Randi J. Hagerman

2.2k total citations
31 papers, 1.6k citations indexed

About

Randi J. Hagerman is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Randi J. Hagerman has authored 31 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 24 papers in Cognitive Neuroscience and 17 papers in Molecular Biology. Recurrent topics in Randi J. Hagerman's work include Genetics and Neurodevelopmental Disorders (31 papers), Autism Spectrum Disorder Research (24 papers) and Congenital heart defects research (7 papers). Randi J. Hagerman is often cited by papers focused on Genetics and Neurodevelopmental Disorders (31 papers), Autism Spectrum Disorder Research (24 papers) and Congenital heart defects research (7 papers). Randi J. Hagerman collaborates with scholars based in United States, Australia and France. Randi J. Hagerman's co-authors include Flora Tassone, Khaled M. A. Amiri, Amy Cronister, Claudia Bagni, Giovanni Neri, William E. Sobesky, Paul J. Hagerman, Louise W. Gane, Annette K. Taylor and Michael D. Wittenberger and has published in prestigious journals such as Journal of Clinical Investigation, PEDIATRICS and Scientific Reports.

In The Last Decade

Randi J. Hagerman

28 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Randi J. Hagerman United States 19 1.4k 947 852 182 91 31 1.6k
Richard J. Schroer United States 24 1.3k 0.9× 795 0.8× 976 1.1× 208 1.1× 173 1.9× 39 2.0k
P. J. Hagerman United States 9 1.1k 0.8× 667 0.7× 754 0.9× 171 0.9× 104 1.1× 9 1.2k
Richard J. Simensen United States 21 1.2k 0.9× 638 0.7× 912 1.1× 82 0.5× 108 1.2× 50 1.9k
Susan Harris United States 9 1.1k 0.8× 821 0.9× 595 0.7× 108 0.6× 80 0.9× 13 1.2k
Amber Hogart United States 10 1.2k 0.9× 627 0.7× 972 1.1× 115 0.6× 28 0.3× 10 1.5k
Reymundo Lozano United States 20 819 0.6× 519 0.5× 552 0.6× 100 0.5× 40 0.4× 44 1.1k
Michele Ono United States 10 808 0.6× 691 0.7× 461 0.5× 87 0.5× 65 0.7× 12 1.0k
Ave M. Lachiewicz United States 23 1.6k 1.1× 1.2k 1.3× 784 0.9× 115 0.6× 50 0.5× 38 1.9k
Jennifer Reichert United States 15 1.5k 1.1× 1.6k 1.6× 869 1.0× 190 1.0× 61 0.7× 17 2.3k
Karin Ziliotto Dias Brazil 10 1.1k 0.8× 854 0.9× 649 0.8× 116 0.6× 24 0.3× 19 1.4k

Countries citing papers authored by Randi J. Hagerman

Since Specialization
Citations

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

Fields of papers citing papers by Randi J. Hagerman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Randi J. Hagerman. 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 Randi J. Hagerman. The network helps show where Randi J. Hagerman may publish in the future.

