Parneet Kaur

772 total citations
32 papers, 343 citations indexed

About

Parneet Kaur is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Parneet Kaur has authored 32 papers receiving a total of 343 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Neurology. Recurrent topics in Parneet Kaur's work include Genomics and Rare Diseases (4 papers), Neurological diseases and metabolism (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Parneet Kaur is often cited by papers focused on Genomics and Rare Diseases (4 papers), Neurological diseases and metabolism (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Parneet Kaur collaborates with scholars based in India, United States and China. Parneet Kaur's co-authors include Arunachalam Muthuraman, Pradeep Kumar, Manjinder Kaur, Saurabh Kulshrestha, Anju Shukla, Katta M. Girisha, Sanjay K. S. Patel, Yung‐Hun Yang, Xiangkai Li and Shashi Kant Bhatia and has published in prestigious journals such as SHILAP Revista de lepidopterología, Pharmacology Biochemistry and Behavior and Human Genetics.

In The Last Decade

Parneet Kaur

29 papers receiving 339 citations

Peers

Parneet Kaur
Wenlin Zhang China
Yuqin Peng China
Yuji Tanaka Japan
Feng-fei Li China
Yue‐Feng Zhang China
Wen Zheng China
Caixia Li China
Chan Liu China
Wenlin Zhang China
Parneet Kaur
Citations per year, relative to Parneet Kaur Parneet Kaur (= 1×) peers Wenlin Zhang

Countries citing papers authored by Parneet Kaur

Since Specialization
Citations

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

Fields of papers citing papers by Parneet Kaur

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Parneet Kaur

This figure shows the co-authorship network connecting the top 25 collaborators of Parneet Kaur. A scholar is included among the top collaborators of Parneet Kaur 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 Parneet Kaur. Parneet Kaur 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.
Sharma, Gaurav Kumar, et al.. (2024). In silico screening and evaluation of antiviral peptides as inhibitors against ORF9b protein of SARS-CoV-2. 3 Biotech. 14(9). 192–192. 1 indexed citations
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Guo, Xinyu, Yoshiko Murakami, Taroh Kinoshita, et al.. (2022). C18orf32 loss-of-function is associated with a neurodevelopmental disorder with hypotonia and contractures. Human Genetics. 141(8). 1423–1429. 3 indexed citations
6.
Kaur, Parneet, Joshi Stephen, Rajagopal Kadavigere, et al.. (2021). Bi‐allelic missense variant, p. Ser35Leu in EXOSC1 is associated with pontocerebellar hypoplasia. Clinical Genetics. 99(4). 594–600. 15 indexed citations
7.
Kaur, Parneet, et al.. (2021). Acrania-exencephaly-anencephaly sequence. SHILAP Revista de lepidopterología. 10(4). 282–285. 2 indexed citations
8.
Bijarnia‐Mahay, Sunita, et al.. (2021). Growth and neurodevelopmental disorder with arthrogryposis, microcephaly and structural brain anomalies caused by Bi-allelic partial deletion of SMPD4 gene. Journal of Human Genetics. 67(3). 133–136. 5 indexed citations
9.
Narayanan, Dhanya Lakshmi, Parneet Kaur, Suvasini Sharma, et al.. (2021). Multilocus disease-causing genomic variations for Mendelian disorders: role of systematic phenotyping and implications on genetic counselling. European Journal of Human Genetics. 29(12). 1774–1780. 8 indexed citations
10.
Joseph, Joseph, et al.. (2021). Osteoporosis Complications in Crohn's Disease Patients: Factors, Pathogenesis, and Treatment Outlines. Cureus. 13(12). e20564–e20564. 4 indexed citations
11.
Kaur, Parneet, et al.. (2021). Nanomaterial conjugated lignocellulosic waste: cost-effective production of sustainable bioenergy using enzymes. 3 Biotech. 11(11). 480–480. 11 indexed citations
12.
Kaur, Parneet, et al.. (2021). Further evidence of muscle involvement in neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy. Annals of Human Genetics. 86(2). 94–101. 3 indexed citations
13.
Kaur, Parneet, et al.. (2020). Spastic Paraplegia Type 56 in a Young Child. The Indian Journal of Pediatrics. 87(8). 650–651. 1 indexed citations
14.
Thakur, Vikram, et al.. (2020). Blood clots in COVID-19 patients: Simplifying the curious mystery. Medical Hypotheses. 146. 110371–110371. 42 indexed citations
15.
Kaur, Parneet, et al.. (2019). Basal cell carcinoma of eyelid. 4(1). 102–104. 1 indexed citations
16.
Kaur, Parneet, et al.. (2019). Homozygous variant, p.(Arg643Trp) in VAC14 causes striatonigral degeneration: report of a novel variant and review of VAC14-related disorders. Journal of Human Genetics. 64(12). 1237–1242. 10 indexed citations
17.
Kaur, Parneet, et al.. (2019). Identification of a novel homozygous variant confirms ITPA as a developmental and epileptic encephalopathy gene. American Journal of Medical Genetics Part A. 179(5). 857–861. 12 indexed citations
18.
Muthuraman, Arunachalam & Parneet Kaur. (2015). Renin-Angiotensin-Aldosterone System: A Current Drug Target for the Management of Neuropathic Pain. Current Drug Targets. 17(2). 178–195. 11 indexed citations
19.
Muthuraman, Arunachalam, et al.. (2015). Investigation of the role of non-selective calcium channel blocker (flunarizine) on cerebral ischemic–reperfusion associated cognitive dysfunction in aged mice. Pharmacology Biochemistry and Behavior. 131. 26–32. 10 indexed citations
20.
Kaur, Parneet, et al.. (1988). Impact of education in the knowledge and practices of rural mothers and key family members on diarrhoea and its treatment at home.. PubMed. 6(1). 15–20. 4 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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