Armando Reyes‐Engel

1.7k total citations · 1 hit paper
42 papers, 1.2k citations indexed

About

Armando Reyes‐Engel is a scholar working on Rheumatology, Surgery and Molecular Biology. According to data from OpenAlex, Armando Reyes‐Engel has authored 42 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Rheumatology, 9 papers in Surgery and 8 papers in Molecular Biology. Recurrent topics in Armando Reyes‐Engel's work include Folate and B Vitamins Research (12 papers), Pregnancy and preeclampsia studies (5 papers) and Prenatal Screening and Diagnostics (4 papers). Armando Reyes‐Engel is often cited by papers focused on Folate and B Vitamins Research (12 papers), Pregnancy and preeclampsia studies (5 papers) and Prenatal Screening and Diagnostics (4 papers). Armando Reyes‐Engel collaborates with scholars based in Spain, United States and Sweden. Armando Reyes‐Engel's co-authors include Pirjo Pakarinen, Kristiina Aittomäki, Albert de la Chapelle, Ilpo Huhtaniemi, Eeva-Marja Sankila, Juha S. Tapanainen, Eberhard Nieschlag, Heikki Lehväslaiho, M.J. Gaitán and Antônio Alonso and has published in prestigious journals such as Cell, The Lancet and Nucleic Acids Research.

In The Last Decade

Armando Reyes‐Engel

40 papers receiving 1.2k 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.

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

1995 699 citations Kristiina Aittomäki, Pirjo Pakarinen et al. Cell profile →

Peers

Armando Reyes‐Engel

PHEOH

GENET

EDM

Kazuhiro Tamura Japan

Ayumi Takakura United States

Kenneth A. Steingold United States

Alicia Belgorosky Argentina

H. G. Bohnet Germany

Yardena Tenenbaum‐Rakover Israel

Hervé Mittre France

Mirja Nurmio Finland

Yoshito Ibuki Japan

Sylvie Brailly France

Kazuhiro Tamura Japan

Armando Reyes‐Engel

198 ×0.5

PHEOH

380 ×0.9

331 ×0.8

218 ×0.6

GENET

157 ×0.7

EDM

Citations per year, relative to Armando Reyes‐Engel Armando Reyes‐Engel (= 1×) peers Kazuhiro Tamura

Countries citing papers authored by Armando Reyes‐Engel

Since Specialization

Citations

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

Fields of papers citing papers by Armando Reyes‐Engel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Armando Reyes‐Engel. 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 Armando Reyes‐Engel. The network helps show where Armando Reyes‐Engel may publish in the future.

Co-authorship network of co-authors of Armando Reyes‐Engel

This figure shows the co-authorship network connecting the top 25 collaborators of Armando Reyes‐Engel. A scholar is included among the top collaborators of Armando Reyes‐Engel 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 Armando Reyes‐Engel. Armando Reyes‐Engel 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

Real, Luís Miguel, Itziar de Rojas, Adriana Castro‐Zavala, et al.. (2023). A Functional Pipeline of Genome-Wide Association Data Leads to Midostaurin as a Repurposed Drug for Alzheimer’s Disease. International Journal of Molecular Sciences. 24(15). 12079–12079. 3 indexed citations

Alvero‐Cruz, José Ramón, Emilio Alarcón‐Martín, Jerónimo García-Romero, et al.. (2022). Moderate exercise reveals the influence of ACTN3 R577X and ACE I/D polymorphisms on physical performance in non-athlete active subjects. Gene. 850. 146958–146958. 1 indexed citations

Reyes‐Engel, Armando, et al.. (2021). MAOB rs3027452 Modifies Mood Improvement After Tryptophan Supplementation. International Journal of General Medicine. Volume 14. 1751–1756. 3 indexed citations

Castellano‐Castillo, Daniel, José Luís Royo, Lidia Sánchez‐Alcoholado, et al.. (2019). Effects of SHBG rs1799941 Polymorphism on Free Testosterone Levels and Hypogonadism Risk in Young Non-Diabetic Obese Males. Journal of Clinical Medicine. 8(8). 1136–1136. 5 indexed citations

