Jai Rup Singh

2.7k total citations
47 papers, 795 citations indexed

About

Jai Rup Singh is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Jai Rup Singh has authored 47 papers receiving a total of 795 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 24 papers in Molecular Biology and 6 papers in Plant Science. Recurrent topics in Jai Rup Singh's work include Connexins and lens biology (12 papers), Genetic Associations and Epidemiology (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Jai Rup Singh is often cited by papers focused on Connexins and lens biology (12 papers), Genetic Associations and Epidemiology (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Jai Rup Singh collaborates with scholars based in India, United States and Germany. Jai Rup Singh's co-authors include Vanita Vanita, Daljit Singh, Karl Sperling, Anupam Kaur, Raymonda Varon, Peter N. Robinson, Dharambir K. Sanghera, Sarju Ralhan, Gurpreet Singh Wander and Varinderpal S. Dhillon and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and British Journal of Dermatology.

In The Last Decade

Jai Rup Singh

46 papers receiving 726 citations

Peers

Jai Rup Singh

GENET

OPHTH

SURGE

Gita Akots United States

Klea Lamnissou Greece

Joelle Mbatchou United States

Shiyang Zhang China

L. Bassas Spain

Qiuling Liu China

James Amos‐Landgraf United States

Diego G. Ogando United States

X. Li United States

Gita Akots United States

Jai Rup Singh

405 ×0.9

363 ×0.9

GENET

15 ×0.1

OPHTH

29 ×0.3

152 ×2.5

SURGE

Citations per year, relative to Jai Rup Singh Jai Rup Singh (= 1×) peers Gita Akots

Countries citing papers authored by Jai Rup Singh

Since Specialization

Citations

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

Fields of papers citing papers by Jai Rup Singh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jai Rup Singh. 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 Jai Rup Singh. The network helps show where Jai Rup Singh may publish in the future.

Co-authorship network of co-authors of Jai Rup Singh

This figure shows the co-authorship network connecting the top 25 collaborators of Jai Rup Singh. A scholar is included among the top collaborators of Jai Rup Singh 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 Jai Rup Singh. Jai Rup Singh 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

Singh, Jai Rup, et al.. (2024). Polygenic Risk Score Assessment for Coronary Artery Disease in Asian Indians. Journal of Cardiovascular Translational Research. 17(5). 1086–1096. 2 indexed citations

Singh, Jai Rup, et al.. (2024). Novel and known variants in GJA3 and LIM2 in congenital cataract families from North India. BMC Genomics. 25(1). 31–31. 1 indexed citations

Singh, Jai Rup, et al.. (2023). Mutation screening in autosomal dominant congenital cataract families from North India. Molecular Genetics and Genomics. 298(6). 1279–1288. 1 indexed citations

Sapkota, Bishwa R., Ruth Hopkins, Andrew Bjonnes, et al.. (2015). Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study. The Journal of Steroid Biochemistry and Molecular Biology. 158. 149–156. 39 indexed citations

Robinson, Peter N., et al.. (2012). A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family. Experimental Eye Research. 104. 82–88. 18 indexed citations

Been, Latonya, Aparna Shankar, Christopher E. Aston, et al.. (2011). A low frequency variant within the GWAS locus of MTNR1B affects fasting glucose concentrations: Genetic risk is modulated by obesity. Nutrition Metabolism and Cardiovascular Diseases. 22(11). 944–951. 27 indexed citations

Sanghera, Dharambir K., Latonya Been, Sarju Ralhan, et al.. (2011). Genome-Wide Linkage Scan to Identify Loci Associated with Type 2 Diabetes and Blood Lipid Phenotypes in the Sikh Diabetes Study. PLoS ONE. 6(6). e21188–e21188. 18 indexed citations

Vanita, Vanita, et al.. (2009). Novel EXT1 and EXT2 Mutations in Hereditary Multiple Exostoses Families of Indian Origin. Genetic Testing and Molecular Biomarkers. 13(1). 43–49. 6 indexed citations

Vanita, Vanita, Jai Rup Singh, Daljit Singh, Raymonda Varon, & Karl Sperling. (2008). A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.. PubMed. 14. 1171–5. 24 indexed citations

10.

Vanita, Vanita, Jai Rup Singh, Daljit Singh, Raymonda Varon, & Karl Sperling. (2008). A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.. PubMed. 14. 323–6. 36 indexed citations

11.

Sanghera, Dharambir K., Swapan K. Nath, Xana Kim-Howard, et al.. (2008). TCF7L2 Polymorphisms are Associated with Type 2 Diabetes in Khatri Sikhs from North India: Genetic Variation Affects Lipid Levels. Annals of Human Genetics. 72(4). 499–509. 57 indexed citations

12.

Singh, Arvind R., Anupam Kaur, & Jai Rup Singh. (2008). POEMS Syndrome: A Case Report from Punjab. International Journal of Human Genetics. 8(3). 257–261. 1 indexed citations

13.

Vanita, Vanita, Hans Christian Hennies, Daljit Singh, et al.. (2006). A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.. PubMed. 12. 1217–22. 35 indexed citations

14.

Sanghera, Dharambir K., Jasvinder Singh Bhatti, Gurjit Kaur Bhatti, et al.. (2006). The Khatri Sikh Diabetes Study (SDS): Study Design, Methodology, Sample Collection, and Initial Results. Human Biology. 78(1). 43–63. 30 indexed citations

15.

Vanita, Vanita, Daljit Singh, Peter N. Robinson, Karl Sperling, & Jai Rup Singh. (2006). A novel mutation in the DNA‐binding domain of MAF at 16q23.1 associated with autosomal dominant “cerulean cataract” in an Indian family. American Journal of Medical Genetics Part A. 140A(6). 558–566. 67 indexed citations

16.

Bashamboo, Anu, et al.. (2003). Molecular characterization of a Y-derived marker chromosome and identification of indels in the DYS1 region in a patient with stigmata of Turner syndrome. Current Science. 84(2). 219–22425. 7 indexed citations

17.

Kaur, Anupam, et al.. (2003). Cytogenetic Profile of Individuals with Mental Retardation. International Journal of Human Genetics. 3(1). 13–16. 9 indexed citations

18.

Kaur, Inderjeet, Sangita Roy, Subhabrata Chakrabarti, et al.. (2002). Genomic Diversities and Affinities among Four Endogamous Groups of Punjab (India) Based on Autosomal and Mitochondrial DNA Polymorphisms. Human Biology. 74(6). 819–836. 14 indexed citations

19.

Singh, Jai Rup, Virinder Kaur Sarhadi, Daljit Singh, et al.. (2001). A Novel Form of “Central Pouchlike” Cataract, with Sutural Opacities, Maps to Chromosome 15q21-22. The American Journal of Human Genetics. 68(2). 509–514. 21 indexed citations

20.

Singh, Jai Rup, et al.. (1983). Normal Values for Interpupillary, Inner Canthal and Outer Canthal Distances in an Indian Population. Human Heredity. 33(5). 326–328. 25 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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