Sumita Danda

2.4k total citations
122 papers, 1.0k citations indexed

About

Sumita Danda is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Sumita Danda has authored 122 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 36 papers in Genetics and 26 papers in Physiology. Recurrent topics in Sumita Danda's work include Metabolism and Genetic Disorders (16 papers), Lysosomal Storage Disorders Research (13 papers) and Vasculitis and related conditions (11 papers). Sumita Danda is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Lysosomal Storage Disorders Research (13 papers) and Vasculitis and related conditions (11 papers). Sumita Danda collaborates with scholars based in India, United States and United Kingdom. Sumita Danda's co-authors include Alka V. Ekbote, Debashish Danda, Maya Thomas, Sangeetha Yoganathan, Gautham Arunachal, Ruchika Goel, Atanu Kumar Dutta, George Joseph, Ashwin Dalal and Sniya Sudhakar and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Sumita Danda

104 papers receiving 984 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sumita Danda India 16 489 269 196 128 111 122 1.0k
Qiji Liu China 22 899 1.8× 232 0.9× 232 1.2× 90 0.7× 137 1.2× 87 1.6k
Lamei Yuan China 19 551 1.1× 268 1.0× 78 0.4× 106 0.8× 74 0.7× 83 1.0k
Guy Helman United States 19 692 1.4× 108 0.4× 96 0.5× 156 1.2× 78 0.7× 41 1.0k
Anas M. Alazami Saudi Arabia 22 857 1.8× 584 2.2× 63 0.3× 156 1.2× 100 0.9× 55 1.5k
Davide Tonduti Italy 19 728 1.5× 183 0.7× 81 0.4× 87 0.7× 51 0.5× 64 1.1k
Masato Hoshi Japan 21 876 1.8× 184 0.7× 116 0.6× 132 1.0× 117 1.1× 43 1.6k
Claudio Graziano Italy 20 695 1.4× 325 1.2× 55 0.3× 73 0.6× 96 0.9× 77 1.2k
Isabelle Thiffault United States 23 822 1.7× 482 1.8× 73 0.4× 64 0.5× 88 0.8× 65 1.4k
Khushnooda Ramzan Saudi Arabia 18 644 1.3× 320 1.2× 55 0.3× 236 1.8× 112 1.0× 79 1.2k
Mark D. Ludman Canada 20 446 0.9× 386 1.4× 332 1.7× 31 0.2× 173 1.6× 41 1.2k

Countries citing papers authored by Sumita Danda

Since Specialization
Citations

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

Fields of papers citing papers by Sumita Danda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sumita Danda

This figure shows the co-authorship network connecting the top 25 collaborators of Sumita Danda. A scholar is included among the top collaborators of Sumita Danda 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 Sumita Danda. Sumita Danda 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
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Thomas, Nihal, et al.. (2025). COL1A1 and COL1A2 Gene Variants Causing Osteogenesis Imperfecta in a Major Referral Center of India. American Journal of Medical Genetics Part A. 197(7). e64023–e64023. 1 indexed citations
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Singh, Swati, Sumita Danda, Neetu Sharma, et al.. (2024). Biallelic variants in CCN2 underlie an autosomal recessive kyphomelic dysplasia. European Journal of Human Genetics. 33(1). 30–37. 1 indexed citations
6.
Danda, Debashish, Ruchika Goel, Jayakanthan Kabeerdoss, et al.. (2023). Angiogenesis related genes in Takayasu Arteritis (TAK): robust association with Tag SNPs of IL-18 and FGF-2 in a South Asian Cohort. Journal of Human Genetics. 69(1). 13–18. 3 indexed citations
7.
Danda, Sumita, et al.. (2022). First reported cases with Xia‐Gibbs syndrome from India harboring novel variants in AHDC1. American Journal of Medical Genetics Part A. 188(8). 2501–2504. 2 indexed citations
8.
Thomas, Niranjan, et al.. (2022). Novel Mutations in CRLF1: Case Reports with Crisponi Syndrome. The Indian Journal of Pediatrics. 89(11). 1148–1150. 2 indexed citations
9.
Chapla, Aaron, et al.. (2022). Genotype of autosomal recessive congenital ichthyosis from a tertiary care center in India. Pediatric Dermatology. 39(3). 420–424. 3 indexed citations
10.
Saxena, Deepti, Madhulika Kabra, Neerja Gupta, et al.. (2022). Genotype-phenotype spectrum of 130 unrelated Indian families with Mucopolysaccharidosis type II. European Journal of Medical Genetics. 65(3). 104447–104447. 3 indexed citations
11.
Danda, Sumita, et al.. (2022). Spectrum of Chromosomal Abnormalities Detected by Conventional Cytogenetic Analysis Following Invasive Prenatal Testing of Fetuses with Abnormal Ultrasound Scans. The Journal of Obstetrics and Gynecology of India. 72(S1). 209–216. 1 indexed citations
12.
Muthusamy, Karthik, et al.. (2022). Clustering of Juvenile Canavan disease in an Indian community due to population bottleneck and isolation: genomic signatures of a founder event. European Journal of Human Genetics. 31(1). 73–80. 2 indexed citations
13.
Mistry, Pramod K., Elena Lukina, Hadhami Ben Turkia, et al.. (2021). Clinical outcomes after 4.5 years of eliglustat therapy for Gaucher disease type 1: Phase 3 ENGAGE trial final results. American Journal of Hematology. 96(9). 1156–1165. 31 indexed citations
14.
Chaudhary, Ajay Kumar, Hampapathalu Adimurthy Nagarajaram, Ashwin Dalal, et al.. (2021). Ectodysplasin pathogenic variants affecting the furin‐cleavage site and unusual clinical features define X‐linked hypohidrotic ectodermal dysplasia in India. American Journal of Medical Genetics Part A. 188(3). 788–805. 2 indexed citations
15.
Kumar, Atin, Arun Kumar Gupta, Neetu Bhari, et al.. (2020). Mutation Spectrum of Tuberous Sclerosis Complex Patients in Indian Population. Journal of Pediatric Genetics. 10(4). 274–283. 4 indexed citations
16.
Tamhankar, Parag, Lakshmi Vasudevan, Rita Christopher, et al.. (2020). Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1. Journal of Pediatric Genetics. 10(3). 213–221. 5 indexed citations
17.
Muthusamy, Karthik, Ankan Gupta, Meenakshi Malhotra, et al.. (2020). Co‐occurrence of Aicardi–Goutières syndrome type 6 and dyschromatosis symmetrica hereditaria due to compound heterozygous pathogenic variants in ADAR1 : a case series from India. Clinical and Experimental Dermatology. 46(4). 704–709. 5 indexed citations
18.
Danda, Sumita, Atanu Kumar Dutta, Sheela Nampoothiri, et al.. (2020). Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India. Clinical Rheumatology. 39(9). 2743–2749. 2 indexed citations
19.
Nair, Aswin, Ruchika Goel, Jayakanthan Kabeerdoss, et al.. (2017). C‐reactive protein gene polymorphisms (rs1205) in Asian Indian patients with Takayasu arteritis: Associations and phenotype correlations. International Journal of Rheumatic Diseases. 21(3). 732–739. 5 indexed citations
20.
Danda, Sumita, Shubha R. Phadke, & S. S. Agarwal. (1997). Acromesomelic dwarfism: report of a family with two affected siblings.. PubMed. 34(12). 1127–30. 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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