Royo, José Luís, et al.. (2018). Sperm count and motility are quantitatively affected by functional polymorphisms of HTR2A , MAOA and SLC18A. Reproductive BioMedicine Online. 36(5). 560–567. 6 indexed citations

Martinez, Francisco Eduardo, et al.. (2013). Genetic polymorphisms of serotonin transporter and receptor 1A could influence success during embryo implantation and maintenance of pregnancy. Fertility and Sterility. 99(7). 2009–2016.e2. 5 indexed citations

Benito, Carmen, et al.. (2012). Evaluation of a low cost cryopreservation system on the biology of human amniotic fluid-derived mesenchymal stromal cells. Cryobiology. 64(3). 160–166. 11 indexed citations

Benito, Carmen, et al.. (2011). Lifespan of human amniotic fluid-derived multipotent mesenchymal stromal cells. Cytotherapy. 13(5). 572–581. 27 indexed citations

Reyes‐Engel, Armando, et al.. (2011). Genetic polymorphisms in folate pathway enzymes, DRD4 and GSTM1 are related to temporomandibular disorder. BMC Medical Genetics. 12(1). 75–75. 30 indexed citations

10.

Gaitán, M.J., et al.. (2008). Human genetic selection on the MTHFR 677C>T polymorphism. BMC Medical Genetics. 9(1). 104–104. 41 indexed citations

11.

Redondo, Maximino, Armando Reyes‐Engel, Emilio Perea‐Milla, et al.. (2007). Association between polymorphisms of folate-metabolizing enzymes and risk of prostate cancer. European Journal of Surgical Oncology. 34(7). 805–810. 41 indexed citations

12.

García‐Pinilla, José Manuel, Juan José Gómez‐Doblas, Manuel F. Jiménez‐Navarro, et al.. (2006). Influence of high homocysteine and low folate plasmatic levels in medium-term prognosis after acute coronary syndromes. International Journal of Cardiology. 118(2). 220–226. 6 indexed citations

13.

Tournev, Ivailo, Velina Guergueltcheva, И. В. Литвиненко, et al.. (2005). Congenital myasthenic syndrome type Ia - Clinical phenotyping and genetic epidemiology. 45(3). 1 indexed citations

14.

Reyes‐Engel, Armando. (2002). Implications on human fertility of the 677C->T and 1298A->C polymorphisms of the MTHFR gene: consequences of a possible genetic selection. Molecular Human Reproduction. 8(10). 952–957. 62 indexed citations

15.

Romero, María Soledad, et al.. (2001). Efecto del ácido levofolínico sobre las concentraciones de homocisteína plasmática en la mujer joven y sana en la consulta preconcepcional. Medicina Clínica. 117(6). 211–215. 5 indexed citations

16.

Teresa–Galván, Eduardo de, et al.. (2001). Both alleles of the M235T polymorphism of the angiotensinogen gene can be a risk factor for myocardial infarction. Clinical Genetics. 60(1). 52–57. 39 indexed citations

17.

Teresa–Galván, Eduardo de, et al.. (1999). The genotype interactions of methylenetetrahydrofolate reductase and renin-angiotensin system genes are associated with myocardial infarction. Atherosclerosis. 145(2). 293–300. 31 indexed citations

18.

Reyes‐Engel, Armando, et al.. (1996). Increased expression of scavenger receptor type I gene in human peripheral blood from hyperlipidemic patients determined by quantitative additive RT-PCR. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 1300(2). 135–141. 12 indexed citations

19.

Aittomäki, Kristiina, Pirjo Pakarinen, Juha S. Tapanainen, et al.. (1995). Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell. 82(6). 959–968. 699 indexed citations breakdown →

20.

Bleecker, Jan De & Armando Reyes‐Engel. (1994). Expression of CD45 isoforms on T cells in inflammatory myopathies. Ghent University Academic Bibliography (Ghent University). 3 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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