Co-authorship network of co-authors of Randi J. Hagerman

This figure shows the co-authorship network connecting the top 25 collaborators of Randi J. Hagerman. A scholar is included among the top collaborators of Randi J. Hagerman 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 Randi J. Hagerman. Randi J. Hagerman 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.
Caruana, Giovanni, et al.. (2025). Involvement of the Cerebellar Peduncles in FMR1 Premutation Carriers: A Pictorial Review of Their Anatomy, Imaging, and Pathology. International Journal of Molecular Sciences. 26(9). 4402–4402.
2.
Zhu, Yiting, Dongyun Li, Chunchun Hu, et al.. (2025). Effects of Metformin on children with Fragile X Syndrome: a randomized, double-blind, placebo-controlled trial. Molecular Autism. 16(1). 57–57.
3.
Wang, Jun Yi, Laia Rodríguez‐Revenga, Kyoungmi Kim, et al.. (2024). Enlarged perivascular spaces and their association with motor, cognition, MRI markers and cerebrovascular risk factors in male fragile X premutation carriers. Journal of the Neurological Sciences. 461. 123056–123056. 1 indexed citations
4.
Maltman, Nell, et al.. (2024). Language use predicts symptoms of fragile X-associated tremor/ataxia syndrome in men and women with the FMR1 premutation. Scientific Reports. 14(1). 20707–20707. 1 indexed citations
5.
Hagerman, Randi J., Sébastien Jacquemont, Elizabeth Berry‐Kravis, et al.. (2018). Mavoglurant in Fragile X Syndrome: Results of two open-label, extension trials in adults and adolescents. Scientific Reports. 8(1). 16970–16970. 40 indexed citations
6.
Hagerman, Randi J.. (2014). Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers. PubMed. 3(2). 38 indexed citations
7.
Bagni, Claudia, Flora Tassone, Giovanni Neri, & Randi J. Hagerman. (2012). Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics. Journal of Clinical Investigation. 122(12). 4314–4322. 247 indexed citations
8.
Yrigollen, Carolyn M., Blythe Durbin‐Johnson, Louise W. Gane, et al.. (2012). AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome. Genetics in Medicine. 14(8). 729–736. 134 indexed citations
9.
Gane, Louise W., et al.. (2012). A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male. American Journal of Medical Genetics Part A. 158A(5). 1221–1224. 6 indexed citations
10.
Godler, David E., Howard R. Slater, Minh Bui, et al.. (2011). FMR1 Intron 1 Methylation Predicts FMRP Expression in Blood of Female Carriers of Expanded FMR1 Alleles. Journal of Molecular Diagnostics. 13(5). 528–536. 37 indexed citations
11.
Napoli, Eleonora, Catherine Ross‐Inta, Sarah Wong, et al.. (2011). Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndrome. Human Molecular Genetics. 20(15). 3079–3092. 91 indexed citations
12.
Tassone, Flora & Randi J. Hagerman. (2011). The Fragile X-Associated Tremor Ataxia Syndrome. Results and problems in cell differentiation. 54. 337–357. 31 indexed citations
13.
Chavez, Alyssa, et al.. (2011). Clinical phenotypes of a juvenile sibling pair carrying the fragile X premutation. American Journal of Medical Genetics Part A. 155(3). 519–525. 13 indexed citations
14.
Hall, Deborah A., et al.. (2008). Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease. Parkinsonism & Related Disorders. 15(2). 156–159. 50 indexed citations
15.
Sobesky, William E., Annette K. Taylor, Bruce F. Pennington, et al.. (1996). Molecular/clinical correlations in females with fragile X. American Journal of Medical Genetics. 64(2). 340–345. 71 indexed citations
16.
Hagerman, Randi J., et al.. (1994). A survey of fluoxetine therapy in fragile X syndrome. 7. 155–164. 29 indexed citations
17.
Sobesky, William E., Louise W. Staley, Elizabeth Berry‐Kravis, et al.. (1994). Fragile X Syndrome in a Normal IQ Male with Learning and Emotional Problems. Journal of the American Academy of Child & Adolescent Psychiatry. 33(9). 1316–1321. 32 indexed citations
18.
Hagerman, Randi J., et al.. (1992). Girls With Fragile X Syndrome: Physical and Neurocognitive Status and Outcome. PEDIATRICS. 89(3). 395–400. 120 indexed citations
19.
Goldson, Edward & Randi J. Hagerman. (1992). The Fragile X Syndrome. Developmental Medicine & Child Neurology. 34(9). 826–832. 18 indexed citations
20.
Hagerman, Randi J., Khaled M. A. Amiri, & Amy Cronister. (1991). Fragile X checklist. American Journal of Medical Genetics. 38(2-3). 283–287. 124 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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