Shivaram Shastri

849 total citations
22 papers, 571 citations indexed

About

Shivaram Shastri is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Shivaram Shastri has authored 22 papers receiving a total of 571 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pulmonary and Respiratory Medicine, 5 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Shivaram Shastri's work include Cystic Fibrosis Research Advances (8 papers), Pancreatitis Pathology and Treatment (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Shivaram Shastri is often cited by papers focused on Cystic Fibrosis Research Advances (8 papers), Pancreatitis Pathology and Treatment (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Shivaram Shastri collaborates with scholars based in India, Sweden and United States. Shivaram Shastri's co-authors include Madhulika Kabra, Rakesh Lodha, Pramod Kumar Garg, S. K. Kabra, P.S.N. Menon, Manju Ghosh, Shallu Midha, Sushil Kumar Kabra, Vishal Kapoor and S. K. Kabra and has published in prestigious journals such as Gut, Pharmacological Research and Journal of Clinical Gastroenterology.

In The Last Decade

Shivaram Shastri

22 papers receiving 559 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shivaram Shastri India 14 268 149 104 94 56 22 571
Meghana Sathe United States 13 251 0.9× 120 0.8× 98 0.9× 25 0.3× 44 0.8× 42 515
Jae‐Hyung Chang United States 10 34 0.1× 104 0.7× 119 1.1× 34 0.4× 24 0.4× 17 562
Meshell Johnson United States 12 431 1.6× 122 0.8× 298 2.9× 13 0.1× 53 0.9× 15 779
Yat‐Ching Tong Taiwan 17 75 0.3× 190 1.3× 97 0.9× 17 0.2× 99 1.8× 55 688
Hinda Kopelman Canada 17 449 1.7× 252 1.7× 181 1.7× 59 0.6× 48 0.9× 25 776
Hongxing Dang China 12 134 0.5× 66 0.4× 99 1.0× 18 0.2× 61 1.1× 41 346
Cristina Mayordomo Spain 8 173 0.6× 36 0.2× 194 1.9× 71 0.8× 111 2.0× 12 549
Deborah A. Elder United States 17 88 0.3× 297 2.0× 109 1.0× 49 0.5× 51 0.9× 43 658
Giovanna De Cunto Italy 15 287 1.1× 33 0.2× 174 1.7× 9 0.1× 53 0.9× 23 597
George Yanni United States 10 51 0.2× 214 1.4× 55 0.5× 41 0.4× 122 2.2× 26 457

Countries citing papers authored by Shivaram Shastri

Since Specialization
Citations

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

Fields of papers citing papers by Shivaram Shastri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shivaram Shastri

This figure shows the co-authorship network connecting the top 25 collaborators of Shivaram Shastri. A scholar is included among the top collaborators of Shivaram Shastri 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 Shivaram Shastri. Shivaram Shastri 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.
Jain, Vandana, Anil Kumar, Manisha Jana, et al.. (2019). Genetic polymorphisms associated with obesity and non-alcoholic fatty liver disease in Asian Indian adolescents. Journal of Pediatric Endocrinology and Metabolism. 32(7). 749–758. 13 indexed citations
2.
Lodha, Rakesh, et al.. (2019). Aquagenic Wrinkling of Skin: A Screening Test for Cystic Fibrosis. Indian Pediatrics. 56(2). 109–113. 8 indexed citations
3.
Singh, Pawan Kumar, Manju Ghosh, Shipra Sharma, et al.. (2017). Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India. The Indian Journal of Medical Research. 145(4). 492–497. 5 indexed citations
4.
Kumar, Lalit, Sameer Bakhshi, Atul Sharma, et al.. (2017). Influence of MDR1 and CYP3A5 genetic polymorphisms on trough levels and therapeutic response of imatinib in newly diagnosed patients with chronic myeloid leukemia. Pharmacological Research. 120. 138–145. 23 indexed citations
5.
Kumar, Lalit, Sameer Bakhshi, Atul Sharma, et al.. (2017). Do polymorphisms inMDR1andCYP3A5genes influence the risk of cytogenetic relapse in patients with chronic myeloid leukemia on imatinib therapy?. Leukemia & lymphoma. 58(9). 2218–2226. 4 indexed citations
6.
Sahi, Puneet Kaur, Shivaram Shastri, Rakesh Lodha, et al.. (2016). ADRB2 polymorphism and salbutamol responsiveness in Northern Indian children with mild to moderate exacerbation of asthma. Indian Pediatrics. 53(3). 211–215. 6 indexed citations
7.
Lodha, Rakesh, Shivaram Shastri, Savita Saini, et al.. (2015). Zinc Supplementation for One Year Among Children with Cystic Fibrosis Does Not Decrease Pulmonary Infection. Respiratory Care. 61(1). 78–84. 23 indexed citations
8.
Gulati, Sheffali, Puneet Jain, Shivaram Shastri, et al.. (2015). Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapy. Neurology India. 63(1). 35–35. 12 indexed citations
9.
Gupta, Neerja, Pawan Kumar Singh, Manoj Kumar, et al.. (2014). Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian Patients. JIMD Reports. 21. 45–55. 24 indexed citations
10.
Ghosh, Manju, Shipra Sharma, Shivaram Shastri, et al.. (2012). Norrie Disease: First Mutation Report and Prenatal Diagnosis in an Indian Family. The Indian Journal of Pediatrics. 79(11). 1529–1531. 3 indexed citations
11.
Tripathi, Manjari, et al.. (2011). Association of Angiotensin-Converting Enzyme Insertion(I)/Deletion (D) Genotype in Alzheimer's Disease Patients of North Indian Population. International Journal of Neuroscience. 121(10). 557–561. 10 indexed citations
12.
13.
Garg, Pramod Kumar, et al.. (2009). Association of SPINK1 Gene Mutation and CFTR Gene Polymorphisms in Patients With Pancreas Divisum Presenting With Idiopathic Pancreatitis. Journal of Clinical Gastroenterology. 43(9). 848–852. 53 indexed citations
14.
Kabra, S. K., et al.. (2009). Long-term daily high and low doses of azithromycin in children with cystic fibrosis: A randomized controlled trial. Journal of Cystic Fibrosis. 9(1). 17–23. 24 indexed citations
15.
Shastri, Shivaram, Madhulika Kabra, Sushil Kumar Kabra, Ravindra Mohan Pandey, & P.S.N. Menon. (2007). Characterisation of mutations and genotype–phenotype correlation in cystic fibrosis: Experience from India. Journal of Cystic Fibrosis. 7(2). 110–115. 39 indexed citations
16.
Kabra, S. K., Madhulika Kabra, Rakesh Lodha, & Shivaram Shastri. (2007). Cystic fibrosis in India. Pediatric Pulmonology. 42(12). 1087–1094. 47 indexed citations
17.
Kabra, S. K., Madhulika Kabra, Shivaram Shastri, & Rakesh Lodha. (2006). Diagnosing and managing cystic fibrosis in the developing world. Paediatric Respiratory Reviews. 7. S147–S150. 23 indexed citations
18.
Kapoor, Vishal, Shivaram Shastri, Madhulika Kabra, et al.. (2005). Carrier frequency of F508del mutation of cystic fibrosis in Indian population. Journal of Cystic Fibrosis. 5(1). 43–46. 40 indexed citations
19.
Maheshwari, M., et al.. (2003). Screening of families with autosomal recessive non‐syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario. American Journal of Medical Genetics Part A. 120A(2). 180–184. 55 indexed citations
20.
Kabra, Madhulika, et al.. (2002). Prenatal diagnosis of haemoglobinopathies.. PubMed. 14(6). 340–2. 5 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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