V. Cusí

1.7k total citations
38 papers, 703 citations indexed

About

V. Cusí is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Cell Biology. According to data from OpenAlex, V. Cusí has authored 38 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Pediatrics, Perinatology and Child Health and 7 papers in Cell Biology. Recurrent topics in V. Cusí's work include Metabolism and Genetic Disorders (6 papers), Prenatal Screening and Diagnostics (5 papers) and Mitochondrial Function and Pathology (3 papers). V. Cusí is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Prenatal Screening and Diagnostics (5 papers) and Mitochondrial Function and Pathology (3 papers). V. Cusí collaborates with scholars based in Spain, United Kingdom and France. V. Cusí's co-authors include M. Torrents, J. M. Carrera, Isidró Ferrer, M. Pineda, Carlos Mortera, Xavier Krauel, Pilar Póo, Jaume Campistol, Ana Muñoz and Lourdes Ibáñez and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and PEDIATRICS.

In The Last Decade

V. Cusí

36 papers receiving 687 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. Cusí Spain 17 217 168 156 135 94 38 703
Akiko Matsumoto Japan 18 225 1.0× 171 1.0× 185 1.2× 120 0.9× 94 1.0× 52 950
A Martínez-Bermejo Spain 14 274 1.3× 114 0.7× 146 0.9× 32 0.2× 120 1.3× 40 650
K Zuppinger Switzerland 18 299 1.4× 171 1.0× 101 0.6× 66 0.5× 294 3.1× 75 957
Tatsuro Izumi Japan 16 225 1.0× 184 1.1× 223 1.4× 57 0.4× 97 1.0× 70 895
Francesca Menni Italy 17 271 1.2× 173 1.0× 113 0.7× 115 0.9× 162 1.7× 46 1.0k
Maie Kaarsoo Herrick United States 15 246 1.1× 160 1.0× 82 0.5× 95 0.7× 52 0.6× 25 730
Albert Larbrisseau Canada 16 214 1.0× 180 1.1× 174 1.1× 206 1.5× 84 0.9× 24 995
A. G. Kasselberg United States 15 283 1.3× 160 1.0× 29 0.2× 163 1.2× 92 1.0× 23 831
Vincenzo Antona Italy 19 428 2.0× 117 0.7× 145 0.9× 56 0.4× 307 3.3× 57 821
Todor Arsov Australia 18 255 1.2× 86 0.5× 73 0.5× 220 1.6× 340 3.6× 41 1.1k

Countries citing papers authored by V. Cusí

Since Specialization
Citations

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

Fields of papers citing papers by V. Cusí

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Cusí

This figure shows the co-authorship network connecting the top 25 collaborators of V. Cusí. A scholar is included among the top collaborators of V. Cusí 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 V. Cusí. V. Cusí 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.
Lorenzo, David, et al.. (2023). The reuse of genetic information in research and informed consent. European Journal of Human Genetics. 31(12). 1393–1397.
2.
Esquerda, Montse, et al.. (2020). Ethical questions concerning newborn genetic screening. Clinical Genetics. 99(1). 93–98. 12 indexed citations
3.
Martín‐Solé, Oriol, et al.. (2016). Effects of Platelet-Rich Plasma (PRP) on a Model of Renal Ischemia-Reperfusion in Rats. PLoS ONE. 11(8). e0160703–e0160703. 27 indexed citations
4.
Cusí, V.. (2014). Consentimiento informado dinámico versus consentimiento amplio en biobancos. Dialnet (Universidad de la Rioja). 21(74). 14–19.
5.
Arias, Daniel Palanca, Àngels García‐Cazorla, Cristina Jou, et al.. (2012). cblE-Type Homocystinuria Presenting with Features of Haemolytic-Uremic Syndrome in the Newborn Period. JIMD Reports. 8. 57–62. 6 indexed citations
6.
Alarcón, Ana, Lourdes Ibáñez, Pilar Póo, et al.. (2011). Impact of histological chorioamnionitis, funisitis and clinical chorioamnionitis on neurodevelopmental outcome of preterm infants. Early Human Development. 87(4). 253–257. 71 indexed citations
7.
Vicente, Asunción, Maria C. Bolling, María Antonia González-Enseñat, et al.. (2011). Extensive acantholysis as the major histological feature of a severe case of Dowling Meara-epidermolysis bullosa simplex: a reappraisal of acantholysis in the newborn. European Journal of Dermatology. 21(6). 966–971. 5 indexed citations
8.
Font, Aida, Frederic Tort, Aleix Navarro‐Sastre, et al.. (2011). Quantitative Analysis of mtDNA Content in Formalin-Fixed Paraffin-Embedded Muscle Tissue. JIMD Reports. 1. 125–129. 1 indexed citations
9.
Mariné, Meritxell, C. Olivé, Montserrat Alsina, et al.. (2010). The prevalence of coeliac disease is significantly higher in children compared with adults. Alimentary Pharmacology & Therapeutics. 33(4). 477–486. 64 indexed citations
10.
Campistol, Jaume, et al.. (2010). Disfunción neurológica inducida por bilirrubina. Neurología. 27(4). 202–211. 11 indexed citations
11.
Pérez‐Dueñas, Belén, Àngels García‐Cazorla, M. Pineda, et al.. (2008). Long-term evolution of eight Spanish patients with CDG type Ia: Typical and atypical manifestations. European Journal of Paediatric Neurology. 13(5). 444–451. 36 indexed citations
12.
María, Belén De José, et al.. (2000). Management of tracheal agenesis. Pediatric Anesthesia. 10(4). 441–444. 16 indexed citations
13.
Pàmpols, Teresa, M. Pineda, M. Girós, et al.. (1999). Neuronopathic juvenile glucosylceramidosis due to sap -C deficiency: clinical course, neuropathology and brain lipid composition in this Gaucher disease variant. Acta Neuropathologica. 97(1). 91–97. 38 indexed citations
14.
Comas, C., M. Carrera, Ana Muñoz, et al.. (1997). Early detection of reversed diastolic umbilical flow: should we offer karyotyping?. Ultrasound in Obstetrics and Gynecology. 10(6). 400–402. 15 indexed citations
15.
Pineda, Mercè, Jaume Campistol, Marina Vilaseca, et al.. (1995). An atypical French form of pyruvate carboxylase deficiency. Brain and Development. 17(4). 276–279. 15 indexed citations
16.
Carrera, J. M., M. Torrents, Carlos Mortera, V. Cusí, & Ana Muñoz. (1995). Routine prenatal ultrasound screening for fetal abnormalities: 22 years' experience. Ultrasound in Obstetrics and Gynecology. 5(3). 174–179. 41 indexed citations
17.
Manzanares, Rafael González, et al.. (1995). Schinzel‐Giedion syndrome: Report of two sibs. American Journal of Medical Genetics. 59(1). 96–99. 24 indexed citations
18.
Minguella, J. & V. Cusí. (1992). Macrodactyly of the hands and feet. International Orthopaedics. 16(3). 245–9. 14 indexed citations
19.
Ferrer, Isidró, et al.. (1988). FOCAL DENDRITIC SWELLINGS IN PURKINJE CELLS IN MUCOPOLYSACCHARIDOSES TYPES I, II AND III. A GOLGI AND ULTRASTRUCTURAL STUDY. Neuropathology and Applied Neurobiology. 14(4). 315–323. 26 indexed citations
20.
Ferrer, Isidró, et al.. (1987). Dégénérescence systématisée optico-cochléo-dentelée. Journal of Neurology. 234(6). 416–420. 5 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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