Allan L. Reiss

71.5k total citations · 11 hit papers
529 papers, 53.3k citations indexed

About

Allan L. Reiss is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Allan L. Reiss has authored 529 papers receiving a total of 53.3k indexed citations (citations by other indexed papers that have themselves been cited), including 238 papers in Genetics, 236 papers in Cognitive Neuroscience and 123 papers in Molecular Biology. Recurrent topics in Allan L. Reiss's work include Genetics and Neurodevelopmental Disorders (193 papers), Autism Spectrum Disorder Research (132 papers) and Congenital heart defects research (89 papers). Allan L. Reiss is often cited by papers focused on Genetics and Neurodevelopmental Disorders (193 papers), Autism Spectrum Disorder Research (132 papers) and Congenital heart defects research (89 papers). Allan L. Reiss collaborates with scholars based in United States, United Kingdom and Japan. Allan L. Reiss's co-authors include Vinod Menon, Michael D. Greicius, Gary H. Glover, Alan F. Schatzberg, Heather A. Kenna, Jennifer Keller, Gaurav Srivastava, William W. Seeley, Stéphan Eliez and Xu Cui and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Nature Communications.

In The Last Decade

Allan L. Reiss

522 papers receiving 52.0k citations

Hit Papers

Dissociable Intrinsic Connectivity Networks for Salience ... 2001 2026 2009 2017 2007 2002 2004 2007 2001 1000 2.0k 3.0k 4.0k 5.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Allan L. Reiss United States 108 32.8k 11.4k 8.7k 8.5k 7.3k 529 53.3k
Jay N. Giedd United States 106 24.6k 0.8× 4.5k 0.4× 8.9k 1.0× 12.2k 1.4× 3.6k 0.5× 263 48.4k
Daniel R. Weinberger United States 141 33.9k 1.0× 10.4k 0.9× 9.4k 1.1× 25.5k 3.0× 17.1k 2.3× 719 83.1k
René S. Kahn Netherlands 108 19.3k 0.6× 4.2k 0.4× 7.9k 0.9× 16.3k 1.9× 5.6k 0.8× 734 45.5k
Judith L. Rapoport United States 102 20.8k 0.6× 3.9k 0.3× 5.7k 0.7× 16.9k 2.0× 3.5k 0.5× 413 43.3k
Eric Courchesne United States 96 24.5k 0.7× 9.2k 0.8× 2.3k 0.3× 4.8k 0.6× 4.2k 0.6× 200 31.3k
Declan Murphy United Kingdom 93 15.1k 0.5× 5.2k 0.5× 3.7k 0.4× 6.1k 0.7× 3.9k 0.5× 541 31.2k
Nancy C. Andreasen United States 120 22.3k 0.7× 3.4k 0.3× 9.6k 1.1× 29.2k 3.4× 3.9k 0.5× 515 56.9k
Raquel E. Gur United States 107 22.0k 0.7× 2.5k 0.2× 7.4k 0.8× 13.5k 1.6× 3.7k 0.5× 620 42.3k
Matcheri S. Keshavan United States 98 16.5k 0.5× 3.2k 0.3× 5.7k 0.7× 18.0k 2.1× 3.3k 0.5× 911 42.0k
Andreas Meyer‐Lindenberg Germany 96 15.5k 0.5× 3.0k 0.3× 4.1k 0.5× 7.1k 0.8× 3.7k 0.5× 459 34.8k

Countries citing papers authored by Allan L. Reiss

Since Specialization
Citations

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

Fields of papers citing papers by Allan L. Reiss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Allan L. Reiss. 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 Allan L. Reiss. The network helps show where Allan L. Reiss may publish in the future.

