Andreína Cattani

509 total citations
19 papers, 335 citations indexed

About

Andreína Cattani is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Andreína Cattani has authored 19 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Andreína Cattani's work include Sexual Differentiation and Disorders (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Hormonal and reproductive studies (3 papers). Andreína Cattani is often cited by papers focused on Sexual Differentiation and Disorders (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Hormonal and reproductive studies (3 papers). Andreína Cattani collaborates with scholars based in Chile, United States and United Kingdom. Andreína Cattani's co-authors include Cristián García, Helena Poggi, Oscar M. Navarro, Hernán G. García, Alan Daneman, Alejandro Martínez‐Aguayo, Marcela Lagos, L A Valdivia, A Foradori and Carlos Fardella and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of Bone and Mineral Research and The Journal of Pediatrics.

In The Last Decade

Andreína Cattani

19 papers receiving 323 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreína Cattani Chile 8 163 121 112 106 61 19 335
José María Cantú Mexico 10 199 1.2× 129 1.1× 62 0.6× 87 0.8× 7 0.1× 17 377
Stanisław Zajączek Poland 10 198 1.2× 129 1.1× 28 0.3× 29 0.3× 26 0.4× 36 354
Jo A. Kelly United Kingdom 8 185 1.1× 114 0.9× 49 0.4× 86 0.8× 5 0.1× 9 323
H. U. Tietze Germany 10 318 2.0× 144 1.2× 56 0.5× 88 0.8× 5 0.1× 21 475
Hagit Schayek Israel 13 227 1.4× 110 0.9× 67 0.6× 62 0.6× 6 0.1× 23 363
Josefina Muñoz Spain 11 175 1.1× 38 0.3× 87 0.8× 18 0.2× 19 0.3× 11 453
Eva Maria Cutiongco Philippines 7 168 1.0× 180 1.5× 15 0.1× 28 0.3× 5 0.1× 7 327
S M Farrow United Kingdom 11 91 0.6× 77 0.6× 165 1.5× 45 0.4× 4 0.1× 17 285
Mary H. Waziri United States 8 216 1.3× 182 1.5× 24 0.2× 10 0.1× 9 0.1× 10 341
Liangfeng Shi China 10 89 0.5× 70 0.6× 36 0.3× 155 1.5× 11 0.2× 16 340

Countries citing papers authored by Andreína Cattani

Since Specialization
Citations

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

Fields of papers citing papers by Andreína Cattani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreína Cattani

This figure shows the co-authorship network connecting the top 25 collaborators of Andreína Cattani. A scholar is included among the top collaborators of Andreína Cattani 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 Andreína Cattani. Andreína Cattani is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Cerda, Jaime, et al.. (2022). ¿Cuál es el mejor método de estimación de talla final en pacientes con pubertad precoz?. Andes pediatrica. 93(2). 214–221. 1 indexed citations
2.
Poggi, Helena, Marcela Lagos, Cecília Mellado, et al.. (2015). A Deletion of More than 800 kb Is the Most Recurrent Mutation in Chilean Patients with <b><i>SHOX</i></b> Gene Defects. Hormone Research in Paediatrics. 84(4). 254–257. 7 indexed citations
3.
Borzutzky, Arturo, Mirentxu Iruretagoyena, Alejandro Martínez‐Aguayo, et al.. (2014). A126: Clusters of Autoimmune Diseases in Children and the Role of PTPN22 C1858T Gene Polymorphism in Pediatric Polyautoimmunity. Arthritis & Rheumatology. 66(S3). 1 indexed citations
4.
Martínez‐Aguayo, Alejandro, et al.. (2013). A novel insertion in the FOXL2 gene in a Chilean patient with blepharophimosis ptosis epicanthus inversus syndrome type I. Journal of Pediatric Endocrinology and Metabolism. 27(1-2). 181–4. 2 indexed citations
5.
Cattani, Andreína, et al.. (2010). A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type Ia and normal serum calcium and phosphate levels. Arquivos Brasileiros de Endocrinologia & Metabologia. 54(8). 728–731. 4 indexed citations
6.
González, Ángel, Erick Riquelme, Cristián A. Carvajal, et al.. (2008). A Novel Adrenocorticotropin Receptor Mutation Alters Its Structure and Function, Causing Familial Glucocorticoid Deficiency. The Journal of Clinical Endocrinology & Metabolism. 93(8). 3097–3105. 10 indexed citations
7.
Carvajal, Cristián A., et al.. (2008). Marcadores de inflamación endotelial subclínica en una familia con hiperaldosteronismo familiar tipo I por mutación de novo. Revista médica de Chile. 136(9). 1134–40. 5 indexed citations
8.
Martínez‐Aguayo, Alejandro, et al.. (2007). Testicular Adrenal Rest Tumors and Leydig and Sertoli Cell Function in Boys with Classical Congenital Adrenal Hyperplasia. The Journal of Clinical Endocrinology & Metabolism. 92(12). 4583–4589. 77 indexed citations
9.
Malloy, Peter J., et al.. (2004). A Unique Insertion/Substitution in Helix H1 of the Vitamin D Receptor Ligand Binding Domain in a Patient With Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets. Journal of Bone and Mineral Research. 19(6). 1018–1024. 27 indexed citations
10.
Mancilla, Edna E., Helena Poggi, Gabriela M. Repetto, et al.. (2003). Y Chromosome Sequences in Turner's Syndrome: Association with Virilization and Gonadoblastoma. Journal of Pediatric Endocrinology and Metabolism. 16(8). 1157–63. 26 indexed citations
11.
Cattani, Andreína, et al.. (2002). Bone metabolism in children with epidermolysis bullosa. The Journal of Pediatrics. 140(4). 467–469. 28 indexed citations
12.
Fardella, Carlos, et al.. (2000). Mutations in the CYP21B gene in a Chilean population with simple virilizing congenital adrenal hyperplasia. Journal of Endocrinological Investigation. 23(6). 412–416. 7 indexed citations
13.
García, Cristián, et al.. (2000). Breast US in Children and Adolescents. Radiographics. 20(6). 1605–1612. 98 indexed citations
14.
15.
Fardella, Carlos, et al.. (1998). Salt-Wasting Congenital Adrenal Hyperplasia: Detection of Mutations in CYP21B Gene in a Chilean Population1. The Journal of Clinical Endocrinology & Metabolism. 83(9). 3357–3360. 34 indexed citations
16.
Fardella, Carlos, et al.. (1997). [Molecular diagnosis of salt wasting congenital adrenal hyperplasia, caused by deficit of 21-hydroxylase, in the Chilean population].. PubMed. 125(9). 987–92. 1 indexed citations
17.
Youlton, R, et al.. (1992). 22 RESPONSE TO THE GRF TEST IN PATIENTS WITH GROWTH HORMONE DEFICTT. Pediatric Research. 32(2). 252–252. 1 indexed citations
18.
Youlton, R, et al.. (1990). PREMATURE TELARCHE (PT): STUDY OF ITS FRECUENCY AND ETIOLOGICAL FACTORS. PRELIMINARY REPORT. Pediatric Research. 28(4). 421–421. 1 indexed citations
19.
Arteaga, Eugenio, et al.. (1989). The paradoxical response of growth hormone (GH) to thyrotropin-releasing hormone (TRH) in constitutionally tall children involves a cholinergic pathway. Journal of Endocrinological Investigation. 12(8). 543–548. 1 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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