Avinaash Maharaj

499 total citations
24 papers, 148 citations indexed

About

Avinaash Maharaj is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Avinaash Maharaj has authored 24 papers receiving a total of 148 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Endocrinology, Diabetes and Metabolism and 8 papers in Genetics. Recurrent topics in Avinaash Maharaj's work include Sphingolipid Metabolism and Signaling (7 papers), Genetic Syndromes and Imprinting (6 papers) and Growth Hormone and Insulin-like Growth Factors (6 papers). Avinaash Maharaj is often cited by papers focused on Sphingolipid Metabolism and Signaling (7 papers), Genetic Syndromes and Imprinting (6 papers) and Growth Hormone and Insulin-like Growth Factors (6 papers). Avinaash Maharaj collaborates with scholars based in United Kingdom, Spain and Türkiye. Avinaash Maharaj's co-authors include Louise Metherell, Rathi Prasad, Li F. Chan, Jack Williams, Indraneel Banerjee, Tülay Güran, Helen L. Storr, Débora Braslavsky, Leonardo Guasti and Federica Buonocore and has published in prestigious journals such as Nature Communications, The Journal of Clinical Endocrinology & Metabolism and European Journal of Endocrinology.

In The Last Decade

Avinaash Maharaj

21 papers receiving 147 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Avinaash Maharaj United Kingdom 7 87 50 36 36 16 24 148
Lotte Krogh Denmark 6 75 0.9× 46 0.9× 33 0.9× 54 1.5× 37 2.3× 15 179
Yuki Murayama Japan 7 83 1.0× 30 0.6× 27 0.8× 16 0.4× 19 1.2× 18 142
Jon Celay Spain 8 47 0.5× 30 0.6× 28 0.8× 25 0.7× 9 0.6× 13 131
Jordi Rodó Spain 6 38 0.4× 20 0.4× 36 1.0× 35 1.0× 29 1.8× 7 115
H. Serap Kalkanoğlu Türkiye 10 93 1.1× 21 0.4× 46 1.3× 20 0.6× 39 2.4× 17 216
Jose Efren Barragan Avila United Kingdom 4 60 0.7× 29 0.6× 46 1.3× 8 0.2× 15 0.9× 4 161
Sylvia Stoeckler-Ipsiroglu Austria 8 121 1.4× 39 0.8× 68 1.9× 20 0.6× 12 0.8× 11 247
Nathalie Chami United States 6 86 1.0× 17 0.3× 42 1.2× 71 2.0× 27 1.7× 7 202
Rebecca Gelfer United States 3 135 1.6× 31 0.6× 61 1.7× 9 0.3× 41 2.6× 4 197

