Paula Scaglia

701 total citations
27 papers, 471 citations indexed

About

Paula Scaglia is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics and Molecular Biology. According to data from OpenAlex, Paula Scaglia has authored 27 papers receiving a total of 471 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Endocrinology, Diabetes and Metabolism, 17 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in Paula Scaglia's work include Growth Hormone and Insulin-like Growth Factors (19 papers), Genetic Syndromes and Imprinting (10 papers) and Metabolism and Genetic Disorders (5 papers). Paula Scaglia is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (19 papers), Genetic Syndromes and Imprinting (10 papers) and Metabolism and Genetic Disorders (5 papers). Paula Scaglia collaborates with scholars based in Argentina, United States and Denmark. Paula Scaglia's co-authors include Horacio M. Domené, Héctor Jasper, María Gabriela Ropelato, Alicia S. Martínez, Juan J. Heinrich, Sonia V. Bengolea, P. Pennisi, Marı́a Gabriela Ballerini, Mariana Gutiérrez and Jan Frystyk and has published in prestigious journals such as New England Journal of Medicine, The Journal of Clinical Endocrinology & Metabolism and Human Molecular Genetics.

In The Last Decade

Paula Scaglia

26 papers receiving 461 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Paula Scaglia Argentina	10	378	236	162	71	43	27	471
Sonia V. Bengolea Argentina	11	352 0.9×	181 0.8×	180 1.1×	71 1.0×	70 1.6×	17	462
Jérôme Dulon France	14	271 0.7×	214 0.9×	385 2.4×	16 0.2×	71 1.7×	28	737
Ricardo Gracía Spain	11	183 0.5×	241 1.0×	277 1.7×	14 0.2×	37 0.9×	17	461
Wu Xiang Liao Singapore	11	66 0.2×	204 0.9×	257 1.6×	30 0.4×	12 0.3×	15	606
Maria Maniati-Christidi Greece	12	314 0.8×	131 0.6×	267 1.6×	24 0.3×	54 1.3×	16	421
David R. Clemmons United States	7	314 0.8×	61 0.3×	168 1.0×	58 0.8×	16 0.4×	8	379
Tinka Hovnik Slovenia	10	81 0.2×	91 0.4×	132 0.8×	14 0.2×	47 1.1×	25	290
Haruhiko Isotani Japan	9	103 0.3×	67 0.3×	183 1.1×	22 0.3×	47 1.1×	24	363
Ashwini Mallappa United States	18	653 1.7×	186 0.8×	690 4.3×	14 0.2×	121 2.8×	45	938
KUMIKO ASAKAWA Japan	13	431 1.1×	113 0.5×	181 1.1×	35 0.5×	11 0.3×	29	527

Countries citing papers authored by Paula Scaglia

Since Specialization

Citations

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

Fields of papers citing papers by Paula Scaglia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paula Scaglia

This figure shows the co-authorship network connecting the top 25 collaborators of Paula Scaglia. A scholar is included among the top collaborators of Paula Scaglia 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 Paula Scaglia. Paula Scaglia 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

Jørgensen, Flemming Steen, Roxana Marino, Natalia Pérez Garrido, et al.. (2025). A Novel POR G88S Mutation Causes Severe PORD and Establishes a Critical Pharmacogenomic Risk Profile. The Journal of Clinical Endocrinology & Metabolism. 1 indexed citations

Keselman, Ana, et al.. (2024). Case report: Novel SIN3A loss-of-function variant as causative for hypogonadotropic hypogonadism in Witteveen–Kolk syndrome. Frontiers in Genetics. 15. 1354715–1354715.

Karabatas, Liliana, Tomás Gómez, Paula Scaglia, et al.. (2023). An in vivo functional assay to characterize human STAT5B genetic variants during zebrafish development. Human Molecular Genetics. 32(15). 2473–2484. 1 indexed citations

Grinspon, Romina P., et al.. (2023). Identification of a Novel Variant in Myelin Regulatory Growth Factor by Next-Generation Sequencing Led to the Detection of a Clinically Inapparent Congenital Heart Defect in a Patient with a 46,XY Disorder of Sex Development. Journal of Personalized Medicine. 13(7). 1158–1158. 2 indexed citations

Brunello, F., Gabriela Sansó, Paula Scaglia, et al.. (2022). Delayed Puberty Due to a WDR11 Truncation at Its N-Terminal Domain Leading to a Mild Form of Ciliopathy Presenting With Dissociated Central Hypogonadism: Case Report. Frontiers in Pediatrics. 10. 887658–887658. 1 indexed citations

