Saba Samad Memon

481 total citations
66 papers, 270 citations indexed

About

Saba Samad Memon is a scholar working on Endocrinology, Diabetes and Metabolism, Surgery and Molecular Biology. According to data from OpenAlex, Saba Samad Memon has authored 66 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Endocrinology, Diabetes and Metabolism, 29 papers in Surgery and 15 papers in Molecular Biology. Recurrent topics in Saba Samad Memon's work include Adrenal and Paraganglionic Tumors (20 papers), Pituitary Gland Disorders and Treatments (19 papers) and Parathyroid Disorders and Treatments (12 papers). Saba Samad Memon is often cited by papers focused on Adrenal and Paraganglionic Tumors (20 papers), Pituitary Gland Disorders and Treatments (19 papers) and Parathyroid Disorders and Treatments (12 papers). Saba Samad Memon collaborates with scholars based in India, United Kingdom and United States. Saba Samad Memon's co-authors include Tushar Bandgar, Anurag Lila, Virendra Patil, Nalini S. Shah, Vijaya Sarathi, Swati Jadhav, Gaurav Malhotra, Manjunath Goroshi, Ambarish Kunwar and Priyanka Verma and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Clinical Endocrinology.

In The Last Decade

Saba Samad Memon

52 papers receiving 268 citations

Peers

Saba Samad Memon

SURGE

EDM

EPIDE

Crystal Kamilaris United States

Giancarlo Candela Italy

Shun‐Yu Chi Taiwan

Piotr Glinicki Poland

Tarek Abdel‐Aziz United Kingdom

Benjamin Chevalier France

Chiara Offi Italy

Neslihan Çuhacı Türkiye

H. P. H. Neumann Germany

Nami Takada Japan

Crystal Kamilaris United States

Saba Samad Memon

133 ×1.0

SURGE

126 ×1.0

EDM

47 ×1.0

103 ×2.3

EPIDE

35 ×1.0

Citations per year, relative to Saba Samad Memon Saba Samad Memon (= 1×) peers Crystal Kamilaris

Countries citing papers authored by Saba Samad Memon

Since Specialization

Citations

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

Fields of papers citing papers by Saba Samad Memon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Saba Samad Memon. 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 Saba Samad Memon. The network helps show where Saba Samad Memon may publish in the future.

Co-authorship network of co-authors of Saba Samad Memon

This figure shows the co-authorship network connecting the top 25 collaborators of Saba Samad Memon. A scholar is included among the top collaborators of Saba Samad Memon 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 Saba Samad Memon. Saba Samad Memon 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

Lila, Anurag, Saba Samad Memon, Virendra Patil, et al.. (2025). Bilateral macronodular adrenocortical disease: a single centre experience. Endocrine Connections. 14(3).

Lila, Anurag, et al.. (2025). Insights in non-CAH pediatric primary adrenal insufficiency: a single-center experience from India. Journal of Pediatric Endocrinology and Metabolism. 38(4). 383–390. 2 indexed citations

Rao, Archana, Anurag Lila, Vijaya Sarathi, et al.. (2025). Clinical and radiological insights into secondary hypophysitis: A single-center experience with a focus on tuberculosis. Endocrine. 90(1). 266–275. 1 indexed citations

Memon, Saba Samad, Vijaya Sarathi, Anurag Lila, et al.. (2025). Pediatric and adolescent von Hippel-Lindau disease: tumor profiles, genotype-phenotype correlation and comparison with adults. Journal of Endocrinological Investigation. 48(7). 1635–1647.

Memon, Saba Samad, et al.. (2025). Adolescent primary hyperparathyroidism. Best Practice & Research Clinical Endocrinology & Metabolism. 39(2). 101975–101975.

Memon, Saba Samad, Anurag Lila, Vijaya Sarathi, et al.. (2024). Diagnostic performance of various imaging modalities in localizing ectopic ACTH syndrome: A systematic review. Annales d Endocrinologie. 85(6). 596–603. 1 indexed citations

Memon, Saba Samad, Anurag Lila, Vijaya Sarathi, et al.. (2024). Pituitary apoplexy: a comprehensive analysis of 93 cases across functioning and non-functioning pituitary adenomas from a single-center. Pituitary. 27(5). 705–713. 1 indexed citations

Memon, Saba Samad, et al.. (2024). Efficacy and safety of burosumab compared with conventional therapy in patients with X-linked hypophosphatemia: A systematic review. Archives of Endocrinology and Metabolism. 68. e230242–e230242. 3 indexed citations

Memon, Saba Samad, Vijaya Sarathi, Anurag Lila, et al.. (2024). Pituitary apoplexy in cushing’s disease: a single center study and systematic literature review. Pituitary. 27(4). 335–344. 2 indexed citations

10.

Memon, Saba Samad, Manjunath Goroshi, Virendra C. Patil, et al.. (2024). The polar vessel sign: insights from CT imaging analysis in Asian Indian primary hyperparathyroidism. Endocrine. 87(2). 800–809. 2 indexed citations

11.

Sarathi, Vijaya, Anurag Lila, Saba Samad Memon, et al.. (2024). Steroidogenic acute regulatory protein (STAR) deficiency: Our experience and systematic review for phenotype–genotype correlation. Clinical Endocrinology. 100(5). 431–440. 7 indexed citations

12.

Patil, Virendra, Vijaya Sarathi, Nilendu Purandare, et al.. (2023). Dual-phase computed tomography for localization of parathyroid lesions in children and adolescents with primary hyperparathyroidism. Annales d Endocrinologie. 84(4). 446–453. 4 indexed citations

13.

Memon, Saba Samad, Vijaya Sarathi, Anurag Lila, et al.. (2023). 46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters. Annales d Endocrinologie. 85(1). 48–55. 1 indexed citations

14.

Memon, Saba Samad, Anurag Lila, Mustafa Khan, et al.. (2023). Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review. Calcified Tissue International. 114(2). 137–146. 1 indexed citations

15.

Jamale, Tukaram, et al.. (2023). Acquired disorders of phosphaturia: Beyond tumor-induced osteomalacia. Best Practice & Research Clinical Endocrinology & Metabolism. 38(2). 101839–101839.

16.

Memon, Saba Samad, Anurag Lila, Vijaya Sarathi, et al.. (2022). Genotype–Phenotype Correlations in Asian Indian Children and Adolescents with Primary Hyperparathyroidism. Calcified Tissue International. 111(3). 229–241. 5 indexed citations

17.

Patil, Virendra, Anurag Lila, Nalini S. Shah, et al.. (2022). Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review. Pituitary. 25(3). 444–453. 4 indexed citations

18.

Memon, Saba Samad, Anurag Lila, Manjunath Goroshi, et al.. (2021). Prevalence of primary aldosteronism in type 2 diabetes mellitus and hypertension: A prospective study from Western India. Clinical Endocrinology. 96(4). 539–548. 10 indexed citations

19.

Patil, Virendra, Anurag Lila, Nalini S. Shah, et al.. (2021). <b><i>GNRH1</i></b> Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review. Neuroendocrinology. 112(8). 723–732. 3 indexed citations

20.

Lila, Anurag, Vijaya Sarathi, Saba Samad Memon, et al.. (2021). Clinical, Hormonal, Genetic, and Molecular Characteristics in Androgen Insensitivity Syndrome in an Asian Indian Cohort from a Single Centre in Western India. Sexual Development. 15(4). 253–261. 3 indexed citations

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