Countries citing papers authored by Avinaash Maharaj

Since Specialization
Citations

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

Fields of papers citing papers by Avinaash Maharaj

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Avinaash Maharaj

This figure shows the co-authorship network connecting the top 25 collaborators of Avinaash Maharaj. A scholar is included among the top collaborators of Avinaash Maharaj 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 Avinaash Maharaj. Avinaash Maharaj 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.
Abdullah, Mohamed Ahmed, Omer Babiker, Claire E. Hutchison, et al.. (2025). Novel recurrent mutations and genetic diversity in Sudanese children with adrenal insufficiency. European Journal of Endocrinology. 192(3). 277–289. 1 indexed citations
2.
Maharaj, Avinaash, Miho Ishida, Anna Rybak, et al.. (2024). QSOX2 Deficiency-induced short stature, gastrointestinal dysmotility and immune dysfunction. Nature Communications. 15(1). 8420–8420. 2 indexed citations
3.
Maharaj, Avinaash, Thatchawan Thanasupawat, Sjoerd D. Joustra, et al.. (2024). Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome. JCI Insight. 9(6). 3 indexed citations
4.
Maharaj, Avinaash. (2023). Familial Glucocorticoid Deficiency: the changing landscape of an eponymous syndrome. Frontiers in Endocrinology. 14. 1268345–1268345.
5.
Maharaj, Avinaash, Jack Williams, Katharina Schilbach, et al.. (2023). Characterization of dominant-negative growth hormone receptor variants reveals a potential therapeutic target for short stature. European Journal of Endocrinology. 188(4). 353–365.
6.
Williams, Jack, Chris Smith, Charlotte Hall, et al.. (2023). Elevated sphingosine-1-phosphate lyase leads to increased metabolism and reduced survival in adrenocortical carcinoma. European Journal of Endocrinology. 188(1). 67–77. 5 indexed citations
7.
Maharaj, Avinaash, et al.. (2022). Can Digenic, Tri-Allelic Inheritance of Variants in STAR and CYP11A1 Give Rise to Primary Adrenal Insufficiency? A Case Report. Frontiers in Endocrinology. 13. 860055–860055. 4 indexed citations
8.
Maharaj, Avinaash, Tülay Güran, Federica Buonocore, et al.. (2022). Insights From Long-term Follow-up of a Girl With Adrenal Insufficiency and Sphingosine-1-Phosphate Lyase Deficiency. Journal of the Endocrine Society. 6(5). bvac020–bvac020. 6 indexed citations
9.
Maharaj, Avinaash, Jack Williams, Sumana Chatterjee, et al.. (2021). Growth Hormone Receptor (GHR) 6Ω Pseudoexon Activation: A Novel Cause of Severe Growth Hormone Insensitivity. The Journal of Clinical Endocrinology & Metabolism. 107(1). e401–e416. 5 indexed citations
10.
Maharaj, Avinaash, Sumana Chatterjee, Pratik Shah, et al.. (2021). Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity Syndromes. The Journal of Clinical Endocrinology & Metabolism. 106(11). e4716–e4733. 13 indexed citations
11.
Maharaj, Avinaash, Jack Williams, Sumana Chatterjee, et al.. (2021). Growth hormone receptor 6Ω pseudoexon activation: a novel cause of severe growth hormone insensitivity. Endocrine Abstracts. 1 indexed citations
12.
Maharaj, Avinaash, et al.. (2021). Sphingosine 1- Phosphate Lyase Insufficiency Syndrome (SPLIS); A Role in Multiple Endocrinopathies. Journal of the Endocrine Society. 5(Supplement_1). A662–A662. 1 indexed citations
13.
Smith, Christopher A., Avinaash Maharaj, Jordan E. Read, et al.. (2021). In Vitro Splicing Assay Proves the Pathogenicity of Intronic Variants in MRAP. Journal of the Endocrine Society. 5(Supplement_1). A85–A86. 1 indexed citations
14.
Maharaj, Avinaash, Federica Buonocore, Gabriel Ángel Martos‐Moreno, et al.. (2021). Missplicing due to a synonymous, T96= exonic substitution in the T-box transcription factor TBX19 resulting in isolated ACTH deficiency. Endocrinology Diabetes and Metabolism Case Reports. 2021. 4 indexed citations
15.
Williams, Jack, Anju Paudyal, Sherine Awad, et al.. (2020). Mylk3null C57BL/6N mice develop cardiomyopathy, whereasNntnull C57BL/6J mice do not. Life Science Alliance. 3(4). e201900593–e201900593. 25 indexed citations
16.
Maharaj, Avinaash, et al.. (2020). A Sphingosine-1-Phosphate Lyase Mutation Associated With Congenital Nephrotic Syndrome and Multiple Endocrinopathy. Frontiers in Pediatrics. 8. 151–151. 19 indexed citations
17.
Chatterjee, Sumana, Stephen Rose, Talat Mushtaq, et al.. (2020). GHR gene transcript heterogeneity may explain phenotypic variability in GHR pseudoexon (6Ψ) patients. Endocrine Connections. 9(3). 211–222. 4 indexed citations
18.
Maharaj, Avinaash, Jack Williams, Teisha Y. Bradshaw, et al.. (2020). Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction. The Journal of Steroid Biochemistry and Molecular Biology. 202. 105730–105730. 22 indexed citations
19.
Maharaj, Avinaash, et al.. (2019). Isolated glucocorticoid deficiency: Genetic causes and animal models. The Journal of Steroid Biochemistry and Molecular Biology. 189. 73–80. 21 indexed citations
20.
Prasad, Rathi, Avinaash Maharaj, Eirini Meimaridou, et al.. (2016). Mutations in SGPL1, encoding sphingosine-1-phosphate lyase, cause a novel form of primary adrenal insufficiency with steroid resistant nephrotic syndrome. Endocrine Abstracts. 1 indexed citations

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