Kalpana Gowrishankar

1.3k total citations
23 papers, 305 citations indexed

About

Kalpana Gowrishankar is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Kalpana Gowrishankar has authored 23 papers receiving a total of 305 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Genetics and 3 papers in Infectious Diseases. Recurrent topics in Kalpana Gowrishankar's work include Connective tissue disorders research (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Renal Diseases and Glomerulopathies (3 papers). Kalpana Gowrishankar is often cited by papers focused on Connective tissue disorders research (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Renal Diseases and Glomerulopathies (3 papers). Kalpana Gowrishankar collaborates with scholars based in India, Portugal and United Kingdom. Kalpana Gowrishankar's co-authors include Sarala Rajajee, Sheela Nampoothiri, Katta M. Girisha, Shubha R. Phadke, Maria Rita Passos‐Bueno, Salomé de Almeida, Ernst Reichenberger, Cassio Menezes Raposo do Amaral, I‐Ping Chen and Valdenize Tiziani and has published in prestigious journals such as PLoS ONE, Journal of Cellular Biochemistry and Cytogenetic and Genome Research.

In The Last Decade

Kalpana Gowrishankar

22 papers receiving 298 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kalpana Gowrishankar India 10 172 94 45 33 32 23 305
XL Zhang China 12 182 1.1× 57 0.6× 21 0.5× 23 0.7× 46 1.4× 31 382
Bruce Castle United Kingdom 13 186 1.1× 197 2.1× 21 0.5× 48 1.5× 15 0.5× 16 386
Valentina Broshtilova Bulgaria 8 89 0.5× 77 0.8× 54 1.2× 12 0.4× 33 1.0× 44 347
Natália D. Linhares Brazil 10 168 1.0× 102 1.1× 89 2.0× 9 0.3× 29 0.9× 21 350
Pietro Sirleto Italy 12 221 1.3× 137 1.5× 28 0.6× 31 0.9× 44 1.4× 25 399
Shady Younis United States 12 188 1.1× 66 0.7× 66 1.5× 11 0.3× 39 1.2× 22 355
L. Alexander Liggett United States 7 193 1.1× 92 1.0× 110 2.4× 79 2.4× 32 1.0× 7 446
Katherine Neas New Zealand 12 214 1.2× 103 1.1× 50 1.1× 25 0.8× 21 0.7× 22 430
Nela Maksimović Serbia 11 139 0.8× 42 0.4× 40 0.9× 42 1.3× 16 0.5× 39 345
ShunJiang Yu Canada 15 270 1.6× 97 1.0× 44 1.0× 12 0.4× 47 1.5× 18 492

Countries citing papers authored by Kalpana Gowrishankar

Since Specialization
Citations

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

Fields of papers citing papers by Kalpana Gowrishankar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kalpana Gowrishankar

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

All Works

20 of 20 papers shown
1.
Gowrishankar, Kalpana, et al.. (2023). Laron syndrome in South Indian children – A descriptive study. 2. 109–113.
2.
Gowrishankar, Kalpana, et al.. (2021). Lethal Restrictive Dermopathy with ZMPSTE24 Mutation. Pediatric and Developmental Pathology. 25(3). 327–329. 1 indexed citations
3.
Bhat, Meenakshi, et al.. (2020). Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations. BMC Medical Genetics. 21(1). 50–50. 50 indexed citations
4.
Jacob, Prince, Shalini S. Nayak, Kalpana Gowrishankar, et al.. (2020). Digital clubbing as the predominant manifestation of hypertrophic osteoarthropathy caused by pathogenic variants in HPGD in three Indian families. Clinical Dysmorphology. 29(3). 123–126. 3 indexed citations
5.
Narayanan, Dhanya Lakshmi, Neerja Gupta, Madhulika Kabra, et al.. (2019). Spectrum of ARSA variations in Asian Indian patients with Arylsulfatase A deficient metachromatic leukodystrophy. Journal of Human Genetics. 64(4). 323–331. 15 indexed citations
6.
Girisha, Katta M., Sheela Nampoothiri, Kalpana Gowrishankar, et al.. (2018). Locus and allelic heterogeneity and phenotypic variability in Waardenburg syndrome. Clinical Genetics. 95(3). 398–402. 17 indexed citations
7.
Venkatesan, Vettriselvi, et al.. (2018). Novel variations in NPHS1 gene in children of South Indian population and its association with primary nephrotic syndrome. Journal of Cellular Biochemistry. 119(12). 10143–10150. 3 indexed citations
8.
Cho, Tae‐Joon, Shubha R. Phadke, Kalpana Gowrishankar, et al.. (2017). Additional three patients with Smith‐McCort dysplasia due to novel RAB33B mutations. American Journal of Medical Genetics Part A. 173(3). 588–595. 15 indexed citations
9.
Venkatesan, Vettriselvi, et al.. (2016). Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children. Clinical and Experimental Nephrology. 21(1). 127–133. 7 indexed citations
10.
Mohan, Shruthi, et al.. (2016). Subtelomeric rearrangements in Indian children with idiopathic intellectual disability/developmental delay. The Indian Journal of Medical Research. 144(2). 206–214. 2 indexed citations
11.
Venkatesan, Vettriselvi, et al.. (2015). Association of ACE and MDR1 Gene Polymorphisms with Steroid Resistance in Children with Idiopathic Nephrotic Syndrome. Genetic Testing and Molecular Biomarkers. 19(8). 454–456. 8 indexed citations
12.
Bhavani, Gandham SriLakshmi, Hitesh Shah, Anju Shukla, et al.. (2015). Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy. American Journal of Medical Genetics Part A. 170(2). 410–417. 23 indexed citations
13.
Gowrishankar, Kalpana, et al.. (2015). Genetic disorders with heterotopic ossificans. Indian Journal of Orthopaedics. 49(3). 361–364. 2 indexed citations
14.
Kumar, R. Ashok, et al.. (2015). Class II Analphoid Chromosome in a Child with Aberrant Chromosome 7: A Rare Cytogenetic Association. Cytogenetic and Genome Research. 146(2). 120–123. 5 indexed citations
15.
Hu, Ying, I‐Ping Chen, Salomé de Almeida, et al.. (2013). A Novel Autosomal Recessive GJA1 Missense Mutation Linked to Craniometaphyseal Dysplasia. PLoS ONE. 8(8). e73576–e73576. 52 indexed citations
16.
Uppuluri, Ramya, et al.. (2013). Crossed polydactyly and Greig cephalopolysyndactyly syndrome. Indian Pediatrics. 50(10). 967–968. 1 indexed citations
17.
Dalal, Ashwin, Gandham SriLakshmi Bhavani, Padma Priya Togarrati, et al.. (2012). Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia. American Journal of Medical Genetics Part A. 158A(11). 2820–2828. 47 indexed citations
18.
Vasanthi, Thiruvengadam, et al.. (2011). Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic association. Indian journal of human genetics. 17(3). 241–241. 2 indexed citations
19.
Ganesh, Ramaswamy, et al.. (2009). Thiamine responsive megaloblastic anemia syndrome. The Indian Journal of Pediatrics. 76(3). 313–314. 13 indexed citations
20.
Gowrishankar, Kalpana & Sarala Rajajee. (1994). Varied manifestations of viral myocarditis. The Indian Journal of Pediatrics. 61(1). 75–80. 11 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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