Preeti Paliwal

712 total citations
33 papers, 520 citations indexed

About

Preeti Paliwal is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Preeti Paliwal has authored 33 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 11 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Preeti Paliwal's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Corneal Surgery and Treatments (5 papers). Preeti Paliwal is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Corneal Surgery and Treatments (5 papers). Preeti Paliwal collaborates with scholars based in India, United States and Australia. Preeti Paliwal's co-authors include Irina M. Conboy, Arundhati Sharma, Radhika Tandon, Novalia Pishesha, Rasik B. Vajpayee, Seema Sen, Namrata Sharma, Lukasz J. Bugaj, Vegesna Radha and Michael J. Conboy and has published in prestigious journals such as SHILAP Revista de lepidopterología, Circulation Research and Biophysical Journal.

In The Last Decade

Preeti Paliwal

30 papers receiving 500 citations

Peers

Preeti Paliwal

RNMI

OPHTH

GENET

PHYSI

Anne Katrine Wiencke Denmark

Prasuna Paluru United States

Lijie Dong China

Jessica Wilson United States

Kazutaka Hirabayashi Japan

Cécile Cauquil France

John R. Ainsworth United Kingdom

Alex Malandrini Italy

Oscar F. Chacón‐Camacho Mexico

Graziana Esposito Italy

Anne Katrine Wiencke Denmark

Preeti Paliwal

175 ×0.7

107 ×0.7

RNMI

209 ×2.2

OPHTH

21 ×0.3

GENET

56 ×1.0

PHYSI

Citations per year, relative to Preeti Paliwal Preeti Paliwal (= 1×) peers Anne Katrine Wiencke

Countries citing papers authored by Preeti Paliwal

Since Specialization

Citations

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

Fields of papers citing papers by Preeti Paliwal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Preeti Paliwal

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

All Works

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20 of 20 papers shown

Paliwal, Preeti, et al.. (2025). Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of 300 Indian Patients. The Indian Journal of Pediatrics. 93(1). 36–47.

Paliwal, Preeti, et al.. (2024). In vitro treatment with liposome-encapsulated Mannose-1-phosphate restores N-glycosylation in PMM2-CDG patient-derived fibroblasts. Molecular Genetics and Metabolism. 143(1-2). 108531–108531. 2 indexed citations

Hartman, James J., Darren T. Hwee, Julien Robert‐Paganin, et al.. (2024). Aficamten is a small-molecule cardiac myosin inhibitor designed to treat hypertrophic cardiomyopathy. Nature Cardiovascular Research. 3(8). 1003–1016. 29 indexed citations

Bijarnia‐Mahay, Sunita, et al.. (2023). A Rare Case of Mosaic 3pter and 5pter Deletion-Duplication with Autism Spectrum Disorder and Dyskinesia. SHILAP Revista de lepidopterología. 2023. 1–9.

Paliwal, Preeti, et al.. (2021). Prenatal Diagnosis by Chromosome Microarray Analysis, An Indian Experience. The Journal of Obstetrics and Gynecology of India. 71(2). 156–167. 5 indexed citations

Hartman, James J., Darren T. Hwee, Jingying Wang, et al.. (2020). Characterization of the Cardiac Myosin Inhibitor CK-3773274: a Potential Therapeutic Approach for Hypertrophic Cardiomyopathy. Biophysical Journal. 118(3). 596a–596a. 8 indexed citations

Verma, Ishwar C., Preeti Paliwal, & Kanika Singh. (2017). Genetic Testing in Pediatric Ophthalmology. The Indian Journal of Pediatrics. 85(3). 228–236. 15 indexed citations

Gupta, Ranjan, Preeti Paliwal, Radhika Tandon, et al.. (2015). Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India.. PubMed. 21. 1252–60. 23 indexed citations

Bansal, Virinder Kumar, Arundhati Sharma, Preeti Paliwal, et al.. (2014). Prospective Case–Control Study to Evaluate the Role of Glutathione S Transferases (GSTT1 and GSTM1) Gene Deletion in Breast Carcinoma and Its Prognostic Significance. Indian Journal of Surgery. 77(S3). 1067–1072. 10 indexed citations

10.

Paliwal, Preeti, Arundhati Sharma, Radhika Tandon, et al.. (2012). Molecular Genetic Analysis of Macular Corneal Dystrophy Patients from North India. Ophthalmic Research. 48(1). 28–32. 9 indexed citations

11.

Paliwal, Preeti & Irina M. Conboy. (2011). Inhibitors of Tyrosine Phosphatases and Apoptosis Reprogram Lineage-Marked Differentiated Muscle to Myogenic Progenitor Cells. Chemistry & Biology. 18(9). 1153–1166. 14 indexed citations

12.

Paliwal, Preeti, Anshul Sharma, Shweta Birla, et al.. (2011). Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotype. Molecular Human Reproduction. 17(6). 372–378. 20 indexed citations

13.

Paliwal, Preeti, et al.. (2011). A Novel <i>TGFBI</i> Phenotype with Amyloid Deposits and Arg124Leu Mutation. Ophthalmic Research. 46(3). 164–167. 2 indexed citations

14.

Paliwal, Preeti, Radhika Tandon, Divya Dube, Punit Kaur, & Arundhati Sharma. (2011). Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus.. PubMed. 17. 481–5. 28 indexed citations

15.

Paliwal, Preeti, Arundhati Sharma, Radhika Tandon, et al.. (2010). TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophies.. PubMed. 16. 1429–38. 21 indexed citations

16.

Paliwal, Preeti, et al.. (2010). An unusual association of hypospadias with partial deletion of chromosome 1q. Fertility and Sterility. 93(7). 2413.e11–2413.e13. 2 indexed citations

17.

Shivaprasad, C, Preeti Paliwal, Rajesh Khadgawat, & Ankur Sharma. (2010). Identification of a novel mutation in an Indian patient with CAII deficiency syndrome. Journal of Postgraduate Medicine. 56(4). 290–292. 2 indexed citations

18.

Biswas, Ahitagni, Tarun Puri, Shikha Goyal, et al.. (2009). Spinal Myxopapillary Ependymoma With Down Syndrome: Exploring an Unusual Association. Journal of Pediatric Hematology/Oncology. 32(1). e38–e41. 5 indexed citations

19.

Paliwal, Preeti. (2009). Clinical and Genetic Profile of Avellino Corneal Dystrophy in 2 Families From North India. Archives of Ophthalmology. 127(10). 1373–1373. 21 indexed citations

20.

Paliwal, Preeti, Vegesna Radha, & G. Swarup. (2007). Regulation of p73 by Hck through kinase-dependent and independent mechanisms. BMC Molecular Biology. 8(1). 45–45. 30 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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