Arti Pandya

5.0k total citations
75 papers, 2.7k citations indexed

About

Arti Pandya is a scholar working on Molecular Biology, Sensory Systems and Cognitive Neuroscience. According to data from OpenAlex, Arti Pandya has authored 75 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 32 papers in Sensory Systems and 19 papers in Cognitive Neuroscience. Recurrent topics in Arti Pandya's work include Hearing, Cochlea, Tinnitus, Genetics (32 papers), Connexins and lens biology (16 papers) and Hearing Loss and Rehabilitation (16 papers). Arti Pandya is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (32 papers), Connexins and lens biology (16 papers) and Hearing Loss and Rehabilitation (16 papers). Arti Pandya collaborates with scholars based in United States, Türkiye and Japan. Arti Pandya's co-authors include Kathleen S. Arnos, Walter E. Nance, Mustafa Tekin, Susan H. Blanton, Katherine O. Welch, Virginia W. Norris, Xia Xia, Nathaniel H. Robin, Heidi L. Rehm and Christine Yoshinaga‐Itano and has published in prestigious journals such as The Lancet, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Arti Pandya

70 papers receiving 2.6k citations

Peers

Arti Pandya

SURGE

GENET

Henricus P. M. Kunst Netherlands

Maria Bitner‐Glindzicz United Kingdom

Kunihiro Fukushima Japan

Kimia Kahrizi Iran

Karen Brøndum‐Nielsen Denmark

Hideichi Shinkawa Japan

Jinsei Jung South Korea

Theo Peters Netherlands

Moien Kanaan Israel

Michael B. Petersen Greece

Henricus P. M. Kunst Netherlands

Arti Pandya

987 ×0.8

999 ×0.8

985 ×1.9

SURGE

376 ×0.8

253 ×0.6

GENET

Citations per year, relative to Arti Pandya Arti Pandya (= 1×) peers Henricus P. M. Kunst

Countries citing papers authored by Arti Pandya

Since Specialization

Citations

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

Fields of papers citing papers by Arti Pandya

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arti Pandya

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Blatt, Julie, et al.. (2023). Repurposing of antiangiogenic agents for treatment of vascular anomalies. Pharmacology & Therapeutics. 250. 108520–108520. 1 indexed citations

Li, Marilyn M., Ahmad Abou Tayoun, Marina T. DiStefano, et al.. (2022). Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 24(7). 1392–1406. 37 indexed citations

Blatt, Julie, et al.. (2019). Cancer Risk in Klippel–Trenaunay Syndrome. Lymphatic Research and Biology. 17(6). 630–636. 17 indexed citations

Marchuk, Daniel S., Laurie D. Smith, Alexandra Arreola, et al.. (2017). Co‐occurring Down syndrome and SUCLA2‐related mitochondrial depletion syndrome. American Journal of Medical Genetics Part A. 173(10). 2720–2724.

Dominguez, Laura M., et al.. (2013). Risk Factors Associated With Unilateral Hearing Loss. JAMA Otolaryngology–Head & Neck Surgery. 139(1). 59–59. 19 indexed citations

Anderson, Paula, et al.. (2012). Performance Evaluation of Two Methods Using Commercially Available Reagents for PCR-Based Detection of FMR1 Mutation. Journal of Molecular Diagnostics. 14(5). 476–486. 14 indexed citations

Dodson, Kelley M., Bich Hong Nguyen, Aristides Sismanis, et al.. (2012). Etiology of unilateral hearing loss in a national hereditary deafness repository. American Journal of Otolaryngology. 33(5). 590–594. 34 indexed citations

Rendtorff, Nanna Dahl, Marianne Lodahl, Houda Boulahbel, et al.. (2011). Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment. American Journal of Medical Genetics Part A. 155(6). 1298–1313. 89 indexed citations

Arnos, Kathleen S., Katherine O. Welch, Mustafa Tekin, et al.. (2008). A Comparative Analysis of the Genetic Epidemiology of Deafness in the United States in Two Sets of Pedigrees Collected More than a Century Apart. The American Journal of Human Genetics. 83(2). 200–207. 30 indexed citations

10.

Welch, Katherine O., et al.. (2007). Compound heterozygosity for dominant and recessive GJB2 mutations: Effect on phenotype and review of the literature. American Journal of Medical Genetics Part A. 143A(14). 1567–1573. 31 indexed citations

11.

Arnos, Kathleen S., et al.. (2006). A focus group study of consumer attitudes toward genetic testing and newborn screening for deafness. Genetics in Medicine. 8(12). 779–783. 34 indexed citations

12.

Welch, Katherine O., Mustafa Tekin, Walter E. Nance, et al.. (2003). Chudley‐McCullough syndrome: Expanded phenotype and review of the literature. American Journal of Medical Genetics Part A. 119A(1). 71–76. 11 indexed citations

13.

Cabral, Wayne A., Elena Makareeva, Alain Colige, et al.. (2003). Type I Collagen Triplet Duplication Mutation in Lethal Osteogenesis Imperfecta Shifts Register of α Chains throughout the Helix and Disrupts Incorporation of Mutant Helices into Fibrils and Extracellular Matrix. Journal of Biological Chemistry. 278(12). 10006–10012. 27 indexed citations

14.

Tekin, Mustafa, Kathleen S. Arnos, & Arti Pandya. (2001). Advances in hereditary deafness. The Lancet. 358(9287). 1082–1090. 121 indexed citations

15.

Tekin, Mustafa, et al.. (2001). W44C mutation in the connexin 26 gene associated with dominant non‐syndromic deafness. Clinical Genetics. 59(4). 269–273. 18 indexed citations

16.

Lu, Kangmo, E. Starr Hazard, Angela Brooks‐Wilson, et al.. (2001). Two Genes That Map to the STSL Locus Cause Sitosterolemia: Genomic Structure and Spectrum of Mutations Involving Sterolin-1 and Sterolin-2, Encoded by ABCG5 and ABCG8, Respectively. The American Journal of Human Genetics. 69(2). 278–290. 282 indexed citations

17.

Marcus, Dennis M., et al.. (1999). Discordant retinoblastoma in monozygotic twins. American Journal of Ophthalmology. 128(4). 524–526. 5 indexed citations

18.

Fisch, Gene S., Nancy J. Carpenter, Jeanette J. A. Holden, et al.. (1999). Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: Growth, development, and profiles. American Journal of Medical Genetics. 83(4). 257–263. 36 indexed citations

19.

Pandya, Arti, et al.. (1997). Implications of Molecular Diagnostic Testing in Families with Hereditary Pancreatitis. Genetic Testing. 1(3). 207–211. 4 indexed citations

20.

Pandya, Arti, et al.. (1995). Interstitial deletion of the long arm of chromosome 6 associated with unusual limb anomalies: Report of two new patients and review of the literature. American Journal of Medical Genetics. 59(1). 38–43. 21 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.

Explore authors with similar magnitude of impact