Vasantha Gowda

627 total citations
15 papers, 204 citations indexed

About

Vasantha Gowda is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Vasantha Gowda has authored 15 papers receiving a total of 204 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Surgery. Recurrent topics in Vasantha Gowda's work include Neurogenetic and Muscular Disorders Research (8 papers), Muscle Physiology and Disorders (5 papers) and Congenital Anomalies and Fetal Surgery (5 papers). Vasantha Gowda is often cited by papers focused on Neurogenetic and Muscular Disorders Research (8 papers), Muscle Physiology and Disorders (5 papers) and Congenital Anomalies and Fetal Surgery (5 papers). Vasantha Gowda collaborates with scholars based in United Kingdom, United States and Ireland. Vasantha Gowda's co-authors include Heinz Jungbluth, Conrad Smith, A O'Rourke, Carl Fratter, Joanna Poulton, Caroline A. Sewry, Mariacristina Scoto, S. Robb, Rahul Phadke and Lorenzo Maggi and has published in prestigious journals such as Neurology, PEDIATRICS and Human Molecular Genetics.

In The Last Decade

Vasantha Gowda

11 papers receiving 199 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vasantha Gowda United Kingdom	6	157	75	57	41	23	15	204
Elke Hobbiebrunken Germany	8	133 0.8×	45 0.6×	35 0.6×	17 0.4×	76 3.3×	11	268
Ludo van der Pol Netherlands	6	89 0.6×	29 0.4×	16 0.3×	38 0.9×	12 0.5×	8	144
Marjorie Illingworth United Kingdom	5	142 0.9×	93 1.2×	18 0.3×	22 0.5×	25 1.1×	8	239
Caroline Espil‐Taris France	10	113 0.7×	31 0.4×	24 0.4×	16 0.4×	20 0.9×	20	211
A. Nascimento Osorio Spain	8	164 1.0×	56 0.7×	39 0.7×	6 0.1×	42 1.8×	14	213
Giuseppina Vitiello Italy	8	131 0.8×	27 0.4×	14 0.2×	10 0.2×	49 2.1×	16	260
Jennie Sheehan United Kingdom	4	141 0.9×	37 0.5×	71 1.2×	4 0.1×	10 0.4×	6	191
Ksenija Gorni Italy	5	99 0.6×	20 0.3×	16 0.3×	14 0.3×	8 0.3×	10	129
C. Cini United Kingdom	5	103 0.7×	35 0.5×	40 0.7×	5 0.1×	10 0.4×	5	148
Ana Kosać Serbia	7	82 0.5×	53 0.7×	16 0.3×	9 0.2×	4 0.2×	15	120

Countries citing papers authored by Vasantha Gowda

Since Specialization

Citations

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

Fields of papers citing papers by Vasantha Gowda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vasantha Gowda

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

15 of 15 papers shown

Munot, Pinki, et al.. (2024). Risk-benefit profile of onasemnogene abeparvovec in older and heavier children with spinal muscular atrophy type 1. Neuromuscular Disorders. 42. 22–26.

Sheehan, Jennie, et al.. (2024). Spinal presentations in children with spinal muscular atrophy type 1 following gene therapy treatment with onasemnogene abeparvovec – The SMA REACH UK network experience. Neuromuscular Disorders. 44. 104451–104451. 1 indexed citations

Sárközy, Anna, Mário Sá, Deborah Ridout, et al.. (2023). Long-term Natural History of Pediatric Dominant and Recessive RYR1 -Related Myopathy. Neurology. 101(15). e1495–e1508. 4 indexed citations

Gowda, Vasantha, et al.. (2023). Gene therapy for spinal muscular atrophy. Archives of Disease in Childhood Education & Practice. 108(5). 347–350.

Gowda, Vasantha, et al.. (2022). New treatments in spinal muscular atrophy. Archives of Disease in Childhood. 108(7). 511–517. 18 indexed citations

Gowda, Vasantha, Elizabeth Wraige, Min Ong, et al.. (2022). Real-world experience of gene therapy with onasemnogene-abeparvovec (Zolgensma®) for patients with SMA-type1 in UK. Journal of Neurology Neurosurgery & Psychiatry. 93(9). e2.1–e2.1. 2 indexed citations

Gowda, Vasantha, Miguel Ángel Luque-Fernández, Anne‐Marie Childs, et al.. (2021). Prediagnosis pathway benchmarking audit in patients with Duchenne muscular dystrophy. Archives of Disease in Childhood. 107(2). 160–165.

Sabir, Ataf, Jameela Sheikh, Vasantha Gowda, et al.. (2021). KIAA0753-related skeletal ciliopathy: a ninth case, extending the phenotype and reporting a novel variant. Clinical Dysmorphology. 30(3). 142–146. 1 indexed citations

Allen, Nicholas M., et al.. (2018). Unusual Presentations of Dystrophinopathies in Childhood. PEDIATRICS. 141(Supplement_5). S510–S514. 5 indexed citations

10.

Nakou, Vasiliki, et al.. (2017). Bladder involvement in presentation of mitofusin-2 (MFN-2) associated sensory-motor axonal neuropathy. European Journal of Paediatric Neurology. 21. e237–e237.

11.

Jungbluth, Heinz, et al.. (2016). Treatment with Zoledronic Acid in Children with Duchenne Muscular Dystrophy. 86. 1 indexed citations

12.

Colombo, Irene, Mariacristina Scoto, Adnan Y. Manzur, et al.. (2014). Congenital myopathies. Neurology. 84(1). 28–35. 85 indexed citations

13.

Uusimaa, Johanna, Vasantha Gowda, Conrad Smith, et al.. (2013). Prospective study of POLG mutations presenting in children with intractable epilepsy: Prevalence and clinical features. Epilepsia. 54(6). 1002–1011. 34 indexed citations

14.

Gowda, Vasantha, Jeremy Parr, & Sandeep Jayawant. (2008). Evaluation of the floppy infant. Paediatrics and Child Health. 18(1). 17–21. 8 indexed citations

15.

Ashley, Neil, A O'Rourke, Conrad Smith, et al.. (2008). Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations. Human Molecular Genetics. 17(16). 2496–2506. 45 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