Joseph G. Gleeson

21.2k total citations · 3 hit papers
127 papers, 9.5k citations indexed

About

Joseph G. Gleeson is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Joseph G. Gleeson has authored 127 papers receiving a total of 9.5k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Molecular Biology, 56 papers in Genetics and 32 papers in Cell Biology. Recurrent topics in Joseph G. Gleeson's work include Genetics and Neurodevelopmental Disorders (24 papers), Neurogenesis and neuroplasticity mechanisms (23 papers) and Genomics and Rare Diseases (19 papers). Joseph G. Gleeson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (24 papers), Neurogenesis and neuroplasticity mechanisms (23 papers) and Genomics and Rare Diseases (19 papers). Joseph G. Gleeson collaborates with scholars based in United States, Egypt and United Kingdom. Joseph G. Gleeson's co-authors include Christopher A. Walsh, Lisa A. Flanagan, Peter T. Lin, Teruyuki Tanaka, Li‐Huei Tsai, Holden Higginbotham, Hiroyuki Koizumi, William B. Dobyns, Kristina M. Allen and Madeline A. Lancaster and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Joseph G. Gleeson

120 papers receiving 9.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Doublecortin Is a Microtubule-Associated Protein and Is Expressed Widely by Migrating Neurons

1999 1.1k citations Joseph G. Gleeson, Christopher A. Walsh et al. profile →
doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein

1998 801 citations Joseph G. Gleeson, William B. Dobyns et al. profile →
De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly

2012 463 citations Jennifer L. Silhavy, Sangwoo Kim et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Joseph G. Gleeson United States	48	5.2k	2.8k	2.4k	2.2k	2.1k	127	9.5k
Jamel Chelly France	50	5.8k 1.1×	2.4k 0.9×	1.4k 0.6×	1.9k 0.9×	1.8k 0.9×	128	9.7k
Katsuhiko Mikoshiba Japan	65	9.0k 1.7×	1.6k 0.6×	1.2k 0.5×	2.0k 0.9×	2.5k 1.2×	205	12.6k
Terry Magnuson United States	70	12.5k 2.4×	4.2k 1.5×	1.1k 0.5×	1.8k 0.8×	1.8k 0.9×	198	18.0k
Noriko Osumi Japan	53	6.2k 1.2×	1.7k 0.6×	2.0k 0.9×	774 0.3×	1.8k 0.9×	223	9.0k
Robert F. Hevner United States	62	6.5k 1.3×	2.1k 0.8×	4.7k 2.0×	877 0.4×	3.9k 1.9×	130	11.9k
Kazunori Nakajima Japan	57	5.9k 1.1×	1.9k 0.7×	5.7k 2.4×	1.6k 0.7×	5.5k 2.7×	249	13.3k
Hiroshi Kiyonari Japan	62	7.7k 1.5×	1.5k 0.5×	806 0.3×	2.3k 1.0×	1.6k 0.8×	251	13.0k
Jane E. Johnson United States	55	8.4k 1.6×	1.5k 0.5×	3.2k 1.4×	1.2k 0.5×	2.6k 1.3×	141	12.8k
Julie R. Korenberg United States	51	5.5k 1.1×	2.5k 0.9×	2.2k 0.9×	522 0.2×	1.4k 0.7×	167	10.5k
Orly Reiner Israel	42	3.9k 0.8×	1.1k 0.4×	1.7k 0.7×	2.4k 1.1×	1.5k 0.7×	117	6.9k

Countries citing papers authored by Joseph G. Gleeson

Since Specialization

Citations

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

Fields of papers citing papers by Joseph G. Gleeson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph G. Gleeson. 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 Joseph G. Gleeson. The network helps show where Joseph G. Gleeson may publish in the future.

