Jordan T. Gladman

673 total citations
13 papers, 406 citations indexed

About

Jordan T. Gladman is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Jordan T. Gladman has authored 13 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Genetics. Recurrent topics in Jordan T. Gladman's work include Muscle Physiology and Disorders (5 papers), RNA Research and Splicing (5 papers) and RNA modifications and cancer (4 papers). Jordan T. Gladman is often cited by papers focused on Muscle Physiology and Disorders (5 papers), RNA Research and Splicing (5 papers) and RNA modifications and cancer (4 papers). Jordan T. Gladman collaborates with scholars based in United States, France and Australia. Jordan T. Gladman's co-authors include Roderick A. Corriveau, Marian Emr, Salina P. Waddy, Claudia S. Moy, Walter J. Koroshetz, Francesca Bosetti, James I. Koenig, Dawn S. Chandler, Mani S. Mahadevan and Ramesh S. Yadava and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Human Genetics.

In The Last Decade

Jordan T. Gladman

13 papers receiving 402 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jordan T. Gladman United States	10	210	104	76	64	51	13	406
Maria Àngels Font Spain	8	105 0.5×	94 0.9×	47 0.6×	50 0.8×	45 0.9×	20	390
Gui Zhang China	11	240 1.1×	41 0.4×	70 0.9×	63 1.0×	64 1.3×	26	509
Bernadette T. Majda Australia	11	232 1.1×	54 0.5×	174 2.3×	45 0.7×	72 1.4×	15	530
Marine Poittevin France	10	132 0.6×	179 1.7×	32 0.4×	93 1.5×	50 1.0×	11	472
Meriel McEntagart United Kingdom	14	273 1.3×	77 0.7×	157 2.1×	29 0.5×	49 1.0×	24	576
Da‐Lin Yao United States	10	168 0.8×	91 0.9×	126 1.7×	42 0.7×	63 1.2×	12	546
Longxiao Wei China	11	117 0.6×	67 0.6×	51 0.7×	25 0.4×	61 1.2×	23	346
Nicolas Dupré France	12	150 0.7×	82 0.8×	62 0.8×	32 0.5×	199 3.9×	23	429
Dong Broquères-You France	9	100 0.5×	55 0.5×	59 0.8×	112 1.8×	26 0.5×	16	358
Taro Komuro Japan	12	223 1.1×	35 0.3×	77 1.0×	147 2.3×	132 2.6×	37	467

Countries citing papers authored by Jordan T. Gladman

Since Specialization

Citations

This map shows the geographic impact of Jordan T. Gladman'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 Jordan T. Gladman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jordan T. Gladman more than expected).

Fields of papers citing papers by Jordan T. Gladman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jordan T. Gladman. 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 Jordan T. Gladman. The network helps show where Jordan T. Gladman may publish in the future.

Co-authorship network of co-authors of Jordan T. Gladman

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

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Yadava, Ramesh S., et al.. (2019). MBNL1 overexpression is not sufficient to rescue the phenotypes in a mouse model of RNA toxicity. Human Molecular Genetics. 28(14). 2330–2338. 17 indexed citations

Gladman, Jordan T., Roderick A. Corriveau, Stéphanie Debette, et al.. (2019). Vascular contributions to cognitive impairment and dementia: Research consortia that focus on etiology and treatable targets to lessen the burden of dementia worldwide. Alzheimer s & Dementia Translational Research & Clinical Interventions. 5(1). 789–796. 27 indexed citations

Corriveau, Roderick A., Francesca Bosetti, Marian Emr, et al.. (2016). The Science of Vascular Contributions to Cognitive Impairment and Dementia (VCID): A Framework for Advancing Research Priorities in the Cerebrovascular Biology of Cognitive Decline. Cellular and Molecular Neurobiology. 36(2). 281–288. 173 indexed citations

Yadava, Ramesh S., Erin P. Foff, Qing Yu, et al.. (2016). TWEAK Regulates Muscle Functions in a Mouse Model of RNA Toxicity. PLoS ONE. 11(2). e0150192–e0150192. 8 indexed citations

Yadava, Ramesh S., Erin P. Foff, Qing Yu, et al.. (2014). TWEAK/Fn14, a pathway and novel therapeutic target in myotonic dystrophy. Human Molecular Genetics. 24(7). 2035–2048. 32 indexed citations

Rehman, Shagufta, Jordan T. Gladman, Ammasi Periasamy, Yuansheng Sun, & Mani S. Mahadevan. (2014). Development of an AP-FRET Based Analysis for Characterizing RNA-Protein Interactions in Myotonic Dystrophy (DM1). PLoS ONE. 9(4). e95957–e95957. 13 indexed citations

Gladman, Jordan T., et al.. (2014). NKX2-5, a modifier of skeletal muscle pathology due to RNA toxicity. Human Molecular Genetics. 24(1). 251–264. 8 indexed citations

Gladman, Jordan T., et al.. (2013). Age of Onset of RNA Toxicity Influences Phenotypic Severity: Evidence from an Inducible Mouse Model of Myotonic Dystrophy (DM1). PLoS ONE. 8(9). e72907–e72907. 15 indexed citations

Jacob, Aishwarya G., Ravi K. Singh, Daniel F. Comiskey, et al.. (2013). Stress-Induced Isoforms of MDM2 and MDM4 Correlate with High-Grade Disease and an Altered Splicing Network in Pediatric Rhabdomyosarcoma. Neoplasia. 15(9). 1049–IN8. 21 indexed citations

10.

Pierson, Christopher R., Andrew Snyder, Jordan T. Gladman, et al.. (2011). Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype. Human Molecular Genetics. 21(4). 811–825. 53 indexed citations

11.

Bebee, Thomas W., Jordan T. Gladman, & Dawn S. Chandler. (2011). Generation of a tamoxifen inducible SMN mouse for temporal SMN replacement. genesis. 49(12). 927–934. 1 indexed citations

12.

Gladman, Jordan T., Thomas W. Bebee, Xueyong Wang, et al.. (2010). A humanized Smn gene containing the SMN2 nucleotide alteration in exon 7 mimics SMN2 splicing and the SMA disease phenotype. Human Molecular Genetics. 19(21). 4239–4252. 23 indexed citations

13.

Gladman, Jordan T. & Dawn S. Chandler. (2009). Intron 7 conserved sequence elements regulate the splicing of the SMN genes. Human Genetics. 126(6). 833–841. 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.

Explore authors with similar magnitude of impact