Laura Audı́

2.1k total citations
64 papers, 1.4k citations indexed

About

Laura Audı́ is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Laura Audı́ has authored 64 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Endocrinology, Diabetes and Metabolism, 35 papers in Molecular Biology and 18 papers in Genetics. Recurrent topics in Laura Audı́'s work include Growth Hormone and Insulin-like Growth Factors (26 papers), Sexual Differentiation and Disorders (22 papers) and Birth, Development, and Health (9 papers). Laura Audı́ is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (26 papers), Sexual Differentiation and Disorders (22 papers) and Birth, Development, and Health (9 papers). Laura Audı́ collaborates with scholars based in Spain, United States and Germany. Laura Audı́'s co-authors include Antonio Carrascosa, Mónica Fernández‐Cancio, Pilar Andaluz, Diego Yeste, Cristina Estéban, Miquel Gussinyé, Anna Sanmartı́, Núria Torán, I. Salinas and Anna Lucas and has published in prestigious journals such as The Journal of Immunology, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Laura Audı́

62 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laura Audı́ Spain 22 627 537 424 175 171 64 1.4k
Zeynep Şıklar Türkiye 20 432 0.7× 404 0.8× 389 0.9× 163 0.9× 137 0.8× 140 1.4k
Mohd Shazli Draman United Kingdom 21 686 1.1× 305 0.6× 272 0.6× 112 0.6× 222 1.3× 36 1.4k
Zehra Aycan Türkiye 24 886 1.4× 687 1.3× 559 1.3× 223 1.3× 124 0.7× 220 2.2k
Zoran Gucev North Macedonia 19 805 1.3× 820 1.5× 417 1.0× 322 1.8× 172 1.0× 111 2.0k
Ece Böber Türkiye 23 580 0.9× 394 0.7× 467 1.1× 202 1.2× 131 0.8× 145 1.7k
Gi Baroncelli Italy 21 506 0.8× 351 0.7× 299 0.7× 149 0.9× 133 0.8× 53 1.2k
N Yordam Türkiye 20 523 0.8× 290 0.5× 232 0.5× 167 1.0× 151 0.9× 51 1.1k
Dorothy I. Shulman United States 20 1.0k 1.6× 472 0.9× 602 1.4× 232 1.3× 97 0.6× 69 1.9k
Giacomo Colussi Italy 22 244 0.4× 1.1k 2.0× 299 0.7× 155 0.9× 207 1.2× 79 2.4k
F. De Luca Italy 25 924 1.5× 463 0.9× 382 0.9× 259 1.5× 63 0.4× 76 2.0k

