Jeffrey R. Gruen

8.0k total citations
93 papers, 3.0k citations indexed

About

Jeffrey R. Gruen is a scholar working on Genetics, Developmental and Educational Psychology and Molecular Biology. According to data from OpenAlex, Jeffrey R. Gruen has authored 93 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Genetics, 33 papers in Developmental and Educational Psychology and 31 papers in Molecular Biology. Recurrent topics in Jeffrey R. Gruen's work include Reading and Literacy Development (30 papers), Genetics and Neurodevelopmental Disorders (25 papers) and Language Development and Disorders (13 papers). Jeffrey R. Gruen is often cited by papers focused on Reading and Literacy Development (30 papers), Genetics and Neurodevelopmental Disorders (25 papers) and Language Development and Disorders (13 papers). Jeffrey R. Gruen collaborates with scholars based in United States, Canada and United Kingdom. Jeffrey R. Gruen's co-authors include Vineet Bhandari, Sherman M. Weissman, Joel Gelernter, Grier P. Page, Heping Zhang, Haiying Meng, Matthew J. Bizzarro, John D. Eicher, Laura R. Ment and Henry R. Kranzler and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and SHILAP Revista de lepidopterología.

In The Last Decade

Jeffrey R. Gruen

90 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jeffrey R. Gruen United States 32 996 865 725 449 446 93 3.0k
Johannes Schumacher Germany 23 528 0.5× 646 0.7× 547 0.8× 118 0.3× 184 0.4× 83 1.9k
Colleen A. Morris United States 40 276 0.3× 1.4k 1.6× 1.8k 2.5× 343 0.8× 535 1.2× 67 5.8k
Herbert A. Lubs United States 46 878 0.9× 3.5k 4.0× 2.8k 3.9× 117 0.3× 970 2.2× 141 6.8k
Thomas Scerri United Kingdom 19 770 0.8× 853 1.0× 606 0.8× 54 0.1× 443 1.0× 24 1.8k
Isabelle Jambaqué France 33 364 0.4× 628 0.7× 778 1.1× 313 0.7× 1.0k 2.3× 88 4.2k
Ann Swillen Belgium 29 139 0.1× 1.6k 1.9× 3.0k 4.2× 1.2k 2.7× 691 1.5× 119 4.0k
Janine A. Lamb United Kingdom 25 259 0.3× 937 1.1× 928 1.3× 50 0.1× 673 1.5× 56 2.6k
Lisbeth Tranebjærg Denmark 43 147 0.1× 2.3k 2.6× 3.6k 5.0× 281 0.6× 417 0.9× 163 6.7k
David P. Roeltgen United States 35 422 0.4× 1.3k 1.5× 777 1.1× 90 0.2× 1.1k 2.5× 62 2.9k
Silvia Paracchini United Kingdom 28 1.3k 1.3× 1.6k 1.8× 813 1.1× 29 0.1× 1.0k 2.3× 63 3.1k

Countries citing papers authored by Jeffrey R. Gruen

Since Specialization
Citations

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

Fields of papers citing papers by Jeffrey R. Gruen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffrey R. Gruen. 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 Jeffrey R. Gruen. The network helps show where Jeffrey R. Gruen may publish in the future.

