María L. Couce

7.0k total citations
242 papers, 3.6k citations indexed

About

María L. Couce is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, María L. Couce has authored 242 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 83 papers in Clinical Biochemistry, 76 papers in Molecular Biology and 65 papers in Physiology. Recurrent topics in María L. Couce's work include Metabolism and Genetic Disorders (83 papers), Lysosomal Storage Disorders Research (35 papers) and Mitochondrial Function and Pathology (32 papers). María L. Couce is often cited by papers focused on Metabolism and Genetic Disorders (83 papers), Lysosomal Storage Disorders Research (35 papers) and Mitochondrial Function and Pathology (32 papers). María L. Couce collaborates with scholars based in Spain, United States and United Kingdom. María L. Couce's co-authors include Ana Fernández‐Marmiesse, José M. Fraga, Luis Aldámiz‐Echevarría, Rosaura Leis, Sofía Gouveia, Paula Sánchez‐Pintos, José A. Cocho, Daisy Castiñeiras, Fernando Andrade and Alejandro Pérez‐Muñuzuri and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

María L. Couce

230 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
María L. Couce Spain 30 1.2k 1.2k 916 651 590 242 3.6k
Hsiang‐Yu Lin Taiwan 30 115 0.1× 711 0.6× 1.4k 1.5× 506 0.8× 444 0.8× 167 3.1k
Barry I. Hudson United States 31 2.8k 2.3× 1.2k 1.0× 458 0.5× 79 0.1× 43 0.1× 65 4.5k
Salvatore Scacco Italy 37 462 0.4× 2.2k 1.9× 654 0.7× 101 0.2× 51 0.1× 119 3.8k
Rita Castro Portugal 20 139 0.1× 1.2k 1.0× 251 0.3× 817 1.3× 290 0.5× 42 2.4k
Jiin‐Haur Chuang Taiwan 34 227 0.2× 1.3k 1.0× 329 0.4× 126 0.2× 152 0.3× 166 3.6k
Masanobu Kawakami Japan 41 99 0.1× 1.4k 1.2× 960 1.0× 156 0.2× 94 0.2× 193 5.2k
Edmund J. Miller United States 33 334 0.3× 1.5k 1.3× 391 0.4× 105 0.2× 65 0.1× 112 5.1k
Daniel Landau Israel 33 123 0.1× 1.3k 1.1× 224 0.2× 141 0.2× 353 0.6× 125 3.5k
Neerja Gupta India 24 145 0.1× 804 0.7× 283 0.3× 152 0.2× 292 0.5× 206 2.2k
Guangju Zhai Canada 33 95 0.1× 1.4k 1.1× 617 0.7× 2.4k 3.7× 62 0.1× 92 4.5k

Countries citing papers authored by María L. Couce

Since Specialization
Citations

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

Fields of papers citing papers by María L. Couce

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by María L. Couce. 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 María L. Couce. The network helps show where María L. Couce may publish in the future.