Co-authorship network of co-authors of Joseph G. Gleeson

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph G. Gleeson. A scholar is included among the top collaborators of Joseph G. Gleeson 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 Joseph G. Gleeson. Joseph G. Gleeson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Chung, Changuk, Xiaoxu Yang, Robert F. Hevner, et al.. (2024). Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain. Nature. 629(8011). 384–392. 16 indexed citations

Ziegler, Alban, Joanne Carroll, Jennifer Bain, et al.. (2024). Antisense oligonucleotide therapy in an individual with KIF1A-associated neurological disorder. Nature Medicine. 30(10). 2782–2786. 14 indexed citations

Gleeson, Joseph G., Laurence Mignon, Winston X. Yan, et al.. (2024). A framework for N-of-1 trials of individualized gene-targeted therapies for genetic diseases. Nature Communications. 15(1). 9802–9802. 7 indexed citations

Heffner, Caleb, Sangmoon Lee, Pablo Lara-González, et al.. (2023). TMEM161B modulates radial glial scaffolding in neocortical development. Proceedings of the National Academy of Sciences. 120(4). e2209983120–e2209983120. 5 indexed citations

Owen, Mallory, Meredith S. Wright, Serge Batalov, et al.. (2023). Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing. JAMA Network Open. 6(2). e2254069–e2254069. 22 indexed citations

Zaki, Maha S., Abdelrahim A. Sadek, Mona L. Essawi, et al.. (2023). Clinical and molecular spectrum of a large Egyptian cohort with ALS2 ‐related disorders of infantile‐onset of clinical continuum IAHSP / JPLS. Clinical Genetics. 104(2). 238–244. 1 indexed citations

Breuss, Martin W., Xiaoxu Yang, Valentina Stanley, et al.. (2022). Unbiased mosaic variant assessment in sperm: a cohort study to test predictability of transmission. eLife. 11. 7 indexed citations

Regla-Nava, José Ángel, Ying-Ting Wang, Camila R. Fontes-Garfias, et al.. (2022). A Zika virus mutation enhances transmission potential and confers escape from protective dengue virus immunity. Cell Reports. 39(2). 110655–110655. 32 indexed citations

Rapaport, Franck, Bertrand Boisson, Anne Gregor, et al.. (2021). Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance. Proceedings of the National Academy of Sciences. 118(3). 18 indexed citations

10.

Chai, Guoliang, Frederike L. Harms, Christian Casar, et al.. (2021). Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation. Brain. 145(4). 1551–1563. 11 indexed citations

11.

Zaki, Maha S., Katherine Johnson, Jennifer McEvoy‐Venneri, et al.. (2020). Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability. Journal of Medical Genetics. 58(4). 237–246. 5 indexed citations

12.

Hanzlíková, Hana, Evgeniia Prokhorova, Kateřina Krejčíková, et al.. (2020). Pathogenic ARH3 mutations result in ADP-ribose chromatin scars during DNA strand break repair. Nature Communications. 11(1). 3391–3391. 35 indexed citations

13.

Haute, Lindsey Van, Song-Yi Lee, Christopher A. Powell, et al.. (2019). NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs. Nucleic Acids Research. 47(16). 8720–8733. 116 indexed citations

14.

Castro, Cecilia, Robert F. Harvey, Matthias Heiß, et al.. (2019). Cytosine-5 RNA methylation links protein synthesis to cell metabolism. PLoS Biology. 17(6). e3000297–e3000297. 98 indexed citations

15.

Baek, Seung Tae, Brett Copeland, Eun-Jin Yun, et al.. (2015). An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development. Nature Medicine. 21(12). 1445–1454. 91 indexed citations

16.

Martínez, Fernando J., Jeong Ho Lee, Ji Eun Lee, et al.. (2012). Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome. Journal of Medical Genetics. 49(6). 380–385. 183 indexed citations

17.

Silhavy, Jennifer L., Stephanie Bielas, Bobby G. Ng, et al.. (2010). SRD5A3 is required for the conversion of polyprenol to dolichol, essential for N-linked protein glycosylation. 133(11). 3210–3220. 1 indexed citations

18.

Gleeson, Joseph G., Sharon Minnerath, Ruben Kuzniecky, et al.. (2000). Somatic and Germline Mosaic Mutations in the doublecortin Gene Are Associated with Variable Phenotypes. The American Journal of Human Genetics. 67(3). 574–581. 87 indexed citations

19.

Wilson, John A., John A. Wilson, Yuen‐Sum Lau, et al.. (1991). The action of MPTP on synaptic transmission is affected by changes in Ca2+ concentrations. Brain Research. 541(2). 342–346. 6 indexed citations

20.

Gleeson, Joseph G. & Jack Price. (1988). Controlled trial of budesonide given by the nebuhaler in preschool children with asthma.. BMJ. 297(6642). 163–166. 61 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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