MA Vilaseca

429 total citations
8 papers, 252 citations indexed

About

MA Vilaseca is a scholar working on Clinical Biochemistry, Rheumatology and Surgery. According to data from OpenAlex, MA Vilaseca has authored 8 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Clinical Biochemistry, 4 papers in Rheumatology and 2 papers in Surgery. Recurrent topics in MA Vilaseca's work include Metabolism and Genetic Disorders (5 papers), Folate and B Vitamins Research (4 papers) and Amino Acid Enzymes and Metabolism (1 paper). MA Vilaseca is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Folate and B Vitamins Research (4 papers) and Amino Acid Enzymes and Metabolism (1 paper). MA Vilaseca collaborates with scholars based in Spain, Czechia and Portugal. MA Vilaseca's co-authors include Nilo Lambruschini, Rafael Artuch, D Moyano, Josep M. Campistol, Rosa Gassió, Belén Pérez‐Dueñas, Carme Valls, Laura Gort, Aleix Navarro‐Sastre and Linda De Meırleır and has published in prestigious journals such as European Journal of Clinical Nutrition, Acta Paediatrica and Clinical Genetics.

In The Last Decade

MA Vilaseca

8 papers receiving 247 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
MA Vilaseca Spain	8	165	103	94	85	43	8	252
D. Asplin United Kingdom	9	302 1.8×	231 2.2×	102 1.1×	56 0.7×	46 1.1×	9	329
Hülya Gökmen Özel Türkiye	9	250 1.5×	186 1.8×	130 1.4×	65 0.8×	22 0.5×	32	312
Bożena Didycz Poland	8	187 1.1×	118 1.1×	103 1.1×	59 0.7×	19 0.4×	19	221
Masoud Mahdavi Rashed Iran	8	107 0.6×	174 1.7×	89 0.9×	23 0.3×	17 0.4×	28	316
Valentina Rovelli Italy	10	185 1.1×	131 1.3×	133 1.4×	31 0.4×	15 0.3×	19	300
Catherine Ashmore United Kingdom	12	255 1.5×	202 2.0×	115 1.2×	49 0.6×	27 0.6×	47	332
David Gil Spain	9	105 0.6×	84 0.8×	115 1.2×	31 0.4×	13 0.3×	21	300
T. Bottiglieri United States	6	25 0.2×	24 0.2×	60 0.6×	116 1.4×	44 1.0×	9	248
Hina Ayesha Pakistan	8	70 0.4×	61 0.6×	48 0.5×	21 0.2×	12 0.3×	24	227
Jim Bonham United Kingdom	6	58 0.4×	39 0.4×	28 0.3×	67 0.8×	16 0.4×	7	168

Countries citing papers authored by MA Vilaseca

Since Specialization

Citations

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

Fields of papers citing papers by MA Vilaseca

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of MA Vilaseca

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

All Works

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8 of 8 papers shown

1.

Espinós, Carmen, Àngels García‐Cazorla, Dolores Martínez‐Rubio, et al.. (2010). Ancient origin of the CTH alelle carrying the c.200C>T (p.T67I) variant in patients with cystathioninuria. Clinical Genetics. 78(6). 554–559. 9 indexed citations

2.

Urreizti, Roser, Almudena Pino‐Ángeles, Mónica Cozar, et al.. (2010). Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiency. Clinical Genetics. 78(5). 441–448. 15 indexed citations

3.

Quintana, Ester, Laura Gort, C. Busquets, et al.. (2009). Mutational study in thePDHA1gene of 40 patients suspected of pyruvate dehydrogenase complex deficiency. Clinical Genetics. 77(5). 474–482. 31 indexed citations

4.

Colomé, Catrina, Rafael Artuch, Cristina Sierra, et al.. (2003). Plasma thiols and their determinants in phenylketonuria. European Journal of Clinical Nutrition. 57(8). 964–968. 10 indexed citations

5.

Gassió, Rosa, et al.. (2003). Do adult patients with phenylketonuria improve their quality of life after introduction/resumption of a phenylalanine‐restricted diet?. Acta Paediatrica. 92(12). 1474–1478. 59 indexed citations

6.

Pérez‐Dueñas, Belén, et al.. (2002). New approach to osteopenia in phenylketonuric patients. Acta Paediatrica. 91(8). 899–904. 46 indexed citations

7.

Moyano, D, MA Vilaseca, Rafael Artuch, Carme Valls, & Nilo Lambruschini. (1998). Plasma total-homocysteine in anorexia nervosa. European Journal of Clinical Nutrition. 52(3). 172–175. 23 indexed citations

8.

Moyano, D, MA Vilaseca, Rafael Artuch, & Nilo Lambruschini. (1998). Plasma amino acids in anorexia nervosa. European Journal of Clinical Nutrition. 52(9). 684–689. 59 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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