Ramu Elango

1.9k total citations
76 papers, 1.0k citations indexed

About

Ramu Elango is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Ramu Elango has authored 76 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 26 papers in Genetics and 16 papers in Surgery. Recurrent topics in Ramu Elango's work include Celiac Disease Research and Management (9 papers), Helicobacter pylori-related gastroenterology studies (8 papers) and Inflammatory Bowel Disease (6 papers). Ramu Elango is often cited by papers focused on Celiac Disease Research and Management (9 papers), Helicobacter pylori-related gastroenterology studies (8 papers) and Inflammatory Bowel Disease (6 papers). Ramu Elango collaborates with scholars based in Saudi Arabia, India and United States. Ramu Elango's co-authors include Noor Ahmad Shaik, Babajan Banaganapalli, Jumana Y. Al‐Aama, Zuhier Awan, Kent W. Hunter, Rachel A. Gibson, Fayçal Hentati, Liling Warren, Omar I. Saadah and David E. Housman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Ramu Elango

74 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ramu Elango Saudi Arabia	19	447	263	186	145	112	76	1.0k
Hossein Fakhrai-Rad Sweden	12	764 1.7×	419 1.6×	144 0.8×	222 1.5×	91 0.8×	17	1.4k
Wanqiu Chen United States	21	929 2.1×	199 0.8×	436 2.3×	78 0.5×	87 0.8×	48	1.7k
Alejandro Abuin United States	15	998 2.2×	233 0.9×	135 0.7×	69 0.5×	53 0.5×	17	1.3k
Isabell Greeve Germany	12	402 0.9×	118 0.4×	78 0.4×	134 0.9×	99 0.9×	21	1.1k
Alice Zhao United States	12	642 1.4×	140 0.5×	120 0.6×	75 0.5×	27 0.2×	22	1.1k
Alberto Blázquez Spain	18	750 1.7×	141 0.5×	87 0.5×	37 0.3×	111 1.0×	50	1.1k
V. Wong Canada	18	538 1.2×	128 0.5×	78 0.4×	290 2.0×	55 0.5×	27	1.1k
Teresa C. Ritchie United States	12	433 1.0×	207 0.8×	50 0.3×	64 0.4×	179 1.6×	13	843
Fuyuki Miya Japan	19	509 1.1×	299 1.1×	33 0.2×	126 0.9×	126 1.1×	84	1.0k
Mohammad Fallahi United States	26	1.2k 2.8×	118 0.4×	123 0.7×	69 0.5×	281 2.5×	41	1.9k

Countries citing papers authored by Ramu Elango

Since Specialization

Citations

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

Fields of papers citing papers by Ramu Elango

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ramu Elango

This figure shows the co-authorship network connecting the top 25 collaborators of Ramu Elango. A scholar is included among the top collaborators of Ramu Elango 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 Ramu Elango. Ramu Elango 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

Shaik, Noor Ahmad, et al.. (2024). Nationwide survey on awareness of consanguinity and genetic diseases in Saudi Arabia: challenges and potential solutions to reduce the national healthcare burden. Human Genomics. 18(1). 138–138. 2 indexed citations

Shaik, Noor Ahmad, Mohammad Athar, Ahmed A. Awan, et al.. (2023). Protein structural insights into a rare PCSK9 gain-of-function variant (R496W) causing familial hypercholesterolemia in a Saudi family: whole exome sequencing and computational analysis. Frontiers in Physiology. 14. 1204018–1204018. 2 indexed citations

Shaik, Noor Ahmad, Zuhier Awan, Yousef Qari, et al.. (2023). Rare variant burden analysis from exomes of three consanguineous families reveals LILRB1 and PRSS3 as potential key proteins in inflammatory bowel disease pathogenesis. Frontiers in Medicine. 10. 1164305–1164305. 3 indexed citations

Elsamanoudy, Ayman Z., et al.. (2022). Integrative system biology and mathematical modeling of genetic networks identifies shared biomarkers for obesity and diabetes. Mathematical Biosciences & Engineering. 19(3). 2310–2329. 13 indexed citations

Shaik, Noor Ahmad, et al.. (2021). TagSNP approach for HLA risk allele genotyping of Saudi celiac disease patients: effectiveness and pitfalls. Bioscience Reports. 41(6). 1 indexed citations

