Carlos E. Prada

3.7k total citations · 1 hit paper
91 papers, 1.6k citations indexed

About

Carlos E. Prada is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Carlos E. Prada has authored 91 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 22 papers in Physiology and 15 papers in Genetics. Recurrent topics in Carlos E. Prada's work include Lysosomal Storage Disorders Research (20 papers), Cellular transport and secretion (10 papers) and Chronic Lymphocytic Leukemia Research (8 papers). Carlos E. Prada is often cited by papers focused on Lysosomal Storage Disorders Research (20 papers), Cellular transport and secretion (10 papers) and Chronic Lymphocytic Leukemia Research (8 papers). Carlos E. Prada collaborates with scholars based in United States, Colombia and United Kingdom. Carlos E. Prada's co-authors include Marcos López, Lissette Sanchez-Aranguren, Robert J. Hopkin, Elizabeth K. Schorry, Thomas J. Kipps, Anne M. Lovell, Januario E. Castro, Howard M. Saal, Lisa J. Martin and Olivier Loria and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Carlos E. Prada

78 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Endothelial dysfunction and preeclampsia: role of oxidative stress

2014 343 citations Carlos E. Prada et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Carlos E. Prada United States	21	507	310	292	288	259	91	1.6k
Jung Oh Kim South Korea	20	778 1.5×	186 0.6×	104 0.4×	62 0.2×	64 0.2×	90	1.8k
Tsuyoshi Fukushima Japan	26	820 1.6×	52 0.2×	189 0.6×	30 0.1×	151 0.6×	117	2.1k
Mourad Toporsian Canada	14	437 0.9×	1.3k 4.3×	93 0.3×	945 3.3×	227 0.9×	15	2.2k
Gijs Afink Netherlands	23	609 1.2×	480 1.5×	19 0.1×	357 1.2×	60 0.2×	59	1.6k
Jean-Michel Bidart France	25	735 1.4×	54 0.2×	55 0.2×	104 0.4×	87 0.3×	41	2.4k
Francesc Alameda Spain	26	780 1.5×	150 0.5×	50 0.2×	21 0.1×	157 0.6×	78	1.7k
Anne‐Marie Madec France	23	516 1.0×	33 0.1×	68 0.2×	63 0.2×	167 0.6×	49	1.7k
Peter W. Hewett United Kingdom	24	988 1.9×	629 2.0×	23 0.1×	458 1.6×	143 0.6×	42	2.0k
Fredrika Pekonen Finland	30	670 1.3×	443 1.4×	21 0.1×	290 1.0×	125 0.5×	65	2.5k
Noël Lamandé France	21	865 1.7×	69 0.2×	63 0.2×	40 0.1×	136 0.5×	38	1.6k

Countries citing papers authored by Carlos E. Prada

Since Specialization

Citations

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

Fields of papers citing papers by Carlos E. Prada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carlos E. Prada. 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 Carlos E. Prada. The network helps show where Carlos E. Prada may publish in the future.

Co-authorship network of co-authors of Carlos E. Prada

This figure shows the co-authorship network connecting the top 25 collaborators of Carlos E. Prada. A scholar is included among the top collaborators of Carlos E. Prada 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 Carlos E. Prada. Carlos E. Prada 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

Hostetter, Margaret K., Louis J. Muglia, Javier González del Rey, et al.. (2024). Complete Blood Count Values Over Time in Young Children During the Dengue Virus Epidemic in the Dominican Republic From 2018 to 2020. BioMed Research International. 2024(1). 1 indexed citations

Liu, Andrew C., Yang Shen, Hongzhi He, et al.. (2024). Clinical and functional studies of MTOR variants in Smith-Kingsmore syndrome reveal deficits of circadian rhythm and sleep-wake behavior. Human Genetics and Genomics Advances. 5(4). 100333–100333. 1 indexed citations

Kim, Katherine, et al.. (2023). Treatment-naive and post-treatment glucosylsphingosine (lyso-GL1) levels in a cohort of pediatric patients with Gaucher disease. Molecular Genetics and Metabolism. 141(1). 107736–107736. 4 indexed citations

