Osnat Admoni

811 total citations
22 papers, 555 citations indexed

About

Osnat Admoni is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Osnat Admoni has authored 22 papers receiving a total of 555 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Endocrinology, Diabetes and Metabolism and 7 papers in Genetics. Recurrent topics in Osnat Admoni's work include Thyroid Disorders and Treatments (6 papers), Growth Hormone and Insulin-like Growth Factors (5 papers) and Sexual Differentiation and Disorders (4 papers). Osnat Admoni is often cited by papers focused on Thyroid Disorders and Treatments (6 papers), Growth Hormone and Insulin-like Growth Factors (5 papers) and Sexual Differentiation and Disorders (4 papers). Osnat Admoni collaborates with scholars based in Israel, United States and France. Osnat Admoni's co-authors include Yardena Tenenbaum‐Rakover, Nicolás de Roux, André Iovane, Yardena Rakover, Michal Gur, Carina Levin, Idit Lavi, Daniel Fink, Samuel Refetoff and Ariel Koren and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and Diabetes Care.

In The Last Decade

Osnat Admoni

20 papers receiving 527 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Osnat Admoni Israel 14 245 230 143 140 57 22 555
Michaela Kosmann Germany 8 247 1.0× 108 0.5× 155 1.1× 140 1.0× 10 0.2× 9 703
Canquan Zhou China 16 133 0.5× 35 0.2× 422 3.0× 65 0.5× 7 0.1× 44 720
Andrea Fuhrer Switzerland 6 124 0.5× 92 0.4× 6 0.0× 91 0.7× 36 0.6× 11 433
Brigitte Robert France 15 145 0.6× 61 0.3× 90 0.6× 19 0.1× 19 0.3× 25 499
Frances Collins United Kingdom 16 150 0.6× 252 1.1× 338 2.4× 52 0.4× 14 0.2× 26 743
Norihiro Koyama Japan 10 84 0.3× 67 0.3× 202 1.4× 191 1.4× 29 0.5× 13 504
V. Pérez‐Infante United States 8 158 0.6× 84 0.4× 318 2.2× 144 1.0× 14 0.2× 9 450
Márton Doleschall Hungary 12 140 0.6× 81 0.4× 12 0.1× 211 1.5× 7 0.1× 25 503
Violeta A. Chiauzzi Argentina 12 92 0.4× 106 0.5× 202 1.4× 118 0.8× 4 0.1× 19 427
Massimiliano Cocca Italy 9 91 0.4× 92 0.4× 64 0.4× 19 0.1× 78 1.4× 20 352

Countries citing papers authored by Osnat Admoni

Since Specialization
Citations

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

Fields of papers citing papers by Osnat Admoni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Osnat Admoni

