Roxana Marino

1.2k total citations
39 papers, 722 citations indexed

About

Roxana Marino is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Roxana Marino has authored 39 papers receiving a total of 722 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 20 papers in Genetics and 18 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Roxana Marino's work include Sexual Differentiation and Disorders (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Growth Hormone and Insulin-like Growth Factors (9 papers). Roxana Marino is often cited by papers focused on Sexual Differentiation and Disorders (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Growth Hormone and Insulin-like Growth Factors (9 papers). Roxana Marino collaborates with scholars based in Argentina, United States and Switzerland. Roxana Marino's co-authors include Alicia Belgorosky, Marco A. Rivarola, Gabriela Guercio, Pablo Ramírez, Marta Ciaccio, Nora Saraco, Elisa Vaiani, Esperanza Berensztein, Natalia Pérez Garrido and Mariana Costanzo and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, PEDIATRICS and Clinical Chemistry.

In The Last Decade

Roxana Marino

39 papers receiving 712 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Roxana Marino Argentina	14	388	377	298	112	108	39	722
C Lecointre France	10	336 0.9×	203 0.5×	155 0.5×	119 1.1×	10 0.1×	15	506
M. A. Timmerman Netherlands	14	426 1.1×	119 0.3×	191 0.6×	160 1.4×	16 0.1×	21	646
Susana Belli Argentina	11	150 0.4×	73 0.2×	164 0.6×	123 1.1×	17 0.2×	28	515
Patrick Lim Australia	8	195 0.5×	128 0.3×	141 0.5×	160 1.4×	30 0.3×	13	485
Monique A. de Vroede United States	10	482 1.2×	257 0.7×	441 1.5×	42 0.4×	9 0.1×	12	687
Pavlos Fanis Cyprus	12	283 0.7×	146 0.4×	71 0.2×	50 0.4×	20 0.2×	36	618
Carolina Rosselot United States	13	253 0.7×	120 0.3×	64 0.2×	31 0.3×	32 0.3×	18	425
Hiroko Kawata Japan	13	424 1.1×	177 0.5×	76 0.3×	75 0.7×	69 0.6×	19	777
Mounia Tannour‐Louet United States	10	328 0.8×	253 0.7×	67 0.2×	87 0.8×	20 0.2×	13	569
Sylwia Słuczanowska-Głąbowska Poland	14	142 0.4×	55 0.1×	73 0.2×	49 0.4×	114 1.1×	36	480

Countries citing papers authored by Roxana Marino

Since Specialization

Citations

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

Fields of papers citing papers by Roxana Marino

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roxana Marino

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

All Works

Sort: Min cites: Since: Top N: Style:

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

Garrido, Natalia Pérez, Laura Galluzzo, Mariana Costanzo, et al.. (2023). A Surgical and Clinical Approach to Persistent Müllerian Duct Syndrome: Laparoscopic, Histological, and Molecular Findings. Sexual Development. 17(1). 1–7. 1 indexed citations

Vaiani, Elisa, et al.. (2023). Treatment with TRIAC in pediatric patients with MCT8. Archivos Argentinos de Pediatria. 121(6). e202202968–e202202968. 1 indexed citations

Pino, Mariana del, Natalia Pérez Garrido, Pablo Ramírez, et al.. (2022). Growth in height and body proportion from birth to adulthood in hereditary hypophosphatemic rickets: a retrospective cohort study. Journal of Endocrinological Investigation. 45(7). 1349–1358. 3 indexed citations

Garrido, Natalia Pérez, et al.. (2021). Hereditary hypophosphatemic rickets and craniosynostosis. Journal of Pediatric Endocrinology and Metabolism. 34(9). 1105–1113. 7 indexed citations

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

Marino, Roxana, Natalia Pérez Garrido, Pablo Ramírez, et al.. (2021). Ehlers–Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia. The Journal of Clinical Endocrinology & Metabolism. 106(7). e2789–e2802. 12 indexed citations

Garrido, Natalia Pérez, Roxana Marino, Pablo Ramírez, et al.. (2019). Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort. Journal of Clinical Research in Pediatric Endocrinology. 11(1). 24–33. 10 indexed citations

Costanzo, Mariana, Nora Saraco, Roxana Marino, et al.. (2018). Accelerated Pubertal Tempo in a 46,XY Aromatase-Deficient Patient. Hormone Research in Paediatrics. 90(4). 275–282. 6 indexed citations

10.