Sánchez, A.I., et al.. (2023). Prenatal and infantile diagnosis of craniosynostosis in individuals with RASopathies. American Journal of Medical Genetics Part A. 194(2). 195–202. 2 indexed citations

Mangano, Francesco T., et al.. (2022). International Pediatric Multidisciplinary Management Using Telemedicine to Promote Equitable Care. Telemedicine Journal and e-Health. 29(5). 674–685. 1 indexed citations

Prada, Carlos E., et al.. (2022). Per-Anal Endoscopic Myotomy as Rescue Therapy for Hirschsprung Disease After Unsuccessful Surgical Myectomy. ACG Case Reports Journal. 9(4). e00755–e00755. 3 indexed citations

Weaver, K. Nicole, Jing Chen, Amy Shikany, et al.. (2022). Prevalence of Genetic Diagnoses in a Cohort With Valvar Pulmonary Stenosis. Circulation Genomic and Precision Medicine. 15(4). e003635–e003635. 7 indexed citations

Baker, Elizabeth, Ben Pode‐Shakked, Laura Cross, et al.. (2022). PPP2R1A neurodevelopmental disorder is associated with congenital heart defects. American Journal of Medical Genetics Part A. 188(11). 3262–3277. 7 indexed citations

Beerens, Manu, Lejla Mulahasanovic, Thomas D. Ryan, et al.. (2022). Stx4 is required to regulate cardiomyocyte Ca2+ handling during vertebrate cardiac development. Human Genetics and Genomics Advances. 3(3). 100115–100115. 4 indexed citations

10.

Weaver, K. Nicole, Marguerite M. Caré, Yuri A. Zárate, et al.. (2021). Craniosynostosis is a feature of Costello syndrome. American Journal of Medical Genetics Part A. 188(4). 1280–1286. 3 indexed citations

11.

Muir, Alison M., Kristin G. Monaghan, Ingrid M. Wentzensen, et al.. (2021). A recurrent, de novo pathogenic variant in ARPC4 disrupts actin filament formation and causes microcephaly and speech delay. SHILAP Revista de lepidopterología. 3(1). 100072–100072. 4 indexed citations

12.

Valencia, C. Alexander, et al.. (2020). An international telemedicine program for diagnosis of genetic disorders: Partnership of pediatrician and geneticist. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(4). 996–1008. 8 indexed citations

13.

Serai, Suraj D., et al.. (2018). Correlating liver stiffness with disease severity scoring system (DS3) values in Gaucher disease type 1 (GD1) patients. Molecular Genetics and Metabolism. 123(3). 357–363. 16 indexed citations

14.

Zhang, Wujuan, Carlos E. Prada, Ida Vanessa Döederlein Schwartz, et al.. (2017). A convenient approach to facilitate monitoring Gaucher disease progression and therapeutic response. The Analyst. 142(18). 3380–3387. 12 indexed citations

15.

Prada, Carlos E., Claudia Gonzaga‐Jauregui, Samantha Penney, et al.. (2014). Clinical utility of whole-exome sequencing in rare diseases: Galactosialidosis. European Journal of Medical Genetics. 57(7). 339–344. 20 indexed citations

16.

Herrero, Juan, et al.. (2013). Changes in wild ungulate populations in Aragon, Spain between 2001 and 2010. Galemys Spanish Journal of Mammalogy. 25. 51–57.

17.

Sund, Kristen L., Sarah Zimmerman, Cameron Thomas, et al.. (2012). Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships. Genetics in Medicine. 15(1). 70–78. 61 indexed citations

18.

Prada, Carlos E., et al.. (2011). Lethal presentation of neurofibromatosis and Noonan syndrome. American Journal of Medical Genetics Part A. 155(6). 1360–1366. 16 indexed citations

19.

Diggle, Christine P., Ian Carr, Emanuel Zitt, et al.. (2010). Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy. Lara D. Veeken. 49(6). 1056–1062. 40 indexed citations

20.

Couto, Sérgio, et al.. (2006). Nuevos datos sobre la presencia de marta, Martes martes (Linnaeus, 1758) en el Prepirineo aragonés y navarro. 18(1). 47–50. 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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