Inusha Panigrahi

2.1k total citations
145 papers, 1.0k citations indexed

About

Inusha Panigrahi is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Inusha Panigrahi has authored 145 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Genetics, 44 papers in Molecular Biology and 29 papers in Genetics. Recurrent topics in Inusha Panigrahi's work include Hemoglobinopathies and Related Disorders (20 papers), Iron Metabolism and Disorders (16 papers) and Genetic Syndromes and Imprinting (12 papers). Inusha Panigrahi is often cited by papers focused on Hemoglobinopathies and Related Disorders (20 papers), Iron Metabolism and Disorders (16 papers) and Genetic Syndromes and Imprinting (12 papers). Inusha Panigrahi collaborates with scholars based in India, United Kingdom and United States. Inusha Panigrahi's co-authors include Sarita Agarwal, Ram Kumar Marwaha, Rashmi Ranjan Das, Renu Saxena, Sushree Samiksha Naik, Anjana Munshi, R. K. Marwaha, Sheetal Sharda, Shubha R. Phadke and Renu Suthar and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Inusha Panigrahi

125 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Inusha Panigrahi India 17 335 293 267 254 153 145 1.0k
Athanasios Christoforidis Greece 18 311 0.9× 320 1.1× 129 0.5× 169 0.7× 120 0.8× 80 1.0k
Şule Ünal Türkiye 16 268 0.8× 510 1.7× 241 0.9× 136 0.5× 74 0.5× 80 1.1k
Patrizia Accorsi Italy 21 145 0.4× 289 1.0× 266 1.0× 290 1.1× 280 1.8× 111 1.3k
Bruno Costes France 22 344 1.0× 123 0.4× 512 1.9× 201 0.8× 85 0.6× 40 1.9k
Velu Nair India 16 291 0.9× 323 1.1× 362 1.4× 213 0.8× 46 0.3× 112 1.3k
Lori Steiner United States 22 153 0.5× 225 0.8× 284 1.1× 297 1.2× 57 0.4× 35 1.4k
Sarah E. Strandjord United States 21 263 0.8× 408 1.4× 340 1.3× 93 0.4× 62 0.4× 43 1.6k
G Torelli Italy 22 156 0.5× 348 1.2× 230 0.9× 58 0.2× 76 0.5× 66 1.4k
Helen M. Hansen United States 23 238 0.7× 90 0.3× 845 3.2× 198 0.8× 285 1.9× 66 1.6k
Kimberly A. Kasow United States 18 239 0.7× 400 1.4× 135 0.5× 136 0.5× 210 1.4× 68 1.1k

Countries citing papers authored by Inusha Panigrahi

Since Specialization
Citations

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

Fields of papers citing papers by Inusha Panigrahi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inusha Panigrahi

