Ami Mankodi

5.6k total citations · 3 hit papers
45 papers, 4.0k citations indexed

About

Ami Mankodi is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Ami Mankodi has authored 45 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 24 papers in Cellular and Molecular Neuroscience and 14 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Ami Mankodi's work include Muscle Physiology and Disorders (26 papers), Genetic Neurodegenerative Diseases (23 papers) and Cardiomyopathy and Myosin Studies (12 papers). Ami Mankodi is often cited by papers focused on Muscle Physiology and Disorders (26 papers), Genetic Neurodegenerative Diseases (23 papers) and Cardiomyopathy and Myosin Studies (12 papers). Ami Mankodi collaborates with scholars based in United States, India and United Kingdom. Ami Mankodi's co-authors include Charles A. Thornton, Maurice S. Swanson, Richard T. Moxley, Hong Jiang, Rahul Kanadia, Don Henderson, Codrin Lungu, Xiaoyan Lin, Carolyn McClain and Robert J. White and has published in prestigious journals such as Science, Journal of Biological Chemistry and Molecular Cell.

In The Last Decade

Ami Mankodi

43 papers receiving 3.9k 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.

A Muscleblind Knockout Model for Myotonic Dystrophy

2003 576 citations Rahul Kanadia, Karen A. Johnstone et al. Science profile →
Myotonic Dystrophy in Transgenic Mice Expressing an Expanded CUG Repeat

2000 554 citations Ami Mankodi, Charles A. Thornton et al. Science profile →
Expanded CUG Repeats Trigger Aberrant Splicing of ClC-1 Chloride Channel Pre-mRNA and Hyperexcitability of Skeletal Muscle in Myotonic Dystrophy

2002 513 citations Ami Mankodi, Masanori Takahashi et al. Molecular Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ami Mankodi United States	22	3.3k	2.7k	674	603	301	45	4.0k
Hans Rudolf Brenner Switzerland	33	2.7k 0.8×	1.6k 0.6×	242 0.4×	343 0.6×	166 0.6×	58	3.3k
Mauro Toselli Italy	24	1.9k 0.6×	1.2k 0.4×	122 0.2×	115 0.2×	169 0.6×	49	2.5k
Atle Melberg Sweden	25	1.4k 0.4×	432 0.2×	181 0.3×	285 0.5×	113 0.4×	44	2.1k
Eric Leguern France	20	1.2k 0.4×	993 0.4×	111 0.2×	267 0.4×	90 0.3×	33	2.6k
Harold G. Marks United States	24	840 0.3×	685 0.3×	147 0.2×	239 0.4×	100 0.3×	48	1.6k
Laurent Bernheim Switzerland	35	2.6k 0.8×	1.7k 0.6×	562 0.8×	38 0.1×	193 0.6×	63	3.4k
Franco Laccone Austria	29	1.8k 0.5×	1.2k 0.4×	89 0.1×	597 1.0×	94 0.3×	118	2.9k
Lluı́s Samaranch United States	28	1.0k 0.3×	768 0.3×	109 0.2×	648 1.1×	214 0.7×	49	2.2k
Kathie M. Bishop United States	25	2.6k 0.8×	1.1k 0.4×	81 0.1×	654 1.1×	1.7k 5.7×	53	4.2k
Daniel Rochefort Canada	24	1.4k 0.4×	759 0.3×	49 0.1×	724 1.2×	449 1.5×	45	2.4k

Countries citing papers authored by Ami Mankodi

Since Specialization

Citations

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

Fields of papers citing papers by Ami Mankodi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ami Mankodi. 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 Ami Mankodi. The network helps show where Ami Mankodi may publish in the future.

Co-authorship network of co-authors of Ami Mankodi

This figure shows the co-authorship network connecting the top 25 collaborators of Ami Mankodi. A scholar is included among the top collaborators of Ami Mankodi 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 Ami Mankodi. Ami Mankodi 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

Subedi, Kalpana, Yongmei Zhao, Castle Raley, et al.. (2023). Expression of LIM domain-binding 3 (LDB3), a striated muscle Z-band alternatively spliced PDZ-motif protein in the nervous system. Scientific Reports. 13(1). 270–270. 4 indexed citations

Bulea, Thomas C., et al.. (2022). Simple and economical HandClench Relaxometer device for reliable and sensitive measurement of grip myotonia in myotonic dystrophy. Neuromuscular Disorders. 32(4). 321–331. 4 indexed citations

Deutsch, Gayle K., Katharine A. Hagerman, Jacinda B. Sampson, et al.. (2022). Brief assessment of cognitive function in myotonic dystrophy: Multicenter longitudinal study using computer‐assisted evaluation. Muscle & Nerve. 65(5). 560–567. 4 indexed citations

