Arthavan Selvanathan

435 total citations
22 papers, 290 citations indexed

About

Arthavan Selvanathan is a scholar working on Clinical Biochemistry, Genetics and Molecular Biology. According to data from OpenAlex, Arthavan Selvanathan has authored 22 papers receiving a total of 290 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Clinical Biochemistry, 9 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Arthavan Selvanathan's work include Metabolism and Genetic Disorders (9 papers), Genomics and Rare Diseases (6 papers) and Amino Acid Enzymes and Metabolism (4 papers). Arthavan Selvanathan is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Genomics and Rare Diseases (6 papers) and Amino Acid Enzymes and Metabolism (4 papers). Arthavan Selvanathan collaborates with scholars based in Australia, New Zealand and United Kingdom. Arthavan Selvanathan's co-authors include Kaustuv Bhattacharya, Alissa K. Robbins, Cristina Delgado-Martín, Richard B. Lock, Junior Hall, David T. Teachey, Charles G. Mullighan, Mignon L. Loh, Andrew Wood and Sarah K. Tasian and has published in prestigious journals such as Blood, Nutrients and Genetics in Medicine.

In The Last Decade

Arthavan Selvanathan

21 papers receiving 287 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arthavan Selvanathan Australia 7 128 98 88 68 55 22 290
Walid Al‐Achkar Syria 11 63 0.5× 199 2.0× 108 1.2× 34 0.5× 11 0.2× 52 359
Michelle McBean Australia 12 29 0.2× 109 1.1× 97 1.1× 23 0.3× 8 0.1× 21 262
Camila Matzenbacher Bittar Brazil 11 19 0.1× 35 0.4× 87 1.0× 37 0.5× 48 0.9× 16 267
Céline Bourgne France 9 60 0.5× 44 0.4× 110 1.3× 9 0.1× 39 0.7× 26 271
Eden Haverfield United States 13 20 0.2× 40 0.4× 241 2.7× 95 1.4× 28 0.5× 23 536
Xunqiang Yin China 9 101 0.8× 25 0.3× 126 1.4× 129 1.9× 19 0.3× 16 362
Hagit Baris Feldman Israel 11 16 0.1× 16 0.2× 131 1.5× 67 1.0× 33 0.6× 42 366
Kanwaldeep Mallhi United States 9 25 0.2× 73 0.7× 96 1.1× 20 0.3× 29 0.5× 21 249
Maria Bouvy‐Liivrand Finland 11 54 0.4× 45 0.5× 243 2.8× 9 0.1× 42 0.8× 14 365
Parag Tamhankar India 10 16 0.1× 51 0.5× 95 1.1× 34 0.5× 9 0.2× 32 272

Countries citing papers authored by Arthavan Selvanathan

Since Specialization
Citations

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

Fields of papers citing papers by Arthavan Selvanathan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arthavan Selvanathan

