Pablo Ramírez

693 total citations
25 papers, 381 citations indexed

About

Pablo Ramírez is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Pablo Ramírez has authored 25 papers receiving a total of 381 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Endocrinology, Diabetes and Metabolism and 11 papers in Genetics. Recurrent topics in Pablo Ramírez's work include Sexual Differentiation and Disorders (13 papers), Hormonal and reproductive studies (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Pablo Ramírez is often cited by papers focused on Sexual Differentiation and Disorders (13 papers), Hormonal and reproductive studies (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Pablo Ramírez collaborates with scholars based in Argentina, United States and Switzerland. Pablo Ramírez's co-authors include Alicia Belgorosky, Roxana Marino, Marco A. Rivarola, Gabriela Guercio, Natalia Pérez Garrido, Mariana Costanzo, Marta Ciaccio, Mercedes Maceiras, Esperanza Berensztein and Eduardo Chaler and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Clinical Endocrinology and European Journal of Endocrinology.

In The Last Decade

Pablo Ramírez

25 papers receiving 375 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Pablo Ramírez Argentina	11	260	206	185	62	56	25	381
María Sonia Baquedano Argentina	11	244 0.9×	224 1.1×	200 1.1×	142 2.3×	42 0.8×	19	462
Mariana Costanzo Argentina	10	181 0.7×	156 0.8×	83 0.4×	75 1.2×	55 1.0×	26	284
Zehra Yavaş Abalı Türkiye	9	147 0.6×	82 0.4×	100 0.5×	33 0.5×	8 0.1×	48	243
Matthias Viemann Germany	7	217 0.8×	80 0.4×	160 0.9×	18 0.3×	16 0.3×	10	269
Athanasia Stoupa France	9	161 0.6×	92 0.4×	197 1.1×	26 0.4×	6 0.1×	23	261
Francesca Teofoli Italy	10	150 0.6×	37 0.2×	181 1.0×	16 0.3×	10 0.2×	23	329
Raúl Sánchón Spain	6	102 0.4×	39 0.2×	134 0.7×	224 3.6×	21 0.4×	6	352
Béatrice Sente Belgium	8	150 0.6×	77 0.4×	203 1.1×	99 1.6×	30 0.5×	8	347
Atsumi Tsuji‐Hosokawa Japan	10	165 0.6×	43 0.2×	58 0.3×	11 0.2×	13 0.2×	31	257
Massimo Realacci Italy	11	57 0.2×	66 0.3×	69 0.4×	24 0.4×	35 0.6×	17	321

Countries citing papers authored by Pablo Ramírez

Since Specialization

Citations

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

Fields of papers citing papers by Pablo Ramírez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pablo Ramírez

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

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

Marino, Roxana, Angélica Moresco, Natalia Pérez Garrido, Pablo Ramírez, & Alicia Belgorosky. (2022). Congenital Adrenal Hyperplasia and Ehlers-Danlos Syndrome. Frontiers in Endocrinology. 13. 803226–803226. 13 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

Guercio, Gabriela, Nora Saraco, Mariana Costanzo, et al.. (2020). Estrogens in Human Male Gonadotropin Secretion and Testicular Physiology From Infancy to Late Puberty. Frontiers in Endocrinology. 11. 72–72. 29 indexed citations

Vaiani, Elisa, Pablo Ramírez, Mariana Costanzo, et al.. (2019). The Low-Dose ACTH Test: Usefulness of Combined Analysis of Serum and Salivary Maximum Cortisol Response in Pediatrics. The Journal of Clinical Endocrinology & Metabolism. 104(10). 4323–4330. 6 indexed citations

10.

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

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.

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

14.

Marino, Roxana, Natalia Pérez Garrido, Mariana Costanzo, et al.. (2014). Five New Cases of 46,XX Aromatase Deficiency: Clinical Follow-Up From Birth to Puberty, a Novel Mutation, and a Founder Effect. The Journal of Clinical Endocrinology & Metabolism. 100(2). E301–E307. 29 indexed citations

15.

Baquedano, María Sonia, Gabriela Guercio, Roxana Marino, et al.. (2013). [Novel heterozygous mutation in the steroidogenic acute regulatory protein gene in a 46,XY patient with congenital lipoid adrenal hyperplasia].. PubMed. 73(4). 297–302. 1 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.

Ciaccio, Marta, Mariana Costanzo, Gabriela Guercio, et al.. (2012). Preserved Fertility in a Patient with a 46,XY Disorder of Sex Development due to a New Heterozygous Mutation in the NR5A1/SF-1 Gene: Evidence of 46,XY and 46,XX Gonadal Dysgenesis Phenotype Variability in Multiple Members of an Affected Kindred. Hormone Research in Paediatrics. 78(2). 119–126. 30 indexed citations

18.

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

19.

Costanzo, Mariana, Roxana Marino, Esperanza Berensztein, et al.. (2010). Three New SF-1 (NR5A1) Gene Mutations in Two Unrelated Families with Multiple Affected Members: Within-Family Variability in 46,XY Subjects and Low Ovarian Reserve in Fertile 46,XX Subjects. Hormone Research in Paediatrics. 75(1). 70–77. 53 indexed citations

20.

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

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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