Jaya Punetha

1.8k total citations
15 papers, 437 citations indexed

About

Jaya Punetha is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jaya Punetha has authored 15 papers receiving a total of 437 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jaya Punetha's work include Muscle Physiology and Disorders (7 papers), Cardiomyopathy and Myosin Studies (4 papers) and Genomics and Rare Diseases (3 papers). Jaya Punetha is often cited by papers focused on Muscle Physiology and Disorders (7 papers), Cardiomyopathy and Myosin Studies (4 papers) and Genomics and Rare Diseases (3 papers). Jaya Punetha collaborates with scholars based in United States, Australia and Canada. Jaya Punetha's co-authors include Eric P. Hoffman, Akanchha Kesari, Shalini N. Jhangiani, James R. Lupski, Richard A. Gibbs, Zeynep Coban‐Akdemir, Jawid M. Fatih, Heather Gordish‐Dressman, Erik Henricson and Luca Bello and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and RNA.

In The Last Decade

Jaya Punetha

15 papers receiving 434 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jaya Punetha United States	11	319	139	94	85	51	15	437
Carsten G. Bönnemann United States	3	304 1.0×	64 0.5×	93 1.0×	86 1.0×	45 0.9×	5	368
Kim Shontz United States	5	374 1.2×	133 1.0×	86 0.9×	80 0.9×	46 0.9×	11	445
Véronique Bolduc United States	10	355 1.1×	119 0.9×	95 1.0×	59 0.7×	96 1.9×	19	492
Ryan D. Wuebbles United States	13	404 1.3×	54 0.4×	77 0.8×	81 1.0×	40 0.8×	22	468
Natalie Farra Canada	5	405 1.3×	128 0.9×	62 0.7×	37 0.4×	52 1.0×	6	491
Anne Destrèe Belgium	11	219 0.7×	253 1.8×	68 0.7×	68 0.8×	23 0.5×	13	458
Patrick Frosk Canada	10	495 1.6×	81 0.6×	140 1.5×	59 0.7×	119 2.3×	18	618
Cécile Peccate France	15	560 1.8×	112 0.8×	110 1.2×	86 1.0×	59 1.2×	25	661
Shehla Mohammed United Kingdom	12	497 1.6×	248 1.8×	34 0.4×	55 0.6×	61 1.2×	25	680
Juergen Scharner United Kingdom	13	625 2.0×	81 0.6×	46 0.5×	102 1.2×	40 0.8×	13	712

Countries citing papers authored by Jaya Punetha

Since Specialization

Citations

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

Fields of papers citing papers by Jaya Punetha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jaya Punetha

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

All Works

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15 of 15 papers shown

Posey, Jennifer E., Gail E. Graham, Jaya Punetha, et al.. (2023). Phenotypic heterogeneity associated with KIF21A: Two new cases and review of the literature. American Journal of Medical Genetics Part A. 194(3). e63455–e63455. 1 indexed citations

Punetha, Jaya, Ender Karaca, Alper Gezdirici, et al.. (2019). Biallelic CACNA2D2 variants in epileptic encephalopathy and cerebellar atrophy. Annals of Clinical and Translational Neurology. 6(8). 1395–1406. 20 indexed citations

Coban‐Akdemir, Zeynep, Janson J. White, Xiaofei Song, et al.. (2018). Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles. The American Journal of Human Genetics. 103(2). 171–187. 120 indexed citations

Punetha, Jaya, Tamar Harel, Zeynep Coban‐Akdemir, et al.. (2018). Identification of a pathogenic PMP2 variant in a multi-generational family with CMT type 1: Clinical gene panels versus genome-wide approaches to molecular diagnosis. Molecular Genetics and Metabolism. 125(3). 302–304. 10 indexed citations

Campbell, Ian M., Andrés Hernández, Shalini N. Jhangiani, et al.. (2018). Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning Algorithm. Journal of Pediatric Genetics. 7(4). 164–173. 12 indexed citations

Punetha, Jaya, et al.. (2016). Somatic mosaicism due to a reversion variant causing hemi-atrophy: a novel variant of dystrophinopathy. European Journal of Human Genetics. 24(10). 1511–1514. 5 indexed citations

O’Grady, Gina, Monkol Lek, Shireen R. Lamandé, et al.. (2016). Diagnosis and etiology of congenital muscular dystrophy: We are halfway there. Annals of Neurology. 80(1). 101–111. 49 indexed citations

Punetha, Jaya, Akanchha Kesari, Eric P. Hoffman, et al.. (2016). Novel Col12A1 variant expands the clinical picture of congenital myopathies with extracellular matrix defects. Muscle & Nerve. 55(2). 277–281. 29 indexed citations

Bello, Luca, Heather Gordish‐Dressman, Avital Cnaan, et al.. (2015). Genetic modifiers of ambulation in the CINRG duchenne natural history study.. Annals of Neurology. 3 indexed citations

10.

Bello, Luca, Akanchha Kesari, Heather Gordish‐Dressman, et al.. (2015). Genetic modifiers of ambulation in the cooperative international Neuromuscular research group Duchenne natural history study. Annals of Neurology. 77(4). 684–696. 80 indexed citations

11.

Punetha, Jaya, et al.. (2014). Exome Sequencing Identifies DYNC1H1 Variant Associated With Vertebral Abnormality and Spinal Muscular Atrophy With Lower Extremity Predominance. Pediatric Neurology. 52(2). 239–244. 28 indexed citations

12.

O’Grady, Gina, Heather Best, Emily C. Oates, et al.. (2014). Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spine. European Journal of Human Genetics. 23(6). 883–886. 16 indexed citations

13.

Clarke, Nigel F., Kimberly Amburgey, James W. Teener, et al.. (2013). A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathies. Neuromuscular Disorders. 23(5). 432–436. 29 indexed citations

14.

Punetha, Jaya & Eric P. Hoffman. (2013). Short Read (Next-Generation) Sequencing. Circulation Cardiovascular Genetics. 6(4). 427–434. 17 indexed citations

15.

Lin, Lina, et al.. (2011). Facile synthesis of nucleoside 5′-(α-P-seleno)-triphosphates and phosphoroselenoate RNA transcription. RNA. 17(10). 1932–1938. 18 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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