Co-authorship network of co-authors of María L. Couce

This figure shows the co-authorship network connecting the top 25 collaborators of María L. Couce. A scholar is included among the top collaborators of María L. Couce 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 María L. Couce. María L. Couce 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.
Weinstein, David A., Terry G. J. Derks, David Rodriguez‐Buritica, et al.. (2025). Safety and Efficacy of DTX401 , an AAV8 ‐Mediated Liver‐Directed Gene Therapy, in Adults With Glycogen Storage Disease Type I a ( GSDIa ). Journal of Inherited Metabolic Disease. 48(2). e70014–e70014. 7 indexed citations
2.
Vella, Giovanna, et al.. (2025). Novel Phenotypical and Biochemical Findings in Mucolipidosis Type II. International Journal of Molecular Sciences. 26(6). 2408–2408. 1 indexed citations
3.
Luna, Manuel Sánchez, María L. Couce, & Belén Fernández Colomer. (2024). Recomendaciones de la Sociedad Española de Neonatología para la profilaxis frente a las infecciones graves por virus respiratorio sincitial con nirsevimab, para la estación 2024-2025. Anales de Pediatría. 101(5). 364–366. 2 indexed citations
4.
Löfvendahl, Sofia, Mattias Rudebeck, Peter Lindgren, et al.. (2024). Societal costs and quality of life associated with arginase 1 deficiency in a European setting – a multinational, cross-sectional survey. Journal of Medical Economics. 27(1). 1146–1156. 3 indexed citations
5.
Sánchez‐Pintos, Paula, M. Dolores Bóveda, Sofía Gouveia, et al.. (2024). Clinical and biochemical evolution after partial dietary liberalization of two cases of galactosemia due to galactose mutarotase deficiency. BMC Pediatrics. 24(1). 620–620. 1 indexed citations
6.
Cernada, María, et al.. (2024). Recién nacido pequeño para la edad gestacional: concepto, diagnóstico y caracterización neonatal, seguimiento y recomendaciones. Anales de Pediatría. 101(2). 124–131. 1 indexed citations
7.
Löfvendahl, Sofia, Peter Lindgren, Karolina M. Stępień, et al.. (2024). Disease burden among patients with Arginase 1 deficiency and their caregivers: A multinational, cross‐sectional survey. JIMD Reports. 65(6). 450–460. 1 indexed citations
8.
Cernada, María, et al.. (2024). Small for gestational age: concept, diagnosis and neonatal characterization, follow-up and recommendations. SHILAP Revista de lepidopterología. 101(2). 124–131. 1 indexed citations
9.
10.
Yubero, Dèlia, Fátima Leal, María L. Couce, et al.. (2022). The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1 . Clinical Genetics. 102(1). 40–55. 6 indexed citations
11.
Martínez‐Carballo, Elena, et al.. (2022). Postnatal Exposure to Organic Pollutants in Maternal Milk in North-Western Spain. SSRN Electronic Journal. 4 indexed citations
12.
González‐Lamuño, Domingo, Paula Sánchez‐Pintos, Fernando Andrade, María L. Couce, & Luis Aldámiz‐Echevarría. (2021). Treatment adherence in tyrosinemia type 1 patients. Orphanet Journal of Rare Diseases. 16(1). 256–256. 15 indexed citations
13.
Gouveia, Sofía, M.E. Vázquez-Mosquera, Emiliano González‐Vioque, et al.. (2021). Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome. International Journal of Molecular Sciences. 22(24). 13484–13484. 9 indexed citations
14.
Gouveia, Sofía, Emiliano González‐Vioque, Á. Hermida Ameijeiras, et al.. (2020). Identification of a Novel Variant in EARS2 Associated with a Severe Clinical Phenotype Expands the Clinical Spectrum of LTBL. Genes. 11(9). 1028–1028. 1 indexed citations
15.
Cortès‐Saladelafont, Elisenda, Federico Ramos, María L. Couce, et al.. (2019). Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism. Scientific Reports. 9(1). 9128–9128. 6 indexed citations
16.
Couce, María L., et al.. (2019). Effects of LC-PUFA Supplementation in Patients with Phenylketonuria: A Systematic Review of Controlled Trials. Nutrients. 11(7). 1537–1537. 5 indexed citations
17.
Emperador, Sonia, M. Pilar Bayona‐Bafaluy, Ana Fernández‐Marmiesse, et al.. (2016). Molecular-genetic characterization and rescue of a TSFM mutation causing childhood-onset ataxia and nonobstructive cardiomyopathy. European Journal of Human Genetics. 25(1). 153–156. 16 indexed citations
18.
Posset, Roland, Ángeles García‐Cazorla, Vassili Valayannopoulos, et al.. (2016). Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders. Journal of Inherited Metabolic Disease. 39(5). 661–672. 49 indexed citations
19.
Aldámiz‐Echevarría, Luis, et al.. (2015). Phenylketonuria TreatmentsImpact on Physical Growth:A Spanish RetrospectiveLongitudinal Study. 1(2). 1 indexed citations
20.
Aldámiz‐Echevarría, Luis, María L. Couce, Sergio Lage, et al.. (2013). Tetrahydrobiopterin therapy vs phenylalanine-restricted diet: Impact on growth in PKU. Molecular Genetics and Metabolism. 109(4). 331–338. 23 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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