR1 Mutation. Journal of Molecular Diagnostics. 26(6). 498–509. 2 indexed citations
4.
Schneider, Andrea, et al.. (2024). Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome. Genes. 15(3). 331–331. 3 indexed citations
5.
Aishworiya, Ramkumar, Kyoungmi Kim, Angela John Thurman, et al.. (2023). Intercorrelation of Molecular Biomarkers and Clinical Phenotype Measures in Fragile X Syndrome. Cells. 12(14). 1920–1920. 4 indexed citations
6.
Kim, Kyoungmi, Andrea Schneider, Cecilia Giulivi, et al.. (2023). Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS). Cells. 12(24). 2773–2773. 8 indexed citations
7.
Aishworiya, Ramkumar, et al.. (2023). Fragile X Syndrome and Fetal Alcohol Syndrome: Occurrence of Dual Diagnosis in a Set of Triplets. Journal of Developmental & Behavioral Pediatrics. 44(7). e470–e475.
8.
Hessl, David, Emilio Ferrer, Glenda Espinal, et al.. (2023). FMR1 Carriers Report Executive Function Changes Prior to Fragile X‐Associated Tremor/Ataxia Syndrome: A Longitudinal Study. Movement Disorders. 39(3). 519–525. 3 indexed citations
9.
Espinal, Glenda, Ramkumar Aishworiya, Andrea Schneider, et al.. (2022). Tophaceous gout of the nose in a male FMR1 premutation carrier. SHILAP Revista de lepidopterología. 10(11). e6586–e6586. 1 indexed citations
10.
Schneider, Andrea, Dragana Protić, Jun Yi Wang, et al.. (2020). <p>Rapidly Progressing Neurocognitive Disorder in a Male with FXTAS and Alzheimer’s Disease</p>. Clinical Interventions in Aging. Volume 15. 285–292. 6 indexed citations
12.
Sansone, Stephanie M., Andrea Schneider, Cindy Johnston, et al.. (2016). Psychiatric disorders among women with the fragile X premutation without children affected by fragile X syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(8). 1139–1147. 22 indexed citations
13.
Lozano, Reymundo, Naomi Saito, Andrea Schneider, et al.. (2016). Aging in Fragile X Premutation Carriers. The Cerebellum. 15(5). 587–594. 12 indexed citations
14.
Abrams, Liane, et al.. (2015). Contraction of a Maternal Fragile X Mental Retardation 1 Premutation Allele. Journal of Medical Cases. 6(12). 547–553. 2 indexed citations
15.
Loesch, Danuta Z., Minh Bui, Andrea Schneider, et al.. (2014). Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion. Clinical Genetics. 87(2). 173–178. 35 indexed citations
16.
Wang, Jun Yi, David Hessl, Christine Iwahashi, et al.. (2012). Influence of the fragile X mental retardation (FMR1) gene on the brain and working memory in men with normal FMR1 alleles. NeuroImage. 65. 288–298. 33 indexed citations
17.
Hessl, David, Andrea Schneider, Kami Koldewyn, et al.. (2011). Decreased Fragile X Mental Retardation Protein Expression Underlies Amygdala Dysfunction in Carriers of the Fragile X Premutation. Biological Psychiatry. 70(9). 859–865. 80 indexed citations
18.
Chonchaiya, Weerasak, Jacky Au, Andrea Schneider, et al.. (2011). Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder. Human Genetics. 131(4). 581–589. 86 indexed citations
19.
Schneider, Andrea, Elizabeth Ballinger, Alyssa Chavez, et al.. (2010). Prepulse inhibition in patients with fragile X-associated tremor ataxia syndrome. Neurobiology of Aging. 33(6). 1045–1053. 14 indexed citations
20.
Bourgeois, James A., Andreea L. Seritan, David Hessl, et al.. (2010). Lifetime Prevalence of Mood and Anxiety Disorders in Fragile X Premutation Carriers. The Journal of Clinical Psychiatry. 72(2). 175–182. 145 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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