Co-authorship network of co-authors of Jeffrey R. Gruen

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey R. Gruen. A scholar is included among the top collaborators of Jeffrey R. Gruen 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 Jeffrey R. Gruen. Jeffrey R. Gruen 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.
Kudzi, William, Vivian Paintsil, Catherine Segbefia, et al.. (2025). Elevated serum heme oxygenase‐1 in pediatric sickle cell disease: Insights from the SickleGenAfrica Network. HemaSphere. 9(9). e70209–e70209.
2.
Kaplan, Edward H., et al.. (2024). Optimal evaluation policies to identify students with reading disabilities. Socio-Economic Planning Sciences. 98. 102116–102116.
3.
Li, Miao, Maureen W. Lovett, Joan Bosson‐Heenan, et al.. (2024). Phonological awareness mediates the relationship between DCDC2 and reading performance with home environment. npj Science of Learning. 9(1). 36–36. 1 indexed citations
4.
Petrill, Stephen A., Brett Klamer, Steven Buyske, et al.. (2023). The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait. Genes. 14(9). 1748–1748.
5.
Gabel, Lisa A., et al.. (2022). Orthographic Depth May Influence the Degree of Severity of Maze Learning Performance in Children at Risk for Reading Disorder. Developmental Neuroscience. 44(6). 651–670. 2 indexed citations
6.
Tang, Kevin, et al.. (2020). DCDC2READ1 regulatory element: how temporal processing differences may shape language. Proceedings of the Royal Society B Biological Sciences. 287(1928). 20192712–20192712. 2 indexed citations
7.
Boada, Richard, Dina E. Hill, Lisa A. Jacobson, et al.. (2018). Causal Attribution Profiles as a Function of Reading Skills, Hyperactivity, and Inattention. Scientific Studies of Reading. 23(3). 254–272. 9 indexed citations
8.
Tang, Kevin, Jeffrey G. Malins, Natalie R. Powers, et al.. (2018). Worldwide distribution of theDCDC2READ1 regulatory element and its relationship with phoneme variation across languages. Proceedings of the National Academy of Sciences. 115(19). 4951–4956. 8 indexed citations
9.
Li, Miao, Jeffrey G. Malins, Maureen W. Lovett, et al.. (2018). A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children. npj Science of Learning. 3(1). 20–20. 10 indexed citations
10.
Bhandari, Vineet & Jeffrey R. Gruen. (2015). What is the basis for a genetic approach in neonatal disorders?. Seminars in Perinatology. 39(8). 568–573. 6 indexed citations
11.
Marino, Cecilia, Paola Scifo, Pasquale Anthony Della Rosa, et al.. (2014). The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia. Cortex. 57. 227–243. 39 indexed citations
12.
Douet, Vanessa, Linda Chang, Brian Keating, et al.. (2014). Schizophrenia-risk variant rs6994992 in the neuregulin-1 gene on brain developmental trajectories in typically developing children. Translational Psychiatry. 4(5). e392–e392. 8 indexed citations
13.
Eicher, John D. & Jeffrey R. Gruen. (2013). Imaging-genetics in dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments. Molecular Genetics and Metabolism. 110(3). 201–212. 30 indexed citations
14.
Jamadar, Sharna D., Natalie R. Powers, Shashwath A. Meda, et al.. (2012). Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study. Brain Imaging and Behavior. 7(1). 15–27. 21 indexed citations
15.
Gabel, Lisa A., et al.. (2009). Progress towards a cellular neurobiology of reading disability. Neurobiology of Disease. 38(2). 173–180. 44 indexed citations
16.
Gibson, Christopher J. & Jeffrey R. Gruen. (2008). The human lexinome: Genes of language and reading. Journal of Communication Disorders. 41(5). 409–420. 28 indexed citations
17.
Yang, Bao‐Zhu, Henry R. Kranzler, Hongyu Zhao, et al.. (2007). Association of haplotypic variants in DRD2, ANKK1, TTC12 and NCAM1 to alcohol dependence in independent case–control and family samples. Human Molecular Genetics. 16(23). 2844–2853. 99 indexed citations
18.
Hisama, Fuki M., Jeffrey R. Gruen, Elena L. Grigorenko, et al.. (2001). Human GABAB receptor 1 gene: Eight novel sequence variants. Human Mutation. 17(4). 349–350. 13 indexed citations
19.
Ajioka, Richard S., et al.. (1997). Recombinations defining centromeric and telomeric borders for the hereditary haemochromatosis locus.. Journal of Medical Genetics. 34(1). 28–33. 2 indexed citations
20.
Parimoo, Satish, et al.. (1994). Isolation of novel non-HLA gene fragments from the hemochromatosis region (6p21.3) by cDNA hybridization selection.. PubMed Central. 54(2). 244–51. 15 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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