V. Nathan Subramaniam

5.8k total citations
138 papers, 4.5k citations indexed

About

V. Nathan Subramaniam is a scholar working on Hematology, Genetics and Nutrition and Dietetics. According to data from OpenAlex, V. Nathan Subramaniam has authored 138 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Hematology, 63 papers in Genetics and 42 papers in Nutrition and Dietetics. Recurrent topics in V. Nathan Subramaniam's work include Iron Metabolism and Disorders (78 papers), Hemoglobinopathies and Related Disorders (62 papers) and Trace Elements in Health (41 papers). V. Nathan Subramaniam is often cited by papers focused on Iron Metabolism and Disorders (78 papers), Hemoglobinopathies and Related Disorders (62 papers) and Trace Elements in Health (41 papers). V. Nathan Subramaniam collaborates with scholars based in Australia, Singapore and United States. V. Nathan Subramaniam's co-authors include Daniel F. Wallace, Gautam Rishi, Wanjin Hong, Dorothy H. Crawford, Lawrie W. Powell, Siew Heng Wong, Gregory J. Anderson, Grant A. Ramm, Lesa Summerville and David M. Frazer and has published in prestigious journals such as Nature, Science and The Lancet.

In The Last Decade

V. Nathan Subramaniam

132 papers receiving 4.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. Nathan Subramaniam Australia 39 2.3k 1.9k 1.7k 1.2k 893 138 4.5k
Maura Poli Italy 32 1.4k 0.6× 700 0.4× 825 0.5× 1.3k 1.1× 174 0.2× 77 3.2k
John W. Forstrom United States 18 1.2k 0.5× 417 0.2× 369 0.2× 1.3k 1.1× 244 0.3× 23 3.5k
David M. Koeller United States 30 565 0.2× 312 0.2× 553 0.3× 2.9k 2.5× 162 0.2× 66 4.4k
Onyinye Onyekwere United States 18 798 0.3× 896 0.5× 142 0.1× 2.4k 2.1× 268 0.3× 29 4.4k
Yoshihiro Torimoto Japan 23 676 0.3× 378 0.2× 249 0.1× 916 0.8× 90 0.1× 86 2.8k
Christine Chomienne France 56 6.8k 2.9× 2.0k 1.0× 99 0.1× 10.1k 8.7× 496 0.6× 248 12.8k
Tsz‐Kwong Man United States 28 400 0.2× 425 0.2× 361 0.2× 1.4k 1.2× 86 0.1× 73 2.9k
Raymond Taetle United States 38 1.0k 0.5× 545 0.3× 110 0.1× 2.2k 1.9× 148 0.2× 129 4.4k
Andrew G. Hall United Kingdom 36 863 0.4× 457 0.2× 105 0.1× 2.2k 1.9× 108 0.1× 118 4.0k
David F. Bishop United States 40 310 0.1× 265 0.1× 238 0.1× 2.6k 2.3× 478 0.5× 86 4.2k

Countries citing papers authored by V. Nathan Subramaniam

Since Specialization
Citations

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

Fields of papers citing papers by V. Nathan Subramaniam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. Nathan Subramaniam. 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 V. Nathan Subramaniam. The network helps show where V. Nathan Subramaniam may publish in the future.