Baquedano, María Sonia, Gabriela Guercio, Mariana Costanzo, et al.. (2018). Mutation of HSD3B2 Gene and Fate of Dehydroepiandrosterone. Vitamins and hormones. 108. 75–123. 6 indexed citations

11.

Ciaccio, Marta, Roxana Marino, Pablo Ramírez, et al.. (2017). Two novel heterozygous missense variations within the GLI2 gene in two unrelated Argentine patients.. PubMed. 76(4). 213–8. 3 indexed citations

12.

Garrido, Natalia Pérez, Roxana Marino, Pablo Ramírez, et al.. (2017). Androgen Insensitivity Syndrome at Prepuberty: Marked Loss of Spermatogonial Cells at Early Childhood and Presence of Gonocytes up to Puberty. Sexual Development. 11(5-6). 225–237. 7 indexed citations

13.

Saraco, Nora, Suzana Nesi-França, Roxana Marino, et al.. (2015). An Intron 9 CYP19 Gene Variant (IVS9+5G>A), Present in an Aromatase-Deficient Girl, Affects Normal Splicing and Is Also Present in Normal Human Steroidogenic Tissues. Hormone Research in Paediatrics. 84(4). 275–282. 9 indexed citations

14.

Hwa, Vivian, Horacio M. Domené, Héctor Jasper, et al.. (2015). STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability. European Journal of Endocrinology. 173(3). 291–296. 27 indexed citations

15.

Baquedano, María Sonia, Marta Ciaccio, Roxana Marino, et al.. (2014). A Novel Missense Mutation in theHSD3B2Gene, Underlying Nonsalt-Wasting Congenital Adrenal Hyperplasia. New Insight Into the Structure-Function Relationships of 3β-Hydroxysteroid Dehidrogenase Type II. The Journal of Clinical Endocrinology & Metabolism. 100(1). E191–E196. 10 indexed citations

16.

Baquedano, María Sonia, Gabriela Guercio, Roxana Marino, et al.. (2012). Unique Dominant Negative Mutation in the N-Terminal Mitochondrial Targeting Sequence of StAR, Causing a Variant Form of Congenital Lipoid Adrenal Hyperplasia. The Journal of Clinical Endocrinology & Metabolism. 98(1). E153–E161. 17 indexed citations

17.

Marino, Roxana, Pablo Ramírez, Natalia Pérez Garrido, et al.. (2011). Steroid 21‐hydroxylase gene mutational spectrum in 454 Argentinean patients: genotype–phenotype correlation in a large cohort of patients with congenital adrenal hyperplasia. Clinical Endocrinology. 75(4). 427–435. 65 indexed citations

18.

Pepe, Carolina, Nora Saraco, María Sonia Baquedano, et al.. (2007). The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues. Clinical Endocrinology. 67(5). 698–705. 26 indexed citations

19.

Vaiani, Elisa, Roxana Marino, Pablo Ramírez, et al.. (2006). Unexpected Peripheral Markers of Thyroid Function in a Patient with a Novel Mutation of the MCT8 Thyroid Hormone Transporter Gene. Hormone Research in Paediatrics. 67(1). 1–6. 65 indexed citations

20.

Belgorosky, Alicia, Carolina Pepe, Roxana Marino, et al.. (2003). Hypothalamic-Pituitary-Ovarian Axis during Infancy, Early and Late Prepuberty in an Aromatase-Deficient Girl Who Is a Compound Heterocygote for Two New Point Mutations of the CYP19 Gene. The Journal of Clinical Endocrinology & Metabolism. 88(11). 5127–5131. 69 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.

Explore authors with similar magnitude of impact