Banaganapalli, Babajan, Ahmed N. Sahly, Thoraia Shinawi, et al.. (2021). Molecular differential analysis of uterine leiomyomas and leiomyosarcomas through weighted gene network and pathway tracing approaches. Systems Biology in Reproductive Medicine. 67(3). 209–220. 7 indexed citations

Suganthe, R.C., et al.. (2021). Multiclass Classification of Alzheimer’s Disease Using Hybrid Deep Convolutional Neural Network. NVEO - NATURAL VOLATILES & ESSENTIAL OILS Journal | NVEO. 145–153. 21 indexed citations

Shinawi, Thoraia, Babajan Banaganapalli, Noor Ahmad Shaik, et al.. (2021). Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects. Frontiers in Medicine. 8. 724826–724826. 10 indexed citations

Shaik, Noor Ahmad, et al.. (2020). Molecular modelling and dynamic simulations of sequestosome 1 (SQSTM1) missense mutations linked to Paget disease of bone. Journal of Biomolecular Structure and Dynamics. 39(8). 2873–2884. 8 indexed citations

10.

Banaganapalli, Babajan, et al.. (2020). Molecular profiling of lamellar ichthyosis pathogenic missense mutations on the structural and stability aspects of TGM1 protein. Journal of Biomolecular Structure and Dynamics. 39(14). 4962–4972. 7 indexed citations

11.

Banaganapalli, Babajan, et al.. (2020). Myocardial infarction biomarker discovery with integrated gene expression, pathways and biological networks analysis. Genomics. 112(6). 5072–5085. 20 indexed citations

12.

Edris, Sherif, et al.. (2020). Identification of Causative Variants Contributing to Nonsyndromic Orofacial Clefts Using Whole-Exome Sequencing in a Saudi Family. Genetic Testing and Molecular Biomarkers. 24(11). 723–731. 3 indexed citations

13.

Mohammed, Arif, Aftab Ahmad, Omar I. Saadah, et al.. (2020). Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysis. Scientific Reports. 10(1). 16290–16290. 16 indexed citations

14.

Shaik, Noor Ahmad, Tariq Masoodi, Preetha J. Shetty, et al.. (2019). Molecular modelling and dynamics of CA2 missense mutations causative to carbonic anhydrase 2 deficiency syndrome. Journal of Biomolecular Structure and Dynamics. 38(14). 4067–4080. 21 indexed citations

15.

Hakeem, Khalid Rehman, Noor Ahmad Shaik, Babajan Banaganapalli, & Ramu Elango. (2019). Essentials of Bioinformatics, Volume III In Silico Life Sciences: Agriculture. 1 indexed citations

16.

Sabir, Jamal S. M., Abdelfatteh El Omri, Babajan Banaganapalli, et al.. (2019). Dissecting the Role of NF-κb Protein Family and Its Regulators in Rheumatoid Arthritis Using Weighted Gene Co-Expression Network. Frontiers in Genetics. 10. 1163–1163. 19 indexed citations

17.

Shaik, Noor Ahmad, Zuhier Awan, Prashant Kumar Verma, Ramu Elango, & Babajan Banaganapalli. (2018). Protein phenotype diagnosis of autosomal dominant calmodulin mutations causing irregular heart rhythms. Journal of Cellular Biochemistry. 119(10). 8233–8248. 11 indexed citations

18.

Banaganapalli, Babajan, et al.. (2017). Distribution ofCYP2C8 andCYP2C9 amino acid substitution alleles in South Indian diabetes patients: A genotypic and computational protein phenotype study. Clinical and Experimental Pharmacology and Physiology. 44(12). 1171–1179. 6 indexed citations

19.

Hunter, Kent W., Laura Riba, Leonard C. Schalkwyk, et al.. (1996). Toward the construction of integrated physical and genetic maps of the mouse genome using interspersed repetitive sequence PCR (IRS-PCR) genomics.. Genome Research. 6(4). 290–299. 14 indexed citations

20.

Karayiorgou, Maria, Laura Kasch, Virginia K. Lasseter, et al.. (1994). Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model. American Journal of Medical Genetics. 54(4). 345–353. 18 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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