Pathak, Pankaj, Kalpana Subedi, Ilda B. Molloy, et al.. (2021). Myopathy associated LDB3 mutation causes Z-disc disassembly and protein aggregation through PKCα and TSC2-mTOR downregulation. Communications Biology. 4(1). 355–355. 25 indexed citations

Grunseich, Christopher, Mallory Owen, Alice B. Schindler, et al.. (2021). Improving the efficacy of exome sequencing at a quaternary care referral centre: novel mutations, clinical presentations and diagnostic challenges in rare neurogenetic diseases. Journal of Neurology Neurosurgery & Psychiatry. 92(11). 1186–1196. 12 indexed citations

Todd, Joshua J., Jessica W. Witherspoon, Tokunbor A. Lawal, et al.. (2018). Novel Variants in Individuals with RYR1-Related Congenital Myopathies: Genetic, Laboratory, and Clinical Findings. Frontiers in Neurology. 9. 118–118. 11 indexed citations

Mankodi, Ami, Noura Azzabou, Thomas C. Bulea, et al.. (2017). Concentric exercise effects on skeletal muscle water T2 in Duchenne muscular dystrophy (P2.131). Neurology. 88(16_supplement). 1 indexed citations

Mankodi, Ami, Christopher Grunseich, Lisa Cook, et al.. (2015). Divalent cation-responsive myotonia and muscle paralysis in skeletal muscle sodium channelopathy. Neuromuscular Disorders. 25(11). 908–912. 6 indexed citations

Lin, Xiaoyan, Soojay Banerjee, Joshua D. Kaufman, et al.. (2014). Z-disc-associated, Alternatively Spliced, PDZ Motif-containing Protein (ZASP) Mutations in the Actin-binding Domain Cause Disruption of Skeletal Muscle Actin Filaments in Myofibrillar Myopathy. Journal of Biological Chemistry. 289(19). 13615–13626. 40 indexed citations

10.

Grunseich, Christopher, Laura C. Bott, Carlo Rinaldi, et al.. (2014). Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat. Neuromuscular Disorders. 24(11). 978–981. 35 indexed citations

11.

Dastgir, Jahannaz, Carole Vuillerot, Kathleen A. Harrison, et al.. (2013). P.13.9 Acoustic radiation force impulse imaging for the differentiation of muscle tissue stiffness in neuromuscular disorders. Neuromuscular Disorders. 23(9-10). 811–811. 3 indexed citations

12.

Mankodi, Ami, et al.. (2011). Progressive myopathy in an inducible mouse model of oculopharyngeal muscular dystrophy. Neurobiology of Disease. 45(1). 539–546. 17 indexed citations

13.

Mankodi, Ami. (2008). Myotonic disorders. Neurology India. 56(3). 298–298. 12 indexed citations

14.

Lin, Xiaoyan, Ami Mankodi, Rahul Kanadia, et al.. (2006). Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy. Human Molecular Genetics. 15(13). 2087–2097. 401 indexed citations

15.

Lueck, John D., Ami Mankodi, Maurice S. Swanson, Charles A. Thornton, & Robert T. Dirksen. (2006). Muscle Chloride Channel Dysfunction in Two Mouse Models of Myotonic Dystrophy. The Journal of General Physiology. 129(1). 79–94. 90 indexed citations

16.

Kanadia, Rahul, Karen A. Johnstone, Ami Mankodi, et al.. (2003). A Muscleblind Knockout Model for Myotonic Dystrophy. Science. 302(5652). 1978–1980. 576 indexed citations breakdown →

17.

Filosto, Massimiliano, Michelangelo Mancuso, Yutaka Nishigaki, et al.. (2003). Clinical and Genetic Heterogeneity in Progressive External Ophthalmoplegia Due to Mutations in Polymerase γ. Archives of Neurology. 60(9). 1279–84. 96 indexed citations

18.

Mankodi, Ami, Masanori Takahashi, Hong Jiang, et al.. (2002). Expanded CUG Repeats Trigger Aberrant Splicing of ClC-1 Chloride Channel Pre-mRNA and Hyperexcitability of Skeletal Muscle in Myotonic Dystrophy. Molecular Cell. 10(1). 35–44. 513 indexed citations breakdown →

19.

Mankodi, Ami. (2001). Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2. Human Molecular Genetics. 10(19). 2165–2170. 347 indexed citations

20.

Bhatt, Mohit, et al.. (2000). Posttraumatic akinetic-rigid syndrome resembling Parkinson's disease: A report on three patients. Movement Disorders. 15(2). 313–317. 26 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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