This figure shows the co-authorship network connecting the top 25 collaborators of Osnat Admoni. A scholar is included among the top collaborators of Osnat Admoni 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 Osnat Admoni. Osnat Admoni 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.
Almashanu, Shlomo, et al.. (2024). The natural course of newborns with transient congenital hypothyroidism. Endocrine Connections. 13(12).
2.
Levy‐Shraga, Yael, Osnat Admoni, Kineret Mazor‐Aronovitch, et al.. (2023). Clinical and Molecular Characteristics and Long-term Follow-up of Children With Pseudohypoparathyroidism Type IA. The Journal of Clinical Endocrinology & Metabolism. 109(2). 424–438.
3.
Khayat, Morad, et al.. (2021). Long-Term Outcome of Patients with TPO Mutations. Journal of Clinical Medicine. 10(17). 3898–3898. 2 indexed citations
4.
Tenenbaum‐Rakover, Yardena, Osnat Admoni, Charles Sultan, et al.. (2021). The evolving role of whole-exome sequencing in the management of disorders of sex development. Endocrine Connections. 10(6). 620–629. 13 indexed citations
5.
Admoni, Osnat, et al.. (2020). Long-Term Follow-Up and Outcomes of Autoimmune Thyroiditis in Childhood. Frontiers in Endocrinology. 11. 309–309. 13 indexed citations
6.
Admoni, Osnat, et al.. (2016). A Novel Mutation (S54C) of the <b><i>PAX8</i></b> Gene in a Family with Congenital Hypothyroidism and a High Proportion of Affected Individuals. Hormone Research in Paediatrics. 86(2). 137–142. 11 indexed citations
7.
Garin, Intza, Francesca Marta Elli, Agnès Linglart, et al.. (2015). Novel Microdeletions Affecting the GNAS Locus in Pseudohypoparathyroidism: Characterization of the Underlying Mechanisms. The Journal of Clinical Endocrinology & Metabolism. 100(4). E681–E687. 32 indexed citations
8.
Tenenbaum‐Rakover, Yardena, Shlomo Almashanu, Osnat Admoni, et al.. (2015). Long-Term Outcome of Loss-of-Function Mutations in Thyrotropin Receptor Gene. Thyroid. 25(3). 292–299. 26 indexed citations
9.
Admoni, Osnat, et al.. (2012). Ghrelin and growth hormone secretagogue receptor (GHSR) genes are not commonly involved in growth or weight abnormalities in an Israeli pediatric population. Journal of Pediatric Endocrinology and Metabolism. 25(5-6). 537–40. 2 indexed citations
10.
Tenenbaum‐Rakover, Yardena, et al.. (2010). Can Auxology, IGF-I and IGFBP-3 Measurements Followed by MRI and Genetic Tests Replace GH Stimulation Tests in the Diagnosis of GH Deficiency in Children?. Journal of Pediatric Endocrinology and Metabolism. 23(4). 387–94. 5 indexed citations
11.
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13.
Tenenbaum‐Rakover, Yardena, et al.. (2006). Neuroendocrine Phenotype Analysis in Five Patients with Isolated Hypogonadotropic Hypogonadism due to a L102P Inactivating Mutation of GPR54. The Journal of Clinical Endocrinology & Metabolism. 92(3). 1137–1144. 135 indexed citations
14.
Admoni, Osnat, et al.. (2006). Hyperandrogenism in carriers of CYP21 mutations: the role of genotype. Clinical Endocrinology. 64(6). 645–651. 40 indexed citations
15.
Sagi, Liora, Nehama Zuckerman‐Levin, Aneta Gawlik, et al.. (2006). Clinical Significance of the Parental Origin of the X Chromosome in Turner Syndrome. The Journal of Clinical Endocrinology & Metabolism. 92(3). 846–852. 68 indexed citations
16.
Spiegel, Ronen, et al.. (2005). Secondary Diabetes Mellitus: Late Complication of Glycogen Storage Disease Type 1b. Journal of Pediatric Endocrinology and Metabolism. 18(6). 617–9. 17 indexed citations
17.
Hanukoglu, Aaron, Ilan Dalal, Osnat Admoni, et al.. (2003). Extrapancreatic Autoimmune Manifestations in Type 1 Diabetes Patients and Their First-Degree Relatives. Diabetes Care. 26(4). 1235–1240. 67 indexed citations
18.
Pomponio, Robert J., Thomas Reynolds, Hanna Mandel, et al.. (1997). Profound Biotinidase Deficiency Caused by a Point Mutation That Creates a Downstream Cryptic 3' Splice Acceptor Site Within an Exon of the Human Biotinidase Gene. Human Molecular Genetics. 6(5). 739–745. 21 indexed citations
19.
Bader, David, Orna Blondheim, Richard A. Jonas, et al.. (1996). Decreased ferritin levels, despite iron supplementation, during erythropoietin therapy in anaemia of prematurity. Acta Paediatrica. 85(4). 496–501. 25 indexed citations
20.
Admoni, Osnat, et al.. (1995). Epidemiologilogical, Clinical and Microbiological Features of Shigellosis among Hospitalized Children in Northern Israel. Scandinavian Journal of Infectious Diseases. 27(2). 139–144. 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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