This figure shows the co-authorship network connecting the top 25 collaborators of Arthavan Selvanathan. A scholar is included among the top collaborators of Arthavan Selvanathan 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 Arthavan Selvanathan. Arthavan Selvanathan 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.
Selvanathan, Arthavan, Sanjay Bansal, Emer Fitzpatrick, et al.. (2025). Early postnatal hepatocyte transplantation in a child with molybdenum cofactor deficiency type B. Molecular Genetics and Metabolism. 145(1). 109079–109079. 1 indexed citations
2.
McEwen, Alison, Kirsten Boggs, Carolyn Ellaway, et al.. (2025). An Explorative Qualitative Study of the Role of a Genetic Counsellor to Parents Receiving a Diagnosis After a Positive Newborn Bloodspot Screening. International Journal of Neonatal Screening. 11(2). 32–32.
3.
Selvanathan, Arthavan, et al.. (2024). Hematologic Manifestations in Primary Mitochondrial Diseases. Journal of Pediatric Hematology/Oncology. 46(5). e338–e347. 2 indexed citations
4.
Selvanathan, Arthavan, Nancy van Doorn, Susan Thompson, et al.. (2023). Diagnosis and management of children with McArdle Syndrome (GSD V) in New South Wales. JIMD Reports. 64(5). 327–336. 2 indexed citations
5.
Thompson, Susan, Arthavan Selvanathan, Cathryn M. Lewis, et al.. (2023). Treatment of HMG-CoA Lyase Deficiency—Longitudinal Data on Clinical and Nutritional Management of 10 Australian Cases. Nutrients. 15(3). 531–531. 3 indexed citations
6.
Selvanathan, Arthavan, et al.. (2022). A narrative review of metabolomics in the era of “-omics”: integration into clinical practice for inborn errors of metabolism. Translational Pediatrics. 11(10). 1704–1716. 13 indexed citations
7.
Allcock, Richard J. N., Joy Yaplito‐Lee, Carolyn Ellaway, et al.. (2022). The relationship between beta-ureidopropionase deficiency due to UPB1 variants and human phenotypes is uncertain. Molecular Genetics and Metabolism. 137(1-2). 62–67. 2 indexed citations
8.
Selvanathan, Arthavan, Elizabeth Farnsworth, Michel Tchan, et al.. (2022). Intronic variants in inborn errors of metabolism: Beyond the exome. Frontiers in Genetics. 13. 1031495–1031495. 3 indexed citations
9.
Selvanathan, Arthavan, Gerard De Jong, Drago Bratkovic, et al.. (2022). A serendipitous journey to a promoter variant: The c.‐106C>A variant and its role in late‐onset ornithine transcarbamylase deficiency. JIMD Reports. 63(4). 271–275. 3 indexed citations
10.
Selvanathan, Arthavan, Won‐Tae Kim, Maina Kava, et al.. (2022). 3‐Methylglutaconyl‐CoA hydratase deficiency: When ascertainment bias confounds a biochemical diagnosis. JIMD Reports. 63(6). 568–574. 6 indexed citations
11.
Selvanathan, Arthavan, et al.. (2021). Mitochondrial iron-sulfur cluster biogenesis and neurological disorders. Mitochondrion. 62. 41–49. 13 indexed citations
12.
Riley, Lisa G., Minal Menezes, Andrew Williams, et al.. (2021). FGF21 outperforms GDF15 as a diagnostic biomarker of mitochondrial disease in children. Molecular Genetics and Metabolism. 135(1). 63–71. 15 indexed citations
13.
Selvanathan, Arthavan, Francesca Moore, Robert Wynn, et al.. (2021). Effectiveness of early hematopoietic stem cell transplantation in preventing neurocognitive decline in aspartylglucosaminuria: A case series. JIMD Reports. 61(1). 3–11. 3 indexed citations
14.
Selvanathan, Arthavan, Gareth Baynam, Yemima Berman, et al.. (2021). Paediatric genomic testing: Navigating genomic reports for the general paediatrician. Journal of Paediatrics and Child Health. 58(1). 8–15. 1 indexed citations
15.
Selvanathan, Arthavan, et al.. (2020). Ornithine Transcarbamylase Deficiency Presenting as Acute Liver Failure in Girls. Journal of Pediatric Gastroenterology and Nutrition. 71(2). 208–210. 3 indexed citations
16.
Barlow‐Stewart, Kristine, Arthavan Selvanathan, Tony Roscioli, et al.. (2018). User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia. Journal of Genetic Counseling. 28(2). 240–250. 6 indexed citations
17.
18.
Kirk, Edwin P., Kristine Barlow‐Stewart, Arthavan Selvanathan, et al.. (2018). Beyond the panel: preconception screening in consanguineous couples using the TruSight One “clinical exome”. Genetics in Medicine. 21(3). 608–612. 16 indexed citations
19.
Selvanathan, Arthavan, et al.. (2018). Effectiveness of early hematopoietic stem cell transplantation in preventing neurocognitive decline in mucopolysaccharidosis type II: A case series. Molecular Genetics and Metabolism. 123(2). S127–S128. 1 indexed citations
20.
Maude, Shannon L., Sibasish Dolai, Cristina Delgado-Martín, et al.. (2015). Efficacy of JAK/STAT pathway inhibition in murine xenograft models of early T-cell precursor (ETP) acute lymphoblastic leukemia. Blood. 125(11). 1759–1767. 158 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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