Co-authorship network of co-authors of V. Nathan Subramaniam

This figure shows the co-authorship network connecting the top 25 collaborators of V. Nathan Subramaniam. A scholar is included among the top collaborators of V. Nathan Subramaniam 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 V. Nathan Subramaniam. V. Nathan Subramaniam 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.
Rishi, Gautam, et al.. (2021). Cancer: The role of iron and ferroptosis. The International Journal of Biochemistry & Cell Biology. 141. 106094–106094. 32 indexed citations
2.
Rishi, Gautam & V. Nathan Subramaniam. (2019). Signaling pathways regulating hepcidin. Vitamins and hormones. 110. 47–70. 16 indexed citations
3.
Wankell, Miriam, et al.. (2017). The functional roles of T-cadherin in mammalian biology. SHILAP Revista de lepidopterología. 4(1). 62–81. 10 indexed citations
4.
Wallace, Daniel F. & V. Nathan Subramaniam. (2015). Analysis of IL-22 contribution to hepcidin induction and hypoferremia during the response to LPS in vivo. Queensland's institutional digital repository (The University of Queensland). 6 indexed citations
5.
Goh, Justin B., Daniel F. Wallace, Weifeng Hong, & V. Nathan Subramaniam. (2015). Endofin, a novel BMP-SMAD regulator of the iron-regulatory hormone, hepcidin. QUT ePrints (Queensland University of Technology). 1 indexed citations
6.
Tan, Terrence, Dorothy H. Crawford, V. Nathan Subramaniam, et al.. (2013). Excess iron modulates endoplasmic reticulum stress-associated pathways in a mouse model of alcohol and high-fat diet-induced liver injury. Laboratory Investigation. 93(12). 1295–1312. 93 indexed citations
7.
Wallace, Daniel F., et al.. (2013). New genetic complexity underlying atypical iron disorders. Journal of Gastroenterology and Hepatology. 28. 5–5. 2 indexed citations
8.
Britton, Laurence, Terrence Tan, Andrew D. Clouston, et al.. (2012). The progression of NAFLD to NASH in a mouse model of Hfe(-/-)- associated steatohepatitis is attenuated by co-administration of curcumin and vitamin E. Hepatology. 27. 15–16. 2 indexed citations
9.
Stuart, Katherine, Kim R. Bridle, Therese L. Murphy, et al.. (2011). The Altered Expression of Iron Metabolism Genes in Models of Liver Injury Suggests Iron Deficiency in Cholestasis and Inappropriate Regulation of Hepcidin in Hepatocellular Cirrhosis. Hepatology. 26. 4–4.
10.
Subramaniam, V. Nathan, et al.. (2011). Temporal and tissue-specific analysis of iron loading in mouse models of hereditary haemochromatosis. Journal of Gastroenterology and Hepatology. 26. 7–8. 2 indexed citations
11.
Ruddell, Richard G., Belinda Knight, Janina E. E. Tirnitz‐Parker, et al.. (2009). Lymphotoxin-β receptor signaling regulates hepatic stellate cell function and wound healing in a murine model of chronic liver injury. Murdoch Research Repository (Murdoch University). 1 indexed citations
12.
Crawford, Dorothy H., Therese L. Murphy, Louise E. Ramm, et al.. (2008). Serum hyaluronic acid with serum ferritin accurately predicts cirrhosis and reduces the need for liver biopsy in C282Y hemochromatosis #. Hepatology. 49(2). 418–425. 38 indexed citations
13.
Walsh, Alissa, Jeannette L. Dixon, Grant A. Ramm, et al.. (2006). The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis. Queensland's institutional digital repository (The University of Queensland). 1 indexed citations
14.
Wallace, Daniel F., et al.. (2004). Inactivation of the murine Transferrin Receptor 2 gene using the cre recombinase: loxP system. Faculty of Health. 3 indexed citations
15.
Powell, Lawrie W., Grant A. Ramm, Kym Anderson, et al.. (2002). Phenotypic expression of hfe-associated hemochromatosis in C282Y homozygous relatives: Implications for screening.. Hepatology. 36(4). 2 indexed citations
16.
Subramaniam, V. Nathan, et al.. (2000). Haemochromatosis in the new millennium. Queensland's institutional digital repository (The University of Queensland). 11 indexed citations
17.
Wong, Siew Heng, Yue Xu, Tao Zhang, et al.. (1999). GS32, a Novel Golgi SNARE of 32 kDa, Interacts Preferentially with Syntaxin 6. Molecular Biology of the Cell. 10(1). 119–134. 64 indexed citations
18.
Lowe, Stephen L., et al.. (1997). A SNARE involved in protein transport through the Golgi apparatus. Nature. 389(6653). 881–884. 76 indexed citations
19.
Coe, John G. S., et al.. (1996). YP26, a 26 KDA protein potentially involved in ER-Golgi transport in the yeast S-cerevisiae. Molecular Biology of the Cell. 7. 429–429. 1 indexed citations
20.
Tang, Bor Luen, Siew Heng Wong, Sarah Löw, V. Nathan Subramaniam, & Hong Wu. (1994). Cytosolic factors block antibody binding to the C-terminal cytoplasmic tail of the KDEL receptor. National University of Singapore. 1 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

Breakdown of academic impact, for papers by Maura Poli Breakdown of academic impact, for papers by John W. Forstrom Breakdown of academic impact, for papers by David M. Koeller Breakdown of academic impact, for papers by Onyinye Onyekwere Breakdown of academic impact, for papers by Yoshihiro Torimoto Breakdown of academic impact, for papers by Christine Chomienne Breakdown of academic impact, for papers by Tsz‐Kwong Man Breakdown of academic impact, for papers by Raymond Taetle Breakdown of academic impact, for papers by Andrew G. Hall Breakdown of academic impact, for papers by David F. Bishop
Rankless by CCL
2026