Chitra C. Iyer

635 total citations
17 papers, 462 citations indexed

About

Chitra C. Iyer is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Chitra C. Iyer has authored 17 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 7 papers in Surgery. Recurrent topics in Chitra C. Iyer's work include Neurogenetic and Muscular Disorders Research (12 papers), RNA modifications and cancer (7 papers) and Muscle Physiology and Disorders (7 papers). Chitra C. Iyer is often cited by papers focused on Neurogenetic and Muscular Disorders Research (12 papers), RNA modifications and cancer (7 papers) and Muscle Physiology and Disorders (7 papers). Chitra C. Iyer collaborates with scholars based in United States, Switzerland and Czechia. Chitra C. Iyer's co-authors include Arthur H.M. Burghes, W. David Arnold, Vicki L. McGovern, Stephen J. Kolb, Sara E. Gombash, Kevin D. Foust, Phillip G. Zaworski, Brian C. Clark, Deepti Chugh and Brian K. Kaspar and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Chitra C. Iyer

17 papers receiving 462 citations

Peers

Countries citing papers authored by Chitra C. Iyer

Since Specialization

Citations

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

Fields of papers citing papers by Chitra C. Iyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chitra C. Iyer. 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 Chitra C. Iyer. The network helps show where Chitra C. Iyer may publish in the future.

Co-authorship network of co-authors of Chitra C. Iyer

This figure shows the co-authorship network connecting the top 25 collaborators of Chitra C. Iyer. A scholar is included among the top collaborators of Chitra C. Iyer 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 Chitra C. Iyer. Chitra C. Iyer 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:

17 of 17 papers shown

#	Work	Indexed citations
1	Voluntary wheel running with and without follistatin overexpression improves NMJ transmission but not motor unit loss in late life of C57BL/6J mice 2021 ·Neurobiology of Aging ·Deepti Chugh, Chitra C. Iyer, (unknown), (unknown), Brian K. Kaspar, Kathrin Meyer, Arthur H.M. Burghes, Brian C. Clark, W. David Arnold	12
2	Follistatin-induced muscle hypertrophy in aged mice improves neuromuscular junction innervation and function 2021 ·Neurobiology of Aging ·Chitra C. Iyer, Deepti Chugh, (unknown), (unknown), (unknown), (unknown), Brian K. Kaspar, Kathrin Meyer, Arthur H.M. Burghes, W. David Arnold	17
3	Conditional deletion of SMN in cell culture identifies functional SMN alleles 2020 ·Human Molecular Genetics ·(unknown), Vicki L. McGovern, Thanh T. Le, Chitra C. Iyer, Brian K. Kaspar, Arthur H.M. Burghes	10
4	Intragenic complementation of amino and carboxy terminal SMN missense mutations can rescue Smn null mice 2020 ·Human Molecular Genetics ·Vicki L. McGovern, (unknown), W. David Arnold, Sandra Duqué, Chitra C. Iyer, Aurélie Massoni‐Laporte, Eileen Workman, (unknown), Daniel J. Battle, Arthur H.M. Burghes	3
5	Early‐onset aging and mitochondrial defects associated with loss of histone acetyltransferase 1 (Hat1) 2019 ·Aging Cell ·Prabakaran Nagarajan, (unknown), Chitra C. Iyer, (unknown), W. David Arnold, Mark R. Parthun	28
6	Neuromuscular junction transmission failure is a late phenotype in aging mice 2019 ·Neurobiology of Aging ·Deepti Chugh, Chitra C. Iyer, Xueyong Wang, (unknown), Mark M. Rich, W. David Arnold	34
7	Muscle strength and size are associated with motor unit connectivity in aged mice 2018 ·Neurobiology of Aging ·(unknown), Chitra C. Iyer, (unknown), (unknown), Anna Bratasz, Stephen J. Kolb, Brian C. Clark, Arthur H.M. Burghes, W. David Arnold	87
8	Mild SMN missense alleles are only functional in the presence of SMN2 in mammals 2018 ·Human Molecular Genetics ·Chitra C. Iyer, (unknown), Aurélie Massoni‐Laporte, Sandra Duqué, (unknown), Sarah Tisdale, Vicki L. McGovern, Thanh T. Le, Phillip G. Zaworski, W. David Arnold, Livio Pellizzoni, Arthur H.M. Burghes	9
9	Muscle contractility dysfunction precedes loss of motor unit connectivity in SOD1(G93A) mice 2018 ·Muscle & Nerve ·(unknown), (unknown), (unknown), Chitra C. Iyer, Deepti Chugh, Marilly Palettas, Patrick L. Heilman, David Kline, W. David Arnold, Stephen J. Kolb	15
10	HuD and the Survival Motor Neuron Protein Interact in Motoneurons and Are Essential for Motoneuron Development, Function, and mRNA Regulation 2017 ·Journal of Neuroscience ·(unknown), Phan Q. Duy, Min An, Jared C. Talbot, Chitra C. Iyer, Marc A. Wolman, Christine E. Beattie	38
11	SMN Blood Levels in a Porcine Model of Spinal Muscular Atrophy 2017 ·Journal of Neuromuscular Diseases ·Chitra C. Iyer, Xueqian Wang, Samantha Renusch, Sandra Duqué, Allison Wehr, (unknown), Vicki L. McGovern, W. David Arnold, Arthur H.M. Burghes, Stephen J. Kolb	10
12	Normalization of Patient-Identified Plasma Biomarkers in SMNΔ7 Mice following Postnatal SMN Restoration 2016 ·PLoS ONE ·W. David Arnold, Sandra Duqué, Chitra C. Iyer, Phillip G. Zaworski, Vicki L. McGovern, (unknown), Katharine M. von Herrmann, Dione Kobayashi, Karen Chen, Stephen J. Kolb, Sergey Paushkin, Arthur H.M. Burghes	10
13	SMN expression is required in motor neurons to rescue electrophysiological deficits in the SMNΔ7 mouse model of SMA 2015 ·Human Molecular Genetics ·Vicki L. McGovern, Chitra C. Iyer, W. David Arnold, Sara E. Gombash, Phillip G. Zaworski, (unknown), Kevin D. Foust, Arthur H.M. Burghes	47
14	Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMA 2015 ·Human Molecular Genetics ·Chitra C. Iyer, Vicki L. McGovern, Jason D. Murray, Sara E. Gombash, Phillip G. Zaworski, Kevin D. Foust, Paul M.L. Janssen, Arthur H.M. Burghes	32
15	SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice 2015 ·Human Molecular Genetics ·Sara E. Gombash, Christopher Cowley, Julie C. Fitzgerald, Chitra C. Iyer, David Fried, Vicki L. McGovern, Kent C. Williams, Arthur H.M. Burghes, Fedias L. Christofi, Brian D. Gulbransen, Kevin D. Foust	42
16	Deletion of atrophy enhancing genes fails to ameliorate the phenotype in a mouse model of spinal muscular atrophy 2014 ·Neuromuscular Disorders ·Chitra C. Iyer, Vicki L. McGovern, (unknown), David J. Glass, Arthur H.M. Burghes	9
17	Electrophysiological biomarkers in spinal muscular atrophy: proof of concept 2013 ·Annals of Clinical and Translational Neurology ·W. David Arnold, Paul Porensky, Vicki L. McGovern, Chitra C. Iyer, Sandra Duqué, Xiaobai Li, Kathrin Meyer, Leah Schmelzer, Brian K. Kaspar, Stephen J. Kolb, John T. Kissel, Arthur H.M. Burghes	59

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