Co-authorship network of co-authors of Allan L. Reiss

This figure shows the co-authorship network connecting the top 25 collaborators of Allan L. Reiss. A scholar is included among the top collaborators of Allan L. Reiss 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 Allan L. Reiss. Allan L. Reiss 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.
Gao, Yuanyuan, et al.. (2024). Longitudinal Changes in Functional Neural Activation and Sensitization During Face Processing in Fragile X Syndrome. Biological Psychiatry. 97(5). 499–506. 1 indexed citations
2.
Klabunde, Megan, Tamar Green, David S. Hong, et al.. (2023). Longitudinal investigation of cognition, social competence, and anxiety in children and adolescents with Turner syndrome. Hormones and Behavior. 149. 105300–105300. 3 indexed citations
3.
Li, Rihui, Jennifer L. Bruno, Cindy H. Lee, et al.. (2022). Aberrant brain network and eye gaze patterns during natural social interaction predict multi-domain social-cognitive behaviors in girls with fragile X syndrome. Molecular Psychiatry. 27(9). 3768–3776. 6 indexed citations
4.
Balters, Stephanie, Lara C. Foland‐Ross, Sabrina Brigadoi, et al.. (2022). Towards assessing subcortical “deep brain” biomarkers of PTSD with functional near-infrared spectroscopy. Cerebral Cortex. 33(7). 3969–3984. 5 indexed citations
5.
Lee, Cindy H., et al.. (2021). COVID-19 Pandemic: Mental Health in Girls With and Without Fragile X Syndrome. Journal of Pediatric Psychology. 47(1). 25–36. 4 indexed citations
6.
Bruno, Jennifer L., David S. Hong, Amy A. Lightbody, et al.. (2020). Glucocorticoid regulation and neuroanatomy in fragile x syndrome. Journal of Psychiatric Research. 134. 81–88. 1 indexed citations
7.
Xie, Hua, Iliana I. Karipidis, Amber Howell, et al.. (2020). Finding the neural correlates of collaboration using a three-person fMRI hyperscanning paradigm. Proceedings of the National Academy of Sciences. 117(37). 23066–23072. 41 indexed citations
9.
Kenna, Heather A., Scott S. Hall, Amy A. Lightbody, et al.. (2013). High rates of comorbid depressive and anxiety disorders among women with premutation of the FMR1 gene. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(8). 872–878. 24 indexed citations
10.
Cohen, Jeremy D., et al.. (2013). Insular cortex abnormalities in psychotic major depression: Relationship to gender and psychotic symptoms. Neuroscience Research. 75(4). 331–339. 10 indexed citations
11.
Wolff, Jason J., James W. Bodfish, Heather C. Hazlett, et al.. (2012). Evidence of a Distinct Behavioral Phenotype in Young Boys With Fragile X Syndrome and Autism. Journal of the American Academy of Child & Adolescent Psychiatry. 51(12). 1324–1332. 76 indexed citations
12.
Kelley, Ryan, Amy Garrett, Jeremy D. Cohen, et al.. (2012). Altered brain function underlying verbal memory encoding and retrieval in psychotic major depression. Psychiatry Research Neuroimaging. 211(2). 119–126. 35 indexed citations
13.
Kesler, Shelli R., Charles E. Schwartz, Roger E. Stevenson, & Allan L. Reiss. (2009). The impact of spermine synthase (SMS) mutations on brain morphology. Neurogenetics. 10(4). 299–305. 20 indexed citations
14.
Hall, Scott S., David D. Burns, Amy A. Lightbody, & Allan L. Reiss. (2008). Longitudinal Changes in Intellectual Development in Children with Fragile X Syndrome. Journal of Abnormal Child Psychology. 36(6). 927–939. 61 indexed citations
15.
Greicius, Michael D., Benjamin Flores, Vinod Menon, et al.. (2007). Resting-State Functional Connectivity in Major Depression: Abnormally Increased Contributions from Subgenual Cingulate Cortex and Thalamus. Biological Psychiatry. 62(5). 429–437. 1756 indexed citations breakdown →
16.
Carrión, Victor G., Carl F. Weems, & Allan L. Reiss. (2007). Stress Predicts Brain Changes in Children: A Pilot Longitudinal Study on Youth Stress, Posttraumatic Stress Disorder, and the Hippocampus. PEDIATRICS. 119(3). 509–516. 231 indexed citations
17.
Lightbody, Amy A., Scott S. Hall, & Allan L. Reiss. (2006). Chronological age, but not FMRP levels, predicts neuropsychological performance in girls with fragile X syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(5). 468–472. 16 indexed citations
18.
Johnston, Cindy, Stéphan Eliez, Jennifer Dyer-Friedman, et al.. (2001). Neurobehavioral phenotype in carriers of the fragile X premutation. American Journal of Medical Genetics. 103(4). 314–319. 96 indexed citations
19.
Luo, Shengyuan, J. Courtland Robinson, Allan L. Reiss, & Barbara R. Migeon. (1993). DNA methylation of the fragile X locus in somatic and germ cells during fetal development: Relevance to the fragile X syndrome and X inactivation. Somatic Cell and Molecular Genetics. 19(4). 393–404. 35 indexed citations
20.
Reiss, Allan L.. (1993). Fragile-X syndrome: Diagnosis, treatment and research. The American Journal of Human Genetics. 52(2). 444–445. 31 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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