This figure shows the co-authorship network connecting the top 25 collaborators of Inusha Panigrahi. A scholar is included among the top collaborators of Inusha Panigrahi 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 Inusha Panigrahi. Inusha Panigrahi 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.
Panigrahi, Inusha, et al.. (2025). Microcephalic osteodysplastic primordial dwarfism type II in four Indian children with PCNT variants. Egyptian Journal of Medical Human Genetics. 26(1). 1 indexed citations
2.
Bhatia, Prateek, Inusha Panigrahi, Sameer Vyas, et al.. (2025). Clinical and Genetic Landscape of Children With Congenital Muscular Dystrophies From North India. Journal of Child Neurology. 2022956994–2022956994.
3.
Panigrahi, Inusha, et al.. (2025). P059: Influence of MTHFR polymorphisms and folate pathway metabolites on comorbidities in Down syndrome. Genetics in Medicine Open. 3. 102903–102903.
4.
Kumari, Anu, Devi Dayal, Anupriya Kaur, et al.. (2024). Estrogen Receptor 1 Gene Polymorphism and its Association with Idiopathic Short Stature in North Indian Population. Journal of Clinical Research in Pediatric Endocrinology. 16(3). 0–0.
5.
Kakar, Naseebullah, Gandham SriLakshmi Bhavani, Manisha Goyal, et al.. (2024). Multi‐gene panel sequencing in highly consanguineous families and patients with congenital forms of skeletal dysplasias. Clinical Genetics. 106(1). 47–55. 1 indexed citations
6.
George, Arun, et al.. (2024). Clinical and molecular characterisation of children with monogenic obesity: a case series. Pediatric Endocrinology Diabetes and Metabolism. 30(2). 104–109. 1 indexed citations
7.
Srivastava, Priyanka, et al.. (2023). Neurofibromatosis type 1: Clinical characteristics and mutation spectrum in a North Indian cohort. Heliyon. 10(1). e23685–e23685. 2 indexed citations
8.
9.
Mahajan, Rahul, Dipankar De, Sanjeev Handa, et al.. (2020). Managing syndromic congenital ichthyosis at a tertiary care institute—Genotype‐phenotype correlations, and novel treatments. Dermatologic Therapy. 33(6). e13816–e13816. 5 indexed citations
10.
Kaur, Anit, et al.. (2020). Wolf–Hirschhorn syndrome: A case series from India. American Journal of Medical Genetics Part A. 182(12). 3048–3051. 3 indexed citations
11.
Panigrahi, Inusha, et al.. (2019). Niemann‐Pick Disease: An Underdiagnosed Lysosomal Storage Disorder. SHILAP Revista de lepidopterología. 2019(1). 3108093–3108093. 6 indexed citations
12.
Sheth, Jayesh, et al.. (2017). Quantitative and Qualitative Analysis of Urinary Glycosaminoglycans (GAGs). 1 indexed citations
13.
14.
Kumar, Ravindra, et al.. (2013). GENETIC HETEROGENEITY OF BETA GLOBIN MUTATIONS AMONG ASIAN-INDIANS AND IMPORTANCE IN GENETIC COUNSELLING AND DIAGNOSIS. Mediterranean Journal of Hematology and Infectious Diseases. 5(1). e2013003–e2013003. 11 indexed citations
15.
Jain, Shalu, Inusha Panigrahi, Rekha Gupta, Shubha R. Phadke, & Sarita Agarwal. (2012). Multiplex Quantitative Fluorescent Polymerase Chain Reaction for Detection of Aneuploidies. Genetic Testing and Molecular Biomarkers. 16(6). 624–627. 12 indexed citations
16.
Panigrahi, Inusha, Mani Bhushan, Mukesh Yadav, Niranjan Khandelwal, & Pratibha Singhi. (2011). Macrocephaly–capillary malformation syndrome: Three new cases. Journal of the Neurological Sciences. 313(1-2). 178–181. 3 indexed citations
17.
Oberoi, Sapna, et al.. (2011). Xmn1‐Gγ polymorphism and clinical predictors of severity of disease in β‐thalassemia intermedia. Pediatric Blood & Cancer. 57(6). 1025–1028. 15 indexed citations
18.
Jain, Shalu, Sarita Agarwal, Inusha Panigrahi, Parag Tamhankar, & Shubha R. Phadke. (2010). Diagnosis of Down Syndrome and Detection of Origin of Nondisjunction by Short Tandem Repeat Analysis. Genetic Testing and Molecular Biomarkers. 14(4). 489–491. 16 indexed citations
19.
Panigrahi, Inusha, Rashmi Ranjan Das, & R. K. Marwaha. (2010). Hemifacial microsomia with pulmonary hypoplasia. BMJ Case Reports. 2010. bcr0420091759–bcr0420091759. 2 indexed citations
20.
Panigrahi, Inusha, Ram Kumar Marwaha, & Rashmi Ranjan Das. (2009). Long-term response to deferiprone therapy in Asian Indians. Annals of Hematology. 89(2). 231–231. 1 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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