Countries citing papers authored by Laura Audı́

Since Specialization
Citations

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

Fields of papers citing papers by Laura Audı́

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Audı́

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Audı́. A scholar is included among the top collaborators of Laura Audı́ 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 Laura Audı́. Laura Audı́ 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.
Parween, Shaheena, Mónica Fernández‐Cancio, Sara Benito‐Sanz, et al.. (2020). Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR : Expanding the PORD Phenotype. The Journal of Clinical Endocrinology & Metabolism. 105(4). e1272–e1290. 13 indexed citations
2.
Sanders, Caroline, J. Camille Hall, Arianne B. Dessens, et al.. (2018). Involving Individuals with Disorders of Sex Development and Their Parents in Exploring New Models of Shared Learning: Proceedings from a DSDnet COST Action Workshop. Sexual Development. 12(5). 225–231. 13 indexed citations
3.
Fernández‐Cancio, Mónica, Emilio García García, Gil Guerra‐Júnior, et al.. (2017). Discordant Genotypic Sex and Phenotype Variations in Two Spanish Siblings with 17α-Hydroxylase/17,20-Lyase Deficiency Carrying the Most Prevalent Mutated<b><i> CYP17A1</i></b> Alleles of Brazilian Patients. Sexual Development. 11(2). 70–77. 8 indexed citations
4.
Kholy, Mohamed El, et al.. (2016). Nutritional rickets: vitamin D, calcium, and the genetic make-up. Pediatric Research. 81(2). 356–363. 5 indexed citations
5.
Audı́, Laura. (2014). Past Experiences of Adults with Disorders of Sex Development. Endocrine development. 27. 138–148. 5 indexed citations
6.
Renehan, Andrew G., Marcel Zwahlen, Andrew Whatmore, et al.. (2012). Growth Hormone Receptor Polymorphism and Growth Hormone Therapy Response in Children: A Bayesian Meta-Analysis. American Journal of Epidemiology. 175(9). 867–877. 30 indexed citations
7.
Liao, Lih‐Mei, et al.. (2012). Determinant factors of gender identity: A commentary. Journal of Pediatric Urology. 8(6). 597–601. 12 indexed citations
8.
Andrade, Anenisia C., Dionisios Chrysis, Laura Audı́, & Ola Nilsson. (2011). Methods to Study Cartilage and Bone Development. Endocrine development. 21. 52–66. 12 indexed citations
9.
França, Marcela M., Alexander A.L. Jorge, Kyriaki S. Alatzoglou, et al.. (2011). Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency. The Journal of Clinical Endocrinology & Metabolism. 96(9). E1457–E1460. 11 indexed citations
10.
Yeste, Diego, Joan Vendrell, María Clemente, et al.. (2010). Retinol-Binding Protein 4 Levels in Obese Children and Adolescents with Glucose Intolerance. Hormone Research in Paediatrics. 73(5). 335–340. 12 indexed citations
11.
Ventura, Paula Sol, Cristina Azcona, María Clemente, et al.. (2008). Monoallelic mutations in DUOXA2 are associated with mild permanent hypothyroidism and goiter. 1 indexed citations
12.
Fernández‐Cancio, Mónica, Laura Audı́, Antonio Carrascosa, et al.. (2008). Vitamin D and growth hormone regulate growth hormone/insulin-like growth factor (GH–IGF) axis gene expression in human fetal epiphyseal chondrocytes. Growth Hormone & IGF Research. 19(3). 232–237. 26 indexed citations
13.
Estéban, Cristina, Laura Audı́, Antonio Carrascosa, et al.. (2006). Human growth hormone (GH1) gene polymorphism map in a normal‐statured adult population. Clinical Endocrinology. 66(2). 258–268. 21 indexed citations
14.
15.
Carrascosa, Antonio, et al.. (2004). Fetal growth regulation and intrauterine growth retardation.. PubMed. 17 Suppl 3. 435–43. 13 indexed citations
16.
Fernández‐Cancio, Mónica, Manuel Nistal, Ricardo Gracía, et al.. (2004). Compound Heterozygous Mutations in the SRD5A2 Gene Exon 4 in a Male Pseudohermaphrodite Patient of Chinese Origin. Journal of Andrology. 25(3). 412–416. 28 indexed citations
17.
Audı́, Laura, et al.. (2001). Low sensitivity of IGF-1, IGFBP-3 and urinary GH in the diagnosis of growth hormone insufficiency in slowly-growing short-statured boys. Medicina Clínica. 116(1). 6–11. 4 indexed citations
18.
Burgos, R., Rafael Simó, Laura Audı́, et al.. (1997). Vitreous levels of vascular endothelial growth factor are not influenced by its serum concentrations in diabetic retinopathy. Diabetologia. 40(9). 1107–1109. 86 indexed citations
19.
Larriba, Sara, et al.. (1995). Androgen binding protein is tissue-specifically expressed and biologically active in transgenic mice. The Journal of Steroid Biochemistry and Molecular Biology. 53(1-6). 573–578. 23 indexed citations
20.
Romero, R., et al.. (1992). Comparative effects of captopril versus nifedipine on proteinuria and renal function of type 2 diabetic patients. Diabetes Research and Clinical Practice. 17(3). 191–198. 27 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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