Débora Braslavsky

1.1k total citations
25 papers, 454 citations indexed

About

Débora Braslavsky is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Surgery. According to data from OpenAlex, Débora Braslavsky has authored 25 papers receiving a total of 454 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Endocrinology, Diabetes and Metabolism, 11 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in Débora Braslavsky's work include Growth Hormone and Insulin-like Growth Factors (13 papers), Sexual Differentiation and Disorders (4 papers) and Pituitary Gland Disorders and Treatments (4 papers). Débora Braslavsky is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (13 papers), Sexual Differentiation and Disorders (4 papers) and Pituitary Gland Disorders and Treatments (4 papers). Débora Braslavsky collaborates with scholars based in Argentina, United States and United Kingdom. Débora Braslavsky's co-authors include Ignacio Bergadá, Ana Keselman, Marı́a Gabriela Ballerini, María Gabriela Ropelato, John C. Achermann, Stanley F. Nelson, Esteban C. Dell’Angelica, Abhik K. Banerjee, Rahul Parnaik and Hane Lee and has published in prestigious journals such as Nature Genetics, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Débora Braslavsky

25 papers receiving 450 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Débora Braslavsky 239 187 168 86 73 25 454
Laurence Michel‐Calemard 325 1.4× 295 1.6× 49 0.3× 53 0.6× 57 0.8× 22 438
Roxana Marino 388 1.6× 377 2.0× 298 1.8× 112 1.3× 41 0.6× 39 722
Mounia Tannour‐Louet 328 1.4× 253 1.4× 67 0.4× 87 1.0× 108 1.5× 13 569
Spyridon Gerou 147 0.6× 43 0.2× 57 0.3× 31 0.4× 68 0.9× 31 393
Ioanna Bouba 147 0.6× 202 1.1× 83 0.5× 209 2.4× 35 0.5× 31 561
Carolina Rosselot 253 1.1× 120 0.6× 64 0.4× 31 0.4× 168 2.3× 18 425
Monique A. de Vroede 482 2.0× 257 1.4× 441 2.6× 42 0.5× 105 1.4× 12 687
Ron G. Rosenfeld 243 1.0× 227 1.2× 326 1.9× 29 0.3× 38 0.5× 8 522
Abdulsalam Abu‐Libdeh 187 0.8× 115 0.6× 75 0.4× 24 0.3× 66 0.9× 25 338
Zehra Yavaş Abalı 147 0.6× 82 0.4× 100 0.6× 33 0.4× 26 0.4× 48 243

Countries citing papers authored by Débora Braslavsky

Since Specialization
Citations

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

Fields of papers citing papers by Débora Braslavsky

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Débora Braslavsky

This figure shows the co-authorship network connecting the top 25 collaborators of Débora Braslavsky. A scholar is included among the top collaborators of Débora Braslavsky 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 Débora Braslavsky. Débora Braslavsky 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.
Ballerini, Marı́a Gabriela, María Eugenia Rodríguez, Laura M. De Castro, et al.. (2024). Nocturnal Salivary Cortisol Is an Accurate Non-Invasive Test to Assess Endogenous Hypercortisolism in Children with Obesity and a Clinical Phenotype Suspicious for Cushing’s Syndrome. Hormone Research in Paediatrics. 98(6). 719–727. 2 indexed citations
2.
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
3.
Rey, Rodolfo A., Ignacio Bergadá, Marı́a Gabriela Ballerini, et al.. (2023). Diagnosing and treating anterior pituitary hormone deficiency in pediatric patients. Reviews in Endocrine and Metabolic Disorders. 25(3). 555–573. 4 indexed citations
4.
Mercogliano, María F., Amanda H. Mortensen, Débora Braslavsky, et al.. (2021). Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders. The Journal of Clinical Endocrinology & Metabolism. 106(7). 1956–1976. 13 indexed citations
5.
Grinspon, Romina P., Daniel Yankelevich, María Gabriela Ropelato, et al.. (2021). Development and Validation of a Prediction Rule for Growth Hormone Deficiency Without Need for Pharmacological Stimulation Tests in Children With Risk Factors. Frontiers in Endocrinology. 11. 624684–624684. 5 indexed citations
6.
Maharaj, Avinaash, Jack Williams, Teisha Y. Bradshaw, et al.. (2020). Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction. The Journal of Steroid Biochemistry and Molecular Biology. 202. 105730–105730. 22 indexed citations
7.
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
8.
Pérez‐Millán, María Inés, Alexandre Z. Daly, Juan P. Bustamante, et al.. (2018). Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarism. Molecular Genetics & Genomic Medicine. 6(4). 514–525. 18 indexed citations
9.
Braslavsky, Débora, Laura Prieto, Ana Keselman, et al.. (2017). Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection. Hormone Research in Paediatrics. 88(3-4). 274–280. 13 indexed citations
10.
Bessa, Danielle S., Delanie B. Macedo, Vinícius Nahime Brito, et al.. (2016). High Frequency of <b><i>MKRN3</i></b> Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic. Neuroendocrinology. 105(1). 17–25. 56 indexed citations
11.
Prasad, Rathi, Avinaash Maharaj, Eirini Meimaridou, et al.. (2016). Mutations in SGPL1, encoding sphingosine-1-phosphate lyase, cause a novel form of primary adrenal insufficiency with steroid resistant nephrotic syndrome. Endocrine Abstracts. 1 indexed citations
12.
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
13.
Braslavsky, Débora, Romina P. Grinspon, Marı́a Gabriela Ballerini, et al.. (2015). Hypogonadotropic Hypogonadism in Infants with Congenital Hypopituitarism: A Challenge to Diagnose at an Early Stage. Hormone Research in Paediatrics. 84(5). 289–297. 36 indexed citations
14.
Jullien, Nicolas, Alexandru Saveanu, Ignacio Bergadá, et al.. (2015). Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue. PLoS ONE. 10(5). e0126648–e0126648. 10 indexed citations
15.
Rajagopal, Abbhirami, Débora Braslavsky, James T. Lu, et al.. (2014). Exome Sequencing Identifies a Novel Homozygous Mutation in the Phosphate Transporter SLC34A1 in Hypophosphatemia and Nephrocalcinosis. The Journal of Clinical Endocrinology & Metabolism. 99(11). E2451–E2456. 36 indexed citations
16.
Arboleda, Valerie A., Hane Lee, Rahul Parnaik, et al.. (2012). Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome. Nature Genetics. 44(7). 788–792. 121 indexed citations
17.
Grinspon, Romina P., Débora Braslavsky, Patricia Bedecarrás, et al.. (2012). Sertoli cell markers in the diagnosis of paediatric male hypogonadism. Journal of Pediatric Endocrinology and Metabolism. 25(1-2). 3–11. 21 indexed citations
18.
Braslavsky, Débora, Ana Keselman, Ana Chiesa, & Ignacio Bergadá. (2011). Diagnóstico de endocrinopatía congénita en neonatos con ictericia prolongada e hipoglucemia. Anales de Pediatría. 76(3). 120–126. 3 indexed citations
19.
Gryngarten, Mirta, et al.. (2010). Spontaneous Ovarian Hyperstimulation Syndrome Caused by a Follicle-Stimulating Hormone-Secreting Pituitary Macroadenoma in an Early Pubertal Girl. Hormone Research in Paediatrics. 73(4). 293–298. 26 indexed citations
20.
Neri, Alessandro, et al.. (1986). Enterobius (Oxyuris) vermicularis of the pelvic peritoneum — a cause of infertility. European Journal of Obstetrics & Gynecology and Reproductive Biology. 23(3-4). 239–241. 13 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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