Karabatas, Liliana, Paula Scaglia, Mariana Gutiérrez, et al.. (2020). Expression of acid-labile subunit (ALS) in developing and adult zebrafish and its role in dorso-ventral patterning during development. General and Comparative Endocrinology. 299. 113591–113591. 7 indexed citations

Borges, Maria de Fátima, et al.. (2019). A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING. Revista Paulista de Pediatria. 37(4). 520–524. 1 indexed citations

Braslavsky, Débora, Paula Scaglia, Ana Keselman, et al.. (2019). p.R209H GH1 variant challenges short stature assessment. Growth Hormone & IGF Research. 50. 23–26. 6 indexed citations

Ramírez, Laura, Paula Scaglia, Ana Keselman, et al.. (2019). A novel heterozygous STAT5B variant in a patient with short stature and partial growth hormone insensitivity (GHI). Growth Hormone & IGF Research. 50. 61–70. 8 indexed citations

10.

Gutiérrez, Mariana, Liliana Karabatas, Paula Scaglia, et al.. (2016). Assessment of pathogenicity of natural IGFALS gene variants by in silico bioinformatics tools and in vitro functional studies. Molecular and Cellular Endocrinology. 429. 19–28. 9 indexed citations

11.

Scaglia, Paula, Andrea Sala, Ignacio Bergadá, et al.. (2015). Recurrent IGFALS Gene Mutations p.E35Gfs*17 and p.(L409F; A475V): Hot Spot or Founder Effect?. 1 indexed citations

12.

Scaglia, Paula, Ana Keselman, Liliana Karabatas, et al.. (2014). ALS Deficiency due to a Novel and Two Already Described IGFALS Gene Mutations in an Unusual Non Consanguineous Family: Two Compound Heterozygous (Father and Son) and Two Heterozygous Carriers (Brother and Mother). 1 indexed citations

13.

Domené, Horacio M., Paula Scaglia, Alicia S. Martínez, et al.. (2013). Heterozygous <b><i>IGFALS</i></b> Gene Variants in Idiopathic Short Stature and Normal Children: Impact on Height and the IGF System. Hormone Research in Paediatrics. 80(6). 413–423. 36 indexed citations

14.

Ballerini, Marı́a Gabriela, Horacio M. Domené, Paula Scaglia, et al.. (2013). Association of serum components of the GH-IGFs-IGFBPs system with GHR-exon 3 polymorphism in normal and idiopathic short stature children. Growth Hormone & IGF Research. 23(6). 229–236. 9 indexed citations

15.

Scaglia, Paula, Alicia S. Martínez, Eva Feigerlová, et al.. (2012). A Novel Missense Mutation in the SH2 Domain of theSTAT5BGene Results in a Transcriptionally Inactive STAT5b Associated with Severe IGF-I Deficiency, Immune Dysfunction, and Lack of Pulmonary Disease. The Journal of Clinical Endocrinology & Metabolism. 97(5). E830–E839. 34 indexed citations

16.

Scaglia, Paula, et al.. (2012). Severe congenital non-autoimmune hyperthyroidism associated to a mutation in the extracellular domain of thyrotropin receptor gene. Arquivos Brasileiros de Endocrinologia & Metabologia. 56(8). 513–518. 3 indexed citations

17.

Keselman, Ana, Paula Scaglia, Marı́a Gabriela Ballerini, et al.. (2012). Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus. Arquivos Brasileiros de Endocrinologia & Metabologia. 56(8). 558–563. 4 indexed citations

18.

Ballerini, Marı́a Gabriela, et al.. (2010). 17α-Hydroxyprogesterone and Cortisol Serum Levels in Neonates and Young Children: Influence of Age, Gestational Age, Gender and Methodological Procedures. Journal of Pediatric Endocrinology and Metabolism. 23(1-2). 121–32. 15 indexed citations

19.

Domené, Horacio M., Laura Gruñeiro‐Papendieck, Ana Chiesa, et al.. (2003). The C105fs114X Is the Prevalent Thyrotropin Beta-Subunit Gene Mutation in Argentinean Patients with Congenital Central Hypothyroidism. Hormone Research in Paediatrics. 61(1). 41–46. 26 indexed citations

20.

Puyó, Ana M., Amanda Pellegrino de Iraldi, Liliana Albornoz, et al.. (1998). Atrial natriuretic factor in two kidney--two clip renovascular hypertension in the rat.. PubMed. 58(2). 165–70. 7 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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